more general categories |
information about this item |
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1. Human Genes |
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1. Human Genes |
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A kinase (PRKA) anchor protein 13 [HGNC:AKAP13] (18) |
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ezrin [HGNC:EZR] (32) |
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aldo-keto reductase family 1, member C1 [HGNC:AKR1C1] (148) |
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aldo-keto reductase family 1, member C2 [HGNC:AKR1C2] (134) |
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aldo-keto reductase family 1, member C3 [HGNC:AKR1C3] (128) |
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karyopherin (importin) beta 1 [HGNC:KPNB1] (20) |
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origin recognition complex, subunit 4 [HGNC:ORC4] (8) |
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valosin containing protein [HGNC:VCP] (19) |
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ATPase, aminophospholipid transporter, class I, type 8B, member 1 [HGNC:ATP8B1] (25) |
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ATP-binding cassette, sub-family A (ABC1), member 07 [HGNC:ABCA7] (7) |
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nuclear receptor coactivator 3 [HGNC:NCOA3] (42) |
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transcription factor 04 [HGNC:TCF4] (38) |
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UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 4 [HGNC:B4GALT4] (7) |
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carboxylesterase 2 [HGNC:CES2] (55) |
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cathepsin S [HGNC:CTSS] (14) |
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chemokine (C-C motif) receptor 01 [HGNC:CCR1] (21) |
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endoglin [HGNC:ENG] (11) |
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Fc fragment of IgG, low affinity IIa, receptor (CD032) [HGNC:FCGR2A] (4) |
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integrin, alpha V [HGNC:ITGAV] (33) |
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interleukin 06 receptor [HGNC:IL6R] (55) |
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interleukin 06 signal transducer (gp130, oncostatin M receptor) [HGNC:IL6ST] (38) |
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interleukin 10 receptor, beta [HGNC:IL10RB] (17) |
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toll-like receptor 3 [HGNC:TLR3] (27) |
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tumor necrosis factor (ligand) superfamily, member 10 [HGNC:TNFSF10] (155) |
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chemokine (C-C motif) receptor 01 [HGNC:CCR1] (21) |
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chloride channel, voltage-sensitive 3 [HGNC:CLCN3] (19) |
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chloride intracellular channel 4 [HGNC:CLIC4] (19) |
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collagen, type I, alpha 1 [HGNC:COL1A1] (123) |
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collagen, type I, alpha 2 [HGNC:COL1A2] (43) |
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collagen, type III, alpha 1 [HGNC:COL3A1] (33) |
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collagen, type IV, alpha 2 [HGNC:COL4A2] (26) |
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collagen, type V, alpha 1 [HGNC:COL5A1] (17) |
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collagen, type V, alpha 2 [HGNC:COL5A2] (22) |
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collagen, type VI, alpha 1 [HGNC:COL6A1] (28) |
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collagen, type VI, alpha 2 [HGNC:COL6A2] (21) |
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complement factor H [HGNC:CFH] (9) |
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cyclin-dependent kinase 01 [HGNC:CDK1] (151) |
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cytochrome b-245, alpha polypeptide [HGNC:CYBA] (40) |
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cytochrome P450, family 11, subfamily A, polypeptide 01 [HGNC:CYP11A1] (65) |
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cytochrome P450, family 17, subfamily A, polypeptide 01 [HGNC:CYP17A1] (88) |
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parvalbumin [HGNC:PVALB] (3) |
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chorionic gonadotropin, beta polypeptide [HGNC:CGB] (67) |
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coagulation factor II (thrombin) [HGNC:F2] (95) |
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follicle stimulating hormone, beta polypeptide [HGNC:FSHB] (68) |
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insulin-like 3 (Leydig cell) [HGNC:INSL3] (12) |
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endothelin receptor type A [HGNC:EDNRA] (31) |
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endothelin receptor type B [HGNC:EDNRB] (35) |
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ephrin-B2 [HGNC:EFNB2] (32) |
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Fanconi anemia, complementation group C [HGNC:FANCC] (22) |
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stearoyl-CoA desaturase (delta-9-desaturase) [HGNC:SCD] (78) |
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interleukin 06 signal transducer (gp130, oncostatin M receptor) [HGNC:IL6ST] (38) |
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protein tyrosine phosphatase, receptor type, D [HGNC:PTPRD] (6) |
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EGF containing fibulin-like extracellular matrix protein 2 [HGNC:EFEMP2] (10) |
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F-box protein 40 [HGNC:FBXO40] (2) |
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glutathione S-transferase alpha 2 [HGNC:GSTA2] (44) |
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glutathione S-transferase mu 1 [HGNC:GSTM1] (144) |
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UDP-glucose ceramide glucosyltransferase [HGNC:UGCG] (46) |
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angiogenic factor with G patch and FHA domains 1 [HGNC:AGGF1] (5) |
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heat shock 70kDa protein 01B [HGNC:HSPA1B] (65) |
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heat shock 70kDa protein 04 [HGNC:HSPA4] (49) |
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DnaJ (Hsp40) homolog, subfamily C, member 07 [HGNC:DNAJC7] (8) |
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heat shock protein 90kDa beta (Grp94), member 1 [HGNC:HSP90B1] (53) |
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major histocompatibility complex, class II, DP alpha 1 [HGNC:HLA-DPA1] (13) |
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major histocompatibility complex, class II, DQ alpha 1 [HGNC:HLA-DQA1] (8) |
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major histocompatibility complex, class II, DQ beta 1 [HGNC:HLA-DQB1] (16) |
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prospero homeobox 1 [HGNC:PROX1] (17) |
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zinc finger E-box binding homeobox 1 [HGNC:ZEB1] (33) |
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major histocompatibility complex, class II, DP alpha 1 [HGNC:HLA-DPA1] (13) |
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major histocompatibility complex, class II, DQ alpha 1 [HGNC:HLA-DQA1] (8) |
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major histocompatibility complex, class II, DQ beta 1 [HGNC:HLA-DQB1] (16) |
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palladin, cytoskeletal associated protein [HGNC:PALLD] (22) |
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peroxidasin homolog (Drosophila) [HGNC:PXDN] (12) |
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protein tyrosine phosphatase, receptor type, D [HGNC:PTPRD] (6) |
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Fc fragment of IgG, low affinity IIa, receptor (CD032) [HGNC:FCGR2A] (4) |
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interleukin 06 receptor [HGNC:IL6R] (55) |
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karyopherin (importin) beta 1 [HGNC:KPNB1] (20) |
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integrin, alpha V [HGNC:ITGAV] (33) |
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interleukin 06 receptor [HGNC:IL6R] (55) |
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interleukin 06 signal transducer (gp130, oncostatin M receptor) [HGNC:IL6ST] (38) |
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interleukin 10 receptor, beta [HGNC:IL10RB] (17) |
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nestin [HGNC:NES] (21) |
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nuclear receptor coactivator 3 [HGNC:NCOA3] (42) |
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lysine (K)-specific demethylase 6A [HGNC:KDM6A] (10) |
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lysine (K)-specific methyltransferase 2A [HGNC:KMT2A] (22) |
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latent transforming growth factor beta binding protein 3 [HGNC:LTBP3] (3) |
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lysophosphatidic acid receptor 6 [HGNC:LPAR6] (9) |
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mitochondrial ribosomal protein S06 [HGNC:MRPS6] (22) |
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myosin, heavy chain 03, skeletal muscle, embryonic [HGNC:MYH3] (6) |
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myosin, heavy chain 11, smooth muscle [HGNC:MYH11] (7) |
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RAR-related orphan receptor A [HGNC:RORA] (22) |
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retinoid X receptor, beta [HGNC:RXRB] (31) |
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synuclein, alpha (non A4 component of amyloid precursor) [HGNC:SNCA] (71) |
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chromodomain helicase DNA binding protein 4 [HGNC:CHD4] (7) |
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lysine (K)-specific methyltransferase 2A [HGNC:KMT2A] (22) |
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A kinase (PRKA) anchor protein 13 [HGNC:AKAP13] (18) |
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pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 [HGNC:PLEKHA1] (9) |
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son of sevenless homolog 1 (Drosophila) [HGNC:SOS1] (27) |
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proteasome (prosome, macropain) activator subunit 4 [HGNC:PSME4] (19) |
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protein phosphatase 1, regulatory subunit 03A [HGNC:PPP1R3A] (1) |
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pyruvate dehyrogenase phosphatase catalytic subunit 1 [HGNC:PDP1] (19) |
