GlyCosmos Portal

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Displaying entries **5301 - 5325** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism
DOID:1742	drug psychosis Aliases: Drug-induced psychosis Drug-induced psychotic disorder	ACE CALR COMT GAD1 GAD2 HPGDS	1312 1636 2571 2572 27306 811	Homo sapiens (human)
DOID:9620	vesicoureteral reflux Aliases: vesico-ureteral reflux	ACE COMT EXT1 GFRA1 HPSE2 PIGN PIGQ SDHA SDHB SLC33A1 SLC3A1 SMC3	1312 1636 2131 23556 2674 60495 6389 6390 6519 9091 9126 9197	Homo sapiens (human)
DOID:10930	borderline personality disorder	ACE CACNA2D4 COMT DBT DGKH ETNPPL FADS1 G6PD GAD1 GAD2 GPC1 IMPA2 LDHA LMAN2L MCAT MPPE1 PLCG1 SYNJ1	1312 160851 1629 1636 2539 2571 2572 27349 2817 3613 3939 3992 5335 64850 65258 81562 8867 93589	Homo sapiens (human)
DOID:12401	intermittent explosive disorder Aliases: explosive personality disorder	ACE APRT CACNA2D4 COMT DBT DGKH ETNPPL FADS1 G6PD GAD1 GAD2 GPC1 IMPA2 LDHA LMAN2L MCAT MPPE1 PAFAH1B1 PLCD1 PLCG1 SYNJ1	1312 160851 1629 1636 2539 2571 2572 27349 2817 353 3613 3939 3992 5048 5333 5335 64850 65258 81562 8867 93589	Homo sapiens (human)
DOID:8941	seborrheic infantile dermatitis Aliases: Complement 5 dysfunction Generalized seborrheic dermatitis of infants Infantile seborrheic dermatitis Infantile seborrhoeic dermatitis Pityriasis capitis Seborrhea sicca Seborrhoea capitis Seborrhoeic dermatitis of scalp Seborrhoeic eczema of scalp cradle cap seborrhea capitis	COMT CYP51A1 PIK3CA	1312 1595 5290	Homo sapiens (human)
DOID:715	obsolete T-cell lymphoblastic leukemia/lymphoma	CD209 CD38 CD44 CNTN2 COMT CYP19A1 FCGR3B FUT4 ICAM1 LGALS1 LGALS9 MRC1 MTAP NCAM1 PIK3CA PIK3CB PIK3CD PIK3CG PNP PTEN SACM1L SELL SIGLEC7 SOAT1 TALDO1 TMED9 VCAM1	1312 1588 2215 22908 2526 27036 30835 3383 3956 3965 4360 4507 4684 4860 5290 5291 5293 5294 54732 5728 6402 6646 6888 6900 7412 952 960	Homo sapiens (human)
DOID:12169	carpal tunnel syndrome Aliases: CTS - Carpal tunnel syndrome Median nerve entrapment carpal tunnel median neuropathy	ACAN ACE CHPT1 COMT CYP19A1 OLR1 PTGS2 UMPS	1312 1588 1636 176 4973 56994 5743 7372	Homo sapiens (human)
DOID:799	varicose veins Aliases: Varix Venous ectasia Venous varices varices	ACHE AKR1B10 CALR CHST3 COMT CYP4A11 CYP4F2 DLD G6PC3 ICAM1 PGP PIK3CA PTGS2 SELE STS	1312 1579 1738 283871 3383 412 43 5290 57016 5743 6401 811 8529 92579 9469	Homo sapiens (human)
DOID:2479	central nervous system origin vertigo Aliases: Vertigo of central origin central vestibular vertigo	ACHE COMT CYP3A5 FKRP GCDH GLA GYG1 NAGA NT5E SGSH	1312 1577 2639 2717 2992 43 4668 4907 6448 79147	Homo sapiens (human)
DOID:8645	subacute delirium	ACHE ACSS2 COMT CYP3A5 ENO2 FCGR3B FIG4 LGALS3 PIK3CA PIK3CB PIK3CD PIK3CG PLA2G15 SOAT1 UGCG	1312 1577 2026 2215 23659 3958 43 5290 5291 5293 5294 55902 6646 7357 9896	Homo sapiens (human)
DOID:0060776	congenital diarrhea 5 with tufting enteropathy Aliases: DIAR5 congenital diarrhoea 5 with tufting enteropathy congenital familial intractable diarrhea with epithelial or epithelium abnormalities congenital familial intractable diarrhoea with epithelial or epithelium abnormalities congenital tufting enteropathy tufting enteropathy	COMT CYP2E1 DGAT1 MAG PRNP	1312 1571 4099 5621 8694	Homo sapiens (human)
