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 testosterone enanthate
C004648
 
  
  
  

MeSH Unique Identifier: C004648
Chemical – Gene Interaction

Note 1: Testosterone enanthate affects the expression of ABCA7 mRNA

Note 2: Testosterone enanthate affects the expression of ABHD2 mRNA

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C01. Bacterial Infections and Mycoses: Mycoses [MESH:D009181]
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C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities: Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] > Congenital Abnormalities [MESH:D000013] > Nervous System Malformations [MESH:D009421] > Agenesis of Corpus Callosum [MESH:D061085]
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1. Human Genes 
1. Human Genes
 A-kinase anchor proteins [HGNC:AKAP] (99) 
 A kinase (PRKA) anchor protein 13 [HGNC:AKAP13] (18)
 ezrin [HGNC:EZR] (32)
 Aldo-keto reductases [HGNC:AKR] (282) 
 aldo-keto reductase family 1, member C1 [HGNC:AKR1C1] (148)
 aldo-keto reductase family 1, member C2 [HGNC:AKR1C2] (134)
 aldo-keto reductase family 1, member C3 [HGNC:AKR1C3] (128)
 Armadillo repeat containing [HGNC:ARMC] (176) 
 karyopherin (importin) beta 1 [HGNC:KPNB1] (20)
 ATPases [HGNC:ATP] (106) 
 ATPases, AAA [HGNC:AATP] (69) 
 origin recognition complex, subunit 4 [HGNC:ORC4] (8)
 valosin containing protein [HGNC:VCP] (19)
 ATPases, P-type [HGNC:PATP] (43) 
 ATPase, aminophospholipid transporter, class I, type 8B, member 1 [HGNC:ATP8B1] (25)
 ATP-binding cassette transporters [HGNC:ABC] (821) 
 ATP-binding cassette transporters, subfamily A [HGNC:ABCA] (29) 
 ATP-binding cassette, sub-family A (ABC1), member 07 [HGNC:ABCA7] (7)
 Basic helix-loop-helix [HGNC:BHLH] (618) 
 nuclear receptor coactivator 3 [HGNC:NCOA3] (42)
 transcription factor 04 [HGNC:TCF4] (38)
 Beta 3-glycosyltransferases [HGNC:B3GT] (48) 
 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 4 [HGNC:B4GALT4] (7)
 Carboxylesterases [HGNC:CES] (125) 
 carboxylesterase 2 [HGNC:CES2] (55)
 Cathepsins [HGNC:CTS] (135) 
 cathepsin S [HGNC:CTSS] (14)
 CD molecules [HGNC:CD] (1459) 
 chemokine (C-C motif) receptor 01 [HGNC:CCR1] (21)
 endoglin [HGNC:ENG] (11)
 Fc fragment of IgG, low affinity IIa, receptor (CD032) [HGNC:FCGR2A] (4)
 integrin, alpha V [HGNC:ITGAV] (33)
 interleukin 06 receptor [HGNC:IL6R] (55)
 interleukin 06 signal transducer (gp130, oncostatin M receptor) [HGNC:IL6ST] (38)
 interleukin 10 receptor, beta [HGNC:IL10RB] (17)
 toll-like receptor 3 [HGNC:TLR3] (27)
 tumor necrosis factor (ligand) superfamily, member 10 [HGNC:TNFSF10] (155)
 Chemokine receptors [HGNC:CR] (207) 
 Chemokine (C-C motif) receptors [HGNC:CCR] (92) 
 chemokine (C-C motif) receptor 01 [HGNC:CCR1] (21)
 Chloride channels [HGNC:CLCNS] (69) 
 Chloride channels, voltage-sensitive [HGNC:CLCN] (39) 
 chloride channel, voltage-sensitive 3 [HGNC:CLCN3] (19)
 Chloride intracellular channels [HGNC:CLIC] (39) 
 chloride intracellular channel 4 [HGNC:CLIC4] (19)
 Collagens [HGNC:COL] (230) 
 collagen, type I, alpha 1 [HGNC:COL1A1] (123)
 collagen, type I, alpha 2 [HGNC:COL1A2] (43)
 collagen, type III, alpha 1 [HGNC:COL3A1] (33)
 collagen, type IV, alpha 2 [HGNC:COL4A2] (26)
 collagen, type V, alpha 1 [HGNC:COL5A1] (17)
 collagen, type V, alpha 2 [HGNC:COL5A2] (22)
 collagen, type VI, alpha 1 [HGNC:COL6A1] (28)
 collagen, type VI, alpha 2 [HGNC:COL6A2] (21)
 Complement system [HGNC:complement-systems] (153) 
 complement factor H [HGNC:CFH] (9)
 Cyclin-dependent kinases [HGNC:CDK] (338) 
 cyclin-dependent kinase 01 [HGNC:CDK1] (151)
 Cytochrome b [HGNC:CYB] (73) 
 cytochrome b-245, alpha polypeptide [HGNC:CYBA] (40)
 Cytochrome P450s [HGNC:CYP] (1673) 
 cytochrome P450, family 11, subfamily A, polypeptide 01 [HGNC:CYP11A1] (65)
 cytochrome P450, family 17, subfamily A, polypeptide 01 [HGNC:CYP17A1] (88)
 EF-hand domain containing [HGNC:EFHAND] (226) 
 parvalbumin [HGNC:PVALB] (3)
 Endogenous Ligands [HGNC:ENDOLIG] (1191) 
 chorionic gonadotropin, beta polypeptide [HGNC:CGB] (67)
 coagulation factor II (thrombin) [HGNC:F2] (95)
 follicle stimulating hormone, beta polypeptide [HGNC:FSHB] (68)
 insulin-like 3 (Leydig cell) [HGNC:INSL3] (12)
 Endothelin receptors [HGNC:EDNR] (57) 
 endothelin receptor type A [HGNC:EDNRA] (31)
 endothelin receptor type B [HGNC:EDNRB] (35)
 Ephrins [HGNC:EFN] (55) 
 ephrin-B2 [HGNC:EFNB2] (32)
 Fanconi anemia, complementation groups [HGNC:FANC] (81) 
 Fanconi anemia, complementation group C [HGNC:FANCC] (22)
 Fatty acid desaturases [HGNC:FADS] (108) 
 stearoyl-CoA desaturase (delta-9-desaturase) [HGNC:SCD] (78)
 Fibronectin type III domain containing [HGNC:FN3] (399) 
 interleukin 06 signal transducer (gp130, oncostatin M receptor) [HGNC:IL6ST] (38)
 protein tyrosine phosphatase, receptor type, D [HGNC:PTPRD] (6)
 Fibulins [HGNC:FBLN] (53) 
 EGF containing fibulin-like extracellular matrix protein 2 [HGNC:EFEMP2] (10)
 F-boxes [HGNC:FBX] (66) 
 "F-boxes ""other"" [HGNC:FBXO]" (6) 
 F-box protein 40 [HGNC:FBXO40] (2)
 Glutathione S-transferases [HGNC:GST] (460) 
 Glutathione S-transferases, soluble [HGNC:SGST] (447) 
 glutathione S-transferase alpha 2 [HGNC:GSTA2] (44)
 glutathione S-transferase mu 1 [HGNC:GSTM1] (144)
 Glycosyltransferase family 2 domain containing [HGNC:GLT2] (57) 
 UDP-glucose ceramide glucosyltransferase [HGNC:UGCG] (46)
 G patch domain containing [HGNC:GPATCH] (46) 
 angiogenic factor with G patch and FHA domains 1 [HGNC:AGGF1] (5)
 Heat shock proteins [HGNC:HSP] (390) 
 Heat shock proteins, HSP70 [HGNC:HSP70] (294) 
 heat shock 70kDa protein 01B [HGNC:HSPA1B] (65)
 heat shock 70kDa protein 04 [HGNC:HSPA4] (49)
 Heat shock proteins, DNAJ (HSP40) [HGNC:DNAJ] (88) 
 DnaJ (Hsp40) homolog, subfamily C, member 07 [HGNC:DNAJC7] (8)
 Heat shock proteins, HSPC (HSP90) [HGNC:HSP90] (119) 
 heat shock protein 90kDa beta (Grp94), member 1 [HGNC:HSP90B1] (53)
 Histocompatibility complex [HGNC:HLA] (108) 
 major histocompatibility complex, class II, DP alpha 1 [HGNC:HLA-DPA1] (13)
 major histocompatibility complex, class II, DQ alpha 1 [HGNC:HLA-DQA1] (8)
 major histocompatibility complex, class II, DQ beta 1 [HGNC:HLA-DQB1] (16)
 Homeoboxes [HGNC:homeobox] (219) 
 Homeoboxes, PROS class [HGNC:PROX] (17) 
 prospero homeobox 1 [HGNC:PROX1] (17)
 Homeoboxes, ZF class [HGNC:ZF] (38) 
 zinc finger E-box binding homeobox 1 [HGNC:ZEB1] (33)
 Immunoglobulin superfamily domain containing [HGNC:IGSF] (761) 
 C1-set domain containing [HGNC:C1SET] (121) 
 major histocompatibility complex, class II, DP alpha 1 [HGNC:HLA-DPA1] (13)
 major histocompatibility complex, class II, DQ alpha 1 [HGNC:HLA-DQA1] (8)
 major histocompatibility complex, class II, DQ beta 1 [HGNC:HLA-DQB1] (16)
 I-set domain containing [HGNC:ISET] (447) 
 palladin, cytoskeletal associated protein [HGNC:PALLD] (22)
 peroxidasin homolog (Drosophila) [HGNC:PXDN] (12)
 protein tyrosine phosphatase, receptor type, D [HGNC:PTPRD] (6)
 Immunoglobulin-like domain containing [HGNC:IGD] (645) 
 Fc fragment of IgG, low affinity IIa, receptor (CD032) [HGNC:FCGR2A] (4)
 interleukin 06 receptor [HGNC:IL6R] (55)
 Importins [HGNC:IPO] (35) 
 karyopherin (importin) beta 1 [HGNC:KPNB1] (20)
 Integrins [HGNC:ITG] (284) 
 integrin, alpha V [HGNC:ITGAV] (33)
 Interleukins and interleukin receptors [HGNC:IL] (1294) 
 interleukin 06 receptor [HGNC:IL6R] (55)
 interleukin 06 signal transducer (gp130, oncostatin M receptor) [HGNC:IL6ST] (38)
 interleukin 10 receptor, beta [HGNC:IL10RB] (17)
 Intermediate filaments [HGNC:IF] (273) 
 Type IV [HGNC:] (57) 
 nestin [HGNC:NES] (21)
 K-acetyltransferases [HGNC:KAT] (176) 
 nuclear receptor coactivator 3 [HGNC:NCOA3] (42)
 K-demethylases [HGNC:KDM] (47) 
 lysine (K)-specific demethylase 6A [HGNC:KDM6A] (10)
 K-methyltransferases [HGNC:KMT] (101) 
 lysine (K)-specific methyltransferase 2A [HGNC:KMT2A] (22)
 Latent transforming growth factor, beta binding proteins [HGNC:LTBP] (24) 
 latent transforming growth factor beta binding protein 3 [HGNC:LTBP3] (3)
 Lysophospholipid (LPA) receptors [HGNC:LPAR] (29) 
 lysophosphatidic acid receptor 6 [HGNC:LPAR6] (9)
 Mitochondrial ribosomal proteins [HGNC:MRP] (52) 
 Mitochondrial ribosomal proteins, large subunits [HGNC:MRPL] (52) 
 mitochondrial ribosomal protein S06 [HGNC:MRPS6] (22)
 Myosins [HGNC:myosin] (111) 
 Myosins, class II [HGNC:MYHII] (61) 
 myosin, heavy chain 03, skeletal muscle, embryonic [HGNC:MYH3] (6)
 myosin, heavy chain 11, smooth muscle [HGNC:MYH11] (7)
 Nuclear hormone receptors [HGNC:NR] (1322) 
 RAR-related orphan receptor A [HGNC:RORA] (22)
 retinoid X receptor, beta [HGNC:RXRB] (31)
 Parkinson disease [HGNC:PARK] (136) 
 synuclein, alpha (non A4 component of amyloid precursor) [HGNC:SNCA] (71)
 PHD-type zinc fingers [HGNC:PHF] (103) 
 chromodomain helicase DNA binding protein 4 [HGNC:CHD4] (7)
 lysine (K)-specific methyltransferase 2A [HGNC:KMT2A] (22)
 Pleckstrin homology (PH) domain containing [HGNC:PLEKH] (227) 
 A kinase (PRKA) anchor protein 13 [HGNC:AKAP13] (18)
 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 [HGNC:PLEKHA1] (9)
 son of sevenless homolog 1 (Drosophila) [HGNC:SOS1] (27)
 Proteasome (prosome, macropain) subunits [HGNC:PSM] (98) 
 proteasome (prosome, macropain) activator subunit 4 [HGNC:PSME4] (19)
 Protein phosphatase, catalytic and regulatory subunits [HGNC:PPP-PPM-CTD] (225) 
 Protein phosphatase 1, regulatory subunits [HGNC:PPP1R] (155) 
 protein phosphatase 1, regulatory subunit 03A [HGNC:PPP1R3A] (1)
 Protein phosphatases, Mg2+/Mn2+ dependent [HGNC:PPM] (58) 
 pyruvate dehyrogenase phosphatase catalytic subunit 1 [HGNC:PDP1] (19)
 Protein phosphatases, CTD aspartate-based [HGNC:CTD] (5) 
 CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) phosphatase, subunit 1 [HGNC:CTDP1] (5)
 Protein tyrosine phosphatases, including dual specificity phosphatases [HGNC:PTP] (254) 
 Protein tyrosine phosphatases, Class I Cys-based [HGNC:PTPN] (252) 
 Class I Cys-based PTPs : Transmembrane receptor-like [HGNC:PTPR] (69) 
 protein tyrosine phosphatase, receptor type, D [HGNC:PTPRD] (6)
 Proteoglycans [HGNC:proteoglycan] (70) 
 Proteoglycans, extracellular matrix: small leucine-rich repeats [HGNC:SLRR] (37) 
 asporin [HGNC:ASPN] (3)
 lumican [HGNC:LUM] (17)
 Proteoglycans, extracellular matrix: other [HGNC:ECMPG] (24) 
 structural maintenance of chromosomes 3 [HGNC:SMC3] (17)
 RAB, member RAS oncogene [HGNC:RAB] (69) 
 RAB27A, member RAS oncogene family [HGNC:RAB27A] (8)
 Rho guanine nucleotide exchange factors [HGNC:ARHGEF] (105) 
 A kinase (PRKA) anchor protein 13 [HGNC:AKAP13] (18)
 son of sevenless homolog 1 (Drosophila) [HGNC:SOS1] (27)
 RNA binding motif containing [HGNC:RRM] (251) 
 heterogeneous nuclear ribonucleoprotein R [HGNC:HNRNPR] (8)
 polypyrimidine tract binding protein 1 [HGNC:PTBP1] (13)
 squamous cell carcinoma antigen recognized by T cells 3 [HGNC:SART3] (10)
 transformer 2 alpha homolog (Drosophila) [HGNC:TRA2A] (22)
 RING-type zinc fingers [HGNC:RNF] (151) 
 neuralized homolog (Drosophila) [HGNC:NEURL] (3)
 Secreted frizzled-related proteins [HGNC:SFRP] (46) 
 frizzled-related protein [HGNC:FRZB] (16)
 SH2 domain containing [HGNC:SH2D] (431) 
 hemopoietic cell kinase [HGNC:HCK] (20)
 signal transducer and activator of transcription 1, 91kDa [HGNC:STAT1] (108)
 Short chain dehydrogenase/reductase superfamily [HGNC:SDR] (302) 
 Short chain dehydrogenase/reductase superfamily, Classical fold cluster 2 [HGNC:SDRC2] (140) 
 hydroxysteroid (17-beta) dehydrogenase 06 [HGNC:HSD17B6] (15)
 Short chain dehydrogenase/reductase superfamily, Atypical [HGNC:SDRA] (89) 
 HIV-1 Tat interactive protein 2, 30kDa [HGNC:HTATIP2] (22)
 SMADs [HGNC:SMAD] (84) 
 SMAD family member 4 [HGNC:SMAD4] (22)
 Solute carriers [HGNC:SLC] (716) 
 solute carrier family 16 (monocarboxylate transporter), member 7 [HGNC:SLC16A7] (14)
 solute carrier family 35 (UDP-GlcA/UDP-GalNAc transporter), member D1 [HGNC:SLC35D1] (10)
 SRY (sex determining region Y)-boxes [HGNC:SOX] (95) 
 SRY (sex determining region Y)-box 04 [HGNC:SOX4] (39)
 StAR-related lipid transfer (START) domain containing [HGNC:STARD] (91) 
 steroidogenic acute regulatory protein [HGNC:STAR] (57)
 Structural maintenance of chromosomes proteins [HGNC:SMC] (44) 
 structural maintenance of chromosomes 2 [HGNC:SMC2] (25)
 structural maintenance of chromosomes 3 [HGNC:SMC3] (17)
 T-boxes [HGNC:TBX] (49) 
 T-box 01 [HGNC:TBX1] (7)
 Tetratricopeptide repeat domain containing [HGNC:TTC] (153) 
 DnaJ (Hsp40) homolog, subfamily C, member 07 [HGNC:DNAJC7] (8)
 FK506 binding protein 05 [HGNC:FKBP5] (46)
 G-protein signaling modulator 2 [HGNC:GPSM2] (27)
 interferon-induced protein with tetratricopeptide repeats 3 [HGNC:IFIT3] (35)
 lysine (K)-specific demethylase 6A [HGNC:KDM6A] (10)
 RAN binding protein 2 [HGNC:RANBP2] (16)
 tetratricopeptide repeat domain 09 [HGNC:TTC9] (10)
 Tumor necrosis factor (ligand) superfamily [HGNC:TNFSF] (898) 
 tumor necrosis factor (ligand) superfamily, member 10 [HGNC:TNFSF10] (155)
 Ubiquitin-specific peptidases [HGNC:USP] (24) 
 ubiquitin specific peptidase 02 [HGNC:USP2] (7)
 UBX domain containing [HGNC:UBXN] (16) 
 Fas associated factor family member 2 [HGNC:FAF2] (5)
 WD repeat domain containing [HGNC:WDR] (199) 
 guanine nucleotide binding protein (G protein), beta polypeptide 1 [HGNC:GNB1] (14)
 WD repeat domain 46 [HGNC:WDR46] (7)
 ZINC FINGERS [HGNC:ZNF] (383) 
 Zinc fingers, C2H2-type [HGNC:ZNF] (349) 
 human immunodeficiency virus type I enhancer binding protein 2 [HGNC:HIVEP2] (23)
 zinc finger E-box binding homeobox 1 [HGNC:ZEB1] (33)
 Other zinc fingers [HGNC:] (148) 
 Zinc fingers, FYVE-type [HGNC:ZFYVE ] (31) 
 RUN and FYVE domain containing 3 [HGNC:RUFY3] (11)
2. Interaction: Human Genes and Chemicals 
2. Interaction: Human Genes and Chemicals
 Affects (3990) 
 cotreatment (1499)
 expression (494)
 Decreases (5154) 
 expression (2187)
 reaction (3393)
 response to substance (713)
 Increases (5571) 
 abundance (630)
 activity (2865)
 expression (3238)
 hydrolysis (158)
 metabolic processing (740)
 phosphorylation (1060)
A. Anatomy 
A. Anatomy
 Body Regions [MESH:D001829] (867) 
 Head [MESH:D006257] (523) 
 Ear [MESH:D004423] (236) 
 Meier-Gorlin syndrome [MESH:C538012] (133)
 Musculoskeletal System [MESH:D009141] (1255) 
 Skeleton [MESH:D012863] (1177) 
 Bone and Bones [MESH:D001842] (1112) 
 Bones of Lower Extremity [MESH:D050281] (278) 
 Leg Bones [MESH:D007867] (228) 
 Patella [MESH:D010329] (168) 
 Meier-Gorlin syndrome [MESH:C538012] (133)
 Urogenital System [MESH:D014566] (986) 
 Genitalia [MESH:D005835] (400) 
 Genitalia, Male [MESH:D005837] (297) 
 Testis [MESH:D013737] (92) 
 Leydig Cell Hypoplasia [MESH:C562567] (65)
 Gonads [MESH:D006066] (91) 
 Testis [MESH:D013737] (86) 
 Leydig Cell Hypoplasia [MESH:C562567] (65)
 Endocrine System [MESH:D004703] (206) 
 Endocrine Glands [MESH:D004702] (193) 
 Gonads [MESH:D006066] (99) 
 Testis [MESH:D013737] (87) 
 Leydig Cell Hypoplasia [MESH:C562567] (65)
 Cardiovascular System [MESH:D002319] (1086) 