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CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) phosphatase, subunit 1 [HGNC:CTDP1] (5) |
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protein tyrosine phosphatase, receptor type, D [HGNC:PTPRD] (6) |
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asporin [HGNC:ASPN] (3) |
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lumican [HGNC:LUM] (17) |
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structural maintenance of chromosomes 3 [HGNC:SMC3] (17) |
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RAB27A, member RAS oncogene family [HGNC:RAB27A] (8) |
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A kinase (PRKA) anchor protein 13 [HGNC:AKAP13] (18) |
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son of sevenless homolog 1 (Drosophila) [HGNC:SOS1] (27) |
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heterogeneous nuclear ribonucleoprotein R [HGNC:HNRNPR] (8) |
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polypyrimidine tract binding protein 1 [HGNC:PTBP1] (13) |
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squamous cell carcinoma antigen recognized by T cells 3 [HGNC:SART3] (10) |
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transformer 2 alpha homolog (Drosophila) [HGNC:TRA2A] (22) |
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neuralized homolog (Drosophila) [HGNC:NEURL] (3) |
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frizzled-related protein [HGNC:FRZB] (16) |
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hemopoietic cell kinase [HGNC:HCK] (20) |
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signal transducer and activator of transcription 1, 91kDa [HGNC:STAT1] (108) |
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hydroxysteroid (17-beta) dehydrogenase 06 [HGNC:HSD17B6] (15) |
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HIV-1 Tat interactive protein 2, 30kDa [HGNC:HTATIP2] (22) |
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SMAD family member 4 [HGNC:SMAD4] (22) |
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solute carrier family 16 (monocarboxylate transporter), member 7 [HGNC:SLC16A7] (14) |
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solute carrier family 35 (UDP-GlcA/UDP-GalNAc transporter), member D1 [HGNC:SLC35D1] (10) |
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SRY (sex determining region Y)-box 04 [HGNC:SOX4] (39) |
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steroidogenic acute regulatory protein [HGNC:STAR] (57) |
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structural maintenance of chromosomes 2 [HGNC:SMC2] (25) |
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structural maintenance of chromosomes 3 [HGNC:SMC3] (17) |
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T-box 01 [HGNC:TBX1] (7) |
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DnaJ (Hsp40) homolog, subfamily C, member 07 [HGNC:DNAJC7] (8) |
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FK506 binding protein 05 [HGNC:FKBP5] (46) |
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G-protein signaling modulator 2 [HGNC:GPSM2] (27) |
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interferon-induced protein with tetratricopeptide repeats 3 [HGNC:IFIT3] (35) |
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lysine (K)-specific demethylase 6A [HGNC:KDM6A] (10) |
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RAN binding protein 2 [HGNC:RANBP2] (16) |
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tetratricopeptide repeat domain 09 [HGNC:TTC9] (10) |
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tumor necrosis factor (ligand) superfamily, member 10 [HGNC:TNFSF10] (155) |
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ubiquitin specific peptidase 02 [HGNC:USP2] (7) |
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Fas associated factor family member 2 [HGNC:FAF2] (5) |
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guanine nucleotide binding protein (G protein), beta polypeptide 1 [HGNC:GNB1] (14) |
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WD repeat domain 46 [HGNC:WDR46] (7) |
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human immunodeficiency virus type I enhancer binding protein 2 [HGNC:HIVEP2] (23) |
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zinc finger E-box binding homeobox 1 [HGNC:ZEB1] (33) |
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RUN and FYVE domain containing 3 [HGNC:RUFY3] (11) |
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2. Interaction: Human Genes and Chemicals |
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2. Interaction: Human Genes and Chemicals |
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cotreatment (1499) |
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expression (494) |
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expression (2187) |
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reaction (3393) |
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response to substance (713) |
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abundance (630) |
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activity (2865) |
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expression (3238) |
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hydrolysis (158) |
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metabolic processing (740) |
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phosphorylation (1060) |
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A. Anatomy |
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A. Anatomy |
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Meier-Gorlin syndrome [MESH:C538012] (133) |
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Meier-Gorlin syndrome [MESH:C538012] (133) |
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Leydig Cell Hypoplasia [MESH:C562567] (65) |
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Leydig Cell Hypoplasia [MESH:C562567] (65) |
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Leydig Cell Hypoplasia [MESH:C562567] (65) |
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Aortic Valve, Calcification of [MESH:C562942] (655) |
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Striatal Degeneration, Autosomal Dominant [MESH:C563783] (21) |
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Meier-Gorlin syndrome [MESH:C538012] (133) |
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Basal Laminar Drusen [MESH:C563034] (52) |
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Basal Laminar Drusen [MESH:C563034] (52) |
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Basal Laminar Drusen [MESH:C563034] (52) |
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C01. Bacterial Infections and Mycoses |
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C01. Bacterial Infections and Mycoses |
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Mycoplasma Infections [MESH:D009175] (1947) |
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Meningococcal Infections [MESH:D008589] (242) |
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Mycobacterium Infections, Nontuberculous [MESH:D009165] (480) |
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Paratuberculosis [MESH:D010283] (427) |
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Urinary Tract Infections [MESH:D014552] (984) |
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Peritonitis [MESH:D010538] (800) |
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Shock, Septic [MESH:D012772] (1830) |
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Endotoxemia [MESH:D019446] (1289) |
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Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224) |
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Endotoxemia [MESH:D019446] (1289) |
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Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224) |
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Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224) |
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C02. Virus Diseases |
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C02. Virus Diseases |
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Encephalitis, Herpes Simplex [MESH:D020803] (72) |
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Hepatitis B, Chronic [MESH:D019694] (277) |
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Cytomegalovirus Infections [MESH:D003586] (222) |
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Encephalitis, Herpes Simplex [MESH:D020803] (72) |
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Encephalitis, Herpes Simplex [MESH:D020803] (72) |
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Hepatitis C [MESH:D006526] (1627) |
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Hepatitis B, Chronic [MESH:D019694] (277) |
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Hepatitis C [MESH:D006526] (1627) |
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Influenza, Human [MESH:D007251] (1075) |
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Influenza in Birds [MESH:D005585] (53) |
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HIV Wasting Syndrome [MESH:D019247] (1956) |
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HIV Wasting Syndrome [MESH:D019247] (1956) |
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C03. Parasitic Diseases |
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C03. Parasitic Diseases |
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Liver Diseases, Parasitic [MESH:D008109] (1009) |
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Schistosomiasis mansoni [MESH:D012555] (1033) |
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Malaria [MESH:D008288] (2175) |
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Leishmaniasis, Visceral [MESH:D007898] (2149) |
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C04. Neoplasms |
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C04. Neoplasms |
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Neoplasms, Second Primary [MESH:D016609] (518) |
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Precancerous Conditions [MESH:D011230] (2858) |
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Follicular Cyst [MESH:D005497] (151) |
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Chudley-Mccullough syndrome [MESH:C535459] (45) |
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Polycystic Ovary Syndrome [MESH:D011085] (2186) |
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Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
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Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510) |
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Leukemia, Myelomonocytic, Acute [MESH:D015479] (85) |
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Leukemia, Monocytic, Acute [MESH:D007948] (98) |
