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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source	Last Updated
Alliance of Genome Resources	July 29, 2024
DisGeNET	July 29, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **4276 - 4300** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source ▼
DOID:0060831	Griscelli syndrome Aliases: Chediak-Higashi-like syndrome Griscelli-Prunieras syndrome partial albinism-immunodeficiency syndrome	FCGR3B IDS	2215 3423	Homo sapiens (human)	DisGeNET DisGeNET
DOID:0050632	oculocutaneous albinism	CALR CANX G6PC3 IDS PIK3CA PTEN	3423 5290 5728 811 821 92579	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:2862	glucosephosphate dehydrogenase deficiency Aliases: Glucose-6-phosphate dehydrogenase deficiency deficiency of G-6PD	ABO ACADM AGL AGXT AKR1B1 ALDOA ALG9 APRT CYP4F3 EHHADH ENO3 EPM2A FBP1 G6PC1 G6PC2 G6PC3 G6PD GAA GALE GALK1 GALT GBE1 GLA GPI GYG1 GYG2 GYS2 HADHA HK1 HPGDS ICAM1 IDS IGF2R LDHA LGALS1 LPL MGAM MGAT1 MPDU1 MTM1 NDUFAB1 PFKL PFKM PGAM2 PGK1 PGM1 PYGL PYGM SI SLC2A2 SLC35A2 SLC37A4 SLC3A1 TKT UGP2 UGT1A10 UGT1A1 UGT1A4 UGT1A6 UGT1A7 UGT1A8 UGT8 VCAM1	178 189 1962 2027 2203 226 231 2538 2539 2542 2548 2582 2584 2592 2632 2717 27306 28 2821 2992 2998 3030 3098 3383 34 3423 3482 353 3939 3956 4023 4051 4245 4534 4706 5211 5213 5224 5230 5236 54575 54576 54577 54578 54657 54658 57818 5836 5837 6476 6514 6519 7086 7355 7360 7368 7412 7957 79796 8908 8972 92579 9526	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET
DOID:2747	glycogen storage disease Aliases: glycogenosis	ABO ACADM AGL AGXT AKR1B1 ALDOA ALG9 APRT CYP4F3 EHHADH ENO3 EPM2A FBP1 G6PC1 G6PC2 G6PC3 G6PD GAA GALE GALK1 GALT GBE1 GLA GPI GYG1 GYG2 GYS2 HADHA HK1 HPGDS ICAM1 IDS IGF2R LDHA LGALS1 LPL MGAM MGAT1 MPDU1 MTM1 NDUFAB1 PFKL PFKM PFKP PGAM2 PGK1 PGM1 PHKA1 PHKA2 PHKG2 PRKAG2 PYGL PYGM SI SLC2A2 SLC35A2 SLC37A4 SLC3A1 TKT UGP2 UGT1A10 UGT1A1 UGT1A4 UGT1A6 UGT1A7 UGT1A8 UGT8 VCAM1	178 189 1962 2027 2203 226 231 2538 2539 2542 2548 2582 2584 2592 2632 2717 27306 28 2821 2992 2998 3030 3098 3383 34 3423 3482 353 3939 3956 4023 4051 4245 4534 4706 51422 5211 5213 5214 5224 5230 5236 5255 5256 5261 54575 54576 54577 54578 54657 54658 57818 5836 5837 6476 6514 6519 7086 7355 7360 7368 7412 7957 79796 8908 8972 92579 9526	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:9266	cystinuria	ABO ACADM AGL AGXT AKR1B1 ALDOA ALG9 APRT CYP4F3 EHHADH ENO3 EPM2A FBP1 G6PC1 G6PC2 G6PC3 G6PD GAA GALE GALK1 GALT GBE1 GLA GPI GYG1 GYG2 GYS2 HADHA HK1 HPGDS ICAM1 IDS IGF2R LDHA LGALS1 LPL MGAM MGAT1 MPDU1 MTM1 NDUFAB1 PFKL PFKM PGAM2 PGK1 PGM1 PYGL PYGM SI SLC2A2 SLC35A2 SLC37A4 SLC3A1 TKT UGP2 UGT1A10 UGT1A1 UGT1A4 UGT1A6 UGT1A7 UGT1A8 UGT8 VCAM1	178 189 1962 2027 2203 226 231 2538 2539 2542 2548 2582 2584 2592 2632 2717 27306 28 2821 2992 2998 3030 3098 3383 34 3423 3482 353 3939 3956 4023 4051 4245 4534 4706 5211 5213 5224 5230 5236 54575 54576 54577 54578 54657 54658 57818 5836 5837 6476 6514 6519 7086 7355 7360 7368 7412 7957 79796 8908 8972 92579 9526	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:9870	galactosemia Aliases: Galactosaemia Galactose intolerance	ABO ACADM AGL AGXT AKR1B1 ALDOA ALG9 APRT CD14 CYP4F3 CYP51A1 EHHADH ENO3 EPM2A FBP1 G6PC1 G6PC2 G6PC3 G6PD GAA GALE GALK1 GALM GALT GBE1 GK GLA GP2 