 Heart [MESH:D006321] (904) 
 Heart Valves [MESH:D006351] (666) 
 Aortic Valve [MESH:D001021] (659) 
 Aortic Valve, Calcification of [MESH:C562942] (655)
 Nervous System [MESH:D009420] (587) 
 Central Nervous System [MESH:D002490] (371) 
 Brain [MESH:D001921] (349) 
 Prosencephalon [MESH:D016548] (154) 
 Telencephalon [MESH:D013687] (75) 
 Cerebrum [MESH:D054022] (63) 
 Basal Ganglia [MESH:D001479] (35) 
 Corpus Striatum [MESH:D003342] (28) 
 Striatal Degeneration, Autosomal Dominant [MESH:C563783] (21)
 Sense Organs [MESH:D012679] (1060) 
 Ear [MESH:D004423] (323) 
 Meier-Gorlin syndrome [MESH:C538012] (133)
 Eye [MESH:D005123] (858) 
 Uvea [MESH:D014602] (270) 
 Choroid [MESH:D002829] (54) 
 Bruch Membrane [MESH:D016570] (53) 
 Basal Laminar Drusen [MESH:C563034] (52)
 Tissues [MESH:D014024] (397) 
 Epithelium [MESH:D004848] (92) 
 Basement Membrane [MESH:D001485] (54) 
 Bruch Membrane [MESH:D016570] (53) 
 Basal Laminar Drusen [MESH:C563034] (52)
 Membranes [MESH:D008566] (87) 
 Basement Membrane [MESH:D001485] (57) 
 Bruch Membrane [MESH:D016570] (53) 
 Basal Laminar Drusen [MESH:C563034] (52)
C01. Bacterial Infections and Mycoses 
C01. Bacterial Infections and Mycoses
 Bacterial Infections [MESH:D001424] (3716) 
 Gram-Negative Bacterial Infections [MESH:D016905] (3085) 
 Mycoplasmatales Infections [MESH:D009180] (1949) 
 Mycoplasma Infections [MESH:D009175] (1947)
 Neisseriaceae Infections [MESH:D016870] (273) 
 Meningococcal Infections [MESH:D008589] (242)
 Gram-Positive Bacterial Infections [MESH:D016908] (2434) 
 Actinomycetales Infections [MESH:D000193] (1466) 
 Mycobacterium Infections [MESH:D009164] (1446) 
 Mycobacterium Infections, Nontuberculous [MESH:D009165] (480)
 Paratuberculosis [MESH:D010283] (427)
 Infection [MESH:D007239] (4109) 
 Urinary Tract Infections [MESH:D014552] (984)
 Intraabdominal Infections [MESH:D059413] (958) 
 Peritonitis [MESH:D010538] (800)
 Sepsis [MESH:D018805] (3556) 
 Shock, Septic [MESH:D012772] (1830)
 Bacteremia [MESH:D016470] (1369) 
 Endotoxemia [MESH:D019446] (1289)
 Skin Diseases, Infectious [MESH:D012874] (415) 
 Dermatomycoses [MESH:D003881] (267) 
 Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224)
 Toxemia [MESH:D014115] (1290) 
 Endotoxemia [MESH:D019446] (1289)
 Mycoses [MESH:D009181] (385) 
 Candidiasis [MESH:D002177] (307) 
 Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224)
 Dermatomycoses [MESH:D003881] (267) 
 Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224)
C02. Virus Diseases 
C02. Virus Diseases
 Virus Diseases [MESH:D014777] (4544) 
 Central Nervous System Viral Diseases [MESH:D020805] (1416) 
 Encephalitis [MESH:D004660] (226) 
 Encephalitis, Viral [MESH:D018792] (183) 
 Encephalitis, Herpes Simplex [MESH:D020803] (72)
 DNA Virus Infections [MESH:D004266] (2474) 
 Hepadnaviridae Infections [MESH:D018347] (977) 
 Hepatitis B [MESH:D006509] (976) 
 Hepatitis B, Chronic [MESH:D019694] (277)
 Herpesviridae Infections [MESH:D006566] (1944) 
 Cytomegalovirus Infections [MESH:D003586] (222)
 Encephalitis, Herpes Simplex [MESH:D020803] (72)
 Encephalitis, Viral [MESH:D018792] (183) 
 Encephalitis, Herpes Simplex [MESH:D020803] (72)
 Hepatitis, Viral, Human [MESH:D006525] (1766) 
 Hepatitis C [MESH:D006526] (1627)
 Hepatitis B [MESH:D006509] (976) 
 Hepatitis B, Chronic [MESH:D019694] (277)
 RNA Virus Infections [MESH:D012327] (4215) 
 Flaviviridae Infections [MESH:D018178] (1656) 
 Hepatitis C [MESH:D006526] (1627)
 Orthomyxoviridae Infections [MESH:D009976] (1077) 
 Influenza, Human [MESH:D007251] (1075)
 Influenza in Birds [MESH:D005585] (53)
 Retroviridae Infections [MESH:D012192] (3420) 
 Lentivirus Infections [MESH:D016180] (3408) 
 HIV Infections [MESH:D015658] (3402) 
 HIV Wasting Syndrome [MESH:D019247] (1956)
 Sexually Transmitted Diseases [MESH:D012749] (3305) 
 Sexually Transmitted Diseases, Viral [MESH:D015229] (3304) 
 HIV Infections [MESH:D015658] (3296) 
 HIV Wasting Syndrome [MESH:D019247] (1956)
C03. Parasitic Diseases 
C03. Parasitic Diseases
 Parasitic Diseases [MESH:D010272] (3828) 
 Liver Diseases, Parasitic [MESH:D008109] (1009)
 Helminthiasis [MESH:D006373] (1644) 
 Trematode Infections [MESH:D014201] (1182) 
 Schistosomiasis [MESH:D012552] (1073) 
 Schistosomiasis mansoni [MESH:D012555] (1033)
 Protozoan Infections [MESH:D011528] (3014) 
 Malaria [MESH:D008288] (2175)
 Euglenozoa Infections [MESH:D056986] (2552) 
 Leishmaniasis [MESH:D007896] (2541) 
 Leishmaniasis, Visceral [MESH:D007898] (2149)
C04. Neoplasms 
C04. Neoplasms
 Neoplasms [MESH:D009369] (10293) 
 Neoplasms, Second Primary [MESH:D016609] (518)
 Precancerous Conditions [MESH:D011230] (2858)
 Cysts [MESH:D003560] (2625) 
 Follicular Cyst [MESH:D005497] (151)
 Arachnoid Cysts [MESH:D016080] (50) 
 Chudley-Mccullough syndrome [MESH:C535459] (45)
 Ovarian Cysts [MESH:D010048] (2534) 
 Polycystic Ovary Syndrome [MESH:D011085] (2186)
 Neoplasms by Histologic Type [MESH:D009370] (8793) 
 Leukemia [MESH:D007938] (4576) 
 Leukemia, Lymphoid [MESH:D007945] (3047) 
 Leukemia, B-Cell [MESH:D015448] (2564) 
 Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)
 Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754) 
 Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)
 Leukemia, Myeloid [MESH:D007951] (2773) 
 Leukemia, Myelomonocytic, Acute [MESH:D015479] (85)
 Leukemia, Myeloid, Acute [MESH:D015470] (2176) 
 Leukemia, Monocytic, Acute [MESH:D007948] (98)
 Leukemia, Promyelocytic, Acute [MESH:D015473] (1367)
 Lymphoma [MESH:D008223] (3686) 
 Lymphoma, Non-Hodgkin [MESH:D008228] (3337) 
 Lymphoma, Mantle-Cell [MESH:D020522] (561)
 Lymphoma, B-Cell [MESH:D016393] (2624) 
 Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)
 Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742) 
 Neoplasms, Connective Tissue [MESH:D009372] (3626) 
 Neoplasms, Bone Tissue [MESH:D018213] (2217) 
 Osteosarcoma [MESH:D012516] (2175)
 Neoplasms, Muscle Tissue [MESH:D009379] (1965) 
 Leiomyoma [MESH:D007889] (744)
 Myosarcoma [MESH:D009217] (790) 
 Rhabdomyosarcoma [MESH:D012208] (789)
 Sarcoma [MESH:D012509] (4246) 
 Hemangiosarcoma [MESH:D006394] (1836)
 Osteosarcoma [MESH:D012516] (2175)
 Myosarcoma [MESH:D009217] (790) 
 Rhabdomyosarcoma [MESH:D012208] (789)
 Neoplasms, Germ Cell and Embryonal [MESH:D009373] (5126) 
 Neuroectodermal Tumors [MESH:D017599] (5066) 
 Neoplasms, Neuroepithelial [MESH:D018302] (4487) 
 Glioma [MESH:D005910] (4261) 
 Astrocytoma [MESH:D001254] (2692) 
 Glioblastoma [MESH:D005909] (2554)
 Neuroectodermal Tumors, Primitive [MESH:D018242] (2005) 
 Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433) 
 Neuroblastoma [MESH:D009447] (1420)
 Neuroendocrine Tumors [MESH:D018358] (3633) 
 Melanoma [MESH:D008545] (3508) 
 Uveal melanoma [MESH:C536494] (109)
 Paraganglioma [MESH:D010235] (297) 
 Pheochromocytoma [MESH:D010673] (275)
 Neoplasms, Glandular and Epithelial [MESH:D009375] (7760) 
 Adenoma [MESH:D000236] (4051) 
 Adenoma, Liver Cell [MESH:D018248] (685)
 Adenoma, Oxyphilic [MESH:D018249] (115)
 Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)
 Mesothelioma [MESH:D008654] (2567)
 Prolactinoma [MESH:D015175] (312)
 Adenomatous Polyps [MESH:D018256] (1571) 
 Adenomatous Polyposis Coli [MESH:D011125] (1565)
 Carcinoma [MESH:D002277] (7263) 
 Carcinoma, Transitional Cell [MESH:D002295] (2662)
 Adenocarcinoma [MESH:D000230] (6565) 
 Adenocarcinoma of lung [MESH:C538231] (1487)
 Adenocarcinoma Of Esophagus [MESH:C562730] (1530)
 Carcinoma, Adenoid Cystic [MESH:D003528] (1561)
 Carcinoma, Hepatocellular [MESH:D006528] (5375)
 Carcinoma, Intraductal, Noninfiltrating [MESH:D002285] (500)
 Carcinoma, Renal Cell [MESH:D002292] (2975)
 Cholangiocarcinoma [MESH:D018281] (2398)
 Carcinoma, Ductal [MESH:D044584] (1786) 
 Carcinoma, Ductal, Breast [MESH:D018270] (1112)
 Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)
 Carcinoma in Situ [MESH:D002278] (2111) 
 Prostatic Intraepithelial Neoplasia [MESH:D019048] (1565)
 Carcinoma, Squamous Cell [MESH:D002294] (4294) 
 Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)
 Neoplasms, Ductal, Lobular, and Medullary [MESH:D018299] (1831) 
 Carcinoma, Intraductal, Noninfiltrating [MESH:D002285] (500)
 Carcinoma, Ductal [MESH:D044584] (1786) 
 Carcinoma, Ductal, Breast [MESH:D018270] (1112)
 Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)
 Neoplasms, Mesothelial [MESH:D018301] (2569) 
 Mesothelioma [MESH:D008654] (2567)
 Neoplasms, Neuroepithelial [MESH:D018302] (4487) 
 Glioma [MESH:D005910] (4261) 
 Astrocytoma [MESH:D001254] (2692) 
 Glioblastoma [MESH:D005909] (2554)
 Neuroectodermal Tumors, Primitive [MESH:D018242] (2005) 
 Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433) 
 Neuroblastoma [MESH:D009447] (1420)
 Neoplasms, Squamous Cell [MESH:D018307] (4457) 
 Carcinoma, Squamous Cell [MESH:D002294] (4294) 
 Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)
 Neoplasms, Gonadal Tissue [MESH:D018309] (284) 
 Sex Cord-Gonadal Stromal Tumors [MESH:D018312] (282) 
 Sertoli-Leydig Cell Tumor [MESH:D018310] (272) 
 Leydig Cell Tumor [MESH:D007984] (267)
 Neoplasms, Nerve Tissue [MESH:D009380] (5201) 
 Meningioma [MESH:D008579] (978)
 Neuroectodermal Tumors [MESH:D017599] (5059) 
 Neoplasms, Neuroepithelial [MESH:D018302] (4487) 
 Glioma [MESH:D005910] (4261) 
 Astrocytoma [MESH:D001254] (2692) 
 Glioblastoma [MESH:D005909] (2554)
 Neuroectodermal Tumors, Primitive [MESH:D018242] (2005) 
 Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433) 
 Neuroblastoma [MESH:D009447] (1420)
 Neuroendocrine Tumors [MESH:D018358] (3625) 
 Melanoma [MESH:D008545] (3508) 
 Uveal melanoma [MESH:C536494] (109)
 Paraganglioma [MESH:D010235] (297) 
 Pheochromocytoma [MESH:D010673] (275)
 Neoplasms, Vascular Tissue [MESH:D009383] (2959) 
 Hemangiosarcoma [MESH:D006394] (1836)
 Meningioma [MESH:D008579] (978)
 Hemangioma [MESH:D006391] (690) 
 Hemangioma, Capillary [MESH:D018324] (503) 
 Hemangioblastoma [MESH:D018325] (395)
 Nevi and Melanomas [MESH:D018326] (3572) 
 Melanoma [MESH:D008545] (3508) 
 Uveal melanoma [MESH:C536494] (109)
 Nevus [MESH:D009506] (340) 
 Nevus, Sebaceous of Jadassohn [MESH:D054000] (209)
 Neoplasms by Site [MESH:D009371] (9169) 
 Bone Neoplasms [MESH:D001859] (1334)
 Skin Neoplasms [MESH:D012878] (2992)
 Breast Neoplasms [MESH:D001943] (6077) 
 Breast Neoplasms, Male [MESH:D018567] (650)
 Carcinoma, Ductal, Breast [MESH:D018270] (1112)
 Digestive System Neoplasms [MESH:D004067] (7487) 
 Gastrointestinal Neoplasms [MESH:D005770] (6452) 
 Stomach Neoplasms [MESH:D013274] (4942)
 Esophageal Neoplasms [MESH:D004938] (3737) 
 Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)
 Adenocarcinoma Of Esophagus [MESH:C562730] (1530)
 Intestinal Neoplasms [MESH:D007414] (5358) 
 Cecal Neoplasms [MESH:D002430] (822)
 Colorectal Neoplasms [MESH:D015179] (5294) 
 Adenomatous Polyposis Coli [MESH:D011125] (1565)
 Colonic Neoplasms [MESH:D003110] (4405) 
 Adenomatous Polyposis Coli [MESH:D011125] (1565)
 Liver Neoplasms [MESH:D008113] (6048) 
 Adenoma, Liver Cell [MESH:D018248] (685)
 Carcinoma, Hepatocellular [MESH:D006528] (5375)
 Liver Neoplasms, Experimental [MESH:D008114] (2837)
 Pancreatic Neoplasms [MESH:D010190] (3820) 
 Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)
 Endocrine Gland Neoplasms [MESH:D004701] (4925) 
 Ovarian Neoplasms [MESH:D010051] (3275)
 Thyroid Neoplasms [MESH:D013964] (2040)
 Pancreatic Neoplasms [MESH:D010190] (3820) 
 Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)
 Pituitary Neoplasms [MESH:D010911] (981) 
 Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)
 Prolactinoma [MESH:D015175] (312)
 Testicular Neoplasms [MESH:D013736] (520) 
 Sertoli-Leydig Cell Tumor [MESH:D018310] (272) 
 Leydig Cell Tumor [MESH:D007984] (267)
 Eye Neoplasms [MESH:D005134] (400) 
 Uveal Neoplasms [MESH:D014604] (115) 
 Uveal melanoma [MESH:C536494] (109)
 Head and Neck Neoplasms [MESH:D006258] (4612) 
 Thyroid Neoplasms [MESH:D013964] (2040)
 Esophageal Neoplasms [MESH:D004938] (3737) 
 Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)
 Adenocarcinoma Of Esophagus [MESH:C562730] (1530)
 Mouth Neoplasms [MESH:D009062] (2263) 
 Salivary Gland Neoplasms [MESH:D012468] (968)
 Otorhinolaryngologic Neoplasms [MESH:D010039] (1557) 
 Pharyngeal Neoplasms [MESH:D010610] (1520) 
 Nasopharyngeal Neoplasms [MESH:D009303] (1500)
 Mammary Neoplasms, Animal [MESH:D015674] (3404) 
 Mammary Neoplasms, Experimental [MESH:D008325] (3268)
 Nervous System Neoplasms [MESH:D009423] (3130) 
 Central Nervous System Neoplasms [MESH:D016543] (3055) 
 Brain Neoplasms [MESH:D001932] (2764) 
 Supratentorial Neoplasms [MESH:D015173] (930) 
 Hypothalamic Neoplasms [MESH:D007029] (922) 
 Pituitary Neoplasms [MESH:D010911] (914)
 Central Nervous System Cysts [MESH:D020863] (57) 
 Arachnoid Cysts [MESH:D016080] (50) 
 Chudley-Mccullough syndrome [MESH:C535459] (45)
 Meningeal Neoplasms [MESH:D008577] (984) 
 Meningioma [MESH:D008579] (978)
 Thoracic Neoplasms [MESH:D013899] (6032) 
 Respiratory Tract Neoplasms [MESH:D012142] (6020) 
 Lung Neoplasms [MESH:D008175] (6015) 
 Adenocarcinoma of lung [MESH:C538231] (1487)
 Bronchial Neoplasms [MESH:D001984] (3608) 
 Carcinoma, Bronchogenic [MESH:D002283] (3606) 
 Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)
 Small Cell Lung Carcinoma [MESH:D055752] (1380)
 Urogenital Neoplasms [MESH:D014565] (7002) 
 Genital Neoplasms, Female [MESH:D005833] (2540) 
 Uterine Neoplasms [MESH:D014594] (2431) 
 Endometrial Neoplasms [MESH:D016889] (1987)
 Genital Neoplasms, Male [MESH:D005834] (6224) 
 Penile Neoplasms [MESH:D010412] (890)
 Prostatic Neoplasms [MESH:D011471] (6135)
 Testicular Neoplasms [MESH:D013736] (520) 
 Sertoli-Leydig Cell Tumor [MESH:D018310] (272) 
 Leydig Cell Tumor [MESH:D007984] (267)
 Urologic Neoplasms [MESH:D014571] (5315) 
 Urinary Bladder Neoplasms [MESH:D001749] (4079)
 Kidney Neoplasms [MESH:D007680] (3966) 
 Carcinoma, Renal Cell [MESH:D002292] (2975)
 Neoplasms, Experimental [MESH:D009374] (5218) 
 Liver Neoplasms, Experimental [MESH:D008114] (2837)
 Mammary Neoplasms, Experimental [MESH:D008325] (3268)
 Neoplastic Processes [MESH:D009385] (5317) 
 Anaplasia [MESH:D000708] (348)
 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) 
 Juvenile polyposis syndrome [MESH:C537702] (196)
 Adenomatous Polyposis Coli [MESH:D011125] (1565)
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)
 Bone Diseases, Developmental [MESH:D001848] (3315) 
 Dysostoses [MESH:D004413] (1019) 
 Craniofacial Dysostosis [MESH:D003394] (391) 
 Freeman-Sheldon syndrome [MESH:C535483] (23)
 Mandibulofacial Dysostosis [MESH:D008342] (63)
 Osteochondrodysplasias [MESH:D010009] (2440) 
 Schneckenbecken dysplasia [MESH:C536637] (22)
 Spondyloepimetaphyseal Dysplasia, Pakistani Type [MESH:C567551] (63)
 Hyperostosis, Cortical, Congenital [MESH:D006958] (392)
 Osteosclerosis [MESH:D010026] (356)
 Osteogenesis Imperfecta [MESH:D010013] (481) 
 Osteogenesis imperfecta, type 2A [MESH:C536042] (375)
 Osteogenesis imperfecta, type 3 [MESH:C536044] (375)
