Item 16 of 90 (back to results) previous next   tamibarotene C061133               MeSH Unique Identifier: C061133 Scope Notes: Has retinoid-binding activity Chemical – Gene Interaction Note 1: Tamibarotene affects the expression of SEPT11 mRNA Note 2: Tamibarotene results in decreased expression of SEPT11 mRNA Click here for more information

Current search: C05. Musculoskeletal Diseases: Musculoskeletal Diseases [MESH:D009140] > Bone Diseases [MESH:D001847] > Bone Diseases, Developmental [MESH:D001848] > Osteochondrodysplasias [MESH:D010009] > Osteoglophonic dwarfism [MESH:C536050] × Select any link to see items in a related category. more general categories    information about this item 1. Human Genes  1. Human Genes  A-kinase anchor proteins [HGNC:AKAP] (99)   A kinase (PRKA) anchor protein (yotiao) 9 [HGNC:AKAP9] (21)  Aldo-keto reductases [HGNC:AKR] (282)   potassium voltage-gated channel, shaker-related subfamily, beta member 2 [HGNC:KCNAB2] (7)  Ankyrin repeat domain containing [HGNC:ANKRD] (566)   integrin-linked kinase [HGNC:ILK] (17)  ATPases [HGNC:ATP] (106)   ATPases, V-type [HGNC:VATP] (14)   ATPase, H+ transporting, lysosomal V0 subunit a2 [HGNC:ATP6V0A2] (10)  T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3 [HGNC:TCIRG1] (5)  ATP-binding cassette transporters [HGNC:ABC] (821)   ATP-binding cassette transporters, subfamily B [HGNC:ABCB] (452)   transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) [HGNC:TAP1] (28)  transporter 2, ATP-binding cassette, sub-family B (MDR/TAP) [HGNC:TAP2] (11)  Basic helix-loop-helix [HGNC:BHLH] (618)   basic helix-loop-helix family, member e40 [HGNC:BHLHE40] (42)  v-myc avian myelocytomatosis viral oncogene homolog [HGNC:MYC] (254)  Basic leucine zipper proteins [HGNC:bZIP] (670)   cAMP responsive element binding protein 1 [HGNC:CREB1] (108)  CCAAT/enhancer binding protein (C/EBP), beta [HGNC:CEBPB] (71)  CCAAT/enhancer binding protein (C/EBP), delta [HGNC:CEBPD] (51)  FBJ murine osteosarcoma viral oncogene homolog B [HGNC:FOSB] (45)  nuclear factor, erythroid 2-like 2 [HGNC:NFE2L2] (213)  X-box binding protein 1 [HGNC:XBP1] (79)  Cadherins [HGNC:CDH] (214)   Cadherins, related [HGNC:CDHR] (55)   FAT atypical cadherin 1 [HGNC:FAT1] (20)  S100 calcium binding proteins [HGNC:S100] (110)   S100 calcium binding protein A04 [HGNC:S100A4] (35)  S100 calcium binding protein A08 [HGNC:S100A8] (31)  S100 calcium binding protein A09 [HGNC:S100A9] (33)  Cathepsins [HGNC:CTS] (135)   cathepsin A [HGNC:CTSA] (3)  cathepsin D [HGNC:CTSD] (53)  CD molecules [HGNC:CD] (1459)   chemokine (C-C motif) receptor 01 [HGNC:CCR1] (21)  chemokine (C-X-C motif) receptor 04 [HGNC:CXCR4] (92)  coagulation factor III (thromboplastin, tissue factor) [HGNC:F3] (92)  Fc fragment of IgG, high affinity Ia, receptor (CD064) [HGNC:FCGR1A] (4)  Fc fragment of IgG, low affinity IIb, receptor (CD032) [HGNC:FCGR2B] (10)  fibroblast growth factor receptor 1 [HGNC:FGFR1] (43)  fucosyltransferase 4 (alpha (1,3) fucosyltransferase, myeloid-specific) [HGNC:FUT4] (9)  gamma-glutamyltransferase 1 [HGNC:GGT1] (13)  integrin, alpha 4 (antigen CD49D, alpha 4 subunit of VLA-4 receptor) [HGNC:ITGA4] (22)  integrin, alpha M (complement component 3 receptor 3 subunit) [HGNC:ITGAM] (75)  integrin, beta 2 (complement component 3 receptor 3 and 4 subunit) [HGNC:ITGB2] (58)  intercellular adhesion molecule 3 [HGNC:ICAM3] (20)  interleukin 10 receptor, beta [HGNC:IL10RB] (17)  macrophage scavenger receptor 1 [HGNC:MSR1] (27)  prion protein [HGNC:PRNP] (49)  protein tyrosine phosphatase, receptor type, C [HGNC:PTPRC] (16)  selectin L [HGNC:SELL] (43)  thrombomodulin [HGNC:THBD] (38)  tumor necrosis factor (ligand) superfamily, member 10 [HGNC:TNFSF10] (155)  tumor necrosis factor receptor superfamily, member 14 [HGNC:TNFRSF14] (21)  Chemokine ligands [HGNC:CCL] (472)   chemokine (C-C motif) ligand 04 [HGNC:CCL4] (96)  chemokine (C-C motif) ligand 05 [HGNC:CCL5] (141)  Chemokine receptors [HGNC:CR] (207)   Chemokine (C-C motif) receptors [HGNC:CCR] (92)   chemokine (C-C motif) receptor 01 [HGNC:CCR1] (21)  Chemokine (C-X-C motif) receptors [HGNC:CXCR] (135)   chemokine (C-X-C motif) receptor 04 [HGNC:CXCR4] (92)  Chloride channels [HGNC:CLCNS] (69)   Chloride channels, voltage-sensitive [HGNC:CLCN] (39)   chloride channel, voltage-sensitive Ka [HGNC:CLCNKA] (3)  Collagens [HGNC:COL] (230)   collagen, type XI, alpha 2 [HGNC:COL11A2] (5)  Complement system [HGNC:complement-systems] (153)   integrin, alpha M (complement component 3 receptor 3 subunit) [HGNC:ITGAM] (75)  integrin, beta 2 (complement component 3 receptor 3 and 4 subunit) [HGNC:ITGB2] (58)  Coronins [HGNC:CORO] (22)   coronin, actin binding protein, 1A [HGNC:CORO1A] (7)  Cytochrome b [HGNC:CYB] (73)   cytochrome b-245, alpha polypeptide [HGNC:CYBA] (40)  cytochrome b-245, beta polypeptide [HGNC:CYBB] (27)  Cytochrome P450s [HGNC:CYP] (1673)   cytochrome P450, family 24, subfamily A, polypeptide 01 [HGNC:CYP24A1] (58)  Dyneins, cytoplasmic [HGNC:DYN] (49)   dynein, cytoplasmic 1, light intermediate chain 2 [HGNC:DYNC1LI2] (12)  EF-hand domain containing [HGNC:EFHAND] (226)   S100 calcium binding protein A04 [HGNC:S100A4] (35)  S100 calcium binding protein A08 [HGNC:S100A8] (31)  S100 calcium binding protein A09 [HGNC:S100A9] (33)  Endogenous Ligands [HGNC:ENDOLIG] (1191)   chemokine (C-C motif) ligand 04 [HGNC:CCL4] (96)  chemokine (C-C motif) ligand 05 [HGNC:CCL5] (141)  chorionic gonadotropin, beta polypeptide [HGNC:CGB] (67)  endothelin 1 [HGNC:EDN1] (119)  endothelin 2 [HGNC:EDN2] (20)  Fatty acid desaturases [HGNC:FADS] (108)   stearoyl-CoA desaturase (delta-9-desaturase) [HGNC:SCD] (78)  Fibronectin type III domain containing [HGNC:FN3] (399)   protein tyrosine phosphatase, receptor type, C [HGNC:PTPRC] (16)  protein tyrosine phosphatase, receptor type, F [HGNC:PTPRF] (20)  TYRO3 protein tyrosine kinase [HGNC:TYRO3] (14)  F-boxes [HGNC:FBX] (66)   F-boxes and leucine-rich repeats [HGNC:FBXL] (58)   S-phase kinase-associated protein 2, E3 ubiquitin protein ligase [HGNC:SKP2] (54)  Fucosyltransferases [HGNC:FUT] (16)   fucosyltransferase 4 (alpha (1,3) fucosyltransferase, myeloid-specific) [HGNC:FUT4] (9)  GATA zinc finger domain containing [HGNC:GATAD] (101)   GATA binding protein 2 [HGNC:GATA2] (33)  Gamma-glutamyltransferases [HGNC:GGT] (13)   gamma-glutamyltransferase 1 [HGNC:GGT1] (13)  Glutathione S-transferases [HGNC:GST] (460)   Glutathione S-transferases, soluble [HGNC:SGST] (447)   glutathione S-transferase mu 1 [HGNC:GSTM1] (144)  glutathione S-transferase omega 1 [HGNC:GSTO1] (31)  Glycosyltransferase family 2 domain containing [HGNC:GLT2] (57)   UDP-glucose ceramide glucosyltransferase [HGNC:UGCG] (46)  G patch domain containing [HGNC:GPATCH] (46)   SON DNA binding protein [HGNC:SON] (18)  Heat shock proteins [HGNC:HSP] (390)   Heat shock proteins, DNAJ (HSP40) [HGNC:DNAJ] (88)   spastic ataxia of Charlevoix-Saguenay (sacsin) [HGNC:SACS] (19)  Heat shock proteins, HSPC (HSP90) [HGNC:HSP90] (119)   heat shock protein 90kDa alpha (cytosolic), class B member 1 [HGNC:HSP90AB1] (30)  heat shock protein 90kDa beta (Grp94), member 1 [HGNC:HSP90B1] (53)  Histocompatibility complex [HGNC:HLA] (108)   major histocompatibility complex, class I, C [HGNC:HLA-C] (27)  major histocompatibility complex, class I, E [HGNC:HLA-E] (29)  major histocompatibility complex, class I, G [HGNC:HLA-G] (25)  major histocompatibility complex, class II, DM alpha [HGNC:HLA-DMA] (15)  major histocompatibility complex, class II, DP alpha 1 [HGNC:HLA-DPA1] (13)  major histocompatibility complex, class II, DQ beta 1 [HGNC:HLA-DQB1] (16)  major histocompatibility complex, class II, DR alpha [HGNC:HLA-DRA] (23)  Homeoboxes [HGNC:homeobox] (219)   Homeoboxes, TALE class [HGNC:TALE] (72)   TGFB-induced factor homeobox 1 [HGNC:TGIF1] (37)  IKAROS zinc fingers [HGNC:IKZF] (19)   IKAROS family zinc finger 1 (Ikaros) [HGNC:IKZF1] (11)  Immunoglobulins [HGNC:IG] (25)   IGH locus [HGNC:IGH] (17)   immunoglobulin heavy constant gamma 1 (G1m marker) [HGNC:IGHG1] (11)  Immunoglobulin superfamily domain containing [HGNC:IGSF] (761)   V-set domain containing [HGNC:VSET] (188)   cell adhesion molecule 1 [HGNC:CADM1] (15)  C1-set domain containing [HGNC:C1SET] (121)   major histocompatibility complex, class I, C [HGNC:HLA-C] (27)  major histocompatibility complex, class I, E [HGNC:HLA-E] (29)  major histocompatibility complex, class I, G [HGNC:HLA-G] (25)  major histocompatibility complex, class II, DM alpha [HGNC:HLA-DMA] (15)  major histocompatibility complex, class II, DP alpha 1 [HGNC:HLA-DPA1] (13)  major histocompatibility complex, class II, DQ beta 1 [HGNC:HLA-DQB1] (16)  major histocompatibility complex, class II, DR alpha [HGNC:HLA-DRA] (23)  C2-set domain containing [HGNC:C2SET] (225)   cell adhesion molecule 1 [HGNC:CADM1] (15)  I-set domain containing [HGNC:ISET] (447)   fibroblast growth factor receptor 1 [HGNC:FGFR1] (43)  neurotrophic tyrosine kinase, receptor, type 2 [HGNC:NTRK2] (14)  protein tyrosine phosphatase, receptor type, F [HGNC:PTPRF] (20)  trio Rho guanine nucleotide exchange factor [HGNC:TRIO] (16)  TYRO3 protein tyrosine kinase [HGNC:TYRO3] (14)  Immunoglobulin-like domain containing [HGNC:IGD] (645)   cell adhesion molecule 1 [HGNC:CADM1] (15)  Fc fragment of IgG, high affinity Ia, receptor (CD064) [HGNC:FCGR1A] (4)  Fc fragment of IgG, low affinity IIb, receptor (CD032) [HGNC:FCGR2B] (10)  intercellular adhesion molecule 3 [HGNC:ICAM3] (20)  TYRO3 protein tyrosine kinase [HGNC:TYRO3] (14)  Integrins [HGNC:ITG] (284)   integrin, alpha 4 (antigen CD49D, alpha 4 subunit of VLA-4 receptor) [HGNC:ITGA4] (22)  integrin, alpha M (complement component 3 receptor 3 subunit) [HGNC:ITGAM] (75)  integrin, beta 2 (complement component 3 receptor 3 and 4 subunit) [HGNC:ITGB2] (58)  Interferons and interferon receptors [HGNC:IFN] (684)   interleukin 06 (interferon, beta 2) [HGNC:IL6] (511)  Interleukins and interleukin receptors [HGNC:IL] (1294)   interleukin 01, beta [HGNC:IL1B] (497)  interleukin 06 (interferon, beta 2) [HGNC:IL6] (511)  interleukin 10 receptor, beta [HGNC:IL10RB] (17)  Intermediate filaments [HGNC:IF] (273)   Type III [HGNC:] (100)   vimentin [HGNC:VIM] (77)  Type V. Lamins [HGNC:] (81)   lamin B1 [HGNC:LMNB1] (50)  IP3 receptors [HGNC:ITPR] (60)   inositol 1,4,5-trisphosphate receptor, type 2 [HGNC:ITPR2] (18)  inositol 1,4,5-trisphosphate receptor, type 3 [HGNC:ITPR3] (14)  K-methyltransferases [HGNC:KMT] (101)   lysine (K)-specific methyltransferase 2B [HGNC:KMT2B] (13)  PR domain containing 02, with ZNF domain [HGNC:PRDM2] (21)  Kinesins [HGNC:KIF] (68)   kinesin heavy chain member 2A [HGNC:KIF2A] (13)  Laminins [HGNC:LAM] (93)   laminin, gamma 1 (formerly LAMB2) [HGNC:LAMC1] (29)  Lectins, galactoside-binding [HGNC:LGALS] (92)   lectin, galactoside-binding, soluble, 1 [HGNC:LGALS1] (53)  lectin, galactoside-binding, soluble, 9 [HGNC:LGALS9] (6)  Leukotriene receptors [HGNC:LTNR] (42)   leukotriene B4 receptor [HGNC:LTB4R] (9)  Metallothioneins [HGNC:MT] (183)   metallothionein 1A [HGNC:MT1A] (54)  metallothionein 3 [HGNC:MT3] (42)  Mitochondrial respiratory chain complex assembly factors [HGNC:MITOAF] (42)   ATP synthase mitochondrial F1 complex assembly factor 2 [HGNC:ATPAF2] (4)  surfeit 1 [HGNC:SURF1] (4)  Mitogen-activated protein kinase cascade [HGNC:MAP#K] (854)   Mitogen-activated protein kinases [HGNC:MAPK] (797)   mitogen-activated protein kinase 01 [HGNC:MAPK1] (651)  mitogen-activated protein kinase 03 [HGNC:MAPK3] (644)  mitogen-activated protein kinase 14 [HGNC:MAPK14] (162)  Nuclear hormone receptors [HGNC:NR] (1322)   nuclear receptor subfamily 2, group F, member 2 [HGNC:NR2F2] (22)  retinoic acid receptor, alpha [HGNC:RARA] (73)  retinoic acid receptor, beta [HGNC:RARB] (56)  retinoid X receptor, alpha [HGNC:RXRA] (97)  Nucleotide-binding domain and leucine rich repeat containing [HGNC:NLR] (33)   class II, major histocompatibility complex, transactivator [HGNC:CIITA] (9)  PHD-type zinc fingers [HGNC:PHF] (103)   tripartite motif containing 33 [HGNC:TRIM33] (8)  Pleckstrin homology (PH) domain containing [HGNC:PLEKH] (227)   pleckstrin [HGNC:PLEK] (6)  vav 1 guanine nucleotide exchange factor [HGNC:VAV1] (9)  vav 3 guanine nucleotide exchange factor [HGNC:VAV3] (25)  Potassium channels [HGNC:KCN] (298)   potassium voltage-gated channel, shaker-related subfamily, beta member 2 [HGNC:KCNAB2] (7)  Proteasome (prosome, macropain) subunits [HGNC:PSM] (98)   proteasome (prosome, macropain) activator subunit 2 (PA28 beta) [HGNC:PSME2] (7)  Protein phosphatase, catalytic and regulatory subunits [HGNC:PPP-PPM-CTD] (225)   Protein phosphatase 1, regulatory subunits [HGNC:PPP1R] (155)   axin 1 [HGNC:AXIN1] (9)  Protein phosphatase 2, regulatory subunits [HGNC:PPP2R] (69)   protein phosphatase 2, regulatory subunit A, beta [HGNC:PPP2R1B] (18)  Protein tyrosine phosphatases, including dual specificity phosphatases [HGNC:PTP] (254)   Protein tyrosine phosphatases, Class I Cys-based [HGNC:PTPN] (252)   Class I Cys-based PTPs : Transmembrane receptor-like [HGNC:PTPR] (69)   protein tyrosine phosphatase, receptor type, F [HGNC:PTPRF] (20)  Class I Cys-based PTPs : MAP kinase phosphatases [HGNC:DUSPT] (127)   dual specificity phosphatase 10 [HGNC:DUSP10] (34)  RAB, member RAS oncogene [HGNC:RAB] (69)   RAB05A, member RAS oncogene family [HGNC:RAB5A] (12)  Rho GTPase activating proteins [HGNC:ARHGAP] (76)   histocompatibility (minor) HA-1 [HGNC:HMHA1] (8)  Rho guanine nucleotide exchange factors [HGNC:ARHGEF] (105)   trio Rho guanine nucleotide exchange factor [HGNC:TRIO] (16)  vav 1 guanine nucleotide exchange factor [HGNC:VAV1] (9)  vav 3 guanine nucleotide exchange factor [HGNC:VAV3] (25)  RNA binding motif containing [HGNC:RRM] (251)   serine/arginine-rich splicing factor 10 [HGNC:SRSF10] (12)  splicing factor proline/glutamine-rich [HGNC:SFPQ] (27)  TAF15 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 68kDa [HGNC:TAF15] (12)  S ribosomal proteins [HGNC:RPS] (104)   ribosomal protein S02 [HGNC:RPS2] (11)  Serine/arginine-rich splicing factors [HGNC:SRSF] (62)   serine/arginine-rich splicing factor 10 [HGNC:SRSF10] (12)  Serine (or cysteine) peptidase inhibitors [HGNC:SERPIN] (252)   serpin peptidase inhibitor, clade B (ovalbumin), member 02 [HGNC:SERPINB2] (63)  serpin peptidase inhibitor, clade B (ovalbumin), member 08 [HGNC:SERPINB8] (23)  serpin peptidase inhibitor, clade B (ovalbumin), member 10 [HGNC:SERPINB10] (5)  Serine/threonine phosphatases [HGNC:PPP-PPM-CTD] (43)   A kinase (PRKA) anchor protein (yotiao) 09 [HGNC:AKAP9] (21)  SH2 domain containing [HGNC:SH2D] (431)   FYN oncogene related to SRC, FGR, YES [HGNC:FYN] (47)  hemopoietic cell kinase [HGNC:HCK] (20)  NCK adaptor protein 1 [HGNC:NCK1] (17)  SH2 domain containing 1A [HGNC:SH2D1A] (4)  signal transducer and activator of transcription 1, 91kDa [HGNC:STAT1] (108)  signal transducer and activator of transcription 5B [HGNC:STAT5B] (25)  Src-like-adaptor [HGNC:SLA] (16)  vav 1 guanine nucleotide exchange factor [HGNC:VAV1] (9)  vav 3 guanine nucleotide exchange factor [HGNC:VAV3] (25)  v-yes-1 Yamaguchi sarcoma viral related oncogene homolog [HGNC:LYN] (39)  Short chain dehydrogenase/reductase superfamily [HGNC:SDR] (302)   Short chain dehydrogenase/reductase superfamily, Classical fold cluster 1 [HGNC:SDRC1] (60)   hydroxyprostaglandin dehydrogenase 15-(NAD) [HGNC:HPGD] (44)  SMADs [HGNC:SMAD] (84)   SMAD family member 2 [HGNC:SMAD2] (33)  SMAD family member 4 [HGNC:SMAD4] (22)  Solute carriers [HGNC:SLC] (716)   solute carrier family 02 (facilitated glucose/fructose transporter), member 05 [HGNC:SLC2A5] (21)  solute carrier family 16 (monocarboxylate transporter), member 1 [HGNC:SLC16A1] (43)  solute carrier family 16 (monocarboxylate transporter), member 7 [HGNC:SLC16A7] (14)  solute carrier family 26 (anion exchanger), member 2 [HGNC:SLC26A2] (24)  Tetratricopeptide repeat domain containing [HGNC:TTC] (153)   FK506 binding protein 05 [HGNC:FKBP5] (46)  interferon-induced protein with tetratricopeptide repeats 3 [HGNC:IFIT3] (35)  Transglutaminases [HGNC:TGM] (82)   transglutaminase 5 [HGNC:TGM5] (7)  Tripartite motif containing [HGNC:TRIM] (80)   tripartite motif containing 33 [HGNC:TRIM33] (8)  Tumor necrosis factor (ligand) superfamily [HGNC:TNFSF] (898)   tumor necrosis factor [HGNC:TNF] (795)  tumor necrosis factor (ligand) superfamily, member 10 [HGNC:TNFSF10] (155)  Tumor necrosis factor receptor superfamily [HGNC:TNFRSF] (295)   tumor necrosis factor receptor superfamily, member 14 [HGNC:TNFRSF14] (21)  Ubiquitin-specific peptidases [HGNC:USP] (24)   ubiquitin specific peptidase 13 (isopeptidase T-3) [HGNC:USP13] (14)  WD repeat domain containing [HGNC:WDR] (199)   coronin, actin binding protein, 1A [HGNC:CORO1A] (7)  excision repair cross-complementing rodent repair deficiency, complementation group 8 [HGNC:ERCC8] (6)  SEC31 homolog A (S. cerevisiae) [HGNC:SEC31A] (18)  ZINC FINGERS [HGNC:ZNF] (383)   Zinc fingers, C2H2-type [HGNC:ZNF] (349)   B-cell CLL/lymphoma 11A (zinc finger protein) [HGNC:BCL11A] (14)  early growth response 3 [HGNC:EGR3] (37)  IKAROS family zinc finger 1 (Ikaros) [HGNC:IKZF1] (11)  Zinc fingers, C2H2-type with KRAB domain [HGNC:ZKRAB] (42)   zinc finger protein 267 [HGNC:ZNF267] (12)  Zinc fingers, C2H2-type with BTB/POZ domain [HGNC:ZBTB] (35)   zinc finger and BTB domain containing 16 [HGNC:ZBTB16] (11) 2. Interaction: Human Genes and Chemicals  2. Interaction: Human Genes and Chemicals  Affects (3990)   binding (2423)  cotreatment (1499)  expression (494)  localization (731)  Decreases (5154)   activity (2549)  expression (2187)  phosphorylation (590)  reaction (3393)  response to substance (713)  Increases (5571)   activity (2865)  expression (3238)  phosphorylation (1060)  reaction (1574)  response to substance (641)  secretion (901)  uptake (378) A. Anatomy  A. Anatomy  Body Regions [MESH:D001829] (867)   Head [MESH:D006257] (523)   Ear [MESH:D004423] (236)   Meier-Gorlin syndrome [MESH:C538012] (133)  Musculoskeletal System [MESH:D009141] (1255)   Skeleton [MESH:D012863] (1177)   Bone and Bones [MESH:D001842] (1112)   Bones of Lower Extremity [MESH:D050281] (278)   Leg Bones [MESH:D007867] (228)   Patella [MESH:D010329] (168)   Epiphyseal dysplasia, multiple, 4 [MESH:C535504] (34)  Meier-Gorlin syndrome [MESH:C538012] (133)  Urogenital System [MESH:D014566] (986)   Genitalia [MESH:D005835] (400)   Skeletal Defects, Genital Hypoplasia, And Mental Retardation [MESH:C567306] (52)  Urinary Tract [MESH:D014551] (721)   Kidney [MESH:D007668] (707)   Nephrons [MESH:D009399] (518)   Kidney Tubules [MESH:D007684] (510)   Kidney Tubules, Proximal [MESH:D007687] (504)   Allanson Pantzar McLeod syndrome [MESH:C537048] (503)  Sense Organs [MESH:D012679] (1060)   Ear [MESH:D004423] (323)   Meier-Gorlin syndrome [MESH:C538012] (133)  Eye [MESH:D005123] (858)   Anterior Eye Segment [MESH:D000869] (664)   Cornea [MESH:D003315] (40)   Warburg Sjo Fledelius syndrome [MESH:C536681] (15)  Iris [MESH:D007498] (234)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Uvea [MESH:D014602] (270)   Iris [MESH:D007498] (234)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Cells [MESH:D002477] (1885)   Cellular Structures [MESH:D022082] (1562)   Chromosomes [MESH:D002875] (1300)   Chromosomes, Mammalian [MESH:D033481] (1282)   Chromosomes, Human [MESH:D002877] (1280)   Chromosomes, Human, 4-5 [MESH:D002905] (149)   Chromosomes, Human, Pair 5 [MESH:D002895] (136)   5q- syndrome [MESH:C535323] (131) C01. Bacterial Infections and Mycoses  C01. Bacterial Infections and Mycoses  Bacterial Infections [MESH:D001424] (3716)   Gram-Negative Bacterial Infections [MESH:D016905] (3085)   Chlamydiaceae Infections [MESH:D002694] (1699)   Chlamydia Infections [MESH:D002690] (1696)  Enterobacteriaceae Infections [MESH:D004756] (669)   Salmonella Infections [MESH:D012480] (620)   Salmonella Infections, Animal [MESH:D012481] (604)  Legionellosis [MESH:D007876] (612)   Legionnaires' Disease [MESH:D007877] (611)  Mycoplasmatales Infections [MESH:D009180] (1949)   Mycoplasma Infections [MESH:D009175] (1947)  Gram-Positive Bacterial Infections [MESH:D016908] (2434)   Listeriosis [MESH:D008088] (1622)  Staphylococcal Infections [MESH:D013203] (264)  Actinomycetales Infections [MESH:D000193] (1466)   Mycobacterium Infections [MESH:D009164] (1446)   Mycobacterium Infections, Nontuberculous [MESH:D009165] (480)  Paratuberculosis [MESH:D010283] (427)  Tuberculosis [MESH:D014376] (992)   Tuberculosis, Bovine [MESH:D014380] (380)  Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Infection [MESH:D007239] (4109)   Arthritis, Infectious [MESH:D001170] (1702)  Urinary Tract Infections [MESH:D014552] (984)  Intraabdominal Infections [MESH:D059413] (958)   Appendicitis [MESH:D001064] (774)  Peritonitis [MESH:D010538] (800)  Opportunistic Infections [MESH:D009894] (949)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Sepsis [MESH:D018805] (3556)   Shock, Septic [MESH:D012772] (1830)  Bacteremia [MESH:D016470] (1369)   Endotoxemia [MESH:D019446] (1289)  Sexually Transmitted Diseases [MESH:D012749] (1712)   Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Skin Diseases, Infectious [MESH:D012874] (415)   Dermatomycoses [MESH:D003881] (267)   Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224)  Toxemia [MESH:D014115] (1290)   Endotoxemia [MESH:D019446] (1289)  Mycoses [MESH:D009181] (385)   Candidiasis [MESH:D002177] (307)   Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224)  Dermatomycoses [MESH:D003881] (267)   Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224) C02. Virus Diseases  C02. Virus Diseases  Virus Diseases [MESH:D014777] (4544)   Central Nervous System Viral Diseases [MESH:D020805] (1416)   Encephalitis [MESH:D004660] (226)   Encephalitis, Viral [MESH:D018792] (183)   Subacute Sclerosing Panencephalitis [MESH:D013344] (63)   Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy [MESH:C536329] (61)  Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  DNA Virus Infections [MESH:D004266] (2474)   Hepadnaviridae Infections [MESH:D018347] (977)   Hepatitis B [MESH:D006509] (976)   Hepatitis B, Chronic [MESH:D019694] (277)  Herpesviridae Infections [MESH:D006566] (1944)   Cytomegalovirus Infections [MESH:D003586] (222)  Epstein-Barr Virus Infections [MESH:D020031] (695)   Burkitt Lymphoma [MESH:D002051] (691)  Sarcoma, Kaposi [MESH:D012514] (1578)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Papillomavirus Infections [MESH:D030361] (630)   Warts [MESH:D014860] (172)   WHIM syndrome [MESH:C536697] (148)  Epidermodysplasia Verruciformis [MESH:D004819] (18)  Encephalitis, Viral [MESH:D018792] (183)   Subacute Sclerosing Panencephalitis [MESH:D013344] (63)   Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy [MESH:C536329] (61)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis C [MESH:D006526] (1627)  Hepatitis B [MESH:D006509] (976)   Hepatitis B, Chronic [MESH:D019694] (277)  Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  Opportunistic Infections [MESH:D009894] (949)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  RNA Virus Infections [MESH:D012327] (4215)   Flaviviridae Infections [MESH:D018178] (1656)   Hepatitis C [MESH:D006526] (1627)  Mononegavirales Infections [MESH:D018701] (900)   Paramyxoviridae Infections [MESH:D018184] (889)   Morbillivirus Infections [MESH:D018185] (87)   Measles [MESH:D008457] (83)   Subacute Sclerosing Panencephalitis [MESH:D013344] (63)   Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy [MESH:C536329] (61)  Pneumovirus Infections [MESH:D018186] (853)   Respiratory Syncytial Virus Infections [MESH:D018357] (852)  Orthomyxoviridae Infections [MESH:D009976] (1077)   Influenza, Human [MESH:D007251] (1075)  Picornaviridae Infections [MESH:D010850] (1672)   Cardiovirus Infections [MESH:D018188] (1548)  Retroviridae Infections [MESH:D012192] (3420)   Lentivirus Infections [MESH:D016180] (3408)   HIV Infections [MESH:D015658] (3402)   Acquired Immunodeficiency Syndrome [MESH:D000163] (743)  HIV Wasting Syndrome [MESH:D019247] (1956)  AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Sexually Transmitted Diseases [MESH:D012749] (3305)   Sexually Transmitted Diseases, Viral [MESH:D015229] (3304)   HIV Infections [MESH:D015658] (3296)   Acquired Immunodeficiency Syndrome [MESH:D000163] (743)  HIV Wasting Syndrome [MESH:D019247] (1956)  Skin Diseases, Viral [MESH:D017193] (203)   Warts [MESH:D014860] (172)   WHIM syndrome [MESH:C536697] (148)  Epidermodysplasia Verruciformis [MESH:D004819] (18)  Slow Virus Diseases [MESH:D012897] (782)   Acquired Immunodeficiency Syndrome [MESH:D000163] (743)  Subacute Sclerosing Panencephalitis [MESH:D013344] (63)   Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy [MESH:C536329] (61)  Tumor Virus Infections [MESH:D014412] (1069)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691)  Warts [MESH:D014860] (172)   WHIM syndrome [MESH:C536697] (148)  Epidermodysplasia Verruciformis [MESH:D004819] (18) C03. Parasitic Diseases  C03. Parasitic Diseases  Parasitic Diseases [MESH:D010272] (3828)   Liver Diseases, Parasitic [MESH:D008109] (1009)  Helminthiasis [MESH:D006373] (1644)   Nematode Infections [MESH:D009349] (870)   Adenophorea Infections [MESH:D017188] (808)   Enoplida Infections [MESH:D017189] (807)   Trichuriasis [MESH:D014257] (805)  Trematode Infections [MESH:D014201] (1182)   Schistosomiasis [MESH:D012552] (1073)   Schistosomiasis mansoni [MESH:D012555] (1033)  Opportunistic Infections [MESH:D009894] (949)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Protozoan Infections [MESH:D011528] (3014)   Malaria [MESH:D008288] (2175)  Amebiasis [MESH:D000562] (1711)   Entamoebiasis [MESH:D004749] (1689)  Euglenozoa Infections [MESH:D056986] (2552)   Leishmaniasis [MESH:D007896] (2541)   Leishmaniasis, Visceral [MESH:D007898] (2149)  Leishmaniasis, Cutaneous [MESH:D016773] (2359)   Leishmaniasis, Mucocutaneous [MESH:D007897] (606)  Skin Diseases, Parasitic [MESH:D012876] (2541)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)   Leishmaniasis, Mucocutaneous [MESH:D007897] (606) C04. Neoplasms  C04. Neoplasms  Neoplasms [MESH:D009369] (10293)   Neoplasms, Second Primary [MESH:D016609] (518)  Cysts [MESH:D003560] (2625)   Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Hamartoma [MESH:D006222] (1484)   Tuberous Sclerosis [MESH:D014402] (635)  Neoplasms by Histologic Type [MESH:D009370] (8793)   Leukemia [MESH:D007938] (4576)   Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)  Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Leukemia, Myeloid [MESH:D007951] (2773)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Leukemia, Myelomonocytic, Acute [MESH:D015479] (85)  Leukemia, Myelomonocytic, Juvenile [MESH:D054429] (344)  Leukemia, Myeloid, Acute [MESH:D015470] (2176)   Platelet Disorder, Familial, with Associated Myeloid Malignancy [MESH:C563324] (62)  Leukemia, Promyelocytic, Acute [MESH:D015473] (1367)  Lymphoma [MESH:D008223] (3686)   Lymphoma, Non-Hodgkin [MESH:D008228] (3337)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, Mantle-Cell [MESH:D020522] (561)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Neoplasms, Complex and Mixed [MESH:D018193] (1121)   Carcinosarcoma [MESH:D002296] (581)  Hepatoblastoma [MESH:D018197] (548)  Wilms Tumor [MESH:D009396] (553)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742)   Chondrosarcoma, Extraskeletal Myxoid [MESH:C563195] (98)  Neoplasms, Connective Tissue [MESH:D009372] (3626)   Sarcoma, Synovial [MESH:D013584] (993)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Extraskeletal Myxoid [MESH:C563195] (98)  Chondrosarcoma, Mesenchymal [MESH:D018211] (1161)  Neoplasms, Bone Tissue [MESH:D018213] (2217)   Osteosarcoma [MESH:D012516] (2175)  Neoplasms, Fibrous Tissue [MESH:D018218] (1720)   Fibroma [MESH:D005350] (1578)   Fibromatosis, Abdominal [MESH:D018221] (56)  Fibromatosis, Aggressive [MESH:D018222] (1562)   Desmoid disease, hereditary [MESH:C535944] (58)  Histiocytoma [MESH:D051642] (272)   Histiocytoma, Malignant Fibrous [MESH:D051677] (266)   Histiocytoma, Angiomatoid Fibrous [MESH:C563181] (258)  Neoplasms, Muscle Tissue [MESH:D009379] (1965)   Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)  Sarcoma [MESH:D012509] (4246)   Carcinosarcoma [MESH:D002296] (581)  Hemangiosarcoma [MESH:D006394] (1836)  Osteosarcoma [MESH:D012516] (2175)  Sarcoma, Synovial [MESH:D013584] (993)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Extraskeletal Myxoid [MESH:C563195] (98)  Chondrosarcoma, Mesenchymal [MESH:D018211] (1161)  Histiocytoma, Malignant Fibrous [MESH:D051677] (266)   Histiocytoma, Angiomatoid Fibrous [MESH:C563181] (258)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)  Sarcoma, Kaposi [MESH:D012514] (1578)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Neoplasms, Germ Cell and Embryonal [MESH:D009373] (5126)   Neuroectodermal Tumors [MESH:D017599] (5066)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neuroendocrine Tumors [MESH:D018358] (3633)   Carcinoma, Neuroendocrine [MESH:D018278] (262)   Carcinoma, Medullary [MESH:D018276] (181)  Melanoma [MESH:D008545] (3508)   Uveal melanoma [MESH:C536494] (109)  Neoplasms, Glandular and Epithelial [MESH:D009375] (7760)   Adenoma [MESH:D000236] (4051)   Mesothelioma [MESH:D008654] (2567)  Adenomatous Polyps [MESH:D018256] (1571)   Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Carcinoma [MESH:D002277] (7263)   Thyroid cancer, papillary [MESH:C536915] (111)  Carcinoma, Basal Cell [MESH:D002280] (1628)  Carcinoma, Transitional Cell [MESH:D002295] (2662)  Adenocarcinoma [MESH:D000230] (6565)   Adenocarcinoma of lung [MESH:C538231] (1487)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Adenocarcinoma, Clear Cell [MESH:D018262] (1291)  Carcinoma, Adenoid Cystic [MESH:D003528] (1561)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Cholangiocarcinoma [MESH:D018281] (2398)  Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Carcinoma, Neuroendocrine [MESH:D018278] (262)   Carcinoma, Medullary [MESH:D018276] (181)  Carcinoma in Situ [MESH:D002278] (2111)   Prostatic Intraepithelial Neoplasia [MESH:D019048] (1565)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Neoplasms, Basal Cell [MESH:D018295] (1707)   Carcinoma, Basal Cell [MESH:D002280] (1628)  Neoplasms, Ductal, Lobular, and Medullary [MESH:D018299] (1831)   Carcinoma, Medullary [MESH:D018276] (181)  Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Neoplasms, Mesothelial [MESH:D018301] (2569)   Mesothelioma [MESH:D008654] (2567)  Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neoplasms, Squamous Cell [MESH:D018307] (4457)   Papilloma [MESH:D010212] (2243)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Neoplasms, Nerve Tissue [MESH:D009380] (5201)   Meningioma [MESH:D008579] (978)  Neuroectodermal Tumors [MESH:D017599] (5059)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neuroendocrine Tumors [MESH:D018358] (3625)   Carcinoma, Neuroendocrine [MESH:D018278] (184)   Carcinoma, Medullary [MESH:D018276] (181)  Melanoma [MESH:D008545] (3508)   Uveal melanoma [MESH:C536494] (109)  Neoplasms, Plasma Cell [MESH:D054219] (2772)   Multiple Myeloma [MESH:D009101] (2767)  Neoplasms, Vascular Tissue [MESH:D009383] (2959)   Hemangiosarcoma [MESH:D006394] (1836)  Meningioma [MESH:D008579] (978)  Hemangioma [MESH:D006391] (690)   Sturge-Weber Syndrome [MESH:D013341] (76)  Sarcoma, Kaposi [MESH:D012514] (1578)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Nevi and Melanomas [MESH:D018326] (3572)   Melanoma [MESH:D008545] (3508)   Uveal melanoma [MESH:C536494] (109)  Neoplasms by Site [MESH:D009371] (9169)   Skin Neoplasms [MESH:D012878] (2992)  Soft Tissue Neoplasms [MESH:D012983] (2003)  Abdominal Neoplasms [MESH:D000008] (74)   Desmoid disease, hereditary [MESH:C535944] (58)  Breast Neoplasms [MESH:D001943] (6077)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Digestive System Neoplasms [MESH:D004067] (7487)   Biliary Tract Neoplasms [MESH:D001661] (1165)   Gallbladder Neoplasms [MESH:D005706] (993)  Gastrointestinal Neoplasms [MESH:D005770] (6452)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5358)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Turcot syndrome [MESH:C536928] (159)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)  Rectal Neoplasms [MESH:D012004] (717)  Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)   Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, papillary [MESH:C536915] (111)  Eye Neoplasms [MESH:D005134] (400)   Uveal Neoplasms [MESH:D014604] (115)   Uveal melanoma [MESH:C536494] (109)  Head and Neck Neoplasms [MESH:D006258] (4612)   Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Mouth Neoplasms [MESH:D009062] (2263)   Salivary Gland Neoplasms [MESH:D012468] (968)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, papillary [MESH:C536915] (111)  Mammary Neoplasms, Animal [MESH:D015674] (3404)   Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Nervous System Neoplasms [MESH:D009423] (3130)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)   Turcot syndrome [MESH:C536928] (159)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)  Thoracic Neoplasms [MESH:D013899] (6032)   Respiratory Tract Neoplasms [MESH:D012142] (6020)   Lung Neoplasms [MESH:D008175] (6015)   Adenocarcinoma of lung [MESH:C538231] (1487)  Bronchial Neoplasms [MESH:D001984] (3608)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380)  Urogenital Neoplasms [MESH:D014565] (7002)   Genital Neoplasms, Female [MESH:D005833] (2540)   Uterine Neoplasms [MESH:D014594] (2431)   Endometrial Neoplasms [MESH:D016889] (1987)  Uterine Cervical Neoplasms [MESH:D002583] (978)  Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Neoplasms, Experimental [MESH:D009374] (5218)   Liver Neoplasms, Experimental [MESH:D008114] (2837)  Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Tumor Virus Infections [MESH:D014412] (697)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691)  Neoplasms, Multiple Primary [MESH:D009378] (961)   Tuberous Sclerosis [MESH:D014402] (635)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplasm Metastasis [MESH:D009362] (4441)   Lymphatic Metastasis [MESH:D008207] (917)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Turcot syndrome [MESH:C536928] (159)  Juvenile polyposis syndrome [MESH:C537702] (196)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (260)  Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Tuberous Sclerosis [MESH:D014402] (635)  Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Wilms Tumor [MESH:D009396] (553)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Precancerous Conditions [MESH:D011230] (2858)   Aberrant Crypt Foci [MESH:D058739] (326)  Tumor Virus Infections [MESH:D014412] (759)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691)  Warts [MESH:D014860] (167)   WHIM syndrome [MESH:C536697] (148)  Epidermodysplasia Verruciformis [MESH:D004819] (18) C05. Musculoskeletal Diseases  C05. Musculoskeletal Diseases  Musculoskeletal Diseases [MESH:D009140] (8705)   Cartilage Diseases [MESH:D002357] (438)  