Item 6 of 117 (back to results) previous next   terbufos C012568               MeSH Unique Identifier: C012568 Chemical – Gene Interaction Note 1: Terbufos results in increased methylation of MARC1 promoter Note 2: Terbufos results in increased methylation of A4GALT promoter Click here for more information

Current search: C11. Eye Diseases: Eye Diseases [MESH:D005128] > Eyelid Diseases [MESH:D005141] > Blepharoptosis [MESH:D001763] × Select any link to see items in a related category. more general categories    information about this item 1. Human Genes  1. Human Genes  Acetylcholine receptors, nicotinic [HGNC:CHRN] (130)   cholinergic receptor, nicotinic, alpha 3 (neuronal) [HGNC:CHRNA3] (31)  Actin related protein 2/3 complex subunits [HGNC:ARPC] (15)   actin related protein 2/3 complex, subunit 2, 34kDa [HGNC:ARPC2] (15)  ADAM metallopeptidases with thrombospondin type 1 motif [HGNC:ADAMTS] (53)   ADAM metallopeptidase with thrombospondin type 1 motif, 01 [HGNC:ADAMTS1] (34)  Adenylate kinases [HGNC:AK] (23)   adenylate kinase 5 [HGNC:AK5] (15)  ADP-ribosylation factor GTPase activating proteins [HGNC:ARFGAP] (20)   ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 [HGNC:ARAP3] (11)  Ankyrin repeat domain containing [HGNC:ANKRD] (566)   ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 [HGNC:ARAP3] (11)  B-cell scaffold protein with ankyrin repeats 1 [HGNC:BANK1] (7)  Armadillo repeat containing [HGNC:ARMC] (176)   catenin (cadherin-associated protein), delta 2 [HGNC:CTNND2] (18)  plakophilin 1 (ectodermal dysplasia/skin fragility syndrome) [HGNC:PKP1] (5)  Ataxins [HGNC:ATXN] (46)   ataxin 01 [HGNC:ATXN1] (21)  ATPases [HGNC:ATP] (106)   ATPases, P-type [HGNC:PATP] (43)   ATPase, class V, type 10A [HGNC:ATP10A] (6)  Basic helix-loop-helix [HGNC:BHLH] (618)   neurogenin 3 [HGNC:NEUROG3] (8)  transcription factor binding to IGHM enhancer 3 [HGNC:TFE3] (12)  twist basic helix-loop-helix transcription factor 1 [HGNC:TWIST1] (19)  v-myc avian myelocytomatosis viral oncogene homolog [HGNC:MYC] (254)  v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog [HGNC:MYCN] (29)  Basic leucine zipper proteins [HGNC:bZIP] (670)   FBJ murine osteosarcoma viral oncogene homolog [HGNC:FOS] (277)  jun proto-oncogene [HGNC:JUN] (290)  Blood group antigens [HGNC:blood-group] (97)   complement component (3b/4b) receptor 1 (Knops blood group) [HGNC:CR1] (11)  BRICHOS domain containing [HGNC:BRICD] (28)   surfactant protein C [HGNC:SFTPC] (9)  Cadherins [HGNC:CDH] (214)   Cadherins, major [HGNC:MCDH] (189)   desmocollin 1 [HGNC:DSC1] (12)  desmocollin 3 [HGNC:DSC3] (13)  Cadherins, related [HGNC:CDHR] (55)   cadherin-related family member 1 [HGNC:CDHR1] (4)  calsyntenin 2 [HGNC:CLSTN2] (4)  ret proto-oncogene [HGNC:RET] (37)  S100 calcium binding proteins [HGNC:S100] (110)   S100 calcium binding protein A04 [HGNC:S100A4] (35)  CD molecules [HGNC:CD] (1459)   CD226 molecule [HGNC:CD226] (6)  chemokine (C-C motif) receptor 08 [HGNC:CCR8] (11)  colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) [HGNC:CSF2RB] (11)  complement component (3b/4b) receptor 1 (Knops blood group) [HGNC:CR1] (11)  fms-related tyrosine kinase 3 [HGNC:FLT3] (23)  integrin, alpha 6 [HGNC:ITGA6] (39)  interleukin 01 receptor, type I [HGNC:IL1R1] (52)  leukocyte immunoglobulin-like receptor, subfamily A (with TM domain), member 4 [HGNC:LILRA4] (3)  leukocyte-associated immunoglobulin-like receptor 2 [HGNC:LAIR2] (12)  nerve growth factor receptor [HGNC:NGFR] (24)  neural cell adhesion molecule 1 [HGNC:NCAM1] (15)  poliovirus receptor-related 1 (herpesvirus entry mediator C) [HGNC:PVRL1] (8)  sphingosine-1-phosphate receptor 1 [HGNC:S1PR1] (16)  toll-like receptor 2 [HGNC:TLR2] (55)  Chemokine receptors [HGNC:CR] (207)   Chemokine (C-C motif) receptors [HGNC:CCR] (92)   chemokine (C-C motif) receptor 08 [HGNC:CCR8] (11)  Chloride channels [HGNC:CLCNS] (69)   Chloride intracellular channels [HGNC:CLIC] (39)   chloride intracellular channel 1 [HGNC:CLIC1] (21)  Cholinergic receptors [HGNC:CHR] (184)   cholinergic receptor, nicotinic, alpha 3 (neuronal) [HGNC:CHRNA3] (31)  Claudins [HGNC:CLDN] (76)   claudin 01 [HGNC:CLDN1] (34)  Collagens [HGNC:COL] (230)   collagen, type I, alpha 1 [HGNC:COL1A1] (123)  collagen, type IV, alpha 3 (Goodpasture antigen) [HGNC:COL4A3] (11)  collagen, type VI, alpha 3 [HGNC:COL6A3] (26)  Complement system [HGNC:complement-systems] (153)   complement component (3b/4b) receptor 1 (Knops blood group) [HGNC:CR1] (11)  Cytochrome P450s [HGNC:CYP] (1673)   cytochrome P450, family 26, subfamily A, polypeptide 01 [HGNC:CYP26A1] (32)  Dopamine receptors [HGNC:DRD] (106)   dopamine receptor D1 [HGNC:DRD1] (33)  EF-hand domain containing [HGNC:EFHAND] (226)   follistatin-like 1 [HGNC:FSTL1] (10)  plastin 3 [HGNC:PLS3] (15)  S100 calcium binding protein A04 [HGNC:S100A4] (35)  Endogenous Ligands [HGNC:ENDOLIG] (1191)   proenkephalin [HGNC:PENK] (9)  somatostatin [HGNC:SST] (17)  thyrotropin-releasing hormone [HGNC:TRH] (9)  EPH receptors [HGNC:EPH] (55)   EPH receptor A7 [HGNC:EPHA7] (13)  Fatty acid binding protein family [HGNC:FABP] (151)   cellular retinoic acid binding protein 1 [HGNC:CRABP1] (12)  fatty acid binding protein 5 (psoriasis-associated) [HGNC:FABP5] (29)  fatty acid binding protein 7, brain [HGNC:FABP7] (10)  retinol binding protein 1, cellular [HGNC:RBP1] (28)  Fibronectin type III domain containing [HGNC:FN3] (399)   colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) [HGNC:CSF2RB] (11)  deleted in colorectal carcinoma [HGNC:DCC] (13)  EPH receptor A7 [HGNC:EPHA7] (13)  Kallmann syndrome 1 sequence [HGNC:KAL1] (10)  neural cell adhesion molecule 1 [HGNC:NCAM1] (15)  protein tyrosine phosphatase, receptor type, F [HGNC:PTPRF] (20)  protein tyrosine phosphatase, receptor type, G [HGNC:PTPRG] (17)  protein tyrosine phosphatase, receptor type, K [HGNC:PTPRK] (24)  protein tyrosine phosphatase, receptor type, O [HGNC:PTPRO] (10)  roundabout, axon guidance receptor, homolog 4 (Drosophila) [HGNC:ROBO4] (9)  Fermitins [HGNC:FERMT] (27)   fermitin family member 1 [HGNC:FERMT1] (15)  Forkhead boxes [HGNC:FOX] (139)   forkhead box A1 [HGNC:FOXA1] (30)  forkhead box D3 [HGNC:FOXD3] (5)  forkhead box J1 [HGNC:FOXJ1] (14)  GABA receptors [HGNC:GABR] (118)   GABA(A) receptors [HGNC:GABRA] (105)   gamma-aminobutyric acid (GABA) A receptor, alpha 2 [HGNC:GABRA2] (28)  GATA zinc finger domain containing [HGNC:GATAD] (101)   GATA binding protein 4 [HGNC:GATA4] (13)  Gap junction proteins (connexins) [HGNC:GJ] (78)   gap junction protein, alpha 3, 46kDa [HGNC:GJA3] (5)  gap junction protein, alpha 4, 37kDa [HGNC:GJA4] (10)  gap junction protein, beta 2, 26kDa [HGNC:GJB2] (19)  gap junction protein, gamma 1, 45kDa [HGNC:GJC1] (14)  Glutamate receptors [HGNC:GR] (64)   Glutamate receptors, ionotropic [HGNC:GRI] (38)   glutamate receptor, ionotropic, AMPA 4 [HGNC:GRIA4] (4)  glutamate receptor, ionotropic, kainate 3 [HGNC:GRIK3] (5)  Glutamate receptors, metabotropic [HGNC:GRM] (33)   glutamate receptor, metabotropic 2 [HGNC:GRM2] (7)  glutamate receptor, metabotropic 7 [HGNC:GRM7] (6)  Glutathione S-transferases [HGNC:GST] (460)   Glutathione S-transferases, soluble [HGNC:SGST] (447)   glutathione S-transferase mu 5 [HGNC:GSTM5] (11)  Glycosyltransferase family 8 domain containing [HGNC:GLT8] (16)   like-glycosyltransferase [HGNC:LARGE] (9)  G protein-coupled receptors [HGNC:GPCR] (66)   GPCR class A, orphans [HGNC:GPCRAO] (30)   leucine-rich repeat containing G protein-coupled receptor 5 [HGNC:LGR5] (9)  Heat shock proteins [HGNC:HSP] (390)   Heat shock proteins, HSP70 [HGNC:HSP70] (294)   heat shock 70kDa protein 02 [HGNC:HSPA2] (39)  Histamine receptors [HGNC:HRH] (86)   histamine receptor H2 [HGNC:HRH2] (24)  Histocompatibility complex [HGNC:HLA] (108)   major histocompatibility complex, class II, DM alpha [HGNC:HLA-DMA] (15)  Homeoboxes [HGNC:homeobox] (219)   Homeoboxes, ANTP class [HGNC:HOXL] (152)   HOXL subclass homeoboxes [HGNC:HOXL] (95)   homeobox A02 [HGNC:HOXA2] (7)  homeobox A09 [HGNC:HOXA9] (12)  homeobox A13 [HGNC:HOXA13] (7)  pancreatic and duodenal homeobox 1 [HGNC:PDX1] (16)  NKL subclass homeoboxes [HGNC:NKL] (109)   distal-less homeobox 5 [HGNC:DLX5] (3)  Homeoboxes, LIM class [HGNC:LIM] (23)   LIM homeobox 1 [HGNC:LHX1] (6)  Homeoboxes, PRD class [HGNC:PRD] (60)   ALX homeobox 4 [HGNC:ALX4] (5)  paired box 7 [HGNC:PAX7] (9)  Homeoboxes, SINE class [HGNC:SINE] (20)   SIX homeobox 6 [HGNC:SIX6] (7)  Homeoboxes, TALE class [HGNC:TALE] (72)   iroquois homeobox 4 [HGNC:IRX4] (10)  Hydroxy-carboxylic acid receptors [HGNC:HCAR] (25)   hydroxycarboxylic acid receptor 3 [HGNC:HCAR3] (25)  Hypocretin (orexin) receptors [HGNC:HCRTR] (11)   hypocretin (orexin) receptor 1 [HGNC:HCRTR1] (8)  Immunoglobulin superfamily domain containing [HGNC:IGSF] (761)   V-set domain containing [HGNC:VSET] (188)   CD226 molecule [HGNC:CD226] (6)  junctional adhesion molecule 3 [HGNC:JAM3] (6)  poliovirus receptor-related 1 (herpesvirus entry mediator C) [HGNC:PVRL1] (8)  C1-set domain containing [HGNC:C1SET] (121)   major histocompatibility complex, class II, DM alpha [HGNC:HLA-DMA] (15)  C2-set domain containing [HGNC:C2SET] (225)   poliovirus receptor-related 1 (herpesvirus entry mediator C) [HGNC:PVRL1] (8)  I-set domain containing [HGNC:ISET] (447)   deleted in colorectal carcinoma [HGNC:DCC] (13)  fibroblast growth factor receptor-like 1 [HGNC:FGFRL1] (5)  interleukin 01 receptor, type I [HGNC:IL1R1] (52)  neural cell adhesion molecule 1 [HGNC:NCAM1] (15)  neuregulin 1 [HGNC:NRG1] (47)  neurotrophic tyrosine kinase, receptor, type 3 [HGNC:NTRK3] (16)  protein tyrosine phosphatase, receptor type, F [HGNC:PTPRF] (20)  roundabout, axon guidance receptor, homolog 4 (Drosophila) [HGNC:ROBO4] (9)  Immunoglobulin-like domain containing [HGNC:IGD] (645)   deleted in colorectal carcinoma [HGNC:DCC] (13)  fms-related tyrosine kinase 3 [HGNC:FLT3] (23)  interleukin 01 receptor, type I [HGNC:IL1R1] (52)  junctional adhesion molecule 3 [HGNC:JAM3] (6)  leukocyte immunoglobulin-like receptor, subfamily A (with TM domain), member 4 [HGNC:LILRA4] (3)  leukocyte-associated immunoglobulin-like receptor 2 [HGNC:LAIR2] (12)  poliovirus receptor-related 1 (herpesvirus entry mediator C) [HGNC:PVRL1] (8)  protein tyrosine phosphatase, receptor type, K [HGNC:PTPRK] (24)  Integrins [HGNC:ITG] (284)   integrin, alpha 6 [HGNC:ITGA6] (39)  Interleukins and interleukin receptors [HGNC:IL] (1294)   interleukin 01 receptor, type I [HGNC:IL1R1] (52)  interleukin 10 [HGNC:IL10] (187)  interleukin 17 receptor C [HGNC:IL17RC] (6)  Intermediate filaments [HGNC:IF] (273)   Type II. Keratins (basic) [HGNC:] (106)   keratin 04 [HGNC:KRT4] (9)  K-methyltransferases [HGNC:KMT] (101)   PR domain containing 02, with ZNF domain [HGNC:PRDM2] (21)  Kallikreins [HGNC:KLK] (65)   kallikrein-related peptidase 10 [HGNC:KLK10] (15)  Keratins [HGNC:KRT] (161)   keratin 04 [HGNC:KRT4] (9)  Laminins [HGNC:LAM] (93)   laminin, alpha 2 [HGNC:LAMA2] (11)  Leukocyte-associated Ig-like receptors [HGNC:LAIR] (12)   leukocyte-associated immunoglobulin-like receptor 2 [HGNC:LAIR2] (12)  Leukocyte immunoglobulin-like receptors [HGNC:LILR] (17)   leukocyte immunoglobulin-like receptor, subfamily A (with TM domain), member 4 [HGNC:LILRA4] (3)  Low density lipoprotein receptors [HGNC:LDLR] (71)   retinol binding protein 04, plasma [HGNC:RBP4] (17)  Lysophospholipid (LPA) receptors [HGNC:LPAR] (29)   lysophosphatidic acid receptor 1 [HGNC:LPAR1] (22)  Lysophospholipid (S1P) receptors [HGNC:S1PR] (18)   sphingosine-1-phosphate receptor 1 [HGNC:S1PR1] (16)  Melatonin receptors [HGNC:MTNR] (13)   melatonin receptor 1A [HGNC:MTNR1A] (12)  Metallothioneins [HGNC:MT] (183)   metallothionein 3 [HGNC:MT3] (42)  Netrins [HGNC:NTN] (13)   netrin G2 [HGNC:NTNG2] (9)  Neuropeptide receptors [HGNC:NPR] (30)   Neurotensin receptors [HGNC:NTSR] (8)   neurotensin receptor 1 (high affinity) [HGNC:NTSR1] (8)  Nuclear hormone receptors [HGNC:NR] (1322)   hepatocyte nuclear factor 4, alpha [HGNC:HNF4A] (35)  nuclear receptor subfamily 1, group I, member 2 [HGNC:NR1I2] (328)  nuclear receptor subfamily 2, group E, member 3 [HGNC:NR2E3] (4)  nuclear receptor subfamily 4, group A, member 1 [HGNC:NR4A1] (68)  retinoic acid receptor, alpha [HGNC:RARA] (73)  OTU domain containing [HGNC:OTUD] (88)   tumor necrosis factor, alpha-induced protein 3 [HGNC:TNFAIP3] (88)  Paired boxes [HGNC:PAX] (37)   paired box 7 [HGNC:PAX7] (9)  PHD-type zinc fingers [HGNC:PHF] (103)   SP140 nuclear body protein [HGNC:SP140] (5)  Pleckstrin homology (PH) domain containing [HGNC:PLEKH] (227)   ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 [HGNC:ARAP3] (11)  FERM, RhoGEF (ARHGEF) and pleckstrin domain protein 1 (chondrocyte-derived) [HGNC:FARP1] (20)  fermitin family member 1 [HGNC:FERMT1] (15)  growth factor receptor-bound protein 14 [HGNC:GRB14] (14)  myosin phosphatase Rho interacting protein [HGNC:MPRIP] (16)  Ras protein-specific guanine nucleotide-releasing factor 1 [HGNC:RASGRF1] (11)  spectrin, beta, non-erythrocytic 1 [HGNC:SPTBN1] (28)  Potassium channels [HGNC:KCN] (298)   potassium voltage-gated channel, Isk-related family, member 1 [HGNC:KCNE1] (19)  Potassium channels, two-P [HGNC:KCNK] (40)   potassium channel, subfamily K, member 09 [HGNC:KCNK9] (10)  Potassium channels, voltage-gated [HGNC:Kv] (224)   potassium voltage-gated channel, shaker-related subfamily, member 5 [HGNC:KCNA5] (20)  Prostanoid receptors [HGNC:PTGR] (95)   prostaglandin E receptor 2 (subtype EP2), 53kDa [HGNC:PTGER2] (29)  Protein phosphatase, catalytic and regulatory subunits [HGNC:PPP-PPM-CTD] (225)   Protein phosphatase 1, regulatory subunits [HGNC:PPP1R] (155)   HYDIN, axonemal central pair apparatus protein [HGNC:HYDIN] (5)  protein phosphatase 1, regulatory (inhibitor) subunit 01A [HGNC:PPP1R1A] (12)  Protein tyrosine phosphatases, including dual specificity phosphatases [HGNC:PTP] (254)   Protein tyrosine phosphatases, Asp-based [HGNC:PTPE] (15)   eyes absent homolog 4 (Drosophila) [HGNC:EYA4] (10)  Protein tyrosine phosphatases, Class I Cys-based [HGNC:PTPN] (252)   Class I Cys-based PTPs : Non-receptor [HGNC:PTPN] (75)   protein tyrosine phosphatase, non-receptor type 06 [HGNC:PTPN6] (20)  protein tyrosine phosphatase, non-receptor type 13 (APO-1/CD95 (Fas)-associated phosphatase) [HGNC:PTPN13] (22)  Class I Cys-based PTPs : Transmembrane receptor-like [HGNC:PTPR] (69)   protein tyrosine phosphatase, receptor type, F [HGNC:PTPRF] (20)  protein tyrosine phosphatase, receptor type, G [HGNC:PTPRG] (17)  protein tyrosine phosphatase, receptor type, K [HGNC:PTPRK] (24)  protein tyrosine phosphatase, receptor type, O [HGNC:PTPRO] (10)  Class I Cys-based PTPs : MAP kinase phosphatases [HGNC:DUSPT] (127)   dual specificity phosphatase 06 [HGNC:DUSP6] (50)  RAB, member RAS oncogene [HGNC:RAB] (69)   RAB08A, member RAS