Item 7 of 154 (back to results) previous next   methylselenic acid C008493               MeSH Unique Identifier: C008493 Chemical – Gene Interaction Note 1: AR protein inhibits the reaction [methylselenic acid results in decreased expression of ABCC4 mRNA] Note 2: Methylselenic acid affects the expression of ABCC4 mRNA Click here for more information

Current search: C17. Skin and Connective Tissue Diseases: Skin Diseases [MESH:D012871] > Skin Diseases, Genetic [MESH:D012873] > Dyskeratosis Congenita [MESH:D019871] > Hoyeraal Hreidarsson syndrome [MESH:C536068] × Select any link to see items in a related category. more general categories    information about this item 1. Human Genes  1. Human Genes  A-kinase anchor proteins [HGNC:AKAP] (99)   A kinase (PRKA) anchor protein 12 [HGNC:AKAP12] (34)  Ankyrin repeat domain containing [HGNC:ANKRD] (566)   cyclin-dependent kinase inhibitor 2D (p19, inhibits CDK4) [HGNC:CDKN2D] (29)  nuclear factor of kappa light polypeptide gene enhancer in B-cells 1 [HGNC:NFKB1] (254)  ATP-binding cassette transporters [HGNC:ABC] (821)   ATP-binding cassette transporters, subfamily C [HGNC:ABCC] (458)   ATP-binding cassette, sub-family C (CFTR/MRP), member 4 [HGNC:ABCC4] (88)  Basic helix-loop-helix [HGNC:BHLH] (618)   inhibitor of DNA binding 1, dominant negative helix-loop-helix protein [HGNC:ID1] (63)  inhibitor of DNA binding 2, dominant negative helix-loop-helix protein [HGNC:ID2] (69)  inhibitor of DNA binding 3, dominant negative helix-loop-helix protein [HGNC:ID3] (47)  MAX dimerization protein 1 [HGNC:MXD1] (46)  MAX interactor 1, dimerization protein [HGNC:MXI1] (19)  microphthalmia-associated transcription factor [HGNC:MITF] (28)  nuclear receptor coactivator 1 [HGNC:NCOA1] (71)  nuclear receptor coactivator 2 [HGNC:NCOA2] (50)  v-myc avian myelocytomatosis viral oncogene homolog [HGNC:MYC] (254)  Basic leucine zipper proteins [HGNC:bZIP] (670)   cAMP responsive element binding protein 1 [HGNC:CREB1] (108)  jun B proto-oncogene [HGNC:JUNB] (59)  jun proto-oncogene [HGNC:JUN] (290)  X-box binding protein 1 [HGNC:XBP1] (79)  Beta 3-glycosyltransferases [HGNC:B3GT] (48)   UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 [HGNC:B4GALT1] (22)  Blood group antigens [HGNC:blood-group] (97)   solute carrier family 14 (urea transporter), member 1 [HGNC:SLC14A1] (13)  Cadherins [HGNC:CDH] (214)   Cadherins, major [HGNC:MCDH] (189)   cadherin 07, type 2 [HGNC:CDH7] (5)  cadherin 15, type 1, M-cadherin (myotubule) [HGNC:CDH15] (4)  S100 calcium binding proteins [HGNC:S100] (110)   S100 calcium binding protein A04 [HGNC:S100A4] (35)  Cathepsins [HGNC:CTS] (135)   cathepsin K [HGNC:CTSK] (11)  CD molecules [HGNC:CD] (1459)   integrin, beta 4 [HGNC:ITGB4] (41)  prion protein [HGNC:PRNP] (49)  toll-like receptor 2 [HGNC:TLR2] (55)  Collagens [HGNC:COL] (230)   collagen, type VI, alpha 1 [HGNC:COL6A1] (28)  Coronins [HGNC:CORO] (22)   coronin, actin binding protein, 1A [HGNC:CORO1A] (7)  Cyclin-dependent kinases [HGNC:CDK] (338)   cyclin-dependent kinase 01 [HGNC:CDK1] (151)  cyclin-dependent kinase 02 [HGNC:CDK2] (177)  cyclin-dependent kinase 04 [HGNC:CDK4] (127)  cyclin-dependent kinase 05 [HGNC:CDK5] (21)  cyclin-dependent kinase 06 [HGNC:CDK6] (55)  Dolichyl D-mannosyl phosphate dependent mannosyltransferases [HGNC:DOLPM] (30)   ALG3, alpha-1,3- mannosyltransferase [HGNC:ALG3] (9)  EF-hand domain containing [HGNC:EFHAND] (226)   myosin, light chain 09, regulatory [HGNC:MYL9] (16)  S100 calcium binding protein A04 [HGNC:S100A4] (35)  spectrin, alpha, non-erythrocytic 1 [HGNC:SPTAN1] (30)  Endothelin receptors [HGNC:EDNR] (57)   endothelin receptor type A [HGNC:EDNRA] (31)  endothelin receptor type B [HGNC:EDNRB] (35)  Exostosin glycosyltransferase family [HGNC:EXT] (22)   exostosin glycosyltransferase 1 [HGNC:EXT1] (18)  Fatty acid binding protein family [HGNC:FABP] (151)   cellular retinoic acid binding protein 2 [HGNC:CRABP2] (32)  Fatty acid desaturases [HGNC:FADS] (108)   stearoyl-CoA desaturase (delta-9-desaturase) [HGNC:SCD] (78)  Fibronectin type III domain containing [HGNC:FN3] (399)   fibronectin 1 [HGNC:FN1] (112)  integrin, beta 4 [HGNC:ITGB4] (41)  Fibulins [HGNC:FBLN] (53)   EGF containing fibulin-like extracellular matrix protein 2 [HGNC:EFEMP2] (10)  Forkhead boxes [HGNC:FOX] (139)   forkhead box A1 [HGNC:FOXA1] (30)  forkhead box O3 [HGNC:FOXO3] (41)  Gap junction proteins (connexins) [HGNC:GJ] (78)   gap junction protein, alpha 1, 43kDa [HGNC:GJA1] (48)  G protein-coupled receptors [HGNC:GPCR] (66)   GPCR class B, orphans [HGNC:GPCRBO] (50)   latrophilin 3 [HGNC:LPHN3] (2)  Heat shock proteins [HGNC:HSP] (390)   Heat shock proteins, HSP70 [HGNC:HSP70] (294)   heat shock 70kDa protein 05 (glucose-regulated protein, 78kDa) [HGNC:HSPA5] (148)  Heat shock proteins, HSPB (small) [HGNC:HSPB] (127)   crystallin, alpha B [HGNC:CRYAB] (42)  Heat shock proteins, HSPC (HSP90) [HGNC:HSP90] (119)   heat shock protein 90kDa beta (Grp94), member 1 [HGNC:HSP90B1] (53)  Histones [HGNC:HIST] (173)   Histones, Replication-independent [HGNC:RIH] (148)   H1 histone family, member 0 [HGNC:H1F0] (23)  Homeoboxes [HGNC:homeobox] (219)   Homeoboxes, ANTP class [HGNC:HOXL] (152)   HOXL subclass homeoboxes [HGNC:HOXL] (95)   homeobox A09 [HGNC:HOXA9] (12)  NKL subclass homeoboxes [HGNC:NKL] (109)   NK3 homeobox 1 [HGNC:NKX3-1] (42)  Homeoboxes, TALE class [HGNC:TALE] (72)   pre-B-cell leukemia homeobox 1 [HGNC:PBX1] (24)  Integrins [HGNC:ITG] (284)   integrin, beta 4 [HGNC:ITGB4] (41)  Intermediate filaments [HGNC:IF] (273)   Type I. Keratins (acidic) [HGNC:] (120)   keratin 15 [HGNC:KRT15] (23)  keratin 20 [HGNC:KRT20] (8)  Type III [HGNC:] (100)   vimentin [HGNC:VIM] (77)  Type V. Lamins [HGNC:] (81)   lamin B2 [HGNC:LMNB2] (17)  IP3 receptors [HGNC:ITPR] (60)   inositol 1,4,5-trisphosphate receptor, type 1 [HGNC:ITPR1] (44)  K-acetyltransferases [HGNC:KAT] (176)   nuclear receptor coactivator 1 [HGNC:NCOA1] (71)  nuclear receptor coactivator 2 [HGNC:NCOA2] (50)  Kallikreins [HGNC:KLK] (65)   kallikrein-related peptidase 02 [HGNC:KLK2] (25)  Keratins [HGNC:KRT] (161)   keratin 15 [HGNC:KRT15] (23)  keratin 20 [HGNC:KRT20] (8)  Kinesins [HGNC:KIF] (68)   kinesin family member 11 [HGNC:KIF11] (29)  Kruppel-like transcription factors [HGNC:KLF] (106)   Kruppel-like factor 04 (gut) [HGNC:KLF4] (49)  Laminins [HGNC:LAM] (93)   laminin, beta 3 [HGNC:LAMB3] (30)  MAX dimerization proteins [HGNC:MXD] (65)   MAX dimerization protein 1 [HGNC:MXD1] (46)  MAX interactor 1, dimerization protein [HGNC:MXI1] (19)  Mitochondrial ribosomal proteins [HGNC:MRP] (52)   Mitochondrial ribosomal proteins, large subunits [HGNC:MRPL] (52)   mitochondrial ribosomal protein L19 [HGNC:MRPL19] (5)  Mitogen-activated protein kinase cascade [HGNC:MAP#K] (854)   Mitogen-activated protein kinases [HGNC:MAPK] (797)   mitogen-activated protein kinase 01 [HGNC:MAPK1] (651)  mitogen-activated protein kinase 03 [HGNC:MAPK3] (644)  mitogen-activated protein kinase 08 [HGNC:MAPK8] (234)  mitogen-activated protein kinase 09 [HGNC:MAPK9] (121)  Mitogen-activated protein kinase kinases [HGNC:MAP2K] (157)   mitogen-activated protein kinase kinase 1 [HGNC:MAP2K1] (106)  mitogen-activated protein kinase kinase 5 [HGNC:MAP2K5] (20)  Myocyte enhancer factors [HGNC:MEF2] (41)   myocyte enhancer factor 2C [HGNC:MEF2C] (18)  Myosins [HGNC:myosin] (111)   Myosins, class X [HGNC:MYOX] (22)   myosin X [HGNC:MYO10] (22)  Myosins, light chain [HGNC:MYL] (27)   myosin, light chain 09, regulatory [HGNC:MYL9] (16)  ncRNAs (non-protein coding RNAs) [HGNC:rna] (57)   Long non-coding RNAs [HGNC:LNCRNA] (54)   TP53 target 1 (non-protein coding) [HGNC:TP53TG1] (20)  Nuclear hormone receptors [HGNC:NR] (1322)   estrogen receptor 1 [HGNC:ESR1] (506)  estrogen receptor 2 (ER beta) [HGNC:ESR2] (261)  nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor) [HGNC:NR3C1] (138)  progesterone receptor [HGNC:PGR] (209)  vitamin D (1,25- dihydroxyvitamin D3) receptor [HGNC:VDR] (101)  OTU domain containing [HGNC:OTUD] (88)   tumor necrosis factor, alpha-induced protein 3 [HGNC:TNFAIP3] (88)  PHD-type zinc fingers [HGNC:PHF] (103)   inhibitor of growth family, member 1 [HGNC:ING1] (9)  Potassium channels [HGNC:KCN] (298)   Potassium channels, inwardly rectifying [HGNC:KCNJ] (65)   potassium inwardly-rectifying channel, subfamily J, member 08 [HGNC:KCNJ8] (15)  Potassium channels, voltage-gated [HGNC:Kv] (224)   potassium voltage-gated channel, subfamily H (eag-related), member 2 [HGNC:KCNH2] (164)  Protein phosphatase, catalytic and regulatory subunits [HGNC:PPP-PPM-CTD] (225)   Protein phosphatase 1, regulatory subunits [HGNC:PPP1R] (155)   aurora kinase A [HGNC:AURKA] (52)  Protein phosphatases, Mg2+/Mn2+ dependent [HGNC:PPM] (58)   protein phosphatase, Mg2+/Mn2+ dependent, 1B [HGNC:PPM1B] (14)  Protein tyrosine phosphatases, including dual specificity phosphatases [HGNC:PTP] (254)   Protein tyrosine phosphatases, Class I Cys-based [HGNC:PTPN] (252)   Class I Cys-based PTPs : PTENs [HGNC:DUSPQ] (91)   phosphatase and tensin homolog [HGNC:PTEN] (91)  Class I Cys-based PTPs : MAP kinase phosphatases [HGNC:DUSPT] (127)   dual specificity phosphatase 10 [HGNC:DUSP10] (34)  Receptor accessory proteins [HGNC:REEP] (11)   receptor accessory protein 1 [HGNC:REEP1] (11)  Rho GTPase activating proteins [HGNC:ARHGAP] (76)   deleted in liver cancer 1 [HGNC:DLC1] (22)  RNA binding motif containing [HGNC:RRM] (251)   heterogeneous nuclear ribonucleoprotein A/B [HGNC:HNRNPAB] (14)  L ribosomal proteins [HGNC:RPL] (79)   ribosomal protein L27a [HGNC:RPL27A] (17)  Semaphorins [HGNC:SEMA] (46)   sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A [HGNC:SEMA5A] (6)  Serine peptidases [HGNC:PRSS] (133)   Serine peptidases, transmembrane [HGNC:TMPRSS] (75)   transmembrane protease, serine 02 [HGNC:TMPRSS2] (33)  Serine (or cysteine) peptidase inhibitors [HGNC:SERPIN] (252)   serpin peptidase inhibitor, clade B (ovalbumin), member 05 [HGNC:SERPINB5] (29)  serpin peptidase inhibitor, clade B (ovalbumin), member 06 [HGNC:SERPINB6] (11)  serpin peptidase inhibitor, clade F (alpha-2 antiplasmin, pigment epithelium derived factor), member 1 [HGNC:SERPINF1] (18)  SH2 domain containing [HGNC:SH2D] (431)   FYN oncogene related to SRC, FGR, YES [HGNC:FYN] (47)  SMADs [HGNC:SMAD] (84)   SMAD family member 7 [HGNC:SMAD7] (20)  Snail homologs [HGNC:SNAI] (56)   snail family zinc finger 2 [HGNC:SNAI2] (28)  Solute carriers [HGNC:SLC] (716)   solute carrier family 14 (urea transporter), member 1 [HGNC:SLC14A1] (13)  solute carrier family 16 (monocarboxylate transporter), member 7 [HGNC:SLC16A7] (14)  solute carrier family 19 (folate transporter), member 1 [HGNC:SLC19A1] (30)  Specificity protein transcription factors [HGNC:SP] (109)   Sp1 transcription factor [HGNC:SP1] (106)  StAR-related lipid transfer (START) domain containing [HGNC:STARD] (91)   deleted in liver cancer 1 [HGNC:DLC1] (22)  Tetratricopeptide repeat domain containing [HGNC:TTC] (153)   FK506 binding protein 05 [HGNC:FKBP5] (46)  Tropomyosins [HGNC:TPM] (66)   tropomyosin 1 (alpha) [HGNC:TPM1] (32)  Tudor domain containing [HGNC:TDRD] (64)   staphylococcal nuclease and tudor domain containing 1 [HGNC:SND1] (9)  WD repeat domain containing [HGNC:WDR] (199)   coronin, actin binding protein, 1A [HGNC:CORO1A] (7)  transducin (beta)-like 1X-linked [HGNC:TBL1X] (19)  Wingless-type MMTV integration sites [HGNC:WNT] (82)   wingless-type MMTV integration site family, member 07A [HGNC:WNT7A] (7)  ZINC FINGERS [HGNC:ZNF] (383)   Zinc fingers, C2H2-type [HGNC:ZNF] (349)   Kruppel-like factor 04 (gut) [HGNC:KLF4] (49)  MYC-associated zinc finger protein (purine-binding transcription factor) [HGNC:MAZ] (12)  snail family zinc finger 2 [HGNC:SNAI2] (28)  Sp1 transcription factor [HGNC:SP1] (106)  Zinc fingers, C2H2-type with KRAB domain [HGNC:ZKRAB] (42)   paternally expressed 3 [HGNC:PEG3] (7)  zinc finger protein 267 [HGNC:ZNF267] (12)  Zinc fingers, C2H2-type with SCAN domain [HGNC:ZSCAN] (10)   paternally expressed 3 [HGNC:PEG3] (7)  Zinc fingers, C2H2-type with KRAB and SCAN domain [HGNC:ZKSCAN] (10)   paternally expressed 3 [HGNC:PEG3] (7)  Other zinc fingers [HGNC:] (148)   Zinc fingers, MYM-type [HGNC:ZMYM ] (64)   DEAF1 transcription factor [HGNC:DEAF1] (12) 2. Interaction: Human Genes and Chemicals  2. Interaction: Human Genes and Chemicals  Affects (3990)   binding (2423)  cotreatment (1499)  expression (494)  reaction (624)  response to substance (623)  Decreases (5154)   activity (2549)  degradation (120)  expression (2187)  phosphorylation (590)  reaction (3393)  response to substance (713)  secretion (346)  Increases (5571)   activity (2865)  cleavage (666)  degradation (347)  expression (3238)  metabolic processing (740)  phosphorylation (1060)  reaction (1574)  response to substance (641)  splicing (25) 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 Structurally [STY:T104] (44741)   Organic Chemical [STY:T109] (44144) A. Anatomy  A. Anatomy  Body Regions [MESH:D001829] (867)   Extremities [MESH:D005121] (484)   Upper Extremity [MESH:D034941] (441)   Hand [MESH:D006225] (428)   Fingers [MESH:D005385] (422)   Syndactyly, type 3 [MESH:C538154] (192)  Head [MESH:D006257] (523)   Ear [MESH:D004423] (236)   Meier-Gorlin syndrome [MESH:C538012] (133)  Face [MESH:D005145] (387)   Coffin-Siris syndrome [MESH:C536436] (102)  Neck [MESH:D009333] (107)   Coffin-Siris syndrome [MESH:C536436] (102)  Musculoskeletal System [MESH:D009141] (1255)   Skeleton [MESH:D012863] (1177)   