Bone Diseases [MESH:D001847] (5801)   Bone Diseases, Endocrine [MESH:D001849] (747)  Osteoarthropathy, Primary Hypertrophic [MESH:D010004] (94)  Bone Diseases, Developmental [MESH:D001848] (3315)   Acromicric dysplasia [MESH:C535662] (520)  Skeletal Defects, Genital Hypoplasia, And Mental Retardation [MESH:C567306] (52)  Spondyloepimetaphyseal Dysplasia, Aggrecan Type [MESH:C567558] (35)  Dwarfism [MESH:D004392] (778)   Diastrophic dysplasia [MESH:C536170] (34)  Cockayne Syndrome [MESH:D003057] (107)  Achondroplasia [MESH:D000130] (196)   Achondrogenesis type 1B [MESH:C536016] (34)  Dysostoses [MESH:D004413] (1019)   Synostosis [MESH:D013580] (817)   Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Craniosynostoses [MESH:D003398] (438)   Jackson-Weiss syndrome [MESH:C537559] (149)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Syndactyly [MESH:D013576] (487)   Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Osteochondrodysplasias [MESH:D010009] (2440)   Atelosteogenesis type 2 [MESH:C535395] (34)  Epiphyseal dysplasia, multiple, 4 [MESH:C535504] (34)  Pierre Robin syndrome with fetal chondrodysplasia [MESH:C535776] (16)  Osteoglophonic dwarfism [MESH:C536050] (90)  Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy [MESH:C536329] (61)  Spondyloepiphyseal Dysplasia, Kimberley Type [MESH:C564252] (35)  Camurati-Engelmann Syndrome [MESH:D003966] (492)  Cleidocranial Dysplasia [MESH:D002973] (129)  Achondroplasia [MESH:D000130] (196)   Achondrogenesis type 1B [MESH:C536016] (34)  Chondrodysplasia Punctata [MESH:D002806] (108)   Chondrodysplasia Punctata, Rhizomelic [MESH:D018902] (53)   Rhizomelic chondrodysplasia punctata, type 3 [MESH:C537608] (26)  Osteosclerosis [MESH:D010026] (356)   Osteopetrosis [MESH:D010022] (318)   Osteopetrosis, Autosomal Recessive 1 [MESH:C564915] (29)  Bone Diseases, Metabolic [MESH:D001851] (3492)   Osteoporosis [MESH:D010024] (3037)   Osteoporosis, Postmenopausal [MESH:D015663] (2351)  Bone Resorption [MESH:D001862] (2352)   Osteolysis [MESH:D010014] (1787)  Spinal Diseases [MESH:D013122] (2485)   Intervertebral Disc Degeneration [MESH:D055959] (827)  Spinal Curvatures [MESH:D013121] (742)   Kyphosis [MESH:D007738] (637)  Spondylitis [MESH:D013166] (1924)   Spondylarthritis [MESH:D025241] (1912)   Spondylarthropathies [MESH:D025242] (1909)   Arthritis, Psoriatic [MESH:D015535] (1859)  Spondylitis, Ankylosing [MESH:D013167] (431)  Foot Deformities [MESH:D005530] (553)   Foot Deformities, Congenital [MESH:D005532] (538)   Jackson-Weiss syndrome [MESH:C537559] (149)  Hand Deformities [MESH:D006226] (590)   Hand Deformities, Congenital [MESH:D006228] (587)   Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Jaw Diseases [MESH:D007571] (1601)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)  Micrognathism [MESH:D008844] (230)   Meier-Gorlin syndrome [MESH:C538012] (133)  Pierre Robin Syndrome [MESH:D010855] (101)   Pierre Robin syndrome with fetal chondrodysplasia [MESH:C535776] (16)  Joint Diseases [MESH:D007592] (4657)   Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Osteoarthropathy, Primary Hypertrophic [MESH:D010004] (94)  Ankylosis [MESH:D000844] (479)   Spondylitis, Ankylosing [MESH:D013167] (431)  Arthritis [MESH:D001168] (4416)   Stickler syndrome, type 3 [MESH:C537494] (16)  Arthritis, Experimental [MESH:D001169] (3142)  Arthritis, Infectious [MESH:D001170] (1702)  Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Psoriatic [MESH:D015535] (1859)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Osteoarthritis [MESH:D010003] (1743)  Spondylarthritis [MESH:D025241] (1912)   Spondylarthropathies [MESH:D025242] (1909)   Arthritis, Psoriatic [MESH:D015535] (1859)  Spondylitis, Ankylosing [MESH:D013167] (431)  Contracture [MESH:D003286] (296)   Congenital contractural arachnodactyly [MESH:C536211] (47)  Muscular Diseases [MESH:D009135] (4071)   Erythrocyte Lactate Transporter Defect [MESH:C565449] (106)  Contracture [MESH:D003286] (303)   Congenital contractural arachnodactyly [MESH:C536211] (47)  Mitochondrial Myopathies [MESH:D017240] (2176)   Mitochondrial Encephalomyopathies [MESH:D017237] (1121)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Muscle Spasticity [MESH:D009128] (187)   Spastic ataxia Charlevoix-Saguenay type [MESH:C536787] (37)  Muscular Disorders, Atrophic [MESH:D020966] (1598)   Optic atrophy polyneuropathy deafness [MESH:C537129] (31)  Muscular Dystrophies [MESH:D009136] (1593)   Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Myositis [MESH:D009220] (2071)   Dermatomyositis [MESH:D003882] (1826)  Polymyositis [MESH:D017285] (2007)   Dermatomyositis [MESH:D003882] (1826)  Rhabdomyolysis [MESH:D012206] (465)   Myoglobinuria [MESH:D009212] (96)   Myoglobinuria, Acute Recurrent, Autosomal Recessive [MESH:C564832] (64)  Musculoskeletal Abnormalities [MESH:D009139] (3796)   Craniofacial Abnormalities [MESH:D019465] (3098)   Spondyloepimetaphyseal Dysplasia, Aggrecan Type [MESH:C567558] (35)  Cleidocranial Dysplasia [MESH:D002973] (129)  Loeys-Dietz Syndrome [MESH:D055947] (263)  Craniosynostoses [MESH:D003398] (438)   Jackson-Weiss syndrome [MESH:C537559] (149)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 4 [MESH:C564180] (70)  Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)  Micrognathism [MESH:D008844] (230)   Meier-Gorlin syndrome [MESH:C538012] (133)  Pierre Robin Syndrome [MESH:D010855] (101)   Pierre Robin syndrome with fetal chondrodysplasia [MESH:C535776] (16)  Microcephaly [MESH:D008831] (700)   Warburg Sjo Fledelius syndrome [MESH:C536681] (15)  Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)  Plagiocephaly [MESH:D059041] (440)   Craniosynostoses [MESH:D003398] (438)   Jackson-Weiss syndrome [MESH:C537559] (149)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Limb Deformities, Congenital [MESH:D017880] (1813)   Acromicric dysplasia [MESH:C535662] (520)  Brachydactyly [MESH:D059327] (220)  Arachnodactyly [MESH:D054119] (126)   Congenital contractural arachnodactyly [MESH:C536211] (47)  Lower Extremity Deformities, Congenital [MESH:D038061] (560)   Foot Deformities, Congenital [MESH:D005532] (538)   Jackson-Weiss syndrome [MESH:C537559] (149)  Syndactyly [MESH:D013576] (487)   Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Upper Extremity Deformities, Congenital [MESH:D038062] (604)   Hand Deformities, Congenital [MESH:D006228] (587)   Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Synostosis [MESH:D013580] (817)   Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Craniosynostoses [MESH:D003398] (438)   Jackson-Weiss syndrome [MESH:C537559] (149)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Syndactyly [MESH:D013576] (487)   Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Rheumatic Diseases [MESH:D012216] (4032)   Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Osteoarthritis [MESH:D010003] (1743) C06. Digestive System Diseases  C06. Digestive System Diseases  Digestive System Diseases [MESH:D004066] (9461)   Biliary Tract Diseases [MESH:D001660] (3845)   Bile Duct Diseases [MESH:D001649] (3512)   Cholestasis [MESH:D002779] (3419)   Cholestasis, Intrahepatic [MESH:D002780] (1510)   Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Biliary Tract Neoplasms [MESH:D001661] (1165)   Gallbladder Neoplasms [MESH:D005706] (993)  Gallbladder Diseases [MESH:D005705] (1215)   Gallbladder Neoplasms [MESH:D005706] (993)  Digestive System Abnormalities [MESH:D004065] (2127)   Barrett Esophagus [MESH:D001471] (1930)  Digestive System Neoplasms [MESH:D004067] (7493)   Biliary Tract Neoplasms [MESH:D001661] (1165)   Gallbladder Neoplasms [MESH:D005706] (993)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Turcot syndrome [MESH:C536928] (159)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)  Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Gastrointestinal Diseases [MESH:D005767] (7443)   Esophageal Diseases [MESH:D004935] (4255)   Barrett Esophagus [MESH:D001471] (1930)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Gastroenteritis [MESH:D005759] (4066)   Appendicitis [MESH:D001064] (774)  Mucositis [MESH:D052016] (1238)  Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Enteritis [MESH:D004751] (157)   Ileitis [MESH:D007079] (137)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Gastritis [MESH:D005756] (967)   Gastritis, Atrophic [MESH:D005757] (947)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Inflammatory Bowel Disease 25, Autosomal Recessive [MESH:C567251] (43)  Colitis, Ulcerative [MESH:D003093] (2601)  Crohn Disease [MESH:D003424] (2585)  Gastrointestinal Hemorrhage [MESH:D006471] (815)   Peptic Ulcer Hemorrhage [MESH:D010438] (553)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Turcot syndrome [MESH:C536928] (159)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)  Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Intestinal Diseases [MESH:D007410] (6206)   Cecal Diseases [MESH:D002429] (1330)   Appendicitis [MESH:D001064] (774)  Cecal Neoplasms [MESH:D002430] (822)  Colonic Diseases [MESH:D003108] (5564)   Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Colonic Diseases, Functional [MESH:D003109] (439)   Irritable Bowel Syndrome [MESH:D043183] (429)  Colorectal Neoplasms [MESH:D015179] (5282)   Turcot syndrome [MESH:C536928] (159)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Duodenal Diseases [MESH:D004378] (1982)   Peptic Ulcer [MESH:D010437] (1969)   Duodenal Ulcer [MESH:D004381] (1549)  Enteritis [MESH:D004751] (157)   Ileitis [MESH:D007079] (137)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Ileal Diseases [MESH:D007077] (143)   Ileitis [MESH:D007079] (137)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Inflammatory Bowel Disease 25, Autosomal Recessive [MESH:C567251] (43)  Colitis, Ulcerative [MESH:D003093] (2601)  Crohn Disease [MESH:D003424] (2585)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Turcot syndrome [MESH:C536928] (159)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)  Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Intestinal Polyposis [MESH:D044483] (1610)   Juvenile polyposis syndrome [MESH:C537702] (196)  Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Malabsorption Syndromes [MESH:D008286] (492)   Celiac Disease [MESH:D002446] (340)  Rectal Diseases [MESH:D012002] (4596)   Colorectal Neoplasms [MESH:D015179] (4534)   Turcot syndrome [MESH:C536928] (159)  Rectal Neoplasms [MESH:D012004] (717)  Peptic Ulcer [MESH:D010437] (3172)   Duodenal Ulcer [MESH:D004381] (1549)  Stomach Ulcer [MESH:D013276] (2915)  Stomach Diseases [MESH:D013272] (5325)   Stomach Neoplasms [MESH:D013274] (4942)  Gastritis [MESH:D005756] (967)   Gastritis, Atrophic [MESH:D005757] (947)  Peptic Ulcer [MESH:D010437] (2994)   Stomach Ulcer [MESH:D013276] (2915)  Liver Diseases [MESH:D008107] (8167)   Drug-Induced Liver Injury [MESH:D056486] (4936)  Hepatic Veno-Occlusive Disease [MESH:D006504] (208)  Hepatolenticular Degeneration [MESH:D006527] (473)  Hepatorenal Syndrome [MESH:D006530] (910)  Hypertension, Portal [MESH:D006975] (869)  Liver Diseases, Parasitic [MESH:D008109] (1009)  Cholestasis, Intrahepatic [MESH:D002780] (1510)   Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Fatty Liver [MESH:D005234] (3584)   Non-alcoholic Fatty Liver Disease [MESH:C541083] (1567)  Hepatic Insufficiency [MESH:D048550] (2771)   Liver Failure [MESH:D017093] (2768)   Hepatic Encephalopathy [MESH:D006501] (1795)  Liver Failure, Acute [MESH:D017114] (2404)   Massive Hepatic Necrosis [MESH:D047508] (93)  Hepatitis [MESH:D006505] (3883)   Hepatitis, Alcoholic [MESH:D006519] (1613)  Hepatitis, Chronic [MESH:D006521] (2071)   Hepatitis, Autoimmune [MESH:D019693] (1982)  Hepatitis B, Chronic [MESH:D019694] (277)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis C [MESH:D006526] (1627)  Hepatitis B [MESH:D006509] (976)   Hepatitis B, Chronic [MESH:D019694] (277)  Liver Cirrhosis [MESH:D008103] (5542)   Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Liver Cirrhosis, Experimental [MESH:D008106] (4589)  Liver Diseases, Alcoholic [MESH:D008108] (3243)   Hepatitis, Alcoholic [MESH:D006519] (1613)  Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Diseases [MESH:D010182] (4453)   Cystic Fibrosis [MESH:D003550] (760)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Peritoneal Diseases [MESH:D010532] (1119)   Peritoneal Fibrosis [MESH:D056627] (488)  Peritonitis [MESH:D010538] (800) C07. Stomatognathic Diseases  C07. Stomatognathic Diseases  Stomatognathic Diseases [MESH:D009057] (5348)   Jaw Diseases [MESH:D007571] (1608)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)  Micrognathism [MESH:D008844] (230)   Meier-Gorlin syndrome [MESH:C538012] (133)  Pierre Robin Syndrome [MESH:D010855] (101)   Pierre Robin syndrome with fetal chondrodysplasia [MESH:C535776] (16)  Mouth Diseases [MESH:D009059] (4783)   Behcet Syndrome [MESH:D001528] (1784)  Mucositis [MESH:D052016] (1238)  Oral Submucous Fibrosis [MESH:D009914] (2432)  Oral Ulcer [MESH:D019226] (488)  Lip Diseases [MESH:D008047] (924)   Cleft Lip [MESH:D002971] (914)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)  Cleft Palate [MESH:D002972] (1330)  Mouth Neoplasms [MESH:D009062] (2263)   Salivary Gland Neoplasms [MESH:D012468] (968)  Periodontal Diseases [MESH:D010510] (1001)   Periodontitis [MESH:D010518] (843)  Salivary Gland Diseases [MESH:D012466] (1213)   Salivary Gland Neoplasms [MESH:D012468] (968)  Stomatitis [MESH:D013280] (1235)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Tooth Abnormalities [MESH:D014071] (622)  Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)  Micrognathism [MESH:D008844] (230)   Meier-Gorlin syndrome [MESH:C538012] (133)  Pierre Robin Syndrome [MESH:D010855] (101)   Pierre Robin syndrome with fetal chondrodysplasia [MESH:C535776] (16)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)  Cleft Palate [MESH:D002972] (1330)  Tooth Diseases [MESH:D014076] (742)   Tooth Abnormalities [MESH:D014071] (622) C08. Respiratory Tract Diseases  C08. Respiratory Tract Diseases  Z. Exceptions (1984)   Not Fully Specified [NFS] (1984)  Respiratory Tract Diseases [MESH:D012140] (7881)   Respiratory System Abnormalities [MESH:D015619] (243)  Thoracic Diseases [MESH:D013896] (81)  Bronchial Diseases [MESH:D001982] (4382)   Asthma [MESH:D001249] (4098)  Bronchiectasis [MESH:D001987] (1792)  Bronchitis [MESH:D001991] (993)   Bronchitis, Chronic [MESH:D029481] (569)  Bronchiolitis [MESH:D001988] (617)   Bronchiolitis Obliterans [MESH:D001989] (611)  Lung Diseases [MESH:D008171] (7249)   Cystic Fibrosis [MESH:D003550] (760)  Hypertension, Pulmonary [MESH:D006976] (2000)  Pulmonary Edema [MESH:D011654] (2109)  Pulmonary Embolism [MESH:D011655] (1118)  Pulmonary Fibrosis [MESH:D011658] (3140)  Respiratory Distress Syndrome, Adult [MESH:D012128] (864)  Lung Diseases, Interstitial [MESH:D017563] (2966)   Pneumoconiosis [MESH:D011009] (2789)   Anthracosis [MESH:D055008] (1805)  Asbestosis [MESH:D001195] (935)  Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273)  Lung Diseases, Obstructive [MESH:D008173] (4697)   Asthma [MESH:D001249] (3903)  Bronchitis [MESH:D001991] (993)   Bronchitis, Chronic [MESH:D029481] (569)  Bronchiolitis [MESH:D001988] (617)   Bronchiolitis Obliterans [MESH:D001989] (611)  Pulmonary Disease, Chronic Obstructive [MESH:D029424] (3564)   Bronchitis, Chronic [MESH:D029481] (569)  Pulmonary Emphysema [MESH:D011656] (1259)  Lung Injury [MESH:D055370] (3688)   Acute Lung Injury [MESH:D055371] (1907)  Pneumoconiosis [MESH:D011009] (2789)   Anthracosis [MESH:D055008] (1805)  Asbestosis [MESH:D001195] (935)  Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273)  Ventilator-Induced Lung Injury [MESH:D055397] (1023)   Bronchopulmonary Dysplasia [MESH:D001997] (1021)  Lung Neoplasms [MESH:D008175] (6012)   Adenocarcinoma of lung [MESH:C538231] (1487)  Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380)  Pneumonia [MESH:D011014] (3482)   Pneumonia, Aspiration [MESH:D011015] (824)  Nose Diseases [MESH:D009668] (1504)   Rhinitis [MESH:D012220] (1134)  Pleural Diseases [MESH:D010995] (2240)   Pleurisy [MESH:D010998] (2070)  Respiration Disorders [MESH:D012120] (2218)   Hyperventilation [MESH:D006985] (654)  Respiratory Distress Syndrome, Adult [MESH:D012128] (864)  Apnea [MESH:D001049] (748)   Sleep Apnea Syndromes [MESH:D012891] (570)   Sleep Apnea, Central [MESH:D020182] (347)   Congenital central hypoventilation syndrome [MESH:C536209] (341)  Respiratory Insufficiency [MESH:D012131] (841)   Hypoventilation [MESH:D007040] (360)   Congenital central hypoventilation syndrome [MESH:C536209] (341)  Respiratory Hypersensitivity [MESH:D012130] (4401)   Asthma [MESH:D001249] (4098)  Respiratory Tract Infections [MESH:D012141] (3926)   Influenza, Human [MESH:D007251] (1075)  Pleurisy [MESH:D010998] (2070)  Rhinitis [MESH:D012220] (766)  Bronchitis [MESH:D001991] (588)   Bronchitis, Chronic [MESH:D029481] (569)  Legionellosis [MESH:D007876] (612)   Legionnaires' Disease [MESH:D007877] (611)  Pneumonia [MESH:D011014] (3482)   Pneumonia, Aspiration [MESH:D011015] (824)  Respiratory Tract Neoplasms [MESH:D012142] (6053)   Lung Neoplasms [MESH:D008175] (6013)   Adenocarcinoma of lung [MESH:C538231] (1487)  Bronchial Neoplasms [MESH:D001984] (3608)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380) C09. Otorhinolaryngologic Diseases  C09. Otorhinolaryngologic Diseases  Otorhinolaryngologic Diseases [MESH:D010038] (3827)   Ear Diseases [MESH:D004427] (2522)   Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Deafness [MESH:D003638] (623)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  Deaf-Blind Disorders [MESH:D054062] (132)   Arts syndrome [MESH:C535388] (31)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Deafness, X-Linked 1 [MESH:C564433] (31)  Deafness, Autosomal Recessive 53 [MESH:C566453] (16)  Bartter Syndrome, Type 4A [MESH:C566530] (27)  Deafness, Autosomal Dominant 13 [MESH:C566612] (16)  Bartter Syndrome, Type 4b [MESH:C567762] (14)  Hearing Loss, Central [MESH:D006313] (140)   Optic atrophy polyneuropathy deafness [MESH:C537129] (31)  Retrocochlear Diseases [MESH:D012181] (241)   Auditory Diseases, Central [MESH:D001304] (210)   Hearing Loss, Central [MESH:D006313] (140)   Optic atrophy polyneuropathy deafness [MESH:C537129] (31)  Nose Diseases [MESH:D009668] (1504)   Rhinitis [MESH:D012220] (1134) C10. Nervous System Diseases  C10. Nervous System Diseases  Z. Exceptions (4027)   Not Fully Specified [NFS] (4027)  Nervous System Diseases [MESH:D009422] (13325)   Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Neuromyelitis Optica [MESH:D009471] (248)  Multiple Sclerosis [MESH:D009103] (1716)   Neuromyelitis Optica [MESH:D009471] (248)  Myelitis, Transverse [MESH:D009188] (255)   Neuromyelitis Optica [MESH:D009471] (248)  Nervous System Autoimmune Disease, Experimental [MESH:D020721] (810)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Central Nervous System Diseases [MESH:D002493] (9745)   Brain Diseases [MESH:D001927] (9294)   Brain Edema [MESH:D001929] (1165)  Brain Injuries [MESH:D001930] (3429)  Hypoxia, Brain [MESH:D002534] (134)  Auditory Diseases, Central [MESH:D001304] (210)   Hearing Loss, Central [MESH:D006313] (140)   Optic atrophy polyneuropathy deafness [MESH:C537129] (31)  Basal Ganglia Diseases [MESH:D001480] (4268)   Hepatolenticular Degeneration [MESH:D006527] (473)  Huntington Disease [MESH:D006816] (540)   Huntington Disease-Like 1 [MESH:C566398] (98)  Parkinsonian Disorders [MESH:D020734] (4009)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Brain Diseases, Metabolic [MESH:D001928] (3351)   Hepatic Encephalopathy [MESH:D006501] (1795)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  Galactosemias [MESH:D005693] (69)  Hepatolenticular Degeneration [MESH:D006527] (473)  MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Alexander Disease [MESH:D038261] (168)  Pelizaeus-Merzbacher Disease [MESH:D020371] (103)  Leigh Disease [MESH:D007888] (206)   Leigh syndrome , French Canadian type [MESH:C537004] (35)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Fucosidosis [MESH:D005645] (34)  Sphingolipidoses [MESH:D013106] (582)   Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type A [MESH:D052536] (44)  Niemann-Pick Disease, Type B [MESH:D052537] (44)  Niemann-Pick Disease, Type C [MESH:D052556] (103)   Niemann-Pick disease, type C2 [MESH:C536119] (43)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149)   Pyruvate Dehydrogenase E3-Binding Protein Deficiency [MESH:C565447] (25)  Tyrosinemias [MESH:D020176] (132)   Hawkinsinuria [MESH:C535845] (34)  Brain Neoplasms [MESH:D001932] (2764)   Turcot syndrome [MESH:C536928] (159)  Cerebellar Diseases [MESH:D002526] (736)   Cerebellar Ataxia [MESH:D002524] (542)   Spinocerebellar Ataxias [MESH:D020754] (406)   Spastic ataxia Charlevoix-Saguenay type [MESH:C536787] (37)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxias [MESH:D020754] (322)   Spastic ataxia Charlevoix-Saguenay type [MESH:C536787] (37)  Cerebrovascular Disorders [MESH:D002561] (5542)   Carotid Artery Diseases [MESH:D002340] (1993)  Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Vasospasm, Intracranial [MESH:D020301] (324)  Brain Ischemia [MESH:D002545] (4873)   Ischemic Attack, Transient [MESH:D002546] (1313)  Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Small Vessel Diseases [MESH:D059345] (1292)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  MELAS Syndrome [MESH:D017241] (1061)  Intracranial Arterial Diseases [MESH:D020765] (2463)   Intracranial Aneurysm [MESH:D002532] (158)  Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Amyloid Angiopathy [MESH:D016657] (470)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  Subarachnoid Hemorrhage [MESH:D013345] (1082)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Dementia [MESH:D003704] (4498)   Alzheimer Disease [MESH:D000544] (4275)  Creutzfeldt-Jakob Syndrome [MESH:D007562] (118)  Lewy Body Disease [MESH:D020961] (1143)  Frontotemporal Lobar Degeneration [MESH:D057174] (310)   Frontotemporal Dementia [MESH:D057180] (300)  Huntington Disease [MESH:D006816] (540)   Huntington Disease-Like 1 [MESH:C566398] (98)  Epilepsy [MESH:D004827] (6274)   Seizures [MESH:D012640] (4502)  Status Epilepticus [MESH:D013226] (4014)  Epilepsies, Myoclonic [MESH:D004831] (1344)   Myoclonic Epilepsies, Progressive [MESH:D020191] (1101)   MERRF Syndrome [MESH:D017243] (1053)  Epilepsies, Partial [MESH:D004828] (1267)   Epilepsy, Temporal Lobe [MESH:D004833] (1108)  Epilepsy, Generalized [MESH:D004829] (1431)   Epilepsy, Tonic-Clonic [MESH:D004830] (1042)  Headache Disorders [MESH:D020773] (2337)   Headache Disorders, Primary [MESH:D051270] (2327)   Migraine Disorders [MESH:D008881] (2318)  Leukoencephalopathies [MESH:D056784] (1916)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (822)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Alexander Disease [MESH:D038261] (168)  Pelizaeus-Merzbacher Disease [MESH:D020371] (103)  Central Nervous System Infections [MESH:D002494] (1823)   Central Nervous System Viral Diseases [MESH:D020805] (1416)   Encephalitis [MESH:D004660] (226)   Encephalitis, Viral [MESH:D018792] (183)   Subacute Sclerosing Panencephalitis [MESH:D013344] (63)   Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy [MESH:C536329] (61)  Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  Encephalitis [MESH:D004660] (351)   Encephalitis, Viral [MESH:D018792] (183)   Subacute Sclerosing Panencephalitis [MESH:D013344] (63)   Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy [MESH:C536329] (61)  Meningitis [MESH:D008581] (1506)   Meningitis, Aseptic [MESH:D008582] (1305)  Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  Prion Diseases [MESH:D017096] (488)   Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98)  Creutzfeldt-Jakob Syndrome [MESH:D007562] (118)  Gerstmann-Straussler-Scheinker Disease [MESH:D016098] (98)  Insomnia, Fatal Familial [MESH:D034062] (98)  Scrapie [MESH:D012608] (462)  Movement Disorders [MESH:D009069] (4823)   Hepatolenticular Degeneration [MESH:D006527] (473)  Dyskinesias [MESH:D020820] (1827)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Chorea [MESH:D002819] (651)   Huntington Disease [MESH:D006816] (540)   Huntington Disease-Like 1 [MESH:C566398] (98)  Dystonic Disorders [MESH:D020821] (729)   Dystonia 12 [MESH:C538001] (36)  Parkinsonian Disorders [MESH:D020734] (4009)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Ocular Motility Disorders [MESH:D015835] (364)   Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement [MESH:C567572] (70)  Spinal Cord Diseases [MESH:D013118] (4376)   Spinal Cord Compression [MESH:D013117] (1800)  Spinal Cord Injuries [MESH:D013119] (1674)  Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxias [MESH:D020754] (322)   Spastic ataxia Charlevoix-Saguenay type [MESH:C536787] (37)  Cranial Nerve Diseases [MESH:D003389] (2004)   Ocular Motility Disorders [MESH:D015835] (1697)   Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement [MESH:C567572] (70)  Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Optic Nerve Diseases [MESH:D009901] (1375)   Optic Atrophy [MESH:D009896] (1203)   Warburg Sjo Fledelius syndrome [MESH:C536681] (15)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic atrophy polyneuropathy deafness [MESH:C537129] (31)  Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Optic Neuritis [MESH:D009902] (273)   Neuromyelitis Optica [MESH:D009471] (248)  Demyelinating Diseases [MESH:D003711] (2917)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (2035)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Neuromyelitis Optica [MESH:D009471] (248)  Multiple Sclerosis [MESH:D009103] (1716)   Neuromyelitis Optica [MESH:D009471] (248)  Myelitis, Transverse [MESH:D009188] (255)   Neuromyelitis Optica [MESH:D009471] (248)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Alexander Disease [MESH:D038261] (168)  Pelizaeus-Merzbacher Disease [MESH:D020371] (103)  Nervous System Malformations [MESH:D009421] (3354)   Agenesis of Corpus Callosum [MESH:D061085] (345)   Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 4 [MESH:C564180] (70)  Central Nervous System Vascular Malformations [MESH:D020785] (1031)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Alstrom Syndrome [MESH:D056769] (20)  Malformations of Cortical Development [MESH:D054220] (1406)   Tuberous Sclerosis [MESH:D014402] (635)  Microcephaly [MESH:D008831] (700)   Warburg Sjo Fledelius syndrome [MESH:C536681] (15)  Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)  Neural Tube Defects [MESH:D009436] (2143)   Spinal Dysraphism [MESH:D016135] (1025)   Spina Bifida Cystica [MESH:D016137] (209)  Nervous System Neoplasms [MESH:D009423] (3073)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)   Turcot syndrome [MESH:C536928] (159)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)  Neurocutaneous Syndromes [MESH:D020752] (1230)   Sturge-Weber Syndrome [MESH:D013341] (76)  Tuberous Sclerosis [MESH:D014402] (635)  von Hippel-Lindau Disease [MESH:D006623] (580)  Neurodegenerative Diseases [MESH:D019636] (6613)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243)   Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98)  Alexander Disease [MESH:D038261] (168)  Cockayne Syndrome [MESH:D003057] (107)  Gerstmann-Straussler-Scheinker Disease [MESH:D016098] (98)  Hepatolenticular Degeneration [MESH:D006527] (473)  Tuberous Sclerosis [MESH:D014402] (635)  Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Alstrom Syndrome [MESH:D056769] (20)  Huntington Disease [MESH:D006816] (540)   Huntington Disease-Like 1 [MESH:C566398] (98)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic atrophy polyneuropathy deafness [MESH:C537129] (31)  Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxias [MESH:D020754] (322)   Spastic ataxia Charlevoix-Saguenay type [MESH:C536787] (37)  Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Prion Diseases [MESH:D017096] (475)   Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98)  Gerstmann-Straussler-Scheinker Disease [MESH:D016098] (98)  Insomnia, Fatal Familial [MESH:D034062] (98)  Scrapie [MESH:D012608] (462)  Tauopathies [MESH:D024801] (4289)   Alzheimer Disease [MESH:D000544] (4275)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Frontotemporal Lobar Degeneration [MESH:D057174] (308)   Frontotemporal Dementia [MESH:D057180] (298)  Neurologic Manifestations [MESH:D009461] (8964)   Neurogenic Inflammation [MESH:D020078] (2246)  Seizures [MESH:D012640] (4514)  Dyskinesias [MESH:D020820] (3365)   Catalepsy [MESH:D002375] (1429)  Dystonia [MESH:D004421] (848)  Hyperkinesis [MESH:D006948] (1799)  Ataxia [MESH:D001259] (1138)   Arts syndrome [MESH:C535388] (31)  Cerebellar Ataxia [MESH:D002524] (542)   Spinocerebellar Ataxias [MESH:D020754] (406)   Spastic ataxia Charlevoix-Saguenay type [MESH:C536787] (37)  Neurobehavioral Manifestations [MESH:D019954] (5230)   Lethargy [MESH:D053609] (1035)  Psychomotor Disorders [MESH:D011596] (576)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Intellectual Disability [MESH:D008607] (3054)   Warburg Sjo Fledelius syndrome [MESH:C536681] (15)  Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Skeletal Defects, Genital Hypoplasia, And Mental Retardation [MESH:C567306] (52)  Mental Retardation, X-Linked [MESH:D038901] (1854)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  ATR-X syndrome [MESH:C538258] (59)  Adrenoleukodystrophy [MESH:D000326] (1348)  Coffin-Lowry Syndrome [MESH:D038921] (45)  Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149)   Pyruvate Dehydrogenase E3-Binding Protein Deficiency [MESH:C565447] (25)  WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscular Atrophy [MESH:D009133] (1234)  Muscle Hypertonia [MESH:D009122] (775)   Muscle Spasticity [MESH:D009128] (187)   Spastic ataxia Charlevoix-Saguenay type [MESH:C536787] (37)  Pain [MESH:D010146] (3875)   Headache [MESH:D006261] (1416)  Neuralgia [MESH:D009437] (2074)  Paralysis [MESH:D010243] (2043)   Hemiplegia [MESH:D006429] (184)   Alternating hemiplegia of childhood [MESH:C536589] (70)  Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Sensation Disorders [MESH:D012678] (5011)   Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Deafness [MESH:D003638] (623)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  Deaf-Blind Disorders [MESH:D054062] (132)   Arts syndrome [MESH:C535388] (31)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Deafness, X-Linked 1 [MESH:C564433] (31)  Deafness, Autosomal Recessive 53 [MESH:C566453] (16)  Bartter Syndrome, Type 4A [MESH:C566530] (27)  Deafness, Autosomal Dominant 13 [MESH:C566612] (16)  Bartter Syndrome, Type 4b [MESH:C567762] (14)  Hearing Loss, Central [MESH:D006313] (140)   Optic atrophy polyneuropathy deafness [MESH:C537129] (31)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Vision Disorders [MESH:D014786] (501)   Blindness [MESH:D001766] (252)   Deaf-Blind Disorders [MESH:D054062] (132)   Arts syndrome [MESH:C535388] (31)  Neuromuscular Diseases [MESH:D009468] (7336)   Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Muscular Diseases [MESH:D009135] (3538)   Erythrocyte Lactate Transporter Defect [MESH:C565449] (106)  Muscular Disorders, Atrophic [MESH:D020966] (1594)   Optic atrophy polyneuropathy deafness [MESH:C537129] (31)  Muscular Dystrophies [MESH:D009136] (1589)   Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Mitochondrial Myopathies [MESH:D017240] (2176)   Mitochondrial Encephalomyopathies [MESH:D017237] (1121)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Myositis [MESH:D009220] (2069)   Dermatomyositis [MESH:D003882] (1826)  Polymyositis [MESH:D017285] (2007)   Dermatomyositis [MESH:D003882] (1826)  Muscular Disorders, Atrophic [MESH:D020966] (33)   Optic atrophy polyneuropathy deafness [MESH:C537129] (31)  Peripheral Nervous System Diseases [MESH:D010523] (6151)   Diabetic Neuropathies [MESH:D003929] (2442)  Neuralgia [MESH:D009437] (2078)  Amyloid Neuropathies [MESH:D017772] (139)   Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  Mononeuropathies [MESH:D020422] (604)   Sciatic Neuropathy [MESH:D020426] (477)  Median Neuropathy [MESH:D020423] (153)   Carpal Tunnel Syndrome [MESH:D002349] (147)  Nerve Compression Syndromes [MESH:D009408] (166)   Carpal Tunnel Syndrome [MESH:D002349] (147)  Polyneuropathies [MESH:D011115] (1134)   Optic atrophy polyneuropathy deafness [MESH:C537129] (31)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Alstrom Syndrome [MESH:D056769] (20)  Neurotoxicity Syndromes [MESH:D020258] (4570)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Heavy Metal Poisoning, Nervous System [MESH:D020260] (2912)   Arsenic Poisoning [MESH:D020261] (2540)  Manganese Poisoning [MESH:D020149] (2214)  Sleep Disorders [MESH:D012893] (2050)   Dyssomnias [MESH:D020920] (1417)   Sleep Disorders, Intrinsic [MESH:D020919] (1270)   Disorders of Excessive Somnolence [MESH:D006970] (581)   Narcolepsy [MESH:D009290] (478)  Sleep Apnea Syndromes [MESH:D012891] (570)   Sleep Apnea, Central [MESH:D020182] (347)   Congenital central hypoventilation syndrome [MESH:C536209] (341)  Sleep Initiation and Maintenance Disorders [MESH:D007319] (354)   Insomnia, Fatal Familial [MESH:D034062] (98)  Trauma, Nervous System [MESH:D020196] (3997)   Spinal Cord Injuries [MESH:D013119] (1676)  Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) C11. Eye Diseases  C11. Eye Diseases  Eye Diseases [MESH:D005128] (6245)   Eyelid Diseases [MESH:D005141] (882)  Corneal Diseases [MESH:D003316] (1445)   Corneal Neovascularization [MESH:D016510] (622)  Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Meretoja syndrome [MESH:C537459] (95)  Corneal Dystrophy, Fleck [MESH:C563256] (12)  Eye Abnormalities [MESH:D005124] (1233)   Aniridia [MESH:D015783] (312)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Eye Diseases, Hereditary [MESH:D015785] (1869)   Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement [MESH:C567572] (70)  Graves Ophthalmopathy [MESH:D049970] (165)  Aniridia [MESH:D015783] (312)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Meretoja syndrome [MESH:C537459] (95)  Corneal Dystrophy, Fleck [MESH:C563256] (12)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic atrophy polyneuropathy deafness [MESH:C537129] (31)  Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Retinitis Pigmentosa [MESH:D012174] (414)   Retinitis Pigmentosa 33 [MESH:C563676] (20)  Alstrom Syndrome [MESH:D056769] (20)  Eye Neoplasms [MESH:D005134] (413)   Uveal Neoplasms [MESH:D014604] (115)   Uveal melanoma [MESH:C536494] (109)  Lacrimal Apparatus Diseases [MESH:D007766] (644)   Dry Eye Syndromes [MESH:D015352] (533)  Lens Diseases [MESH:D007905] (900)   Cataract [MESH:D002386] (860)   Warburg Sjo Fledelius syndrome [MESH:C536681] (15)  Ocular Hypertension [MESH:D009798] (1630)   Glaucoma [MESH:D005901] (1458)  Ocular Motility Disorders [MESH:D015835] (1699)   Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement [MESH:C567572] (70)  Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Optic