 Osteogenesis imperfecta, type 4 [MESH:C536045] (375)
 Bruck syndrome 2 [MESH:C537407] (64)
 Osteogenesis Imperfecta, Type IX [MESH:C564921] (46)
 Bone Diseases, Endocrine [MESH:D001849] (747) 
 Acromegaly [MESH:D000172] (466)
 Bone Diseases, Metabolic [MESH:D001851] (3492) 
 Osteoporosis [MESH:D010024] (3037)
 Rickets [MESH:D012279] (341) 
 Rickets, Hypophosphatemic [MESH:D063730] (276) 
 Familial Hypophosphatemic Rickets [MESH:D053098] (274) 
 Hypophosphatemic Rickets, Autosomal Recessive, 2 [MESH:C567647] (48)
 Hyperostosis [MESH:D015576] (493) 
 Hyperostosis, Cortical, Congenital [MESH:D006958] (392)
 Osteitis Deformans [MESH:D010001] (287) 
 Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57)
 Spinal Diseases [MESH:D013122] (2485) 
 Intervertebral Disc Degeneration [MESH:D055959] (827) 
 Intervertebral disc disease [MESH:C535531] (514)
 Intervertebral Disc Displacement [MESH:D007405] (520) 
 Intervertebral disc disease [MESH:C535531] (514)
 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)
 Spondylitis [MESH:D013166] (1924) 
 Spondylarthritis [MESH:D025241] (1912) 
 Spondylarthropathies [MESH:D025242] (1909) 
 Arthritis, Psoriatic [MESH:D015535] (1859)
 Hand Deformities [MESH:D006226] (590) 
 Hand Deformities, Congenital [MESH:D006228] (587) 
 Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)
 Jaw Diseases [MESH:D007571] (1601) 
 Jaw Abnormalities [MESH:D007569] (1435) 
 Cleft Palate [MESH:D002972] (1330)
 Micrognathism [MESH:D008844] (230) 
 Meier-Gorlin syndrome [MESH:C538012] (133)
 Joint Diseases [MESH:D007592] (4657) 
 Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)
 Arthritis [MESH:D001168] (4416) 
 Arthritis, Experimental [MESH:D001169] (3142)
 Arthritis, Psoriatic [MESH:D015535] (1859)
 Arthritis, Rheumatoid [MESH:D001172] (3603)
 Osteoarthritis [MESH:D010003] (1743)
 Spondylarthritis [MESH:D025241] (1912) 
 Spondylarthropathies [MESH:D025242] (1909) 
 Arthritis, Psoriatic [MESH:D015535] (1859)
 Arthrogryposis [MESH:D001176] (329) 
 Bruck syndrome 2 [MESH:C537407] (64)
 Distal arthrogryposis type 2B [MESH:C538400] (85)
 Contracture [MESH:D003286] (296) 
 Bethlem myopathy [MESH:C535436] (108)
 Muscular Diseases [MESH:D009135] (4071) 
 Eosinophilia-Myalgia Syndrome [MESH:D016603] (31)
 Muscle Rigidity [MESH:D009127] (617)
 Arthrogryposis [MESH:D001176] (329) 
 Bruck syndrome 2 [MESH:C537407] (64)
 Distal arthrogryposis type 2B [MESH:C538400] (85)
 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)
 Muscular Dystrophy, Emery-Dreifuss [MESH:D020389] (169)
 Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)
 Muscular Dystrophies, Limb-Girdle [MESH:D049288] (259) 
 Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57)
 Muscular Dystrophy, Limb-Girdle, Type 2G [MESH:C566599] (13)
 Myopathies, Structural, Congenital [MESH:D020914] (272) 
 Myosclerosis, Autosomal Recessive [MESH:C564968] (45)
 Myositis [MESH:D009220] (2071) 
 Myositis, Inclusion Body [MESH:D018979] (103) 
 Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57)
 Musculoskeletal Abnormalities [MESH:D009139] (3796) 
 Arthrogryposis [MESH:D001176] (329) 
 Bruck syndrome 2 [MESH:C537407] (64)
 Distal arthrogryposis type 2B [MESH:C538400] (85)
 Craniofacial Abnormalities [MESH:D019465] (3098) 
 Congenital Cataracts, Facial Dysmorphism, And Neuropathy [MESH:C565822] (17)
 Costello Syndrome [MESH:D056685] (407)
 22q11 Deletion Syndrome [MESH:D058165] (237) 
 DiGeorge Syndrome [MESH:D004062] (236)
 Craniofacial Dysostosis [MESH:D003394] (391) 
 Freeman-Sheldon syndrome [MESH:C535483] (23)
 Mandibulofacial Dysostosis [MESH:D008342] (63)
 Maxillofacial Abnormalities [MESH:D019767] (1447) 
 Jaw Abnormalities [MESH:D007569] (1438) 
 Cleft Palate [MESH:D002972] (1330)
 Micrognathism [MESH:D008844] (230) 
 Meier-Gorlin syndrome [MESH:C538012] (133)
 Microcephaly [MESH:D008831] (700) 
 Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)
 Noonan Syndrome [MESH:D009634] (506) 
 Noonan syndrome 3 [MESH:C537847] (118)
 Noonan Syndrome 4 [MESH:C548082] (37)
 Limb Deformities, Congenital [MESH:D017880] (1813) 
 Brachydactyly [MESH:D059327] (220)
 Upper Extremity Deformities, Congenital [MESH:D038062] (604) 
 Hand Deformities, Congenital [MESH:D006228] (587) 
 Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)
 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) 
 Cholestasis, progressive familial intrahepatic 1 [MESH:C535933] (263)
 Liver Cirrhosis, Biliary [MESH:D008105] (1274)
 Digestive System Abnormalities [MESH:D004065] (2127) 
 Hirschsprung Disease [MESH:D006627] (361)
 Digestive System Neoplasms [MESH:D004067] (7493) 
 Gastrointestinal Neoplasms [MESH:D005770] (6460) 
 Stomach Neoplasms [MESH:D013274] (4942)
 Esophageal Neoplasms [MESH:D004938] (3737) 
 Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)
 Adenocarcinoma Of Esophagus [MESH:C562730] (1530)
 Intestinal Neoplasms [MESH:D007414] (5359) 
 Cecal Neoplasms [MESH:D002430] (822)
 Colorectal Neoplasms [MESH:D015179] (5294) 
 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) 
 Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)
 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) 
 Colitis [MESH:D003092] (3199) 
 Colitis, Ulcerative [MESH:D003093] (2601)
 Enterocolitis [MESH:D004760] (1536) 
 Enterocolitis, Necrotizing [MESH:D020345] (1367)
 Inflammatory Bowel Diseases [MESH:D015212] (3492) 
 Inflammatory Bowel Disease 25, Autosomal Recessive [MESH:C567251] (43)
 Colitis, Ulcerative [MESH:D003093] (2601)
 Crohn Disease [MESH:D003424] (2585)
 Gastrointestinal 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) 
 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) 
 Colitis [MESH:D003092] (3199) 
 Colitis, Ulcerative [MESH:D003093] (2601)
 Colorectal Neoplasms [MESH:D015179] (5282) 
 Colonic Neoplasms [MESH:D003110] (4405) 
 Adenomatous Polyposis Coli [MESH:D011125] (1565)
 Megacolon [MESH:D008531] (386) 
 Hirschsprung Disease [MESH:D006627] (361)
 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) 
 Inflammatory Bowel Disease 25, Autosomal Recessive [MESH:C567251] (43)
 Colitis, Ulcerative [MESH:D003093] (2601)
 Crohn Disease [MESH:D003424] (2585)
 Intestinal Neoplasms [MESH:D007414] (5359) 
 Cecal Neoplasms [MESH:D002430] (822)
 Colorectal Neoplasms [MESH:D015179] (5294) 
 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) 
 Celiac Disease [MESH:D002446] (340)
 Rectal Diseases [MESH:D012002] (4596) 
 Colorectal Neoplasms [MESH:D015179] (4534)
 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) 
 Cholestasis, progressive familial intrahepatic 1 [MESH:C535933] (263)
 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)
 Hepatic Veno-Occlusive Disease [MESH:D006504] (208) 
 Hepatic venoocclusive disease with immunodeficiency [MESH:C537257] (23)
 Hepatitis [MESH:D006505] (3883) 
 Hepatitis, Chronic [MESH:D006521] (2071) 
 Hepatitis B, Chronic [MESH:D019694] (277)
 Hepatitis, Viral, Human [MESH:D006525] (1766) 
 Hepatitis C [MESH:D006526] (1627)
 Hepatitis B [MESH:D006509] (976) 
 Hepatitis B, Chronic [MESH:D019694] (277)
 Liver Cirrhosis [MESH:D008103] (5542) 
 Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)
 Liver Cirrhosis, Biliary [MESH:D008105] (1274)
 Liver Cirrhosis, Experimental [MESH:D008106] (4589)
 Liver Diseases, Alcoholic [MESH:D008108] (3243) 
 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)
 Pancreatic Diseases [MESH:D010182] (4453) 
 Pancreatic Neoplasms [MESH:D010190] (3820) 
 Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)
 Peritoneal Diseases [MESH:D010532] (1119) 
 Peritonitis [MESH:D010538] (800)
C07. Stomatognathic Diseases 
C07. Stomatognathic Diseases
 Stomatognathic Diseases [MESH:D009057] (5348) 
 Jaw Diseases [MESH:D007571] (1608) 
 Jaw Abnormalities [MESH:D007569] (1435) 
 Cleft Palate [MESH:D002972] (1330)
 Micrognathism [MESH:D008844] (230) 
 Meier-Gorlin syndrome [MESH:C538012] (133)
 Mouth Diseases [MESH:D009059] (4783) 
 Behcet Syndrome [MESH:D001528] (1784)
 Oral Submucous Fibrosis [MESH:D009914] (2432)
 Lip Diseases [MESH:D008047] (924) 
 Cleft Lip [MESH:D002971] (914)
 Mouth Abnormalities [MESH:D009056] (1383) 
 Cleft Lip [MESH:D002971] (914)
 Cleft Palate [MESH:D002972] (1330)
 Mouth Neoplasms [MESH:D009062] (2263) 
 Salivary Gland Neoplasms [MESH:D012468] (968)
 Salivary Gland Diseases [MESH:D012466] (1213) 
 Salivary Gland Neoplasms [MESH:D012468] (968)
 Stomatitis [MESH:D013280] (1235) 
 Stevens-Johnson Syndrome [MESH:D013262] (1163)
 Pharyngeal Diseases [MESH:D010608] (1562) 
 Nasopharyngeal Diseases [MESH:D009302] (1508) 
 Nasopharyngeal Neoplasms [MESH:D009303] (1500)
 Pharyngeal Neoplasms [MESH:D010610] (1520) 
 Nasopharyngeal Neoplasms [MESH:D009303] (1500)
 Stomatognathic System Abnormalities [MESH:D018640] (1705) 
 Maxillofacial Abnormalities [MESH:D019767] (1447) 
 Jaw Abnormalities [MESH:D007569] (1438) 
 Cleft Palate [MESH:D002972] (1330)
 Micrognathism [MESH:D008844] (230) 
 Meier-Gorlin syndrome [MESH:C538012] (133)
 Mouth Abnormalities [MESH:D009056] (1383) 
 Cleft Lip [MESH:D002971] (914)
 Cleft Palate [MESH:D002972] (1330)
 Tooth Abnormalities [MESH:D014071] (622) 
 Tooth Agenesis, Selective, 6 [MESH:C567755] (154)
 Tooth Diseases [MESH:D014076] (742) 
 Tooth Abnormalities [MESH:D014071] (622) 
 Tooth Agenesis, Selective, 6 [MESH:C567755] (154)
C08. Respiratory Tract Diseases 
C08. Respiratory Tract Diseases
 Respiratory Tract Diseases [MESH:D012140] (7881) 
 Thoracic Diseases [MESH:D013896] (81)
 Bronchial Diseases [MESH:D001982] (4382) 
 Asthma [MESH:D001249] (4098)
 Lung Diseases [MESH:D008171] (7249) 
 Hypertension, Pulmonary [MESH:D006976] (2000)
 Pulmonary Fibrosis [MESH:D011658] (3140)
 Respiratory Distress Syndrome, Adult [MESH:D012128] (864)
 Lung Diseases, Interstitial [MESH:D017563] (2966) 
 Pneumoconiosis [MESH:D011009] (2789) 
 Asbestosis [MESH:D001195] (935)
 Silicosis [MESH:D012829] (1273)
 Lung Diseases, Obstructive [MESH:D008173] (4697) 
 Asthma [MESH:D001249] (3903)
 Pulmonary Disease, Chronic Obstructive [MESH:D029424] (3564)
 Lung Injury [MESH:D055370] (3688) 
 Pneumoconiosis [MESH:D011009] (2789) 
 Asbestosis [MESH:D001195] (935)
 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)
 Pneumonia [MESH:D011014] (3482) 
 Pneumonia, Aspiration [MESH:D011015] (824)
 Respiration Disorders [MESH:D012120] (2218) 
 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)
 Hyperventilation [MESH:D006985] (654) 
 Pitt-Hopkins syndrome [MESH:C537403] (113)
 Respiratory Hypersensitivity [MESH:D012130] (4401) 
 Asthma [MESH:D001249] (4098)
 Respiratory Tract Infections [MESH:D012141] (3926) 
 Influenza, Human [MESH:D007251] (1075)
 Pneumonia [MESH:D011014] (3482) 
 Pneumonia, Aspiration [MESH:D011015] (824)
 Respiratory Tract Neoplasms [MESH:D012142] (6053) 
 Lung Neoplasms [MESH:D008175] (6013) 
 Adenocarcinoma of lung [MESH:C538231] (1487)
 Bronchial Neoplasms [MESH:D001984] (3608) 
 Carcinoma, Bronchogenic [MESH:D002283] (3606) 
 Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)
 Small Cell Lung Carcinoma [MESH:D055752] (1380)
C09. Otorhinolaryngologic Diseases 
C09. Otorhinolaryngologic Diseases
 Otorhinolaryngologic Diseases [MESH:D010038] (3827) 
 Ear Diseases [MESH:D004427] (2522) 
 Hearing Disorders [MESH:D006311] (2103) 
 Hearing Loss [MESH:D034381] (2068) 
 Deafness [MESH:D003638] (623) 
 Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)
 Hearing Loss, Sensorineural [MESH:D006319] (1227) 
 Chudley-Mccullough syndrome [MESH:C535459] (45)
 Nephropathy with Pretibial Epidermolysis Bullosa and Deafness [MESH:C563798] (43)
 Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)
 Otorhinolaryngologic Neoplasms [MESH:D010039] (1561) 
 Pharyngeal Neoplasms [MESH:D010610] (1520) 
 Nasopharyngeal Neoplasms [MESH:D009303] (1500)
 Pharyngeal Diseases [MESH:D010608] (1605) 
 Nasopharyngeal Diseases [MESH:D009302] (1508) 
 Nasopharyngeal Neoplasms [MESH:D009303] (1500)
 Pharyngeal Neoplasms [MESH:D010610] (1520) 
 Nasopharyngeal Neoplasms [MESH:D009303] (1500)
C10. Nervous System Diseases 
C10. Nervous System Diseases
 Nervous System Diseases [MESH:D009422] (13325) 
 Congenital Cataracts, Facial Dysmorphism, And Neuropathy [MESH:C565822] (17)
 Restless Legs Syndrome [MESH:D012148] (379)
 Autoimmune Diseases of the Nervous System [MESH:D020274] (2238) 
 Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732) 
 Multiple Sclerosis [MESH:D009103] (1716) 
 Multiple Sclerosis, Relapsing-Remitting [MESH:D020529] (170)
 Central Nervous System Diseases [MESH:D002493] (9745) 
 Brain Diseases [MESH:D001927] (9294) 
 Brain Edema [MESH:D001929] (1165)
 Brain Injuries [MESH:D001930] (3429)
 Basal Ganglia Diseases [MESH:D001480] (4268) 
 Hepatolenticular Degeneration [MESH:D006527] (473)
 Parkinsonian Disorders [MESH:D020734] (4009) 
 Lewy Body Disease [MESH:D020961] (1143) 
 Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)
 Parkinson Disease [MESH:D010300] (3595) 
 Progressive supranuclear palsy atypical [MESH:C537240] (142)
 Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)
 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)
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636) 
 Sphingolipidoses [MESH:D013106] (582) 
 Gaucher Disease [MESH:D005776] (299)
 Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)
 Urea Cycle Disorders, Inborn [MESH:D056806] (315) 
 Citrullinemia [MESH:D020159] (99)
 Brain Neoplasms [MESH:D001932] (2764) 
 Supratentorial Neoplasms [MESH:D015173] (930) 
 Hypothalamic Neoplasms [MESH:D007029] (922) 
 Pituitary Neoplasms [MESH:D010911] (914)
 Cerebrovascular Disorders [MESH:D002561] (5542) 
 Brain Ischemia [MESH:D002545] (4873) 
 Ischemic Attack, Transient [MESH:D002546] (1313)
 Brain Infarction [MESH:D020520] (2571) 
 Cerebral Infarction [MESH:D002544] (2458)
 Brain Stem Infarctions [MESH:D020526] (198) 
 Lateral Medullary Syndrome [MESH:D014854] (188)
 Carotid Artery Diseases [MESH:D002340] (1993) 
 Carotid Stenosis [MESH:D016893] (174)
 Cerebral Small Vessel Diseases [MESH:D059345] (1292) 
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 Intracranial Arterial Diseases [MESH:D020765] (2463) 
 Cerebral Arterial Diseases [MESH:D002539] (2440) 
 Cerebral Amyloid Angiopathy [MESH:D016657] (470) 
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 Intracranial Embolism and Thrombosis [MESH:D002542] (490) 
 Intracranial Thrombosis [MESH:D020767] (481) 
 Sinus Thrombosis, Intracranial [MESH:D012851] (356) 
 Sagittal Sinus Thrombosis [MESH:D020225] (223)
 Intracranial Hemorrhages [MESH:D020300] (3269) 
 Subarachnoid Hemorrhage [MESH:D013345] (1082)
 Cerebral Hemorrhage [MESH:D002543] (2873) 
 Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)
 Stroke [MESH:D020521] (3702) 
 Brain Infarction [MESH:D020520] (2571) 
 Cerebral Infarction [MESH:D002544] (2458)
 Brain Stem Infarctions [MESH:D020526] (198) 
 Lateral Medullary Syndrome [MESH:D014854] (188)
 Dementia [MESH:D003704] (4498) 
 Creutzfeldt-Jakob Syndrome [MESH:D007562] (118)
 Alzheimer Disease [MESH:D000544] (4275) 
 Alzheimer disease type 2 [MESH:C536595] (165)