oncogene family [HGNC:RAB8A] (13)  Regulators of G-protein signaling [HGNC:RGS] (98)   regulator of G-protein signaling 17 [HGNC:RGS17] (12)  Rho GTPase activating proteins [HGNC:ARHGAP] (76)   Rho GTPase activating protein 29 [HGNC:ARHGAP29] (25)  Rho guanine nucleotide exchange factors [HGNC:ARHGEF] (105)   FERM, RhoGEF (ARHGEF) and pleckstrin domain protein 1 (chondrocyte-derived) [HGNC:FARP1] (20)  Ras protein-specific guanine nucleotide-releasing factor 1 [HGNC:RASGRF1] (11)  RNA binding motif containing [HGNC:RRM] (251)   deleted in azoospermia-like [HGNC:DAZL] (8)  L ribosomal proteins [HGNC:RPL] (79)   ribosomal protein L31 [HGNC:RPL31] (16)  Ryanodine receptors [HGNC:RYR] (25)   ryanodine receptor 2 (cardiac) [HGNC:RYR2] (10)  Sodium channels [HGNC:SC] (95)   Sodium channels, voltage-gated [HGNC:SCN] (71)   sodium channel, voltage-gated, type IX, alpha subunit [HGNC:SCN9A] (13)  Secreted frizzled-related proteins [HGNC:SFRP] (46)   secreted frizzled-related protein 2 [HGNC:SFRP2] (14)  secreted frizzled-related protein 4 [HGNC:SFRP4] (12)  Serine peptidases [HGNC:PRSS] (133)   Serine peptidases, serine peptidases [HGNC:TMPRSS] (86)   HtrA serine peptidase 1 [HGNC:HTRA1] (22)  mannan-binding lectin serine peptidase 1 (C4/C2 activating component of Ra-reactive factor) [HGNC:MASP1] (13)  protease, serine, 02 (trypsin 2) [HGNC:PRSS2] (11)  protease, serine, 03 [HGNC:PRSS3] (11)  Serine peptidases, transmembrane [HGNC:TMPRSS] (75)   suppression of tumorigenicity 14 (colon carcinoma) [HGNC:ST14] (10)  Serine/threonine phosphatases [HGNC:PPP-PPM-CTD] (43)   FERM, RhoGEF (ARHGEF) and pleckstrin domain protein 1 (chondrocyte-derived) [HGNC:FARP1] (20)  SH2 domain containing [HGNC:SH2D] (431)   growth factor receptor-bound protein 14 [HGNC:GRB14] (14)  phosphoinositide-3-kinase, regulatory subunit 1 (alpha) [HGNC:PIK3R1] (44)  protein tyrosine phosphatase, non-receptor type 06 [HGNC:PTPN6] (20)  suppressor of cytokine signaling 3 [HGNC:SOCS3] (46)  Short chain dehydrogenase/reductase superfamily [HGNC:SDR] (302)   Short chain dehydrogenase/reductase superfamily, Classical fold cluster 3 [HGNC:SDRC3] (75)   hydroxysteroid (17-beta) dehydrogenase 03 [HGNC:HSD17B3] (17)  Short chain dehydrogenase/reductase superfamily, Extended fold [HGNC:SDRE] (92)   hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 [HGNC:HSD3B7] (6)  Sialyltransferases [HGNC:ST3G] (32)   ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 5 [HGNC:ST6GALNAC5] (8)  Solute carriers [HGNC:SLC] (716)   solute carrier family 01 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1 [HGNC:SLC1A1] (24)  solute carrier family 06 (neurotransmitter transporter), member 02 [HGNC:SLC6A2] (29)  solute carrier family 06 (proline IMINO transporter), member 20 [HGNC:SLC6A20] (6)  solute carrier family 08 (sodium/calcium exchanger), member 3 [HGNC:SLC8A3] (6)  solute carrier family 22 (organic cation transporter), member 01 [HGNC:SLC22A1] (52)  solute carrier family 22 (organic cation transporter), member 03 [HGNC:SLC22A3] (71)  solute carrier family 34 (type II sodium/phosphate contransporter), member 2 [HGNC:SLC34A2] (6)  solute carrier organic anion transporter family, member 3A1 [HGNC:SLCO3A1] (15)  uncoupling protein 1 (mitochondrial, proton carrier) [HGNC:UCP1] (12)  Somatostatin receptors [HGNC:SSTR] (22)   somatostatin receptor 2 [HGNC:SSTR2] (13)  SRY (sex determining region Y)-boxes [HGNC:SOX] (95)   SRY (sex determining region Y)-box 02 [HGNC:SOX2] (19)  Sterile alpha motif (SAM) containing [HGNC:SAMD] (92)   ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 [HGNC:ARAP3] (11)  EPH receptor A7 [HGNC:EPHA7] (13)  Sulfotransferases, membrane-bound [HGNC:SULTM] (37)   heparan sulfate (glucosamine) 3-O-sulfotransferase 2 [HGNC:HS3ST2] (4)  Suppressors of cytokine signaling [HGNC:SOCS] (82)   suppressor of cytokine signaling 3 [HGNC:SOCS3] (46)  Tachykinin receptors [HGNC:TACR] (24)   tachykinin receptor 2 [HGNC:TACR2] (9)  T-boxes [HGNC:TBX] (49)   T-box 03 [HGNC:TBX3] (24)  T-box 05 [HGNC:TBX5] (4)  T-box 19 [HGNC:TBX19] (6)  T-box 20 [HGNC:TBX20] (3)  Tumor necrosis factor receptor superfamily [HGNC:TNFRSF] (295)   nerve growth factor receptor [HGNC:NGFR] (24)  tumor necrosis factor receptor superfamily, member 11b [HGNC:TNFRSF11B] (63)  Ubiquitin-conjugating enzymes E2 [HGNC:UBE2] (97)   ubiquitin-conjugating enzyme E2L 6 [HGNC:UBE2L6] (16)  Voltage-gated ion channels [HGNC:VGIC] (79)   Sodium channels, voltage-gated [HGNC:SCN] (71)   sodium channel, voltage-gated, type IX, alpha subunit [HGNC:SCN9A] (13)  WD repeat domain containing [HGNC:WDR] (199)   transducin-like enhancer of split 4 (E(sp1) homolog, Drosophila) [HGNC:TLE4] (16)  WAP four-disulfide core domain containing [HGNC:WFDC] (26)   Kallmann syndrome 1 sequence [HGNC:KAL1] (10)  ZINC FINGERS [HGNC:ZNF] (383)   Zinc fingers, C2H2-type [HGNC:ZNF] (349)   PR domain containing 14 [HGNC:PRDM14] (5)  PR domain containing 16 [HGNC:PRDM16] (8)  sal-like 1 (Drosophila) [HGNC:SALL1] (15)  Zic family member 3 [HGNC:ZIC3] (6)  zinc finger protein 023 [HGNC:ZNF23] (6)  zinc finger protein 365 [HGNC:ZNF365] (6)  Zinc fingers, C2H2-type with KRAB domain [HGNC:ZKRAB] (42)   zinc finger protein 559 [HGNC:ZNF559] (11) 2. Interaction: Human Genes and Chemicals  2. Interaction: Human Genes and Chemicals  Affects (3990)   binding (2423)  Decreases (5154)   methylation (108)  Increases (5571)   activity (2865)  expression (3238)  methylation (105) A. Anatomy  A. Anatomy  Body Regions [MESH:D001829] (867)   Extremities [MESH:D005121] (484)   Lower Extremity [MESH:D035002] (139)   Foot [MESH:D005528] (125)   Forefoot, Human [MESH:D005545] (118)   Toes [MESH:D014034] (115)   Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Upper Extremity [MESH:D034941] (441)   Hand [MESH:D006225] (428)   Fingers [MESH:D005385] (422)   Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Thumb [MESH:D013933] (54)   Townes-Brocks syndrome [MESH:C536974] (28)  Head [MESH:D006257] (523)   Ear [MESH:D004423] (236)   Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Face [MESH:D005145] (387)   Eye [MESH:D005123] (148)   Eyelids [MESH:D005143] (143)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Saethre-Chotzen Syndrome with Eyelid Anomalies [MESH:C566325] (42)  Musculoskeletal System [MESH:D009141] (1255)   Muscles [MESH:D009132] (97)   Muscle, Skeletal [MESH:D018482] (86)   Abdominal Muscles [MESH:D000009] (49)   Carnevale syndrome [MESH:C535586] (45)  Skeleton [MESH:D012863] (1177)   Bone and Bones [MESH:D001842] (1112)   Bones of Upper Extremity [MESH:D001133] (240)   Arm Bones [MESH:D050280] (183)   Ulna [MESH:D014457] (96)   Ulnar-mammary syndrome [MESH:C536937] (57)  Digestive System [MESH:D004064] (421)   Gastrointestinal Tract [MESH:D041981] (364)   Intestines [MESH:D007422] (271)   Intestine, Large [MESH:D007420] (247)   Rectum [MESH:D012007] (69)   Paroxysmal Extreme Pain Disorder [MESH:C563475] (27)  Lower Gastrointestinal Tract [MESH:D041741] (254)   Intestine, Large [MESH:D007420] (247)   Rectum [MESH:D012007] (69)   Paroxysmal Extreme Pain Disorder [MESH:C563475] (27)  Pancreas [MESH:D010179] (61)   Pancreatic Agenesis, Congenital [MESH:C564908] (44)  Urogenital System [MESH:D014566] (986)   Urinary Tract [MESH:D014551] (721)   Kidney [MESH:D007668] (707)   Hereditary renal agenesis [MESH:C536482] (89)  Endocrine System [MESH:D004703] (206)   Endocrine Glands [MESH:D004702] (193)   Thyroid Gland [MESH:D013961] (53)   Thyroid Dyshormonogenesis 5 [MESH:C562771] (7)  Sense Organs [MESH:D012679] (1060)   Ear [MESH:D004423] (323)   Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Eye [MESH:D005123] (858)   Eyelids [MESH:D005143] (146)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Saethre-Chotzen Syndrome with Eyelid Anomalies [MESH:C566325] (42) C01. Bacterial Infections and Mycoses  C01. Bacterial Infections and Mycoses  Bacterial Infections [MESH:D001424] (3716)   Gram-Positive Bacterial Infections [MESH:D016908] (2434)   Actinomycetales Infections [MESH:D000193] (1466)   Mycobacterium Infections [MESH:D009164] (1446)   Leprosy [MESH:D007918] (261)  Skin Diseases, Bacterial [MESH:D017192] (157)   Hidradenitis Suppurativa [MESH:D017497] (120)  Infection [MESH:D007239] (4109)   Sepsis [MESH:D018805] (3556)  Intraabdominal Infections [MESH:D059413] (958)   Appendicitis [MESH:D001064] (774)  Skin Diseases, Infectious [MESH:D012874] (415)   Cellulitis [MESH:D002481] (87)  Skin Diseases, Bacterial [MESH:D017192] (156)   Hidradenitis Suppurativa [MESH:D017497] (120)  Suppuration [MESH:D013492] (219)   Cellulitis [MESH:D002481] (87)  Hidradenitis Suppurativa [MESH:D017497] (120)  Mycoses [MESH:D009181] (385)   Candidiasis [MESH:D002177] (307)   Candidiasis, Oral [MESH:D002180] (77)  Candidiasis, Vulvovaginal [MESH:D002181] (76) C02. Virus Diseases  C02. Virus Diseases  Virus Diseases [MESH:D014777] (4544)   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)   Epstein-Barr Virus Infections [MESH:D020031] (695)   Burkitt Lymphoma [MESH:D002051] (691)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis B [MESH:D006509] (976)   Hepatitis B, Chronic [MESH:D019694] (277)  RNA Virus Infections [MESH:D012327] (4215)   Orthomyxoviridae Infections [MESH:D009976] (1077)   Influenza, Human [MESH:D007251] (1075)  Picornaviridae Infections [MESH:D010850] (1672)   Enterovirus Infections [MESH:D004769] (241)   Coxsackievirus Infections [MESH:D003384] (194)  Retroviridae Infections [MESH:D012192] (3420)   Lentivirus Infections [MESH:D016180] (3408)   HIV Infections [MESH:D015658] (3402)  Sexually Transmitted Diseases [MESH:D012749] (3305)   Sexually Transmitted Diseases, Viral [MESH:D015229] (3304)   HIV Infections [MESH:D015658] (3296)  Tumor Virus Infections [MESH:D014412] (1069)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691) C03. Parasitic Diseases  C03. Parasitic Diseases  Parasitic Diseases [MESH:D010272] (3828)   Protozoan Infections [MESH:D011528] (3014)   Amebiasis [MESH:D000562] (1711)   Entamoebiasis [MESH:D004749] (1689)  Euglenozoa Infections [MESH:D056986] (2552)   Leishmaniasis [MESH:D007896] (2541)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)  Leishmaniasis, Visceral [MESH:D007898] (2149)  Malaria [MESH:D008288] (2175)   Malaria, Falciparum [MESH:D016778] (438)  Skin Diseases, Parasitic [MESH:D012876] (2541)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359) C04. Neoplasms  C04. Neoplasms  Neoplasms [MESH:D009369] (10293)   Neoplasms, Second Primary [MESH:D016609] (518)  Precancerous Conditions [MESH:D011230] (2858)  Cysts [MESH:D003560] (2625)   Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Neoplasms by Histologic Type [MESH:D009370] (8793)   Leukemia [MESH:D007938] (4576)   Leukemia, Lymphoid [MESH:D007945] (3047)   Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)  Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Leukemia, Myeloid [MESH:D007951] (2773)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Leukemia, Myeloid, Acute [MESH:D015470] (2176)   Leukemia, Promyelocytic, Acute [MESH:D015473] (1367)  Lymphoma [MESH:D008223] (3686)   Lymphoma, Non-Hodgkin [MESH:D008228] (3337)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  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)  Lymphoma, T-Cell [MESH:D016399] (1405)   Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Neoplasms, Complex and Mixed [MESH:D018193] (1121)   Wilms Tumor [MESH:D009396] (553)  Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742)   Neoplasms, Connective Tissue [MESH:D009372] (3626)   Neoplasms, Bone Tissue [MESH:D018213] (2217)   Osteosarcoma [MESH:D012516] (2175)  Neoplasms, Muscle Tissue [MESH:D009379] (1965)   Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)   Rhabdomyosarcoma, Alveolar [MESH:D018232] (149)  Sarcoma [MESH:D012509] (4246)   Hemangiosarcoma [MESH:D006394] (1836)  Osteosarcoma [MESH:D012516] (2175)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)   Rhabdomyosarcoma, Alveolar [MESH:D018232] (149)  Neoplasms, Germ Cell and Embryonal [MESH:D009373] (5126)   Testicular Germ Cell Tumor [MESH:C563236] (176)  Neuroectodermal Tumors [MESH:D017599] (5066)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   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)   Melanoma [MESH:D008545] (3508)  Carcinoma, Neuroendocrine [MESH:D018278] (262)   Vipoma [MESH:D003969] (110)  Carcinoma, Medullary [MESH:D018276] (181)   Familial medullary thyroid carcinoma [MESH:C536911] (101)  Paraganglioma [MESH:D010235] (297)   Pheochromocytoma [MESH:D010673] (275)  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)  Carcinoma [MESH:D002277] (7263)   Carcinoma, Basal Cell [MESH:D002280] (1628)  Carcinoma, Large Cell [MESH:D018287] (211)  Carcinoma, Small Cell [MESH:D018288] (1317)  Carcinoma, Transitional Cell [MESH:D002295] (2662)  Adenocarcinoma [MESH:D000230] (6565)   Adenocarcinoma of lung [MESH:C538231] (1487)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Adrenocortical Carcinoma [MESH:D018268] (821)  Carcinoma, Adenoid Cystic [MESH:D003528] (1561)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Carcinoma, Neuroendocrine [MESH:D018278] (262)   Vipoma [MESH:D003969] (110)  Carcinoma, Medullary [MESH:D018276] (181)   Familial medullary thyroid carcinoma [MESH:C536911] (101)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  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)   Familial medullary thyroid carcinoma [MESH:C536911] (101)  Neoplasms, Mesothelial [MESH:D018301] (2569)   Mesothelioma [MESH:D008654] (2567)  Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   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)   Carcinoma, Squamous Cell [MESH:D002294] (4294)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Neoplasms, Nerve Tissue [MESH:D009380] (5201)   Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  Neuroectodermal Tumors [MESH:D017599] (5059)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   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)   Melanoma [MESH:D008545] (3508)  Carcinoma, Neuroendocrine [MESH:D018278] (184)   Carcinoma, Medullary [MESH:D018276] (181)   Familial medullary thyroid carcinoma [MESH:C536911] (101)  Paraganglioma [MESH:D010235] (297)   Pheochromocytoma [MESH:D010673] (275)  Neoplasms, Plasma Cell [MESH:D054219] (2772)   Multiple Myeloma [MESH:D009101] (2767)  Neoplasms, Vascular Tissue [MESH:D009383] (2959)   Hemangiosarcoma [MESH:D006394] (1836)  Hemangioma [MESH:D006391] (690)   Hemangioma, Capillary [MESH:D018324] (503)   Hemangioma, capillary infantile [MESH:C535860] (190)  Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  Nevi and Melanomas [MESH:D018326] (3572)   Melanoma [MESH:D008545] (3508)  Neoplasms by Site [MESH:D009371] (9169)   Bone Neoplasms [MESH:D001859] (1334)  Skin Neoplasms [MESH:D012878] (2992)  Breast Neoplasms [MESH:D001943] (6077)   