Nerve Diseases [MESH:D009901] (1377)   Optic Atrophy [MESH:D009896] (1203)   Warburg Sjo Fledelius syndrome [MESH:C536681] (15)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic atrophy polyneuropathy deafness [MESH:C537129] (31)  Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Optic Neuritis [MESH:D009902] (273)   Neuromyelitis Optica [MESH:D009471] (248)  Orbital Diseases [MESH:D009916] (317)   Exophthalmos [MESH:D005094] (297)   Graves Disease [MESH:D006111] (278)   Graves Ophthalmopathy [MESH:D049970] (165)  Retinal Diseases [MESH:D012164] (3747)   Diabetic Retinopathy [MESH:D003930] (1371)  Retinal Detachment [MESH:D012163] (1639)  Retinal Vein Occlusion [MESH:D012170] (607)  Retinopathy of Prematurity [MESH:D012178] (353)  Retinal Degeneration [MESH:D012162] (2386)   Macular Degeneration [MESH:D008268] (995)   Macular Degeneration, Age-Related, 11 [MESH:C567450] (61)  Macular Edema [MESH:D008269] (557)  Retinal Dystrophies [MESH:D058499] (1315)   Retinitis Pigmentosa [MESH:D012174] (1307)   Retinitis Pigmentosa 33 [MESH:C563676] (20)  Kearns-Sayre Syndrome [MESH:D007625] (1054)  Uveal Diseases [MESH:D014603] (2428)   Choroid Diseases [MESH:D015862] (595)   Choroidal Neovascularization [MESH:D020256] (550)  Iris Diseases [MESH:D007499] (348)   Aniridia [MESH:D015783] (312)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Uveal Neoplasms [MESH:D014604] (115)   Uveal melanoma [MESH:C536494] (109)  Uveitis [MESH:D014605] (2157)   Panuveitis [MESH:D015864] (1805)   Uveitis, Anterior [MESH:D014606] (1791)   Behcet Syndrome [MESH:D001528] (1784)  Vision Disorders [MESH:D014786] (534)   Blindness [MESH:D001766] (259)   Deaf-Blind Disorders [MESH:D054062] (132)   Arts syndrome [MESH:C535388] (31) C12. Male Urogenital Diseases  C12. Male Urogenital Diseases  Male Urogenital Diseases [MESH:D052801] (8891)   Genital Diseases, Male [MESH:D005832] (6794)   Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Infertility [MESH:D007246] (2909)   Infertility, Male [MESH:D007248] (2851)   Azoospermia [MESH:D053713] (1052)  Penile Diseases [MESH:D010409] (1805)   Penile Induration [MESH:D010411] (495)  Prostatic Diseases [MESH:D011469] (6204)   Prostatic Neoplasms [MESH:D011471] (6135)  Prostatitis [MESH:D011472] (424)  Sexual Dysfunction, Physiological [MESH:D012735] (1808)   Erectile Dysfunction [MESH:D007172] (1791)  Sexually Transmitted Diseases [MESH:D012749] (1712)   Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Testicular Diseases [MESH:D013733] (451)   Cryptorchidism [MESH:D003456] (215)   Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Skeletal Defects, Genital Hypoplasia, And Mental Retardation [MESH:C567306] (52)  Urogenital Abnormalities [MESH:D014564] (2065)   Allanson Pantzar McLeod syndrome [MESH:C537048] (503)  Cryptorchidism [MESH:D003456] (215)   Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Skeletal Defects, Genital Hypoplasia, And Mental Retardation [MESH:C567306] (52)  Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   Kallmann Syndrome [MESH:D017436] (147)  WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Urogenital Neoplasms [MESH:D014565] (6932)   Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Urologic Diseases [MESH:D014570] (7792)   Urinary Tract Infections [MESH:D014552] (984)  Kidney Diseases [MESH:D007674] (7242)   Anuria [MESH:D001002] (833)  Diabetic Nephropathies [MESH:D003928] (2301)  Hepatorenal Syndrome [MESH:D006530] (910)  Hyperoxaluria [MESH:D006959] (1498)  Hypertension, Renal [MESH:D006977] (698)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, IGA [MESH:D005922] (897)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Nephrolithiasis [MESH:D053040] (492)   Kidney Calculi [MESH:D007669] (455)  Nephrosis [MESH:D009401] (2228)   Nephrotic Syndrome [MESH:D009404] (1536)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058)   Pseudohypoaldosteronism [MESH:D011546] (232)  Bartter Syndrome [MESH:D001477] (241)   Bartter Syndrome, Type 4A [MESH:C566530] (27)  Bartter Syndrome, Type 4b [MESH:C567762] (14)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)   Atypical hemolytic uremic syndrome [MESH:C538266] (277)  Ureteral Diseases [MESH:D014515] (1024)   Ureteral Obstruction [MESH:D014517] (575)  Urinary Bladder Diseases [MESH:D001745] (4374)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urinary Bladder, Overactive [MESH:D053201] (530)  Cystitis [MESH:D003556] (604)   Cystitis, Interstitial [MESH:D018856] (264)  Urination Disorders [MESH:D014555] (3598)   Anuria [MESH:D001002] (833)  Urinary Retention [MESH:D016055] (411)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394)  Urolithiasis [MESH:D052878] (585)   Nephrolithiasis [MESH:D053040] (492)   Kidney Calculi [MESH:D007669] (455)  Urinary Calculi [MESH:D014545] (521)   Kidney Calculi [MESH:D007669] (455) C13. Female Urogenital Diseases and Pregnancy Complications  C13. Female Urogenital Diseases and Pregnancy Complications  Z. Exceptions (1116)   Not Fully Specified [NFS] (1116)  Female Urogenital Diseases [MESH:D052776] (8724)   Genital Diseases, Female [MESH:D005831] (5563)   Endometriosis [MESH:D004715] (2461)  Adnexal Diseases [MESH:D000291] (4273)   Ovarian Diseases [MESH:D010049] (4255)   Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Ovarian Neoplasms [MESH:D010051] (3281)   Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Infertility [MESH:D007246] (2211)   Infertility, Female [MESH:D007247] (2184)  Sexually Transmitted Diseases [MESH:D012749] (1712)   Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Uterine Diseases [MESH:D014591] (2479)   Endometrial Hyperplasia [MESH:D004714] (263)  Uterine Cervical Diseases [MESH:D002577] (988)   Uterine Cervical Neoplasms [MESH:D002583] (978)  Uterine Neoplasms [MESH:D014594] (2430)   Endometrial Neoplasms [MESH:D016889] (1984)  Uterine Cervical Neoplasms [MESH:D002583] (978)  Urogenital Abnormalities [MESH:D014564] (2043)   Allanson Pantzar McLeod syndrome [MESH:C537048] (503)  Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   Kallmann Syndrome [MESH:D017436] (147)  WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Urogenital Neoplasms [MESH:D014565] (5792)   Genital Neoplasms, Female [MESH:D005833] (3810)   Ovarian Neoplasms [MESH:D010051] (3281)   Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Uterine Neoplasms [MESH:D014594] (2433)   Endometrial Neoplasms [MESH:D016889] (1989)  Uterine Cervical Neoplasms [MESH:D002583] (978)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Urologic Diseases [MESH:D014570] (7793)   Urinary Tract Infections [MESH:D014552] (984)  Kidney Diseases [MESH:D007674] (7242)   Anuria [MESH:D001002] (833)  Diabetic Nephropathies [MESH:D003928] (2301)  Hepatorenal Syndrome [MESH:D006530] (910)  Hyperoxaluria [MESH:D006959] (1498)  Hypertension, Renal [MESH:D006977] (698)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, IGA [MESH:D005922] (897)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Nephrolithiasis [MESH:D053040] (492)   Kidney Calculi [MESH:D007669] (455)  Nephrosis [MESH:D009401] (2228)   Nephrotic Syndrome [MESH:D009404] (1536)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058)   Pseudohypoaldosteronism [MESH:D011546] (232)  Bartter Syndrome [MESH:D001477] (241)   Bartter Syndrome, Type 4A [MESH:C566530] (27)  Bartter Syndrome, Type 4b [MESH:C567762] (14)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)   Atypical hemolytic uremic syndrome [MESH:C538266] (277)  Ureteral Diseases [MESH:D014515] (1024)   Ureteral Obstruction [MESH:D014517] (575)  Urinary Bladder Diseases [MESH:D001745] (4375)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urinary Bladder, Overactive [MESH:D053201] (530)  Cystitis [MESH:D003556] (604)   Cystitis, Interstitial [MESH:D018856] (264)  Urination Disorders [MESH:D014555] (3598)   Anuria [MESH:D001002] (833)  Urinary Retention [MESH:D016055] (411)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394)  Urolithiasis [MESH:D052878] (585)   Nephrolithiasis [MESH:D053040] (492)   Kidney Calculi [MESH:D007669] (455)  Urinary Calculi [MESH:D014545] (521)   Kidney Calculi [MESH:D007669] (455)  Pregnancy Complications [MESH:D011248] (4768)   Abortion, Spontaneous [MESH:D000022] (2780)  Placenta Diseases [MESH:D010922] (1781)  Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)  Fetal Death [MESH:D005313] (464)   Fetal Resorption [MESH:D005327] (302)  Fetal Diseases [MESH:D005315] (1206)   Fetal Growth Retardation [MESH:D005317] (986)  Hypertension, Pregnancy-Induced [MESH:D046110] (1453)   Pre-Eclampsia [MESH:D011225] (1435)  Obstetric Labor Complications [MESH:D007744] (1550)   Obstetric Labor, Premature [MESH:D007752] (1316)  Prenatal Injuries [MESH:D049188] (1314)   Prenatal Exposure Delayed Effects [MESH:D011297] (870) C14. Cardiovascular Diseases  C14. Cardiovascular Diseases  Z. Exceptions (2667)   Not Fully Specified [NFS] (2667)  Cardiovascular Diseases [MESH:D002318] (10123)   Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)  Cardiovascular Abnormalities [MESH:D018376] (3153)   Heart Defects, Congenital [MESH:D006330] (2447)   Ductus Arteriosus, Patent [MESH:D004374] (325)   Aortic aneurysm, familial thoracic 4 [MESH:C537784] (29)  Vascular Malformations [MESH:D054079] (1098)   Arteriovenous Malformations [MESH:D001165] (1058)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Central Nervous System Vascular Malformations [MESH:D020785] (1031)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Heart Diseases [MESH:D006331] (8614)   Heart Arrest [MESH:D006323] (1926)  Heart Failure [MESH:D006333] (4058)  Arrhythmias, Cardiac [MESH:D001145] (4679)   Atrial Fibrillation [MESH:D001281] (1053)  Bradycardia [MESH:D001919] (1899)  Tachycardia [MESH:D013610] (3339)  Long QT Syndrome [MESH:D008133] (693)   Long Qt Syndrome 11 [MESH:C567513] (48)  Cardiomegaly [MESH:D006332] (4081)   Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1t [MESH:C566052] (76)  Cardiomyopathies [MESH:D009202] (5331)   Cardiomyopathy, Alcoholic [MESH:D002310] (354)  Cardiomyopathy, Hypertrophic [MESH:D002312] (1516)  Diabetic Cardiomyopathies [MESH:D058065] (1995)  Endomyocardial Fibrosis [MESH:D004719] (521)  Kearns-Sayre Syndrome [MESH:D007625] (1054)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocarditis [MESH:D009205] (1708)  Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1t [MESH:C566052] (76)  Heart Defects, Congenital [MESH:D006330] (2443)   Ductus Arteriosus, Patent [MESH:D004374] (325)   Aortic aneurysm, familial thoracic 4 [MESH:C537784] (29)  Heart Valve Diseases [MESH:D006349] (3333)   Aortic Valve Insufficiency [MESH:D001022] (1002)  Aortic Valve Stenosis [MESH:D001024] (1742)   Aortic Stenosis, Subvalvular [MESH:D001020] (1455)   Cardiomyopathy, Hypertrophic [MESH:D002312] (1451)  Myocardial Ischemia [MESH:D017202] (5787)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocardial Stunning [MESH:D017682] (1816)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Stable [MESH:D060050] (1702)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Coronary Stenosis [MESH:D023921] (1806)   Coronary Restenosis [MESH:D023903] (1683)  Myocardial Infarction [MESH:D009203] (4122)   Myocardial Stunning [MESH:D017682] (1816)  Ventricular Dysfunction [MESH:D018754] (2348)   Ventricular Dysfunction, Left [MESH:D018487] (1631)  Vascular Diseases [MESH:D014652] (8691)   Angioedema [MESH:D000799] (837)  Hepatic Veno-Occlusive Disease [MESH:D006504] (208)  Hyperemia [MESH:D006940] (2372)  Hypotension [MESH:D007022] (4045)  Retinal Vein Occlusion [MESH:D012170] (607)  Varicose Veins [MESH:D014648] (383)  Vascular System Injuries [MESH:D057772] (2086)  Aneurysm [MESH:D000783] (1886)   Intracranial Aneurysm [MESH:D002532] (158)  Aneurysm, Dissecting [MESH:D000784] (699)   Loeys-Dietz Syndrome [MESH:D055947] (263)  Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Abdominal [MESH:D017544] (1519)  Loeys-Dietz Syndrome [MESH:D055947] (263)  Aortic Aneurysm, Thoracic [MESH:D017545] (781)   Aortic aneurysm, familial thoracic 4 [MESH:C537784] (29)  Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Angiomatosis [MESH:D000798] (620)   Sturge-Weber Syndrome [MESH:D013341] (76)  von Hippel-Lindau Disease [MESH:D006623] (580)  Aortic Diseases [MESH:D001018] (1737)   Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Abdominal [MESH:D017544] (1519)  Loeys-Dietz Syndrome [MESH:D055947] (263)  Aortic Aneurysm, Thoracic [MESH:D017545] (781)   Aortic aneurysm, familial thoracic 4 [MESH:C537784] (29)  Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Arterial Occlusive Diseases [MESH:D001157] (4520)   Arteriosclerosis [MESH:D001161] (4466)   Atherosclerosis [MESH:D050197] (4188)  Coronary Artery Disease [MESH:D003324] (2685)  Arteriovenous Malformations [MESH:D001165] (1058)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Cerebrovascular Disorders [MESH:D002561] (5541)   Carotid Artery Diseases [MESH:D002340] (1993)  Vasospasm, Intracranial [MESH:D020301] (324)  Brain Ischemia [MESH:D002545] (4873)   Ischemic Attack, Transient [MESH:D002546] (1313)  Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Small Vessel Diseases [MESH:D059345] (1292)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  MELAS Syndrome [MESH:D017241] (1061)  Intracranial Arterial Diseases [MESH:D020765] (2468)   Intracranial Aneurysm [MESH:D002532] (158)  Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Amyloid Angiopathy [MESH:D016657] (470)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  Subarachnoid Hemorrhage [MESH:D013345] (1082)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Diabetic Angiopathies [MESH:D003925] (1984)   Diabetic Retinopathy [MESH:D003930] (1371)  Embolism and Thrombosis [MESH:D016769] (3374)   Embolism [MESH:D004617] (1137)   Pulmonary Embolism [MESH:D011655] (1118)  Thrombosis [MESH:D013927] (3101)   Venous Thrombosis [MESH:D020246] (1141)   Retinal Vein Occlusion [MESH:D012170] (607)  Hemostatic Disorders [MESH:D020141] (2894)   Multiple Myeloma [MESH:D009101] (2765)  Telangiectasia, Hereditary Hemorrhagic [MESH:D013683] (75)   Osler-rendu-weber syndrome 2 [MESH:C537139] (34)  Hypertension [MESH:D006973] (5655)   Hypertension, Essential [MESH:C562386] (1308)  Hypertension, Malignant [MESH:D006974] (621)  Hypertension, Renal [MESH:D006977] (698)  Myocardial Ischemia [MESH:D017202] (5791)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocardial Stunning [MESH:D017682] (1816)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Stable [MESH:D060050] (1702)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Coronary Stenosis [MESH:D023921] (1806)   Coronary Restenosis [MESH:D023903] (1683)  Myocardial Infarction [MESH:D009203] (4151)   Myocardial Stunning [MESH:D017682] (1816)  Peripheral Vascular Diseases [MESH:D016491] (1412)   Raynaud Disease [MESH:D011928] (490)  Livedo Reticularis [MESH:D054068] (228)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Telangiectasis [MESH:D013684] (255)   Telangiectasia, Hereditary Hemorrhagic [MESH:D013683] (75)   Osler-rendu-weber syndrome 2 [MESH:C537139] (34)  Vasculitis [MESH:D014657] (2604)   Behcet Syndrome [MESH:D001528] (1784) C15. Hemic and Lymphatic Diseases  C15. Hemic and Lymphatic Diseases  Hematologic Diseases [MESH:D006402] (6174)   Pancytopenia [MESH:D010198] (332)  Anemia [MESH:D000740] (3966)   Anemia, Refractory [MESH:D000753] (1567)  Anemia, Aplastic [MESH:D000741] (1925)   Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)   Fanconi Anemia, Complementation Group D1 [MESH:C563980] (68)  Anemia, Hemolytic [MESH:D000743] (3083)   Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Sickle Cell [MESH:D000755] (1722)  Thalassemia [MESH:D013789] (501)   alpha-Thalassemia [MESH:D017085] (176)   ATR-X syndrome [MESH:C538258] (59)  Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)  Hemolytic-Uremic Syndrome [MESH:D006463] (2435)   Atypical hemolytic uremic syndrome [MESH:C538266] (277)  Anemia, Macrocytic [MESH:D000748] (382)   5q- syndrome [MESH:C535323] (131)  Blood Coagulation Disorders [MESH:D001778] (1828)   Disseminated Intravascular Coagulation [MESH:D004211] (462)  Thrombocythemia, Essential [MESH:D013920] (707)  Blood Coagulation Disorders, Inherited [MESH:D025861] (720)   Platelet Disorder, Familial, with Associated Myeloid Malignancy [MESH:C563324] (62)  Purpura [MESH:D011693] (475)   Purpura, Thrombocytopenic [MESH:D011696] (237)   Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)  Blood Platelet Disorders [MESH:D001791] (3174)   Platelet Disorder, Familial, with Associated Myeloid Malignancy [MESH:C563324] (62)  Platelet Glycoprotein IV Deficiency [MESH:C564245] (173)  Thrombocytopenia [MESH:D013921] (2966)   Thrombotic Microangiopathies [MESH:D057049] (2598)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)   Atypical hemolytic uremic syndrome [MESH:C538266] (277)  Purpura, Thrombocytopenic [MESH:D011696] (237)   Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)  Thrombocytosis [MESH:D013922] (720)   Thrombocythemia, Essential [MESH:D013920] (707)  Blood Protein Disorders [MESH:D001796] (3051)   Agammaglobulinemia [MESH:D000361] (156)   Severe combined immunodeficiency due to adenosine deaminase deficiency [MESH:C531816] (67)  Hypoproteinemia [MESH:D007019] (1335)   Hypoalbuminemia [MESH:D034141] (1332)  Paraproteinemias [MESH:D010265] (2781)   Multiple Myeloma [MESH:D009101] (2765)  Bone Marrow Diseases [MESH:D001855] (2944)   Anemia, Aplastic [MESH:D000741] (1925)   Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)   Fanconi