 Frontotemporal Lobar Degeneration [MESH:D057174] (310) 
 Frontotemporal Dementia [MESH:D057180] (300) 
 Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57)
 Pick Disease of the Brain [MESH:D020774] (184)
 Lewy Body Disease [MESH:D020961] (1143) 
 Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)
 Epilepsy [MESH:D004827] (6274) 
 Seizures [MESH:D012640] (4502)
 Status Epilepticus [MESH:D013226] (4014)
 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) 
 Migraine without Aura [MESH:D020326] (408)
 Hypothalamic Diseases [MESH:D007027] (1833) 
 Hypothalamic Neoplasms [MESH:D007029] (922) 
 Pituitary Neoplasms [MESH:D010911] (914)
 Pituitary Diseases [MESH:D010900] (1808) 
 Hypopituitarism [MESH:D007018] (732)
 Hyperpituitarism [MESH:D006964] (1250) 
 Acromegaly [MESH:D000172] (466)
 Hyperprolactinemia [MESH:D006966] (603)
 Pituitary Neoplasms [MESH:D010911] (981) 
 Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)
 Prolactinoma [MESH:D015175] (312)
 Central Nervous System Infections [MESH:D002494] (1823) 
 Central Nervous System Viral Diseases [MESH:D020805] (1416) 
 Encephalitis [MESH:D004660] (226) 
 Encephalitis, Viral [MESH:D018792] (183) 
 Encephalitis, Herpes Simplex [MESH:D020803] (72)
 Encephalitis [MESH:D004660] (351) 
 Encephalitis, Viral [MESH:D018792] (183) 
 Encephalitis, Herpes Simplex [MESH:D020803] (72)
 Prion Diseases [MESH:D017096] (488) 
 Creutzfeldt-Jakob Syndrome [MESH:D007562] (118)
 Movement Disorders [MESH:D009069] (4823) 
 Hepatolenticular Degeneration [MESH:D006527] (473)
 Parkinsonian Disorders [MESH:D020734] (4009) 
 Lewy Body Disease [MESH:D020961] (1143) 
 Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)
 Parkinson Disease [MESH:D010300] (3595) 
 Progressive supranuclear palsy atypical [MESH:C537240] (142)
 Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)
 Supranuclear Palsy, Progressive [MESH:D013494] (235) 
 Progressive supranuclear palsy atypical [MESH:C537240] (142)
 Spinal Cord Diseases [MESH:D013118] (4376) 
 Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)
 Muscular Atrophy, Spinal [MESH:D009134] (850) 
 Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566) 
 Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)
 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)
 Demyelinating Diseases [MESH:D003711] (2917) 
 Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (2035) 
 Multiple Sclerosis [MESH:D009103] (1716) 
 Multiple Sclerosis, Relapsing-Remitting [MESH:D020529] (170)
 Nervous System Malformations [MESH:D009421] (3354) 
 Agenesis of Corpus Callosum [MESH:D061085] (345) 
 Chudley-Mccullough syndrome [MESH:C535459] (45)
 Central Nervous System Cysts [MESH:D020863] (57) 
 Arachnoid Cysts [MESH:D016080] (50) 
 Chudley-Mccullough syndrome [MESH:C535459] (45)
 Malformations of Cortical Development [MESH:D054220] (1406) 
 Microcephaly [MESH:D008831] (700) 
 Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)
 Nervous System Neoplasms [MESH:D009423] (3073) 
 Central Nervous System Neoplasms [MESH:D016543] (3055) 
 Brain Neoplasms [MESH:D001932] (2764) 
 Supratentorial Neoplasms [MESH:D015173] (930) 
 Hypothalamic Neoplasms [MESH:D007029] (922) 
 Pituitary Neoplasms [MESH:D010911] (914)
 Central Nervous System Cysts [MESH:D020863] (57) 
 Arachnoid Cysts [MESH:D016080] (50) 
 Chudley-Mccullough syndrome [MESH:C535459] (45)
 Meningeal Neoplasms [MESH:D008577] (984) 
 Meningioma [MESH:D008579] (978)
 Neurocutaneous Syndromes [MESH:D020752] (1230) 
 Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome [MESH:C537943] (28)
 Nevus, Sebaceous of Jadassohn [MESH:D054000] (209)
 Neurodegenerative Diseases [MESH:D019636] (6613) 
 Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243) 
 Hepatolenticular Degeneration [MESH:D006527] (473)
 Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566) 
 Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)
 Lewy Body Disease [MESH:D020961] (1143) 
 Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)
 Motor Neuron Disease [MESH:D016472] (3670) 
 Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)
 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)
 Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)
 Tauopathies [MESH:D024801] (4289) 
 Alzheimer Disease [MESH:D000544] (4275) 
 Alzheimer disease type 2 [MESH:C536595] (165)
 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)
 Frontotemporal Lobar Degeneration [MESH:D057174] (308) 
 Frontotemporal Dementia [MESH:D057180] (298) 
 Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57)
 Neurologic Manifestations [MESH:D009461] (8964) 
 Neurogenic Inflammation [MESH:D020078] (2246)
 Pain [MESH:D010146] (3875)
 Seizures [MESH:D012640] (4514)
 Dyskinesias [MESH:D020820] (3365) 
 Catalepsy [MESH:D002375] (1429)
 Neurobehavioral Manifestations [MESH:D019954] (5230) 
 Communication Disorders [MESH:D003147] (2918) 
 Learning Disorders [MESH:D007859] (2727)
 Language Disorders [MESH:D007806] (653) 
 Speech Disorders [MESH:D013064] (482) 
 Articulation Disorders [MESH:D001184] (164) 
 Dysarthria [MESH:D004401] (163)
 Memory Disorders [MESH:D008569] (3233) 
 Amnesia [MESH:D000647] (1911)
 Intellectual Disability [MESH:D008607] (3054) 
 Pitt-Hopkins syndrome [MESH:C537403] (113)
 Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)
 De Lange Syndrome [MESH:D003635] (55)
 Prader-Willi Syndrome [MESH:D011218] (46)
 Mental Retardation, X-Linked [MESH:D038901] (1854) 
 Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)
 ATR-X syndrome [MESH:C538258] (59)
 Fragile X Syndrome [MESH:D005600] (353)
 Mucopolysaccharidosis II [MESH:D016532] (26)
 Neuromuscular Manifestations [MESH:D020879] (2130) 
 Muscular Atrophy [MESH:D009133] (1234)
 Muscle Hypertonia [MESH:D009122] (775) 
 Muscle Rigidity [MESH:D009127] (617)
 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) 
 Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)
 Hearing Loss, Sensorineural [MESH:D006319] (1227) 
 Chudley-Mccullough syndrome [MESH:C535459] (45)
 Nephropathy with Pretibial Epidermolysis Bullosa and Deafness [MESH:C563798] (43)
 Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)
 Somatosensory Disorders [MESH:D020886] (4000) 
 Hyperalgesia [MESH:D006930] (3929)
 Neuromuscular Diseases [MESH:D009468] (7336) 
 Peripheral Nervous System Diseases [MESH:D010523] (6151)
 Motor Neuron Disease [MESH:D016472] (3670) 
 Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)
 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) 
 Eosinophilia-Myalgia Syndrome [MESH:D016603] (31)
 Muscular Disorders, Atrophic [MESH:D020966] (1594) 
 Muscular Dystrophies [MESH:D009136] (1589) 
 Bethlem myopathy [MESH:C535436] (108)
 Scleroatonic muscular dystrophy [MESH:C537521] (108)
 Muscular Dystrophy, Emery-Dreifuss [MESH:D020389] (169)
 Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)
 Muscular Dystrophies, Limb-Girdle [MESH:D049288] (259) 
 Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57)
 Muscular Dystrophy, Limb-Girdle, Type 2G [MESH:C566599] (13)
 Myopathies, Structural, Congenital [MESH:D020914] (272) 
 Myosclerosis, Autosomal Recessive [MESH:C564968] (45)
 Myositis [MESH:D009220] (2069) 
 Myositis, Inclusion Body [MESH:D018979] (103) 
 Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57)
 Neurotoxicity Syndromes [MESH:D020258] (4570) 
 Heavy Metal Poisoning, Nervous System [MESH:D020260] (2912) 
 Arsenic Poisoning [MESH:D020261] (2540)
 Manganese Poisoning [MESH:D020149] (2214)
 Sleep Disorders [MESH:D012893] (2050) 
 Dyssomnias [MESH:D020920] (1417) 
 Sleep Disorders, Intrinsic [MESH:D020919] (1270) 
 Restless Legs Syndrome [MESH:D012148] (379)
 Disorders of Excessive Somnolence [MESH:D006970] (581) 
 Narcolepsy [MESH:D009290] (478)
 Sleep Apnea Syndromes [MESH:D012891] (570) 
 Sleep Apnea, Obstructive [MESH:D020181] (126)
 Parasomnias [MESH:D020447] (453) 
 Restless Legs Syndrome [MESH:D012148] (379)
 Trauma, Nervous System [MESH:D020196] (3997) 
 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 Dystrophies, Hereditary [MESH:D003317] (341) 
 Corneal Dystrophy, Posterior Polymorphous, 3 [MESH:C563788] (60)
 Fuchs' Endothelial Dystrophy [MESH:D005642] (86) 
 Corneal Dystrophy, Fuchs Endothelial, 6 [MESH:C567675] (60)
 Eye Diseases, Hereditary [MESH:D015785] (1869) 
 Basal Laminar Drusen [MESH:C563034] (52)
 Graves Ophthalmopathy [MESH:D049970] (165)
 Albinism [MESH:D000417] (258) 
 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)
 Albinism, Oculocutaneous [MESH:D016115] (234) 
 Oculocutaneous albinism type 3 [MESH:C537731] (40)
 Hermanski-Pudlak Syndrome [MESH:D022861] (82) 
 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)
 Corneal Dystrophies, Hereditary [MESH:D003317] (341) 
 Corneal Dystrophy, Posterior Polymorphous, 3 [MESH:C563788] (60)
 Fuchs' Endothelial Dystrophy [MESH:D005642] (86) 
 Corneal Dystrophy, Fuchs Endothelial, 6 [MESH:C567675] (60)
 Eye Neoplasms [MESH:D005134] (413) 
 Uveal Neoplasms [MESH:D014604] (115) 
 Uveal melanoma [MESH:C536494] (109)
 Lens Diseases [MESH:D007905] (900) 
 Cataract [MESH:D002386] (860) 
 Congenital Cataracts, Facial Dysmorphism, And Neuropathy [MESH:C565822] (17)
 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)
 Retinal Diseases [MESH:D012164] (3747) 
 Retinal Degeneration [MESH:D012162] (2386) 
 Macular Degeneration [MESH:D008268] (995) 
 Fundus Dystrophy, Pseudoinflammatory, Of Sorsby [MESH:C564992] (121)
 Macular Degeneration, Age-Related, 4 [MESH:C565196] (67)
 Macular Degeneration, Age-Related, 1 [MESH:C566411] (276)
 Retinal Drusen [MESH:D015593] (54) 
 Basal Laminar Drusen [MESH:C563034] (52)
 Uveal Diseases [MESH:D014603] (2428) 
 Uveal Neoplasms [MESH:D014604] (115) 
 Uveal melanoma [MESH:C536494] (109)
 Uveitis [MESH:D014605] (2157) 
 Panuveitis [MESH:D015864] (1805) 
 Uveitis, Anterior [MESH:D014606] (1791) 
 Behcet Syndrome [MESH:D001528] (1784)
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) 
 Penile Neoplasms [MESH:D010412] (890)
 Prostatic Neoplasms [MESH:D011471] (6135)
 Testicular Neoplasms [MESH:D013736] (520) 
 Sertoli-Leydig Cell Tumor [MESH:D018310] (272) 
 Leydig Cell Tumor [MESH:D007984] (267)
 Infertility [MESH:D007246] (2909) 
 Infertility, Male [MESH:D007248] (2851) 
 Aromatase deficiency [MESH:C537436] (277)
 Oligospermia [MESH:D009845] (799) 
 Follicle-stimulating hormone deficiency, isolated [MESH:C537070] (185)
 Penile Diseases [MESH:D010409] (1805) 
 Penile Neoplasms [MESH:D010412] (890)
 Hypospadias [MESH:D007021] (798) 
 Hypospadias 1, X-Linked [MESH:C567482] (571)
 Prostatic Diseases [MESH:D011469] (6204) 
 Prostatic Hyperplasia [MESH:D011470] (336)
 Prostatic Neoplasms [MESH:D011471] (6135)
 Sexual Dysfunction, Physiological [MESH:D012735] (1808) 
 Erectile Dysfunction [MESH:D007172] (1791)
 Testicular Diseases [MESH:D013733] (451) 
 Cryptorchidism [MESH:D003456] (215) 
 Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)
 Urogenital Abnormalities [MESH:D014564] (2065) 
 Cryptorchidism [MESH:D003456] (215) 
 Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)
 Disorders of Sex Development [MESH:D012734] (1637) 
 46, XX Disorders of Sex Development [MESH:D058489] (644) 
 Aromatase deficiency [MESH:C537436] (277)
 Gonadal Dysgenesis, 46,XX [MESH:D023961] (56)
 46, XY Disorders of Sex Development [MESH:D058490] (1060) 
 Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)
 Leydig Cell Hypoplasia [MESH:C562567] (65)
 Androgen-Insensitivity Syndrome [MESH:D013734] (567)
 Gonadal Dysgenesis, 46,XY [MESH:D006061] (131)
 Adrenogenital Syndrome [MESH:D047808] (715) 
 Adrenal Hyperplasia, Congenital [MESH:D000312] (674) 
 Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)
 Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223)
 Gonadal Dysgenesis [MESH:D006059] (492) 
 Gonadal Dysgenesis, 46,XX [MESH:D023961] (56)
 Gonadal Dysgenesis, 46,XY [MESH:D006061] (131)
 Sexual Infantilism [MESH:D050035] (277)
 Hypospadias [MESH:D007021] (798) 
 Hypospadias 1, X-Linked [MESH:C567482] (571)
 Urogenital Neoplasms [MESH:D014565] (6932) 
 Genital Neoplasms, Male [MESH:D005834] (6224) 
 Penile Neoplasms [MESH:D010412] (890)
 Prostatic Neoplasms [MESH:D011471] (6135)
 Testicular Neoplasms [MESH:D013736] (520) 
 Sertoli-Leydig Cell Tumor [MESH:D018310] (272) 
 Leydig Cell Tumor [MESH:D007984] (267)
 Urologic Neoplasms [MESH:D014571] (5315) 
 Urinary Bladder Neoplasms [MESH:D001749] (4079)
 Kidney Neoplasms [MESH:D007680] (3966) 
 Carcinoma, Renal Cell [MESH:D002292] (2975)
 Urologic Diseases [MESH:D014570] (7792) 
 Urinary Tract Infections [MESH:D014552] (984)
 Kidney Diseases [MESH:D007674] (7242) 
 Complement Factor H Deficiency [MESH:C562875] (52)
 Nephropathy with Pretibial Epidermolysis Bullosa and Deafness [MESH:C563798] (43)
 Lipoprotein Glomerulopathy [MESH:C567089] (165)
 Diabetic Nephropathies [MESH:D003928] (2301)
 Kidney Neoplasms [MESH:D007680] (3966) 
 Carcinoma, Renal Cell [MESH:D002292] (2975)
 Nephritis [MESH:D009393] (4236) 
 Glomerulonephritis [MESH:D005921] (3758) 
 Glomerulonephritis, IGA [MESH:D005922] (897)
 Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)
 Glomerulonephritis, Membranous [MESH:D015433] (642)
 Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)
 Nephrosis [MESH:D009401] (2228) 
 Nephrotic Syndrome [MESH:D009404] (1536)
 Renal Insufficiency [MESH:D051437] (4951) 
 Acute Kidney Injury [MESH:D058186] (4142)
 Renal Insufficiency, Chronic [MESH:D051436] (2931) 
 Kidney Failure, Chronic [MESH:D007676] (2930)
 Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058) 
 Pseudohypoaldosteronism [MESH:D011546] (232)
 Hypophosphatemia, Familial [MESH:D007015] (276) 
 Familial Hypophosphatemic Rickets [MESH:D053098] (274) 
 Hypophosphatemic Rickets, Autosomal Recessive, 2 [MESH:C567647] (48)
 Uremia [MESH:D014511] (2898) 
 Hemolytic-Uremic Syndrome [MESH:D006463] (2435) 
 Atypical hemolytic uremic syndrome [MESH:C538266] (277)
 Ureteral Diseases [MESH:D014515] (1024) 
 Ureteral Obstruction [MESH:D014517] (575)
 Urinary Bladder Diseases [MESH:D001745] (4374) 
 Urinary Bladder Neoplasms [MESH:D001749] (4079)
 Urination Disorders [MESH:D014555] (3598) 
 Oliguria [MESH:D009846] (307)
 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)
 Sexual Dysfunction, Physiological [MESH:D012735] (270)
 Adnexal Diseases [MESH:D000291] (4273) 
 Ovarian Diseases [MESH:D010049] (4255) 
 Ovarian Neoplasms [MESH:D010051] (3281)
 Ovarian Cysts [MESH:D010048] (2534) 
 Polycystic Ovary Syndrome [MESH:D011085] (2186)
 Primary Ovarian Insufficiency [MESH:D016649] (270) 
 Premature Ovarian Failure 2a [MESH:C564498] (15)
 Premature Ovarian Failure 7 [MESH:C567838] (52)
 Infertility [MESH:D007246] (2211) 
 Infertility, Female [MESH:D007247] (2184)
 Uterine Diseases [MESH:D014591] (2479) 
 Uterine Neoplasms [MESH:D014594] (2430) 
 Endometrial Neoplasms [MESH:D016889] (1984)
 Urogenital Abnormalities [MESH:D014564] (2043) 
 Disorders of Sex Development [MESH:D012734] (1637) 
 46, XX Disorders of Sex Development [MESH:D058489] (644) 
 Aromatase deficiency [MESH:C537436] (277)