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Leukemia, Promyelocytic, Acute [MESH:D015473] (1367) |
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Lymphoma, Mantle-Cell [MESH:D020522] (561) |
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Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) |
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Osteosarcoma [MESH:D012516] (2175) |
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Leiomyoma [MESH:D007889] (744) |
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Rhabdomyosarcoma [MESH:D012208] (789) |
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Hemangiosarcoma [MESH:D006394] (1836) |
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Osteosarcoma [MESH:D012516] (2175) |
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Rhabdomyosarcoma [MESH:D012208] (789) |
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Glioblastoma [MESH:D005909] (2554) |
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Neuroblastoma [MESH:D009447] (1420) |
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Uveal melanoma [MESH:C536494] (109) |
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Pheochromocytoma [MESH:D010673] (275) |
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Adenoma, Liver Cell [MESH:D018248] (685) |
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Adenoma, Oxyphilic [MESH:D018249] (115) |
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Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383) |
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Mesothelioma [MESH:D008654] (2567) |
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Prolactinoma [MESH:D015175] (312) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Carcinoma, Transitional Cell [MESH:D002295] (2662) |
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Adenocarcinoma of lung [MESH:C538231] (1487) |
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Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
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Carcinoma, Adenoid Cystic [MESH:D003528] (1561) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Carcinoma, Intraductal, Noninfiltrating [MESH:D002285] (500) |
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Carcinoma, Renal Cell [MESH:D002292] (2975) |
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Cholangiocarcinoma [MESH:D018281] (2398) |
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Carcinoma, Ductal, Breast [MESH:D018270] (1112) |
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Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
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Prostatic Intraepithelial Neoplasia [MESH:D019048] (1565) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Carcinoma, Intraductal, Noninfiltrating [MESH:D002285] (500) |
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Carcinoma, Ductal, Breast [MESH:D018270] (1112) |
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Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
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Mesothelioma [MESH:D008654] (2567) |
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Glioblastoma [MESH:D005909] (2554) |
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Neuroblastoma [MESH:D009447] (1420) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Leydig Cell Tumor [MESH:D007984] (267) |
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Meningioma [MESH:D008579] (978) |
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Glioblastoma [MESH:D005909] (2554) |
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Neuroblastoma [MESH:D009447] (1420) |
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Uveal melanoma [MESH:C536494] (109) |
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Pheochromocytoma [MESH:D010673] (275) |
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Hemangiosarcoma [MESH:D006394] (1836) |
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Meningioma [MESH:D008579] (978) |
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Hemangioblastoma [MESH:D018325] (395) |
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Uveal melanoma [MESH:C536494] (109) |
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Nevus, Sebaceous of Jadassohn [MESH:D054000] (209) |
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Bone Neoplasms [MESH:D001859] (1334) |
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Skin Neoplasms [MESH:D012878] (2992) |
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Breast Neoplasms, Male [MESH:D018567] (650) |
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Carcinoma, Ductal, Breast [MESH:D018270] (1112) |
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|
|
|
Stomach Neoplasms [MESH:D013274] (4942) |
|
|
Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
|
|
Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
|
|
Cecal Neoplasms [MESH:D002430] (822) |
|
|
Adenomatous Polyposis Coli [MESH:D011125] (1565) |
|
|
Adenomatous Polyposis Coli [MESH:D011125] (1565) |
|
|
Adenoma, Liver Cell [MESH:D018248] (685) |
|
|
Carcinoma, Hepatocellular [MESH:D006528] (5375) |
|
|
Liver Neoplasms, Experimental [MESH:D008114] (2837) |
|
|
Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
|
|
Ovarian Neoplasms [MESH:D010051] (3275) |
|
|
Thyroid Neoplasms [MESH:D013964] (2040) |
|
|
Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
|
|
Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383) |
|
|
Prolactinoma [MESH:D015175] (312) |
|
|
|
|
|
Leydig Cell Tumor [MESH:D007984] (267) |
|
|
|
|
|
Uveal melanoma [MESH:C536494] (109) |
|
|
Thyroid Neoplasms [MESH:D013964] (2040) |
|
|
Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
|
|
Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
|
|
Salivary Gland Neoplasms [MESH:D012468] (968) |
|
|
|
|
|
Nasopharyngeal Neoplasms [MESH:D009303] (1500) |
|
|
Mammary Neoplasms, Experimental [MESH:D008325] (3268) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Pituitary Neoplasms [MESH:D010911] (914) |
|
|
|
|
|
Chudley-Mccullough syndrome [MESH:C535459] (45) |
|
|
Meningioma [MESH:D008579] (978) |
|
|
|
|
|
|
|
|
Adenocarcinoma of lung [MESH:C538231] (1487) |
|
|
|
|
|
Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
|
|
Small Cell Lung Carcinoma [MESH:D055752] (1380) |
|
|
|
|
|
|
|
|
Endometrial Neoplasms [MESH:D016889] (1987) |
|
|
Penile Neoplasms [MESH:D010412] (890) |
|
|
Prostatic Neoplasms [MESH:D011471] (6135) |
|
|
|
|
|
Leydig Cell Tumor [MESH:D007984] (267) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
Liver Neoplasms, Experimental [MESH:D008114] (2837) |
|
|
Mammary Neoplasms, Experimental [MESH:D008325] (3268) |
|
|
Anaplasia [MESH:D000708] (348) |
|
|
Neoplasm Invasiveness [MESH:D009361] (3388) |
|
|
Neoplasm Metastasis [MESH:D009362] (4441) |
|
|
Neoplasm Recurrence, Local [MESH:D009364] (1949) |
|
|
Cell Transformation, Neoplastic [MESH:D002471] (3389) |
|
|
Juvenile polyposis syndrome [MESH:C537702] (196) |
|
|
Adenomatous Polyposis Coli [MESH:D011125] (1565) |
|
 |
C05. Musculoskeletal Diseases |
 |
 |
|
C05. Musculoskeletal Diseases |
|
|
|
|
|
Bone Neoplasms [MESH:D001859] (1334) |
|
|
Bone Resorption [MESH:D001862] (2352) |
|
|
|
|
|
|
|
|
Freeman-Sheldon syndrome [MESH:C535483] (23) |
|
|
Mandibulofacial Dysostosis [MESH:D008342] (63) |
|
|
Schneckenbecken dysplasia [MESH:C536637] (22) |
|
|
Spondyloepimetaphyseal Dysplasia, Pakistani Type [MESH:C567551] (63) |
|
|
Hyperostosis, Cortical, Congenital [MESH:D006958] (392) |
|
|
Osteosclerosis [MESH:D010026] (356) |
|
|
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) |
|
|
Acromegaly [MESH:D000172] (466) |
|
|
Osteoporosis [MESH:D010024] (3037) |
|
|
|
|
|
|
|
|
Hypophosphatemic Rickets, Autosomal Recessive, 2 [MESH:C567647] (48) |
|
|
Hyperostosis, Cortical, Congenital [MESH:D006958] (392) |
|
|
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57) |
|
|
|
|
|
Intervertebral disc disease [MESH:C535531] (514) |
|
|
Intervertebral disc disease [MESH:C535531] (514) |
|
|
Ossification of the posterior longitudinal ligament of the spine [MESH:C537143] (98) |
|
|
Kyphosis [MESH:D007738] (637) |
|
|
|
|
|
|
|
|
Arthritis, Psoriatic [MESH:D015535] (1859) |
|
|
|
|
|
Growth mental deficiency syndrome of Myhre [MESH:C537620] (51) |
|
|
|
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
Meier-Gorlin syndrome [MESH:C538012] (133) |
|
|
Growth mental deficiency syndrome of Myhre [MESH:C537620] (51) |
|
|
Arthritis, Experimental [MESH:D001169] (3142) |
|
|
Arthritis, Psoriatic [MESH:D015535] (1859) |
|
|
Arthritis, Rheumatoid [MESH:D001172] (3603) |
|
|
Osteoarthritis [MESH:D010003] (1743) |
|
|
|
|
|
Arthritis, Psoriatic [MESH:D015535] (1859) |
|
|
Bruck syndrome 2 [MESH:C537407] (64) |
|
|
Distal arthrogryposis type 2B [MESH:C538400] (85) |
|
|
Bethlem myopathy [MESH:C535436] (108) |
|
|
Eosinophilia-Myalgia Syndrome [MESH:D016603] (31) |
|
|
Muscle Rigidity [MESH:D009127] (617) |
|
|
Bruck syndrome 2 [MESH:C537407] (64) |
|
|
Distal arthrogryposis type 2B [MESH:C538400] (85) |
|
|
Bethlem myopathy [MESH:C535436] (108) |
|
|
|
|
|
Bethlem myopathy [MESH:C535436] (108) |
|
|
Scleroatonic muscular dystrophy [MESH:C537521] (108) |
|
|
Muscular Dystrophy, Emery-Dreifuss [MESH:D020389] (169) |
|
|
Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854) |
|
|
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57) |
|
|
Muscular Dystrophy, Limb-Girdle, Type 2G [MESH:C566599] (13) |
|
|
Myosclerosis, Autosomal Recessive [MESH:C564968] (45) |
|
|
|
|
|
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57) |
|
|
|
|
|
Bruck syndrome 2 [MESH:C537407] (64) |
|
|
Distal arthrogryposis type 2B [MESH:C538400] (85) |
|
|
Congenital Cataracts, Facial Dysmorphism, And Neuropathy [MESH:C565822] (17) |
|
|
Costello Syndrome [MESH:D056685] (407) |
|
|
DiGeorge Syndrome [MESH:D004062] (236) |
|
|
Freeman-Sheldon syndrome [MESH:C535483] (23) |
|
|
Mandibulofacial Dysostosis [MESH:D008342] (63) |
|
|
|
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
Meier-Gorlin syndrome [MESH:C538012] (133) |
|
|
Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76) |
|
|
Noonan syndrome 3 [MESH:C537847] (118) |
|
|
Noonan Syndrome 4 [MESH:C548082] (37) |
|
|
Brachydactyly [MESH:D059327] (220) |
|
|
|
|
|
Growth mental deficiency syndrome of Myhre [MESH:C537620] (51) |
|
|
Arthritis, Rheumatoid [MESH:D001172] (3603) |
|
|
Osteoarthritis [MESH:D010003] (1743) |
|
 |
C06. Digestive System Diseases |
 |
 |
|
C06. Digestive System Diseases |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Cholestasis, progressive familial intrahepatic 1 [MESH:C535933] (263) |
|
|
Liver Cirrhosis, Biliary [MESH:D008105] (1274) |
|
|
Hirschsprung Disease [MESH:D006627] (361) |
|
|
|
|
|
Stomach Neoplasms [MESH:D013274] (4942) |
|
|
Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
|
|
Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
|
|
Cecal Neoplasms [MESH:D002430] (822) |
|
|
|
|
|
Adenomatous Polyposis Coli [MESH:D011125] (1565) |
|
|
Adenoma, Liver Cell [MESH:D018248] (685) |
|
|