DOID:10933	obsessive-compulsive disorder Aliases: Anancastic neurosis obsessive compulsive disorder	ABO ACACA ACAN COMT CYP19A1 CYP2C19 DGKD EFNA5 FCGR3B GAD2 HTR2A LCT	1312 1557 1588 176 1946 2215 2572 28 31 3356 3938 8527	Homo sapiens (human)
DOID:9828	neonatal abstinence syndrome Aliases: Drug withdrawal syndrome in newborn	COMT CYP2B6	1312 1555	Homo sapiens (human)
DOID:9974	drug dependence	COMT CYP2B6 NCAM1	1312 1555 4684	Homo sapiens (human)
DOID:0060402	chromosome 17p13.1 deletion syndrome	ALPP ATRNL1 CD33 CD38 COMT CYP2B6 FCN2 OCRL PAFAH1B1 PIGA PIGN PLCB1 PLCE1 PLCG1 PTEN SLC17A5	1312 1555 2220 23236 23556 250 26033 26503 4952 5048 51196 5277 5335 5728 945 952	Homo sapiens (human)
DOID:0110850	xeroderma pigmentosum group B Aliases: XP group B XPB XPBC	CAT COMT CYP1B1 HPGDS HPRT1 OGG1 PTEN SMUG1 TALDO1 XYLT2	1312 1545 23583 27306 3251 4968 5728 64132 6888 847	Homo sapiens (human)
DOID:0110847	xeroderma pigmentosum variant type Aliases: XPV photosensitivity with defective DNA synthesis xeroderma pigmentosum with normal DNA repair rates	CAT COMT CYP1B1 HPGDS HPRT1 OGG1 PTEN SMUG1 TALDO1 XYLT2	1312 1545 23583 27306 3251 4968 5728 64132 6888 847	Homo sapiens (human)
DOID:0110848	xeroderma pigmentosum group F Aliases: XP group F XP6 XPF xeroderma pigmentosum VI	CAT COMT CYP1B1 HPGDS HPRT1 OGG1 PTEN SMUG1 TALDO1 XYLT2	1312 1545 23583 27306 3251 4968 5728 64132 6888 847	Homo sapiens (human)
DOID:0110846	xeroderma pigmentosum group E Aliases: XP group E XP5 XPE xeroderma pigmentosum V	CAT COMT CYP1B1 HPGDS HPRT1 OGG1 PTEN SMUG1 TALDO1 XYLT2	1312 1545 23583 27306 3251 4968 5728 64132 6888 847	Homo sapiens (human)
DOID:0110849	xeroderma pigmentosum group G Aliases: XP group G XP7 XPG xeroderma pigmentosum VII	CAT COMT CYP1B1 HPGDS HPRT1 OGG1 PTEN SMUG1 TALDO1 XYLT2	1312 1545 23583 27306 3251 4968 5728 64132 6888 847	Homo sapiens (human)
DOID:0050427	xeroderma pigmentosum	CAT COMT CYP1B1 HPGDS HPRT1 OGG1 PTEN SMUG1 TALDO1 XYLT2	1312 1545 23583 27306 3251 4968 5728 64132 6888 847	Homo sapiens (human)
DOID:0110844	xeroderma pigmentosum group C Aliases: XP group C XP3 XPC XPCC xeroderma pigmentosum III	CAT COMT CYP1B1 HPGDS HPRT1 MPG OGG1 PIK3CA PIK3CD PIK3CG PTEN PTGS2 SMUG1 TALDO1 XYLT2	1312 1545 23583 27306 3251 4350 4968 5290 5293 5294 5728 5743 64132 6888 847	Homo sapiens (human)
DOID:0110845	xeroderma pigmentosum group D Aliases: XP group D XP group H XP4 XP8 XPD XPDC XPH xeroderma pigmentosum IV xeroderma pigmentosum VIII	CAT COMT CYP1B1 HPGDS HPRT1 ICAM1 OGG1 PTEN SLC35A2 SMUG1 TALDO1 UGGT1 UGT1A10 UGT1A1 UGT1A3 UGT1A4 UGT1A5 UGT1A6 UGT1A7 UGT1A8 UGT1A9 XYLT2	1312 1545 23583 27306 3251 3383 4968 54575 54576 54577 54578 54579 54600 54657 54658 54659 56886 5728 64132 6888 7355 847	Homo sapiens (human)
DOID:11382	corneal neovascularization	COMT CYP1B1 DCN GLB1 ICAM1 LGALS3 NGLY1	1312 1545 1634 2720 3383 3958 55768	Homo sapiens (human)
DOID:0080365	endometrial hyperplasia	AKR1C1 AKR1C3 CHST3 COMT CYP11A1 CYP17A1 CYP19A1 CYP1A1 HSD17B7 MRC1 PIK3CA PKM PNPLA2 PTEN PTGS2 STS SULT1E1 TFF1	1312 1543 1583 1586 1588 1645 412 4360 51478 5290 5315 57104 5728 5743 6783 7031 8644 9469	Homo sapiens (human)

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