 Gonadal Dysgenesis, 46,XX [MESH:D023961] (56)
 46, XY Disorders of Sex Development [MESH:D058490] (1060) 
 Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)
 Leydig Cell Hypoplasia [MESH:C562567] (65)
 Androgen-Insensitivity Syndrome [MESH:D013734] (567)
 Gonadal Dysgenesis, 46,XY [MESH:D006061] (131)
 Adrenogenital Syndrome [MESH:D047808] (715) 
 Adrenal Hyperplasia, Congenital [MESH:D000312] (674) 
 Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)
 Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223)
 Gonadal Dysgenesis [MESH:D006059] (492) 
 Gonadal Dysgenesis, 46,XX [MESH:D023961] (56)
 Gonadal Dysgenesis, 46,XY [MESH:D006061] (131)
 Sexual Infantilism [MESH:D050035] (277)
 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)
 Uterine Neoplasms [MESH:D014594] (2433) 
 Endometrial Neoplasms [MESH:D016889] (1989)
 Urologic Neoplasms [MESH:D014571] (5315) 
 Urinary Bladder Neoplasms [MESH:D001749] (4079)
 Kidney Neoplasms [MESH:D007680] (3966) 
 Carcinoma, Renal Cell [MESH:D002292] (2975)
 Urologic Diseases [MESH:D014570] (7793) 
 Urinary Tract Infections [MESH:D014552] (984)
 Kidney Diseases [MESH:D007674] (7242) 
 Complement Factor H Deficiency [MESH:C562875] (52)
 Nephropathy with Pretibial Epidermolysis Bullosa and Deafness [MESH:C563798] (43)
 Lipoprotein Glomerulopathy [MESH:C567089] (165)
 Diabetic Nephropathies [MESH:D003928] (2301)
 Kidney Neoplasms [MESH:D007680] (3966) 
 Carcinoma, Renal Cell [MESH:D002292] (2975)
 Nephritis [MESH:D009393] (4236) 
 Glomerulonephritis [MESH:D005921] (3758) 
 Glomerulonephritis, IGA [MESH:D005922] (897)
 Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)
 Glomerulonephritis, Membranous [MESH:D015433] (642)
 Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)
 Nephrosis [MESH:D009401] (2228) 
 Nephrotic Syndrome [MESH:D009404] (1536)
 Renal Insufficiency [MESH:D051437] (4951) 
 Acute Kidney Injury [MESH:D058186] (4142)
 Renal Insufficiency, Chronic [MESH:D051436] (2931) 
 Kidney Failure, Chronic [MESH:D007676] (2930)
 Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058) 
 Pseudohypoaldosteronism [MESH:D011546] (232)
 Hypophosphatemia, Familial [MESH:D007015] (276) 
 Familial Hypophosphatemic Rickets [MESH:D053098] (274) 
 Hypophosphatemic Rickets, Autosomal Recessive, 2 [MESH:C567647] (48)
 Uremia [MESH:D014511] (2898) 
 Hemolytic-Uremic Syndrome [MESH:D006463] (2435) 
 Atypical hemolytic uremic syndrome [MESH:C538266] (277)
 Ureteral Diseases [MESH:D014515] (1024) 
 Ureteral Obstruction [MESH:D014517] (575)
 Urinary Bladder Diseases [MESH:D001745] (4375) 
 Urinary Bladder Neoplasms [MESH:D001749] (4079)
 Urination Disorders [MESH:D014555] (3598) 
 Oliguria [MESH:D009846] (307)
 Proteinuria [MESH:D011507] (3293)
 Pregnancy Complications [MESH:D011248] (4768) 
 Abortion, Spontaneous [MESH:D000022] (2780)
 Diabetes, Gestational [MESH:D016640] (1157)
 Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)
 Fetal Death [MESH:D005313] (464) 
 Fetal Resorption [MESH:D005327] (302)
 Fetal Diseases [MESH:D005315] (1206) 
 Fetal Growth Retardation [MESH:D005317] (986)
 Puerperal Disorders [MESH:D011644] (324) 
 Lactation Disorders [MESH:D007775] (235) 
 Galactorrhea [MESH:D005687] (233)
C14. Cardiovascular Diseases 
C14. Cardiovascular Diseases
 Z. Exceptions (2667) 
 Not Fully Specified [NFS] (2667)
 Cardiovascular Diseases [MESH:D002318] (10123) 
 Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)
 Cardiovascular Abnormalities [MESH:D018376] (3153) 
 Heart Defects, Congenital [MESH:D006330] (2447) 
 Cardiofaciocutaneous syndrome [MESH:C535579] (407)
 Heterotaxy Syndrome [MESH:D059446] (84)
 22q11 Deletion Syndrome [MESH:D058165] (237) 
 DiGeorge Syndrome [MESH:D004062] (236)
 Ductus Arteriosus, Patent [MESH:D004374] (325) 
 Aortic aneurysm, familial thoracic 4 [MESH:C537784] (29)
 Noonan Syndrome [MESH:D009634] (506) 
 Noonan syndrome 3 [MESH:C537847] (118)
 Noonan Syndrome 4 [MESH:C548082] (37)
 Heart Diseases [MESH:D006331] (8614) 
 Heart Failure [MESH:D006333] (4058)
 Arrhythmias, Cardiac [MESH:D001145] (4679) 
 Atrial Fibrillation [MESH:D001281] (1053)
 Bradycardia [MESH:D001919] (1899)
 Tachycardia [MESH:D013610] (3339)
 Cardiomegaly [MESH:D006332] (4081) 
 Hypertrophy, Left Ventricular [MESH:D017379] (1430)
 Cardiomyopathy, Dilated [MESH:D002311] (1576) 
 Cardiomyopathy, Dilated, 1N [MESH:C564388] (13)
 Cardiomyopathies [MESH:D009202] (5331) 
 Diabetic Cardiomyopathies [MESH:D058065] (1995)
 Endomyocardial Fibrosis [MESH:D004719] (521)
 Myocardial Reperfusion Injury [MESH:D015428] (3500)
 Cardiomyopathy, Dilated [MESH:D002311] (1576) 
 Cardiomyopathy, Dilated, 1N [MESH:C564388] (13)
 Heart Defects, Congenital [MESH:D006330] (2443) 
 Cardiofaciocutaneous syndrome [MESH:C535579] (407)
 Heterotaxy Syndrome [MESH:D059446] (84)
 22q11 Deletion Syndrome [MESH:D058165] (237) 
 DiGeorge Syndrome [MESH:D004062] (236)
 Ductus Arteriosus, Patent [MESH:D004374] (325) 
 Aortic aneurysm, familial thoracic 4 [MESH:C537784] (29)
 Noonan Syndrome [MESH:D009634] (506) 
 Noonan syndrome 3 [MESH:C537847] (118)
 Noonan Syndrome 4 [MESH:C548082] (37)
 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)
 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 Artery Disease [MESH:D003324] (2685)
 Myocardial Infarction [MESH:D009203] (4122) 
 Myocardial Stunning [MESH:D017682] (1816)
 Ventricular Outflow Obstruction [MESH:D014694] (976) 
 Aortic Valve Stenosis [MESH:D001024] (810) 
 Aortic Valve, Calcification of [MESH:C562942] (655)
 Vascular Diseases [MESH:D014652] (8691) 
 Angioedema [MESH:D000799] (837)
 Arteritis [MESH:D001167] (1084)
 Hyperemia [MESH:D006940] (2372)
 Hypotension [MESH:D007022] (4045)
 Varicose Veins [MESH:D014648] (383)
 Aneurysm [MESH:D000783] (1886) 
 Aneurysm, Dissecting [MESH:D000784] (699)
 Aortic Aneurysm [MESH:D001014] (1721) 
 Aortic Aneurysm, Thoracic [MESH:D017545] (781) 
 Aortic aneurysm, familial thoracic 4 [MESH:C537784] (29)
 Angiomatosis [MESH:D000798] (620) 
 Klippel-Trenaunay-Weber Syndrome [MESH:D007715] (14)
 Aortic Diseases [MESH:D001018] (1737) 
 Aortic Aneurysm [MESH:D001014] (1721) 
 Aortic Aneurysm, Thoracic [MESH:D017545] (781) 
 Aortic aneurysm, familial thoracic 4 [MESH:C537784] (29)
 Arterial Occlusive Diseases [MESH:D001157] (4520) 
 Carotid Stenosis [MESH:D016893] (174)
 Arteriosclerosis [MESH:D001161] (4466) 
 Atherosclerosis [MESH:D050197] (4188)
 Coronary Artery Disease [MESH:D003324] (2685)
 Cerebrovascular Disorders [MESH:D002561] (5541) 
 Brain Ischemia [MESH:D002545] (4873) 
 Ischemic Attack, Transient [MESH:D002546] (1313)
 Brain Infarction [MESH:D020520] (2571) 
 Cerebral Infarction [MESH:D002544] (2458)
 Brain Stem Infarctions [MESH:D020526] (198) 
 Lateral Medullary Syndrome [MESH:D014854] (188)
 Carotid Artery Diseases [MESH:D002340] (1993) 
 Carotid Stenosis [MESH:D016893] (174)
 Cerebral Small Vessel Diseases [MESH:D059345] (1292) 
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 Intracranial Arterial Diseases [MESH:D020765] (2468) 
 Cerebral Arterial Diseases [MESH:D002539] (2440) 
 Cerebral Amyloid Angiopathy [MESH:D016657] (470) 
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 Intracranial Embolism and Thrombosis [MESH:D002542] (550) 
 Intracranial Thrombosis [MESH:D020767] (481) 
 Sinus Thrombosis, Intracranial [MESH:D012851] (356) 
 Sagittal Sinus Thrombosis [MESH:D020225] (223)
 Intracranial Hemorrhages [MESH:D020300] (3269) 
 Subarachnoid Hemorrhage [MESH:D013345] (1082)
 Cerebral Hemorrhage [MESH:D002543] (2873) 
 Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)
 Stroke [MESH:D020521] (3702) 
 Brain Infarction [MESH:D020520] (2571) 
 Cerebral Infarction [MESH:D002544] (2458)
 Brain Stem Infarctions [MESH:D020526] (198) 
 Lateral Medullary Syndrome [MESH:D014854] (188)
 Embolism and Thrombosis [MESH:D016769] (3374) 
 Thromboembolism [MESH:D013923] (732) 
 Venous Thromboembolism [MESH:D054556] (400)
 Intracranial Embolism and Thrombosis [MESH:D002542] (550) 
 Intracranial Thrombosis [MESH:D020767] (481) 
 Sinus Thrombosis, Intracranial [MESH:D012851] (356) 
 Sagittal Sinus Thrombosis [MESH:D020225] (223)
 Thrombosis [MESH:D013927] (3101) 
 Venous Thrombosis [MESH:D020246] (1141)
 Thromboembolism [MESH:D013923] (732) 
 Venous Thromboembolism [MESH:D054556] (400)
 Intracranial Embolism and Thrombosis [MESH:D002542] (550) 
 Intracranial Thrombosis [MESH:D020767] (481) 
 Sinus Thrombosis, Intracranial [MESH:D012851] (356) 
 Sagittal Sinus Thrombosis [MESH:D020225] (223)
 Hemostatic Disorders [MESH:D020141] (2894) 
 Telangiectasia, Hereditary Hemorrhagic [MESH:D013683] (75)
 Ehlers-Danlos Syndrome [MESH:D004535] (491) 
 Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)
 Ehlers-Danlos syndrome type 2 [MESH:C536195] (55)
 Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)
 Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152)
 Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)
 Hepatic Veno-Occlusive Disease [MESH:D006504] (208) 
 Hepatic venoocclusive disease with immunodeficiency [MESH:C537257] (23)
 Hypertension [MESH:D006973] (5655) 
 Hypertension, Essential [MESH:C562386] (1308)
 Hypertension, Malignant [MESH:D006974] (621)
 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 Artery Disease [MESH:D003324] (2685)
 Myocardial Infarction [MESH:D009203] (4151) 
 Myocardial Stunning [MESH:D017682] (1816)
 Peripheral Vascular Diseases [MESH:D016491] (1412) 
 Raynaud Disease [MESH:D011928] (490)
 Reperfusion Injury [MESH:D015427] (4968) 
 Myocardial Reperfusion Injury [MESH:D015428] (3500)
 Telangiectasis [MESH:D013684] (255) 
 Telangiectasia, Hereditary Hemorrhagic [MESH:D013683] (75)
 Vasculitis [MESH:D014657] (2604) 
 Arteritis [MESH:D001167] (1084)
 Behcet Syndrome [MESH:D001528] (1784)
 Mucocutaneous Lymph Node Syndrome [MESH:D009080] (158)
C15. Hemic and Lymphatic Diseases 
C15. Hemic and Lymphatic Diseases
 Hematologic Diseases [MESH:D006402] (6174) 
 Polycythemia [MESH:D011086] (412)
 Anemia [MESH:D000740] (3966) 
 Anemia, Aplastic [MESH:D000741] (1925) 
 Anemia, Hypoplastic, Congenital [MESH:D029502] (1665) 
 Fanconi Anemia [MESH:D005199] (1604)
 Anemia, Hemolytic [MESH:D000743] (3083) 
 Anemia, Hemolytic, Congenital [MESH:D000745] (2001) 
 Anemia, Dyserythropoietic, Congenital [MESH:D000742] (81)
 Spherocytosis, Hereditary [MESH:D013103] (137) 
 Spherocytosis, Type 1 [MESH:C567159] (21)
 Thalassemia [MESH:D013789] (501) 
 alpha-Thalassemia [MESH:D017085] (176) 
 ATR-X syndrome [MESH:C538258] (59)
 Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)
 Hemolytic-Uremic Syndrome [MESH:D006463] (2435) 
 Atypical hemolytic uremic syndrome [MESH:C538266] (277)
 Blood Coagulation Disorders [MESH:D001778] (1828) 
 Disseminated Intravascular Coagulation [MESH:D004211] (462)
 Blood Coagulation Disorders, Inherited [MESH:D025861] (720) 
 Activated Protein C Resistance [MESH:D020016] (140)
 Antithrombin III Deficiency [MESH:D020152] (80)
 Hypoprothrombinemias [MESH:D007020] (157)
 Hermanski-Pudlak Syndrome [MESH:D022861] (82) 
 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)
 Protein C Deficiency [MESH:D020151] (70) 
 Congenital thrombotic disease, due to Protein C deficiency [MESH:C535424] (66)
 Coagulation Protein Disorders [MESH:D020147] (580) 
 Activated Protein C Resistance [MESH:D020016] (140)
 Hypoprothrombinemias [MESH:D007020] (157)
 Platelet Storage Pool Deficiency [MESH:D010981] (84) 
 Hermanski-Pudlak Syndrome [MESH:D022861] (82) 
 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)
 Purpura [MESH:D011693] (475) 
 Purpura Fulminans [MESH:D055665] (69)
 Blood Platelet Disorders [MESH:D001791] (3174) 
 Platelet Storage Pool Deficiency [MESH:D010981] (84) 
 Hermanski-Pudlak Syndrome [MESH:D022861] (82) 
 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)
 Thrombocytopenia [MESH:D013921] (2966) 
 Thrombotic Microangiopathies [MESH:D057049] (2598) 
 Hemolytic-Uremic Syndrome [MESH:D006463] (2435) 
 Atypical hemolytic uremic syndrome [MESH:C538266] (277)
 Blood Protein Disorders [MESH:D001796] (3051) 
 Antithrombin III Deficiency [MESH:D020152] (80)
 Protein C Deficiency [MESH:D020151] (70) 
 Congenital thrombotic disease, due to Protein C deficiency [MESH:C535424] (66)
 Bone Marrow Diseases [MESH:D001855] (2944) 
 Anemia, Aplastic [MESH:D000741] (1925) 
 Anemia, Hypoplastic, Congenital [MESH:D029502] (1665) 
 Fanconi Anemia [MESH:D005199] (1604)
 Myelodysplastic Syndromes [MESH:D009190] (2093) 
 Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)
 Hemoglobinopathies [MESH:D006453] (1863) 
 Thalassemia [MESH:D013789] (511) 
 alpha-Thalassemia [MESH:D017085] (192) 
 ATR-X syndrome [MESH:C538258] (59)
 Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)
 Hemorrhagic Disorders [MESH:D006474] (3359) 
 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)
 Disseminated Intravascular Coagulation [MESH:D004211] (462)
 Hypoprothrombinemias [MESH:D007020] (157)
 Hemostatic Disorders [MESH:D020141] (2932) 
 Telangiectasia, Hereditary Hemorrhagic [MESH:D013683] (75)
 Ehlers-Danlos Syndrome [MESH:D004535] (491) 
 Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)
 Ehlers-Danlos syndrome type 2 [MESH:C536195] (55)
 Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)
 Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152)
 Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)
 Platelet Storage Pool Deficiency [MESH:D010981] (84) 
 Hermanski-Pudlak Syndrome [MESH:D022861] (82) 
 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)
 Leukocyte Disorders [MESH:D007960] (2662) 
 Eosinophilia [MESH:D004802] (537) 
 Eosinophilia-Myalgia Syndrome [MESH:D016603] (31)
 Phagocyte Bactericidal Dysfunction [MESH:D010585] (998) 
 Granulomatous Disease, Chronic [MESH:D006105] (404) 
 Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative [MESH:C565533] (111)
 Thrombophilia [MESH:D019851] (592) 
 Activated Protein C Resistance [MESH:D020016] (140)
 Antithrombin III Deficiency [MESH:D020152] (80)
 Disseminated Intravascular Coagulation [MESH:D004211] (462)
 Protein C Deficiency [MESH:D020151] (70) 
 Congenital thrombotic disease, due to Protein C deficiency [MESH:C535424] (66)
 Lymphatic Diseases [MESH:D008206] (5167) 
 Mucocutaneous Lymph Node Syndrome [MESH:D009080] (158)
 Histiocytosis [MESH:D015614] (336) 
 Histiocytosis, Non-Langerhans-Cell [MESH:D015616] (315) 
 Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)
 Lymphohistiocytosis, Hemophagocytic [MESH:D051359] (76) 
 Hemophagocytic lymphohistiocytosis, familial, 2 [MESH:C537250] (38)
 Lymphatic Abnormalities [MESH:D044148] (251) 
 22q11 Deletion Syndrome [MESH:D058165] (237) 
 DiGeorge Syndrome [MESH:D004062] (236)
 Lymphoproliferative Disorders [MESH:D008232] (4638) 
 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 T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)
 Lymphoma [MESH:D008223] (3684) 
 Lymphoma, Non-Hodgkin [MESH:D008228] (3330) 
 Lymphoma, Mantle-Cell [MESH:D020522] (561)
 Lymphoma, B-Cell [MESH:D016393] (2624) 
 Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)