Inflammatory Breast Neoplasms [MESH:D058922] (43)  Digestive System Neoplasms [MESH:D004067] (7487)   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)   Colorectal Neoplasms [MESH:D015179] (5294)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Islet Cell [MESH:D018273] (115)   Vipoma [MESH:D003969] (110)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Adrenal Gland Neoplasms [MESH:D000310] (917)   Adrenal Cortex Neoplasms [MESH:D000306] (823)   Adrenocortical Carcinoma [MESH:D018268] (821)  Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia Type 2b [MESH:D018814] (75)  Multiple Endocrine Neoplasia Type 2a [MESH:D018813] (102)   Familial medullary thyroid carcinoma [MESH:C536911] (101)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Islet Cell [MESH:D018273] (115)   Vipoma [MESH:D003969] (110)  Testicular Neoplasms [MESH:D013736] (520)   Testicular Germ Cell Tumor [MESH:C563236] (176)  Thyroid Neoplasms [MESH:D013964] (2040)   Familial medullary thyroid carcinoma [MESH:C536911] (101)  Thyroid cancer, medullary [MESH:C536914] (74)  Head and Neck Neoplasms [MESH:D006258] (4612)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  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)   Familial medullary thyroid carcinoma [MESH:C536911] (101)  Thyroid cancer, medullary [MESH:C536914] (74)  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)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  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)  Testicular Neoplasms [MESH:D013736] (520)   Testicular Germ Cell Tumor [MESH:C563236] (176)  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)  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)   Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia Type 2b [MESH:D018814] (75)  Multiple Endocrine Neoplasia Type 2a [MESH:D018813] (102)   Familial medullary thyroid carcinoma [MESH:C536911] (101)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Metastasis [MESH:D009362] (4441)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Hemangioma, capillary infantile [MESH:C535860] (190)  Meningioma, familial [MESH:C537443] (195)  Adenomatous Polyposis Coli [MESH:D011125] (1565)  Wilms Tumor [MESH:D009396] (553)  Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia Type 2b [MESH:D018814] (75)  Multiple Endocrine Neoplasia Type 2a [MESH:D018813] (102)   Familial medullary thyroid carcinoma [MESH:C536911] (101)  Tumor Virus Infections [MESH:D014412] (759)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691) C05. Musculoskeletal Diseases  C05. Musculoskeletal Diseases  Musculoskeletal Diseases [MESH:D009140] (8705)   Cartilage Diseases [MESH:D002357] (438)  Bone Diseases [MESH:D001847] (5801)   Bone Neoplasms [MESH:D001859] (1334)  Bone Diseases, Developmental [MESH:D001848] (3315)   Dysostoses [MESH:D004413] (1019)   Synostosis [MESH:D013580] (817)   Craniosynostoses [MESH:D003398] (438)   Oculopalatoskeletal syndrome [MESH:C537738] (45)  Acrocephalosyndactylia [MESH:D000168] (201)   Saethre-Chotzen Syndrome with Eyelid Anomalies [MESH:C566325] (42)  Syndactyly [MESH:D013576] (487)   Zlotogora-Ogur syndrome [MESH:C536726] (25)  Sclerosteosis [MESH:C537525] (17)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Acrocephalosyndactylia [MESH:D000168] (201)   Saethre-Chotzen Syndrome with Eyelid Anomalies [MESH:C566325] (42)  Osteochondrodysplasias [MESH:D010009] (2440)   Epiphyseal dysplasia, multiple, 5 [MESH:C535505] (18)  Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related [MESH:C563869] (18)  Fibrous Dysplasia of Bone [MESH:D005357] (737)  Hyperostosis, Cortical, Congenital [MESH:D006958] (392)  Osteogenesis Imperfecta [MESH:D010013] (481)   Osteogenesis imperfecta, type 2A [MESH:C536042] (375)  Osteogenesis imperfecta, type 3 [MESH:C536044] (375)  Osteogenesis imperfecta, type 4 [MESH:C536045] (375)  Bruck syndrome 2 [MESH:C537407] (64)  Bone Diseases, Metabolic [MESH:D001851] (3492)   Osteoporosis [MESH:D010024] (3037)  Bone Resorption [MESH:D001862] (2352)   Osteolysis [MESH:D010014] (1787)  Hyperostosis [MESH:D015576] (493)   Sclerosteosis [MESH:C537525] (17)  Hyperostosis, Cortical, Congenital [MESH:D006958] (392)  Spinal Diseases [MESH:D013122] (2485)   Spondylitis [MESH:D013166] (1924)   Spondylarthritis [MESH:D025241] (1912)   Spondylarthropathies [MESH:D025242] (1909)   Spondylitis, Ankylosing [MESH:D013167] (431)  Foot Deformities [MESH:D005530] (553)   Foot Deformities, Congenital [MESH:D005532] (538)   Hand foot uterus syndrome [MESH:C535627] (20)  Hand Deformities [MESH:D006226] (590)   Hand Deformities, Congenital [MESH:D006228] (587)   Hand foot uterus syndrome [MESH:C535627] (20)  Vohwinkel syndrome [MESH:C536457] (68)  Jaw Diseases [MESH:D007571] (1601)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Zlotogora-Ogur syndrome [MESH:C536726] (25)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Joint Diseases [MESH:D007592] (4657)   Ankylosis [MESH:D000844] (479)   Spondylitis, Ankylosing [MESH:D013167] (431)  Arthritis [MESH:D001168] (4416)   Arthritis, Experimental [MESH:D001169] (3142)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Osteoarthritis [MESH:D010003] (1743)  Spondylarthritis [MESH:D025241] (1912)   Spondylarthropathies [MESH:D025242] (1909)   Spondylitis, Ankylosing [MESH:D013167] (431)  Arthrogryposis [MESH:D001176] (329)   Bruck syndrome 2 [MESH:C537407] (64)  Arthropathy, Neurogenic [MESH:D001177] (30)   Arthropathy, progressive pseudorheumatoid, of childhood [MESH:C535387] (8)  Contracture [MESH:D003286] (296)   Bethlem myopathy [MESH:C535436] (108)  Muscular Diseases [MESH:D009135] (4071)   Arthrogryposis [MESH:D001176] (329)   Bruck syndrome 2 [MESH:C537407] (64)  Contracture [MESH:D003286] (303)   Bethlem myopathy [MESH:C535436] (108)  Muscular Disorders, Atrophic [MESH:D020966] (1598)   Muscular Dystrophies [MESH:D009136] (1593)   Bethlem myopathy [MESH:C535436] (108)  Muscular dystrophy congenital, merosin negative [MESH:C537384] (34)  Scleroatonic muscular dystrophy [MESH:C537521] (108)  Muscular Dystrophies, Limb-Girdle [MESH:D049288] (259)   Sarcoglycanopathies [MESH:D058088] (49)   Limb-girdle muscular dystrophy, type 2C [MESH:C535900] (20)  Musculoskeletal Abnormalities [MESH:D009139] (3796)   Arthrogryposis [MESH:D001176] (329)   Bruck syndrome 2 [MESH:C537407] (64)  Craniofacial Abnormalities [MESH:D019465] (3098)   Malpuech facial clefting syndrome [MESH:C535704] (45)  LIG4 Syndrome [MESH:C564694] (24)  Birk-Barel Mental Retardation Dysmorphism Syndrome [MESH:C567357] (20)  Silver-Russell Syndrome [MESH:D056730] (142)  Craniosynostoses [MESH:D003398] (438)   Oculopalatoskeletal syndrome [MESH:C537738] (45)  Acrocephalosyndactylia [MESH:D000168] (201)   Saethre-Chotzen Syndrome with Eyelid Anomalies [MESH:C566325] (42)  Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Zlotogora-Ogur syndrome [MESH:C536726] (25)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Microcephaly [MESH:D008831] (700)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Plagiocephaly [MESH:D059041] (440)   Craniosynostoses [MESH:D003398] (438)   Oculopalatoskeletal syndrome [MESH:C537738] (45)  Acrocephalosyndactylia [MESH:D000168] (201)   Saethre-Chotzen Syndrome with Eyelid Anomalies [MESH:C566325] (42)  Hip Dislocation, Congenital [MESH:D006618] (56)   Carnevale syndrome [MESH:C535586] (45)  Limb Deformities, Congenital [MESH:D017880] (1813)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Lower Extremity Deformities, Congenital [MESH:D038061] (560)   Holt-Oram syndrome [MESH:C535326] (11)  Foot Deformities, Congenital [MESH:D005532] (538)   Hand foot uterus syndrome [MESH:C535627] (20)  Polydactyly [MESH:D017689] (318)   Preaxial deficiency, postaxial polydactyly and hypospadias [MESH:C538278] (20)  Syndactyly [MESH:D013576] (487)   Zlotogora-Ogur syndrome [MESH:C536726] (25)  Sclerosteosis [MESH:C537525] (17)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Acrocephalosyndactylia [MESH:D000168] (201)   Saethre-Chotzen Syndrome with Eyelid Anomalies [MESH:C566325] (42)  Upper Extremity Deformities, Congenital [MESH:D038062] (604)   Holt-Oram syndrome [MESH:C535326] (11)  Hand Deformities, Congenital [MESH:D006228] (587)   Hand foot uterus syndrome [MESH:C535627] (20)  Vohwinkel syndrome [MESH:C536457] (68)  Synostosis [MESH:D013580] (817)   Craniosynostoses [MESH:D003398] (438)   Oculopalatoskeletal syndrome [MESH:C537738] (45)  Acrocephalosyndactylia [MESH:D000168] (201)   Saethre-Chotzen Syndrome with Eyelid Anomalies [MESH:C566325] (42)  Syndactyly [MESH:D013576] (487)   Zlotogora-Ogur syndrome [MESH:C536726] (25)  Sclerosteosis [MESH:C537525] (17)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Acrocephalosyndactylia [MESH:D000168] (201)   Saethre-Chotzen Syndrome with Eyelid Anomalies [MESH:C566325] (42)  Rheumatic Diseases [MESH:D012216] (4032)   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)   Bile acid synthesis defect, congenital, 1 [MESH:C535442] (25)  Cholangitis [MESH:D002761] (203)   Cholangitis, Sclerosing [MESH:D015209] (93)   Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis [MESH:C564365] (78)  Digestive System Abnormalities [MESH:D004065] (2127)   Barrett Esophagus [MESH:D001471] (1930)  Hirschsprung Disease [MESH:D006627] (361)  Anus, Imperforate [MESH:D001006] (140)   Townes-Brocks syndrome [MESH:C536974] (28)  Esophageal Atresia [MESH:D004933] (47)   Microphthalmia, Syndromic 3 [MESH:C565948] (43)  Digestive System Fistula [MESH:D016154] (102)   Esophageal Fistula [MESH:D004937] (89)   Tracheoesophageal Fistula [MESH:D014138] (88)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Digestive System Neoplasms [MESH:D004067] (7493)   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)   Colorectal Neoplasms [MESH:D015179] (5294)   Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Islet Cell [MESH:D018273] (115)   Vipoma [MESH:D003969] (110)  Gastrointestinal Diseases [MESH:D005767] (7443)   Gastrointestinal Hemorrhage [MESH:D006471] (815)  Esophageal Diseases [MESH:D004935] (4255)   Barrett Esophagus [MESH:D001471] (1930)  Deglutition Disorders [MESH:D003680] (1538)  Esophageal and Gastric Varices [MESH:D004932] (83)  Esophageal Atresia [MESH:D004933] (47)   Microphthalmia, Syndromic 3 [MESH:C565948] (43)  Esophageal Fistula [MESH:D004937] (89)   Tracheoesophageal Fistula [MESH:D014138] (88)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  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)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Colitis, Ulcerative [MESH:D003093] (2601)  Crohn Disease [MESH:D003424] (2585)  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)   Colorectal Neoplasms [MESH:D015179] (5294)   Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Intestinal Diseases [MESH:D007410] (6206)   Cecal Diseases [MESH:D002429] (1330)   Appendicitis [MESH:D001064] (774)  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)   Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Megacolon [MESH:D008531] (386)   Hirschsprung Disease [MESH:D006627] (361)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Colitis, Ulcerative [MESH:D003093] (2601)  Crohn Disease [MESH:D003424] (2585)  Intestinal Neoplasms [MESH:D007414] (5359)   Colorectal Neoplasms [MESH:D015179] (5294)   Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Intestinal Polyposis [MESH:D044483] (1610)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Malabsorption Syndromes [MESH:D008286] (492)   Diarrhea 4, Malabsorptive, Congenital [MESH:C563673] (15)  Celiac Disease [MESH:D002446] (340)  Rectal Diseases [MESH:D012002] (4596)   Colorectal Neoplasms [MESH:D015179] (4534)  Peptic Ulcer [MESH:D010437] (3172)   Stomach Ulcer [MESH:D013276] (2915)  Stomach Diseases [MESH:D013272] (5325)   Stomach Neoplasms [MESH:D013274] (4942)  Peptic Ulcer [MESH:D010437] (2994)   Stomach Ulcer [MESH:D013276] (2915)  Liver Diseases [MESH:D008107] (8167)   Drug-Induced Liver Injury [MESH:D056486] (4936)  Fatty Liver [MESH:D005234] (3584)  Liver Diseases, Alcoholic [MESH:D008108] (3243)  Hepatitis [MESH:D006505] (3883)   Hepatitis, Animal [MESH:D006520] (260)  Hepatitis, Chronic [MESH:D006521] (2071)   Hepatitis, Autoimmune [MESH:D019693] (1982)  Hepatitis B, Chronic [MESH:D019694] (277)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis B [MESH:D006509] (976)   Hepatitis B, Chronic [MESH:D019694] (277)  Hypertension, Portal [MESH:D006975] (869)   Esophageal and Gastric Varices [MESH:D004932] (83)  Liver Cirrhosis [MESH:D008103] (5542)   Liver Cirrhosis, Experimental [MESH:D008106] (4589)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Diseases [MESH:D010182] (4453)   Pancreatic Agenesis, Congenital [MESH:C564908] (44)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Islet Cell [MESH:D018273] (115)   Vipoma [MESH:D003969] (110)  Pancreatitis [MESH:D010195] (1924)   Pancreatitis, Chronic [MESH:D050500] (276) 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)   Zlotogora-Ogur syndrome [MESH:C536726] (25)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Mouth Diseases [MESH:D009059] (4783)   Behcet Syndrome [MESH:D001528] (1784)  Candidiasis, Oral [MESH:D002180] (77)  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)   Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Cleft Palate [MESH:D002972] (1330)   Zlotogora-Ogur syndrome [MESH:C536726] (25)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Mouth Neoplasms [MESH:D009062] (2263)   Salivary Gland Neoplasms [MESH:D012468] (968)  Periodontal Diseases [MESH:D010510] (1001)   Poikiloderma of Kindler [MESH:C536321] (64)  Salivary Gland Diseases [MESH:D012466] (1213)   Salivary Gland Neoplasms [MESH:D012468] (968)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Zlotogora-Ogur syndrome [MESH:C536726] (25)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Cleft Palate [MESH:D002972] (1330)   Zlotogora-Ogur syndrome [MESH:C536726] (25)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Tooth Abnormalities [MESH:D014071] (622)   Nance-Horan syndrome [MESH:C538336] (17)  Tooth Diseases [MESH:D014076] (742)   Tooth Abnormalities [MESH:D014071] (622)   Nance-Horan syndrome [MESH:C538336] (17) C08. Respiratory Tract Diseases  C08. Respiratory Tract Diseases  Z. Exceptions (1984)   Not Fully Specified [NFS] (1984)  Respiratory Tract Diseases [MESH:D012140] (7881)   Thoracic Diseases [MESH:D013896] (81)  Bronchial Diseases [MESH:D001982] (4382)   Asthma [MESH:D001249] (4098)   Asthma, Aspirin-Induced [MESH:D055963] (1055)   Asthma, Nasal Polyps, And Aspirin Intolerance [MESH:C565935] (80)  Lung Diseases [MESH:D008171] (7249)   Pulmonary Alveolar Microlithiasis [MESH:C562405] (44)  Plasma Cell Granuloma, Pulmonary [MESH:D016726] (63)  Pneumonia [MESH:D011014] (3482)  Respiratory Distress Syndrome, Newborn [MESH:D012127] (169)  Lung Diseases, Interstitial [MESH:D017563] (2966)   Surfactant Metabolism Dysfunction, Pulmonary, 1 [MESH:C566882] (102)  Surfactant Metabolism Dysfunction, Pulmonary, 2 [MESH:C567048] (48)  Idiopathic Interstitial Pneumonias [MESH:D054988] (314)   Idiopathic Pulmonary Fibrosis [MESH:D054990] (310)  Lung Diseases, Obstructive [MESH:D008173] (4697)   Asthma [MESH:D001249] (3903)  Pulmonary Disease, Chronic Obstructive [MESH:D029424] (3564)  Lung Injury [MESH:D055370] (3688)   Acute Lung Injury [MESH:D055371] (1907)  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)  Pulmonary Alveolar Proteinosis [MESH:D011649] (139)   Surfactant Metabolism Dysfunction, Pulmonary, 1 [MESH:C566882] (102)  Surfactant Metabolism Dysfunction, Pulmonary, 2 [MESH:C567048] (48)  Pulmonary Fibrosis [MESH:D011658] (3140)   Idiopathic Pulmonary Fibrosis [MESH:D054990] (310)  Nose Diseases [MESH:D009668] (1504)   Nasal Polyps [MESH:D009298] (129)   Asthma, Nasal Polyps, And Aspirin Intolerance [MESH:C565935] (80)  Rhinitis [MESH:D012220] (1134)   Rhinitis, Allergic, Perennial [MESH:D012221] (625)   Allergic Rhinitis [MESH:C567078] (181)  Pleural Diseases [MESH:D010995] (2240)   Pleurisy [MESH:D010998] (2070)  Respiration Disorders [MESH:D012120] (2218)   Respiratory Distress Syndrome, Newborn [MESH:D012127] (169)  Apnea [MESH:D001049] (748)   Sleep Apnea Syndromes [MESH:D012891] (570)   Sleep Apnea, Central [MESH:D020182] (347)   Congenital central hypoventilation syndrome [MESH:C536209] (341)  Hyperventilation [MESH:D006985] (654)   Pitt-Hopkins syndrome [MESH:C537403] (113)  Respiratory Insufficiency [MESH:D012131] (841)   Hypoventilation [MESH:D007040] (360)   Congenital central hypoventilation syndrome [MESH:C536209] (341)  Sarcoglycanopathies [MESH:D058088] (49)   Limb-girdle muscular dystrophy, type 2C [MESH:C535900] (20)  Respiratory Hypersensitivity [MESH:D012130] (4401)   Ige Responsiveness, Atopic [MESH:C564133] (267)  Asthma [MESH:D001249] (4098)   Asthma, Aspirin-Induced [MESH:D055963] (1055)   Asthma, Nasal Polyps, And Aspirin Intolerance [MESH:C565935] (80)  Rhinitis, Allergic, Perennial [MESH:D012221] (625)   Allergic Rhinitis [MESH:C567078] (181)  Respiratory Tract Fistula [MESH:D016156] (91)   Tracheoesophageal Fistula [MESH:D014138] (88)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Respiratory Tract Infections [MESH:D012141] (3926)   Influenza, Human [MESH:D007251] (1075)  Pleurisy [MESH:D010998] (2070)  Pneumonia [MESH:D011014] (3482)  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)  Tracheal Diseases [MESH:D014133] (107)   Tracheoesophageal Fistula [MESH:D014138] (88)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58) 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)   Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Deafness [MESH:D003638] (623)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Keratoderma palmoplantar deafness [MESH:C536152] (68)  Vohwinkel syndrome [MESH:C536457] (68)  Townes-Brocks syndrome [MESH:C536974] (28)  Knuckle pads, leuconychia and sensorineural deafness [MESH:C537210] (68)  Deafness, Autosomal Dominant 10 [MESH:C563354] (26)  Cardiomyopathy, Dilated, 1J [MESH:C565337] (26)  Deafness, Autosomal Recessive 1A [MESH:C567134] (88)  Deafness, Autosomal Dominant 3A [MESH:C567277] (77)  Hearing Loss, Noise-Induced [MESH:D006317] (134)  Nose Diseases [MESH:D009668] (1504)   Nasal Polyps [MESH:D009298] (129)   Asthma, Nasal Polyps, And Aspirin Intolerance [MESH:C565935] (80)  Rhinitis [MESH:D012220] (1134)   Rhinitis, Allergic, Perennial [MESH:D012221] (625)   Allergic Rhinitis [MESH:C567078] (181)  Pharyngeal Diseases [MESH:D010608] (1605)   Deglutition Disorders [MESH:D003680] (108) 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)   Myasthenia Gravis [MESH:D009157] (632)  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)  Autonomic Nervous System Diseases [MESH:D001342] (882)   Primary Dysautonomias [MESH:D054969] (775)   Orthostatic Intolerance [MESH:D054971] (720)  Central Nervous System Diseases [MESH:D002493] (9745)   Brain Diseases [MESH:D001927] (9294)   Brain Injuries [MESH:D001930] (3429)  Brain Neoplasms [MESH:D001932] (2764)  Hydrocephalus [MESH:D006849] (276)  Basal Ganglia Diseases [MESH:D001480] (4268)   Parkinsonian Disorders [MESH:D020734] (4009)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Brain Damage, Chronic [MESH:D001925] (311)   Cerebral Palsy [MESH:D002547] (300)   Cerebral Palsy, Spastic Quadriplegic, 1 [MESH:C567853] (99)  Brain Diseases, Metabolic [MESH:D001928] (3351)   Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Sandhoff Disease [MESH:D012497] (73)  Gangliosidoses, GM2 [MESH:D020143] (126)   Sandhoff Disease [MESH:D012497] (73)  Cerebellar Diseases [MESH:D002526] (736)   Joubert syndrome 4 [MESH:C536296] (18)  Cerebellar Ataxia [MESH:D002524] (542)   Dysequilibrium syndrome [MESH:C535731] (83)  Spinocerebellar Ataxias [MESH:D020754] (406)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxias [MESH:D020754] (322)  Cerebrovascular Disorders [MESH:D002561] (5542)   Vasospasm, Intracranial [MESH:D020301] (324)  Brain Ischemia [MESH:D002545] (4873)   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)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Intracranial Arterial Diseases [MESH:D020765] (2463)   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)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  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)  Lewy Body Disease [MESH:D020961] (1143)  Epilepsy [MESH:D004827] (6274)   Seizures [MESH:D012640] (4502)  Status Epilepticus [MESH:D013226] (4014)  Epilepsies, Partial [MESH:D004828] (1267)   Cortical Dysplasia-Focal Epilepsy Syndrome [MESH:C566482] (24)  Epilepsy, Temporal Lobe [MESH:D004833] (1108)  Epilepsy, Generalized [MESH:D004829] (1431)   Generalized Epilepsy With Febrile Seizures Plus, Type 2 [MESH:C565810] (44)  Epilepsy, Absence [MESH:D004832] (222)  Seizures, Febrile [MESH:D003294] (229)   Generalized Epilepsy With Febrile Seizures Plus, Type 2 [MESH:C565810] (44)  Headache Disorders [MESH:D020773] (2337)   Headache Disorders, Primary [MESH:D051270] (2327)   Migraine Disorders [MESH:D008881] (2318)   Migraine without Aura [MESH:D020326] (408)  Hypothalamic Diseases [MESH:D007027] (1833)   Pituitary Diseases [MESH:D010900] (1808)   Hyperpituitarism [MESH:D006964] (1250)   Hyperprolactinemia [MESH:D006966] (603)  Intracranial Hypertension [MESH:D019586] (368)   Hydrocephalus [MESH:D006849] (274)  Leukoencephalopathies [MESH:D056784] (1916)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (822)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Movement Disorders [MESH:D009069] (4823)   Dyskinesias [MESH:D020820] (1827)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Parkinsonian Disorders [MESH:D020734] (4009)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Spinal Cord Diseases [MESH:D013118] (4376)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxias [MESH:D020754] (322)  Cranial Nerve Diseases [MESH:D003389] (2004)   Ocular Motility Disorders [MESH:D015835] (1697)   Nystagmus, Pathologic [MESH:D009759] (128)   Nystagmus, Congenital [MESH:D020417] (29)   Microphthalmia, Isolated, with Cataract 2 [MESH:C565876] (14)  Ophthalmoplegia [MESH:D009886] (1468)   Fibrosis Of Extraocular Muscles, Congenital, 2 [MESH:C566587] (18)  Strabismus [MESH:D013285] (79)   Carnevale syndrome [MESH:C535586] (45)  Optic Nerve Diseases [MESH:D009901] (1375)   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)  Nervous System Malformations [MESH:D009421] (3354)   Microphthalmia, Syndromic 3 [MESH:C565948] (43)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 17 [MESH:C536644] (39)  Malformations of Cortical Development [MESH:D054220] (1406)   Cortical Dysplasia-Focal Epilepsy Syndrome [MESH:C566482] (24)  Microcephaly [MESH:D008831] (700)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Neural Tube Defects [MESH:D009436] (2143)   Encephalocele [MESH:D004677] (151)   Parietal Foramina 2 [MESH:C566510] (9)  Parietal Foramina [MESH:C566826] (42)  Nervous System Neoplasms [MESH:D009423] (3073)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  Neurodegenerative Diseases [MESH:D019636] (6613)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243)   Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 17 [MESH:C536644] (39)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxias [MESH:D020754] (322)  Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  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)  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)  Tremor [MESH:D014202] (840)  Ataxia [MESH:D001259] (1138)   Ataxia with vitamin E deficiency [MESH:C535393] (271)  Cerebellar Ataxia [MESH:D002524] (542)   Dysequilibrium syndrome [MESH:C535731] (83)  Spinocerebellar Ataxias [MESH:D020754] (406)  Neurobehavioral Manifestations [MESH:D019954] (5230)   Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Language Development Disorders [MESH:D007805] (351)  Speech Disorders [MESH:D013064] (482)   Stuttering [MESH:D013342] (38)  Consciousness Disorders [MESH:D003244] (680)   Unconsciousness [MESH:D014474] (660)   Stupor [MESH:D053608] (103)  Coma [MESH:D003128] (524)   Coma, Post-Head Injury [MESH:D020207] (55)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Intellectual Disability [MESH:D008607] (3054)   Dysequilibrium syndrome [MESH:C535731] (83)  Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Zlotogora-Ogur syndrome [MESH:C536726] (25)  Pitt-Hopkins syndrome [MESH:C537403] (113)  Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Histidinemia [MESH:C538320] (87)  Birk-Barel Mental Retardation Dysmorphism Syndrome [MESH:C567357] (20)  Cri-du-Chat Syndrome [MESH:D003410] (139)  Prader-Willi Syndrome [MESH:D011218] (46)  Mental Retardation, X-Linked [MESH:D038901] (1854)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  ATR-X syndrome [MESH:C538258] (59)  Fragile X Syndrome [MESH:D005600] (353)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscle Hypotonia [MESH:D009123] (258)   Birk-Barel Mental Retardation Dysmorphism Syndrome [MESH:C567357] (20)  Pain [MESH:D010146] (3875)   Paroxysmal Extreme Pain Disorder [MESH:C563475] (27)  Neuralgia [MESH:D009437] (2074)   Neuralgia, Postherpetic [MESH:D051474] (742)  Paralysis [MESH:D010243] (2043)   Ophthalmoplegia [MESH:D009886] (1468)   Fibrosis Of Extraocular Muscles, Congenital, 2 [MESH:C566587] (18)  Sensation Disorders [MESH:D012678] (5011)   Olfaction Disorders [MESH:D000857] (105)  Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Deafness [MESH:D003638] (623)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Keratoderma palmoplantar deafness [MESH:C536152] (68)  Vohwinkel syndrome [MESH:C536457] (68)  Townes-Brocks syndrome [MESH:C536974] (28)  Knuckle pads, leuconychia and sensorineural deafness [MESH:C537210] (68)  Deafness, Autosomal Dominant 10 [MESH:C563354] (26)  Cardiomyopathy, Dilated, 1J [MESH:C565337] (26)  Deafness, Autosomal Recessive 1A [MESH:C567134] (88)  Deafness, Autosomal Dominant 3A [MESH:C567277] (77)  Hearing Loss, Noise-Induced [MESH:D006317] (134)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Vision Disorders [MESH:D014786] (501)   Enhanced S-Cone Syndrome [MESH:C564835] (11)  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)   Muscular Disorders, Atrophic [MESH:D020966] (1594)   Muscular Dystrophies [MESH:D009136] (1589)   Bethlem myopathy [MESH:C535436] (108)  Muscular dystrophy congenital, merosin negative [MESH:C537384] (34)  Scleroatonic muscular dystrophy [MESH:C537521] (108)  Muscular Dystrophies, Limb-Girdle [MESH:D049288] (259)   Sarcoglycanopathies [MESH:D058088] (49)   Limb-girdle muscular dystrophy, type 2C [MESH:C535900] (20)  Neuromuscular Junction Diseases [MESH:D020511] (712)   Myasthenia Gravis [MESH:D009157] (632)  Peripheral Nervous System Diseases [MESH:D010523] (6151)   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)  Neuralgia [MESH:D009437] (2078)   Neuralgia, Postherpetic [MESH:D051474] (742)  Pain Insensitivity, Congenital [MESH:D000699] (29)   Indifference to Pain, Congenital, Autosomal Recessive [MESH:C565467] (27)  Polyneuropathies [MESH:D011115] (1134)   Tangier Disease [MESH:D013631] (170)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 17 [MESH:C536644] (39)  Neurotoxicity Syndromes [MESH:D020258] (4570)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Heavy Metal Poisoning, Nervous System [MESH:D020260] (2912)   Arsenic Poisoning [MESH:D020261] (2540)  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)  Trauma, Nervous System [MESH:D020196] (3997)   Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431)  Coma, Post-Head Injury [MESH:D020207] (55) C11. Eye Diseases  C11. Eye Diseases  Eye Diseases [MESH:D005128] (6245)   Corneal Diseases [MESH:D003316] (1445)   Keratitis [MESH:D007634] (168)  Eye Abnormalities [MESH:D005124] (1233)   Oculopalatoskeletal syndrome [MESH:C537738] (45)  Anophthalmos [MESH:D000853] (63)  Microphthalmos [MESH:D008850] (273)   Microphthalmia, Isolated, with Cataract 2 [MESH:C565876] (14)  Microphthalmia, Syndromic 3 [MESH:C565948] (43)  Eye Diseases, Hereditary [MESH:D015785] (1869)   Enhanced S-Cone Syndrome [MESH:C564835] (11)  Hypomagnesemia 5, Renal, with Ocular Involvement [MESH:C565423] (10)  Fibrosis Of Extraocular Muscles, Congenital, 2 [MESH:C566587] (18)  Albinism [MESH:D000417] (258)   Albinism, Oculocutaneous [MESH:D016115] (234)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Hermansky Pudlak syndrome 2 [MESH:C537709] (16)  Leber Congenital Amaurosis [MESH:D057130] (157)   Amaurosis congenita of Leber, type 1 [MESH:C536600] (11)  Retinitis Pigmentosa [MESH:D012174] (414)   Retinal cone dystrophy 2 [MESH:C538363] (11)  Cone-Rod Dystrophy 5 [MESH:C563415] (19)  Retinitis Pigmentosa 37 [MESH:C567005] (11)  Eyelid Diseases [MESH:D005141] (882)   Blepharoptosis [MESH:D001763] (117)   Carnevale syndrome [MESH:C535586] (45)  Fibrosis Of Extraocular Muscles, Congenital, 2 [MESH:C566587] (18)  Lens Diseases [MESH:D007905] (900)   Cataract [MESH:D002386] (860)   Nance-Horan syndrome [MESH:C538336] (15)  Cataract, Pulverulent, Juvenile-Onset [MESH:C565703] (69)  Microphthalmia, Isolated, with Cataract 2 [MESH:C565876] (14)  Cataract, Zonular Pulverulent 3 [MESH:C566608] (20)  Cataract, Juvenile, With Microcornea And Glucosuria [MESH:C567434] (26)  Ocular Motility Disorders [MESH:D015835] (1699)   Nystagmus, Pathologic [MESH:D009759] (128)   Nystagmus, Congenital [MESH:D020417] (29)   Microphthalmia, Isolated, with Cataract 2 [MESH:C565876] (14)  Ophthalmoplegia [MESH:D009886] (1468)   Fibrosis Of Extraocular Muscles, Congenital, 2 [MESH:C566587] (18)  Strabismus [MESH:D013285] (79)   Carnevale syndrome [MESH:C535586] (45)  Optic Nerve Diseases [MESH:D009901] (1377)   Optic Neuritis [MESH:D009902] (273)   Neuromyelitis Optica [MESH:D009471] (248)  Refractive Errors [MESH:D012030] (457)   Myopia [MESH:D009216] (349)  Retinal Diseases [MESH:D012164] (3747)   Leber Congenital Amaurosis [MESH:D057130] (157)   Amaurosis congenita of Leber, type 1 [MESH:C536600] (11)  Retinal Degeneration [MESH:D012162] (2386)   Joubert syndrome 4 [MESH:C536296] (18)  Enhanced S-Cone Syndrome [MESH:C564835] (11)  Macular Degeneration [MESH:D008268] (995)   Macular Degeneration, Age-Related, 7 [MESH:C565718] (60)  Macular Degeneration, Age-Related, 1 [MESH:C566411] (276)  Retinal Dystrophies [MESH:D058499] (1315)   Retinitis Pigmentosa [MESH:D012174] (1307)   Retinal cone dystrophy 2 [MESH:C538363] (11)  Cone-Rod Dystrophy 5 [MESH:C563415] (19)  Retinitis Pigmentosa 37 [MESH:C567005] (11)  Uveal Diseases [MESH:D014603] (2428)   Uveitis [MESH:D014605] (2157)   Panuveitis [MESH:D015864] (1805)   Uveitis, Anterior [MESH:D014606] (1791)   Behcet Syndrome [MESH:D001528] (1784)  Vision Disorders [MESH:D014786] (534)   Enhanced S-Cone Syndrome [MESH:C564835] (11) C12. Male Urogenital Diseases  C12. Male Urogenital Diseases  Male Urogenital Diseases [MESH:D052801] (8891)   Genital Diseases, Male [MESH:D005832] (6794)   Infertility [MESH:D007246] (2909)  Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Testicular Neoplasms [MESH:D013736] (520)   Testicular Germ Cell Tumor [MESH:C563236] (176)  Penile Diseases [MESH:D010409] (1805)   Hypospadias [MESH:D007021] (798)   Preaxial deficiency, postaxial polydactyly and hypospadias [MESH:C538278] (20)  Prostatic Diseases [MESH:D011469] (6204)   Prostatic Neoplasms [MESH:D011471] (6135)  Prostatitis [MESH:D011472] (424)  Testicular Diseases [MESH:D013733] (451)   Testicular Microlithiasis [MESH:C566478] (44)  Cryptorchidism [MESH:D003456] (215)   Carnevale syndrome [MESH:C535586] (45)  Urogenital Abnormalities [MESH:D014564] (2065)   Hand foot uterus syndrome [MESH:C535627] (20)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Cryptorchidism [MESH:D003456] (215)   Carnevale syndrome [MESH:C535586] (45)  Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   17-Hydroxysteroid Dehydrogenase Deficiency [MESH:C537805] (52)  Kallmann Syndrome [MESH:D017436] (147)  Hypospadias [MESH:D007021] (798)   Preaxial deficiency, postaxial polydactyly and hypospadias [MESH:C538278] (20)  Nephritis, Hereditary [MESH:D009394] (62)   Alport syndrome, recessive type [MESH:C536587] (35)  Urogenital Neoplasms [MESH:D014565] (6932)   Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Testicular Neoplasms [MESH:D013736] (520)   Testicular Germ Cell Tumor [MESH:C563236] (176)  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)  Urologic Diseases [MESH:D014570] (7792)   Kidney Diseases [MESH:D007674] (7242)   Hereditary renal agenesis [MESH:C536482] (89)  Kidney Diseases, Cystic [MESH:D052177] (1009)   Joubert syndrome 4 [MESH:C536296] (18)  Nephronophthisis, familial juvenile [MESH:C537699] (18)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, Membranous [MESH:D015433] (642)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Nephritis, Hereditary [MESH:D009394] (62)   Alport syndrome, recessive type [MESH:C536587] (35)  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)   Iminoglycinuria [MESH:C536285] (38)  Hypomagnesemia 5, Renal, with Ocular Involvement [MESH:C565423] (10)  Glycosuria, Renal [MESH:D006030] (50)   Cataract, Juvenile, With Microcornea And Glucosuria [MESH:C567434] (26)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)   Atypical hemolytic uremic syndrome [MESH:C538266] (277)  Urinary Bladder Diseases [MESH:D001745] (4374)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urination Disorders [MESH:D014555] (3598)   Proteinuria [MESH:D011507] (3293)  Glycosuria [MESH:D006029] (100)   Glycosuria, Renal [MESH:D006030] (50)   Cataract, Juvenile, With Microcornea And Glucosuria [MESH:C567434] (26)  Hematuria [MESH:D006417] (477)   Hematuria, Benign Familial [MESH:C562476] (25) 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 Neoplasms [MESH:D010051] (3281)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Infertility [MESH:D007246] (2211)   Infertility, Female [MESH:D007247] (2184)  Uterine Diseases [MESH:D014591] (2479)   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)  Vaginal Diseases [MESH:D014623] (446)   Vaginitis [MESH:D014627] (88)   Vulvovaginitis [MESH:D014848] (79)   Candidiasis, Vulvovaginal [MESH:D002181] (76)  Vulvar Diseases [MESH:D014845] (873)   Vulvitis [MESH:D014847] (83)   Vulvovaginitis [MESH:D014848] (79)   Candidiasis, Vulvovaginal [MESH:D002181] (76)  Urogenital Abnormalities [MESH:D014564] (2043)   Hand foot uterus syndrome [MESH:C535627] (20)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   17-Hydroxysteroid Dehydrogenase Deficiency [MESH:C537805] (52)  Kallmann Syndrome [MESH:D017436] (147)  Hypospadias [MESH:D007021] (798)   Preaxial deficiency, postaxial polydactyly and hypospadias [MESH:C538278] (20)  Nephritis, Hereditary [MESH:D009394] (62)   Alport syndrome, recessive type [MESH:C536587] (35)  Urogenital Neoplasms [MESH:D014565] (5792)   Genital Neoplasms, Female [MESH:D005833] (3810)   Ovarian Neoplasms [MESH:D010051] (3281)  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)  Urologic Diseases [MESH:D014570] (7793)   Kidney Diseases [MESH:D007674] (7242)   Hereditary renal agenesis [MESH:C536482] (89)  Kidney Diseases, Cystic [MESH:D052177] (1009)   Joubert syndrome 4 [MESH:C536296] (18)  Nephronophthisis, familial juvenile [MESH:C537699] (18)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, Membranous [MESH:D015433] (642)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Nephritis, Hereditary [MESH:D009394] (62)   Alport syndrome, recessive type [MESH:C536587] (35)  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)   Iminoglycinuria [MESH:C536285] (38)  Hypomagnesemia 5, Renal, with Ocular Involvement [MESH:C565423] (10)  Glycosuria, Renal [MESH:D006030] (50)   Cataract, Juvenile, With Microcornea And Glucosuria [MESH:C567434] (26)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)   Atypical hemolytic uremic syndrome [MESH:C538266] (277)  Urinary Bladder Diseases [MESH:D001745] (4375)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urination Disorders [MESH:D014555] (3598)   Proteinuria [MESH:D011507] (3293)  Glycosuria [MESH:D006029] (100)   Glycosuria, Renal [MESH:D006030] (50)   Cataract, Juvenile, With Microcornea And Glucosuria [MESH:C567434] (26)  Hematuria [MESH:D006417] (477)   Hematuria, Benign Familial [MESH:C562476] (25)  Pregnancy Complications [MESH:D011248] (4768)   Abortion, Spontaneous [MESH:D000022] (2780)  Diabetes, Gestational [MESH:D016640] (1157)  Fetal Death [MESH:D005313] (464)  Placenta Diseases [MESH:D010922] (1781)  Polyhydramnios [MESH:D006831] (123)  Fetal Diseases [MESH:D005315] (1206)   Fetal Growth Retardation [MESH:D005317] (986)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Obstetric Labor Complications [MESH:D007744] (1550)   Obstetric Labor, Premature [MESH:D007752] (1316)   Premature Birth [MESH:D047928] (118)  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)   Cardiovascular Abnormalities [MESH:D018376] (3153)   Heart Defects, Congenital [MESH:D006330] (2447)   Holt-Oram syndrome [MESH:C535326] (11)  Malpuech facial clefting syndrome [MESH:C535704] (45)  Arrhythmogenic Right Ventricular Dysplasia [MESH:D019571] (241)   Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 [MESH:C563409] (51)  Dextrocardia [MESH:D003914] (61)   Heterotaxy, visceral, X-linked [MESH:C538116] (22)  Heart Septal Defects [MESH:D006343] (385)   Heart Septal Defects, Atrial [MESH:D006344] (209)   Holt-Oram syndrome [MESH:C535326] (11)  Atrial septal defect 2 [MESH:C538263] (69)  Atrial Septal Defect 4 [MESH:C566963] (13)  Heterotaxy Syndrome [MESH:D059446] (84)   Heterotaxy, visceral, X-linked [MESH:C538116] (22)  Heart Diseases [MESH:D006331] (8614)   Heart Failure [MESH:D006333] (4058)  Arrhythmias, Cardiac [MESH:D001145] (4679)   Bradycardia [MESH:D001919] (1899)  Atrial Fibrillation [MESH:D001281] (1053)   Atrial Fibrillation, Familial, 7 [MESH:C567389] (39)  Long QT Syndrome [MESH:D008133] (693)   Long Qt Syndrome 5 [MESH:C566766] (40)  Jervell-Lange Nielsen Syndrome [MESH:D029593] (64)  Tachycardia [MESH:D013610] (3339)   Tachycardia, Ventricular [MESH:D017180] (1386)   Polymorphic catecholergic ventricular tachycardia [MESH:C536334] (64)  Cardiomegaly [MESH:D006332] (4081)   Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1D [MESH:C563306] (50)  Cardiomyopathy, Dilated, 1J [MESH:C565337] (26)  Cardiomyopathies [MESH:D009202] (5331)   Diabetic Cardiomyopathies [MESH:D058065] (1995)  Myocarditis [MESH:D009205] (1708)  Arrhythmogenic Right Ventricular Dysplasia [MESH:D019571] (241)   Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 [MESH:C563409] (51)  Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1D [MESH:C563306] (50)  Cardiomyopathy, Dilated, 1J [MESH:C565337] (26)  Cardiomyopathy, Hypertrophic [MESH:D002312] (1516)   Cardiomyopathy, Hypertrophic, Familial [MESH:D024741] (339)   Cardiomyopathy, Familial Hypertrophic, 2 [MESH:C566171] (50)  Cardiomyopathy, Restrictive [MESH:D002313] (94)   Cardiomyopathy, Familial Restrictive, 3 [MESH:C567316] (50)  Sarcoglycanopathies [MESH:D058088] (49)   Limb-girdle muscular dystrophy, type 2C [MESH:C535900] (20)  Heart Defects, Congenital [MESH:D006330] (2443)   Holt-Oram syndrome [MESH:C535326] (11)  Malpuech facial clefting syndrome [MESH:C535704] (45)  Arrhythmogenic Right Ventricular Dysplasia [MESH:D019571] (241)   Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 [MESH:C563409] (51)  Dextrocardia [MESH:D003914] (61)   Heterotaxy, visceral, X-linked [MESH:C538116] (22)  Heart Septal Defects [MESH:D006343] (385)   Heart Septal Defects, Atrial [MESH:D006344] (209)   Holt-Oram syndrome [MESH:C535326] (11)  Atrial septal defect 2 [MESH:C538263] (69)  Atrial Septal Defect 4 [MESH:C566963] (13)  Heterotaxy Syndrome [MESH:D059446] (84)   Heterotaxy, visceral, X-linked [MESH:C538116] (22)  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 Infarction [MESH:D009203] (4122)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Coronary Stenosis [MESH:D023921] (1806)  Ventricular Dysfunction [MESH:D018754] (2348)   Ventricular Dysfunction, Left [MESH:D018487] (1631)  Vascular Diseases [MESH:D014652] (8691)   Arteritis [MESH:D001167] (1084)  Hyperemia [MESH:D006940] (2372)  Hypertension [MESH:D006973] (5655)  Hypotension [MESH:D007022] (4045)  Reperfusion Injury [MESH:D015427] (4968)  Vascular System Injuries [MESH:D057772] (2086)  Aneurysm [MESH:D000783] (1886)   Aneurysm, Dissecting [MESH:D000784] (699)  Arterial Occlusive Diseases [MESH:D001157] (4520)   Arteriosclerosis [MESH:D001161] (4466)   Atherosclerosis [MESH:D050197] (4188)  Coronary Artery Disease [MESH:D003324] (2685)  Cerebrovascular Disorders [MESH:D002561] (5541)   Vasospasm, Intracranial [MESH:D020301] (324)  Brain Ischemia [MESH:D002545] (4873)   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)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Intracranial Arterial Diseases [MESH:D020765] (2468)   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)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Embolism and Thrombosis [MESH:D016769] (3374)   Thromboembolism [MESH:D013923] (732)   Venous Thromboembolism [MESH:D054556] (400)  Thrombosis [MESH:D013927] (3101)   Venous Thrombosis [MESH:D020246] (1141)  Thromboembolism [MESH:D013923] (732)   Venous Thromboembolism [MESH:D054556] (400)  Hemostatic Disorders [MESH:D020141] (2894)   Multiple Myeloma [MESH:D009101] (2765)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Myocardial Ischemia [MESH:D017202] (5791)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Infarction [MESH:D009203] (4151)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Coronary Stenosis [MESH:D023921] (1806)  Peripheral Vascular Diseases [MESH:D016491] (1412)   Erythromelalgia [MESH:D004916] (35)  Vasculitis [MESH:D014657] (2604)   Arteritis [MESH:D001167] (1084)  Behcet Syndrome [MESH:D001528] (1784) C15. Hemic and Lymphatic Diseases  C15. Hemic and Lymphatic Diseases  Hematologic Diseases [MESH:D006402] (6174)   Anemia [MESH:D000740] (3966)   Anemia, Aplastic [MESH:D000741] (1925)  Anemia, Hemolytic [MESH:D000743] (3083)   Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   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)  Blood Coagulation Disorders [MESH:D001778] (1828)   Disseminated Intravascular Coagulation [MESH:D004211] (462)  Blood Coagulation Disorders, Inherited [MESH:D025861] (720)   Wiskott-Aldrich Syndrome [MESH:D014923] (28)  Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Hermansky Pudlak syndrome 2 [MESH:C537709] (16)  Protein C Deficiency [MESH:D020151] (70)   Congenital thrombotic disease, due to Protein C deficiency [MESH:C535424] (66)  Platelet Storage Pool Deficiency [MESH:D010981] (84)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Hermansky Pudlak syndrome 2 [MESH:C537709] (16)  Purpura [MESH:D011693] (475)   Purpura Fulminans [MESH:D055665] (69)  Blood Platelet Disorders [MESH:D001791] (3174)   Platelet Storage Pool Deficiency [MESH:D010981] (84)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Hermansky Pudlak syndrome 2 [MESH:C537709] (16)  Thrombocytopenia [MESH:D013921] (2966)   Thrombotic Microangiopathies [MESH:D057049] (2598)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)   Atypical hemolytic uremic syndrome [MESH:C538266] (277)  Blood Protein Disorders [MESH:D001796] (3051)   Paraproteinemias [MESH:D010265] (2781)   Multiple Myeloma [MESH:D009101] (2765)  Protein C Deficiency [MESH:D020151] (70)   Congenital thrombotic disease, due to Protein C deficiency [MESH:C535424] (66)  Bone Marrow Diseases [MESH:D001855] (2944)   Anemia, Aplastic [MESH:D000741] (1925)  Myelodysplastic Syndromes [MESH:D009190] (2093)   Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)  Myeloproliferative Disorders [MESH:D009196] (1492)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Hemoglobinopathies [MESH:D006453] (1863)   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)  Wiskott-Aldrich Syndrome [MESH:D014923] (28)  Hemostatic Disorders [MESH:D020141] (2932)   Multiple Myeloma [MESH:D009101] (2765)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Platelet Storage Pool Deficiency [MESH:D010981] (84)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Hermansky Pudlak syndrome 2 [MESH:C537709] (16)  Leukocyte Disorders [MESH:D007960] (2662)   Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis [MESH:C564365] (78)  Leukopenia [MESH:D007970] (1921)   Agranulocytosis [MESH:D000380] (1675)   Neutropenia [MESH:D009503] (1629)   Neutropenia, Severe Congenital, X-Linked [MESH:C564539] (27)  Lymphopenia [MESH:D008231] (990)   Wiskott-Aldrich Syndrome [MESH:D014923] (28)  