Carcinoma, Hepatocellular [MESH:D006528] (5375) |
|
|
Liver Neoplasms, Experimental [MESH:D008114] (2837) |
|
|
Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
|
|
|
|
|
|
|
|
Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
|
|
Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
|
|
|
|
|
Colitis, Ulcerative [MESH:D003093] (2601) |
|
|
Enterocolitis, Necrotizing [MESH:D020345] (1367) |
|
|
Inflammatory Bowel Disease 25, Autosomal Recessive [MESH:C567251] (43) |
|
|
Colitis, Ulcerative [MESH:D003093] (2601) |
|
|
Crohn Disease [MESH:D003424] (2585) |
|
|
Stomach Neoplasms [MESH:D013274] (4942) |
|
|
Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
|
|
Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
|
|
Cecal Neoplasms [MESH:D002430] (822) |
|
|
|
|
|
Adenomatous Polyposis Coli [MESH:D011125] (1565) |
|
|
|
|
|
Cecal Neoplasms [MESH:D002430] (822) |
|
|
|
|
|
Colitis, Ulcerative [MESH:D003093] (2601) |
|
|
|
|
|
Adenomatous Polyposis Coli [MESH:D011125] (1565) |
|
|
Hirschsprung Disease [MESH:D006627] (361) |
|
|
|
|
|
Duodenal Ulcer [MESH:D004381] (1549) |
|
|
Enterocolitis, Necrotizing [MESH:D020345] (1367) |
|
|
Inflammatory Bowel Disease 25, Autosomal Recessive [MESH:C567251] (43) |
|
|
Colitis, Ulcerative [MESH:D003093] (2601) |
|
|
Crohn Disease [MESH:D003424] (2585) |
|
|
Cecal Neoplasms [MESH:D002430] (822) |
|
|
|
|
|
Adenomatous Polyposis Coli [MESH:D011125] (1565) |
|
|
Juvenile polyposis syndrome [MESH:C537702] (196) |
|
|
Adenomatous Polyposis Coli [MESH:D011125] (1565) |
|
|
Celiac Disease [MESH:D002446] (340) |
|
|
Colorectal Neoplasms [MESH:D015179] (4534) |
|
|
Duodenal Ulcer [MESH:D004381] (1549) |
|
|
Stomach Ulcer [MESH:D013276] (2915) |
|
|
Stomach Neoplasms [MESH:D013274] (4942) |
|
|
Stomach Ulcer [MESH:D013276] (2915) |
|
|
Drug-Induced Liver Injury [MESH:D056486] (4936) |
|
|
Hepatolenticular Degeneration [MESH:D006527] (473) |
|
|
Liver Diseases, Parasitic [MESH:D008109] (1009) |
|
|
Cholestasis, progressive familial intrahepatic 1 [MESH:C535933] (263) |
|
|
Liver Cirrhosis, Biliary [MESH:D008105] (1274) |
|
|
Non-alcoholic Fatty Liver Disease [MESH:C541083] (1567) |
|
|
|
|
|
Liver Failure, Acute [MESH:D017114] (2404) |
|
|
Hepatic venoocclusive disease with immunodeficiency [MESH:C537257] (23) |
|
|
|
|
|
Hepatitis B, Chronic [MESH:D019694] (277) |
|
|
Hepatitis C [MESH:D006526] (1627) |
|
|
Hepatitis B, Chronic [MESH:D019694] (277) |
|
|
Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
|
|
Liver Cirrhosis, Biliary [MESH:D008105] (1274) |
|
|
Liver Cirrhosis, Experimental [MESH:D008106] (4589) |
|
|
Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
|
|
Adenoma, Liver Cell [MESH:D018248] (685) |
|
|
Carcinoma, Hepatocellular [MESH:D006528] (5375) |
|
|
Liver Neoplasms, Experimental [MESH:D008114] (2837) |
|
|
|
|
|
Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
|
|
Peritonitis [MESH:D010538] (800) |
|
 |
C07. Stomatognathic Diseases |
 |
 |
|
C07. Stomatognathic Diseases |
|
|
|
|
|
|
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
Meier-Gorlin syndrome [MESH:C538012] (133) |
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
|
Oral Submucous Fibrosis [MESH:D009914] (2432) |
|
|
Cleft Lip [MESH:D002971] (914) |
|
|
Cleft Lip [MESH:D002971] (914) |
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
Salivary Gland Neoplasms [MESH:D012468] (968) |
|
|
Salivary Gland Neoplasms [MESH:D012468] (968) |
|
|
Stevens-Johnson Syndrome [MESH:D013262] (1163) |
|
|
|
|
|
Nasopharyngeal Neoplasms [MESH:D009303] (1500) |
|
|
Nasopharyngeal Neoplasms [MESH:D009303] (1500) |
|
|
|
|
|
|
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
Meier-Gorlin syndrome [MESH:C538012] (133) |
|
|
Cleft Lip [MESH:D002971] (914) |
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
Tooth Agenesis, Selective, 6 [MESH:C567755] (154) |
|
|
|
|
|
Tooth Agenesis, Selective, 6 [MESH:C567755] (154) |
|
 |
C08. Respiratory Tract Diseases |
 |
 |
|
C08. Respiratory Tract Diseases |
|
|
Thoracic Diseases [MESH:D013896] (81) |
|
|
Asthma [MESH:D001249] (4098) |
|
|
Hypertension, Pulmonary [MESH:D006976] (2000) |
|
|
Pulmonary Fibrosis [MESH:D011658] (3140) |
|
|
Respiratory Distress Syndrome, Adult [MESH:D012128] (864) |
|
|
|
|
|
Asbestosis [MESH:D001195] (935) |
|
|
Silicosis [MESH:D012829] (1273) |
|
|
Asthma [MESH:D001249] (3903) |
|
|
Pulmonary Disease, Chronic Obstructive [MESH:D029424] (3564) |
|
|
|
|
|
Asbestosis [MESH:D001195] (935) |
|
|
Silicosis [MESH:D012829] (1273) |
|
|
Adenocarcinoma of lung [MESH:C538231] (1487) |
|
|
Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
|
|
Small Cell Lung Carcinoma [MESH:D055752] (1380) |
|
|
Pneumonia, Aspiration [MESH:D011015] (824) |
|
|
Respiratory Distress Syndrome, Adult [MESH:D012128] (864) |
|
|
Respiratory Insufficiency [MESH:D012131] (841) |
|
|
|
|
|
Sleep Apnea, Obstructive [MESH:D020181] (126) |
|
|
Pitt-Hopkins syndrome [MESH:C537403] (113) |
|
|
Asthma [MESH:D001249] (4098) |
|
|
Influenza, Human [MESH:D007251] (1075) |
|
|
Pneumonia, Aspiration [MESH:D011015] (824) |
|
|
|
|
|
Adenocarcinoma of lung [MESH:C538231] (1487) |
|
|
|
|
|
Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
|
|
Small Cell Lung Carcinoma [MESH:D055752] (1380) |
|
 |
C09. Otorhinolaryngologic Diseases |
 |
 |
|
C09. Otorhinolaryngologic Diseases |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59) |
|
|
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) |
|
|
|
|
|
Nasopharyngeal Neoplasms [MESH:D009303] (1500) |
|
|
|
|
|
Nasopharyngeal Neoplasms [MESH:D009303] (1500) |
|
|
Nasopharyngeal Neoplasms [MESH:D009303] (1500) |
|
 |
C10. Nervous System Diseases |
 |
 |
|
C10. Nervous System Diseases |
|
|
Congenital Cataracts, Facial Dysmorphism, And Neuropathy [MESH:C565822] (17) |
|
|
Restless Legs Syndrome [MESH:D012148] (379) |
|
|
|
|
|
|
|
|
Multiple Sclerosis, Relapsing-Remitting [MESH:D020529] (170) |
|
|
|
|
|
Brain Edema [MESH:D001929] (1165) |
|
|
Brain Injuries [MESH:D001930] (3429) |
|
|
Hepatolenticular Degeneration [MESH:D006527] (473) |
|
|
|
|
|
Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136) |
|
|
Progressive supranuclear palsy atypical [MESH:C537240] (142) |
|
|
Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136) |
|
|
Progressive supranuclear palsy atypical [MESH:C537240] (142) |
|
|
|
|
|
Hepatolenticular Degeneration [MESH:D006527] (473) |
|
|
Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333) |
|
|
|
|
|
Gaucher Disease [MESH:D005776] (299) |
|
|
Sea-Blue Histiocyte Syndrome [MESH:D012618] (165) |
|
|
Citrullinemia [MESH:D020159] (99) |
|
|
|
|
|
|
|
|
Pituitary Neoplasms [MESH:D010911] (914) |
|
|
|
|
|
Ischemic Attack, Transient [MESH:D002546] (1313) |
|
|
Cerebral Infarction [MESH:D002544] (2458) |
|
|
Lateral Medullary Syndrome [MESH:D014854] (188) |
|
|
Carotid Stenosis [MESH:D016893] (174) |
|
|
|
|
|
Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333) |
|
|
|
|
|
|
|
|
|
|
|
Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333) |
|
|
|
|
|
|
|
|
Sagittal Sinus Thrombosis [MESH:D020225] (223) |
|
|
Subarachnoid Hemorrhage [MESH:D013345] (1082) |
|
|
Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333) |
|
|
|
|
|
Cerebral Infarction [MESH:D002544] (2458) |
|
|
Lateral Medullary Syndrome [MESH:D014854] (188) |
|
|
Creutzfeldt-Jakob Syndrome [MESH:D007562] (118) |
|
|
Alzheimer disease type 2 [MESH:C536595] (165) |
|
|
|
|
|
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57) |
|
|
Pick Disease of the Brain [MESH:D020774] (184) |
|
|
Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136) |
|
|
Seizures [MESH:D012640] (4502) |
|
|
Status Epilepticus [MESH:D013226] (4014) |
|
|
Epilepsy, Tonic-Clonic [MESH:D004830] (1042) |
|
|
|
|
|
|
|
|
Migraine without Aura [MESH:D020326] (408) |
|
|
|
|
|
Pituitary Neoplasms [MESH:D010911] (914) |
|
|
Hypopituitarism [MESH:D007018] (732) |
|
|
Acromegaly [MESH:D000172] (466) |
|
|
Hyperprolactinemia [MESH:D006966] (603) |
|
|
Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383) |
|
|
Prolactinoma [MESH:D015175] (312) |
|
|
|
|
|
|
|
|
|
|
|
Encephalitis, Herpes Simplex [MESH:D020803] (72) |
|
|
|
|
|
Encephalitis, Herpes Simplex [MESH:D020803] (72) |
|
|
Creutzfeldt-Jakob Syndrome [MESH:D007562] (118) |
|
|
Hepatolenticular Degeneration [MESH:D006527] (473) |
|
|
|
|
|
Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136) |
|
|
Progressive supranuclear palsy atypical [MESH:C537240] (142) |
|
|
Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136) |
|
|
Progressive supranuclear palsy atypical [MESH:C537240] (142) |
|
|
Amyotrophic Lateral Sclerosis [MESH:D000690] (3296) |
|
|
|
|
|
Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565) |
|
|
|
|
|
|
|
|
|
|
|
Progressive supranuclear palsy atypical [MESH:C537240] (142) |
|
|
|
|
|
|
|
|
Multiple Sclerosis, Relapsing-Remitting [MESH:D020529] (170) |
|
|
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|
|
Chudley-Mccullough syndrome [MESH:C535459] (45) |
|
|
|
|
|
Chudley-Mccullough syndrome [MESH:C535459] (45) |
|
|
|
|
|
Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Pituitary Neoplasms [MESH:D010911] (914) |
|
|
|
|
|
Chudley-Mccullough syndrome [MESH:C535459] (45) |
|
|
Meningioma [MESH:D008579] (978) |
|
|
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome [MESH:C537943] (28) |
|
|
Nevus, Sebaceous of Jadassohn [MESH:D054000] (209) |
|
|
|
|
|
Hepatolenticular Degeneration [MESH:D006527] (473) |
|
|
Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565) |
|
|
Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136) |
|
|
Amyotrophic Lateral Sclerosis [MESH:D000690] (3296) |
|
|
|
|
|
Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565) |
|
|
Progressive supranuclear palsy atypical [MESH:C537240] (142) |
|
|
Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136) |
|
|
|
|
|
Alzheimer disease type 2 [MESH:C536595] (165) |
|
|
Progressive supranuclear palsy atypical [MESH:C537240] (142) |
|
|
Amyotrophic Lateral Sclerosis [MESH:D000690] (3296) |
|
|
|
|
|
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57) |
|
|
Neurogenic Inflammation [MESH:D020078] (2246) |
|
|
Pain [MESH:D010146] (3875) |
|
|
Seizures [MESH:D012640] (4514) |
|
|
Catalepsy [MESH:D002375] (1429) |
|
|
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|
|
Learning Disorders [MESH:D007859] (2727) |
|
|
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|
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|
|
|
Dysarthria [MESH:D004401] (163) |
|
|
Amnesia [MESH:D000647] (1911) |
|
|
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-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) |
|
|
Muscular Atrophy [MESH:D009133] (1234) |
|
|
Muscle Rigidity [MESH:D009127] (617) |
|
|
|
|
|
|
|
|
Progressive supranuclear palsy atypical [MESH:C537240] (142) |
|
|
|
|
|
|
|
|
|
|
|
Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59) |
|
|
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) |
|
|
Hyperalgesia [MESH:D006930] (3929) |
|
|
Peripheral Nervous System Diseases [MESH:D010523] (6151) |
|
|
Amyotrophic Lateral Sclerosis [MESH:D000690] (3296) |
|
|
|
|
|
Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565) |