Bone and Bones [MESH:D001842] (1112)   Bones of Lower Extremity [MESH:D050281] (278)   Leg Bones [MESH:D007867] (228)   Patella [MESH:D010329] (168)   Meier-Gorlin syndrome [MESH:C538012] (133)  Pelvic Bones [MESH:D010384] (41)   Al Awadi syndrome [MESH:C535612] (30)  Epiphyses [MESH:D004838] (98)   Wolcott-Rallison syndrome [MESH:C536739] (92)  Spine [MESH:D013131] (258)   VACTERL hydrocephaly [MESH:C536521] (151)  Digestive System [MESH:D004064] (421)   Gastrointestinal Tract [MESH:D041981] (364)   Intestines [MESH:D007422] (271)   Intestine, Large [MESH:D007420] (247)   Anal Canal [MESH:D001003] (217)   VACTERL hydrocephaly [MESH:C536521] (151)  Lower Gastrointestinal Tract [MESH:D041741] (254)   Intestine, Large [MESH:D007420] (247)   Anal Canal [MESH:D001003] (217)   VACTERL hydrocephaly [MESH:C536521] (151)  Upper Gastrointestinal Tract [MESH:D041742] (236)   Esophagus [MESH:D004947] (200)   VACTERL hydrocephaly [MESH:C536521] (151)  Respiratory System [MESH:D012137] (321)   Trachea [MESH:D014132] (190)   VACTERL hydrocephaly [MESH:C536521] (151)  Urogenital System [MESH:D014566] (986)   Genitalia [MESH:D005835] (400)   Genitalia, Female [MESH:D005836] (66)   Uterus [MESH:D014599] (43)   Al Awadi syndrome [MESH:C535612] (30)  Urinary Tract [MESH:D014551] (721)   Kidney [MESH:D007668] (707)   VACTERL hydrocephaly [MESH:C536521] (151)  Cardiovascular System [MESH:D002319] (1086)   Heart [MESH:D006321] (904)   Heart Conduction System [MESH:D006329] (263)   Short QT Syndrome 1 [MESH:C566506] (189)  Heart Valves [MESH:D006351] (666)   Aortic Valve [MESH:D001021] (659)   Aortic Valve, Calcification of [MESH:C562942] (655)  Sense Organs [MESH:D012679] (1060)   Ear [MESH:D004423] (323)   Meier-Gorlin syndrome [MESH:C538012] (133)  Eye [MESH:D005123] (858)   Anterior Eye Segment [MESH:D000869] (664)   Iris [MESH:D007498] (234)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Uvea [MESH:D014602] (270)   Iris [MESH:D007498] (234)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Cells [MESH:D002477] (1885)   Cellular Structures [MESH:D022082] (1562)   Chromosomes [MESH:D002875] (1300)   Chromosomes, Mammalian [MESH:D033481] (1282)   Chromosomes, Human [MESH:D002877] (1280)   Chromosomes, Human, 4-5 [MESH:D002905] (149)   Chromosomes, Human, Pair 5 [MESH:D002895] (136)   5q- syndrome [MESH:C535323] (131) C01. Bacterial Infections and Mycoses  C01. Bacterial Infections and Mycoses  Bacterial Infections [MESH:D001424] (3716)   Gram-Negative Bacterial Infections [MESH:D016905] (3085)   Helicobacter Infections [MESH:D016481] (579)  Mycoplasmatales Infections [MESH:D009180] (1949)   Mycoplasma Infections [MESH:D009175] (1947)  Gram-Positive Bacterial Infections [MESH:D016908] (2434)   Actinomycetales Infections [MESH:D000193] (1466)   Mycobacterium Infections [MESH:D009164] (1446)   Leprosy [MESH:D007918] (261)  Paratuberculosis [MESH:D010283] (427)  Tuberculosis [MESH:D014376] (992)  Infection [MESH:D007239] (4109)   Sepsis [MESH:D018805] (3556)  Eye Infections [MESH:D015817] (86)   Corneal Ulcer [MESH:D003320] (61)  Intraabdominal Infections [MESH:D059413] (958)   Peritonitis [MESH:D010538] (800)  Opportunistic Infections [MESH:D009894] (949)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914) C02. Virus Diseases  C02. Virus Diseases  Virus Diseases [MESH:D014777] (4544)   DNA Virus Infections [MESH:D004266] (2474)   Papillomavirus Infections [MESH:D030361] (630)  Herpesviridae Infections [MESH:D006566] (1944)   Epstein-Barr Virus Infections [MESH:D020031] (695)   Burkitt Lymphoma [MESH:D002051] (691)  Sarcoma, Kaposi [MESH:D012514] (1578)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Opportunistic Infections [MESH:D009894] (949)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  RNA Virus Infections [MESH:D012327] (4215)   Orthomyxoviridae Infections [MESH:D009976] (1077)   Influenza, Human [MESH:D007251] (1075)  Retroviridae Infections [MESH:D012192] (3420)   Lentivirus Infections [MESH:D016180] (3408)   HIV Infections [MESH:D015658] (3402)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Sexually Transmitted Diseases [MESH:D012749] (3305)   Sexually Transmitted Diseases, Viral [MESH:D015229] (3304)   HIV Infections [MESH:D015658] (3296)  Tumor Virus Infections [MESH:D014412] (1069)   Papillomavirus Infections [MESH:D030361] (537)  Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691) C03. Parasitic Diseases  C03. Parasitic Diseases  Parasitic Diseases [MESH:D010272] (3828)   Liver Diseases, Parasitic [MESH:D008109] (1009)  Opportunistic Infections [MESH:D009894] (949)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914) 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)  Hamartoma [MESH:D006222] (1484)   Hamartoma Syndrome, Multiple [MESH:D006223] (262)   Proteus Syndrome [MESH:D016715] (152)  Neoplasms by Histologic Type [MESH:D009370] (8793)   Leukemia [MESH:D007938] (4576)   Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)  Leukemia, Myeloid [MESH:D007951] (2773)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Leukemia, Myeloid, Acute [MESH:D015470] (2176)   Leukemia, Megakaryoblastic, Acute [MESH:D007947] (279)  Leukemia, Promyelocytic, Acute [MESH:D015473] (1367)  Lymphoma [MESH:D008223] (3686)   Lymphoma, Non-Hodgkin [MESH:D008228] (3337)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, Mantle-Cell [MESH:D020522] (561)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1405)   Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)  Neoplasms, Complex and Mixed [MESH:D018193] (1121)   Carcinosarcoma [MESH:D002296] (581)  Hepatoblastoma [MESH:D018197] (548)  Wilms Tumor [MESH:D009396] (553)  Rhabdoid Tumor [MESH:D018335] (61)   Rhabdoid Tumor Predisposition Syndrome 2 [MESH:C567643] (43)  Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742)   Neoplasms, Adipose Tissue [MESH:D018205] (677)   Lipoma [MESH:D008067] (159)  Liposarcoma [MESH:D008080] (612)   Liposarcoma, Myxoid [MESH:D018208] (358)  Neoplasms, Connective Tissue [MESH:D009372] (3626)   Sarcoma, Synovial [MESH:D013584] (993)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Mesenchymal [MESH:D018211] (1161)  Neoplasms, Bone Tissue [MESH:D018213] (2217)   Osteosarcoma [MESH:D012516] (2175)  Osteochondroma [MESH:D015831] (157)   Osteochondromatosis [MESH:D018216] (155)   Exostoses, Multiple Hereditary [MESH:D005097] (154)  Neoplasms, Fibrous Tissue [MESH:D018218] (1720)   Histiocytoma [MESH:D051642] (272)   Histiocytoma, Malignant Fibrous [MESH:D051677] (266)   Histiocytoma, Angiomatoid Fibrous [MESH:C563181] (258)  Neoplasms, Muscle Tissue [MESH:D009379] (1965)   Leiomyoma [MESH:D007889] (744)  Smooth Muscle Tumor [MESH:D018235] (132)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)   Rhabdomyosarcoma, Embryonal [MESH:D018233] (98)  Sarcoma [MESH:D012509] (4246)   Carcinosarcoma [MESH:D002296] (581)  Hemangiosarcoma [MESH:D006394] (1836)  Osteosarcoma [MESH:D012516] (2175)  Sarcoma, Synovial [MESH:D013584] (993)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Mesenchymal [MESH:D018211] (1161)  Histiocytoma, Malignant Fibrous [MESH:D051677] (266)   Histiocytoma, Angiomatoid Fibrous [MESH:C563181] (258)  Liposarcoma [MESH:D008080] (612)   Liposarcoma, Myxoid [MESH:D018208] (358)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)   Rhabdomyosarcoma, Embryonal [MESH:D018233] (98)  Phyllodes Tumor [MESH:D003557] (113)   Phyllodes Tumor of the Prostate [MESH:C549759] (110)  Sarcoma, Kaposi [MESH:D012514] (1578)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  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)   Retinoblastoma [MESH:D012175] (319)  Glioma [MESH:D005910] (4261)   Medulloblastoma [MESH:D008527] (1282)  Astrocytoma [MESH:D001254] (2692)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neuroendocrine Tumors [MESH:D018358] (3633)   Carcinoma, Neuroendocrine [MESH:D018278] (262)   Vipoma [MESH:D003969] (110)  Melanoma [MESH:D008545] (3508)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Neoplasms, Glandular and Epithelial [MESH:D009375] (7760)   Adenoma [MESH:D000236] (4051)   ACTH-Secreting Pituitary Adenoma [MESH:D049913] (169)  Adenoma, Liver Cell [MESH:D018248] (685)  Mesothelioma [MESH:D008654] (2567)  Prolactinoma [MESH:D015175] (312)  Adenoma, Islet Cell [MESH:D007516] (31)   Insulinoma [MESH:D007340] (27)  Adenomatous Polyps [MESH:D018256] (1571)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Carcinoma [MESH:D002277] (7263)   Pancreatic cancer, adult [MESH:C535836] (572)  Carcinoma, Lewis Lung [MESH:D018827] (248)  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)  Adenocarcinoma, Clear Cell [MESH:D018262] (1291)  Carcinoma, Adenoid Cystic [MESH:D003528] (1561)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Cholangiocarcinoma [MESH:D018281] (2398)  Adenocarcinoma, Follicular [MESH:D018263] (677)   Thyroid cancer, follicular [MESH:C572845] (674)  Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Carcinoma, Islet Cell [MESH:D018273] (30)   Gastrinoma [MESH:D015408] (26)  Glucagonoma [MESH:D005935] (26)  Carcinoma, Neuroendocrine [MESH:D018278] (262)   Vipoma [MESH:D003969] (110)  Carcinoma in Situ [MESH:D002278] (2111)   Prostatic Intraepithelial Neoplasia [MESH:D019048] (1565)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Neoplasms, Ductal, Lobular, and Medullary [MESH:D018299] (1831)   Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Neoplasms, Mesothelial [MESH:D018301] (2569)   Mesothelioma [MESH:D008654] (2567)  Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Retinoblastoma [MESH:D012175] (319)  Glioma [MESH:D005910] (4261)   Medulloblastoma [MESH:D008527] (1282)  Astrocytoma [MESH:D001254] (2692)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neoplasms, Squamous Cell [MESH:D018307] (4457)   Papilloma [MESH:D010212] (2243)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   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)   Retinoblastoma [MESH:D012175] (319)  Glioma [MESH:D005910] (4261)   Medulloblastoma [MESH:D008527] (1282)  Astrocytoma [MESH:D001254] (2692)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  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)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  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)   Hemangioblastoma [MESH:D018325] (395)  Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  Sarcoma, Kaposi [MESH:D012514] (1578)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Nevi and Melanomas [MESH:D018326] (3572)   Melanoma [MESH:D008545] (3508)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Neoplasms by Site [MESH:D009371] (9169)   Bone Neoplasms [MESH:D001859] (1334)  Soft Tissue Neoplasms [MESH:D012983] (2003)  Breast Neoplasms [MESH:D001943] (6077)   Breast Neoplasms, Male [MESH:D018567] (650)  Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Digestive System Neoplasms [MESH:D004067] (7487)   Biliary Tract Neoplasms [MESH:D001661] (1165)   Gallbladder Neoplasms [MESH:D005706] (993)  Gastrointestinal Neoplasms [MESH:D005770] (6452)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5358)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Turcot syndrome [MESH:C536928] (159)  Adenomatous Polyposis Coli [MESH:D011125] (1565)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)  Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Liver Neoplasms [MESH:D008113] (6048)   Adenoma, Liver Cell [MESH:D018248] (685)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572)  Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Adenoma, Islet Cell [MESH:D007516] (31)   Insulinoma [MESH:D007340] (27)  Carcinoma, Islet Cell [MESH:D018273] (115)   Gastrinoma [MESH:D015408] (26)  Glucagonoma [MESH:D005935] (26)  Vipoma [MESH:D003969] (110)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia, Type IV [MESH:C567059] (297)  Multiple Endocrine Neoplasia Type 1 [MESH:D018761] (26)  Ovarian Neoplasms [MESH:D010051] (3275)   Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572)  Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Adenoma, Islet Cell [MESH:D007516] (31)   Insulinoma [MESH:D007340] (27)  Carcinoma, Islet Cell [MESH:D018273] (115)   Gastrinoma [MESH:D015408] (26)  Glucagonoma [MESH:D005935] (26)  Vipoma [MESH:D003969] (110)  Pituitary Neoplasms [MESH:D010911] (981)   ACTH-Secreting Pituitary Adenoma [MESH:D049913] (172)  Prolactinoma [MESH:D015175] (312)  Testicular Neoplasms [MESH:D013736] (520)   Testicular Germ Cell Tumor [MESH:C563236] (176)  Eye Neoplasms [MESH:D005134] (400)   Retinal Neoplasms [MESH:D019572] (320)   Retinoblastoma [MESH:D012175] (319)  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)  Tongue Neoplasms [MESH:D014062] (1518)  Otorhinolaryngologic Neoplasms [MESH:D010039] (1557)   Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Mammary Neoplasms, Animal [MESH:D015674] (3404)   Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Nervous System Neoplasms [MESH:D009423] (3130)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)   Turcot syndrome [MESH:C536928] (159)  Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  Skin Neoplasms [MESH:D012878] (2992)   Familial cylindromatosis [MESH:C536611] (35)  Thoracic Neoplasms [MESH:D013899] (6032)   Respiratory Tract Neoplasms [MESH:D012142] (6020)   Lung Neoplasms [MESH:D008175] (6015)   Adenocarcinoma of lung [MESH:C538231] (1487)  Bronchial Neoplasms [MESH:D001984] (3608)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380)  Urogenital Neoplasms [MESH:D014565] (7002)   Genital Neoplasms, Female [MESH:D005833] (2540)   Uterine Neoplasms [MESH:D014594] (2431)   Endometrial Neoplasms [MESH:D016889] (1987)  Uterine Cervical Neoplasms [MESH:D002583] (978)  Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)   Prostate cancer, familial [MESH:C537243] (264)  Phyllodes Tumor of the Prostate [MESH:C549759] (110)  Testicular Neoplasms [MESH:D013736] (520)   Testicular Germ Cell Tumor [MESH:C563236] (176)  Urologic Neoplasms [MESH:D014571] (5315)   Ureteral Neoplasms [MESH:D014516] (574)  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)   Carcinoma, Lewis Lung [MESH:D018827] (248)  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)   Hamartoma Syndrome, Multiple [MESH:D006223] (262)   Proteus Syndrome [MESH:D016715] (152)  Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia, Type IV [MESH:C567059] (297)  Multiple Endocrine Neoplasia Type 1 [MESH:D018761] (26)  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)   Familial cylindromatosis [MESH:C536611] (35)  Turcot syndrome [MESH:C536928] (159)  Meningioma, familial [MESH:C537443] (195)  Juvenile polyposis syndrome [MESH:C537702] (196)  Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Adenomatous Polyposis Coli [MESH:D011125] (1565)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (260)  Exostoses, Multiple Hereditary [MESH:D005097] (154)  Hamartoma Syndrome, Multiple [MESH:D006223] (260)  Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Li-Fraumeni Syndrome [MESH:D016864] (859)  Wilms Tumor [MESH:D009396] (553)  Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia, Type IV [MESH:C567059] (297)  Multiple Endocrine Neoplasia Type 1 [MESH:D018761] (26)  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)   Bone Diseases [MESH:D001847] (5801)   Bone Neoplasms [MESH:D001859] (1334)  Bone Resorption [MESH:D001862] (2352)  Osteitis Deformans [MESH:D010001] (287)  Bone Diseases, Developmental [MESH:D001848] (3315)   Acromicric dysplasia [MESH:C535662] (520)  Marfan Syndrome [MESH:D008382] (646)  Proteus Syndrome [MESH:D016715] (152)  Dysostoses [MESH:D004413] (1019)   Craniofacial Dysostosis [MESH:D003394] (391)   Hallermann's Syndrome [MESH:D006210] (193)  Synostosis [MESH:D013580] (817)   Syndactyly [MESH:D013576] (487)   Syndactyly, type 3 [MESH:C538154] (192)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Osteochondrodysplasias [MESH:D010009] (2440)   Wolcott-Rallison syndrome [MESH:C536739] (92)  Ghosal Hematodiaphyseal Dysplasia [MESH:C565551] (58)  Camurati-Engelmann Syndrome [MESH:D003966] (492)  Pycnodysostosis [MESH:D058631] (73)  Osteochondroma [MESH:D015831] (157)   Osteochondromatosis [MESH:D018216] (155)   Exostoses, Multiple Hereditary [MESH:D005097] (154)  Bone Diseases, Endocrine [MESH:D001849] (747)   Acromegaly [MESH:D000172] (466)  Bone Diseases, Metabolic [MESH:D001851] (3492)   Osteoporosis [MESH:D010024] (3037)   Osteoporosis, Postmenopausal [MESH:D015663] (2351)  Rickets [MESH:D012279] (341)   Rickets, Hypophosphatemic [MESH:D063730] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D-Dependent Rickets, Type 2A [MESH:C562794] (137)  Hyperostosis [MESH:D015576] (493)   Exostoses [MESH:D005096] (160)   Exostoses, Multiple Hereditary [MESH:D005097] (154)  Spinal Diseases [MESH:D013122] (2485)   Intervertebral Disc Degeneration [MESH:D055959] (827)  Ossification of Posterior Longitudinal Ligament [MESH:D017887] (99)   Ossification of the posterior longitudinal ligament of the spine [MESH:C537143] (98)  Spinal Curvatures [MESH:D013121] (742)   Kyphosis [MESH:D007738] (637)  Foot Deformities [MESH:D005530] (553)   Foot Deformities, Congenital [MESH:D005532] (538)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Hand Deformities [MESH:D006226] (590)   Hand Deformities, Congenital [MESH:D006228] (587)   Coffin-Siris syndrome [MESH:C536436] (102)  Jaw Diseases [MESH:D007571] (1601)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Orofacial Cleft 11 [MESH:C567410] (101)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Meier-Gorlin syndrome [MESH:C538012] (133)  Joint Diseases [MESH:D007592] (4657)   Arthritis [MESH:D001168] (4416)   Arthritis, Experimental [MESH:D001169] (3142)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Osteoarthritis [MESH:D010003] (1743)  Arthrogryposis [MESH:D001176] (329)   Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Contracture [MESH:D003286] (296)   Bethlem myopathy [MESH:C535436] (108)  Muscular Diseases [MESH:D009135] (4071)   Alpha-B Crystallinopathy [MESH:C563848] (135)  Arthrogryposis [MESH:D001176] (329)   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)  Scleroatonic muscular dystrophy [MESH:C537521] (108)  Filaminopathy, autosomal dominant [MESH:C537932] (40)  Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Musculoskeletal Abnormalities [MESH:D009139] (3796)   Arthrogryposis [MESH:D001176] (329)   Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Craniofacial Abnormalities [MESH:D019465] (3098)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Costello Syndrome [MESH:D056685] (407)  Holoprosencephaly [MESH:D016142] (218)  LEOPARD Syndrome [MESH:D044542] (299)  Noonan Syndrome [MESH:D009634] (506)  Craniofacial Dysostosis [MESH:D003394] (391)   Hallermann's Syndrome [MESH:D006210] (193)  Loeys-Dietz Syndrome [MESH:D055947] (263)   Aortic aneurysm, familial thoracic 3 [MESH:C537783] (107)  Loeys-Dietz Syndrome, Type 1b [MESH:C567181] (107)  Macrocephaly [MESH:D058627] (264)   Macrocephaly Autism Syndrome [MESH:C565342] (151)  Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Orofacial Cleft 11 [MESH:C567410] (101)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Meier-Gorlin syndrome [MESH:C538012] (133)  Microcephaly [MESH:D008831] (700)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Limb Deformities, Congenital [MESH:D017880] (1813)   Acromicric dysplasia [MESH:C535662] (520)  VACTERL hydrocephaly [MESH:C536521] (151)  Microphthalmia, Syndromic 6 [MESH:C566440] (101)  Polydactyly [MESH:D017689] (318)  Proteus Syndrome [MESH:D016715] (152)  Ectromelia [MESH:D004480] (108)   Al Awadi syndrome [MESH:C535612] (30)  Lower Extremity Deformities, Congenital [MESH:D038061] (560)   Foot Deformities, Congenital [MESH:D005532] (538)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Syndactyly [MESH:D013576] (487)   Syndactyly, type 3 [MESH:C538154] (192)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Upper Extremity Deformities, Congenital [MESH:D038062] (604)   Hand Deformities, Congenital [MESH:D006228] (587)   Coffin-Siris syndrome [MESH:C536436] (102)  Synostosis [MESH:D013580] (817)   Syndactyly [MESH:D013576] (487)   Syndactyly, type 3 [MESH:C538154] (192)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  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)   Cholestasis, Intrahepatic [MESH:D002780] (1510)   Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Biliary Tract Neoplasms [MESH:D001661] (1165)   Gallbladder Neoplasms [MESH:D005706] (993)  Cholelithiasis [MESH:D002769] (373)   Gallstones [MESH:D042882] (350)  Gallbladder Diseases [MESH:D005705] (1215)   Gallbladder Neoplasms [MESH:D005706] (993)  Cholecystolithiasis [MESH:D041761] (353)   Gallstones [MESH:D042882] (350)  Digestive System Abnormalities [MESH:D004065] (2127)   Hirschsprung Disease [MESH:D006627] (361)  Digestive System Neoplasms [MESH:D004067] (7493)   Biliary Tract Neoplasms [MESH:D001661] (1165)   Gallbladder Neoplasms [MESH:D005706] (993)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Turcot syndrome [MESH:C536928] (159)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)  Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Liver Neoplasms [MESH:D008113] (6048)   Adenoma, Liver Cell [MESH:D018248] (685)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572)  Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Adenoma, Islet Cell [MESH:D007516] (31)   Insulinoma [MESH:D007340] (27)  Carcinoma, Islet Cell [MESH:D018273] (115)   Gastrinoma [MESH:D015408] (26)  Glucagonoma [MESH:D005935] (26)  Vipoma [MESH:D003969] (110)  Gastrointestinal Diseases [MESH:D005767] (7443)   Esophageal Diseases [MESH:D004935] (4255)   Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Gastroenteritis [MESH:D005759] (4066)   Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   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)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Turcot syndrome [MESH:C536928] (159)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)  Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Intestinal Diseases [MESH:D007410] (6206)   Cecal Diseases [MESH:D002429] (1330)   Cecal Neoplasms [MESH:D002430] (822)  Colonic Diseases [MESH:D003108] (5564)   Colorectal Neoplasms [MESH:D015179] (5282)   Turcot syndrome [MESH:C536928] (159)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Megacolon [MESH:D008531] (386)   Hirschsprung Disease [MESH:D006627] (361)  Duodenal Diseases [MESH:D004378] (1982)   Peptic Ulcer [MESH:D010437] (1969)   Duodenal Ulcer [MESH:D004381] (1549)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Crohn Disease [MESH:D003424] (2585)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Turcot syndrome [MESH:C536928] (159)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)  Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Intestinal Polyposis [MESH:D044483] (1610)   Juvenile polyposis syndrome [MESH:C537702] (196)  Adenomatous Polyposis Coli [MESH:D011125] (1565)  Malabsorption Syndromes [MESH:D008286] (492)   Lactose Intolerance [MESH:D007787] (113)   Lactose Intolerance, Adult Type [MESH:C562601] (112)  Rectal Diseases [MESH:D012002] (4596)   Colorectal Neoplasms [MESH:D015179] (4534)   Turcot syndrome [MESH:C536928] (159)  Rectal Neoplasms [MESH:D012004] (717)  Peptic Ulcer [MESH:D010437] (3172)   Duodenal Ulcer [MESH:D004381] (1549)  Stomach Ulcer [MESH:D013276] (2915)  Stomach Diseases [MESH:D013272] (5325)   Stomach Neoplasms [MESH:D013274] (4942)  Peptic Ulcer [MESH:D010437] (2994)   Stomach Ulcer [MESH:D013276] (2915)  Liver Diseases [MESH:D008107] (8167)   Drug-Induced Liver Injury [MESH:D056486] (4936)  Hepatolenticular Degeneration [MESH:D006527] (473)  Liver Diseases, Parasitic [MESH:D008109] (1009)  Cholestasis, Intrahepatic [MESH:D002780] (1510)   Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Fatty Liver [MESH:D005234] (3584)   Non-alcoholic Fatty Liver Disease [MESH:C541083] (1567)  Hepatic Insufficiency [MESH:D048550] (2771)   Liver Failure [MESH:D017093] (2768)   Liver Failure, Acute [MESH:D017114] (2404)  Hepatitis [MESH:D006505] (3883)   Hepatitis, Chronic [MESH:D006521] (2071)   Hepatitis, Autoimmune [MESH:D019693] (1982)  Liver Cirrhosis [MESH:D008103] (5542)   Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Liver Cirrhosis, Experimental [MESH:D008106] (4589)  Liver Diseases, Alcoholic [MESH:D008108] (3243)   Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Neoplasms [MESH:D008113] (6048)   Adenoma, Liver Cell [MESH:D018248] (685)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria, Acute Hepatic [MESH:C562618] (99)  Pancreatic Diseases [MESH:D010182] (4453)   Cystic Fibrosis [MESH:D003550] (760)  Pancreatitis [MESH:D010195] (1924)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572)  Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Adenoma, Islet Cell [MESH:D007516] (31)   Insulinoma [MESH:D007340] (27)  Carcinoma, Islet Cell [MESH:D018273] (115)   Gastrinoma [MESH:D015408] (26)  Glucagonoma [MESH:D005935] (26)  Vipoma [MESH:D003969] (110)  Peritoneal Diseases [MESH:D010532] (1119)   Peritoneal Fibrosis [MESH:D056627] (488)  Peritonitis [MESH:D010538] (800) C07. Stomatognathic Diseases  C07. Stomatognathic Diseases  Stomatognathic Diseases [MESH:D009057] (5348)   Jaw Diseases [MESH:D007571] (1608)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Orofacial Cleft 11 [MESH:C567410] (101)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Meier-Gorlin syndrome [MESH:C538012] (133)  Periapical Diseases [MESH:D010483] (186)   Periapical Periodontitis [MESH:D010485] (183)  Mouth Diseases [MESH:D009059] (4783)   Oral Submucous Fibrosis [MESH:D009914] (2432)  Lip Diseases [MESH:D008047] (924)   Cleft Lip [MESH:D002971] (914)   Orofacial Cleft 11 [MESH:C567410] (101)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Orofacial Cleft 11 [MESH:C567410] (101)  Cleft Palate [MESH:D002972] (1330)   Orofacial Cleft 11 [MESH:C567410] (101)  Mouth Neoplasms [MESH:D009062] (2263)   Salivary Gland Neoplasms [MESH:D012468] (968)  Tongue Neoplasms [MESH:D014062] (1518)  Periodontal Diseases [MESH:D010510] (1001)   Periapical Diseases [MESH:D010483] (186)   Periapical Periodontitis [MESH:D010485] (183)  Periodontitis [MESH:D010518] (843)   Periapical Periodontitis [MESH:D010485] (183)  Salivary Gland Diseases [MESH:D012466] (1213)   Salivary Gland Neoplasms [MESH:D012468] (968)  Tongue Diseases [MESH:D014060] (1544)   Tongue Neoplasms [MESH:D014062] (1518)  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)   Orofacial Cleft 11 [MESH:C567410] (101)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Meier-Gorlin syndrome [MESH:C538012] (133)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Orofacial Cleft 11 [MESH:C567410] (101)  Cleft Palate [MESH:D002972] (1330)   Orofacial Cleft 11 [MESH:C567410] (101)  Tooth Abnormalities [MESH:D014071] (622)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Tooth Diseases [MESH:D014076] (742)   Tooth Abnormalities [MESH:D014071] (622)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192) C08. Respiratory Tract Diseases  C08. Respiratory Tract Diseases  Respiratory Tract Diseases [MESH:D012140] (7881)   Respiratory System Abnormalities [MESH:D015619] (243)  Bronchial Diseases [MESH:D001982] (4382)   Asthma [MESH:D001249] (4098)  Lung Diseases [MESH:D008171] (7249)   Cystic Fibrosis [MESH:D003550] (760)  Hypertension, Pulmonary [MESH:D006976] (2000)  Pneumonia [MESH:D011014] (3482)  Pulmonary Fibrosis [MESH:D011658] (3140)  Respiratory Distress Syndrome, Adult [MESH:D012128] (864)  Lung Diseases, Interstitial [MESH:D017563] (2966)   Pneumoconiosis [MESH:D011009] (2789)   Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273)  Lung Diseases, Obstructive [MESH:D008173] (4697)   Asthma [MESH:D001249] (3903)  Pulmonary Disease, Chronic Obstructive [MESH:D029424] (3564)   Pulmonary Emphysema [MESH:D011656] (1259)  Lung Injury [MESH:D055370] (3688)   Acute Lung Injury [MESH:D055371] (1907)  Pneumoconiosis [MESH:D011009] (2789)   Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273)  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)  Respiration Disorders [MESH:D012120] (2218)   Hyperventilation [MESH:D006985] (654)  Respiratory Distress Syndrome, Adult [MESH:D012128] (864)  Respiratory Insufficiency [MESH:D012131] (841)  Apnea [MESH:D001049] (748)   Sleep Apnea Syndromes [MESH:D012891] (570)   Sleep Apnea, Obstructive [MESH:D020181] (126)  Respiratory Hypersensitivity [MESH:D012130] (4401)   Asthma [MESH:D001249] (4098)  Respiratory Tract Infections [MESH:D012141] (3926)   Influenza, Human [MESH:D007251] (1075)  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) C09. Otorhinolaryngologic Diseases  C09. Otorhinolaryngologic Diseases  Otorhinolaryngologic Diseases [MESH:D010038] (3827)   Ear Diseases [MESH:D004427] (2522)   Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Deafness [MESH:D003638] (623)   Tietz syndrome [MESH:C536919] (42)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Albinism ocular late onset sensorineural deafness [MESH:C537043] (137)  Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)  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)   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)   Chronobiology Disorders [MESH:D021081] (970)  Demyelinating Diseases [MESH:D003711] (2917)  Central Nervous System Diseases [MESH:D002493] (9745)   Brain Diseases [MESH:D001927] (9294)   Brain Edema [MESH:D001929] (1165)  Brain Injuries [MESH:D001930] (3429)  Hypoxia, Brain [MESH:D002534] (134)  Basal Ganglia Diseases [MESH:D001480] (4268)   Hepatolenticular Degeneration [MESH:D006527] (473)  Huntington Disease [MESH:D006816] (540)   Huntington Disease-Like 1 [MESH:C566398] (98)  Parkinsonian Disorders [MESH:D020734] (4009)   Parkinson Disease [MESH:D010300] (3595)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Supranuclear Palsy, Progressive [MESH:D013494] (235)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Brain Diseases, Metabolic [MESH:D001928] (3351)   Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Hyperglycinemia, Nonketotic [MESH:D020158] (67)  Peroxisomal Disorders [MESH:D018901] (1472)   Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   3-methylcrotonyl CoA carboxylase 2 deficiency [MESH:C535309] (32)  Brain Neoplasms [MESH:D001932] (2764)   Turcot syndrome [MESH:C536928] (159)  Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Cerebellar Diseases [MESH:D002526] (736)   Cerebellar Ataxia [MESH:D002524] (542)   Spinocerebellar Ataxias [MESH:D020754] (406)   Spinocerebellar Ataxia 15 [MESH:C564685] (90)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxia 29 [MESH:C537206] (90)  Spinocerebellar Ataxias [MESH:D020754] (322)   Spinocerebellar Ataxia 15 [MESH:C564685] (90)  Cerebrovascular Disorders [MESH:D002561] (5542)   Vasospasm, Intracranial [MESH:D020301] (324)  Brain Ischemia [MESH:D002545] (4873)   Ischemic Attack, Transient [MESH:D002546] (1313)  Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Intracranial Arterial Diseases [MESH:D020765] (2463)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  Subarachnoid Hemorrhage [MESH:D013345] (1082)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Dementia [MESH:D003704] (4498)   Alzheimer Disease [MESH:D000544] (4275)  Creutzfeldt-Jakob Syndrome [MESH:D007562] (118)  Frontotemporal Lobar Degeneration [MESH:D057174] (310)   Frontotemporal Dementia [MESH:D057180] (300)   Pick Disease of the Brain [MESH:D020774] (184)  Huntington Disease [MESH:D006816] (540)   Huntington Disease-Like 1 [MESH:C566398] (98)  Epilepsy [MESH:D004827] (6274)   Seizures [MESH:D012640] (4502)  Status Epilepticus [MESH:D013226] (4014)  Epilepsies, Partial [MESH:D004828] (1267)   Epilepsy, Temporal Lobe [MESH:D004833] (1108)  Epilepsy, Generalized [MESH:D004829] (1431)   Epilepsy, Tonic-Clonic [MESH:D004830] (1042)  Headache Disorders [MESH:D020773] (2337)   Headache Disorders, Primary [MESH:D051270] (2327)   Migraine Disorders [MESH:D008881] (2318)  Hydrocephalus [MESH:D006849] (276)   VACTERL hydrocephaly [MESH:C536521] (151)  Hypothalamic Diseases [MESH:D007027] (1833)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Pituitary Diseases [MESH:D010900] (1808)   Hyperpituitarism [MESH:D006964] (1250)   Acromegaly [MESH:D000172] (466)  Pituitary Neoplasms [MESH:D010911] (981)   ACTH-Secreting Pituitary Adenoma [MESH:D049913] (172)  Prolactinoma [MESH:D015175] (312)  Intracranial Hypertension [MESH:D019586] (368)   Hydrocephalus [MESH:D006849] (274)   VACTERL hydrocephaly [MESH:C536521] (151)  Leukoencephalopathies [MESH:D056784] (1916)   Ribose 5-Phosphate Isomerase Deficiency [MESH:C563212] (34)  Central Nervous System Infections [MESH:D002494] (1823)   Prion Diseases [MESH:D017096] (488)   Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98)  Creutzfeldt-Jakob Syndrome [MESH:D007562] (118)  Gerstmann-Straussler-Scheinker Disease [MESH:D016098] (98)  Insomnia, Fatal Familial [MESH:D034062] (98)  Scrapie [MESH:D012608] (462)  Movement Disorders [MESH:D009069] (4823)   Hepatolenticular Degeneration [MESH:D006527] (473)  Dyskinesias [MESH:D020820] (1827)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Chorea [MESH:D002819] (651)   Huntington Disease [MESH:D006816] (540)   Huntington Disease-Like 1 [MESH:C566398] (98)  Parkinsonian Disorders [MESH:D020734] (4009)   Parkinson Disease [MESH:D010300] (3595)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Supranuclear Palsy, Progressive [MESH:D013494] (235)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Spinal Cord Diseases [MESH:D013118] (4376)   Spinal Cord Injuries [MESH:D013119] (1674)  Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxia 29 [MESH:C537206] (90)  Spinocerebellar Ataxias [MESH:D020754] (322)   Spinocerebellar Ataxia 15 [MESH:C564685] (90)  Cranial Nerve Diseases [MESH:D003389] (2004)   Ocular Motility Disorders [MESH:D015835] (1697)   Ophthalmoplegia [MESH:D009886] (1468)   Supranuclear Palsy, Progressive [MESH:D013494] (235)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Nervous System Malformations [MESH:D009421] (3354)   Microphthalmia, Syndromic 6 [MESH:C566440] (101)  Neural Tube Defects [MESH:D009436] (2143)  Agenesis of Corpus Callosum [MESH:D061085] (345)   Holoprosencephaly [MESH:D016142] (218)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic Paraplegia 31, Autosomal Dominant [MESH:C565210] (20)  Malformations of Cortical Development [MESH:D054220] (1406)   Lissencephaly [MESH:D054082] (218)   Classical Lissencephalies and Subcortical Band Heterotopias [MESH:D054221] (114)  Macrocephaly [MESH:D058627] (264)   Macrocephaly Autism Syndrome [MESH:C565342] (151)  Microcephaly [MESH:D008831] (700)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Neuronal Migration Disorders [MESH:D054081] (264)   Classical Lissencephalies and Subcortical Band Heterotopias [MESH:D054221] (114)  Nervous System Neoplasms [MESH:D009423] (3073)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)   Turcot syndrome [MESH:C536928] (159)  Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  Neurocutaneous Syndromes [MESH:D020752] (1230)   von Hippel-Lindau Disease [MESH:D006623] (580)  Neurodegenerative Diseases [MESH:D019636] (6613)   Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243)   Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98)  Gerstmann-Straussler-Scheinker Disease [MESH:D016098] (98)  Hepatolenticular Degeneration [MESH:D006527] (473)  Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic Paraplegia 31, Autosomal Dominant [MESH:C565210] (20)  Huntington Disease [MESH:D006816] (540)   Huntington Disease-Like 1 [MESH:C566398] (98)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxia 29 [MESH:C537206] (90)  Spinocerebellar Ataxias [MESH:D020754] (322)   Spinocerebellar Ataxia 15 [MESH:C564685] (90)  Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Parkinson Disease [MESH:D010300] (3595)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Prion Diseases [MESH:D017096] (475)   Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98)  Gerstmann-Straussler-Scheinker Disease [MESH:D016098] (98)  Insomnia, Fatal Familial [MESH:D034062] (98)  Scrapie [MESH:D012608] (462)  Tauopathies [MESH:D024801] (4289)   Alzheimer Disease [MESH:D000544] (4275)  Supranuclear Palsy, Progressive [MESH:D013494] (235)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Frontotemporal Lobar Degeneration [MESH:D057174] (308)   Frontotemporal Dementia [MESH:D057180] (298)  Neurologic Manifestations [MESH:D009461] (8964)   Pain [MESH:D010146] (3875)  Seizures [MESH:D012640] (4514)  Dyskinesias [MESH:D020820] (3365)   Catalepsy [MESH:D002375] (1429)  Hyperkinesis [MESH:D006948] (1799)  Hypokinesia [MESH:D018476] (279)  Tics [MESH:D020323] (62)  Ataxia [MESH:D001259] (1138)   Cerebellar Ataxia [MESH:D002524] (542)   Spinocerebellar Ataxias [MESH:D020754] (406)   Spinocerebellar Ataxia 15 [MESH:C564685] (90)  Neurobehavioral Manifestations [MESH:D019954] (5230)   Memory Disorders [MESH:D008569] (3233)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Language Development Disorders [MESH:D007805] (351)  Consciousness Disorders [MESH:D003244] (680)   Unconsciousness [MESH:D014474] (660)  Intellectual Disability [MESH:D008607] (3054)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Coffin-Siris syndrome [MESH:C536436] (102)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Mental Retardation, Autosomal Dominant 3 [MESH:C567241] (14)  Down Syndrome [MESH:D004314] (1287)  Mental Retardation, X-Linked [MESH:D038901] (1854)   Mucopolysaccharidosis II [MESH:D016532] (26)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscular Atrophy [MESH:D009133] (1234)  Paralysis [MESH:D010243] (2043)   Ophthalmoplegia [MESH:D009886] (1468)   Supranuclear Palsy, Progressive [MESH:D013494] (235)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Sensation Disorders [MESH:D012678] (5011)   Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Deafness [MESH:D003638] (623)   Tietz syndrome [MESH:C536919] (42)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Albinism ocular late onset sensorineural deafness [MESH:C537043] (137)  Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  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 Atrophy, Spinal [MESH:D009134] (850)   Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Muscular Diseases [MESH:D009135] (3538)   Alpha-B Crystallinopathy [MESH:C563848] (135)  Muscular Disorders, Atrophic [MESH:D020966] (1594)   Muscular Dystrophies [MESH:D009136] (1589)   Bethlem myopathy [MESH:C535436] (108)  Scleroatonic muscular dystrophy [MESH:C537521] (108)  Filaminopathy, autosomal dominant [MESH:C537932] (40)  Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Peripheral Nervous System Diseases [MESH:D010523] (6151)   Diabetic Neuropathies [MESH:D003929] (2442)  Polyneuropathies [MESH:D011115] (1134)   Ribose 5-Phosphate Isomerase Deficiency [MESH:C563212] (34)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic Paraplegia 31, Autosomal Dominant [MESH:C565210] (20)  Neurotoxicity Syndromes [MESH:D020258] (4570)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Heavy Metal Poisoning, Nervous System [MESH:D020260] (2912)   Arsenic Poisoning [MESH:D020261] (2540)  Lead Poisoning, Nervous System [MESH:D020263] (102)  Sleep Disorders [MESH:D012893] (2050)   Dyssomnias [MESH:D020920] (1417)   Sleep Disorders, Intrinsic [MESH:D020919] (1270)   Sleep Apnea Syndromes [MESH:D012891] (570)   Sleep Apnea, Obstructive [MESH:D020181] (126)  Sleep Initiation and Maintenance Disorders [MESH:D007319] (354)   Insomnia, Fatal Familial [MESH:D034062] (98)  Trauma, Nervous System [MESH:D020196] (3997)   Spinal Cord Injuries [MESH:D013119] (1676)  Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) C11. Eye Diseases  C11. Eye Diseases  Eye Diseases [MESH:D005128] (6245)   Corneal Diseases [MESH:D003316] (1445)   Corneal Neovascularization [MESH:D016510] (622)  Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Corneal dystrophy, gelatinous drop-like [MESH:C535480] (37)  Meretoja syndrome [MESH:C537459] (95)  Keratitis [MESH:D007634] (168)   Corneal Ulcer [MESH:D003320] (61)  Eye Abnormalities [MESH:D005124] (1233)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Microphthalmos [MESH:D008850] (273)   Microphthalmia, Syndromic 6 [MESH:C566440] (101)  Eye Diseases, Hereditary [MESH:D015785] (1869)   Graves Ophthalmopathy [MESH:D049970] (165)  Albinism [MESH:D000417] (258)   Albinism, Ocular [MESH:D016117] (157)   Albinism ocular late onset sensorineural deafness [MESH:C537043] (137)  Albinism, Oculocutaneous [MESH:D016115] (234)   Tietz syndrome [MESH:C536919] (42)  Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Corneal dystrophy, gelatinous drop-like [MESH:C535480] (37)  Meretoja syndrome [MESH:C537459] (95)  Eye Infections [MESH:D015817] (110)   Corneal Ulcer [MESH:D003320] (61)  Eye Neoplasms [MESH:D005134] (413)   Retinal Neoplasms [MESH:D019572] (320)   Retinoblastoma [MESH:D012175] (319)  Lacrimal Apparatus Diseases [MESH:D007766] (644)   Dry Eye Syndromes [MESH:D015352] (533)  Lens Diseases [MESH:D007905] (900)   Cataract [MESH:D002386] (860)   Alpha-B Crystallinopathy [MESH:C563848] (135)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Cataract, Pulverulent, Juvenile-Onset [MESH:C565703] (69)  Ocular Hypertension [MESH:D009798] (1630)   Glaucoma [MESH:D005901] (1458)   Glaucoma, Open-Angle [MESH:D005902] (1281)   Glaucoma, Primary Open Angle [MESH:C562750] (466)  Ocular Motility Disorders [MESH:D015835] (1699)   Ophthalmoplegia [MESH:D009886] (1468)   Supranuclear Palsy, Progressive [MESH:D013494] (235)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Orbital Diseases [MESH:D009916] (317)   Exophthalmos [MESH:D005094] (297)   Graves Disease [MESH:D006111] (278)   Graves Ophthalmopathy [MESH:D049970] (165)  Refractive Errors [MESH:D012030] (457)   Anisometropia [MESH:D015858] (152)  Retinal Diseases [MESH:D012164] (3747)   Retinal Degeneration [MESH:D012162] (2386)  Retinal Detachment [MESH:D012163] (1639)  Retinal Neoplasms [MESH:D019572] (320)   Retinoblastoma [MESH:D012175] (319)  Uveal Diseases [MESH:D014603] (2428)   Uveitis [MESH:D014605] (2157) C12. Male Urogenital Diseases  C12. Male Urogenital Diseases  Male Urogenital Diseases [MESH:D052801] (8891)   Genital Diseases, Male [MESH:D005832] (6794)   Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)   Prostate cancer, familial [MESH:C537243] (264)  Phyllodes Tumor of the Prostate [MESH:C549759] (110)  Testicular Neoplasms [MESH:D013736] (520)   Testicular Germ Cell Tumor [MESH:C563236] (176)  Infertility [MESH:D007246] (2909)   Infertility, Male [MESH:D007248] (2851)   Azoospermia [MESH:D053713] (1052)  Oligospermia [MESH:D009845] (799)  Penile Diseases [MESH:D010409] (1805)   Penile Induration [MESH:D010411] (495)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Prostatic Diseases [MESH:D011469] (6204)   Prostatic Neoplasms [MESH:D011471] (6135)   Prostate cancer, familial [MESH:C537243] (264)  Phyllodes Tumor of the Prostate [MESH:C549759] (110)  Sexual Dysfunction, Physiological [MESH:D012735] (1808)   Erectile Dysfunction [MESH:D007172] (1791)  Urogenital Abnormalities [MESH:D014564] (2065)   Microphthalmia, Syndromic 6 [MESH:C566440] (101)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Urogenital Neoplasms [MESH:D014565] (6932)   Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)   Prostate cancer, familial [MESH:C537243] (264)  Phyllodes Tumor of the Prostate [MESH:C549759] (110)  Testicular Neoplasms [MESH:D013736] (520)   Testicular Germ Cell Tumor [MESH:C563236] (176)  Urologic Neoplasms [MESH:D014571] (5315)   Ureteral Neoplasms [MESH:D014516] (574)  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)   Diabetic Nephropathies [MESH:D003928] (2301)  Hydronephrosis [MESH:D006869] (956)  Hyperoxaluria [MESH:D006959] (1498)  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, IGA [MESH:D005922] (897)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)   Glomerulopathy with fibronectin deposits [MESH:C536826] (244)  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)   Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D-Dependent Rickets, Type 2A [MESH:C562794] (137)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Ureteral Diseases [MESH:D014515] (1024)   Ureteral Neoplasms [MESH:D014516] (574)  Ureteral Obstruction [MESH:D014517] (575)  Urinary Bladder Diseases [MESH:D001745] (4374)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urination Disorders [MESH:D014555] (3598)   Polyuria [MESH:D011141] (279)  Proteinuria [MESH:D011507] (3293) C13. Female Urogenital Diseases and Pregnancy Complications  C13. Female Urogenital Diseases and Pregnancy Complications  Z. Exceptions (1116)   Not Fully Specified [NFS] (1116)  Female Urogenital Diseases [MESH:D052776] (8724)   Genital Diseases, Female [MESH:D005831] (5563)   Endometriosis [MESH:D004715] (2461)  Adnexal Diseases [MESH:D000291] (4273)   Ovarian Diseases [MESH:D010049] (4255)   Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Ovarian Neoplasms [MESH:D010051] (3281)   Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Infertility [MESH:D007246] (2211)   Infertility, Female [MESH:D007247] (2184)  Uterine Diseases [MESH:D014591] (2479)   Endometrial Hyperplasia [MESH:D004714] (263)  Uterine Cervical Diseases [MESH:D002577] (988)   Uterine Cervical Neoplasms [MESH:D002583] (978)  Uterine Neoplasms [MESH:D014594] (2430)   Endometrial Neoplasms [MESH:D016889] (1984)  Uterine Cervical Neoplasms [MESH:D002583] (978)  Vulvar Diseases [MESH:D014845] (873)   Vulvar Lichen Sclerosus [MESH:D007724] (825)  Urogenital Abnormalities [MESH:D014564] (2043)   Microphthalmia, Syndromic 6 [MESH:C566440] (101)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Urogenital Neoplasms [MESH:D014565] (5792)   Genital Neoplasms, Female [MESH:D005833] (3810)   Ovarian Neoplasms [MESH:D010051] (3281)   Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Uterine Neoplasms [MESH:D014594] (2433)   Endometrial Neoplasms [MESH:D016889] (1989)  Uterine Cervical Neoplasms [MESH:D002583] (978)  Urologic Neoplasms [MESH:D014571] (5315)   Ureteral Neoplasms [MESH:D014516] (574)  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)   Diabetic Nephropathies [MESH:D003928] (2301)  Hydronephrosis [MESH:D006869] (956)  Hyperoxaluria [MESH:D006959] (1498)  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, IGA [MESH:D005922] (897)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)   Glomerulopathy with fibronectin deposits [MESH:C536826] (244)  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)   Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D-Dependent Rickets, Type 2A [MESH:C562794] (137)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Ureteral Diseases [MESH:D014515] (1024)   Ureteral Neoplasms [MESH:D014516] (574)  Ureteral Obstruction [MESH:D014517] (575)  Urinary Bladder Diseases [MESH:D001745] (4375)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urination Disorders [MESH:D014555] (3598)   Polyuria [MESH:D011141] (279)  Proteinuria [MESH:D011507] (3293)  Pregnancy Complications [MESH:D011248] (4768)   Abortion, Spontaneous [MESH:D000022] (2780)  Diabetes, Gestational [MESH:D016640] (1157)  Fetal Diseases [MESH:D005315] (1206)   Fetal Growth Retardation [MESH:D005317] (986)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Prenatal Injuries [MESH:D049188] (1314)   Prenatal Exposure Delayed Effects [MESH:D011297] (870) C14. Cardiovascular Diseases  C14. Cardiovascular Diseases  Cardiovascular Diseases [MESH:D002318] (10123)   Cardiovascular Abnormalities [MESH:D018376] (3153)   Heart Defects, Congenital [MESH:D006330] (2447)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  VACTERL hydrocephaly [MESH:C536521] (151)  Short QT Syndrome 1 [MESH:C566506] (189)  Hypoplastic Left Heart Syndrome [MESH:D018636] (194)  LEOPARD Syndrome [MESH:D044542] (299)  Marfan Syndrome [MESH:D008382] (646)  Noonan Syndrome [MESH:D009634] (506)  Heart Diseases [MESH:D006331] (8614)   Heart Failure [MESH:D006333] (4058)  Arrhythmias, Cardiac [MESH:D001145] (4679)   Short QT Syndrome 1 [MESH:C566506] (189)  Cardiac Arrhythmia, Ankyrin-B-Related [MESH:C566996] (32)  Ventricular Fibrillation [MESH:D014693] (624)  Long QT Syndrome [MESH:D008133] (693)   Long Qt Syndrome 2 [MESH:C563614] (189)  Tachycardia [MESH:D013610] (3339)   Tachycardia, Ventricular [MESH:D017180] (1386)   Torsades de Pointes [MESH:D016171] (880)  Cardiomegaly [MESH:D006332] (4081)   Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1y [MESH:C567507] (103)  Cardiomyopathies [MESH:D009202] (5331)   Alpha-B Crystallinopathy [MESH:C563848] (135)  Diabetic Cardiomyopathies [MESH:D058065] (1995)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1y [MESH:C567507] (103)  Cardiomyopathy, Hypertrophic [MESH:D002312] (1516)   Cardiomyopathy, Hypertrophic, Familial [MESH:D024741] (339)   Cardiomyopathy, Familial Hypertrophic, 3 [MESH:C566170] (103)  Heart Defects, Congenital [MESH:D006330] (2443)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  VACTERL hydrocephaly [MESH:C536521] (151)  Short QT Syndrome 1 [MESH:C566506] (189)  Hypoplastic Left Heart Syndrome [MESH:D018636] (194)  LEOPARD Syndrome [MESH:D044542] (299)  Marfan Syndrome [MESH:D008382] (646)  Noonan Syndrome [MESH:D009634] (506)  Heart Valve Diseases [MESH:D006349] (3333)   Aortic Valve Insufficiency [MESH:D001022] (1002)  Aortic Valve Stenosis [MESH:D001024] (1742)   Aortic Valve, Calcification of [MESH:C562942] (655)  Aortic Stenosis, Subvalvular [MESH:D001020] (1455)   Cardiomyopathy, Hypertrophic [MESH:D002312] (1451)  Pulmonary Valve Stenosis [MESH:D011666] (360)   LEOPARD Syndrome [MESH:D044542] (299)  Myocardial Ischemia [MESH:D017202] (5787)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocardial Stunning [MESH:D017682] (1816)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Coronary Disease [MESH:D003327] (3439)   Coronary Aneurysm [MESH:D003323] (204)  Coronary Artery Disease [MESH:D003324] (2685)  Myocardial Infarction [MESH:D009203] (4122)   Myocardial Stunning [MESH:D017682] (1816)  Ventricular Dysfunction [MESH:D018754] (2348)   Ventricular Dysfunction, Left [MESH:D018487] (1631)  Ventricular Outflow Obstruction [MESH:D014694] (976)   Aortic Valve Stenosis [MESH:D001024] (810)   Aortic Valve, Calcification of [MESH:C562942] (655)  Vascular Diseases [MESH:D014652] (8691)   Hypertension [MESH:D006973] (5655)  Aneurysm [MESH:D000783] (1886)   Coronary Aneurysm [MESH:D003323] (204)  Aneurysm, Dissecting [MESH:D000784] (699)   Loeys-Dietz Syndrome [MESH:D055947] (263)   Aortic aneurysm, familial thoracic 3 [MESH:C537783] (107)  Loeys-Dietz Syndrome, Type 1b [MESH:C567181] (107)  Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Thoracic [MESH:D017545] (781)   Aortic aneurysm, familial thoracic 3 [MESH:C537783] (107)  Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Loeys-Dietz Syndrome, Type 1b [MESH:C567181] (107)  Loeys-Dietz Syndrome [MESH:D055947] (263)   Aortic aneurysm, familial thoracic 3 [MESH:C537783] (107)  Loeys-Dietz Syndrome, Type 1b [MESH:C567181] (107)  Angiomatosis [MESH:D000798] (620)   von Hippel-Lindau Disease [MESH:D006623] (580)  Aortic Diseases [MESH:D001018] (1737)   Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Thoracic [MESH:D017545] (781)   Aortic aneurysm, familial thoracic 3 [MESH:C537783] (107)  Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Loeys-Dietz Syndrome, Type 1b [MESH:C567181] (107)  Loeys-Dietz Syndrome [MESH:D055947] (263)   Aortic aneurysm, familial thoracic 3 [MESH:C537783] (107)  Loeys-Dietz Syndrome, Type 1b [MESH:C567181] (107)  Arterial Occlusive Diseases [MESH:D001157] (4520)   Arteriosclerosis [MESH:D001161] (4466)   Atherosclerosis [MESH:D050197] (4188)  Coronary Artery Disease [MESH:D003324] (2685)  Cerebrovascular Disorders [MESH:D002561] (5541)   Vasospasm, Intracranial [MESH:D020301] (324)  Brain Ischemia [MESH:D002545] (4873)   Ischemic Attack, Transient [MESH:D002546] (1313)  Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Intracranial Arterial Diseases [MESH:D020765] (2468)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  Subarachnoid Hemorrhage [MESH:D013345] (1082)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Hemostatic Disorders [MESH:D020141] (2894)   Multiple Myeloma [MESH:D009101] (2765)  Myocardial Ischemia [MESH:D017202] (5791)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocardial Stunning [MESH:D017682] (1816)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Coronary Disease [MESH:D003327] (3439)   Coronary Aneurysm [MESH:D003323] (204)  Coronary Artery Disease [MESH:D003324] (2685)  Myocardial Infarction [MESH:D009203] (4151)   Myocardial Stunning [MESH:D017682] (1816)  Peripheral Vascular Diseases [MESH:D016491] (1412)   Livedo Reticularis [MESH:D054068] (228)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500) C15. Hemic and Lymphatic Diseases  C15. Hemic and Lymphatic Diseases  Hematologic Diseases [MESH:D006402] (6174)   Pancytopenia [MESH:D010198] (332)  Anemia [MESH:D000740] (3966)   Anemia, Aplastic [MESH:D000741] (1925)   Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)   Fanconi Anemia, Complementation Group D1 [MESH:C563980] (68)  Anemia, Hemolytic [MESH:D000743] (3083)   Anemia, Hemolytic, Autoimmune [MESH:D000744] (117)  Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Anemia, Macrocytic [MESH:D000748] (382)   5q- syndrome [MESH:C535323] (131)  Anemia, Megaloblastic [MESH:D000749] (288)  Anemia, Refractory [MESH:D000753] (1567)   Ghosal Hematodiaphyseal Dysplasia [MESH:C565551] (58)  Blood Coagulation Disorders [MESH:D001778] (1828)   Thrombocythemia, Essential [MESH:D013920] (707)  Blood Platelet Disorders [MESH:D001791] (3174)   Thrombocytopenia [MESH:D013921] (2966)   Thrombotic Microangiopathies [MESH:D057049] (2598)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Thrombocytosis [MESH:D013922] (720)   Thrombocythemia, Essential [MESH:D013920] (707)  Blood Protein Disorders [MESH:D001796] (3051)   Paraproteinemias [MESH:D010265] (2781)   Multiple Myeloma [MESH:D009101] (2765)  Bone Marrow Diseases [MESH:D001855] (2944)   Anemia, Aplastic [MESH:D000741] (1925)   Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)   Fanconi Anemia, Complementation Group D1 [MESH:C563980] (68)  Myelodysplastic Syndromes [MESH:D009190] (2093)   Anemia, Refractory [MESH:D000753] (1567)   Ghosal Hematodiaphyseal Dysplasia [MESH:C565551] (58)  Myeloproliferative Disorders [MESH:D009196] (1492)   Myeloproliferative Disorder, Chronic, with Eosinophilia [MESH:C565054] (134)  Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Thrombocytosis [MESH:D013922] (720)   Thrombocythemia, Essential [MESH:D013920] (707)  Hemorrhagic Disorders [MESH:D006474] (3359)   Thrombocythemia, Essential [MESH:D013920] (707)  Hemostatic Disorders [MESH:D020141] (2932)   Multiple Myeloma [MESH:D009101] (2765)  Leukocyte Disorders [MESH:D007960] (2662)   Eosinophilia [MESH:D004802] (537)   Myeloproliferative Disorder, Chronic, with Eosinophilia [MESH:C565054] (134)  Leukopenia [MESH:D007970] (1921)   Agranulocytosis [MESH:D000380] (1675)   Neutropenia [MESH:D009503] (1629)  Lymphatic Diseases [MESH:D008206] (5167)   Splenic Diseases [MESH:D013158] (1323)  Lymphoproliferative Disorders [MESH:D008232] (4638)   Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Sarcoidosis [MESH:D012507] (895)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)  Lymphoma [MESH:D008223] (3684)   Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, Mantle-Cell [MESH:D020522] (561)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1204)   Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912) 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)   Respiratory System Abnormalities [MESH:D015619] (244)  Abnormalities, Multiple [MESH:D000015] (3192)   Coffin-Siris syndrome [MESH:C536436] (102)  Desmosterolosis [MESH:C566555] (85)  Beckwith-Wiedemann Syndrome [MESH:D001506] (193)  Costello Syndrome [MESH:D056685] (407)  Down Syndrome [MESH:D004314] (1287)  Holoprosencephaly [MESH:D016142] (218)  LEOPARD Syndrome [MESH:D044542] (299)  Marfan Syndrome [MESH:D008382] (646)  Proteus Syndrome [MESH:D016715] (152)  Ectodermal Dysplasia [MESH:D004476] (938)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Loeys-Dietz Syndrome [MESH:D055947] (263)   Aortic aneurysm, familial thoracic 3 [MESH:C537783] (107)  Loeys-Dietz Syndrome, Type 1b [MESH:C567181] (107)  Waardenburg Syndrome [MESH:D014849] (243)   ABCD syndrome [MESH:C535334] (143)  Waardenburg syndrome type 2 [MESH:C536463] (55)  Waardenburg syndrome type 2A [MESH:C536464] (42)  Waardenburg Syndrome, Type 2D [MESH:C563839] (48)  Cardiovascular Abnormalities [MESH:D018376] (3294)   Heart Defects, Congenital [MESH:D006330] (2611)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  VACTERL hydrocephaly [MESH:C536521] (151)  Short QT Syndrome 1 [MESH:C566506] (189)  Hypoplastic Left Heart Syndrome [MESH:D018636] (194)  LEOPARD Syndrome [MESH:D044542] (299)  Marfan Syndrome [MESH:D008382] (646)  Noonan Syndrome [MESH:D009634] (506)  Long QT Syndrome [MESH:D008133] (693)   Long Qt Syndrome 2 [MESH:C563614] (189)  Chromosome Disorders [MESH:D025063] (2030)   Mosaic variegated aneuploidy syndrome [MESH:C536987] (95)  Beckwith-Wiedemann Syndrome [MESH:D001506] (193)  Down Syndrome [MESH:D004314] (1287)  Holoprosencephaly [MESH:D016142] (218)  Digestive System Abnormalities [MESH:D004065] (507)   Hirschsprung Disease [MESH:D006627] (361)  Eye Abnormalities [MESH:D005124] (1233)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Microphthalmos [MESH:D008850] (273)   Microphthalmia, Syndromic 6 [MESH:C566440] (101)  Musculoskeletal Abnormalities [MESH:D009139] (3779)   Arthrogryposis [MESH:D001176] (329)   Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Craniofacial Abnormalities [MESH:D019465] (3064)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Holoprosencephaly [MESH:D016142] (218)  LEOPARD Syndrome [MESH:D044542] (299)  Noonan Syndrome [MESH:D009634] (506)  Craniofacial Dysostosis [MESH:D003394] (391)   Hallermann's Syndrome [MESH:D006210] (193)  Macrocephaly [MESH:D058627] (264)   Macrocephaly Autism Syndrome [MESH:C565342] (151)  Maxillofacial Abnormalities [MESH:D019767] (1448)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Orofacial Cleft 11 [MESH:C567410] (101)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Meier-Gorlin syndrome [MESH:C538012] (133)  Microcephaly [MESH:D008831] (700)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Limb Deformities, Congenital [MESH:D017880] (1813)   Acromicric dysplasia [MESH:C535662] (520)  VACTERL hydrocephaly [MESH:C536521] (151)  Microphthalmia, Syndromic 6 [MESH:C566440] (101)  Polydactyly [MESH:D017689] (318)  Proteus Syndrome [MESH:D016715] (152)  Ectromelia [MESH:D004480] (108)   Al Awadi syndrome [MESH:C535612] (30)  Foot Deformities, Congenital [MESH:D005532] (538)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Hand Deformities, Congenital [MESH:D006228] (587)   Coffin-Siris syndrome [MESH:C536436] (102)  Syndactyly [MESH:D013576] (487)   Syndactyly, type 3 [MESH:C538154] (192)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Synostosis [MESH:D013580] (817)   Syndactyly [MESH:D013576] (487)   Syndactyly, type 3 [MESH:C538154] (192)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Nervous System Malformations [MESH:D009421] (3354)   Microphthalmia, Syndromic 6 [MESH:C566440] (101)  Holoprosencephaly [MESH:D016142] (218)  Neural Tube Defects [MESH:D009436] (2143)  Agenesis of Corpus Callosum [MESH:D061085] (345)   Holoprosencephaly [MESH:D016142] (218)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic Paraplegia 31, Autosomal Dominant [MESH:C565210] (20)  Malformations of Cortical Development [MESH:D054220] (1406)   Lissencephaly [MESH:D054082] (218)   Classical Lissencephalies and Subcortical Band Heterotopias [MESH:D054221] (114)  Macrocephaly [MESH:D058627] (264)   Macrocephaly Autism Syndrome [MESH:C565342] (151)  Microcephaly [MESH:D008831] (700)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Neuronal Migration Disorders [MESH:D054081] (264)   Classical Lissencephalies and Subcortical Band Heterotopias [MESH:D054221] (114)  Skin Abnormalities [MESH:D012868] (1723)   Dyskeratosis Congenita [MESH:D019871] (185)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Epidermolysis Bullosa [MESH:D004820] (260)   Epidermolysis Bullosa Simplex [MESH:D016110] (140)  Epidermolysis Bullosa, Junctional [MESH:D016109] (152)   Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150)  Ichthyosis [MESH:D007057] (481)   Keratosis Follicularis Spinulosa Decalvans, X-Linked [MESH:C536159] (78)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Orofacial Cleft 11 [MESH:C567410] (101)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Meier-Gorlin syndrome [MESH:C538012] (133)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Orofacial Cleft 11 [MESH:C567410] (101)  Cleft Palate [MESH:D002972] (1330)   Orofacial Cleft 11 [MESH:C567410] (101)  Tooth Abnormalities [MESH:D014071] (622)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Urogenital Abnormalities [MESH:D014564] (2064)   Microphthalmia, Syndromic 6 [MESH:C566440] (101)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Fetal Diseases [MESH:D005315] (1205)   Fetal Growth Retardation [MESH:D005317] (986)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Genetic Diseases, Inborn [MESH:D030342] (9766)   Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Camurati-Engelmann Syndrome [MESH:D003966] (492)  Costello Syndrome [MESH:D056685] (407)  Cystic Fibrosis [MESH:D003550] (760)  Marfan Syndrome [MESH:D008382] (646)  Pycnodysostosis [MESH:D058631] (73)  Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)   Fanconi Anemia, Complementation Group D1 [MESH:C563980] (68)  Cardiomyopathy, Hypertrophic, Familial [MESH:D024741] (339)   Cardiomyopathy, Familial Hypertrophic, 3 [MESH:C566170] (103)  Chromosome Disorders [MESH:D025063] (2030)   Mosaic variegated aneuploidy syndrome [MESH:C536987] (95)  Beckwith-Wiedemann Syndrome [MESH:D001506] (193)  Down Syndrome [MESH:D004314] (1287)  Holoprosencephaly [MESH:D016142] (218)  Eye Diseases, Hereditary [MESH:D015785] (1867)   Albinism [MESH:D000417] (359)   Piebaldism [MESH:D016116] (167)  Albinism, Ocular [MESH:D016117] (157)   Albinism ocular late onset sensorineural deafness [MESH:C537043] (137)  Albinism, Oculocutaneous [MESH:D016115] (234)   Tietz syndrome [MESH:C536919] (42)  Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Corneal dystrophy, gelatinous drop-like [MESH:C535480] (37)  Meretoja syndrome [MESH:C537459] (95)  Genetic Diseases, X-Linked [MESH:D040181] (3028)   Keratosis Follicularis Spinulosa Decalvans, X-Linked [MESH:C536159] (78)  Hypospadias 1, X-Linked [MESH:C567482] (571)  Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Dyskeratosis Congenita [MESH:D019871] (185)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Mental Retardation, X-Linked [MESH:D038901] (1867)   Classical Lissencephalies and Subcortical Band Heterotopias [MESH:D054221] (114)  Mucopolysaccharidosis II [MESH:D016532] (26)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465)   Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98)  Gerstmann-Straussler-Scheinker Disease [MESH:D016098] (98)  Hepatolenticular Degeneration [MESH:D006527] (473)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic Paraplegia 31, Autosomal Dominant [MESH:C565210] (20)  Huntington Disease [MESH:D006816] (540)   Huntington Disease-Like 1 [MESH:C566398] (98)  Mental Retardation, X-Linked [MESH:D038901] (1848)   Mucopolysaccharidosis II [MESH:D016532] (26)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxia 29 [MESH:C537206] (90)  Spinocerebellar Ataxias [MESH:D020754] (322)   Spinocerebellar Ataxia 15 [MESH:C564685] (90)  Loeys-Dietz Syndrome [MESH:D055947] (263)   Aortic aneurysm, familial thoracic 3 [MESH:C537783] (107)  Loeys-Dietz Syndrome, Type 1b [MESH:C567181] (107)  Metabolism, Inborn Errors [MESH:D008661] (6032)   Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565)   Methylmalonic acidemia [MESH:C537358] (764)  Hyperglycinemia, Nonketotic [MESH:D020158] (67)  Albinism [MESH:D000417] (359)   Piebaldism [MESH:D016116] (167)  Albinism, Ocular [MESH:D016117] (157)   Albinism ocular late onset sensorineural deafness [MESH:C537043] (137)  Albinism, Oculocutaneous [MESH:D016115] (234)   Tietz syndrome [MESH:C536919] (42)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   3-methylcrotonyl CoA carboxylase 2 deficiency [MESH:C535309] (32)  Amyloidosis, Familial [MESH:D028226] (696)   Corneal dystrophy, gelatinous drop-like [MESH:C535480] (37)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Hyperglycinemia, Nonketotic [MESH:D020158] (67)  Peroxisomal Disorders [MESH:D018901] (1472)   Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   3-methylcrotonyl CoA carboxylase 2 deficiency [MESH:C535309] (32)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Ribose 5-Phosphate Isomerase Deficiency [MESH:C563212] (34)  Congenital Disorders of Glycosylation [MESH:D018981] (188)   Congenital disorder of glycosylation type 1D [MESH:C535742] (18)  Congenital disorder of glycosylation type 1H [MESH:C535746] (19)  Congenital disorder of glycosylation type 2D [MESH:C535753] (40)  Lactose Intolerance [MESH:D007787] (113)   Lactose Intolerance, Adult Type [MESH:C562601] (112)  Mucopolysaccharidoses [MESH:D009083] (164)   Mucopolysaccharidosis II [MESH:D016532] (26)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Desmosterolosis [MESH:C566555] (85)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Lysosomal Storage Diseases [MESH:D016464] (761)   Pycnodysostosis [MESH:D058631] (73)  Mucopolysaccharidoses [MESH:D009083] (164)   Mucopolysaccharidosis II [MESH:D016532] (26)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hepatolenticular Degeneration [MESH:D006527] (473)  Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D-Dependent Rickets, Type 2A [MESH:C562794] (137)  Peroxisomal Disorders [MESH:D018901] (1788)   Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria, Acute Hepatic [MESH:C562618] (99)  Purine-Pyrimidine Metabolism, Inborn Errors [MESH:D011686] (496)   Dihydropyrimidine Dehydrogenase Deficiency [MESH:D054067] (88)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1027)   Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D-Dependent Rickets, Type 2A [MESH:C562794] (137)  Muscular Dystrophies [MESH:D009136] (1597)   Bethlem myopathy [MESH:C535436] (108)  Scleroatonic muscular dystrophy [MESH:C537521] (108)  Filaminopathy, autosomal dominant [MESH:C537932] (40)  Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Familial cylindromatosis [MESH:C536611] (35)  Turcot syndrome [MESH:C536928] (159)  Meningioma, familial [MESH:C537443] (195)  Juvenile polyposis syndrome [MESH:C537702] (196)  Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Adenomatous Polyposis Coli [MESH:D011125] (1565)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (260)  Exostoses, Multiple Hereditary [MESH:D005097] (154)  Hamartoma Syndrome, Multiple [MESH:D006223] (260)  Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Li-Fraumeni Syndrome [MESH:D016864] (859)  Wilms Tumor [MESH:D009396] (553)  Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia, Type