Thrombophilia [MESH:D019851] (592)   Disseminated Intravascular Coagulation [MESH:D004211] (462)  Protein C Deficiency [MESH:D020151] (70)   Congenital thrombotic disease, due to Protein C deficiency [MESH:C535424] (66)  Lymphatic Diseases [MESH:D008206] (5167)   Lymphoproliferative Disorders [MESH:D008232] (4638)   Leukemia, Lymphoid [MESH:D007945] (3047)   Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)  Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Lymphoma [MESH:D008223] (3684)   Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  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)  Splenic Diseases [MESH:D013158] (1323)   Heterotaxy Syndrome [MESH:D059446] (84)   Heterotaxy, visceral, X-linked [MESH:C538116] (22) 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)   Hereditary renal agenesis [MESH:C536482] (89)  Abnormalities, Multiple [MESH:D000015] (3192)   Holt-Oram syndrome [MESH:C535326] (11)  Hand foot uterus syndrome [MESH:C535627] (20)  Malpuech facial clefting syndrome [MESH:C535704] (45)  Vohwinkel syndrome [MESH:C536457] (68)  Ulnar-mammary syndrome [MESH:C536937] (57)  Townes-Brocks syndrome [MESH:C536974] (28)  Knuckle pads, leuconychia and sensorineural deafness [MESH:C537210] (68)  Preaxial deficiency, postaxial polydactyly and hypospadias [MESH:C538278] (20)  Beckwith-Wiedemann Syndrome [MESH:D001506] (193)  Cri-du-Chat Syndrome [MESH:D003410] (139)  Netherton Syndrome [MESH:D056770] (43)  Prader-Willi Syndrome [MESH:D011218] (46)  Silver-Russell Syndrome [MESH:D056730] (142)  Ectodermal Dysplasia [MESH:D004476] (938)   Ectodermal dysplasia/ skin fragility syndrome [MESH:C536183] (20)  Zlotogora-Ogur syndrome [MESH:C536726] (25)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Heterotaxy Syndrome [MESH:D059446] (84)   Heterotaxy, visceral, X-linked [MESH:C538116] (22)  Cardiovascular Abnormalities [MESH:D018376] (3294)   Heart Defects, Congenital [MESH:D006330] (2611)   Holt-Oram syndrome [MESH:C535326] (11)  Malpuech facial clefting syndrome [MESH:C535704] (45)  Arrhythmogenic Right Ventricular Dysplasia [MESH:D019571] (241)   Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 [MESH:C563409] (51)  Dextrocardia [MESH:D003914] (61)   Heterotaxy, visceral, X-linked [MESH:C538116] (22)  Heart Septal Defects [MESH:D006343] (385)   Heart Septal Defects, Atrial [MESH:D006344] (209)   Holt-Oram syndrome [MESH:C535326] (11)  Atrial septal defect 2 [MESH:C538263] (69)  Atrial Septal Defect 4 [MESH:C566963] (13)  Heterotaxy Syndrome [MESH:D059446] (84)   Heterotaxy, visceral, X-linked [MESH:C538116] (22)  Long QT Syndrome [MESH:D008133] (693)   Long Qt Syndrome 5 [MESH:C566766] (40)  Jervell-Lange Nielsen Syndrome [MESH:D029593] (64)  Chromosome Disorders [MESH:D025063] (2030)   Beckwith-Wiedemann Syndrome [MESH:D001506] (193)  Cri-du-Chat Syndrome [MESH:D003410] (139)  Prader-Willi Syndrome [MESH:D011218] (46)  Silver-Russell Syndrome [MESH:D056730] (142)  Sex Chromosome Disorders [MESH:D025064] (479)   Fragile X Syndrome [MESH:D005600] (353)  Digestive System Abnormalities [MESH:D004065] (507)   Hirschsprung Disease [MESH:D006627] (361)  Anus, Imperforate [MESH:D001006] (140)   Townes-Brocks syndrome [MESH:C536974] (28)  Esophageal Atresia [MESH:D004933] (47)   Microphthalmia, Syndromic 3 [MESH:C565948] (43)  Eye Abnormalities [MESH:D005124] (1233)   Oculopalatoskeletal syndrome [MESH:C537738] (45)  Anophthalmos [MESH:D000853] (63)  Microphthalmos [MESH:D008850] (273)   Microphthalmia, Isolated, with Cataract 2 [MESH:C565876] (14)  Microphthalmia, Syndromic 3 [MESH:C565948] (43)  Musculoskeletal Abnormalities [MESH:D009139] (3779)   Arthrogryposis [MESH:D001176] (329)   Bruck syndrome 2 [MESH:C537407] (64)  Craniofacial Abnormalities [MESH:D019465] (3064)   Malpuech facial clefting syndrome [MESH:C535704] (45)  LIG4 Syndrome [MESH:C564694] (24)  Birk-Barel Mental Retardation Dysmorphism Syndrome [MESH:C567357] (20)  Craniosynostoses [MESH:D003398] (438)   Oculopalatoskeletal syndrome [MESH:C537738] (45)  Acrocephalosyndactylia [MESH:D000168] (201)   Saethre-Chotzen Syndrome with Eyelid Anomalies [MESH:C566325] (42)  Maxillofacial Abnormalities [MESH:D019767] (1448)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Zlotogora-Ogur syndrome [MESH:C536726] (25)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Microcephaly [MESH:D008831] (700)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Plagiocephaly [MESH:D059041] (440)   Craniosynostoses [MESH:D003398] (438)   Oculopalatoskeletal syndrome [MESH:C537738] (45)  Acrocephalosyndactylia [MESH:D000168] (201)   Saethre-Chotzen Syndrome with Eyelid Anomalies [MESH:C566325] (42)  Hip Dislocation, Congenital [MESH:D006618] (56)   Carnevale syndrome [MESH:C535586] (45)  Limb Deformities, Congenital [MESH:D017880] (1813)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Foot Deformities, Congenital [MESH:D005532] (538)   Hand foot uterus syndrome [MESH:C535627] (20)  Hand Deformities, Congenital [MESH:D006228] (587)   Hand foot uterus syndrome [MESH:C535627] (20)  Vohwinkel syndrome [MESH:C536457] (68)  Lower Extremity Deformities, Congenital [MESH:D038061] (81)   Holt-Oram syndrome [MESH:C535326] (11)  Polydactyly [MESH:D017689] (318)   Preaxial deficiency, postaxial polydactyly and hypospadias [MESH:C538278] (20)  Syndactyly [MESH:D013576] (487)   Zlotogora-Ogur syndrome [MESH:C536726] (25)  Sclerosteosis [MESH:C537525] (17)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Acrocephalosyndactylia [MESH:D000168] (201)   Saethre-Chotzen Syndrome with Eyelid Anomalies [MESH:C566325] (42)  Upper Extremity Deformities, Congenital [MESH:D038062] (44)   Holt-Oram syndrome [MESH:C535326] (11)  Synostosis [MESH:D013580] (817)   Craniosynostoses [MESH:D003398] (438)   Oculopalatoskeletal syndrome [MESH:C537738] (45)  Acrocephalosyndactylia [MESH:D000168] (201)   Saethre-Chotzen Syndrome with Eyelid Anomalies [MESH:C566325] (42)  Syndactyly [MESH:D013576] (487)   Zlotogora-Ogur syndrome [MESH:C536726] (25)  Sclerosteosis [MESH:C537525] (17)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Acrocephalosyndactylia [MESH:D000168] (201)   Saethre-Chotzen Syndrome with Eyelid Anomalies [MESH:C566325] (42)  Nervous System Malformations [MESH:D009421] (3354)   Microphthalmia, Syndromic 3 [MESH:C565948] (43)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 17 [MESH:C536644] (39)  Malformations of Cortical Development [MESH:D054220] (1406)   Cortical Dysplasia-Focal Epilepsy Syndrome [MESH:C566482] (24)  Microcephaly [MESH:D008831] (700)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Neural Tube Defects [MESH:D009436] (2143)   Encephalocele [MESH:D004677] (151)   Parietal Foramina 2 [MESH:C566510] (9)  Parietal Foramina [MESH:C566826] (42)  Situs Inversus [MESH:D012857] (88)   Dextrocardia [MESH:D003914] (61)   Heterotaxy, visceral, X-linked [MESH:C538116] (22)  Skin Abnormalities [MESH:D012868] (1723)   Dyskeratosis Congenita [MESH:D019871] (185)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Dyskeratosis Congenita, Autosomal Dominant [MESH:C565079] (130)  Ectodermal Dysplasia [MESH:D004476] (958)   Ectodermal dysplasia/ skin fragility syndrome [MESH:C536183] (20)  Zlotogora-Ogur syndrome [MESH:C536726] (25)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Epidermolysis Bullosa [MESH:D004820] (260)   Poikiloderma of Kindler [MESH:C536321] (20)  Ichthyosis [MESH:D007057] (481)   Ichthyosis with hypotrichosis, autosomal recessive [MESH:C536273] (32)  Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis [MESH:C564365] (78)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Netherton Syndrome [MESH:D056770] (43)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Zlotogora-Ogur syndrome [MESH:C536726] (25)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Cleft Palate [MESH:D002972] (1330)   Zlotogora-Ogur syndrome [MESH:C536726] (25)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Tooth Abnormalities [MESH:D014071] (622)   Nance-Horan syndrome [MESH:C538336] (15)  Urogenital Abnormalities [MESH:D014564] (2064)   Hand foot uterus syndrome [MESH:C535627] (20)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Cryptorchidism [MESH:D003456] (215)   Carnevale syndrome [MESH:C535586] (45)  Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   17-Hydroxysteroid Dehydrogenase Deficiency [MESH:C537805] (52)  Kallmann Syndrome [MESH:D017436] (147)  Hypospadias [MESH:D007021] (798)   Preaxial deficiency, postaxial polydactyly and hypospadias [MESH:C538278] (20)  Nephritis, Hereditary [MESH:D009394] (62)   Alport syndrome, recessive type [MESH:C536587] (35)  Fetal Diseases [MESH:D005315] (1205)   Fetal Growth Retardation [MESH:D005317] (986)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Genetic Diseases, Inborn [MESH:D030342] (9766)   Pulmonary Alveolar Microlithiasis [MESH:C562405] (44)  ACTH Deficiency, Isolated [MESH:C562707] (124)  Kallmann Syndrome [MESH:D017436] (147)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Thalassemia [MESH:D013789] (501)   alpha-Thalassemia [MESH:D017085] (176)   ATR-X syndrome [MESH:C538258] (59)  Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)  Blood Coagulation Disorders, Inherited [MESH:D025861] (722)   Wiskott-Aldrich Syndrome [MESH:D014923] (28)  Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Hermansky Pudlak syndrome 2 [MESH:C537709] (16)  Protein C Deficiency [MESH:D020151] (70)   Congenital thrombotic disease, due to Protein C deficiency [MESH:C535424] (66)  Cardiomyopathy, Hypertrophic, Familial [MESH:D024741] (339)   Cardiomyopathy, Familial Hypertrophic, 2 [MESH:C566171] (50)  Chromosome Disorders [MESH:D025063] (2030)   Beckwith-Wiedemann Syndrome [MESH:D001506] (193)  Cri-du-Chat Syndrome [MESH:D003410] (139)  Prader-Willi Syndrome [MESH:D011218] (46)  Silver-Russell Syndrome [MESH:D056730] (142)  Sex Chromosome Disorders [MESH:D025064] (479)   Fragile X Syndrome [MESH:D005600] (353)  Dwarfism [MESH:D004392] (783)   Silver-Russell Syndrome [MESH:D056730] (142)  Eye Diseases, Hereditary [MESH:D015785] (1867)   Enhanced S-Cone Syndrome [MESH:C564835] (11)  Hypomagnesemia 5, Renal, with Ocular Involvement [MESH:C565423] (10)  Fibrosis Of Extraocular Muscles, Congenital, 2 [MESH:C566587] (18)  Albinism [MESH:D000417] (359)   Albinism, Oculocutaneous [MESH:D016115] (234)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Hermansky Pudlak syndrome 2 [MESH:C537709] (16)  Retinitis Pigmentosa [MESH:D012174] (442)   Retinal cone dystrophy 2 [MESH:C538363] (11)  Cone-Rod Dystrophy 5 [MESH:C563415] (19)  Retinitis Pigmentosa 37 [MESH:C567005] (11)  Genetic Diseases, X-Linked [MESH:D040181] (3028)   Heterotaxy, visceral, X-linked [MESH:C538116] (22)  Nance-Horan syndrome [MESH:C538336] (15)  Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)  Neutropenia, Severe Congenital, X-Linked [MESH:C564539] (27)  Wiskott-Aldrich Syndrome [MESH:D014923] (28)  Dyskeratosis Congenita [MESH:D019871] (185)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Dyskeratosis Congenita, Autosomal Dominant [MESH:C565079] (130)  Mental Retardation, X-Linked [MESH:D038901] (1867)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  ATR-X syndrome [MESH:C538258] (59)  Fragile X Syndrome [MESH:D005600] (353)  Hemoglobinopathies [MESH:D006453] (1863)   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)   Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 17 [MESH:C536644] (39)  Mental Retardation, X-Linked [MESH:D038901] (1848)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  ATR-X syndrome [MESH:C538258] (59)  Fragile X Syndrome [MESH:D005600] (353)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxias [MESH:D020754] (322)  Metabolism, Inborn Errors [MESH:D008661] (6032)   Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565)   Histidinemia [MESH:C538320] (87)  Albinism [MESH:D000417] (359)   Albinism, Oculocutaneous [MESH:D016115] (234)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Hermansky Pudlak syndrome 2 [MESH:C537709] (16)  Amyloidosis, Familial [MESH:D028226] (696)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Amyloidosis, familial visceral [MESH:C538249] (285)  Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Sandhoff Disease [MESH:D012497] (73)  Gangliosidoses, GM2 [MESH:D020143] (126)   Sandhoff Disease [MESH:D012497] (73)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Glycogen Storage Disease [MESH:D006008] (530)   Glycogen Storage Disease XIV [MESH:C567859] (42)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Hyperlipoproteinemia Type II [MESH:D006938] (707)  Hypolipoproteinemias [MESH:D007009] (365)   Hypoalphalipoproteinemias [MESH:D052456] (323)   Familial HDL deficiency [MESH:C538394] (170)  Tangier Disease [MESH:D013631] (170)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Gangliosidoses, GM2 [MESH:D020143] (126)   Sandhoff Disease [MESH:D012497] (73)  Lysosomal Storage Diseases [MESH:D016464] (761)   Aspartylglucosaminuria [MESH:D054880] (25)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Gangliosidoses, GM2 [MESH:D020143] (126)   Sandhoff Disease [MESH:D012497] (73)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Molybdenum cofactor deficiency [MESH:C535811] (57)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1027)   Iminoglycinuria [MESH:C536285] (38)  Hypomagnesemia 5, Renal, with Ocular Involvement [MESH:C565423] (10)  Glycosuria, Renal [MESH:D006030] (50)   Cataract, Juvenile, With Microcornea And Glucosuria [MESH:C567434] (26)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Bile acid synthesis defect, congenital, 1 [MESH:C535442] (25)  17-Hydroxysteroid Dehydrogenase Deficiency [MESH:C537805] (52)  Muscular Dystrophies [MESH:D009136] (1597)   Bethlem myopathy [MESH:C535436] (108)  Muscular dystrophy congenital, merosin negative [MESH:C537384] (34)  Scleroatonic muscular dystrophy [MESH:C537521] (108)  Muscular Dystrophies, Limb-Girdle [MESH:D049288] (259)   Sarcoglycanopathies [MESH:D058088] (49)   Limb-girdle muscular dystrophy, type 2C [MESH:C535900] (20)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Hemangioma, capillary infantile [MESH:C535860] (190)  Meningioma, familial [MESH:C537443] (195)  Adenomatous Polyposis Coli [MESH:D011125] (1565)  Wilms Tumor [MESH:D009396] (553)  Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia Type 2b [MESH:D018814] (75)  Multiple Endocrine Neoplasia Type 2a [MESH:D018813] (102)   Familial medullary thyroid carcinoma [MESH:C536911] (101)  Osteogenesis Imperfecta [MESH:D010013] (481)   Osteogenesis imperfecta, type 2A [MESH:C536042] (375)  Osteogenesis imperfecta, type 3 [MESH:C536044] (375)  Osteogenesis imperfecta, type 4 [MESH:C536045] (375)  Bruck syndrome 2 [MESH:C537407] (64)  Pain Insensitivity, Congenital [MESH:D000699] (29)   Indifference to Pain, Congenital, Autosomal Recessive [MESH:C565467] (27)  Skin