|
|
Eosinophilia-Myalgia Syndrome [MESH:D016603] (31) |
|
|
|
|
|
Bethlem myopathy [MESH:C535436] (108) |
|
|
Scleroatonic muscular dystrophy [MESH:C537521] (108) |
|
|
Muscular Dystrophy, Emery-Dreifuss [MESH:D020389] (169) |
|
|
Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854) |
|
|
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57) |
|
|
Muscular Dystrophy, Limb-Girdle, Type 2G [MESH:C566599] (13) |
|
|
Myosclerosis, Autosomal Recessive [MESH:C564968] (45) |
|
|
|
|
|
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57) |
|
|
|
|
|
Arsenic Poisoning [MESH:D020261] (2540) |
|
|
Manganese Poisoning [MESH:D020149] (2214) |
|
|
|
|
|
|
|
|
Restless Legs Syndrome [MESH:D012148] (379) |
|
|
Narcolepsy [MESH:D009290] (478) |
|
|
Sleep Apnea, Obstructive [MESH:D020181] (126) |
|
|
Restless Legs Syndrome [MESH:D012148] (379) |
|
|
|
|
|
Brain Injuries [MESH:D001930] (3431) |
|
 |
C11. Eye Diseases |
 |
 |
|
C11. Eye Diseases |
|
|
|
|
|
|
|
|
Corneal Dystrophy, Posterior Polymorphous, 3 [MESH:C563788] (60) |
|
|
Corneal Dystrophy, Fuchs Endothelial, 6 [MESH:C567675] (60) |
|
|
Basal Laminar Drusen [MESH:C563034] (52) |
|
|
Graves Ophthalmopathy [MESH:D049970] (165) |
|
|
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74) |
|
|
Oculocutaneous albinism type 3 [MESH:C537731] (40) |
|
|
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74) |
|
|
Corneal Dystrophy, Posterior Polymorphous, 3 [MESH:C563788] (60) |
|
|
Corneal Dystrophy, Fuchs Endothelial, 6 [MESH:C567675] (60) |
|
|
|
|
|
Uveal melanoma [MESH:C536494] (109) |
|
|
|
|
|
Congenital Cataracts, Facial Dysmorphism, And Neuropathy [MESH:C565822] (17) |
|
|
|
|
|
|
|
|
Progressive supranuclear palsy atypical [MESH:C537240] (142) |
|
|
|
|
|
|
|
|
Graves Ophthalmopathy [MESH:D049970] (165) |
|
|
|
|
|
|
|
|
Fundus Dystrophy, Pseudoinflammatory, Of Sorsby [MESH:C564992] (121) |
|
|
Macular Degeneration, Age-Related, 4 [MESH:C565196] (67) |
|
|
Macular Degeneration, Age-Related, 1 [MESH:C566411] (276) |
|
|
Basal Laminar Drusen [MESH:C563034] (52) |
|
|
|
|
|
Uveal melanoma [MESH:C536494] (109) |
|
|
|
|
|
|
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
 |
C12. Male Urogenital Diseases |
 |
 |
|
C12. Male Urogenital Diseases |
|
|
|
|
|
|
|
|
Penile Neoplasms [MESH:D010412] (890) |
|
|
Prostatic Neoplasms [MESH:D011471] (6135) |
|
|
|
|
|
Leydig Cell Tumor [MESH:D007984] (267) |
|
|
|
|
|
Aromatase deficiency [MESH:C537436] (277) |
|
|
Follicle-stimulating hormone deficiency, isolated [MESH:C537070] (185) |
|
|
Penile Neoplasms [MESH:D010412] (890) |
|
|
Hypospadias 1, X-Linked [MESH:C567482] (571) |
|
|
Prostatic Hyperplasia [MESH:D011470] (336) |
|
|
Prostatic Neoplasms [MESH:D011471] (6135) |
|
|
Erectile Dysfunction [MESH:D007172] (1791) |
|
|
|
|
|
Growth mental deficiency syndrome of Myhre [MESH:C537620] (51) |
|
|
|
|
|
Growth mental deficiency syndrome of Myhre [MESH:C537620] (51) |
|
|
|
|
|
Aromatase deficiency [MESH:C537436] (277) |
|
|
Gonadal Dysgenesis, 46,XX [MESH:D023961] (56) |
|
|
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) |
|
|
|
|
|
Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
|
|
Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223) |
|
|
Gonadal Dysgenesis, 46,XX [MESH:D023961] (56) |
|
|
Gonadal Dysgenesis, 46,XY [MESH:D006061] (131) |
|
|
Sexual Infantilism [MESH:D050035] (277) |
|
|
Hypospadias 1, X-Linked [MESH:C567482] (571) |
|
|
|
|
|
Penile Neoplasms [MESH:D010412] (890) |
|
|
Prostatic Neoplasms [MESH:D011471] (6135) |
|
|
|
|
|
Leydig Cell Tumor [MESH:D007984] (267) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
Urinary Tract Infections [MESH:D014552] (984) |
|
|
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) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
|
|
|
Glomerulonephritis, IGA [MESH:D005922] (897) |
|
|
Glomerulonephritis, Membranoproliferative [MESH:D015432] (770) |
|
|
Glomerulonephritis, Membranous [MESH:D015433] (642) |
|
|
Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754) |
|
|
Nephrotic Syndrome [MESH:D009404] (1536) |
|
|
Acute Kidney Injury [MESH:D058186] (4142) |
|
|
Kidney Failure, Chronic [MESH:D007676] (2930) |
|
|
Pseudohypoaldosteronism [MESH:D011546] (232) |
|
|
|
|
|
Hypophosphatemic Rickets, Autosomal Recessive, 2 [MESH:C567647] (48) |
|
|
|
|
|
Atypical hemolytic uremic syndrome [MESH:C538266] (277) |
|
|
Ureteral Obstruction [MESH:D014517] (575) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Oliguria [MESH:D009846] (307) |
|
|
Proteinuria [MESH:D011507] (3293) |
|
 |
C13. Female Urogenital Diseases and Pregnancy Complications |
 |
 |
|
C13. Female Urogenital Diseases and Pregnancy Complications |
|
|
Not Fully Specified [NFS] (1116) |
|
|
|
|
|
Endometriosis [MESH:D004715] (2461) |
|
|
Sexual Dysfunction, Physiological [MESH:D012735] (270) |
|
|
|
|
|
Ovarian Neoplasms [MESH:D010051] (3281) |
|
|
Polycystic Ovary Syndrome [MESH:D011085] (2186) |
|
|
Premature Ovarian Failure 2a [MESH:C564498] (15) |
|
|
Premature Ovarian Failure 7 [MESH:C567838] (52) |
|
|
Infertility, Female [MESH:D007247] (2184) |
|
|
|
|
|
Endometrial Neoplasms [MESH:D016889] (1984) |
|
|
|
|
|
|
|
|
Aromatase deficiency [MESH:C537436] (277) |
|
|
Gonadal Dysgenesis, 46,XX [MESH:D023961] (56) |
|
|
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) |
|
|
|
|
|
Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
|
|
Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223) |
|
|
Gonadal Dysgenesis, 46,XX [MESH:D023961] (56) |
|
|
Gonadal Dysgenesis, 46,XY [MESH:D006061] (131) |
|
|
Sexual Infantilism [MESH:D050035] (277) |
|
|
Hypospadias 1, X-Linked [MESH:C567482] (571) |
|
|
|
|
|
Ovarian Neoplasms [MESH:D010051] (3281) |
|
|
Endometrial Neoplasms [MESH:D016889] (1989) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
Urinary Tract Infections [MESH:D014552] (984) |
|
|
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) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
|
|
|
Glomerulonephritis, IGA [MESH:D005922] (897) |
|
|
Glomerulonephritis, Membranoproliferative [MESH:D015432] (770) |
|
|
Glomerulonephritis, Membranous [MESH:D015433] (642) |
|
|
Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754) |
|
|
Nephrotic Syndrome [MESH:D009404] (1536) |
|
|
Acute Kidney Injury [MESH:D058186] (4142) |
|
|
Kidney Failure, Chronic [MESH:D007676] (2930) |
|
|
Pseudohypoaldosteronism [MESH:D011546] (232) |
|
|
|
|
|
Hypophosphatemic Rickets, Autosomal Recessive, 2 [MESH:C567647] (48) |
|
|
|
|
|
Atypical hemolytic uremic syndrome [MESH:C538266] (277) |
|
|
Ureteral Obstruction [MESH:D014517] (575) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Oliguria [MESH:D009846] (307) |
|
|
Proteinuria [MESH:D011507] (3293) |
|
|
Abortion, Spontaneous [MESH:D000022] (2780) |
|
|
Diabetes, Gestational [MESH:D016640] (1157) |
|
|
Pregnancy Complications, Cardiovascular [MESH:D011249] (1994) |
|
|
Fetal Resorption [MESH:D005327] (302) |
|
|
Fetal Growth Retardation [MESH:D005317] (986) |
|
|
|
|
|
Galactorrhea [MESH:D005687] (233) |
|
 |
C14. Cardiovascular Diseases |
 |
 |
|
C14. Cardiovascular Diseases |
|
|
Not Fully Specified [NFS] (2667) |
|
|
Pregnancy Complications, Cardiovascular [MESH:D011249] (1994) |
|
|
|
|
|
Cardiofaciocutaneous syndrome [MESH:C535579] (407) |
|
|
Heterotaxy Syndrome [MESH:D059446] (84) |
|
|
DiGeorge Syndrome [MESH:D004062] (236) |
|
|
Aortic aneurysm, familial thoracic 4 [MESH:C537784] (29) |
|
|
Noonan syndrome 3 [MESH:C537847] (118) |
|
|
Noonan Syndrome 4 [MESH:C548082] (37) |
|
|
Heart Failure [MESH:D006333] (4058) |
|
|
Atrial Fibrillation [MESH:D001281] (1053) |
|
|
Bradycardia [MESH:D001919] (1899) |
|
|
Tachycardia [MESH:D013610] (3339) |
|
|
Hypertrophy, Left Ventricular [MESH:D017379] (1430) |
|
|
Cardiomyopathy, Dilated, 1N [MESH:C564388] (13) |
|
|
Diabetic Cardiomyopathies [MESH:D058065] (1995) |
|
|
Endomyocardial Fibrosis [MESH:D004719] (521) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Cardiomyopathy, Dilated, 1N [MESH:C564388] (13) |
|
|
Cardiofaciocutaneous syndrome [MESH:C535579] (407) |
|
|
Heterotaxy Syndrome [MESH:D059446] (84) |
|
|
DiGeorge Syndrome [MESH:D004062] (236) |
|
|
Aortic aneurysm, familial thoracic 4 [MESH:C537784] (29) |
|
|
Noonan syndrome 3 [MESH:C537847] (118) |
|
|
Noonan Syndrome 4 [MESH:C548082] (37) |
|
|
Aortic Valve Insufficiency [MESH:D001022] (1002) |
|
|
Aortic Valve, Calcification of [MESH:C562942] (655) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Myocardial Stunning [MESH:D017682] (1816) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Coronary Artery Disease [MESH:D003324] (2685) |
|
|
Myocardial Stunning [MESH:D017682] (1816) |
|
|
|
|
|
Aortic Valve, Calcification of [MESH:C562942] (655) |
|
|
Angioedema [MESH:D000799] (837) |
|
|
Arteritis [MESH:D001167] (1084) |
|
|
Hyperemia [MESH:D006940] (2372) |
|
|
Hypotension [MESH:D007022] (4045) |
|
|
Varicose Veins [MESH:D014648] (383) |
|
|
Aneurysm, Dissecting [MESH:D000784] (699) |
|
|
|
|
|
Aortic aneurysm, familial thoracic 4 [MESH:C537784] (29) |
|
|
Klippel-Trenaunay-Weber Syndrome [MESH:D007715] (14) |
|
|
|
|
|
|
|
|
Aortic aneurysm, familial thoracic 4 [MESH:C537784] (29) |
|
|
Carotid Stenosis [MESH:D016893] (174) |
|
|
Atherosclerosis [MESH:D050197] (4188) |
|
|
Coronary Artery Disease [MESH:D003324] (2685) |
|
|
|
|
|
Ischemic Attack, Transient [MESH:D002546] (1313) |
|
|
Cerebral Infarction [MESH:D002544] (2458) |
|
|
Lateral Medullary Syndrome [MESH:D014854] (188) |
|
|
Carotid Stenosis [MESH:D016893] (174) |
|
|
|
|
|
Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333) |
|
|
|
|
|
|
|
|
|
|
|
Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333) |
|
|
|
|
|
|
|
|
Sagittal Sinus Thrombosis [MESH:D020225] (223) |
|
|
Subarachnoid Hemorrhage [MESH:D013345] (1082) |
|
|
Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333) |
|
|
|
|
|
Cerebral Infarction [MESH:D002544] (2458) |
|
|
Lateral Medullary Syndrome [MESH:D014854] (188) |
|
|
|
|
|
Venous Thromboembolism [MESH:D054556] (400) |
|
|
|
|
|
|
|
|
Sagittal Sinus Thrombosis [MESH:D020225] (223) |
|
|
Venous Thrombosis [MESH:D020246] (1141) |
|
|
Venous Thromboembolism [MESH:D054556] (400) |
|
|
|
|
|
|
|
|
Sagittal Sinus Thrombosis [MESH:D020225] (223) |
|
|
Telangiectasia, Hereditary Hemorrhagic [MESH:D013683] (75) |
|
|
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 venoocclusive disease with immunodeficiency [MESH:C537257] (23) |
|
|
Hypertension, Essential [MESH:C562386] (1308) |
|
|
Hypertension, Malignant [MESH:D006974] (621) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Myocardial Stunning [MESH:D017682] (1816) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Coronary Artery Disease [MESH:D003324] (2685) |
|
|
Myocardial Stunning [MESH:D017682] (1816) |
|
|
Raynaud Disease [MESH:D011928] (490) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Telangiectasia, Hereditary Hemorrhagic [MESH:D013683] (75) |
|
|
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 |
|
|
Polycythemia [MESH:D011086] (412) |
|
|
|
|
|
|
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
|
|
|
Anemia, Dyserythropoietic, Congenital [MESH:D000742] (81) |
|
|