IV [MESH:C567059] (297)  Multiple Endocrine Neoplasia Type 1 [MESH:D018761] (26)  Skin Diseases, Genetic [MESH:D012873] (3456)   Keratosis Follicularis Spinulosa Decalvans, X-Linked [MESH:C536159] (78)  Darier Disease [MESH:D007644] (125)  Albinism [MESH:D000417] (359)   Piebaldism [MESH:D016116] (167)  Albinism, Ocular [MESH:D016117] (157)   Albinism ocular late onset sensorineural deafness [MESH:C537043] (137)  Albinism, Oculocutaneous [MESH:D016115] (234)   Tietz syndrome [MESH:C536919] (42)  Dyskeratosis Congenita [MESH:D019871] (185)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Epidermolysis Bullosa [MESH:D004820] (259)   Epidermolysis Bullosa Simplex [MESH:D016110] (140)  Epidermolysis Bullosa, Junctional [MESH:D016109] (152)   Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150)  Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria, Acute Hepatic [MESH:C562618] (99)  Infant, Newborn, Diseases [MESH:D007232] (3064)   Cystic Fibrosis [MESH:D003550] (760)  Ichthyosis [MESH:D007057] (476)   Keratosis Follicularis Spinulosa Decalvans, X-Linked [MESH:C536159] (78) C17. Skin and Connective Tissue Diseases  C17. Skin and Connective Tissue Diseases  Connective Tissue Diseases [MESH:D003240] (4490)   Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Marfan Syndrome [MESH:D008382] (646)  Noonan Syndrome [MESH:D009634] (506)  Penile Induration [MESH:D010411] (495)  Scleroderma, Systemic [MESH:D012595] (199)  Collagen Diseases [MESH:D003095] (1267)   Keloid [MESH:D007627] (1111)  Mucinoses [MESH:D017520] (177)   Mucopolysaccharidoses [MESH:D009083] (164)   Mucopolysaccharidosis II [MESH:D016532] (26)  Rheumatic Diseases [MESH:D012216] (3619)   Arthritis, Rheumatoid [MESH:D001172] (3603)  Skin Diseases [MESH:D012871] (8774)   Lipomatosis [MESH:D008068] (182)  Nephrogenic Fibrosing Dermopathy [MESH:D054989] (452)  Scleroderma, Systemic [MESH:D012595] (199)  Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Breast Diseases [MESH:D001941] (6148)   Breast Neoplasms [MESH:D001943] (6077)   Breast Neoplasms, Male [MESH:D018567] (650)  Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Dermatitis [MESH:D003872] (4530)   Eczema [MESH:D004485] (235)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Facial Dermatoses [MESH:D005148] (1336)   Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Hair Diseases [MESH:D006201] (1891)   Hypotrichosis [MESH:D007039] (1513)   Alopecia [MESH:D000505] (1453)  Keratosis [MESH:D007642] (1941)   Darier Disease [MESH:D007644] (125)  Ichthyosis [MESH:D007057] (481)   Keratosis Follicularis Spinulosa Decalvans, X-Linked [MESH:C536159] (78)  Pigmentation Disorders [MESH:D010859] (1215)   Cafe-au-Lait Spots [MESH:D019080] (186)  Hyperpigmentation [MESH:D017495] (523)   Melanosis [MESH:D008548] (459)   Lentigo [MESH:D007911] (329)   LEOPARD Syndrome [MESH:D044542] (299)  Hypopigmentation [MESH:D017496] (718)   Vitiligo [MESH:D014820] (504)  Albinism [MESH:D000417] (359)   Piebaldism [MESH:D016116] (167)  Albinism, Ocular [MESH:D016117] (157)   Albinism ocular late onset sensorineural deafness [MESH:C537043] (137)  Albinism, Oculocutaneous [MESH:D016115] (234)   Tietz syndrome [MESH:C536919] (42)  Skin Abnormalities [MESH:D012868] (1709)   Dyskeratosis Congenita [MESH:D019871] (185)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Epidermolysis Bullosa [MESH:D004820] (260)   Epidermolysis Bullosa Simplex [MESH:D016110] (140)  Epidermolysis Bullosa, Junctional [MESH:D016109] (152)   Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150)  Ichthyosis [MESH:D007057] (481)   Keratosis Follicularis Spinulosa Decalvans, X-Linked [MESH:C536159] (78)  Skin Diseases, Eczematous [MESH:D017443] (3740)   Eczema [MESH:D004485] (235)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Skin Diseases, Genetic [MESH:D012873] (3481)   Keratosis Follicularis Spinulosa Decalvans, X-Linked [MESH:C536159] (78)  Darier Disease [MESH:D007644] (125)  Albinism [MESH:D000417] (359)   Piebaldism [MESH:D016116] (167)  Albinism, Ocular [MESH:D016117] (157)   Albinism ocular late onset sensorineural deafness [MESH:C537043] (137)  Albinism, Oculocutaneous [MESH:D016115] (234)   Tietz syndrome [MESH:C536919] (42)  Dyskeratosis Congenita [MESH:D019871] (185)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Epidermolysis Bullosa [MESH:D004820] (260)   Epidermolysis Bullosa Simplex [MESH:D016110] (140)  Epidermolysis Bullosa, Junctional [MESH:D016109] (152)   Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150)  Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria, Acute Hepatic [MESH:C562618] (99)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Lipodystrophy [MESH:D008060] (930)   Lipodystrophy, Partial, Acquired [MESH:C562448] (26)  Lipodystrophy, Familial Partial [MESH:D052496] (589)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria, Acute Hepatic [MESH:C562618] (99)  Skin Diseases, Papulosquamous [MESH:D017444] (3392)   Psoriasis [MESH:D011565] (3278)  Skin Diseases, Vascular [MESH:D017445] (3288)   Urticaria [MESH:D014581] (2668)  Livedo Reticularis [MESH:D054068] (228)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Skin Diseases, Vesiculobullous [MESH:D012872] (1754)   Epidermolysis Bullosa [MESH:D004820] (260)   Epidermolysis Bullosa Simplex [MESH:D016110] (140)  Epidermolysis Bullosa, Junctional [MESH:D016109] (152)   Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150)  Skin Neoplasms [MESH:D012878] (2991)   Familial cylindromatosis [MESH:C536611] (35) C18. Nutritional and Metabolic Diseases  C18. Nutritional and Metabolic Diseases  Metabolic Diseases [MESH:D008659] (9025)   Brain Diseases, Metabolic [MESH:D001928] (3350)   Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Hyperglycinemia, Nonketotic [MESH:D020158] (67)  Peroxisomal Disorders [MESH:D018901] (1472)   Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   3-methylcrotonyl CoA carboxylase 2 deficiency [MESH:C535309] (32)  Calcium Metabolism Disorders [MESH:D002128] (3634)   Calcinosis [MESH:D002114] (2989)   Aortic Valve, Calcification of [MESH:C562942] (655)  Rickets [MESH:D012279] (341)   Rickets, Hypophosphatemic [MESH:D063730] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D-Dependent Rickets, Type 2A [MESH:C562794] (137)  DNA Repair-Deficiency Disorders [MESH:D049914] (2245)   Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)  Li-Fraumeni Syndrome [MESH:D016864] (859)  Fanconi Anemia [MESH:D005199] (1604)   Fanconi Anemia, Complementation Group D1 [MESH:C563980] (68)  Glucose Metabolism Disorders [MESH:D044882] (6122)   Hyperglycemia [MESH:D006943] (1858)  Diabetes Mellitus [MESH:D003920] (5891)   Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Diabetes, Gestational [MESH:D016640] (1152)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)   Wolcott-Rallison syndrome [MESH:C536739] (92)  Hyperinsulinism [MESH:D006946] (3586)   Insulin Resistance [MESH:D007333] (3511)  Lipid Metabolism Disorders [MESH:D052439] (3225)   Dyslipidemias [MESH:D050171] (2428)  Lipomatosis [MESH:D008068] (182)  Lipid Metabolism, Inborn Errors [MESH:D008052] (461)   Desmosterolosis [MESH:C566555] (85)  Lipodystrophy [MESH:D008060] (930)   Lipodystrophy, Partial, Acquired [MESH:C562448] (26)  Lipodystrophy, Familial Partial [MESH:D052496] (589)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Malabsorption Syndromes [MESH:D008286] (1869)   Lactose Intolerance [MESH:D007787] (113)   Lactose Intolerance, Adult Type [MESH:C562601] (112)  Metabolism, Inborn Errors [MESH:D008661] (6028)   Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559)   Methylmalonic acidemia [MESH:C537358] (764)  Hyperglycinemia, Nonketotic [MESH:D020158] (67)  Albinism [MESH:D000417] (359)   Piebaldism [MESH:D016116] (167)  Albinism, Ocular [MESH:D016117] (157)   Albinism ocular late onset sensorineural deafness [MESH:C537043] (137)  Albinism, Oculocutaneous [MESH:D016115] (234)   Tietz syndrome [MESH:C536919] (42)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   3-methylcrotonyl CoA carboxylase 2 deficiency [MESH:C535309] (32)  Amyloidosis, Familial [MESH:D028226] (696)   Corneal dystrophy, gelatinous drop-like [MESH:C535480] (37)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Hyperglycinemia, Nonketotic [MESH:D020158] (67)  Peroxisomal Disorders [MESH:D018901] (1472)   Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   3-methylcrotonyl CoA carboxylase 2 deficiency [MESH:C535309] (32)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Ribose 5-Phosphate Isomerase Deficiency [MESH:C563212] (34)  Congenital Disorders of Glycosylation [MESH:D018981] (188)   Congenital disorder of glycosylation type 1D [MESH:C535742] (18)  Congenital disorder of glycosylation type 1H [MESH:C535746] (19)  Congenital disorder of glycosylation type 2D [MESH:C535753] (40)  Lactose Intolerance [MESH:D007787] (113)   Lactose Intolerance, Adult Type [MESH:C562601] (112)  Mucopolysaccharidoses [MESH:D009083] (164)   Mucopolysaccharidosis II [MESH:D016532] (26)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Desmosterolosis [MESH:C566555] (85)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Lysosomal Storage Diseases [MESH:D016464] (761)   Pycnodysostosis [MESH:D058631] (73)  Mucopolysaccharidoses [MESH:D009083] (164)   Mucopolysaccharidosis II [MESH:D016532] (26)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hepatolenticular Degeneration [MESH:D006527] (473)  Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D-Dependent Rickets, Type 2A [MESH:C562794] (137)  Peroxisomal Disorders [MESH:D018901] (1788)   Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria, Acute Hepatic [MESH:C562618] (99)  Purine-Pyrimidine Metabolism, Inborn Errors [MESH:D011686] (496)   Dihydropyrimidine Dehydrogenase Deficiency [MESH:D054067] (88)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1026)   Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D-Dependent Rickets, Type 2A [MESH:C562794] (137)  Phosphorus Metabolism Disorders [MESH:D010760] (711)   Hypophosphatemia [MESH:D017674] (640)   Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D-Dependent Rickets, Type 2A [MESH:C562794] (137)  Rickets, Hypophosphatemic [MESH:D063730] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D-Dependent Rickets, Type 2A [MESH:C562794] (137)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria, Acute Hepatic [MESH:C562618] (99)  Proteostasis Deficiencies [MESH:D057165] (3522)   Amyloidosis [MESH:D000686] (791)   Meretoja syndrome [MESH:C537459] (95)  Amyloidosis, Familial [MESH:D028226] (696)   Corneal dystrophy, gelatinous drop-like [MESH:C535480] (37)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Frontotemporal Lobar Degeneration [MESH:D057174] (308)   Frontotemporal Dementia [MESH:D057180] (298)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Lipodystrophy [MESH:D008060] (930)   Lipodystrophy, Partial, Acquired [MESH:C562448] (26)  Lipodystrophy, Familial Partial [MESH:D052496] (589)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria, Acute Hepatic [MESH:C562618] (99)  Water-Electrolyte Imbalance [MESH:D014883] (2790)   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)  Vitamin B Deficiency [MESH:D014804] (1817)   Folic Acid Deficiency [MESH:D005494] (134)  Vitamin D Deficiency [MESH:D014808] (360)   Rickets [MESH:D012279] (341)   Rickets, Hypophosphatemic [MESH:D063730] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D-Dependent Rickets, Type 2A [MESH:C562794] (137)  Overnutrition [MESH:D044343] (4463)   Obesity [MESH:D009765] (4462) C19. Endocrine System Diseases  C19. Endocrine System Diseases  Endocrine System Diseases [MESH:D004700] (8062)   Diabetes Mellitus [MESH:D003920] (6159)   Diabetes, Gestational [MESH:D016640] (1152)  Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Diabetes Complications [MESH:D048909] (4129)   Diabetic Cardiomyopathies [MESH:D058065] (1995)  Diabetic Nephropathies [MESH:D003928] (2301)  Diabetic Neuropathies [MESH:D003929] (2443)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)   Wolcott-Rallison syndrome [MESH:C536739] (92)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia, Type IV [MESH:C567059] (297)  Multiple Endocrine Neoplasia Type 1 [MESH:D018761] (26)  Ovarian Neoplasms [MESH:D010051] (3275)   Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572)  Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Adenoma, Islet Cell [MESH:D007516] (31)   Insulinoma [MESH:D007340] (27)  Carcinoma, Islet Cell [MESH:D018273] (115)   Gastrinoma [MESH:D015408] (26)  Glucagonoma [MESH:D005935] (26)  Vipoma [MESH:D003969] (110)  Pituitary Neoplasms [MESH:D010911] (981)   ACTH-Secreting Pituitary Adenoma [MESH:D049913] (172)  Prolactinoma [MESH:D015175] (312)  Testicular Neoplasms [MESH:D013736] (520)   Testicular Germ Cell Tumor [MESH:C563236] (176)  Gonadal Disorders [MESH:D006058] (5088)   Puberty, Precocious [MESH:D011629] (1147)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Ovarian Diseases [MESH:D010049] (4253)   Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Ovarian Neoplasms [MESH:D010051] (3281)   Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Testicular Diseases [MESH:D013733] (777)   Testicular Neoplasms [MESH:D013736] (520)   Testicular Germ Cell Tumor [MESH:C563236] (176)  Parathyroid Diseases [MESH:D010279] (1604)   Hyperparathyroidism [MESH:D006961] (1475)  Pituitary Diseases [MESH:D010900] (1829)   Hyperpituitarism [MESH:D006964] (1259)   Acromegaly [MESH:D000172] (466)  Pituitary