Anemia, Complementation Group D1 [MESH:C563980] (68)  Myelodysplastic-Myeloproliferative Diseases [MESH:D054437] (376)   Leukemia, Myelomonocytic, Juvenile [MESH:D054429] (344)  Myelodysplastic Syndromes [MESH:D009190] (2093)   Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)  Anemia, Refractory [MESH:D000753] (1567)  Myeloproliferative Disorders [MESH:D009196] (1492)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Thrombocytosis [MESH:D013922] (720)   Thrombocythemia, Essential [MESH:D013920] (707)  Hemoglobinopathies [MESH:D006453] (1863)   Anemia, Sickle Cell [MESH:D000755] (1722)  Thalassemia [MESH:D013789] (511)   alpha-Thalassemia [MESH:D017085] (192)   ATR-X syndrome [MESH:C538258] (59)  Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)  Hemorrhagic Disorders [MESH:D006474] (3359)   Disseminated Intravascular Coagulation [MESH:D004211] (462)  Thrombocythemia, Essential [MESH:D013920] (707)  Hemostatic Disorders [MESH:D020141] (2932)   Multiple Myeloma [MESH:D009101] (2765)  Telangiectasia, Hereditary Hemorrhagic [MESH:D013683] (75)   Osler-rendu-weber syndrome 2 [MESH:C537139] (34)  Leukocyte Disorders [MESH:D007960] (2662)   Leukocytosis [MESH:D007964] (988)  Leukopenia [MESH:D007970] (1921)   Lymphopenia [MESH:D008231] (990)  Agranulocytosis [MESH:D000380] (1675)   Neutropenia [MESH:D009503] (1629)  Phagocyte Bactericidal Dysfunction [MESH:D010585] (998)   Job Syndrome [MESH:D007589] (772)  Granulomatous Disease, Chronic [MESH:D006105] (404)   Granulomatous Disease, Chronic, X-Linked [MESH:C564417] (111)  Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I [MESH:C565532] (142)  Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative [MESH:C565533] (111)  Thrombophilia [MESH:D019851] (592)   Disseminated Intravascular Coagulation [MESH:D004211] (462)  Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)  Lymphatic Diseases [MESH:D008206] (5167)   Lymphedema [MESH:D008209] (162)  Histiocytosis [MESH:D015614] (336)   Histiocytosis, Non-Langerhans-Cell [MESH:D015616] (315)   Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type A [MESH:D052536] (44)  Niemann-Pick Disease, Type B [MESH:D052537] (44)  Niemann-Pick Disease, Type C [MESH:D052556] (103)   Niemann-Pick disease, type C2 [MESH:C536119] (43)  Lymphoproliferative Disorders [MESH:D008232] (4638)   Giant Lymph Node Hyperplasia [MESH:D005871] (1013)  Sarcoidosis [MESH:D012507] (895)  Agammaglobulinemia [MESH:D000361] (156)   Severe combined immunodeficiency due to adenosine deaminase deficiency [MESH:C531816] (67)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)  Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Lymphoma [MESH:D008223] (3684)   Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, Mantle-Cell [MESH:D020522] (561)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] (12152)   Congenital Abnormalities [MESH:D000013] (8109)   Caudal Duplication Anomaly [MESH:C564315] (29)  Respiratory System Abnormalities [MESH:D015619] (244)  Abnormalities, Multiple [MESH:D000015] (3192)   Warburg Sjo Fledelius syndrome [MESH:C536681] (15)  Alstrom Syndrome [MESH:D056769] (20)  Cockayne Syndrome [MESH:D003057] (107)  Loeys-Dietz Syndrome [MESH:D055947] (263)  Deaf-Blind Disorders [MESH:D054062] (132)   Arts syndrome [MESH:C535388] (31)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 4 [MESH:C564180] (70)  Cardiovascular Abnormalities [MESH:D018376] (3294)   Heart Defects, Congenital [MESH:D006330] (2611)   Ductus Arteriosus, Patent [MESH:D004374] (325)   Aortic aneurysm, familial thoracic 4 [MESH:C537784] (29)  Long QT Syndrome [MESH:D008133] (693)   Long Qt Syndrome 11 [MESH:C567513] (48)  Vascular Malformations [MESH:D054079] (1108)   Arteriovenous Malformations [MESH:D001165] (1058)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Central Nervous System Vascular Malformations [MESH:D020785] (1018)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Telangiectasia, Hereditary Hemorrhagic [MESH:D013683] (75)   Osler-rendu-weber syndrome 2 [MESH:C537139] (34)  Chromosome Disorders [MESH:D025063] (2030)   Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 4 [MESH:C564180] (70)  WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Eye Abnormalities [MESH:D005124] (1233)   Aniridia [MESH:D015783] (312)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Musculoskeletal Abnormalities [MESH:D009139] (3779)   Craniofacial Abnormalities [MESH:D019465] (3064)   Spondyloepimetaphyseal Dysplasia, Aggrecan Type [MESH:C567558] (35)  Cleidocranial Dysplasia [MESH:D002973] (129)  Craniosynostoses [MESH:D003398] (438)   Jackson-Weiss syndrome [MESH:C537559] (149)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 4 [MESH:C564180] (70)  Maxillofacial Abnormalities [MESH:D019767] (1448)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)  Micrognathism [MESH:D008844] (230)   Meier-Gorlin syndrome [MESH:C538012] (133)  Pierre Robin Syndrome [MESH:D010855] (101)   Pierre Robin syndrome with fetal chondrodysplasia [MESH:C535776] (16)  Microcephaly [MESH:D008831] (700)   Warburg Sjo Fledelius syndrome [MESH:C536681] (15)  Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)  Plagiocephaly [MESH:D059041] (440)   Craniosynostoses [MESH:D003398] (438)   Jackson-Weiss syndrome [MESH:C537559] (149)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Limb Deformities, Congenital [MESH:D017880] (1813)   Acromicric dysplasia [MESH:C535662] (520)  Brachydactyly [MESH:D059327] (220)  Arachnodactyly [MESH:D054119] (126)   Congenital contractural arachnodactyly [MESH:C536211] (47)  Foot Deformities, Congenital [MESH:D005532] (538)   Jackson-Weiss syndrome [MESH:C537559] (149)  Hand Deformities, Congenital [MESH:D006228] (587)   Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Syndactyly [MESH:D013576] (487)   Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Synostosis [MESH:D013580] (817)   Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Craniosynostoses [MESH:D003398] (438)   Jackson-Weiss syndrome [MESH:C537559] (149)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Syndactyly [MESH:D013576] (487)   Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Nervous System Malformations [MESH:D009421] (3354)   Agenesis of Corpus Callosum [MESH:D061085] (345)   Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 4 [MESH:C564180] (70)  Central Nervous System Vascular Malformations [MESH:D020785] (1031)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Alstrom Syndrome [MESH:D056769] (20)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 4 [MESH:C564180] (70)  Malformations of Cortical Development [MESH:D054220] (1406)   Tuberous Sclerosis [MESH:D014402] (635)  Microcephaly [MESH:D008831] (700)   Warburg Sjo Fledelius syndrome [MESH:C536681] (15)  Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)  Neural Tube Defects [MESH:D009436] (2143)   Spinal Dysraphism [MESH:D016135] (1025)   Spina Bifida Cystica [MESH:D016137] (209)  Skin Abnormalities [MESH:D012868] (1723)   Port-Wine Stain [MESH:D019339] (86)  Ichthyosis [MESH:D007057] (481)   Keratosis Follicularis Spinulosa Decalvans, X-Linked [MESH:C536159] (78)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Tooth Abnormalities [MESH:D014071] (622)  Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)  Micrognathism [MESH:D008844] (230)   Meier-Gorlin syndrome [MESH:C538012] (133)  Pierre Robin Syndrome [MESH:D010855] (101)   Pierre Robin syndrome with fetal chondrodysplasia [MESH:C535776] (16)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)  Cleft Palate [MESH:D002972] (1330)  Urogenital Abnormalities [MESH:D014564] (2064)   Allanson Pantzar McLeod syndrome [MESH:C537048] (503)  Cryptorchidism [MESH:D003456] (215)   Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Skeletal Defects, Genital Hypoplasia, And Mental Retardation [MESH:C567306] (52)  Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   Kallmann Syndrome [MESH:D017436] (147)  WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Fetal Diseases [MESH:D005315] (1205)   Fetal Growth Retardation [MESH:D005317] (986)  Genetic Diseases, Inborn [MESH:D030342] (9766)   Platelet Glycoprotein IV Deficiency [MESH:C564245] (173)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Camurati-Engelmann Syndrome [MESH:D003966] (492)  Cystic Fibrosis [MESH:D003550] (760)  Kallmann Syndrome [MESH:D017436] (147)  Loeys-Dietz Syndrome [MESH:D055947] (263)  Osteoarthropathy, Primary Hypertrophic [MESH:D010004] (94)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Sickle Cell [MESH:D000755] (1722)  Thalassemia [MESH:D013789] (501)   alpha-Thalassemia [MESH:D017085] (176)   ATR-X syndrome [MESH:C538258] (59)  Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)  Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)   Fanconi Anemia, Complementation Group D1 [MESH:C563980] (68)  Blood Coagulation Disorders, Inherited [MESH:D025861] (722)   Platelet Disorder, Familial, with Associated Myeloid Malignancy [MESH:C563324] (62)  Chromosome Disorders [MESH:D025063] (2030)   Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 4 [MESH:C564180] (70)  WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Dwarfism [MESH:D004392] (783)   Diastrophic dysplasia [MESH:C536170] (34)  Cockayne Syndrome [MESH:D003057] (107)  Achondroplasia [MESH:D000130] (196)   Achondrogenesis type 1B [MESH:C536016] (34)  Eye Diseases, Hereditary [MESH:D015785] (1867)   Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement [MESH:C567572] (70)  Aniridia [MESH:D015783] (312)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Meretoja syndrome [MESH:C537459] (95)  Corneal Dystrophy, Fleck [MESH:C563256] (12)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic atrophy polyneuropathy deafness [MESH:C537129] (31)  Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Retinitis Pigmentosa [MESH:D012174] (442)   Retinitis Pigmentosa 33 [MESH:C563676] (20)  Alstrom Syndrome [MESH:D056769] (20)  Genetic Diseases, X-Linked [MESH:D040181] (3028)   Arts syndrome [MESH:C535388] (31)  Keratosis Follicularis Spinulosa Decalvans, X-Linked [MESH:C536159] (78)  Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked [MESH:C562780] (31)  Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)  Deafness, X-Linked 1 [MESH:C564433] (31)  Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Pelizaeus-Merzbacher Disease [MESH:D020371] (103)  X-Linked Combined Immunodeficiency Diseases [MESH:D053632] (42)  Granulomatous Disease, Chronic [MESH:D006105] (404)   Granulomatous Disease, Chronic, X-Linked [MESH:C564417] (111)  Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I [MESH:C565532] (142)  Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative [MESH:C565533] (111)  Mental Retardation, X-Linked [MESH:D038901] (1867)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  ATR-X syndrome [MESH:C538258] (59)  Adrenoleukodystrophy [MESH:D000326] (1348)  Coffin-Lowry Syndrome [MESH:D038921] (45)  Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149)   Pyruvate Dehydrogenase E3-Binding Protein Deficiency [MESH:C565447] (25)  Hemoglobinopathies [MESH:D006453] (1863)   Anemia, Sickle Cell [MESH:D000755] (1722)  Thalassemia [MESH:D013789] (511)   alpha-Thalassemia [MESH:D017085] (192)   ATR-X syndrome [MESH:C538258] (59)  Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465)   Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98)  Alexander Disease [MESH:D038261] (168)  Cockayne Syndrome [MESH:D003057] (107)  Gerstmann-Straussler-Scheinker Disease [MESH:D016098] (98)  Hepatolenticular Degeneration [MESH:D006527] (473)  Tuberous Sclerosis [MESH:D014402] (635)  Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Alstrom Syndrome [MESH:D056769] (20)  Huntington Disease [MESH:D006816] (540)   Huntington Disease-Like 1 [MESH:C566398] (98)  Mental Retardation, X-Linked [MESH:D038901] (1848)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  ATR-X syndrome [MESH:C538258] (59)  Adrenoleukodystrophy [MESH:D000326] (1348)  Coffin-Lowry Syndrome [MESH:D038921] (45)  Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149)   Pyruvate Dehydrogenase E3-Binding Protein Deficiency [MESH:C565447] (25)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic atrophy polyneuropathy deafness [MESH:C537129] (31)  Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxias [MESH:D020754] (322)   Spastic ataxia Charlevoix-Saguenay type [MESH:C536787] (37)  Metabolism, Inborn Errors [MESH:D008661] (6032)   Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565)   Glutathionuria [MESH:C536836] (96)  Methylmalonic acidemia [MESH:C537358] (764)  Hyperhomocysteinemia [MESH:D020138] (1724)  Tyrosinemias [MESH:D020176] (132)   Hawkinsinuria [MESH:C535845] (34)  Amyloidosis, Familial [MESH:D028226] (696)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  Galactosemias [MESH:D005693] (69)  Hepatolenticular Degeneration [MESH:D006527] (473)  MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Alexander Disease [MESH:D038261] (168)  Pelizaeus-Merzbacher Disease [MESH:D020371] (103)  Leigh Disease [MESH:D007888] (206)   Leigh syndrome , French Canadian type [MESH:C537004] (35)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Fucosidosis [MESH:D005645] (34)  Sphingolipidoses [MESH:D013106] (582)   Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type A [MESH:D052536] (44)  Niemann-Pick Disease, Type B [MESH:D052537] (44)  Niemann-Pick Disease, Type C [MESH:D052556] (103)   Niemann-Pick disease, type C2 [MESH:C536119] (43)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149)   Pyruvate Dehydrogenase E3-Binding Protein Deficiency [MESH:C565447] (25)  Tyrosinemias [MESH:D020176] (132)   Hawkinsinuria [MESH:C535845] (34)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Fucosidosis [MESH:D005645] (34)  Galactosemias [MESH:D005693] (69)  Fructose Metabolism, Inborn Errors [MESH:D015318] (125)   Fructose-1,6-Diphosphatase Deficiency [MESH:D015319] (72)  Pyruvate Metabolism, Inborn Errors [MESH:D015323] (324)   Leigh Disease [MESH:D007888] (206)   Leigh syndrome , French Canadian type [MESH:C537004] (35)  Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149)   Pyruvate Dehydrogenase E3-Binding Protein Deficiency [MESH:C565447] (25)  Cytochrome-c Oxidase Deficiency [MESH:D030401] (48)   Leigh syndrome , French Canadian type [MESH:C537004] (35)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)  Sphingolipidoses [MESH:D013106] (582)   Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type A [MESH:D052536] (44)  Niemann-Pick Disease, Type B [MESH:D052537] (44)  Niemann-Pick Disease, Type C [MESH:D052556] (103)   Niemann-Pick disease, type C2 [MESH:C536119] (43)  Lysosomal Storage Diseases [MESH:D016464] (761)   Neuraminidase deficiency with beta-galactosidase deficiency [MESH:C536411] (21)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Fucosidosis [MESH:D005645] (34)  Sphingolipidoses [MESH:D013106] (582)   Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type A [MESH:D052536] (44)  Niemann-Pick Disease, Type B [MESH:D052537] (44)  Niemann-Pick Disease, Type C [MESH:D052556] (103)   Niemann-Pick disease, type C2 [MESH:C536119] (43)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hemochromatosis [MESH:D006432] (1694)  Hepatolenticular Degeneration [MESH:D006527] (473)  Peroxisomal Disorders [MESH:D018901] (1788)   Adrenoleukodystrophy [MESH:D000326] (1348)  Chondrodysplasia Punctata, Rhizomelic [MESH:D018902] (53)   Rhizomelic chondrodysplasia punctata, type 3 [MESH:C537608] (26)  Porphyrias [MESH:D011164] (917)   Porphyria, Erythropoietic [MESH:D017092] (16)  Purine-Pyrimidine Metabolism, Inborn Errors [MESH:D011686] (496)   Phosphoribosylpyrophosphate Synthetase Superactivity [MESH:C567064] (31)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1027)   Pseudohypoaldosteronism [MESH:D011546] (232)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Muscular Dystrophies [MESH:D009136] (1597)   Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Turcot syndrome [MESH:C536928] (159)  Juvenile polyposis syndrome [MESH:C537702] (196)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (260)  Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Tuberous Sclerosis [MESH:D014402] (635)  Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Wilms Tumor [MESH:D009396] (553)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Skin Diseases, Genetic [MESH:D012873] (3456)   Keratosis Follicularis Spinulosa Decalvans, X-Linked [MESH:C536159] (78)  Peeling Skin Syndrome [MESH:C564818] (9)  Dermatitis, Atopic [MESH:D003876] (2052)  Porphyria, Erythropoietic [MESH:D017092] (16)  Cutis Laxa [MESH:D003483] (177)   Wrinkly skin syndrome [MESH:C536750] (24)  Cutis Laxa, Autosomal Recessive, Type IIA [MESH:C562632] (24)  Infant, Newborn, Diseases [MESH:D007232] (3064)   Cystic Fibrosis [MESH:D003550] (760)  Ichthyosis [MESH:D007057] (476)   Keratosis Follicularis Spinulosa Decalvans, X-Linked [MESH:C536159] (78)  Infant, Premature, Diseases [MESH:D007235] (1292)   Bronchopulmonary Dysplasia [MESH:D001997] (1021)  Retinopathy of Prematurity [MESH:D012178] (353)  Severe Combined Immunodeficiency [MESH:D016511] (315)   Severe combined immunodeficiency due to adenosine deaminase deficiency [MESH:C531816] (67)  Bare lymphocyte syndrome 2 [MESH:C537079] (61)  Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell -Positive, NK Cell-Negative [MESH:C563440] (79)  Bare Lymphocyte Syndrome, Type I [MESH:C565759] (101)  X-Linked Combined Immunodeficiency Diseases [MESH:D053632] (42) C17. Skin and Connective Tissue