 Splenic Diseases [MESH:D013158] (1323) 
 Heterotaxy Syndrome [MESH:D059446] (84)
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) 
 Situs Inversus [MESH:D012857] (88)
 Abnormalities, Multiple [MESH:D000015] (3192) 
 Beta-Hydroxyisobutyryl CoA Deacylase Deficiency [MESH:C562803] (33)
 Insulin-Like Growth Factor I, Resistance To [MESH:C564816] (141)
 Desmosterolosis [MESH:C566555] (85)
 Costello Syndrome [MESH:D056685] (407)
 De Lange Syndrome [MESH:D003635] (55)
 Heterotaxy Syndrome [MESH:D059446] (84)
 Nevus, Sebaceous of Jadassohn [MESH:D054000] (209)
 Prader-Willi Syndrome [MESH:D011218] (46)
 22q11 Deletion Syndrome [MESH:D058165] (237) 
 DiGeorge Syndrome [MESH:D004062] (236)
 Ectodermal Dysplasia [MESH:D004476] (938) 
 Cardiofaciocutaneous syndrome [MESH:C535579] (407)
 Neurocutaneous Syndromes [MESH:D020752] (39) 
 Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome [MESH:C537943] (28)
 Waardenburg Syndrome [MESH:D014849] (243) 
 ABCD syndrome [MESH:C535334] (143)
 Cardiovascular Abnormalities [MESH:D018376] (3294) 
 Heart Defects, Congenital [MESH:D006330] (2611) 
 Cardiofaciocutaneous syndrome [MESH:C535579] (407)
 Heterotaxy Syndrome [MESH:D059446] (84)
 22q11 Deletion Syndrome [MESH:D058165] (237) 
 DiGeorge Syndrome [MESH:D004062] (236)
 Ductus Arteriosus, Patent [MESH:D004374] (325) 
 Aortic aneurysm, familial thoracic 4 [MESH:C537784] (29)
 Noonan Syndrome [MESH:D009634] (506) 
 Noonan syndrome 3 [MESH:C537847] (118)
 Noonan Syndrome 4 [MESH:C548082] (37)
 Vascular Malformations [MESH:D054079] (1108) 
 Telangiectasia, Hereditary Hemorrhagic [MESH:D013683] (75)
 Chromosome Disorders [MESH:D025063] (2030) 
 Mosaic variegated aneuploidy syndrome [MESH:C536987] (95)
 De Lange Syndrome [MESH:D003635] (55)
 Prader-Willi Syndrome [MESH:D011218] (46)
 22q11 Deletion Syndrome [MESH:D058165] (237) 
 DiGeorge Syndrome [MESH:D004062] (236)
 Sex Chromosome Disorders [MESH:D025064] (479) 
 Fragile X Syndrome [MESH:D005600] (353)
 Digestive System Abnormalities [MESH:D004065] (507) 
 Hirschsprung Disease [MESH:D006627] (361)
 Lymphatic Abnormalities [MESH:D044148] (251) 
 22q11 Deletion Syndrome [MESH:D058165] (237) 
 DiGeorge Syndrome [MESH:D004062] (236)
 Musculoskeletal Abnormalities [MESH:D009139] (3779) 
 Arthrogryposis [MESH:D001176] (329) 
 Bruck syndrome 2 [MESH:C537407] (64)
 Distal arthrogryposis type 2B [MESH:C538400] (85)
 Craniofacial Abnormalities [MESH:D019465] (3064) 
 Congenital Cataracts, Facial Dysmorphism, And Neuropathy [MESH:C565822] (17)
 22q11 Deletion Syndrome [MESH:D058165] (237) 
 DiGeorge Syndrome [MESH:D004062] (236)
 Craniofacial Dysostosis [MESH:D003394] (391) 
 Freeman-Sheldon syndrome [MESH:C535483] (23)
 Mandibulofacial Dysostosis [MESH:D008342] (63)
 Maxillofacial Abnormalities [MESH:D019767] (1448) 
 Jaw Abnormalities [MESH:D007569] (1435) 
 Cleft Palate [MESH:D002972] (1330)
 Micrognathism [MESH:D008844] (230) 
 Meier-Gorlin syndrome [MESH:C538012] (133)
 Microcephaly [MESH:D008831] (700) 
 Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)
 Noonan Syndrome [MESH:D009634] (506) 
 Noonan syndrome 3 [MESH:C537847] (118)
 Noonan Syndrome 4 [MESH:C548082] (37)
 Limb Deformities, Congenital [MESH:D017880] (1813) 
 Brachydactyly [MESH:D059327] (220)
 Hand Deformities, Congenital [MESH:D006228] (587) 
 Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)
 Nervous System Malformations [MESH:D009421] (3354) 
 Agenesis of Corpus Callosum [MESH:D061085] (345) 
 Chudley-Mccullough syndrome [MESH:C535459] (45)
 Central Nervous System Cysts [MESH:D020863] (57) 
 Arachnoid Cysts [MESH:D016080] (50) 
 Chudley-Mccullough syndrome [MESH:C535459] (45)
 Malformations of Cortical Development [MESH:D054220] (1406) 
 Microcephaly [MESH:D008831] (700) 
 Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)
 Skin Abnormalities [MESH:D012868] (1723) 
 Ectodermal Dysplasia [MESH:D004476] (958) 
 Cardiofaciocutaneous syndrome [MESH:C535579] (407)
 Neurocutaneous Syndromes [MESH:D020752] (39) 
 Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome [MESH:C537943] (28)
 Ehlers-Danlos Syndrome [MESH:D004535] (491) 
 Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)
 Ehlers-Danlos syndrome type 2 [MESH:C536195] (55)
 Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)
 Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152)
 Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)
 Epidermolysis Bullosa [MESH:D004820] (260) 
 Nephropathy with Pretibial Epidermolysis Bullosa and Deafness [MESH:C563798] (43)
 Stomatognathic System Abnormalities [MESH:D018640] (1705) 
 Maxillofacial Abnormalities [MESH:D019767] (1447) 
 Jaw Abnormalities [MESH:D007569] (1438) 
 Cleft Palate [MESH:D002972] (1330)
 Micrognathism [MESH:D008844] (230) 
 Meier-Gorlin syndrome [MESH:C538012] (133)
 Mouth Abnormalities [MESH:D009056] (1383) 
 Cleft Lip [MESH:D002971] (914)
 Cleft Palate [MESH:D002972] (1330)
 Tooth Abnormalities [MESH:D014071] (622) 
 Tooth Agenesis, Selective, 6 [MESH:C567755] (19)
 Urogenital Abnormalities [MESH:D014564] (2064) 
 Cryptorchidism [MESH:D003456] (215) 
 Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)
 Disorders of Sex Development [MESH:D012734] (1637) 
 46, XX Disorders of Sex Development [MESH:D058489] (644) 
 Aromatase deficiency [MESH:C537436] (277)
 Gonadal Dysgenesis, 46,XX [MESH:D023961] (56)
 46, XY Disorders of Sex Development [MESH:D058490] (1060) 
 Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)
 Leydig Cell Hypoplasia [MESH:C562567] (65)
 Androgen-Insensitivity Syndrome [MESH:D013734] (567)
 Gonadal Dysgenesis, 46,XY [MESH:D006061] (131)
 Adrenogenital Syndrome [MESH:D047808] (715) 
 Adrenal Hyperplasia, Congenital [MESH:D000312] (674) 
 Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)
 Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223)
 Gonadal Dysgenesis [MESH:D006059] (492) 
 Gonadal Dysgenesis, 46,XX [MESH:D023961] (56)
 Gonadal Dysgenesis, 46,XY [MESH:D006061] (131)
 Sexual Infantilism [MESH:D050035] (277)
 Hypospadias [MESH:D007021] (798) 
 Hypospadias 1, X-Linked [MESH:C567482] (571)
 Fetal Diseases [MESH:D005315] (1205) 
 Fetal Growth Retardation [MESH:D005317] (986)
 Genetic Diseases, Inborn [MESH:D030342] (9766) 
 Costello Syndrome [MESH:D056685] (407)
 Adrenal Hyperplasia, Congenital [MESH:D000312] (674) 
 Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)
 Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223)
 Anemia, Hemolytic, Congenital [MESH:D000745] (2001) 
 Anemia, Dyserythropoietic, Congenital [MESH:D000742] (81)
 Spherocytosis, Hereditary [MESH:D013103] (137) 
 Spherocytosis, Type 1 [MESH:C567159] (21)
 Thalassemia [MESH:D013789] (501) 
 alpha-Thalassemia [MESH:D017085] (176) 
 ATR-X syndrome [MESH:C538258] (59)
 Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)
 Anemia, Hypoplastic, Congenital [MESH:D029502] (1665) 
 Fanconi Anemia [MESH:D005199] (1604)
 Blood Coagulation Disorders, Inherited [MESH:D025861] (722) 
 Activated Protein C Resistance [MESH:D020016] (140)
 Antithrombin III Deficiency [MESH:D020152] (80)
 Hypoprothrombinemias [MESH:D007020] (157)
 Hermanski-Pudlak Syndrome [MESH:D022861] (82) 
 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)
 Protein C Deficiency [MESH:D020151] (70) 
 Congenital thrombotic disease, due to Protein C deficiency [MESH:C535424] (66)
 Chromosome Disorders [MESH:D025063] (2030) 
 Mosaic variegated aneuploidy syndrome [MESH:C536987] (95)
 De Lange Syndrome [MESH:D003635] (55)
 Prader-Willi Syndrome [MESH:D011218] (46)
 22q11 Deletion Syndrome [MESH:D058165] (237) 
 DiGeorge Syndrome [MESH:D004062] (236)
 Sex Chromosome Disorders [MESH:D025064] (479) 
 Fragile X Syndrome [MESH:D005600] (353)
 Eye Diseases, Hereditary [MESH:D015785] (1867) 
 Basal Laminar Drusen [MESH:C563034] (52)
 Albinism [MESH:D000417] (359) 
 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)
 Albinism, Oculocutaneous [MESH:D016115] (234) 
 Oculocutaneous albinism type 3 [MESH:C537731] (40)
 Hermanski-Pudlak Syndrome [MESH:D022861] (82) 
 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)
 Piebaldism [MESH:D016116] (167) 
 Griscelli syndrome type 2 [MESH:C537302] (30)
 Corneal Dystrophies, Hereditary [MESH:D003317] (341) 
 Corneal Dystrophy, Posterior Polymorphous, 3 [MESH:C563788] (60)
 Fuchs' Endothelial Dystrophy [MESH:D005642] (86) 
 Corneal Dystrophy, Fuchs Endothelial, 6 [MESH:C567675] (60)
 Genetic Diseases, X-Linked [MESH:D040181] (3028) 
 Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)
 Premature Ovarian Failure 2a [MESH:C564498] (15)
 Hypospadias 1, X-Linked [MESH:C567482] (571)
 Androgen-Insensitivity Syndrome [MESH:D013734] (567)
 Muscular Dystrophy, Emery-Dreifuss [MESH:D020389] (169)
 Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566) 
 Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)
 Granulomatous Disease, Chronic [MESH:D006105] (404) 
 Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative [MESH:C565533] (111)
 Mental Retardation, X-Linked [MESH:D038901] (1867) 
 Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)
 ATR-X syndrome [MESH:C538258] (59)
 Fragile X Syndrome [MESH:D005600] (353)
 Mucopolysaccharidosis II [MESH:D016532] (26)
 Hemoglobinopathies [MESH:D006453] (1863) 
 Thalassemia [MESH:D013789] (511) 
 alpha-Thalassemia [MESH:D017085] (192) 
 ATR-X syndrome [MESH:C538258] (59)
 Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)
 Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465) 
 Hepatolenticular Degeneration [MESH:D006527] (473)
 Mental Retardation, X-Linked [MESH:D038901] (1848) 
 Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)
 ATR-X syndrome [MESH:C538258] (59)
 Fragile X Syndrome [MESH:D005600] (353)
 Mucopolysaccharidosis II [MESH:D016532] (26)
 Metabolism, Inborn Errors [MESH:D008661] (6032) 
 Aromatase deficiency [MESH:C537436] (277)
 3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency [MESH:C567784] (102)
 Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565) 
 Alpha-ketoglutarate dehydrogenase deficiency [MESH:C536582] (59)
 Methylmalonic acidemia [MESH:C537358] (764)
 Beta-Hydroxyisobutyryl CoA Deacylase Deficiency [MESH:C562803] (33)
 Albinism [MESH:D000417] (359) 
 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)
 Albinism, Oculocutaneous [MESH:D016115] (234) 
 Oculocutaneous albinism type 3 [MESH:C537731] (40)
 Hermanski-Pudlak Syndrome [MESH:D022861] (82) 
 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)
 Piebaldism [MESH:D016116] (167) 
 Griscelli syndrome type 2 [MESH:C537302] (30)
 Multiple Carboxylase Deficiency [MESH:D009100] (51) 
 Biotinidase Deficiency [MESH:D028921] (31)
 Urea Cycle Disorders, Inborn [MESH:D056806] (315) 
 Citrullinemia [MESH:D020159] (99)
 Amyloidosis, Familial [MESH:D028226] (696) 
 Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634) 
 Hepatolenticular Degeneration [MESH:D006527] (473)
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636) 
 Sphingolipidoses [MESH:D013106] (582) 
 Gaucher Disease [MESH:D005776] (299)
 Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)
 Urea Cycle Disorders, Inborn [MESH:D056806] (315) 
 Citrullinemia [MESH:D020159] (99)
 Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100) 
 Mucopolysaccharidoses [MESH:D009083] (164) 
 Mucopolysaccharidosis II [MESH:D016532] (26)
 Multiple Carboxylase Deficiency [MESH:D009100] (51) 
 Biotinidase Deficiency [MESH:D028921] (31)
 Lipid Metabolism, Inborn Errors [MESH:D008052] (2071) 
 Desmosterolosis [MESH:C566555] (85)
 Hyperlipoproteinemia Type II [MESH:D006938] (707)
 Hyperlipoproteinemia Type III [MESH:D006952] (181)
 Lipidoses [MESH:D008064] (1655) 
 Sphingolipidoses [MESH:D013106] (582) 
 Gaucher Disease [MESH:D005776] (299)
 Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)
 Lipodystrophy, Congenital Generalized [MESH:D052497] (168) 
 Lipodystrophy, Congenital Generalized, Type 4 [MESH:C567642] (38)
 Lysosomal Storage Diseases [MESH:D016464] (761) 
 Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636) 
 Sphingolipidoses [MESH:D013106] (582) 
 Gaucher Disease [MESH:D005776] (299)
 Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)
 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) 
 Hypophosphatemic Rickets, Autosomal Recessive, 2 [MESH:C567647] (48)
 Renal Tubular Transport, Inborn Errors [MESH:D015499] (1027) 
 Pseudohypoaldosteronism [MESH:D011546] (232)
 Hypophosphatemia, Familial [MESH:D007015] (276) 
 Familial Hypophosphatemic Rickets [MESH:D053098] (274) 
 Hypophosphatemic Rickets, Autosomal Recessive, 2 [MESH:C567647] (48)
 Steroid Metabolism, Inborn Errors [MESH:D043202] (962) 
 Adrenal Hyperplasia, Congenital [MESH:D000312] (674) 
 Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)
 Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223)
 Muscular Dystrophies [MESH:D009136] (1597) 
 Bethlem myopathy [MESH:C535436] (108)
 Scleroatonic muscular dystrophy [MESH:C537521] (108)
 Muscular Dystrophy, Emery-Dreifuss [MESH:D020389] (169)
 Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)
 Muscular Dystrophies, Limb-Girdle [MESH:D049288] (259) 
 Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57)
 Muscular Dystrophy, Limb-Girdle, Type 2G [MESH:C566599] (13)
 Neoplastic Syndromes, Hereditary [MESH:D009386] (2578) 
 Juvenile polyposis syndrome [MESH:C537702] (196)
 Adenomatous Polyposis Coli [MESH:D011125] (1565)
 Osteogenesis Imperfecta [MESH:D010013] (481) 
 Osteogenesis imperfecta, type 2A [MESH:C536042] (375)
 Osteogenesis imperfecta, type 3 [MESH:C536044] (375)
 Osteogenesis imperfecta, type 4 [MESH:C536045] (375)
 Bruck syndrome 2 [MESH:C537407] (64)
 Osteogenesis Imperfecta, Type IX [MESH:C564921] (46)
 Skin Diseases, Genetic [MESH:D012873] (3456) 
 Albinism [MESH:D000417] (359) 
 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)
 Albinism, Oculocutaneous [MESH:D016115] (234) 
 Oculocutaneous albinism type 3 [MESH:C537731] (40)
 Hermanski-Pudlak Syndrome [MESH:D022861] (82) 
 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)
 Piebaldism [MESH:D016116] (167) 
 Griscelli syndrome type 2 [MESH:C537302] (30)
 Ectodermal Dysplasia [MESH:D004476] (958) 
 Cardiofaciocutaneous syndrome [MESH:C535579] (407)
 Neurocutaneous Syndromes [MESH:D020752] (39) 
 Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome [MESH:C537943] (28)
 Ehlers-Danlos Syndrome [MESH:D004535] (491) 
 Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)
 Ehlers-Danlos syndrome type 2 [MESH:C536195] (55)
 Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)
 Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152)
 Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)
 Epidermolysis Bullosa [MESH:D004820] (259) 
 Nephropathy with Pretibial Epidermolysis Bullosa and Deafness [MESH:C563798] (43)
 Keratoderma, Palmoplantar [MESH:D007645] (287) 
 Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome [MESH:C537943] (28)
 Porokeratosis [MESH:D017499] (59) 
 Porokeratosis, disseminated superficial actinic 1 [MESH:C536339] (52)
 Infant, Newborn, Diseases [MESH:D007232] (3064) 