Neoplasms [MESH:D010911] (981)   ACTH-Secreting Pituitary Adenoma [MESH:D049913] (172)  Prolactinoma [MESH:D015175] (312)  Thyroid Diseases [MESH:D013959] (2808)   Goiter [MESH:D006042] (359)   Graves Disease [MESH:D006111] (278)   Graves Ophthalmopathy [MESH:D049970] (165)  Hyperthyroidism [MESH:D006980] (1191)   Graves Disease [MESH:D006111] (278)   Graves Ophthalmopathy [MESH:D049970] (165) C20. Immune System Diseases  C20. Immune System Diseases  Immune System Diseases [MESH:D007154] (7674)   Autoimmune Diseases [MESH:D001327] (5067)   Anemia, Hemolytic, Autoimmune [MESH:D000744] (117)  Arthritis, Rheumatoid [MESH:D001172] (3601)  Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Glomerulonephritis, IGA [MESH:D005922] (897)  Hepatitis, Autoimmune [MESH:D019693] (1982)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Diabetes Mellitus, Type 1 [MESH:D003922] (1893)   Wolcott-Rallison syndrome [MESH:C536739] (92)  Graves Disease [MESH:D006111] (278)   Graves Ophthalmopathy [MESH:D049970] (165)  Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)   Glomerulopathy with fibronectin deposits [MESH:C536826] (244)  Hypersensitivity [MESH:D006967] (5873)   Drug Hypersensitivity [MESH:D004342] (4000)  Hypersensitivity, Delayed [MESH:D006968] (3408)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Hypersensitivity, Immediate [MESH:D006969] (4980)   Urticaria [MESH:D014581] (2668)  Food Hypersensitivity [MESH:D005512] (608)   Peanut Hypersensitivity [MESH:D021183] (572)  Respiratory Hypersensitivity [MESH:D012130] (4250)   Asthma [MESH:D001249] (3914)  Immunologic Deficiency Syndromes [MESH:D007153] (3788)   HIV Infections [MESH:D015658] (3402)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Immunoproliferative Disorders [MESH:D007160] (4761)   Lymphoproliferative Disorders [MESH:D008232] (4734)   Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Multiple Myeloma [MESH:D009101] (2767)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)  Lymphoma [MESH:D008223] (3684)   Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, Mantle-Cell [MESH:D020522] (561)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1382)   Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)  Paraproteinemias [MESH:D010265] (2791)   Multiple Myeloma [MESH:D009101] (2765) C22. Animal Diseases  C22. Animal Diseases  Animal Diseases [MESH:D000820] (3656)   Disease Models, Animal [MESH:D004195] (2058)  Mammary Neoplasms, Animal [MESH:D015674] (2735)  Paratuberculosis [MESH:D010283] (427)  Sheep Diseases [MESH:D012757] (473)   Scrapie [MESH:D012608] (462) C23. Pathological Conditions, Signs and Symptoms  C23. Pathological Conditions, Signs and Symptoms  Pathological Conditions, Anatomical [MESH:D020763] (6074)   Alopecia [MESH:D000505] (1383)  Plaque, Atherosclerotic [MESH:D058226] (696)  Ventricular Remodeling [MESH:D020257] (686)  Atrophy [MESH:D001284] (2603)   Muscular Atrophy [MESH:D009133] (1234)  Calculi [MESH:D002137] (756)   Gallstones [MESH:D042882] (350)  Hernia [MESH:D006547] (2825)   Hernia, Diaphragmatic [MESH:D006548] (2647)  Hernia, Abdominal [MESH:D046449] (208)   Hernia, Inguinal [MESH:D006552] (111)  Hypertrophy [MESH:D006984] (4476)   Splenomegaly [MESH:D013163] (1258)  Cardiomegaly [MESH:D006332] (3802)   Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Polyps [MESH:D011127] (1633)   Intestinal Polyps [MESH:D007417] (1592)  Pathologic Processes [MESH:D010335] (9863)   Gliosis [MESH:D005911] (1419)  Hyperammonemia [MESH:D022124] (322)  Hyperplasia [MESH:D006965] (2463)  Ischemia [MESH:D007511] (3049)  Lithiasis [MESH:D020347] (345)  Necrosis [MESH:D009336] (4019)  Nerve Degeneration [MESH:D009410] (4061)  Ulcer [MESH:D014456] (392)  Arrhythmias, Cardiac [MESH:D001145] (4658)   Short QT Syndrome 1 [MESH:C566506] (189)  Cardiac Arrhythmia, Ankyrin-B-Related [MESH:C566996] (32)  Ventricular Fibrillation [MESH:D014693] (624)  Long QT Syndrome [MESH:D008133] (691)   Long Qt Syndrome 2 [MESH:C563614] (189)  Tachycardia [MESH:D013610] (3339)   Tachycardia, Ventricular [MESH:D017180] (1386)   Torsades de Pointes [MESH:D016171] (880)  Chromosome Aberrations [MESH:D002869] (2352)   Chromosomal Instability [MESH:D043171] (67)  Translocation, Genetic [MESH:D014178] (557)  Aneuploidy [MESH:D000782] (1237)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  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)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Macrocephaly Autism Syndrome [MESH:C565342] (151)  Fibrosis [MESH:D005355] (3133)   Nephrogenic Fibrosing Dermopathy [MESH:D054989] (452)  Peritoneal Fibrosis [MESH:D056627] (488)  Cicatrix [MESH:D002921] (1115)   Keloid [MESH:D007627] (1110)  Genomic Instability [MESH:D042822] (184)   Chromosomal Instability [MESH:D043171] (67)  Microsatellite Instability [MESH:D053842] (141)  Growth Disorders [MESH:D006130] (2438)   Meier-Gorlin syndrome [MESH:C538012] (133)  Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)  Fetal Growth Retardation [MESH:D005317] (986)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Hemorrhage [MESH:D006470] (4451)   Intracranial Hemorrhages [MESH:D020300] (3241)   Cerebral Hemorrhage [MESH:D002543] (2872)  Subarachnoid Hemorrhage [MESH:D013345] (1081)  Inflammation [MESH:D007249] (5241)   Systemic Inflammatory Response Syndrome [MESH:D018746] (3563)   Sepsis [MESH:D018805] (3562)  Menstruation Disturbances [MESH:D008599] (926)   Amenorrhea [MESH:D000568] (817)   Al Awadi syndrome [MESH:C535612] (30)  Metaplasia [MESH:D008679] (1469)   Neovascularization, Pathologic [MESH:D009389] (829)  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)  Ossification, Heterotopic [MESH:D009999] (187)   Ossification of Posterior Longitudinal Ligament [MESH:D017887] (99)   Ossification of the posterior longitudinal ligament of the spine [MESH:C537143] (98)  Postoperative Complications [MESH:D011183] (5311)   Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Sclerosis [MESH:D012598] (224)   Scleroatonic muscular dystrophy [MESH:C537521] (108)  Signs and Symptoms [MESH:D012816] (10659)   Cyanosis [MESH:D003490] (288)  Edema [MESH:D004487] (3726)  Fatigue [MESH:D005221] (437)  Feminization [MESH:D005262] (655)  Body Weight [MESH:D001835] (4972)   Body Weight Changes [MESH:D001836] (3206)   Weight Gain [MESH:D015430] (2595)  Overweight [MESH:D050177] (4455)   Obesity [MESH:D009765] (4454)  Failure to Thrive [MESH:D005183] (415)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Neurologic Manifestations [MESH:D009461] (8702)   Pain [MESH:D010146] (3869)  Seizures [MESH:D012640] (4502)  Dyskinesias [MESH:D020820] (3285)   Catalepsy [MESH:D002375] (1429)  Hyperkinesis [MESH:D006948] (1799)  Hypokinesia [MESH:D018476] (279)  Tics [MESH:D020323] (62)  Ataxia [MESH:D001259] (984)   Cerebellar Ataxia [MESH:D002524] (289)  Neurobehavioral Manifestations [MESH:D019954] (4706)   Memory Disorders [MESH:D008569] (3233)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Language Development Disorders [MESH:D007805] (351)  Consciousness Disorders [MESH:D003244] (677)   Unconsciousness [MESH:D014474] (657)  Intellectual Disability [MESH:D008607] (1476)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Coffin-Siris syndrome [MESH:C536436] (102)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Mental Retardation, Autosomal Dominant 3 [MESH:C567241] (14)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscular Atrophy [MESH:D009133] (1234)  Paralysis [MESH:D010243] (2298)   Ophthalmoplegia [MESH:D009886] (1468)   Supranuclear Palsy, Progressive [MESH:D013494] (235)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Sensation Disorders [MESH:D012678] (5009)   Hearing Disorders [MESH:D006311] (2101)   Hearing Loss [MESH:D034381] (2066)   Deafness [MESH:D003638] (593)   Tietz syndrome [MESH:C536919] (42)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Albinism ocular late onset sensorineural deafness [MESH:C537043] (137)  Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Pain [MESH:D010146] (4511)   Chest Pain [MESH:D002637] (2642)   Angina Pectoris [MESH:D000787] (2568)   Acute Coronary Syndrome [MESH:D054058] (2286)  Signs and Symptoms, Digestive [MESH:D012817] (3095)   Anorexia [MESH:D000855] (854)  Diarrhea [MESH:D003967] (858)  Signs and Symptoms, Respiratory [MESH:D012818] (2724)   Anoxia [MESH:D000860] (1698)  Hyperoxia [MESH:D018496] (694)  Hyperventilation [MESH:D006985] (652)  Skin Manifestations [MESH:D012877] (1250)   Cafe-au-Lait Spots [MESH:D019080] (186)  Livedo Reticularis [MESH:D054068] (228)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Urological Manifestations [MESH:D020924] (3532)   Polyuria [MESH:D011141] (279)  Proteinuria [MESH:D011507] (3293) C24. Occupational Diseases  C24. Occupational Diseases  Z. Exceptions (1530)   Not Fully Specified [NFS] (1530)  Occupational Diseases [MESH:D009784] (3402)   Pneumoconiosis [MESH:D011009] (2670)   Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273) C25. Chemically-Induced Disorders  C25. Chemically-Induced Disorders  Drug-Related Side Effects and Adverse Reactions [MESH:D064420] (5839)   Drug Hypersensitivity [MESH:D004342] (4001)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Poisoning [MESH:D011041] (6703)   Arsenic Poisoning [MESH:D020261] (2540)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Psychoses, Substance-Induced [MESH:D011605] (2053)  Lead Poisoning [MESH:D007855] (515)   Lead Poisoning, Nervous System [MESH:D020263] (102)  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)  Marijuana Abuse [MESH:D002189] (1132)  Phencyclidine Abuse [MESH:D010623] (288)  Psychoses, Substance-Induced [MESH:D011605] (2052)  Substance Withdrawal Syndrome [MESH:D013375] (2956)  Alcohol-Related Disorders [MESH:D019973] (3869)   Alcohol-Induced Disorders [MESH:D020751] (3350)   Liver Diseases, Alcoholic [MESH:D008108] (3243)   Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Opioid-Related Disorders [MESH:D009293] (1491)   Morphine Dependence [MESH:D009021] (855) C26. Wounds and Injuries  C26. Wounds and Injuries  Z. Exceptions (2454)   Not Fully Specified [NFS] (2454)  Wounds and Injuries [MESH:D014947] (5171)   Fractures, Bone [MESH:D050723] (597)  Spinal Cord Injuries [MESH:D013119] (2688)  Craniocerebral Trauma [MESH:D006259] (3523)   Brain Injuries [MESH:D001930] (3431)  Radiation Injuries [MESH:D011832] (2718)   Radiation Injuries, Experimental [MESH:D011833] (2662)  Thoracic Injuries [MESH:D013898] (1831)   Lung Injury [MESH:D055370] (1814)  Trauma, Nervous System [MESH:D020196] (3535)   Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) D02. Organic Chemicals  D02. Organic Chemicals  Organic Chemicals [MESH:D009930] (75987)   Organoselenium Compounds [MESH:D016566] (268) 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)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Macrocephaly Autism Syndrome [MESH:C565342] (151) 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)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Coffin-Siris syndrome [MESH:C536436] (102)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Mental Retardation, Autosomal Dominant 3 [MESH:C567241] (14)  Mental Disorders [MESH:D001523] (2063)   Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98)  Delirium, Dementia, Amnestic, Cognitive Disorders [MESH:D019965] (487)   Cognition Disorders [MESH:D003072] (115)   Huntington Disease [MESH:D006816] (102)   Huntington Disease-Like 1 [MESH:C566398] (98)  Dementia [MESH:D003704] (471)   Huntington Disease [MESH:D006816] (102)   Huntington Disease-Like 1 [MESH:C566398] (98)  Mental Disorders Diagnosed in Childhood [MESH:D019952] (1245)   Child Development Disorders, Pervasive [MESH:D002659] (157)   Autistic Disorder [MESH:D001321] (154)   Macrocephaly Autism Syndrome [MESH:C565342] (151)  Intellectual Disability [MESH:D008607] (1109)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Coffin-Siris syndrome [MESH:C536436] (102)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Mental Retardation, Autosomal Dominant 3 [MESH:C567241] (14)  Mood Disorders [MESH:D019964] (257)   Affective Disorders, Psychotic [MESH:D000341] (248)   Bipolar Disorder [MESH:D001714] (247)   Major Affective Disorder 1 [MESH:C565111] (237)  Major Affective Disorder 7 [MESH:C567529] (136) G. Phenomena and Processes  G. Phenomena and Processes  Genetic Phenomena [MESH:D055614] (1922)   Genetic Processes [MESH:D039361] (1336)   Mutagenesis [MESH:D016296] (1150)   Sequence Deletion [MESH:D017384] (1120)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  Genetic Structures [MESH:D040342] (1612)   Chromosomes [MESH:D002875] (1304)   Chromosomes, Mammalian [MESH:D033481] (1282)   Chromosomes, Human [MESH:D002877] (1280)   Chromosomes, Human, 4-5 [MESH:D002905] (149)   Chromosomes, Human, Pair 5 [MESH:D002895] (136)   5q- syndrome [MESH:C535323] (131)  Genetic Variation [MESH:D014644] (1337)   Mutation [MESH:D009154] (1327)   Allelic Imbalance [MESH:D022981] (1120)   Loss of Heterozygosity [MESH:D019656] (1119)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  Chromosome Aberrations [MESH:D002869] (1297)   Aneuploidy [MESH:D000782] (1220)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  Mosaicism [MESH:D009030] (116)   Mosaic variegated aneuploidy syndrome [MESH:C536987] (95)  Sequence Deletion [MESH:D017384] (1120)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  Ploidies [MESH:D011003] (1227)   Aneuploidy [MESH:D000782] (1220)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)