Spherocytosis, Type 1 [MESH:C567159] (21) |
|
|
|
|
|
ATR-X syndrome [MESH:C538258] (59) |
|
|
Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59) |
|
|
Atypical hemolytic uremic syndrome [MESH:C538266] (277) |
|
|
Disseminated Intravascular Coagulation [MESH:D004211] (462) |
|
|
Activated Protein C Resistance [MESH:D020016] (140) |
|
|
Antithrombin III Deficiency [MESH:D020152] (80) |
|
|
Hypoprothrombinemias [MESH:D007020] (157) |
|
|
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74) |
|
|
Congenital thrombotic disease, due to Protein C deficiency [MESH:C535424] (66) |
|
|
Activated Protein C Resistance [MESH:D020016] (140) |
|
|
Hypoprothrombinemias [MESH:D007020] (157) |
|
|
|
|
|
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74) |
|
|
Purpura Fulminans [MESH:D055665] (69) |
|
|
|
|
|
|
|
|
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74) |
|
|
|
|
|
|
|
|
Atypical hemolytic uremic syndrome [MESH:C538266] (277) |
|
|
Antithrombin III Deficiency [MESH:D020152] (80) |
|
|
Congenital thrombotic disease, due to Protein C deficiency [MESH:C535424] (66) |
|
|
|
|
|
|
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59) |
|
|
|
|
|
|
|
|
ATR-X syndrome [MESH:C538258] (59) |
|
|
Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59) |
|
|
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74) |
|
|
Disseminated Intravascular Coagulation [MESH:D004211] (462) |
|
|
Hypoprothrombinemias [MESH:D007020] (157) |
|
|
Telangiectasia, Hereditary Hemorrhagic [MESH:D013683] (75) |
|
|
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) |
|
|
|
|
|
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74) |
|
|
|
|
|
Eosinophilia-Myalgia Syndrome [MESH:D016603] (31) |
|
|
|
|
|
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative [MESH:C565533] (111) |
|
|
Activated Protein C Resistance [MESH:D020016] (140) |
|
|
Antithrombin III Deficiency [MESH:D020152] (80) |
|
|
Disseminated Intravascular Coagulation [MESH:D004211] (462) |
|
|
Congenital thrombotic disease, due to Protein C deficiency [MESH:C535424] (66) |
|
|
Mucocutaneous Lymph Node Syndrome [MESH:D009080] (158) |
|
|
|
|
|
Sea-Blue Histiocyte Syndrome [MESH:D012618] (165) |
|
|
Hemophagocytic lymphohistiocytosis, familial, 2 [MESH:C537250] (38) |
|
|
|
|
|
DiGeorge Syndrome [MESH:D004062] (236) |
|
|
|
|
|
|
|
|
Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
|
|
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510) |
|
|
|
|
|
Lymphoma, Mantle-Cell [MESH:D020522] (561) |
|
|
Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) |
|
|
Heterotaxy Syndrome [MESH:D059446] (84) |
|
 |
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
 |
 |
|
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
|
|
|
|
|
Situs Inversus [MESH:D012857] (88) |
|
|
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) |
|
|
DiGeorge Syndrome [MESH:D004062] (236) |
|
|
Cardiofaciocutaneous syndrome [MESH:C535579] (407) |
|
|
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome [MESH:C537943] (28) |
|
|
ABCD syndrome [MESH:C535334] (143) |
|
|
|
|
|
Cardiofaciocutaneous syndrome [MESH:C535579] (407) |
|
|
Heterotaxy Syndrome [MESH:D059446] (84) |
|
|
DiGeorge Syndrome [MESH:D004062] (236) |
|
|
Aortic aneurysm, familial thoracic 4 [MESH:C537784] (29) |
|
|
Noonan syndrome 3 [MESH:C537847] (118) |
|
|
Noonan Syndrome 4 [MESH:C548082] (37) |
|
|
Telangiectasia, Hereditary Hemorrhagic [MESH:D013683] (75) |
|
|
Mosaic variegated aneuploidy syndrome [MESH:C536987] (95) |
|
|
De Lange Syndrome [MESH:D003635] (55) |
|
|
Prader-Willi Syndrome [MESH:D011218] (46) |
|
|
DiGeorge Syndrome [MESH:D004062] (236) |
|
|
Fragile X Syndrome [MESH:D005600] (353) |
|
|
Hirschsprung Disease [MESH:D006627] (361) |
|
|
|
|
|
DiGeorge Syndrome [MESH:D004062] (236) |
|
|
|
|
|
Bruck syndrome 2 [MESH:C537407] (64) |
|
|
Distal arthrogryposis type 2B [MESH:C538400] (85) |
|
|
Congenital Cataracts, Facial Dysmorphism, And Neuropathy [MESH:C565822] (17) |
|
|
DiGeorge Syndrome [MESH:D004062] (236) |
|
|
Freeman-Sheldon syndrome [MESH:C535483] (23) |
|
|
Mandibulofacial Dysostosis [MESH:D008342] (63) |
|
|
|
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
Meier-Gorlin syndrome [MESH:C538012] (133) |
|
|
Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76) |
|
|
Noonan syndrome 3 [MESH:C537847] (118) |
|
|
Noonan Syndrome 4 [MESH:C548082] (37) |
|
|
Brachydactyly [MESH:D059327] (220) |
|
|
Growth mental deficiency syndrome of Myhre [MESH:C537620] (51) |
|
|
|
|
|
Chudley-Mccullough syndrome [MESH:C535459] (45) |
|
|
|
|
|
Chudley-Mccullough syndrome [MESH:C535459] (45) |
|
|
|
|
|
Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76) |
|
|
|
|
|
Cardiofaciocutaneous syndrome [MESH:C535579] (407) |
|
|
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome [MESH:C537943] (28) |
|
|
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) |
|
|
Nephropathy with Pretibial Epidermolysis Bullosa and Deafness [MESH:C563798] (43) |
|
|
|
|
|
|
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
Meier-Gorlin syndrome [MESH:C538012] (133) |
|
|
Cleft Lip [MESH:D002971] (914) |
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
Tooth Agenesis, Selective, 6 [MESH:C567755] (19) |
|
|
|
|
|
Growth mental deficiency syndrome of Myhre [MESH:C537620] (51) |
|
|
|
|
|
Aromatase deficiency [MESH:C537436] (277) |
|
|
Gonadal Dysgenesis, 46,XX [MESH:D023961] (56) |
|
|
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) |
|
|
|
|
|
Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
|
|
Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223) |
|
|
Gonadal Dysgenesis, 46,XX [MESH:D023961] (56) |
|
|
Gonadal Dysgenesis, 46,XY [MESH:D006061] (131) |
|
|
Sexual Infantilism [MESH:D050035] (277) |
|
|
Hypospadias 1, X-Linked [MESH:C567482] (571) |
|
|
Fetal Growth Retardation [MESH:D005317] (986) |
|
|
Costello Syndrome [MESH:D056685] (407) |
|
|
Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
|
|
Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223) |
|
|
Anemia, Dyserythropoietic, Congenital [MESH:D000742] (81) |
|
|
Spherocytosis, Type 1 [MESH:C567159] (21) |
|
|
|
|
|
ATR-X syndrome [MESH:C538258] (59) |
|
|
Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59) |
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
Activated Protein C Resistance [MESH:D020016] (140) |
|
|
Antithrombin III Deficiency [MESH:D020152] (80) |
|
|
Hypoprothrombinemias [MESH:D007020] (157) |
|
|
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74) |
|
|
Congenital thrombotic disease, due to Protein C deficiency [MESH:C535424] (66) |
|
|
Mosaic variegated aneuploidy syndrome [MESH:C536987] (95) |
|
|
De Lange Syndrome [MESH:D003635] (55) |
|
|
Prader-Willi Syndrome [MESH:D011218] (46) |
|
|
DiGeorge Syndrome [MESH:D004062] (236) |
|
|
Fragile X Syndrome [MESH:D005600] (353) |
|
|
Basal Laminar Drusen [MESH:C563034] (52) |
|
|
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74) |
|
|
Oculocutaneous albinism type 3 [MESH:C537731] (40) |
|
|
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74) |
|
|
Griscelli syndrome type 2 [MESH:C537302] (30) |
|
|
Corneal Dystrophy, Posterior Polymorphous, 3 [MESH:C563788] (60) |
|
|
Corneal Dystrophy, Fuchs Endothelial, 6 [MESH:C567675] (60) |
|
|
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) |
|
|
Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565) |
|
|
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative [MESH:C565533] (111) |
|
|
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) |
|
|
|
|
|
|
|
|
ATR-X syndrome [MESH:C538258] (59) |
|
|
Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59) |
|
|
Hepatolenticular Degeneration [MESH:D006527] (473) |
|
|
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) |
|
|
Aromatase deficiency [MESH:C537436] (277) |
|
|
3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency [MESH:C567784] (102) |
|
|
Alpha-ketoglutarate dehydrogenase deficiency [MESH:C536582] (59) |
|
|
Methylmalonic acidemia [MESH:C537358] (764) |
|
|
Beta-Hydroxyisobutyryl CoA Deacylase Deficiency [MESH:C562803] (33) |
|
|
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74) |
|
|
Oculocutaneous albinism type 3 [MESH:C537731] (40) |
|
|
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74) |
|
|
Griscelli syndrome type 2 [MESH:C537302] (30) |
|
|
Biotinidase Deficiency [MESH:D028921] (31) |
|
|
Citrullinemia [MESH:D020159] (99) |
|
|
Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333) |
|
|
Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333) |
|
|
Hepatolenticular Degeneration [MESH:D006527] (473) |
|
|
Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333) |
|
|
|
|
|
Gaucher Disease [MESH:D005776] (299) |
|
|
Sea-Blue Histiocyte Syndrome [MESH:D012618] (165) |
|
|
Citrullinemia [MESH:D020159] (99) |
|
|
|
|
|
Mucopolysaccharidosis II [MESH:D016532] (26) |
|
|
Biotinidase Deficiency [MESH:D028921] (31) |
|
|
Desmosterolosis [MESH:C566555] (85) |
|
|
Hyperlipoproteinemia Type II [MESH:D006938] (707) |
|
|
Hyperlipoproteinemia Type III [MESH:D006952] (181) |
|
|
|
|
|
Gaucher Disease [MESH:D005776] (299) |
|
|
Sea-Blue Histiocyte Syndrome [MESH:D012618] (165) |
|
|
Lipodystrophy, Congenital Generalized, Type 4 [MESH:C567642] (38) |
|
|
|
|
|
|
|
|
Gaucher Disease [MESH:D005776] (299) |
|
|
Sea-Blue Histiocyte Syndrome [MESH:D012618] (165) |
|
|
Mucopolysaccharidosis II [MESH:D016532] (26) |
|
|
Hepatolenticular Degeneration [MESH:D006527] (473) |
|
|
|
|
|
Hypophosphatemic Rickets, Autosomal Recessive, 2 [MESH:C567647] (48) |
|
|
Pseudohypoaldosteronism [MESH:D011546] (232) |
|
|
|
|
|
Hypophosphatemic Rickets, Autosomal Recessive, 2 [MESH:C567647] (48) |
|
|
|
|
|
Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
|
|
Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223) |
|
|
Bethlem myopathy [MESH:C535436] (108) |
|
|
Scleroatonic muscular dystrophy [MESH:C537521] (108) |
|
|
Muscular Dystrophy, Emery-Dreifuss [MESH:D020389] (169) |
|
|
Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854) |
|
|
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57) |
|
|
Muscular Dystrophy, Limb-Girdle, Type 2G [MESH:C566599] (13) |
|
|
Juvenile polyposis syndrome [MESH:C537702] (196) |
|
|
Adenomatous Polyposis Coli [MESH:D011125] (1565) |
|
|
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) |
|
|
|
|
|
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74) |
|
|
Oculocutaneous albinism type 3 [MESH:C537731] (40) |
|
|
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74) |
|
|
Griscelli syndrome type 2 [MESH:C537302] (30) |
|
|
Cardiofaciocutaneous syndrome [MESH:C535579] (407) |
|
|
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome [MESH:C537943] (28) |
|
|
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) |
|
|
Nephropathy with Pretibial Epidermolysis Bullosa and Deafness [MESH:C563798] (43) |
|
|
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome [MESH:C537943] (28) |
|
|
Porokeratosis, disseminated superficial actinic 1 [MESH:C536339] (52) |
|
|
Hyperostosis, Cortical, Congenital [MESH:D006958] (392) |
|
 |
C17. Skin and Connective Tissue Diseases |
 |
 |
|
C17. Skin and Connective Tissue Diseases |