 Hyperostosis, Cortical, Congenital [MESH:D006958] (392)
C17. Skin and Connective Tissue Diseases 
C17. Skin and Connective Tissue Diseases
 Connective Tissue Diseases [MESH:D003240] (4490) 
 Lupus Erythematosus, Systemic [MESH:D008180] (2317)
 Scleroderma, Systemic [MESH:D012595] (199)
 Collagen Diseases [MESH:D003095] (1267) 
 Keloid [MESH:D007627] (1111)
 Ehlers-Danlos Syndrome [MESH:D004535] (491) 
 Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)
 Ehlers-Danlos syndrome type 2 [MESH:C536195] (55)
 Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)
 Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152)
 Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)
 Osteogenesis Imperfecta [MESH:D010013] (481) 
 Osteogenesis imperfecta, type 2A [MESH:C536042] (375)
 Osteogenesis imperfecta, type 3 [MESH:C536044] (375)
 Osteogenesis imperfecta, type 4 [MESH:C536045] (375)
 Bruck syndrome 2 [MESH:C537407] (64)
 Osteogenesis Imperfecta, Type IX [MESH:C564921] (46)
 Mucinoses [MESH:D017520] (177) 
 Mucopolysaccharidoses [MESH:D009083] (164) 
 Mucopolysaccharidosis II [MESH:D016532] (26)
 Noonan Syndrome [MESH:D009634] (506) 
 Noonan syndrome 3 [MESH:C537847] (118)
 Noonan Syndrome 4 [MESH:C548082] (37)
 Rheumatic Diseases [MESH:D012216] (3619) 
 Arthritis, Rheumatoid [MESH:D001172] (3603)
 Skin Diseases [MESH:D012871] (8774) 
 Exanthema [MESH:D005076] (301)
 Nephrogenic Fibrosing Dermopathy [MESH:D054989] (452)
 Scleroderma, Systemic [MESH:D012595] (199)
 Skin Neoplasms [MESH:D012878] (2991)
 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)
 Gynecomastia [MESH:D006177] (484) 
 Aromatase deficiency [MESH:C537436] (277)
 Lactation Disorders [MESH:D007775] (235) 
 Galactorrhea [MESH:D005687] (233)
 Dermatitis [MESH:D003872] (4530) 
 Dermatitis, Contact [MESH:D003877] (3394) 
 Dermatitis, Allergic Contact [MESH:D017449] (3241)
 Drug Eruptions [MESH:D003875] (2697) 
 Stevens-Johnson Syndrome [MESH:D013262] (1163)
 Erythema [MESH:D004890] (1330) 
 Erythema Multiforme [MESH:D004892] (1185) 
 Stevens-Johnson Syndrome [MESH:D013262] (1163)
 Facial Dermatoses [MESH:D005148] (1336) 
 Acneiform Eruptions [MESH:D017486] (1312) 
 Chloracne [MESH:D054506] (1274)
 Hair Diseases [MESH:D006201] (1891) 
 Hypotrichosis [MESH:D007039] (1513) 
 Hypotrichosis simplex [MESH:C537160] (92)
 Alopecia [MESH:D000505] (1453)
 Keratosis [MESH:D007642] (1941) 
 Keratoderma, Palmoplantar [MESH:D007645] (287) 
 Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome [MESH:C537943] (28)
 Porokeratosis [MESH:D017499] (59) 
 Porokeratosis, disseminated superficial actinic 1 [MESH:C536339] (52)
 Pigmentation Disorders [MESH:D010859] (1215) 
 Hypopigmentation [MESH:D017496] (718) 
 Albinism [MESH:D000417] (359) 
 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)
 Albinism, Oculocutaneous [MESH:D016115] (234) 
 Oculocutaneous albinism type 3 [MESH:C537731] (40)
 Hermanski-Pudlak Syndrome [MESH:D022861] (82) 
 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)
 Piebaldism [MESH:D016116] (167) 
 Griscelli syndrome type 2 [MESH:C537302] (30)
 Skin Abnormalities [MESH:D012868] (1709) 
 Ectodermal Dysplasia [MESH:D004476] (958) 
 Cardiofaciocutaneous syndrome [MESH:C535579] (407)
 Neurocutaneous Syndromes [MESH:D020752] (39) 
 Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome [MESH:C537943] (28)
 Ehlers-Danlos Syndrome [MESH:D004535] (491) 
 Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)
 Ehlers-Danlos syndrome type 2 [MESH:C536195] (55)
 Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)
 Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152)
 Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)
 Epidermolysis Bullosa [MESH:D004820] (260) 
 Nephropathy with Pretibial Epidermolysis Bullosa and Deafness [MESH:C563798] (43)
 Skin Diseases, Eczematous [MESH:D017443] (3740) 
 Dermatitis, Contact [MESH:D003877] (3394) 
 Dermatitis, Allergic Contact [MESH:D017449] (3241)
 Skin Diseases, Genetic [MESH:D012873] (3481) 
 Albinism [MESH:D000417] (359) 
 Albinism, Oculocutaneous [MESH:D016115] (234) 
 Oculocutaneous albinism type 3 [MESH:C537731] (40)
 Hermanski-Pudlak Syndrome [MESH:D022861] (82) 
 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)
 Piebaldism [MESH:D016116] (167) 
 Griscelli syndrome type 2 [MESH:C537302] (30)
 Ectodermal Dysplasia [MESH:D004476] (958) 
 Cardiofaciocutaneous syndrome [MESH:C535579] (407)
 Neurocutaneous Syndromes [MESH:D020752] (39) 
 Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome [MESH:C537943] (28)
 Ehlers-Danlos Syndrome [MESH:D004535] (491) 
 Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)
 Ehlers-Danlos syndrome type 2 [MESH:C536195] (55)
 Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)
 Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152)
 Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)
 Epidermolysis Bullosa [MESH:D004820] (260) 
 Nephropathy with Pretibial Epidermolysis Bullosa and Deafness [MESH:C563798] (43)
 Keratoderma, Palmoplantar [MESH:D007645] (287) 
 Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome [MESH:C537943] (28)
 Porokeratosis [MESH:D017499] (59) 
 Porokeratosis, disseminated superficial actinic 1 [MESH:C536339] (52)
 Skin Diseases, Infectious [MESH:D012874] (2684) 
 Dermatomycoses [MESH:D003881] (267) 
 Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224)
 Skin Diseases, Metabolic [MESH:D012875] (1574) 
 Lipodystrophy [MESH:D008060] (930) 
 Lipodystrophy, Congenital Generalized [MESH:D052497] (168) 
 Lipodystrophy, Congenital Generalized, Type 4 [MESH:C567642] (38)
 Skin Diseases, Papulosquamous [MESH:D017444] (3392) 
 Psoriasis [MESH:D011565] (3278) 
 Arthritis, Psoriatic [MESH:D015535] (1859)
 Skin Diseases, Vascular [MESH:D017445] (3288) 
 Behcet Syndrome [MESH:D001528] (1784)
 Mucocutaneous Lymph Node Syndrome [MESH:D009080] (158)
 Urticaria [MESH:D014581] (2668) 
 Angioedema [MESH:D000799] (837)
 Skin Diseases, Vesiculobullous [MESH:D012872] (1754) 
 Epidermolysis Bullosa [MESH:D004820] (260) 
 Nephropathy with Pretibial Epidermolysis Bullosa and Deafness [MESH:C563798] (43)
 Erythema Multiforme [MESH:D004892] (1185) 
 Stevens-Johnson Syndrome [MESH:D013262] (1163)
C18. Nutritional and Metabolic Diseases 
C18. Nutritional and Metabolic Diseases
 Metabolic Diseases [MESH:D008659] (9025) 
 Acid-Base Imbalance [MESH:D000137] (854) 
 Acidosis [MESH:D000138] (626) 
 Acidosis, Lactic [MESH:D000140] (204) 
 Pyruvate dehydrogenase phosphatase deficiency [MESH:C536258] (40)
 Brain Diseases, Metabolic [MESH:D001928] (3350) 
 Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634) 
 Hepatolenticular Degeneration [MESH:D006527] (473)
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636) 
 Sphingolipidoses [MESH:D013106] (582) 
 Gaucher Disease [MESH:D005776] (299)
 Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)
 Urea Cycle Disorders, Inborn [MESH:D056806] (315) 
 Citrullinemia [MESH:D020159] (99)
 Calcium Metabolism Disorders [MESH:D002128] (3634) 
 Calcinosis [MESH:D002114] (2989) 
 Aortic Valve, Calcification of [MESH:C562942] (655)
 Vascular Calcification [MESH:D061205] (138) 
 Arterial calcification of infancy [MESH:C537440] (48)
 Rickets [MESH:D012279] (341) 
 Rickets, Hypophosphatemic [MESH:D063730] (276) 
 Familial Hypophosphatemic Rickets [MESH:D053098] (274) 
 Hypophosphatemic Rickets, Autosomal Recessive, 2 [MESH:C567647] (48)
 DNA Repair-Deficiency Disorders [MESH:D049914] (2245) 
 Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)
 Fanconi Anemia [MESH:D005199] (1604)
 Glucose Metabolism Disorders [MESH:D044882] (6122) 
 Diabetes Mellitus [MESH:D003920] (5891) 
 Diabetes Mellitus, Experimental [MESH:D003921] (4771)
 Diabetes Mellitus, Type 1 [MESH:D003922] (1897)
 Diabetes Mellitus, Type 2 [MESH:D003924] (4219)
 Diabetes, Gestational [MESH:D016640] (1152)
 Hyperglycemia [MESH:D006943] (1858) 
 Glucose Intolerance [MESH:D018149] (605)
 Hyperinsulinism [MESH:D006946] (3586) 
 Insulin Resistance [MESH:D007333] (3511)
 Hypoglycemia [MESH:D007003] (2420) 
 3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency [MESH:C567784] (102)
 Lipid Metabolism Disorders [MESH:D052439] (3225) 
 Dyslipidemias [MESH:D050171] (2428) 
 Hyperlipidemias [MESH:D006949] (1908) 
 Hypercholesterolemia [MESH:D006937] (1404)
 Hyperlipoproteinemias [MESH:D006951] (903) 
 Hyperlipoproteinemia Type II [MESH:D006938] (707)
 Hyperlipoproteinemia Type III [MESH:D006952] (181)
 Lipid Metabolism, Inborn Errors [MESH:D008052] (461) 
 Desmosterolosis [MESH:C566555] (85)
 Lipodystrophy [MESH:D008060] (930) 
 Lipodystrophy, Congenital Generalized [MESH:D052497] (168) 
 Lipodystrophy, Congenital Generalized, Type 4 [MESH:C567642] (38)
 Lipidoses [MESH:D008064] (1655) 
 Sphingolipidoses [MESH:D013106] (582) 
 Gaucher Disease [MESH:D005776] (299)
 Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)
 Malabsorption Syndromes [MESH:D008286] (1869) 
 Celiac Disease [MESH:D002446] (340)
 Metabolism, Inborn Errors [MESH:D008661] (6028) 
 Aromatase deficiency [MESH:C537436] (277)
 3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency [MESH:C567784] (102)
 Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559) 
 Alpha-ketoglutarate dehydrogenase deficiency [MESH:C536582] (59)
 Methylmalonic acidemia [MESH:C537358] (764)
 Beta-Hydroxyisobutyryl CoA Deacylase Deficiency [MESH:C562803] (33)
 Albinism [MESH:D000417] (359) 
 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)
 Albinism, Oculocutaneous [MESH:D016115] (234) 
 Oculocutaneous albinism type 3 [MESH:C537731] (40)
 Hermanski-Pudlak Syndrome [MESH:D022861] (82) 
 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)
 Piebaldism [MESH:D016116] (167) 
 Griscelli syndrome type 2 [MESH:C537302] (30)
 Multiple Carboxylase Deficiency [MESH:D009100] (51) 
 Biotinidase Deficiency [MESH:D028921] (31)
 Urea Cycle Disorders, Inborn [MESH:D056806] (315) 
 Citrullinemia [MESH:D020159] (99)
 Amyloidosis, Familial [MESH:D028226] (696) 
 Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634) 
 Hepatolenticular Degeneration [MESH:D006527] (473)
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636) 
 Sphingolipidoses [MESH:D013106] (582) 
 Gaucher Disease [MESH:D005776] (299)
 Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)
 Urea Cycle Disorders, Inborn [MESH:D056806] (315) 
 Citrullinemia [MESH:D020159] (99)
 Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100) 
 Mucopolysaccharidoses [MESH:D009083] (164) 
 Mucopolysaccharidosis II [MESH:D016532] (26)
 Multiple Carboxylase Deficiency [MESH:D009100] (51) 
 Biotinidase Deficiency [MESH:D028921] (31)
 Lipid Metabolism, Inborn Errors [MESH:D008052] (2071) 
 Desmosterolosis [MESH:C566555] (85)
 Hyperlipoproteinemia Type II [MESH:D006938] (707)
 Hyperlipoproteinemia Type III [MESH:D006952] (181)
 Lipidoses [MESH:D008064] (1655) 
 Sphingolipidoses [MESH:D013106] (582) 
 Gaucher Disease [MESH:D005776] (299)
 Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)
 Lipodystrophy, Congenital Generalized [MESH:D052497] (168) 
 Lipodystrophy, Congenital Generalized, Type 4 [MESH:C567642] (38)
 Lysosomal Storage Diseases [MESH:D016464] (761) 
 Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636) 
 Sphingolipidoses [MESH:D013106] (582) 
 Gaucher Disease [MESH:D005776] (299)
 Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)
 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) 
 Hypophosphatemic Rickets, Autosomal Recessive, 2 [MESH:C567647] (48)
 Renal Tubular Transport, Inborn Errors [MESH:D015499] (1026) 
 Pseudohypoaldosteronism [MESH:D011546] (232)
 Hypophosphatemia, Familial [MESH:D007015] (276) 
 Familial Hypophosphatemic Rickets [MESH:D053098] (274) 
 Hypophosphatemic Rickets, Autosomal Recessive, 2 [MESH:C567647] (48)
 Steroid Metabolism, Inborn Errors [MESH:D043202] (962) 
 Adrenal Hyperplasia, Congenital [MESH:D000312] (674) 
 Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)
 Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223)
 Mitochondrial Diseases [MESH:D028361] (2561) 
 3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency [MESH:C567784] (102)
 Phosphorus Metabolism Disorders [MESH:D010760] (711) 
 Hypophosphatemia [MESH:D017674] (640) 
 Hypophosphatemia, Familial [MESH:D007015] (276) 
 Familial Hypophosphatemic Rickets [MESH:D053098] (274) 
 Hypophosphatemic Rickets, Autosomal Recessive, 2 [MESH:C567647] (48)
 Rickets, Hypophosphatemic [MESH:D063730] (276) 
 Familial Hypophosphatemic Rickets [MESH:D053098] (274) 
 Hypophosphatemic Rickets, Autosomal Recessive, 2 [MESH:C567647] (48)
 Proteostasis Deficiencies [MESH:D057165] (3522) 
 Amyloidosis [MESH:D000686] (791) 
 Amyloidosis, Familial [MESH:D028226] (696) 
 Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 Cerebral Amyloid Angiopathy [MESH:D016657] (470) 
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 TDP-43 Proteinopathies [MESH:D057177] (3337) 
 Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)
 Frontotemporal Lobar Degeneration [MESH:D057174] (308) 
 Frontotemporal Dementia [MESH:D057180] (298) 
 Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57)
 Skin Diseases, Metabolic [MESH:D012875] (1574) 
 Lipodystrophy [MESH:D008060] (930) 
 Lipodystrophy, Congenital Generalized [MESH:D052497] (168) 
 Lipodystrophy, Congenital Generalized, Type 4 [MESH:C567642] (38)
 Wasting Syndrome [MESH:D019282] (1959) 
 HIV Wasting Syndrome [MESH:D019247] (1956)
 Water-Electrolyte Imbalance [MESH:D014883] (2790) 
 Hyperkalemia [MESH:D006947] (485)
 Nutrition Disorders [MESH:D009748] (4945) 
 Malnutrition [MESH:D044342] (2754) 
 Deficiency Diseases [MESH:D003677] (2742) 
 Avitaminosis [MESH:D001361] (2304) 
 Vitamin D Deficiency [MESH:D014808] (360) 
 Rickets [MESH:D012279] (341) 
 Rickets, Hypophosphatemic [MESH:D063730] (276) 
 Familial Hypophosphatemic Rickets [MESH:D053098] (274) 
 Hypophosphatemic Rickets, Autosomal Recessive, 2 [MESH:C567647] (48)
 Overnutrition [MESH:D044343] (4463) 
 Obesity [MESH:D009765] (4462) 
 Prader-Willi Syndrome [MESH:D011218] (46)
 Wasting Syndrome [MESH:D019282] (1959) 
 HIV Wasting Syndrome [MESH:D019247] (1956)
C19. Endocrine System Diseases 
C19. Endocrine System Diseases
 Endocrine System Diseases [MESH:D004700] (8062) 
 Adrenal Gland Diseases [MESH:D000307] (2397) 
 Adrenal Insufficiency [MESH:D000309] (1599)
 Adrenal Hyperplasia, Congenital [MESH:D000312] (674) 
 Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)
 Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223)
 Diabetes Mellitus [MESH:D003920] (6159) 
 Diabetes, Gestational [MESH:D016640] (1152)
 Diabetes Mellitus, Experimental [MESH:D003921] (4771)
 Diabetes Mellitus, Type 1 [MESH:D003922] (1897)
 Diabetes Mellitus, Type 2 [MESH:D003924] (4219)
 Diabetes Complications [MESH:D048909] (4129) 
 Diabetic Cardiomyopathies [MESH:D058065] (1995)
 Diabetic Nephropathies [MESH:D003928] (2301)
 Endocrine Gland Neoplasms [MESH:D004701] (4925) 
 Ovarian Neoplasms [MESH:D010051] (3275)
 Thyroid Neoplasms [MESH:D013964] (2040)