Diseases  C17. Skin and Connective Tissue Diseases  Connective Tissue Diseases [MESH:D003240] (4490)   Stickler syndrome, type 3 [MESH:C537494] (16)  Cartilage Diseases [MESH:D002357] (438)  Dermatomyositis [MESH:D003882] (1826)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Penile Induration [MESH:D010411] (495)  Scleroderma, Localized [MESH:D012594] (1597)  Scleroderma, Systemic [MESH:D012595] (199)  Collagen Diseases [MESH:D003095] (1267)   Keloid [MESH:D007627] (1111)  Cutis Laxa [MESH:D003483] (177)   Wrinkly skin syndrome [MESH:C536750] (24)  Cutis Laxa, Autosomal Recessive, Type IIA [MESH:C562632] (24)  Rheumatic Diseases [MESH:D012216] (3619)   Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Skin Diseases [MESH:D012871] (8774)   Dermatomyositis [MESH:D003882] (1826)  Nephrogenic Fibrosing Dermopathy [MESH:D054989] (452)  Scleroderma, Localized [MESH:D012594] (1597)  Scleroderma, Systemic [MESH:D012595] (199)  Skin Neoplasms [MESH:D012878] (2991)  Skin Ulcer [MESH:D012883] (229)  Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Breast Diseases [MESH:D001941] (6148)   Breast Neoplasms [MESH:D001943] (6077)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Dermatitis [MESH:D003872] (4530)   Dermatitis, Atopic [MESH:D003876] (2052)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Dermatitis, Occupational [MESH:D009783] (311)  Dermatitis, Exfoliative [MESH:D003873] (42)   Peeling skin syndrome, acral type [MESH:C536316] (9)  Peeling Skin Syndrome [MESH:C564818] (9)  Drug Eruptions [MESH:D003875] (2697)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Erythema [MESH:D004890] (1330)   Erythema Multiforme [MESH:D004892] (1185)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Facial Dermatoses [MESH:D005148] (1336)   Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Hair Diseases [MESH:D006201] (1891)   Hypotrichosis [MESH:D007039] (1513)   Hypotrichosis simplex [MESH:C537160] (92)  Keratosis [MESH:D007642] (1941)   Ichthyosis [MESH:D007057] (481)   Keratosis Follicularis Spinulosa Decalvans, X-Linked [MESH:C536159] (78)  Pigmentation Disorders [MESH:D010859] (1215)   Peeling skin syndrome, acral type [MESH:C536316] (9)  Hypopigmentation [MESH:D017496] (718)   Vitiligo [MESH:D014820] (504)  Skin Abnormalities [MESH:D012868] (1709)   Port-Wine Stain [MESH:D019339] (86)  Ichthyosis [MESH:D007057] (481)   Keratosis Follicularis Spinulosa Decalvans, X-Linked [MESH:C536159] (78)  Skin Diseases, Eczematous [MESH:D017443] (3740)   Dermatitis, Atopic [MESH:D003876] (2052)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Dermatitis, Occupational [MESH:D009783] (311)  Dermatitis, Exfoliative [MESH:D003873] (42)   Peeling skin syndrome, acral type [MESH:C536316] (9)  Peeling Skin Syndrome [MESH:C564818] (9)  Skin Diseases, Genetic [MESH:D012873] (3481)   Keratosis Follicularis Spinulosa Decalvans, X-Linked [MESH:C536159] (78)  Peeling Skin Syndrome [MESH:C564818] (9)  Dermatitis, Atopic [MESH:D003876] (2052)  Porphyria, Erythropoietic [MESH:D017092] (16)  Cutis Laxa [MESH:D003483] (177)   Wrinkly skin syndrome [MESH:C536750] (24)  Cutis Laxa, Autosomal Recessive, Type IIA [MESH:C562632] (24)  Skin Diseases, Infectious [MESH:D012874] (2684)   Dermatomycoses [MESH:D003881] (267)   Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224)  Skin Diseases, Parasitic [MESH:D012876] (2526)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)   Leishmaniasis, Mucocutaneous [MESH:D007897] (606)  Skin Diseases, Viral [MESH:D017193] (203)   Warts [MESH:D014860] (172)   WHIM syndrome [MESH:C536697] (148)  Epidermodysplasia Verruciformis [MESH:D004819] (18)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Lipodystrophy [MESH:D008060] (930)   Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy [MESH:C536329] (61)  Porphyrias [MESH:D011164] (917)   Porphyria, Erythropoietic [MESH:D017092] (16)  Skin Diseases, Papulosquamous [MESH:D017444] (3392)   Lichenoid Eruptions [MESH:D017512] (1324)  Parapsoriasis [MESH:D010267] (49)  Psoriasis [MESH:D011565] (3278)   Arthritis, Psoriatic [MESH:D015535] (1859)  Skin Diseases, Vascular [MESH:D017445] (3288)   Behcet Syndrome [MESH:D001528] (1784)  Livedo Reticularis [MESH:D054068] (228)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Urticaria [MESH:D014581] (2668)   Angioedema [MESH:D000799] (837)  Skin Diseases, Vesiculobullous [MESH:D012872] (1754)   Erythema Multiforme [MESH:D004892] (1185)   Stevens-Johnson Syndrome [MESH:D013262] (1163) C18. Nutritional and Metabolic Diseases  C18. Nutritional and Metabolic Diseases  Metabolic Diseases [MESH:D008659] (9025)   Metabolic Syndrome X [MESH:D024821] (2151)  Acid-Base Imbalance [MESH:D000137] (854)   Alkalosis [MESH:D000471] (384)  Acidosis [MESH:D000138] (626)   Acidosis, Lactic [MESH:D000140] (204)   Pyruvate Dehydrogenase E3-Binding Protein Deficiency [MESH:C565447] (25)  Brain Diseases, Metabolic [MESH:D001928] (3350)   Hepatic Encephalopathy [MESH:D006501] (1795)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  Galactosemias [MESH:D005693] (69)  Hepatolenticular Degeneration [MESH:D006527] (473)  MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Alexander Disease [MESH:D038261] (168)  Pelizaeus-Merzbacher Disease [MESH:D020371] (103)  Leigh Disease [MESH:D007888] (206)   Leigh syndrome , French Canadian type [MESH:C537004] (35)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Fucosidosis [MESH:D005645] (34)  Sphingolipidoses [MESH:D013106] (582)   Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type A [MESH:D052536] (44)  Niemann-Pick Disease, Type B [MESH:D052537] (44)  Niemann-Pick Disease, Type C [MESH:D052556] (103)   Niemann-Pick disease, type C2 [MESH:C536119] (43)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149)   Pyruvate Dehydrogenase E3-Binding Protein Deficiency [MESH:C565447] (25)  Tyrosinemias [MESH:D020176] (132)   Hawkinsinuria [MESH:C535845] (34)  Calcium Metabolism Disorders [MESH:D002128] (3634)   Calcinosis [MESH:D002114] (2989)  Hypercalcemia [MESH:D006934] (1999)  DNA Repair-Deficiency Disorders [MESH:D049914] (2245)   Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)  Cockayne Syndrome [MESH:D003057] (107)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)  Fanconi Anemia [MESH:D005199] (1604)   Fanconi Anemia, Complementation Group D1 [MESH:C563980] (68)  Severe Combined Immunodeficiency [MESH:D016511] (294)   Severe combined immunodeficiency due to adenosine deaminase deficiency [MESH:C531816] (67)  Bare lymphocyte syndrome 2 [MESH:C537079] (61)  Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell -Positive, NK Cell-Negative [MESH:C563440] (79)  Bare Lymphocyte Syndrome, Type I [MESH:C565759] (101)  Glucose Metabolism Disorders [MESH:D044882] (6122)   Diabetes Mellitus [MESH:D003920] (5891)   Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Hyperglycemia [MESH:D006943] (1858)   Glucose Intolerance [MESH:D018149] (605)  Hyperinsulinism [MESH:D006946] (3586)   Hyperinsulinemic hypoglycemia, familial, 7 [MESH:C538376] (106)  Insulin Resistance [MESH:D007333] (3511)   Metabolic Syndrome X [MESH:D024821] (2151)  Hypoglycemia [MESH:D007003] (2420)   Hyperinsulinemic hypoglycemia, familial, 7 [MESH:C538376] (106)  Iron Metabolism Disorders [MESH:D019189] (2139)   Iron Overload [MESH:D019190] (1772)   Hemochromatosis [MESH:D006432] (1694)  Lipid Metabolism Disorders [MESH:D052439] (3225)   Dyslipidemias [MESH:D050171] (2428)   Hyperlipidemias [MESH:D006949] (1908)   Hypercholesterolemia [MESH:D006937] (1404)  Lipodystrophy [MESH:D008060] (930)   Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy [MESH:C536329] (61)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)  Sphingolipidoses [MESH:D013106] (582)   Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type A [MESH:D052536] (44)  Niemann-Pick Disease, Type B [MESH:D052537] (44)  Niemann-Pick Disease, Type C [MESH:D052556] (103)   Niemann-Pick disease, type C2 [MESH:C536119] (43)  Malabsorption Syndromes [MESH:D008286] (1869)   Celiac Disease [MESH:D002446] (340)  Hyperhomocysteinemia [MESH:D020138] (1716)  Metabolism, Inborn Errors [MESH:D008661] (6028)   Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559)   Glutathionuria [MESH:C536836] (96)  Methylmalonic acidemia [MESH:C537358] (764)  Hyperhomocysteinemia [MESH:D020138] (1724)  Tyrosinemias [MESH:D020176] (132)   Hawkinsinuria [MESH:C535845] (34)  Amyloidosis, Familial [MESH:D028226] (696)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  Galactosemias [MESH:D005693] (69)  Hepatolenticular Degeneration [MESH:D006527] (473)  MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Alexander Disease [MESH:D038261] (168)  Pelizaeus-Merzbacher Disease [MESH:D020371] (103)  Leigh Disease [MESH:D007888] (206)   Leigh syndrome , French Canadian type [MESH:C537004] (35)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Fucosidosis [MESH:D005645] (34)  Sphingolipidoses [MESH:D013106] (582)   Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type A [MESH:D052536] (44)  Niemann-Pick Disease, Type B [MESH:D052537] (44)  Niemann-Pick Disease, Type C [MESH:D052556] (103)   Niemann-Pick disease, type C2 [MESH:C536119] (43)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149)   Pyruvate Dehydrogenase E3-Binding Protein Deficiency [MESH:C565447] (25)  Tyrosinemias [MESH:D020176] (132)   Hawkinsinuria [MESH:C535845] (34)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Fucosidosis [MESH:D005645] (34)  Galactosemias [MESH:D005693] (69)  Fructose Metabolism, Inborn Errors [MESH:D015318] (125)   Fructose-1,6-Diphosphatase Deficiency [MESH:D015319] (72)  Pyruvate Metabolism, Inborn Errors [MESH:D015323] (324)   Leigh Disease [MESH:D007888] (206)   Leigh syndrome , French Canadian type [MESH:C537004] (35)  Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149)   Pyruvate Dehydrogenase E3-Binding Protein Deficiency [MESH:C565447] (25)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)  Sphingolipidoses [MESH:D013106] (582)   Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type A [MESH:D052536] (44)  Niemann-Pick Disease, Type B [MESH:D052537] (44)  Niemann-Pick Disease, Type C [MESH:D052556] (103)   Niemann-Pick disease, type C2 [MESH:C536119] (43)  Lysosomal Storage Diseases [MESH:D016464] (761)   Neuraminidase deficiency with beta-galactosidase deficiency [MESH:C536411] (21)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Fucosidosis [MESH:D005645] (34)  Sphingolipidoses [MESH:D013106] (582)   Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type A [MESH:D052536] (44)  Niemann-Pick Disease, Type B [MESH:D052537] (44)  Niemann-Pick Disease, Type C [MESH:D052556] (103)   Niemann-Pick disease, type C2 [MESH:C536119] (43)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hemochromatosis [MESH:D006432] (1694)  Hepatolenticular Degeneration [MESH:D006527] (473)  Peroxisomal Disorders [MESH:D018901] (1788)   Adrenoleukodystrophy [MESH:D000326] (1348)  Chondrodysplasia Punctata, Rhizomelic [MESH:D018902] (53)   Rhizomelic chondrodysplasia punctata, type 3 [MESH:C537608] (26)  Porphyrias [MESH:D011164] (917)   Porphyria, Erythropoietic [MESH:D017092] (16)  Purine-Pyrimidine Metabolism, Inborn Errors [MESH:D011686] (496)   Phosphoribosylpyrophosphate Synthetase Superactivity [MESH:C567064] (31)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1026)   Pseudohypoaldosteronism [MESH:D011546] (232)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Mitochondrial Diseases [MESH:D028361] (2561)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Cytochrome-c Oxidase Deficiency [MESH:D030401] (48)   Leigh syndrome , French Canadian type [MESH:C537004] (35)  Leigh Disease [MESH:D007888] (206)   Leigh syndrome , French Canadian type [MESH:C537004] (35)  Mitochondrial Myopathies [MESH:D017240] (2176)   Mitochondrial Encephalomyopathies [MESH:D017237] (1121)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149)   Pyruvate Dehydrogenase E3-Binding Protein Deficiency [MESH:C565447] (25)  Porphyrias [MESH:D011164] (917)   Porphyria, Erythropoietic [MESH:D017092] (16)  Proteostasis Deficiencies [MESH:D057165] (3522)   Amyloidosis [MESH:D000686] (791)   Meretoja syndrome [MESH:C537459] (95)  Amyloid Neuropathies [MESH:D017772] (139)   Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  Amyloidosis, Familial [MESH:D028226] (696)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  Cerebral Amyloid Angiopathy [MESH:D016657] (470)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Frontotemporal Lobar Degeneration [MESH:D057174] (308)   Frontotemporal Dementia [MESH:D057180] (298)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Lipodystrophy [MESH:D008060] (930)   Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy [MESH:C536329] (61)  Porphyrias [MESH:D011164] (917)   Porphyria, Erythropoietic [MESH:D017092] (16)  Wasting Syndrome [MESH:D019282] (1959)   HIV Wasting Syndrome [MESH:D019247] (1956)  Water-Electrolyte Imbalance [MESH:D014883] (2790)   Hypercalcemia [MESH:D006934] (1999)  Hypokalemia [MESH:D007008] (1041)  Hyponatremia [MESH:D007010] (789)  Nutrition Disorders [MESH:D009748] (4945)   Malnutrition [MESH:D044342] (2754)   Deficiency Diseases [MESH:D003677] (2742)   Avitaminosis [MESH:D001361] (2304)   Vitamin B Deficiency [MESH:D014804] (1817)   Hyperhomocysteinemia [MESH:D020138] (1716)  Overnutrition [MESH:D044343] (4463)   Obesity [MESH:D009765] (4462)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Obesity, Morbid [MESH:D009767] (515)  Wasting Syndrome [MESH:D019282] (1959)   HIV Wasting Syndrome [MESH:D019247] (1956) C19. Endocrine System Diseases  C19. Endocrine System Diseases  Endocrine System Diseases [MESH:D004700] (8062)   Bone Diseases, Endocrine [MESH:D001849] (173)  Adrenal Gland Diseases [MESH:D000307] (2397)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Adrenal Insufficiency [MESH:D000309] (1599)   Addison Disease [MESH:D000224] (40)  Adrenoleukodystrophy [MESH:D000326] (1348)  Adrenocortical Hyperfunction [MESH:D000308] (618)   Hyperaldosteronism [MESH:D006929] (419)   Bartter Syndrome [MESH:D001477] (241)   Bartter Syndrome, Type 4A [MESH:C566530] (27)  Bartter Syndrome, Type 4b [MESH:C567762] (14)  Diabetes Mellitus [MESH:D003920] (6159)   Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Diabetes Complications [MESH:D048909] (4129)   Diabetic Cardiomyopathies [MESH:D058065] (1995)  Diabetic Nephropathies [MESH:D003928] (2301)  Diabetic Neuropathies [MESH:D003929] (2443)  Diabetic Angiopathies [MESH:D003925] (1984)   Diabetic Retinopathy [MESH:D003930] (1371)  Dwarfism [MESH:D004392] (698)   Diastrophic dysplasia [MESH:C536170] (34)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)   Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, papillary [MESH:C536915] (111)  Gonadal Disorders [MESH:D006058] (5088)   Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   Kallmann Syndrome [MESH:D017436] (147)  WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Hypogonadism [MESH:D007006] (1123)   Warburg Sjo Fledelius syndrome [MESH:C536681] (15)  Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  Kallmann Syndrome [MESH:D017436] (147)  Ovarian Diseases [MESH:D010049] (4253)   Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Ovarian Neoplasms [MESH:D010051] (3281)   Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Testicular Diseases [MESH:D013733] (777)   Cryptorchidism [MESH:D003456] (215)   Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Skeletal Defects, Genital Hypoplasia, And Mental Retardation [MESH:C567306] (52)  Parathyroid Diseases [MESH:D010279] (1604)   Hyperparathyroidism [MESH:D006961] (1475)   Hyperparathyroidism, Secondary [MESH:D006962] (1138)  Polyendocrinopathies, Autoimmune [MESH:D016884] (40)   Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked [MESH:C562780] (31)  Thyroid Diseases [MESH:D013959] (2808)   Goiter [MESH:D006042] (359)   Graves Disease [MESH:D006111] (278)   Graves Ophthalmopathy [MESH:D049970] (165)  Hyperthyroidism [MESH:D006980] (1191)   Graves Disease [MESH:D006111] (278)   Graves Ophthalmopathy [MESH:D049970] (165)  Hyperthyroxinemia [MESH:D006981] (659)   Dystransthyretinemic Euthyroidal Hyperthyroxinemia [MESH:C567719] (136)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, papillary [MESH:C536915] (111) C20. Immune System Diseases  C20. Immune System Diseases  Immune System Diseases [MESH:D007154] (7674)   Graft vs Host Disease [MESH:D006086] (674)  Autoimmune Diseases [MESH:D001327] (5067)   Addison Disease [MESH:D000224] (40)  Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3601)  Diabetes Mellitus, Type 1 [MESH:D003922] (1893)  Glomerulonephritis, IGA [MESH:D005922] (897)  Hepatitis, Autoimmune [MESH:D019693] (1982)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Neuromyelitis Optica [MESH:D009471] (248)  Multiple Sclerosis [MESH:D009103] (1716)   Neuromyelitis Optica [MESH:D009471] (248)  Myelitis, Transverse [MESH:D009188] (255)   Neuromyelitis Optica [MESH:D009471] (248)  Nervous System Autoimmune Disease, Experimental [MESH:D020721] (810)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Graves Disease [MESH:D006111] (278)   Graves Ophthalmopathy [MESH:D049970] (165)  Polyendocrinopathies, Autoimmune [MESH:D016884] (40)   Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked [MESH:C562780] (31)  Hypersensitivity [MESH:D006967] (5873)   Drug Hypersensitivity [MESH:D004342] (4000)   Drug Eruptions [MESH:D003875] (2695)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Hypersensitivity, Delayed [MESH:D006968] (3408)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Hypersensitivity, Immediate [MESH:D006969] (4980)   Anaphylaxis [MESH:D000707] (299)  Dermatitis, Atopic [MESH:D003876] (2052)  Respiratory Hypersensitivity [MESH:D012130] (4250)   Asthma [MESH:D001249] (3914)  Urticaria [MESH:D014581] (2668)   Angioedema [MESH:D000799] (837)  Immunologic Deficiency Syndromes [MESH:D007153] (3788)   WHIM syndrome [MESH:C536697] (148)  Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked [MESH:C562780] (31)  MYD88 Deficiency [MESH:C567379] (79)  Leukocyte-Adhesion Deficiency Syndrome [MESH:D018370] (106)  Lymphopenia [MESH:D008231] (990)  Agammaglobulinemia [MESH:D000361] (156)   Severe combined immunodeficiency due to adenosine deaminase deficiency [MESH:C531816] (67)  HIV Infections [MESH:D015658] (3402)   Acquired Immunodeficiency Syndrome [MESH:D000163] (743)  HIV Wasting Syndrome [MESH:D019247] (1956)  AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Phagocyte Bactericidal Dysfunction [MESH:D010585] (999)   Job Syndrome [MESH:D007589] (772)  Granulomatous Disease, Chronic [MESH:D006105] (404)   Granulomatous Disease, Chronic, X-Linked [MESH:C564417] (111)  Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I [MESH:C565532] (142)  Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative [MESH:C565533] (111)  Severe Combined Immunodeficiency [MESH:D016511] (315)   Severe combined immunodeficiency due to adenosine deaminase deficiency [MESH:C531816] (67)  Bare lymphocyte syndrome 2 [MESH:C537079] (61)  Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell -Positive, NK Cell-Negative [MESH:C563440] (79)  Bare Lymphocyte Syndrome, Type I [MESH:C565759] (101)  X-Linked Combined Immunodeficiency Diseases [MESH:D053632] (42)  Immunoproliferative Disorders [MESH:D007160] (4761)   Lymphoproliferative Disorders [MESH:D008232] (4734)   Giant Lymph Node Hyperplasia [MESH:D005871] (1013)  Multiple Myeloma [MESH:D009101] (2767)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)  Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Lymphoma [MESH:D008223] (3684)   Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, Mantle-Cell [MESH:D020522] (561)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Paraproteinemias [MESH:D010265] (2791)   Multiple Myeloma [MESH:D009101] (2765) C22. Animal Diseases  C22. Animal Diseases  Animal Diseases [MESH:D000820] (3656)   Disease Models, Animal [MESH:D004195] (2058)  Mammary Neoplasms, Animal [MESH:D015674] (2735)  Paratuberculosis [MESH:D010283] (427)  Salmonella Infections, Animal [MESH:D012481] (604)  Cattle Diseases [MESH:D002418] (416)   Tuberculosis, Bovine [MESH:D014380] (380)  Sheep Diseases [MESH:D012757] (473)   Scrapie [MESH:D012608] (462) C23. Pathological Conditions, Signs and Symptoms  C23. Pathological Conditions, Signs and Symptoms  Pathological Conditions, Anatomical [MESH:D020763] (6074)   Ventricular Remodeling [MESH:D020257] (686)  Atrophy [MESH:D001284] (2603)   Muscular Atrophy [MESH:D009133] (1234)  Calculi [MESH:D002137] (756)   Urinary Calculi [MESH:D014545] (521)   Kidney Calculi [MESH:D007669] (455)  Hernia [MESH:D006547] (2825)   Hernia, Diaphragmatic [MESH:D006548] (2647)  Hypertrophy [MESH:D006984] (4476)   Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Splenomegaly [MESH:D013163] (1258)  Cardiomegaly [MESH:D006332] (3802)   Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Polyps [MESH:D011127] (1633)   Intestinal Polyps [MESH:D007417] (1592)   Colonic Polyps [MESH:D003111] (210)  Prolapse [MESH:D011391] (60)   Pelvic Organ Prolapse [MESH:D056887] (59)  Pathologic Processes [MESH:D010335] (9863)   Emphysema [MESH:D004646] (1096)  Gliosis [MESH:D005911] (1419)  Hyperbilirubinemia [MESH:D006932] (1860)  Hyperplasia [MESH:D006965] (2463)  Ischemia [MESH:D007511] (3049)  Leukocytosis [MESH:D007964] (978)  Necrosis [MESH:D009336] (4019)  Neointima [MESH:D058426] (814)  Nerve Degeneration [MESH:D009410] (4061)  Arrhythmias, Cardiac [MESH:D001145] (4658)   Atrial Fibrillation [MESH:D001281] (1053)  Bradycardia [MESH:D001919] (1899)  Tachycardia [MESH:D013610] (3339)  Long QT Syndrome [MESH:D008133] (691)   Long Qt Syndrome 11 [MESH:C567513] (48)  Chromosome Aberrations [MESH:D002869] (2352)   Chromosome Breakage [MESH:D019457] (139)  Micronuclei, Chromosome-Defective [MESH:D048629] (1013)  Translocation, Genetic [MESH:D014178] (557)  Aneuploidy [MESH:D000782] (1237)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  Death [MESH:D003643] (1328)   Death, Sudden [MESH:D003645] (725)  Fetal Death [MESH:D005313] (464)   Fetal Resorption [MESH:D005327] (302)  Disease Attributes [MESH:D020969] (3654)   Disease Progression [MESH:D018450] (2868)  Recurrence [MESH:D012008] (830)  Disease Susceptibility [MESH:D004198] (1200)   Genetic Predisposition to Disease [MESH:D020022] (966)  Facies [MESH:D019066] (738)   Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Fibrosis [MESH:D005355] (3133)   Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement [MESH:C567572] (70)  Nephrogenic Fibrosing Dermopathy [MESH:D054989] (452)  Peritoneal Fibrosis [MESH:D056627] (488)  Cicatrix [MESH:D002921] (1115)   Keloid [MESH:D007627] (1110)  Growth Disorders [MESH:D006130] (2438)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Meier-Gorlin syndrome [MESH:C538012] (133)  Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)  Fetal Growth Retardation [MESH:D005317] (986)  Hemorrhage [MESH:D006470] (4451)   Shock, Hemorrhagic [MESH:D012771] (2042)  Gastrointestinal Hemorrhage [MESH:D006471] (815)   Peptic Ulcer Hemorrhage [MESH:D010438] (553)  Intracranial Hemorrhages [MESH:D020300] (3241)   Cerebral Hemorrhage [MESH:D002543] (2872)  Subarachnoid Hemorrhage [MESH:D013345] (1081)  Purpura [MESH:D011693] (475)   Purpura, Thrombocytopenic [MESH:D011696] (237)   Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)  Inflammation [MESH:D007249] (5241)   Neurogenic Inflammation [MESH:D020078] (2246)  Systemic Inflammatory Response Syndrome [MESH:D018746] (3563)   Sepsis [MESH:D018805] (3562)   Shock, Septic [MESH:D012772] (1830)  Bacteremia [MESH:D016470] (1369)   Endotoxemia [MESH:D019446] (1289)  Menstruation Disturbances [MESH:D008599] (926)   Amenorrhea [MESH:D000568] (817)  Metaplasia [MESH:D008679] (1469)   Neovascularization, Pathologic [MESH:D009389] (829)   Choroidal Neovascularization [MESH:D020256] (550)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplasm Metastasis [MESH:D009362] (4441)   Lymphatic Metastasis [MESH:D008207] (917)  Postoperative Complications [MESH:D011183] (5311)   Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Shock [MESH:D012769] (2550)   Multiple Organ Failure [MESH:D009102] (1836)  Shock, Hemorrhagic [MESH:D012771] (2042)  Systemic Inflammatory Response Syndrome [MESH:D018746] (1832)   Shock, Septic [MESH:D012772] (1830)  Signs and Symptoms [MESH:D012816] (10659)   Chills [MESH:D023341] (644)  Cyanosis [MESH:D003490] (288)  Edema [MESH:D004487] (3726)  Body Temperature Changes [MESH:D001832] (3130)   Fever [MESH:D005334] (2856)  Hypothermia [MESH:D007035] (2075)  Body Weight [MESH:D001835] (4972)   Body Weight Changes [MESH:D001836] (3206)   Weight Gain [MESH:D015430] (2595)  Weight Loss [MESH:D015431] (2512)   Emaciation [MESH:D004614] (2285)   Cachexia [MESH:D002100] (2283)  Overweight [MESH:D050177] (4455)   Obesity [MESH:D009765] (4454)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Obesity, Morbid [MESH:D009767] (515)  Neurologic Manifestations [MESH:D009461] (8702)   Seizures [MESH:D012640] (4502)  Sleep Disorders [MESH:D012893] (1301)  Dyskinesias [MESH:D020820] (3285)   Catalepsy [MESH:D002375] (1429)  Dystonia [MESH:D004421] (848)  Hyperkinesis [MESH:D006948] (1799)  Ataxia [MESH:D001259] (984)   Arts syndrome [MESH:C535388] (31)  Neurobehavioral Manifestations [MESH:D019954] (4706)   Lethargy [MESH:D053609] (1035)  Psychomotor Disorders [MESH:D011596] (576)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Intellectual Disability [MESH:D008607] (1476)   Warburg Sjo Fledelius syndrome [MESH:C536681] (15)  Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Skeletal Defects, Genital Hypoplasia, And Mental Retardation [MESH:C567306] (52)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscular Atrophy [MESH:D009133] (1234)  Muscle Hypertonia [MESH:D009122] (775)   Muscle Spasticity [MESH:D009128] (187)   Spastic ataxia Charlevoix-Saguenay type [MESH:C536787] (37)  Pain [MESH:D010146] (3869)   Headache [MESH:D006261] (1417)  Neuralgia [MESH:D009437] (2074)  Paralysis [MESH:D010243] (2298)   Hemiplegia [MESH:D006429] (184)   Alternating hemiplegia of childhood [MESH:C536589] (70)  Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Sensation Disorders [MESH:D012678] (5009)   Hearing Disorders [MESH:D006311] (2101)   Hearing Loss [MESH:D034381] (2066)   Deafness [MESH:D003638] (593)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  Deaf-Blind Disorders [MESH:D054062] (52)   Arts syndrome [MESH:C535388] (31)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Deafness, X-Linked 1 [MESH:C564433] (31)  Deafness, Autosomal Recessive 53 [MESH:C566453] (16)  Bartter Syndrome, Type 4A [MESH:C566530] (27)  Deafness, Autosomal Dominant 13 [MESH:C566612] (16)  Bartter Syndrome, Type 4b [MESH:C567762] (14)  Hearing Loss, Central [MESH:D006313] (140)   Optic atrophy polyneuropathy deafness [MESH:C537129] (31)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Vision Disorders [MESH:D014786] (444)   Blindness [MESH:D001766] (178)   Deaf-Blind Disorders [MESH:D054062] (52)   Arts syndrome [MESH:C535388] (31)  Pain [MESH:D010146] (4511)   Headache [MESH:D006261] (1417)  Neuralgia [MESH:D009437] (2074)  Chest Pain [MESH:D002637] (2642)   Angina Pectoris [MESH:D000787] (2568)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Stable [MESH:D060050] (1702)  Signs and Symptoms, Digestive [MESH:D012817] (3095)   Hyperphagia [MESH:D006963] (206)  Nausea [MESH:D009325] (2300)  Vomiting [MESH:D014839] (1354)  Diarrhea [MESH:D003967] (858)   Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked [MESH:C562780] (31)  Signs and Symptoms, Respiratory [MESH:D012818] (2724)   Anoxia [MESH:D000860] (1698)  Hyperventilation [MESH:D006985] (652)  Respiratory Sounds [MESH:D012135] (713)  Hypoventilation [MESH:D007040] (359)   Congenital central hypoventilation syndrome [MESH:C536209] (341)  Skin Manifestations [MESH:D012877] (1250)   Livedo Reticularis [MESH:D054068] (228)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Purpura [MESH:D011693] (475)   Purpura, Thrombocytopenic [MESH:D011696] (237)   Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)  Urological Manifestations [MESH:D020924] (3532)   Lower Urinary Tract Symptoms [MESH:D059411] (612)   Urinary Bladder, Overactive [MESH:D053201] (530)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394) C24. Occupational Diseases  C24. Occupational Diseases  Occupational Diseases [MESH:D009784] (3402)   Dermatitis, Occupational [MESH:D009783] (311)  Pneumoconiosis [MESH:D011009] (2670)   Asbestosis [MESH:D001195] (935)  Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273) C25. Chemically-Induced Disorders  C25. Chemically-Induced Disorders  Drug-Related Side Effects and Adverse Reactions [MESH:D064420] (5839)   Drug-Induced Liver Injury [MESH:D056486] (4936)  Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Drug Hypersensitivity [MESH:D004342] (4001)   Drug Eruptions [MESH:D003875] (2697)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Poisoning [MESH:D011041] (6703)   Arsenic Poisoning [MESH:D020261] (2540)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Manganese Poisoning [MESH:D020149] (2214)  Neurotoxicity Syndromes [MESH:D020258] (3323)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Substance-Related Disorders [MESH:D019966] (6308)   Amphetamine-Related Disorders [MESH:D019969] (2858)  Cocaine-Related Disorders [MESH:D019970] (3054)  Drug Overdose [MESH:D062787] (513)  Substance Withdrawal Syndrome [MESH:D013375] (2956)  Tobacco Use Disorder [MESH:D014029] (628)  Alcohol-Related Disorders [MESH:D019973] (3869)   Alcoholism [MESH:D000437] (1519)  Alcohol-Induced Disorders [MESH:D020751] (3350)   Cardiomyopathy, Alcoholic [MESH:D002310] (354)  Liver Diseases, Alcoholic [MESH:D008108] (3243)   Hepatitis, Alcoholic [MESH:D006519] (1613)  Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Opioid-Related Disorders [MESH:D009293] (1491)   Heroin Dependence [MESH:D006556] (950)  Morphine Dependence [MESH:D009021] (855) C26. Wounds and Injuries  C26. Wounds and Injuries  Z. Exceptions (2454)   Not Fully Specified [NFS] (2454)  Wounds and Injuries [MESH:D014947] (5171)   Burns [MESH:D002056] (2565)  Vascular System Injuries [MESH:D057772] (2086)  Craniocerebral Trauma [MESH:D006259] (3523)   Brain Injuries [MESH:D001930] (3431)  Radiation Injuries [MESH:D011832] (2718)   Radiation Injuries, Experimental [MESH:D011833] (2662)  Spinal Cord Injuries [MESH:D013119] (2688)   Spinal Cord Compression [MESH:D013117] (1800)  Sprains and Strains [MESH:D013180] (153)   Cumulative Trauma Disorders [MESH:D012090] (151)   Carpal Tunnel Syndrome [MESH:D002349] (147)  Thoracic Injuries [MESH:D013898] (1831)   Lung Injury [MESH:D055370] (1814)  Trauma, Nervous System [MESH:D020196] (3535)   Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) D02. Organic Chemicals  D02. Organic Chemicals  Organic Chemicals [MESH:D009930] (75987)   Carboxylic Acids [MESH:D002264] (13103)   Acids, Carbocyclic [MESH:D000146] (5074)   Benzoates [MESH:D001565] (3081)  Hydrocarbons [MESH:D006838] (35762)   Hydrocarbons, Cyclic [MESH:D006844] (22983)   Hydrocarbons, Aromatic [MESH:D006841] (19108)   Benzene Derivatives [MESH:D001555] (10684)   Benzoates [MESH:D001565] (3081)  Polycyclic Hydrocarbons, Aromatic [MESH:D011084] (8627)   Naphthalenes [MESH:D009281] (3103)   Tetrahydronaphthalenes [MESH:D013764] (651) D04. Polycyclic Compounds  D04. Polycyclic Compounds  Polycyclic Compounds [MESH:D011083] (22048)   Polycyclic Hydrocarbons, Aromatic [MESH:D011084] (9200)   Naphthalenes [MESH:D009281] (3156)   Tetrahydronaphthalenes [MESH:D013764] (651) E. Analytical, Diagnostic and Therapeutic Techniques and Equipment  E. Analytical, Diagnostic and Therapeutic Techniques and Equipment  Diagnosis [MESH:D003933] (1924)   Diagnostic Techniques and Procedures [MESH:D019937] (1902)   Physical Examination [MESH:D010808] (1041)   Body Constitution [MESH:D001824] (450)   Body Weights and Measures [MESH:D001837] (448)   Body Size [MESH:D049628] (439)   Body Weight [MESH:D001835] (433)   Overweight [MESH:D050177] (428)   Obesity [MESH:D009765] (427)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Facies [MESH:D019066] (704)   Growth mental deficiency syndrome of Myhre [MESH:C537620] (51) F. Psychiatry and Psychology  F. Psychiatry and Psychology  Behavior and Behavior Mechanisms [MESH:D001520] (1594)   Neurobehavioral Manifestations [MESH:D019954] (1206)   Intellectual Disability [MESH:D008607] (1109)   Warburg Sjo Fledelius syndrome [MESH:C536681] (15)  Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Skeletal Defects, Genital Hypoplasia, And Mental Retardation [MESH:C567306] (52)  Mental Disorders [MESH:D001523] (2063)   Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98)  Delirium, Dementia, Amnestic, Cognitive Disorders [MESH:D019965] (487)   Cognition Disorders [MESH:D003072] (115)   Huntington Disease [MESH:D006816] (102)   Huntington Disease-Like 1 [MESH:C566398] (98)  Dementia [MESH:D003704] (471)   Huntington Disease [MESH:D006816] (102)   Huntington Disease-Like 1 [MESH:C566398] (98)  Mental Disorders Diagnosed in Childhood [MESH:D019952] (1245)   Intellectual Disability [MESH:D008607] (1109)   Warburg Sjo Fledelius syndrome [MESH:C536681] (15)  Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Skeletal Defects, Genital Hypoplasia, And Mental Retardation [MESH:C567306] (52)  Mood Disorders [MESH:D019964] (257)   Affective Disorders, Psychotic [MESH:D000341] (248)   Bipolar Disorder [MESH:D001714] (247)   Major Affective Disorder 1 [MESH:C565111] (237)  Major Affective Disorder 7 [MESH:C567529] (136) G. Phenomena and Processes  G. Phenomena and Processes  Genetic Phenomena [MESH:D055614] (1922)   Genetic Processes [MESH:D039361] (1336)   Mutagenesis [MESH:D016296] (1150)   Sequence Deletion [MESH:D017384] (1120)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  Genetic Structures [MESH:D040342] (1612)   Chromosomes [MESH:D002875] (1304)   Chromosomes, Mammalian [MESH:D033481] (1282)   Chromosomes, Human [MESH:D002877] (1280)   Chromosomes, Human, 4-5 [MESH:D002905] (149)   Chromosomes, Human, Pair 5 [MESH:D002895] (136)   5q- syndrome [MESH:C535323] (131)  Genetic Variation [MESH:D014644] (1337)   Mutation [MESH:D009154] (1327)   Allelic Imbalance [MESH:D022981] (1120)   Loss of Heterozygosity [MESH:D019656] (1119)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  Chromosome Aberrations [MESH:D002869] (1297)   Aneuploidy [MESH:D000782] (1220)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  Sequence Deletion [MESH:D017384] (1120)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  Ploidies [MESH:D011003] (1227)   Aneuploidy [MESH:D000782] (1220)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  Physiological Phenomena [MESH:D010829] (788)   Body Constitution [MESH:D001824] (453)   Body Weights and Measures [MESH:D001837] (444)   Body Size [MESH:D049628] (438)   Body Weight [MESH:D001835] (433)   Overweight [MESH:D050177] (428)   Obesity [MESH:D009765] (427)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)