Diseases, Genetic [MESH:D012873] (3456)   Leukokeratosis, Hereditary Mucosal [MESH:D053529] (51)  Netherton Syndrome [MESH:D056770] (43)  Albinism [MESH:D000417] (359)   Albinism, Oculocutaneous [MESH:D016115] (234)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Hermansky Pudlak syndrome 2 [MESH:C537709] (16)  Dermatitis, Atopic [MESH:D003876] (2052)   Dermatitis, Atopic, 4 [MESH:C565291] (130)  Dyskeratosis Congenita [MESH:D019871] (185)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Dyskeratosis Congenita, Autosomal Dominant [MESH:C565079] (130)  Ectodermal Dysplasia [MESH:D004476] (958)   Ectodermal dysplasia/ skin fragility syndrome [MESH:C536183] (20)  Zlotogora-Ogur syndrome [MESH:C536726] (25)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Epidermolysis Bullosa [MESH:D004820] (259)   Poikiloderma of Kindler [MESH:C536321] (20)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Netherton Syndrome [MESH:D056770] (43)  Keratoderma, Palmoplantar [MESH:D007645] (287)   Keratoderma palmoplantar deafness [MESH:C536152] (68)  Vohwinkel syndrome [MESH:C536457] (68)  Knuckle pads, leuconychia and sensorineural deafness [MESH:C537210] (68)  Infant, Newborn, Diseases [MESH:D007232] (3064)   Hyperostosis, Cortical, Congenital [MESH:D006958] (392)  Ichthyosis [MESH:D007057] (476)   Ichthyosis with hypotrichosis, autosomal recessive [MESH:C536273] (32)  Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis [MESH:C564365] (78)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Netherton Syndrome [MESH:D056770] (43)  Infant, Premature, Diseases [MESH:D007235] (1292)   Respiratory Distress Syndrome, Newborn [MESH:D012127] (169)  Nystagmus, Congenital [MESH:D020417] (29)   Microphthalmia, Isolated, with Cataract 2 [MESH:C565876] (14) C17. Skin and Connective Tissue Diseases  C17. Skin and Connective Tissue Diseases  Connective Tissue Diseases [MESH:D003240] (4490)   Cartilage Diseases [MESH:D002357] (438)  Cellulitis [MESH:D002481] (88)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Collagen Diseases [MESH:D003095] (1267)   Keloid [MESH:D007627] (1111)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Nephritis, Hereditary [MESH:D009394] (62)   Alport syndrome, recessive type [MESH:C536587] (35)  Osteogenesis Imperfecta [MESH:D010013] (481)   Osteogenesis imperfecta, type 2A [MESH:C536042] (375)  Osteogenesis imperfecta, type 3 [MESH:C536044] (375)  Osteogenesis imperfecta, type 4 [MESH:C536045] (375)  Bruck syndrome 2 [MESH:C537407] (64)  Rheumatic Diseases [MESH:D012216] (3619)   Arthritis, Rheumatoid [MESH:D001172] (3603)  Skin Diseases [MESH:D012871] (8774)   Ectodermal dysplasia/ skin fragility syndrome [MESH:C536183] (20)  Nephrogenic Fibrosing Dermopathy [MESH:D054989] (452)  Skin Neoplasms [MESH:D012878] (2991)  Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Breast Diseases [MESH:D001941] (6148)   Ulnar-mammary syndrome [MESH:C536937] (57)  Breast Neoplasms [MESH:D001943] (6077)   Inflammatory Breast Neoplasms [MESH:D058922] (43)  Gynecomastia [MESH:D006177] (484)   17-Hydroxysteroid Dehydrogenase Deficiency [MESH:C537805] (52)  Dermatitis [MESH:D003872] (4530)   Drug Eruptions [MESH:D003875] (2697)  Dermatitis, Atopic [MESH:D003876] (2052)   Dermatitis, Atopic, 4 [MESH:C565291] (130)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Dermatitis, Occupational [MESH:D009783] (311)  Facial Dermatoses [MESH:D005148] (1336)   Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Hair Diseases [MESH:D006201] (1891)   Hypotrichosis [MESH:D007039] (1513)   Ichthyosis with hypotrichosis, autosomal recessive [MESH:C536273] (32)  Hypotrichosis And Recurrent Skin Vesicles [MESH:C567751] (17)  Alopecia [MESH:D000505] (1453)   Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis [MESH:C564365] (78)  Keratosis [MESH:D007642] (1941)   Ichthyosis [MESH:D007057] (481)   Ichthyosis with hypotrichosis, autosomal recessive [MESH:C536273] (32)  Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis [MESH:C564365] (78)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Netherton Syndrome [MESH:D056770] (43)  Keratoderma, Palmoplantar [MESH:D007645] (287)   Keratoderma palmoplantar deafness [MESH:C536152] (68)  Vohwinkel syndrome [MESH:C536457] (68)  Knuckle pads, leuconychia and sensorineural deafness [MESH:C537210] (68)  Photosensitivity Disorders [MESH:D010787] (272)   Poikiloderma of Kindler [MESH:C536321] (20)  Pigmentation Disorders [MESH:D010859] (1215)   Hypopigmentation [MESH:D017496] (718)   Albinism [MESH:D000417] (359)   Albinism, Oculocutaneous [MESH:D016115] (234)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Hermansky Pudlak syndrome 2 [MESH:C537709] (16)  Skin Abnormalities [MESH:D012868] (1709)   Dyskeratosis Congenita [MESH:D019871] (185)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Dyskeratosis Congenita, Autosomal Dominant [MESH:C565079] (130)  Ectodermal Dysplasia [MESH:D004476] (958)   Ectodermal dysplasia/ skin fragility syndrome [MESH:C536183] (20)  Zlotogora-Ogur syndrome [MESH:C536726] (25)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Epidermolysis Bullosa [MESH:D004820] (260)   Poikiloderma of Kindler [MESH:C536321] (20)  Ichthyosis [MESH:D007057] (481)   Ichthyosis with hypotrichosis, autosomal recessive [MESH:C536273] (32)  Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis [MESH:C564365] (78)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Netherton Syndrome [MESH:D056770] (43)  Skin Diseases, Eczematous [MESH:D017443] (3740)   Dermatitis, Atopic [MESH:D003876] (2052)   Dermatitis, Atopic, 4 [MESH:C565291] (130)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Dermatitis, Occupational [MESH:D009783] (311)  Skin Diseases, Genetic [MESH:D012873] (3481)   Leukokeratosis, Hereditary Mucosal [MESH:D053529] (51)  Netherton Syndrome [MESH:D056770] (43)  Albinism [MESH:D000417] (359)   Albinism, Oculocutaneous [MESH:D016115] (234)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Hermansky Pudlak syndrome 2 [MESH:C537709] (16)  Dermatitis, Atopic [MESH:D003876] (2052)   Dermatitis, Atopic, 4 [MESH:C565291] (130)  Dyskeratosis Congenita [MESH:D019871] (185)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Dyskeratosis Congenita, Autosomal Dominant [MESH:C565079] (130)  Ectodermal Dysplasia [MESH:D004476] (958)   Ectodermal dysplasia/ skin fragility syndrome [MESH:C536183] (20)  Zlotogora-Ogur syndrome [MESH:C536726] (25)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Epidermolysis Bullosa [MESH:D004820] (260)   Poikiloderma of Kindler [MESH:C536321] (20)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Netherton Syndrome [MESH:D056770] (43)  Keratoderma, Palmoplantar [MESH:D007645] (287)   Keratoderma palmoplantar deafness [MESH:C536152] (68)  Vohwinkel syndrome [MESH:C536457] (68)  Knuckle pads, leuconychia and sensorineural deafness [MESH:C537210] (68)  Skin Diseases, Infectious [MESH:D012874] (2684)   Skin Diseases, Bacterial [MESH:D017192] (156)   Hidradenitis Suppurativa [MESH:D017497] (120)  Skin Diseases, Parasitic [MESH:D012876] (2526)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)  Skin Diseases, Papulosquamous [MESH:D017444] (3392)   Psoriasis [MESH:D011565] (3278)  Skin Diseases, Vascular [MESH:D017445] (3288)   Behcet Syndrome [MESH:D001528] (1784)  Skin Diseases, Vesiculobullous [MESH:D012872] (1754)   Blister [MESH:D001768] (93)   Poikiloderma of Kindler [MESH:C536321] (20)  Hypotrichosis And Recurrent Skin Vesicles [MESH:C567751] (17)  Epidermolysis Bullosa [MESH:D004820] (260)   Poikiloderma of Kindler [MESH:C536321] (20)  Sweat Gland Diseases [MESH:D013543] (231)   Hidradenitis [MESH:D016575] (121)   Hidradenitis Suppurativa [MESH:D017497] (120) 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)   Acidosis [MESH:D000138] (626)   Succinyl-CoA:3-oxoacid CoA transferase deficiency [MESH:C537527] (38)  Brain Diseases, Metabolic [MESH:D001928] (3350)   Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Sandhoff Disease [MESH:D012497] (73)  Gangliosidoses, GM2 [MESH:D020143] (126)   Sandhoff Disease [MESH:D012497] (73)  Calcium Metabolism Disorders [MESH:D002128] (3634)   Hypercalcemia [MESH:D006934] (1999)  Calcinosis [MESH:D002114] (2989)   Pulmonary Alveolar Microlithiasis [MESH:C562405] (44)  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, Gestational [MESH:D016640] (1152)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)   Maturity-Onset Diabetes of the Young, Type 4 [MESH:C563451] (44)  Maturity-Onset Diabetes of the Young, Type 1 [MESH:C565101] (293)  Glycosuria [MESH:D006029] (100)   Glycosuria, Renal [MESH:D006030] (50)   Cataract, Juvenile, With Microcornea And Glucosuria [MESH:C567434] (26)  Hyperinsulinism [MESH:D006946] (3586)   Insulin Resistance [MESH:D007333] (3511)   Metabolic Syndrome X [MESH:D024821] (2151)  Hypoglycemia [MESH:D007003] (2420)   ACTH Deficiency, Isolated [MESH:C562707] (124)  Lipid Metabolism Disorders [MESH:D052439] (3225)   Dyslipidemias [MESH:D050171] (2428)   Hyperlipidemias [MESH:D006949] (1908)   Hypercholesterolemia [MESH:D006937] (1404)  Hyperlipoproteinemias [MESH:D006951] (903)   Hyperlipoproteinemia Type II [MESH:D006938] (707)  Hypolipoproteinemias [MESH:D007009] (409)   Hypoalphalipoproteinemias [MESH:D052456] (323)   Familial HDL deficiency [MESH:C538394] (170)  Tangier Disease [MESH:D013631] (170)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Gangliosidoses, GM2 [MESH:D020143] (126)   Sandhoff Disease [MESH:D012497] (73)  Malabsorption Syndromes [MESH:D008286] (1869)   Diarrhea 4, Malabsorptive, Congenital [MESH:C563673] (15)  Celiac Disease [MESH:D002446] (340)  Metabolism, Inborn Errors [MESH:D008661] (6028)   Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559)   Histidinemia [MESH:C538320] (87)  Albinism [MESH:D000417] (359)   Albinism, Oculocutaneous [MESH:D016115] (234)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Hermansky Pudlak syndrome 2 [MESH:C537709] (16)  Amyloidosis, Familial [MESH:D028226] (696)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Amyloidosis, familial visceral [MESH:C538249] (285)  Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Sandhoff Disease [MESH:D012497] (73)  Gangliosidoses, GM2 [MESH:D020143] (126)   Sandhoff Disease [MESH:D012497] (73)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Glycogen Storage Disease [MESH:D006008] (530)   Glycogen Storage Disease XIV [MESH:C567859] (42)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Hyperlipoproteinemia Type II [MESH:D006938] (707)  Hypolipoproteinemias [MESH:D007009] (365)   Hypoalphalipoproteinemias [MESH:D052456] (323)   Familial HDL deficiency [MESH:C538394] (170)  Tangier Disease [MESH:D013631] (170)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Gangliosidoses, GM2 [MESH:D020143] (126)   Sandhoff Disease [MESH:D012497] (73)  Lysosomal Storage Diseases [MESH:D016464] (761)   Aspartylglucosaminuria [MESH:D054880] (25)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Gangliosidoses, GM2 [MESH:D020143] (126)   Sandhoff Disease [MESH:D012497] (73)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Molybdenum cofactor deficiency [MESH:C535811] (57)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1026)   Iminoglycinuria [MESH:C536285] (38)  Hypomagnesemia 5, Renal, with Ocular Involvement [MESH:C565423] (10)  Glycosuria, Renal [MESH:D006030] (50)   Cataract, Juvenile, With Microcornea And Glucosuria [MESH:C567434] (26)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Bile acid synthesis defect, congenital, 1 [MESH:C535442] (25)  17-Hydroxysteroid Dehydrogenase Deficiency [MESH:C537805] (52)  Phosphorus Metabolism Disorders [MESH:D010760] (711)   Hypophosphatemia [MESH:D017674] (640)  Proteostasis Deficiencies [MESH:D057165] (3522)   Amyloidosis [MESH:D000686] (791)   Amyloid Neuropathies [MESH:D017772] (139)   Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  Amyloidosis, Familial [MESH:D028226] (696)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Amyloidosis, familial visceral [MESH:C538249] (285)  Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Cerebral Amyloid Angiopathy [MESH:D016657] (470)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Water-Electrolyte Imbalance [MESH:D014883] (2790)   Hypercalcemia [MESH:D006934] (1999)  Hypokalemia [MESH:D007008] (1041)  Nutrition Disorders [MESH:D009748] (4945)   Malnutrition [MESH:D044342] (2754)   Deficiency Diseases [MESH:D003677] (2742)   Avitaminosis [MESH:D001361] (2304)   Vitamin A Deficiency [MESH:D014802] (705)   Keratomalacia [MESH:C536156] (61)  Vitamin E Deficiency [MESH:D014811] (274)   Ataxia with vitamin E deficiency [MESH:C535393] (271)  Overnutrition [MESH:D044343] (4463)   Obesity [MESH:D009765] (4462)   Obesity, Morbid [MESH:D009767] (515)  Prader-Willi Syndrome [MESH:D011218] (46) C19. Endocrine System Diseases  C19. Endocrine System Diseases  Z. Exceptions (123)   Not Fully Specified [NFS] (123)  Endocrine System Diseases [MESH:D004700] (8062)   ACTH Deficiency, Isolated [MESH:C562707] (124)  Adrenal Gland Diseases [MESH:D000307] (2397)   Adrenal Cortex Diseases [MESH:D000303] (969)   Adrenal Cortex Neoplasms [MESH:D000306] (823)   Adrenocortical Carcinoma [MESH:D018268] (821)  Adrenal Gland Neoplasms [MESH:D000310] (917)   Adrenal Cortex Neoplasms [MESH:D000306] (823)   Adrenocortical Carcinoma [MESH:D018268] (821)  Diabetes Mellitus [MESH:D003920] (6159)   Diabetes, Gestational [MESH:D016640] (1152)  Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)  Diabetes Complications [MESH:D048909] (4129)   Diabetic Cardiomyopathies [MESH:D058065] (1995)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)   Maturity-Onset Diabetes of the Young, Type 4 [MESH:C563451] (44)  Maturity-Onset Diabetes of the Young, Type 1 [MESH:C565101] (293)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Adrenal Gland Neoplasms [MESH:D000310] (917)   Adrenal Cortex Neoplasms [MESH:D000306] (823)   Adrenocortical Carcinoma [MESH:D018268] (821)  Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia Type 2b [MESH:D018814] (75)  Multiple Endocrine Neoplasia Type 2a [MESH:D018813] (102)   Familial medullary thyroid carcinoma [MESH:C536911] (101)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Islet Cell [MESH:D018273] (115)   Vipoma [MESH:D003969] (110)  Testicular Neoplasms [MESH:D013736] (520)   Testicular Germ Cell Tumor [MESH:C563236] (176)  Thyroid Neoplasms [MESH:D013964] (2040)   Familial medullary thyroid carcinoma [MESH:C536911] (101)  Thyroid cancer, medullary [MESH:C536914] (74)  Gonadal Disorders [MESH:D006058] (5088)   Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   17-Hydroxysteroid Dehydrogenase Deficiency [MESH:C537805] (52)  Kallmann Syndrome [MESH:D017436] (147)  Hypogonadism [MESH:D007006] (1123)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  Kallmann Syndrome [MESH:D017436] (147)  Ovarian Diseases [MESH:D010049] (4253)   Ovarian Neoplasms [MESH:D010051] (3281)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Testicular Diseases [MESH:D013733] (777)   Testicular Microlithiasis [MESH:C566478] (44)  Cryptorchidism [MESH:D003456] (215)   Carnevale syndrome [MESH:C535586] (45)  Testicular Neoplasms [MESH:D013736] (520)   Testicular Germ Cell Tumor [MESH:C563236] (176)  Pituitary Diseases [MESH:D010900] (1829)   Hyperpituitarism [MESH:D006964] (1259)   Hyperprolactinemia [MESH:D006966] (603)  Thyroid Diseases [MESH:D013959] (2808)   Hyperthyroidism [MESH:D006980] (1191)  Hyperthyroxinemia [MESH:D006981] (659)   Dystransthyretinemic Euthyroidal Hyperthyroxinemia [MESH:C567719] (136)  Hypothyroidism [MESH:D007037] (496)   Thyroid Dyshormonogenesis 5 [MESH:C562771] (7)  Thyroid Neoplasms [MESH:D013964] (2040)   Familial medullary thyroid carcinoma [MESH:C536911] (101)  Thyroid cancer, medullary [MESH:C536914] (74) C20. Immune System Diseases  C20. Immune System Diseases  Immune System Diseases [MESH:D007154] (7674)   Autoimmune Diseases [MESH:D001327] (5067)   Arthritis, Rheumatoid [MESH:D001172] (3601)  Diabetes Mellitus, Type 1 [MESH:D003922] (1893)  Glomerulonephritis, Membranous [MESH:D015433] (642)  Hepatitis, Autoimmune [MESH:D019693] (1982)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Myasthenia Gravis [MESH:D009157] (632)  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)  Hypersensitivity [MESH:D006967] (5873)   Drug Hypersensitivity [MESH:D004342] (4000)   Drug Eruptions [MESH:D003875] (2695)  Asthma, Aspirin-Induced [MESH:D055963] (1055)   Asthma, Nasal Polyps, And Aspirin Intolerance [MESH:C565935] (80)  Hypersensitivity, Delayed [MESH:D006968] (3408)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Hypersensitivity, Immediate [MESH:D006969] (4980)   Asthma, Aspirin-Induced [MESH:D055963] (1055)   Asthma, Nasal Polyps, And Aspirin Intolerance [MESH:C565935] (80)  Dermatitis, Atopic [MESH:D003876] (2052)   Dermatitis, Atopic, 4 [MESH:C565291] (130)  Respiratory Hypersensitivity [MESH:D012130] (4250)   Ige Responsiveness, Atopic [MESH:C564133] (267)  Asthma [MESH:D001249] (3914)  Rhinitis, Allergic, Perennial [MESH:D012221] (625)   Allergic Rhinitis [MESH:C567078] (181)  Immunologic Deficiency Syndromes [MESH:D007153] (3788)   CD8 Deficiency, Familial [MESH:C563824] (41)  LIG4 Syndrome [MESH:C564694] (24)  HIV Infections [MESH:D015658] (3402)  Wiskott-Aldrich Syndrome [MESH:D014923] (28)  Lymphopenia [MESH:D008231] (990)   Wiskott-Aldrich Syndrome [MESH:D014923] (28)  Immunoproliferative Disorders [MESH:D007160] (4761)   Lymphoproliferative Disorders [MESH:D008232] (4734)   Multiple Myeloma [MESH:D009101] (2767)  Leukemia, Lymphoid [MESH:D007945] (3047)   Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)  Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Lymphoma [MESH:D008223] (3684)   Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  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)  Lymphoma, T-Cell [MESH:D016399] (1382)   Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  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)  Hepatitis, Animal [MESH:D006520] (260)  Mammary Neoplasms, Animal [MESH:D015674] (2735) C23. Pathological Conditions, Signs and Symptoms  C23. Pathological Conditions, Signs and Symptoms  Pathological Conditions, Anatomical [MESH:D020763] (6074)   Atrophy [MESH:D001284] (2603)  Facial Asymmetry [MESH:D005146] (31)  Plaque, Amyloid [MESH:D058225] (334)  Alopecia [MESH:D000505] (1383)   Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis [MESH:C564365] (78)  Blister [MESH:D001768] (93)   Poikiloderma of Kindler [MESH:C536321] (20)  Hypotrichosis And Recurrent Skin Vesicles [MESH:C567751] (17)  Calculi [MESH:D002137] (756)   Testicular Microlithiasis [MESH:C566478] (44)  Fistula [MESH:D005402] (130)   Digestive System Fistula [MESH:D016154] (102)   Esophageal Fistula [MESH:D004937] (89)   Tracheoesophageal Fistula [MESH:D014138] (88)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Hernia [MESH:D006547] (2825)   Encephalocele [MESH:D004677] (151)   Parietal Foramina 2 [MESH:C566510] (9)  Parietal Foramina [MESH:C566826] (42)  Hernia, Diaphragmatic [MESH:D006548] (2647)   Congenital diaphragmatic hernia [MESH:C538080] (381)  Hypertrophy [MESH:D006984] (4476)   Cardiomegaly [MESH:D006332] (3802)   Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Polyps [MESH:D011127] (1633)   Intestinal Polyps [MESH:D007417] (1592)  Nasal Polyps [MESH:D009298] (129)   Asthma, Nasal Polyps, And Aspirin Intolerance [MESH:C565935] (80)  Pathologic Processes [MESH:D010335] (9863)   Extravasation of Diagnostic and Therapeutic Materials [MESH:D005119] (506)  Hyperuricemia [MESH:D033461] (82)  Ischemia [MESH:D007511] (3049)  Necrosis [MESH:D009336] (4019)  Nerve Degeneration [MESH:D009410] (4061)  Arrhythmias, Cardiac [MESH:D001145] (4658)   Bradycardia [MESH:D001919] (1899)  Atrial Fibrillation [MESH:D001281] (1053)   Atrial Fibrillation, Familial, 7 [MESH:C567389] (39)  Long QT Syndrome [MESH:D008133] (691)   Long Qt Syndrome 5 [MESH:C566766] (40)  Tachycardia [MESH:D013610] (3339)   Tachycardia, Ventricular [MESH:D017180] (1386)   Polymorphic catecholergic ventricular tachycardia [MESH:C536334] (64)  Channelopathies [MESH:D053447] (28)   Indifference to Pain, Congenital, Autosomal Recessive [MESH:C565467] (27)  Death [MESH:D003643] (1328)   Fetal Death [MESH:D005313] (464)  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)   Pitt-Hopkins syndrome [MESH:C537403] (113)  Fibrosis [MESH:D005355] (3133)   Fibrosis Of Extraocular Muscles, Congenital, 2 [MESH:C566587] (18)  Nephrogenic Fibrosing Dermopathy [MESH:D054989] (452)  Cicatrix [MESH:D002921] (1115)   Keloid [MESH:D007627] (1110)  Granuloma [MESH:D006099] (587)   Granuloma, Plasma Cell [MESH:D006104] (58)  Growth Disorders [MESH:D006130] (2438)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  LIG4 Syndrome [MESH:C564694] (24)  Fetal Growth Retardation [MESH:D005317] (986)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Hemorrhage [MESH:D006470] (4451)   Gastrointestinal Hemorrhage [MESH:D006471] (815)  Hematuria [MESH:D006417] (477)   Hematuria, Benign Familial [MESH:C562476] (25)  Intracranial Hemorrhages [MESH:D020300] (3241)   Cerebral Hemorrhage [MESH:D002543] (2872)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Purpura [MESH:D011693] (475)   Purpura Fulminans [MESH:D055665] (69)  Inflammation [MESH:D007249] (5241)   Neurogenic Inflammation [MESH:D020078] (2246)  Suppuration [MESH:D013492] (117)   Cellulitis [MESH:D002481] (87)  Systemic Inflammatory Response Syndrome [MESH:D018746] (3563)   Sepsis [MESH:D018805] (3562)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Metastasis [MESH:D009362] (4441)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Postoperative Complications [MESH:D011183] (5311)   Reperfusion Injury [MESH:D015427] (4968)  Sclerosis [MESH:D012598] (224)   Scleroatonic muscular dystrophy [MESH:C537521] (108)  Shock [MESH:D012769] (2550)   Multiple Organ Failure [MESH:D009102] (1836)  Signs and Symptoms [MESH:D012816] (10659)   Edema [MESH:D004487] (3726)  Body Temperature Changes [MESH:D001832] (3130)   Hypothermia [MESH:D007035] (2075)  Body Weight [MESH:D001835] (4972)   Body Weight Changes [MESH:D001836] (3206)   Weight Gain [MESH:D015430] (2595)  Overweight [MESH:D050177] (4455)   Obesity [MESH:D009765] (4454)   Obesity, Morbid [MESH:D009767] (515)  Neurologic Manifestations [MESH:D009461] (8702)   Orthostatic Intolerance [MESH:D054971] (64)  Seizures [MESH:D012640] (4502)  Dyskinesias [MESH:D020820] (3285)   Catalepsy [MESH:D002375] (1429)  Dystonia [MESH:D004421] (848)  Hyperkinesis [MESH:D006948] (1799)  Tremor [MESH:D014202] (840)  Ataxia [MESH:D001259] (984)   Ataxia with vitamin E deficiency [MESH:C535393] (271)  Cerebellar Ataxia [MESH:D002524] (289)   Dysequilibrium syndrome [MESH:C535731] (83)  Neurobehavioral Manifestations [MESH:D019954] (4706)   Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Language Development Disorders [MESH:D007805] (351)  Speech Disorders [MESH:D013064] (482)   Stuttering [MESH:D013342] (38)  Consciousness Disorders [MESH:D003244] (677)   Unconsciousness [MESH:D014474] (657)   Stupor [MESH:D053608] (103)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Intellectual Disability [MESH:D008607] (1476)   Dysequilibrium syndrome [MESH:C535731] (83)  Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Zlotogora-Ogur syndrome [MESH:C536726] (25)  Pitt-Hopkins syndrome [MESH:C537403] (113)  Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Histidinemia [MESH:C538320] (87)  Birk-Barel Mental Retardation Dysmorphism Syndrome [MESH:C567357] (20)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscle Hypotonia [MESH:D009123] (258)   Birk-Barel Mental Retardation Dysmorphism Syndrome [MESH:C567357] (20)  Pain [MESH:D010146] (3869)   Paroxysmal Extreme Pain Disorder [MESH:C563475] (27)  Neuralgia [MESH:D009437] (2074)   Neuralgia, Postherpetic [MESH:D051474] (742)  Paralysis [MESH:D010243] (2298)   Ophthalmoplegia [MESH:D009886] (1468)   Fibrosis Of Extraocular Muscles, Congenital, 2 [MESH:C566587] (18)  Sensation Disorders [MESH:D012678] (5009)   Olfaction Disorders [MESH:D000857] (105)  Hearing Disorders [MESH:D006311] (2101)   Hearing Loss [MESH:D034381] (2066)   Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Deafness [MESH:D003638] (593)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Keratoderma palmoplantar deafness [MESH:C536152] (68)  Vohwinkel syndrome [MESH:C536457] (68)  Townes-Brocks syndrome [MESH:C536974] (28)  Knuckle pads, leuconychia and sensorineural deafness [MESH:C537210] (68)  Deafness, Autosomal Dominant 10 [MESH:C563354] (26)  Cardiomyopathy, Dilated, 1J [MESH:C565337] (26)  Deafness, Autosomal Recessive 1A [MESH:C567134] (88)  Deafness, Autosomal Dominant 3A [MESH:C567277] (77)  Hearing Loss, Noise-Induced [MESH:D006317] (134)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Vision Disorders [MESH:D014786] (444)   Enhanced S-Cone Syndrome [MESH:C564835] (11)  Pain [MESH:D010146] (4511)   Paroxysmal Extreme Pain Disorder [MESH:C563475] (27)  Chest Pain [MESH:D002637] (2642)   Angina Pectoris [MESH:D000787] (2568)   Acute Coronary Syndrome [MESH:D054058] (2286)  Neuralgia [MESH:D009437] (2074)   Neuralgia, Postherpetic [MESH:D051474] (742)  Signs and Symptoms, Digestive [MESH:D012817] (3095)   Diarrhea [MESH:D003967] (858)   Diarrhea 4, Malabsorptive, Congenital [MESH:C563673] (15)  Signs and Symptoms, Respiratory [MESH:D012818] (2724)   Anoxia [MESH:D000860] (1698)  Respiratory Sounds [MESH:D012135] (713)  Hyperventilation [MESH:D006985] (652)   Pitt-Hopkins syndrome [MESH:C537403] (113)  Hypoventilation [MESH:D007040] (359)   Congenital central hypoventilation syndrome [MESH:C536209] (341)  Skin Manifestations [MESH:D012877] (1250)   Purpura [MESH:D011693] (475)   Purpura Fulminans [MESH:D055665] (69)  Urological Manifestations [MESH:D020924] (3532)   Proteinuria [MESH:D011507] (3293) C24. Occupational Diseases  C24. Occupational Diseases  Occupational Diseases [MESH:D009784] (3402)   Agricultural Workers' Diseases [MESH:D000382] (193)  Dermatitis, Occupational [MESH:D009783] (311) 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)  Asthma, Aspirin-Induced [MESH:D055963] (1055)   Asthma, Nasal Polyps, And Aspirin Intolerance [MESH:C565935] (80)  Poisoning [MESH:D011041] (6703)   Arsenic Poisoning [MESH:D020261] (2540)  Carbon Tetrachloride Poisoning [MESH:D002252] (102)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Psychoses, Substance-Induced [MESH:D011605] (2053)  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)  Psychoses, Substance-Induced [MESH:D011605] (2052)  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)   Liver Diseases, Alcoholic [MESH:D008108] (3243)  Opioid-Related Disorders [MESH:D009293] (1491)   Heroin Dependence [MESH:D006556] (950) 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)  Extravasation of Diagnostic and Therapeutic Materials [MESH:D005119] (506)  Fractures, Bone [MESH:D050723] (597)  Vascular System Injuries [MESH:D057772] (2086)  Craniocerebral Trauma [MESH:D006259] (3523)   Brain Injuries [MESH:D001930] (3431)  Coma, Post-Head Injury [MESH:D020207] (55)  Sprains and Strains [MESH:D013180] (153)   Cumulative Trauma Disorders [MESH:D012090] (151)   Carpal Tunnel Syndrome [MESH:D002349] (147)  Thoracic Injuries [MESH:D013898] (1831)   Heart Injuries [MESH:D006335] (82)  Trauma, Nervous System [MESH:D020196] (3535)   Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431)  Coma, Post-Head Injury [MESH:D020207] (55) D02. Organic Chemicals  D02. Organic Chemicals  Organic Chemicals [MESH:D009930] (75987)   Organophosphorus Compounds [MESH:D009943] (2593)   Organothiophosphorus Compounds [MESH:D009946] (291)  Sulfur Compounds [MESH:D013457] (10450)   Organothiophosphorus Compounds [MESH:D009946] (291) 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)   Facies [MESH:D019066] (704)   Pitt-Hopkins syndrome [MESH:C537403] (113) 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)   Dysequilibrium syndrome [MESH:C535731] (83)  Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Zlotogora-Ogur syndrome [MESH:C536726] (25)  Pitt-Hopkins syndrome [MESH:C537403] (113)  Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Histidinemia [MESH:C538320] (87)  Birk-Barel Mental Retardation Dysmorphism Syndrome [MESH:C567357] (20)  Psychological Phenomena and Processes [MESH:D011579] (294)   Psychophysiology [MESH:D011603] (86)   Sensation [MESH:D012677] (53)   Pain [MESH:D010146] (32)   Paroxysmal Extreme Pain Disorder [MESH:C563475] (27)  Mental Disorders [MESH:D001523] (2063)   Mental Disorders Diagnosed in Childhood [MESH:D019952] (1245)   Developmental Disabilities [MESH:D002658] (151)   Malpuech facial clefting syndrome [MESH:C535704] (45)  Intellectual Disability [MESH:D008607] (1109)   Dysequilibrium syndrome [MESH:C535731] (83)  Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Zlotogora-Ogur syndrome [MESH:C536726] (25)  Pitt-Hopkins syndrome [MESH:C537403] (113)  Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Histidinemia [MESH:C538320] (87)  Birk-Barel Mental Retardation Dysmorphism Syndrome [MESH:C567357] (20)  Sexual and Gender Disorders [MESH:D019968] (624)   Disorders of Sex Development [MESH:D012734] (609)   46, XY Disorders of Sex Development [MESH:D058490] (388)   17-Hydroxysteroid Dehydrogenase Deficiency [MESH:C537805] (52) G. Phenomena and Processes  G. Phenomena and Processes  Musculoskeletal and Neural Physiological Phenomena [MESH:D055687] (260)   Nervous System Physiological Phenomena [MESH:D009424] (141)   Nervous System Physiological Processes [MESH:D052778] (113)   Sensation [MESH:D012677] (56)   Pain [MESH:D010146] (33)   Paroxysmal Extreme Pain Disorder [MESH:C563475] (27)