 Pancreatic Neoplasms [MESH:D010190] (3820) 
 Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)
 Pituitary Neoplasms [MESH:D010911] (981) 
 Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)
 Prolactinoma [MESH:D015175] (312)
 Testicular Neoplasms [MESH:D013736] (520) 
 Sertoli-Leydig Cell Tumor [MESH:D018310] (272) 
 Leydig Cell Tumor [MESH:D007984] (267)
 Gonadal Disorders [MESH:D006058] (5088) 
 Puberty, Delayed [MESH:D011628] (449)
 Disorders of Sex Development [MESH:D012734] (1637) 
 46, XX Disorders of Sex Development [MESH:D058489] (644) 
 Aromatase deficiency [MESH:C537436] (277)
 Gonadal Dysgenesis, 46,XX [MESH:D023961] (56)
 46, XY Disorders of Sex Development [MESH:D058490] (1060) 
 Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)
 Leydig Cell Hypoplasia [MESH:C562567] (65)
 Androgen-Insensitivity Syndrome [MESH:D013734] (567)
 Gonadal Dysgenesis, 46,XY [MESH:D006061] (131)
 Adrenogenital Syndrome [MESH:D047808] (715) 
 Adrenal Hyperplasia, Congenital [MESH:D000312] (674) 
 Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)
 Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223)
 Gonadal Dysgenesis [MESH:D006059] (492) 
 Gonadal Dysgenesis, 46,XX [MESH:D023961] (56)
 Gonadal Dysgenesis, 46,XY [MESH:D006061] (131)
 Sexual Infantilism [MESH:D050035] (277)
 Hypogonadism [MESH:D007006] (1123) 
 Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)
 Sexual Infantilism [MESH:D050035] (277)
 Ovarian Diseases [MESH:D010049] (4253) 
 Ovarian Neoplasms [MESH:D010051] (3281)
 Ovarian Cysts [MESH:D010048] (2534) 
 Polycystic Ovary Syndrome [MESH:D011085] (2186)
 Primary Ovarian Insufficiency [MESH:D016649] (270) 
 Premature Ovarian Failure 2a [MESH:C564498] (15)
 Premature Ovarian Failure 7 [MESH:C567838] (52)
 Puberty, Precocious [MESH:D011629] (1147) 
 Familial Testotoxicosis [MESH:C536961] (65)
 Testicular Diseases [MESH:D013733] (777) 
 Cryptorchidism [MESH:D003456] (215) 
 Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)
 Testicular Neoplasms [MESH:D013736] (520) 
 Sertoli-Leydig Cell Tumor [MESH:D018310] (272) 
 Leydig Cell Tumor [MESH:D007984] (267)
 Parathyroid Diseases [MESH:D010279] (1604) 
 Hypoparathyroidism [MESH:D007011] (376) 
 22q11 Deletion Syndrome [MESH:D058165] (237) 
 DiGeorge Syndrome [MESH:D004062] (236)
 Pituitary Diseases [MESH:D010900] (1829) 
 Hypopituitarism [MESH:D007018] (732)
 Hyperpituitarism [MESH:D006964] (1259) 
 Acromegaly [MESH:D000172] (466)
 Hyperprolactinemia [MESH:D006966] (603)
 Pituitary Neoplasms [MESH:D010911] (981) 
 Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)
 Prolactinoma [MESH:D015175] (312)
 Thyroid Diseases [MESH:D013959] (2808) 
 Thyroid Neoplasms [MESH:D013964] (2040)
 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) 
 Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)
 Autoimmune Diseases [MESH:D001327] (5067) 
 Arthritis, Rheumatoid [MESH:D001172] (3601)
 Diabetes Mellitus, Type 1 [MESH:D003922] (1893)
 Glomerulonephritis, IGA [MESH:D005922] (897)
 Glomerulonephritis, Membranous [MESH:D015433] (642)
 Lupus Erythematosus, Systemic [MESH:D008180] (2317)
 Autoimmune Diseases of the Nervous System [MESH:D020274] (2238) 
 Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732) 
 Multiple Sclerosis [MESH:D009103] (1716) 
 Multiple Sclerosis, Relapsing-Remitting [MESH:D020529] (170)
 Graves Disease [MESH:D006111] (278) 
 Graves Ophthalmopathy [MESH:D049970] (165)
 Hypersensitivity [MESH:D006967] (5873) 
 Immune Complex Diseases [MESH:D007105] (782)
 Drug Hypersensitivity [MESH:D004342] (4000) 
 Drug Eruptions [MESH:D003875] (2695) 
 Stevens-Johnson Syndrome [MESH:D013262] (1163)
 Hypersensitivity, Delayed [MESH:D006968] (3408) 
 Dermatitis, Allergic Contact [MESH:D017449] (3241)
 Hypersensitivity, Immediate [MESH:D006969] (4980) 
 Respiratory Hypersensitivity [MESH:D012130] (4250) 
 Asthma [MESH:D001249] (3914)
 Urticaria [MESH:D014581] (2668) 
 Angioedema [MESH:D000799] (837)
 Immunologic Deficiency Syndromes [MESH:D007153] (3788) 
 Hepatic venoocclusive disease with immunodeficiency [MESH:C537257] (23)
 Griscelli syndrome type 2 [MESH:C537302] (30)
 HIV Infections [MESH:D015658] (3402) 
 HIV Wasting Syndrome [MESH:D019247] (1956)
 Phagocyte Bactericidal Dysfunction [MESH:D010585] (999) 
 Granulomatous Disease, Chronic [MESH:D006105] (404) 
 Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative [MESH:C565533] (111)
 Immunoproliferative Disorders [MESH:D007160] (4761) 
 Lymphoproliferative Disorders [MESH:D008232] (4734) 
 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 T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)
 Lymphoma [MESH:D008223] (3684) 
 Lymphoma, Non-Hodgkin [MESH:D008228] (3330) 
 Lymphoma, Mantle-Cell [MESH:D020522] (561)
 Lymphoma, B-Cell [MESH:D016393] (2624) 
 Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)
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)
 Bird Diseases [MESH:D001715] (67) 
 Influenza in Birds [MESH:D005585] (53)
 Poultry Diseases [MESH:D011201] (58) 
 Influenza in Birds [MESH:D005585] (53)
C23. Pathological Conditions, Signs and Symptoms 
C23. Pathological Conditions, Signs and Symptoms
 Pathological Conditions, Anatomical [MESH:D020763] (6074) 
 Alopecia [MESH:D000505] (1383)
 Plaque, Amyloid [MESH:D058225] (334)
 Plaque, Atherosclerotic [MESH:D058226] (696)
 Agenesis of Corpus Callosum [MESH:D061085] (197) 
 Chudley-Mccullough syndrome [MESH:C535459] (45)
 Atrophy [MESH:D001284] (2603) 
 Muscular Atrophy [MESH:D009133] (1234)
 Hernia [MESH:D006547] (2825) 
 Hernia, Diaphragmatic [MESH:D006548] (2647) 
 Congenital diaphragmatic hernia [MESH:C538080] (381)
 Intervertebral Disc Displacement [MESH:D007405] (520) 
 Intervertebral disc disease [MESH:C535531] (514)
 Hypertrophy [MESH:D006984] (4476) 
 Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)
 Splenomegaly [MESH:D013163] (1258)
 Cardiomegaly [MESH:D006332] (3802) 
 Hypertrophy, Left Ventricular [MESH:D017379] (1430)
 Pathologic Processes [MESH:D010335] (9863) 
 Gliosis [MESH:D005911] (1419)
 Hyperplasia [MESH:D006965] (2463)
 Arrhythmias, Cardiac [MESH:D001145] (4658) 
 Atrial Fibrillation [MESH:D001281] (1053)
 Bradycardia [MESH:D001919] (1899)
 Tachycardia [MESH:D013610] (3339)
 Chromosome Aberrations [MESH:D002869] (2352) 
 Micronuclei, Chromosome-Defective [MESH:D048629] (1013)
 Death [MESH:D003643] (1328) 
 Fetal Death [MESH:D005313] (464) 
 Fetal Resorption [MESH:D005327] (302)
 Disease Attributes [MESH:D020969] (3654) 
 Critical Illness [MESH:D016638] (296)
 Disease Progression [MESH:D018450] (2868)
 Disease Susceptibility [MESH:D004198] (1200) 
 Genetic Predisposition to Disease [MESH:D020022] (966)
 Facies [MESH:D019066] (738) 
 Cardiofaciocutaneous syndrome [MESH:C535579] (407)
 Pitt-Hopkins syndrome [MESH:C537403] (113)
 Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)
 Fibrosis [MESH:D005355] (3133) 
 Nephrogenic Fibrosing Dermopathy [MESH:D054989] (452)
 Cicatrix [MESH:D002921] (1115) 
 Keloid [MESH:D007627] (1110)
 Granuloma [MESH:D006099] (587) 
 Granuloma, Plasma Cell [MESH:D006104] (58)
 Growth Disorders [MESH:D006130] (2438) 
 Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)
 Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)
 Meier-Gorlin syndrome [MESH:C538012] (133)
 Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)
 Insulin-Like Growth Factor I, Resistance To [MESH:C564816] (141)
 Spondyloepimetaphyseal Dysplasia, Pakistani Type [MESH:C567551] (63)
 Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)
 Fetal Growth Retardation [MESH:D005317] (986)
 Hemorrhage [MESH:D006470] (4451) 
 Intracranial Hemorrhages [MESH:D020300] (3241) 
 Subarachnoid Hemorrhage [MESH:D013345] (1081)
 Cerebral Hemorrhage [MESH:D002543] (2872) 
 Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)
 Purpura [MESH:D011693] (475) 
 Purpura Fulminans [MESH:D055665] (69)
 Inflammation [MESH:D007249] (5241) 
 Neurogenic Inflammation [MESH:D020078] (2246)
 Systemic Inflammatory Response Syndrome [MESH:D018746] (3563) 
 Sepsis [MESH:D018805] (3562) 
 Shock, Septic [MESH:D012772] (1830)
 Bacteremia [MESH:D016470] (1369) 
 Endotoxemia [MESH:D019446] (1289)
 Ischemia [MESH:D007511] (3049) 
 Infarction [MESH:D007238] (298)
 Menstruation Disturbances [MESH:D008599] (926) 
 Amenorrhea [MESH:D000568] (817)
 Oligomenorrhea [MESH:D009839] (228)
 Metaplasia [MESH:D008679] (1469) 
 Neovascularization, Pathologic [MESH:D009389] (829)
 Necrosis [MESH:D009336] (4019) 
 Infarction [MESH:D007238] (298)
 Neoplastic Processes [MESH:D009385] (5317) 
 Anaplasia [MESH:D000708] (348)
 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)
 Nerve Degeneration [MESH:D009410] (4061) 
 Striatal Degeneration, Autosomal Dominant [MESH:C563783] (21)
 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)
 Shock [MESH:D012769] (2550) 
 Systemic Inflammatory Response Syndrome [MESH:D018746] (1832) 
 Shock, Septic [MESH:D012772] (1830)
 Signs and Symptoms [MESH:D012816] (10659) 
 Edema [MESH:D004487] (3726)
 Feminization [MESH:D005262] (655)
 Body Temperature Changes [MESH:D001832] (3130) 
 Fever [MESH:D005334] (2856)
 Hypothermia [MESH:D007035] (2075)
 Body Weight [MESH:D001835] (4972) 
 Birth Weight [MESH:D001724] (377)
 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)
 Neurobehavioral Manifestations [MESH:D019954] (4706) 
 Communication Disorders [MESH:D003147] (2918) 
 Learning Disorders [MESH:D007859] (2727)
 Language Disorders [MESH:D007806] (653) 
 Speech Disorders [MESH:D013064] (482) 
 Articulation Disorders [MESH:D001184] (164) 
 Dysarthria [MESH:D004401] (163)
 Memory Disorders [MESH:D008569] (3233) 
 Amnesia [MESH:D000647] (1911)
 Intellectual Disability [MESH:D008607] (1476) 
 Pitt-Hopkins syndrome [MESH:C537403] (113)
 Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)
 Neuromuscular Manifestations [MESH:D020879] (2130) 
 Muscular Atrophy [MESH:D009133] (1234)
 Muscle Hypertonia [MESH:D009122] (775) 
 Muscle Rigidity [MESH:D009127] (617)
 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) 
 Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)
 Hearing Loss, Sensorineural [MESH:D006319] (1227) 
 Chudley-Mccullough syndrome [MESH:C535459] (45)
 Nephropathy with Pretibial Epidermolysis Bullosa and Deafness [MESH:C563798] (43)
 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, Respiratory [MESH:D012818] (2724) 
 Hyperventilation [MESH:D006985] (652) 
 Pitt-Hopkins syndrome [MESH:C537403] (113)
 Skin Manifestations [MESH:D012877] (1250) 
 Purpura [MESH:D011693] (475) 
 Purpura Fulminans [MESH:D055665] (69)
 Urological Manifestations [MESH:D020924] (3532) 
 Oliguria [MESH:D009846] (307)
 Proteinuria [MESH:D011507] (3293)
C24. Occupational Diseases 
C24. Occupational Diseases
 Occupational Diseases [MESH:D009784] (3402) 
 Pneumoconiosis [MESH:D011009] (2670) 
 Asbestosis [MESH:D001195] (935)
 Silicosis [MESH:D012829] (1273)
C25. Chemically-Induced Disorders 
C25. Chemically-Induced Disorders
 Drug-Related Side Effects and Adverse Reactions [MESH:D064420] (5839) 
 Drug-Induced Liver Injury [MESH:D056486] (4936)
 Drug Hypersensitivity [MESH:D004342] (4001) 
 Drug Eruptions [MESH:D003875] (2697) 
 Stevens-Johnson Syndrome [MESH:D013262] (1163)
 Poisoning [MESH:D011041] (6703) 
 Arsenic Poisoning [MESH:D020261] (2540)
 Drug-Induced Liver Injury [MESH:D056486] (4936)
 Manganese Poisoning [MESH:D020149] (2214)
 Mercury Poisoning [MESH:D008630] (193)
 Neurotoxicity Syndromes [MESH:D020258] (3323)
 Psychoses, Substance-Induced [MESH:D011605] (2053)
 Substance-Related Disorders [MESH:D019966] (6308) 
 Amphetamine-Related Disorders [MESH:D019969] (2858)
 Cocaine-Related Disorders [MESH:D019970] (3054)
 Marijuana Abuse [MESH:D002189] (1132)
 Opioid-Related Disorders [MESH:D009293] (1491)
 Phencyclidine Abuse [MESH:D010623] (288)
 Psychoses, Substance-Induced [MESH:D011605] (2052)
 Substance Withdrawal Syndrome [MESH:D013375] (2956)
 Alcohol-Related Disorders [MESH:D019973] (3869) 
 Alcoholism [MESH:D000437] (1519)
 Alcohol-Induced Disorders [MESH:D020751] (3350) 
 Liver Diseases, Alcoholic [MESH:D008108] (3243) 
 Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)
C26. Wounds and Injuries 
C26. Wounds and Injuries
 Wounds and Injuries [MESH:D014947] (5171) 
 Burns [MESH:D002056] (2565)
 Craniocerebral Trauma [MESH:D006259] (3523) 
 Brain Injuries [MESH:D001930] (3431)
 Radiation Injuries [MESH:D011832] (2718) 
 Radiation Injuries, Experimental [MESH:D011833] (2662)
 Trauma, Nervous System [MESH:D020196] (3535) 
 Craniocerebral Trauma [MESH:D006259] (3507) 
 Brain Injuries [MESH:D001930] (3431)
D04. Polycyclic Compounds 
D04. Polycyclic Compounds
 Polycyclic Compounds [MESH:D011083] (22048) 
 Steroids [MESH:D013256] (6272) 
 Androstanes [MESH:D000731] (757) 
 Androstenes [MESH:D000736] (507) 
 Androstenols [MESH:D000737] (258) 
 Testosterone [MESH:D013739] (118)
D06. Hormones, Hormone Substitutes, and Hormone Antagonists 
D06. Hormones, Hormone Substitutes, and Hormone Antagonists
 Hormones [MESH:D006728] (4254) 
 Gonadal Hormones [MESH:D042341] (1226) 
 Gonadal Steroid Hormones [MESH:D012739] (1172) 
 Testosterone Congeners [MESH:D045165] (359) 
 Testosterone [MESH:D013739] (91)
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)
 Pitt-Hopkins syndrome [MESH:C537403] (113)
 Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)
F. Psychiatry and Psychology 
F. Psychiatry and Psychology
 Behavior and Behavior Mechanisms [MESH:D001520] (1594) 
 Neurobehavioral Manifestations [MESH:D019954] (1206) 
 Intellectual Disability [MESH:D008607] (1109) 
 Pitt-Hopkins syndrome [MESH:C537403] (113)
 Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)
 Mental Disorders [MESH:D001523] (2063) 
 Delirium, Dementia, Amnestic, Cognitive Disorders [MESH:D019965] (487) 
 Dementia [MESH:D003704] (471) 
 Alzheimer Disease [MESH:D000544] (242) 
 Alzheimer disease type 2 [MESH:C536595] (165)
 Frontotemporal Lobar Degeneration [MESH:D057174] (112) 
 Frontotemporal Dementia [MESH:D057180] (109) 
 Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57)
 Lewy Body Disease [MESH:D020961] (139) 
 Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)
 Mental Disorders Diagnosed in Childhood [MESH:D019952] (1245) 
 Intellectual Disability [MESH:D008607] (1109) 
 Pitt-Hopkins syndrome [MESH:C537403] (113)
 Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)
 Sexual and Gender Disorders [MESH:D019968] (624) 
 Disorders of Sex Development [MESH:D012734] (609) 
 46, XX Disorders of Sex Development [MESH:D058489] (375) 
 Aromatase deficiency [MESH:C537436] (277)
 46, XY Disorders of Sex Development [MESH:D058490] (388) 
 Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)
 Leydig Cell Hypoplasia [MESH:C562567] (65)
G. Phenomena and Processes 
G. Phenomena and Processes
 Genetic Phenomena [MESH:D055614] (1922) 
 Genetic Variation [MESH:D014644] (1337) 
 Mutation [MESH:D009154] (1327) 
 Chromosome Aberrations [MESH:D002869] (1297) 
 Mosaicism [MESH:D009030] (116) 
 Mosaic variegated aneuploidy syndrome [MESH:C536987] (95)