Item 13 of 25 (back to results) previous next   Fonofos D004397               MeSH Unique Identifier: D004397 Scope Notes: An organothiophosphorus cholinesterase inhibitor that is used as an insecticide. Chemical – Gene Interaction Note 1: Fonofos results in increased methylation of MARC1 promoter Note 2: Fonofos results in increased methylation of A4GALT promoter Click here for more information

Current search: C05. Musculoskeletal Diseases: Musculoskeletal Diseases [MESH:D009140] > Bone Diseases [MESH:D001847] > Bone Diseases, Developmental [MESH:D001848] > Dysostoses [MESH:D004413] > Synostosis [MESH:D013580] > Syndactyly [MESH:D013576] > Rosselli-Gulienetti Syndrome [MESH:C563117] × 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 neuroblastoma derived homolog [HGNC:MYCN] (29)  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 01, subfamily A, polypeptide 02 [HGNC:CYP1A2] (466)  cytochrome P450, family 03, subfamily A, polypeptide 04 [HGNC:CYP3A4] (612)  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 2, group E, member 3 [HGNC:NR2E3] (4)  retinoic acid receptor, alpha [HGNC:RARA] (73)  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)  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)  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)   response to substance (623)  Decreases (5154)   activity (2549)  methylation (108)  reaction (3393)  Increases (5571)   chemical synthesis (464)  metabolic processing (740)  methylation (105) 4. Semantic Terms  4. Semantic Terms  Entity [STY:T071] (48056)   Physical Object [STY:T072] (47583)   Substance [STY:T167] (46174)   Chemical [STY:T103] (46110)   Chemical Viewed Functionally [STY:T120] (28747)   Hazardous or Poisonous Substance [STY:T131] (590)  Chemical Viewed Structurally [STY:T104] (44741)   Organic Chemical [STY:T109] (44144)   Organophosphorus Compound [STY:T115] (306) 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 C [MESH:D006526] (1627)  Hepatitis B [MESH:D006509] (976)   Hepatitis B, Chronic [MESH:D019694] (277)  RNA Virus Infections [MESH:D012327] (4215)   Flaviviridae Infections [MESH:D018178] (1656)   Hepatitis C [MESH:D006526] (1627)  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)  Otorhinolaryngologic Neoplasms [MESH:D010039] (1557)   Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  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)   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)  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)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  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)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  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)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Craniofacial Abnormalities [MESH:D019465] (3098)   Malpuech facial clefting syndrome [MESH:C535704] (45)  LIG4 Syndrome [MESH:C564694] (24)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  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)  Hepatomegaly [MESH:D006529] (1169)  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 C [MESH:D006526] (1627)  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)  Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  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)   Neuroendocrine Carcinoma of Salivary Glands, Sensorineural Hearing Loss, and Enamel Hypoplasia [MESH:C566352] (437)  Periodontal Diseases [MESH:D010510] (1001)   Poikiloderma of Kindler [MESH:C536321] (64)  Salivary Gland Diseases [MESH:D012466] (1213)   Salivary Gland Neoplasms [MESH:D012468] (968)   Neuroendocrine Carcinoma of Salivary Glands, Sensorineural Hearing Loss, and Enamel Hypoplasia [MESH:C566352] (437)  Pharyngeal Diseases [MESH:D010608] (1562)   Nasopharyngeal Diseases [MESH:D009302] (1508)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  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 Agenesis, Selective, 6 [MESH:C567755] (154)  Tooth Diseases [MESH:D014076] (742)   Tooth Abnormalities [MESH:D014071] (622)   Nance-Horan syndrome [MESH:C538336] (17)  Tooth Agenesis, Selective, 6 [MESH:C567755] (154) 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)  Otorhinolaryngologic Neoplasms [MESH:D010039] (1561)   Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Pharyngeal Diseases [MESH:D010608] (1605)   Deglutition Disorders [MESH:D003680] (108)  Nasopharyngeal Diseases [MESH:D009302] (1508)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198) 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)  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)   Stroke [MESH:D020521] (3702)  Vasospasm, Intracranial [MESH:D020301] (324)  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)   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)  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)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  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)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  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)   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)   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)  Torsades de Pointes [MESH:D016171] (880)  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)   Stroke [MESH:D020521] (3702)  Vasospasm, Intracranial [MESH:D020301] (324)  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)   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)  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)   Methemoglobinemia [MESH:D008708] (850)  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)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Craniofacial Abnormalities [MESH:D019465] (3064)   Malpuech facial clefting syndrome [MESH:C535704] (45)  LIG4 Syndrome [MESH:C564694] (24)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  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)  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)  Lysosomal Storage Diseases [MESH:D016464] (761)   Aspartylglucosaminuria [MESH:D054880] (25)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Molybdenum cofactor deficiency [MESH:C535811] (57)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  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)   Dermatitis, Atopic [MESH:D003876] (2052)  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)  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)  Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  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)  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)   Dermatitis, Atopic [MESH:D003876] (2052)  Drug Eruptions [MESH:D003875] (2697)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Dermatitis, Occupational [MESH:D009783] (311)  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, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Dermatitis, Occupational [MESH:D009783] (311)  Skin Diseases, Genetic [MESH:D012873] (3481)   Dermatitis, Atopic [MESH:D003876] (2052)  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)  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)  Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  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, Metabolic [MESH:D012875] (1574)   Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  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)  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)  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)  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)  Lysosomal Storage Diseases [MESH:D016464] (761)   Aspartylglucosaminuria [MESH:D054880] (25)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Molybdenum cofactor deficiency [MESH:C535811] (57)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  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)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  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)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  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)   Dermatitis, Atopic [MESH:D003876] (2052)  Asthma, Aspirin-Induced [MESH:D055963] (1055)   Asthma, Nasal Polyps, And Aspirin Intolerance [MESH:C565935] (80)  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)   Hepatomegaly [MESH:D006529] (1169)  Splenomegaly [MESH:D013163] (1258)  Cardiomegaly [MESH:D006332] (3802)   Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Polyps [MESH:D011127] (1633)   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)  Torsades de Pointes [MESH:D016171] (880)  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)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  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)   Organophosphonates [MESH:D063065] (506)   Organothiophosphonates [MESH:D063085] (9)   Fonofos [MESH:D004397] (3)  Organothiophosphorus Compounds [MESH:D009946] (291)   Organothiophosphonates [MESH:D063085] (9)   Fonofos [MESH:D004397] (3)  Sulfur Compounds [MESH:D013457] (10450)   Organothiophosphorus Compounds [MESH:D009946] (291)   Organothiophosphonates [MESH:D063085] (9)   Fonofos [MESH:D004397] (3) 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)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  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)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  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)