|
|
Lupus Erythematosus, Systemic [MESH:D008180] (2317) |
|
|
Scleroderma, Systemic [MESH:D012595] (199) |
|
|
Keloid [MESH:D007627] (1111) |
|
|
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, 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) |
|
|
|
|
|
Mucopolysaccharidosis II [MESH:D016532] (26) |
|
|
Noonan syndrome 3 [MESH:C537847] (118) |
|
|
Noonan Syndrome 4 [MESH:C548082] (37) |
|
|
Arthritis, Rheumatoid [MESH:D001172] (3603) |
|
|
Exanthema [MESH:D005076] (301) |
|
|
Nephrogenic Fibrosing Dermopathy [MESH:D054989] (452) |
|
|
Scleroderma, Systemic [MESH:D012595] (199) |
|
|
Skin Neoplasms [MESH:D012878] (2991) |
|
|
Chloracne [MESH:D054506] (1274) |
|
|
|
|
|
Breast Neoplasms, Male [MESH:D018567] (650) |
|
|
Carcinoma, Ductal, Breast [MESH:D018270] (1112) |
|
|
Aromatase deficiency [MESH:C537436] (277) |
|
|
Galactorrhea [MESH:D005687] (233) |
|
|
|
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
Stevens-Johnson Syndrome [MESH:D013262] (1163) |
|
|
|
|
|
Stevens-Johnson Syndrome [MESH:D013262] (1163) |
|
|
|
|
|
Chloracne [MESH:D054506] (1274) |
|
|
|
|
|
Hypotrichosis simplex [MESH:C537160] (92) |
|
|
Alopecia [MESH:D000505] (1453) |
|
|
|
|
|
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome [MESH:C537943] (28) |
|
|
Porokeratosis, disseminated superficial actinic 1 [MESH:C536339] (52) |
|
|
|
|
|
|
|
|
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74) |
|
|
Oculocutaneous albinism type 3 [MESH:C537731] (40) |
|
|
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74) |
|
|
Griscelli syndrome type 2 [MESH:C537302] (30) |
|
|
|
|
|
Cardiofaciocutaneous syndrome [MESH:C535579] (407) |
|
|
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome [MESH:C537943] (28) |
|
|
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) |
|
|
Nephropathy with Pretibial Epidermolysis Bullosa and Deafness [MESH:C563798] (43) |
|
|
|
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
|
|
|
|
|
|
Oculocutaneous albinism type 3 [MESH:C537731] (40) |
|
|
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74) |
|
|
Griscelli syndrome type 2 [MESH:C537302] (30) |
|
|
Cardiofaciocutaneous syndrome [MESH:C535579] (407) |
|
|
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome [MESH:C537943] (28) |
|
|
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) |
|
|
Nephropathy with Pretibial Epidermolysis Bullosa and Deafness [MESH:C563798] (43) |
|
|
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome [MESH:C537943] (28) |
|
|
Porokeratosis, disseminated superficial actinic 1 [MESH:C536339] (52) |
|
|
|
|
|
Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224) |
|
|
|
|
|
|
|
|
Lipodystrophy, Congenital Generalized, Type 4 [MESH:C567642] (38) |
|
|
|
|
|
Arthritis, Psoriatic [MESH:D015535] (1859) |
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
|
Mucocutaneous Lymph Node Syndrome [MESH:D009080] (158) |
|
|
Angioedema [MESH:D000799] (837) |
|
|
|
|
|
Nephropathy with Pretibial Epidermolysis Bullosa and Deafness [MESH:C563798] (43) |
|
|
Stevens-Johnson Syndrome [MESH:D013262] (1163) |
|
 |
C18. Nutritional and Metabolic Diseases |
 |
 |
|
C18. Nutritional and Metabolic Diseases |
|
|
|
|
|
|
|
|
|
|
|
Pyruvate dehydrogenase phosphatase deficiency [MESH:C536258] (40) |
|
|
|
|
|
Hepatolenticular Degeneration [MESH:D006527] (473) |
|
|
Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333) |
|
|
|
|
|
Gaucher Disease [MESH:D005776] (299) |
|
|
Sea-Blue Histiocyte Syndrome [MESH:D012618] (165) |
|
|
Citrullinemia [MESH:D020159] (99) |
|
|
|
|
|
Aortic Valve, Calcification of [MESH:C562942] (655) |
|
|
Arterial calcification of infancy [MESH:C537440] (48) |
|
|
|
|
|
|
|
|
Hypophosphatemic Rickets, Autosomal Recessive, 2 [MESH:C567647] (48) |
|
|
Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76) |
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
|
|
|
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) |
|
|
Glucose Intolerance [MESH:D018149] (605) |
|
|
Insulin Resistance [MESH:D007333] (3511) |
|
|
3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency [MESH:C567784] (102) |
|
|
|
|
|
|
|
|
Hypercholesterolemia [MESH:D006937] (1404) |
|
|
Hyperlipoproteinemia Type II [MESH:D006938] (707) |
|
|
Hyperlipoproteinemia Type III [MESH:D006952] (181) |
|
|
Desmosterolosis [MESH:C566555] (85) |
|
|
|
|
|
Lipodystrophy, Congenital Generalized, Type 4 [MESH:C567642] (38) |
|
|
|
|
|
Gaucher Disease [MESH:D005776] (299) |
|
|
Sea-Blue Histiocyte Syndrome [MESH:D012618] (165) |
|
|
Celiac Disease [MESH:D002446] (340) |
|
|
Aromatase deficiency [MESH:C537436] (277) |
|
|
3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency [MESH:C567784] (102) |
|
|
Alpha-ketoglutarate dehydrogenase deficiency [MESH:C536582] (59) |
|
|
Methylmalonic acidemia [MESH:C537358] (764) |
|
|
Beta-Hydroxyisobutyryl CoA Deacylase Deficiency [MESH:C562803] (33) |
|
|
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74) |
|
|
Oculocutaneous albinism type 3 [MESH:C537731] (40) |
|
|
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74) |
|
|
Griscelli syndrome type 2 [MESH:C537302] (30) |
|
|
Biotinidase Deficiency [MESH:D028921] (31) |
|
|
Citrullinemia [MESH:D020159] (99) |
|
|
Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333) |
|
|
Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333) |
|
|
Hepatolenticular Degeneration [MESH:D006527] (473) |
|
|
Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333) |
|
|
|
|
|
Gaucher Disease [MESH:D005776] (299) |
|
|
Sea-Blue Histiocyte Syndrome [MESH:D012618] (165) |
|
|
Citrullinemia [MESH:D020159] (99) |
|
|
|
|
|
Mucopolysaccharidosis II [MESH:D016532] (26) |
|
|
Biotinidase Deficiency [MESH:D028921] (31) |
|
|
Desmosterolosis [MESH:C566555] (85) |
|
|
Hyperlipoproteinemia Type II [MESH:D006938] (707) |
|
|
Hyperlipoproteinemia Type III [MESH:D006952] (181) |
|
|
|
|
|
Gaucher Disease [MESH:D005776] (299) |
|
|
Sea-Blue Histiocyte Syndrome [MESH:D012618] (165) |
|
|
Lipodystrophy, Congenital Generalized, Type 4 [MESH:C567642] (38) |
|
|
|
|
|
|
|
|
Gaucher Disease [MESH:D005776] (299) |
|
|
Sea-Blue Histiocyte Syndrome [MESH:D012618] (165) |
|
|
Mucopolysaccharidosis II [MESH:D016532] (26) |
|
|
Hepatolenticular Degeneration [MESH:D006527] (473) |
|
|
|
|
|
Hypophosphatemic Rickets, Autosomal Recessive, 2 [MESH:C567647] (48) |
|
|
Pseudohypoaldosteronism [MESH:D011546] (232) |
|
|
|
|
|
Hypophosphatemic Rickets, Autosomal Recessive, 2 [MESH:C567647] (48) |
|
|
|
|
|
Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
|
|
Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223) |
|
|
3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency [MESH:C567784] (102) |
|
|
|
|
|
|
|
|
|
|
|
Hypophosphatemic Rickets, Autosomal Recessive, 2 [MESH:C567647] (48) |
|
|
|
|
|
Hypophosphatemic Rickets, Autosomal Recessive, 2 [MESH:C567647] (48) |
|
|
|
|
|
|
|
|
Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333) |
|
|
Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333) |
|
|
|
|
|
Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333) |
|
|
Amyotrophic Lateral Sclerosis [MESH:D000690] (3296) |
|
|
|
|
|
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57) |
|
|
|
|
|
|
|
|
Lipodystrophy, Congenital Generalized, Type 4 [MESH:C567642] (38) |
|
|
HIV Wasting Syndrome [MESH:D019247] (1956) |
|
|
Hyperkalemia [MESH:D006947] (485) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Hypophosphatemic Rickets, Autosomal Recessive, 2 [MESH:C567647] (48) |
|
|
|
|
|
Prader-Willi Syndrome [MESH:D011218] (46) |
|
|
HIV Wasting Syndrome [MESH:D019247] (1956) |
|
 |
C19. Endocrine System Diseases |
 |
 |
|
C19. Endocrine System Diseases |
|
|
|
|
|
Adrenal Insufficiency [MESH:D000309] (1599) |
|
|
Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
|
|
Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223) |
|
|
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) |
|
|
Diabetic Cardiomyopathies [MESH:D058065] (1995) |
|
|
Diabetic Nephropathies [MESH:D003928] (2301) |
|
|
Ovarian Neoplasms [MESH:D010051] (3275) |
|
|
Thyroid Neoplasms [MESH:D013964] (2040) |
|
|
Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
|
|
Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383) |
|
|
Prolactinoma [MESH:D015175] (312) |
|
|
|
|
|
Leydig Cell Tumor [MESH:D007984] (267) |
|
|
Puberty, Delayed [MESH:D011628] (449) |
|
|
|
|
|
Aromatase deficiency [MESH:C537436] (277) |
|
|
Gonadal Dysgenesis, 46,XX [MESH:D023961] (56) |
|
|
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) |
|
|
|
|
|
Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
|
|
Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223) |
|
|
Gonadal Dysgenesis, 46,XX [MESH:D023961] (56) |
|
|
Gonadal Dysgenesis, 46,XY [MESH:D006061] (131) |
|
|
Sexual Infantilism [MESH:D050035] (277) |
|
|
Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59) |
|
|
Sexual Infantilism [MESH:D050035] (277) |
|
|
Ovarian Neoplasms [MESH:D010051] (3281) |
|
|
Polycystic Ovary Syndrome [MESH:D011085] (2186) |
|
|
Premature Ovarian Failure 2a [MESH:C564498] (15) |
|
|
Premature Ovarian Failure 7 [MESH:C567838] (52) |
|
|
Familial Testotoxicosis [MESH:C536961] (65) |
|
|
|
|
|
Growth mental deficiency syndrome of Myhre [MESH:C537620] (51) |
|
|
|
|
|
Leydig Cell Tumor [MESH:D007984] (267) |
|
|
|
|
|
|
|
|
DiGeorge Syndrome [MESH:D004062] (236) |
|
|
Hypopituitarism [MESH:D007018] (732) |
|
|
Acromegaly [MESH:D000172] (466) |
|
|
Hyperprolactinemia [MESH:D006966] (603) |
|
|
Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383) |
|
|
Prolactinoma [MESH:D015175] (312) |
|
|
Thyroid Neoplasms [MESH:D013964] (2040) |
|
|
|
|
|
Graves Ophthalmopathy [MESH:D049970] (165) |
|
|
|
|
|
Graves Ophthalmopathy [MESH:D049970] (165) |
|
 |
C20. Immune System Diseases |
 |
 |
|
C20. Immune System Diseases |
|
|
Glomerulonephritis, Membranoproliferative [MESH:D015432] (770) |
|
|
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) |
|
|
|
|
|
|
|
|
Multiple Sclerosis, Relapsing-Remitting [MESH:D020529] (170) |
|
|
Graves Ophthalmopathy [MESH:D049970] (165) |
|
|
Immune Complex Diseases [MESH:D007105] (782) |
|
|
|
|
|
Stevens-Johnson Syndrome [MESH:D013262] (1163) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
|
|
|
Asthma [MESH:D001249] (3914) |
|
|
Angioedema [MESH:D000799] (837) |
|
|
Hepatic venoocclusive disease with immunodeficiency [MESH:C537257] (23) |
|
|
Griscelli syndrome type 2 [MESH:C537302] (30) |
|
|
HIV Wasting Syndrome [MESH:D019247] (1956) |
|
|
|
|
|
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative [MESH:C565533] (111) |
|
|
|
|
|
|
|
|
|
|
|
Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
|
|
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510) |
|
|
|
|
|
Lymphoma, Mantle-Cell [MESH:D020522] (561) |
|
|
Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) |
|
 |
C22. Animal Diseases |
 |
 |
|
C22. Animal Diseases |
|
|
Disease Models, Animal [MESH:D004195] (2058) |
|
|
Mammary Neoplasms, Animal [MESH:D015674] (2735) |
|
|
Paratuberculosis [MESH:D010283] (427) |
|
|
Influenza in Birds [MESH:D005585] (53) |
|
|
Influenza in Birds [MESH:D005585] (53) |
|
 |
C23. Pathological Conditions, Signs and Symptoms |
 |
 |
|
C23. Pathological Conditions, Signs and Symptoms |
|
|
Alopecia [MESH:D000505] (1383) |
|
|
Plaque, Amyloid [MESH:D058225] (334) |
|
|
Plaque, Atherosclerotic [MESH:D058226] (696) |
|
|
Chudley-Mccullough syndrome [MESH:C535459] (45) |
|
|
Muscular Atrophy [MESH:D009133] (1234) |
|
|
|
|
|
Congenital diaphragmatic hernia [MESH:C538080] (381) |
|
|
Intervertebral disc disease [MESH:C535531] (514) |
|
|
Growth mental deficiency syndrome of Myhre [MESH:C537620] (51) |
|
|
Splenomegaly [MESH:D013163] (1258) |
|
|
Hypertrophy, Left Ventricular [MESH:D017379] (1430) |
|
|
Gliosis [MESH:D005911] (1419) |
|
|
Hyperplasia [MESH:D006965] (2463) |
|
|
Atrial Fibrillation [MESH:D001281] (1053) |
|
|
Bradycardia [MESH:D001919] (1899) |
|
|
Tachycardia [MESH:D013610] (3339) |
|
|
Micronuclei, Chromosome-Defective [MESH:D048629] (1013) |
|
|
|
|
|
Fetal Resorption [MESH:D005327] (302) |
|
|
Critical Illness [MESH:D016638] (296) |
|
|
Disease Progression [MESH:D018450] (2868) |
|
|
Genetic Predisposition to Disease [MESH:D020022] (966) |
|
|
Cardiofaciocutaneous syndrome [MESH:C535579] (407) |
|
|
Pitt-Hopkins syndrome [MESH:C537403] (113) |
|
|
Growth mental deficiency syndrome of Myhre [MESH:C537620] (51) |
|
|
Nephrogenic Fibrosing Dermopathy [MESH:D054989] (452) |
|
|
Keloid [MESH:D007627] (1110) |
|
|
Granuloma, Plasma Cell [MESH:D006104] (58) |
|
|
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) |
|
|
|
|
|
Subarachnoid Hemorrhage [MESH:D013345] (1081) |
|
|
Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333) |
|
|
Purpura Fulminans [MESH:D055665] (69) |
|
|
Neurogenic Inflammation [MESH:D020078] (2246) |
|
|
|
|
|
Shock, Septic [MESH:D012772] (1830) |
|
|
Endotoxemia [MESH:D019446] (1289) |
|
|
Infarction [MESH:D007238] (298) |
|
|
Amenorrhea [MESH:D000568] (817) |
|
|
Oligomenorrhea [MESH:D009839] (228) |
|
|
Neovascularization, Pathologic [MESH:D009389] (829) |
|
|
Infarction [MESH:D007238] (298) |
|
|
Anaplasia [MESH:D000708] (348) |
|
|
Neoplasm Invasiveness [MESH:D009361] (3388) |
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Neoplasm Metastasis [MESH:D009362] (4441) |
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Neoplasm Recurrence, Local [MESH:D009364] (1949) |
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Cell Transformation, Neoplastic [MESH:D002471] (3389) |
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Striatal Degeneration, Autosomal Dominant [MESH:C563783] (21) |
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Ossification of the posterior longitudinal ligament of the spine [MESH:C537143] (98) |
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Myocardial Reperfusion Injury [MESH:D015428] (3500) |
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Scleroatonic muscular dystrophy [MESH:C537521] (108) |
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Shock, Septic [MESH:D012772] (1830) |
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Edema [MESH:D004487] (3726) |
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Feminization [MESH:D005262] (655) |
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Fever [MESH:D005334] (2856) |
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Hypothermia [MESH:D007035] (2075) |
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Birth Weight [MESH:D001724] (377) |
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Weight Gain [MESH:D015430] (2595) |
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Obesity [MESH:D009765] (4454) |
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Cardiofaciocutaneous syndrome [MESH:C535579] (407) |
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Pain [MESH:D010146] (3869) |
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Seizures [MESH:D012640] (4502) |
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Catalepsy [MESH:D002375] (1429) |
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Learning Disorders [MESH:D007859] (2727) |
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Dysarthria [MESH:D004401] (163) |
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Amnesia [MESH:D000647] (1911) |
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Pitt-Hopkins syndrome [MESH:C537403] (113) |
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Growth mental deficiency syndrome of Myhre [MESH:C537620] (51) |
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Muscular Atrophy [MESH:D009133] (1234) |
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Muscle Rigidity [MESH:D009127] (617) |
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Progressive supranuclear palsy atypical [MESH:C537240] (142) |
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Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59) |
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Chudley-Mccullough syndrome [MESH:C535459] (45) |
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Nephropathy with Pretibial Epidermolysis Bullosa and Deafness [MESH:C563798] (43) |
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Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346) |
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Hyperalgesia [MESH:D006930] (3929) |
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Acute Coronary Syndrome [MESH:D054058] (2286) |
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Pitt-Hopkins syndrome [MESH:C537403] (113) |
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Purpura Fulminans [MESH:D055665] (69) |
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Oliguria [MESH:D009846] (307) |
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Proteinuria [MESH:D011507] (3293) |
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C24. Occupational Diseases |
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C24. Occupational Diseases |
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Asbestosis [MESH:D001195] (935) |
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Silicosis [MESH:D012829] (1273) |
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C25. Chemically-Induced Disorders |
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C25. Chemically-Induced Disorders |
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Drug-Induced Liver Injury [MESH:D056486] (4936) |
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Stevens-Johnson Syndrome [MESH:D013262] (1163) |
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Arsenic Poisoning [MESH:D020261] (2540) |
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Drug-Induced Liver Injury [MESH:D056486] (4936) |
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Manganese Poisoning [MESH:D020149] (2214) |
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Mercury Poisoning [MESH:D008630] (193) |
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Neurotoxicity Syndromes [MESH:D020258] (3323) |
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Psychoses, Substance-Induced [MESH:D011605] (2053) |
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Amphetamine-Related Disorders [MESH:D019969] (2858) |
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Cocaine-Related Disorders [MESH:D019970] (3054) |
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Marijuana Abuse [MESH:D002189] (1132) |
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Opioid-Related Disorders [MESH:D009293] (1491) |
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Phencyclidine Abuse [MESH:D010623] (288) |
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Psychoses, Substance-Induced [MESH:D011605] (2052) |
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Substance Withdrawal Syndrome [MESH:D013375] (2956) |
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Alcoholism [MESH:D000437] (1519) |
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Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
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C26. Wounds and Injuries |
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C26. Wounds and Injuries |
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Burns [MESH:D002056] (2565) |
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Brain Injuries [MESH:D001930] (3431) |
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Radiation Injuries, Experimental [MESH:D011833] (2662) |
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Brain Injuries [MESH:D001930] (3431) |
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D04. Polycyclic Compounds |
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D04. Polycyclic Compounds |
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Testosterone [MESH:D013739] (118) |
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D06. Hormones, Hormone Substitutes, and Hormone Antagonists |
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D06. Hormones, Hormone Substitutes, and Hormone Antagonists |
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Testosterone [MESH:D013739] (91) |
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E. Analytical, Diagnostic and Therapeutic Techniques and Equipment |
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E. Analytical, Diagnostic and Therapeutic Techniques and Equipment |
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Cardiofaciocutaneous syndrome [MESH:C535579] (407) |
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Pitt-Hopkins syndrome [MESH:C537403] (113) |
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Growth mental deficiency syndrome of Myhre [MESH:C537620] (51) |
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F. Psychiatry and Psychology |
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F. Psychiatry and Psychology |
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Pitt-Hopkins syndrome [MESH:C537403] (113) |
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Growth mental deficiency syndrome of Myhre [MESH:C537620] (51) |
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Alzheimer disease type 2 [MESH:C536595] (165) |
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Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57) |
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Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136) |
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Pitt-Hopkins syndrome [MESH:C537403] (113) |
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Growth mental deficiency syndrome of Myhre [MESH:C537620] (51) |
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Aromatase deficiency [MESH:C537436] (277) |
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Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
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Leydig Cell Hypoplasia [MESH:C562567] (65) |
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G. Phenomena and Processes |
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G. Phenomena and Processes |
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Mosaic variegated aneuploidy syndrome [MESH:C536987] (95) |
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