GPI GYG1 GYG2 GYS2 HADHA HK1 HPGDS ICAM1 IDS IGF2R LDHA LGALS1 LPL MGAM MGAT1 MPDU1 MTM1 NDUFAB1 PFKL PFKM PGAM2 PGK1 PGM1 PTEN PYGL PYGM SI SLC2A2 SLC35A2 SLC37A4 SLC3A1 SLC5A1 TKT UGP2 UGT1A10 UGT1A1 UGT1A4 UGT1A6 UGT1A7 UGT1A8 UGT8 VCAM1	130589 1595 178 189 1962 2027 2203 226 231 2538 2539 2542 2548 2582 2584 2592 2632 2710 2717 27306 28 2813 2821 2992 2998 3030 3098 3383 34 3423 3482 353 3939 3956 4023 4051 4245 4534 4706 5211 5213 5224 5230 5236 54575 54576 54577 54578 54657 54658 5728 57818 5836 5837 6476 6514 6519 6523 7086 7355 7360 7368 7412 7957 79796 8908 8972 92579 929 9526	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:2749	glycogen storage disease Ia	ABO ACADM AGL AGXT AKR1B1 ALDOA ALG9 APRT ARSA CYP4F3 EHHADH ENO3 EPM2A FBP1 G6PC1 G6PC2 G6PC3 G6PD GAA GALE GALK1 GALT GBE1 GLA GPI GYG1 GYG2 GYS2 HADHA HK1 HPGDS ICAM1 IDS IGF2R LDHA LGALS1 LPL MGAM MGAT1 MPDU1 MTM1 NDUFAB1 PFKL PFKM PGAM2 PGK1 PGM1 PYGL PYGM SI SLC2A2 SLC2A4 SLC35A2 SLC37A4 SLC3A1 TKT UGP2 UGT1A10 UGT1A1 UGT1A4 UGT1A6 UGT1A7 UGT1A8 UGT8 VCAM1	178 189 1962 2027 2203 226 231 2538 2539 2542 2548 2582 2584 2592 2632 2717 27306 28 2821 2992 2998 3030 3098 3383 34 3423 3482 353 3939 3956 4023 4051 410 4245 4534 4706 5211 5213 5224 5230 5236 54575 54576 54577 54578 54657 54658 57818 5836 5837 6476 6514 6517 6519 7086 7355 7360 7368 7412 7957 79796 8908 8972 92579 9526	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:4267	akinetic mutism Aliases: Coma vigilans	PRNP	5621	Homo sapiens (human)	DisGeNET
DOID:12987	agranulocytosis Aliases: Granulocytopenic disorder Granulopenia granulocytopenia	ABO ACE AGA ALDH2 B3GAT1 CD177 CD33 CEL CHPT1 COG4 CYP1B1 CYP2B6 CYP2C19 CYP2C8 CYP2C9 CYP39A1 CYP3A5 DHDDS FCGR3B FH G6PC1 G6PC3 HMMR IDUA LPIN2 MBL2 MMUT NAMPT NCAM1 PARP1 PARP9 PCCA PCCB PGM3 PIK3CA PIK3CB PIK3CD PIK3CG SELP SLC17A5 SLC27A5 SLC35A1 SLC35A2 SLC37A4 TMTC3 TNFRSF10C UGGT1 UGT1A10 UGT1A1 UGT1A3 UGT1A4 UGT1A5 UGT1A6 UGT1A7 UGT1A8 UGT1A9 UMPS	10135 10559 1056 10998 142 1545 1555 1557 1558 1559 1577 160418 1636 175 217 2215 2271 2538 2542 25839 26503 27087 28 3161 3425 4153 4594 4684 5095 5096 51302 5238 5290 5291 5293 5294 54575 54576 54577 54578 54579 54600 54657 54658 54659 56886 56994 57126 6403 7355 7372 79947 83666 8794 92579 945 9663	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET
DOID:1227	neutropenia	ABO ACE AGA ALDH2 B3GAT1 CD177 CD33 CEL CHPT1 COG4 CYP1B1 CYP2B6 CYP2C19 CYP2C8 CYP2C9 CYP39A1 CYP3A5 DHDDS FCGR3B FH G6PC1 G6PC3 HMMR IDUA LPIN2 MBL2 MMUT NAMPT NCAM1 PARP1 PARP9 PCCA PCCB PGM3 PIK3CA PIK3CB PIK3CD PIK3CG SELP SLC17A5 SLC27A5 SLC35A1 SLC35A2 SLC37A4 TMTC3 TNF TNFRSF10C UGGT1 UGT1A10 UGT1A1 UGT1A3 UGT1A4 UGT1A5 UGT1A6 UGT1A7 UGT1A8 UGT1A9 UMPS	10135 10559 1056 10998 142 1545 1555 1557 1558 1559 1577 160418 1636 175 217 2215 2271 2538 2542 25839 26503 27087 28 3161 3425 4153 4594 4684 5095 5096 51302 5238 5290 5291 5293 5294 54575 54576 54577 54578 54579 54600 54657 54658 54659 56886 56994 57126 6403 7124 7355 7372 79947 83666 8794 92579 945 9663	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:0050590	severe congenital neutropenia	ABO ACE AGA B3GAT1 CD177 CD33 CEL CHPT1 COG4 CYP1B1 CYP2B6 CYP2C19 CYP2C8 CYP2C9 CYP39A1 CYP3A5 DHDDS FCGR3B FH G6PC1 G6PC3 HMMR IDUA LPIN2 MBL2 MMUT NAMPT NCAM1 PARP1 PARP9 PCCA PCCB PGM3 PIK3CA PIK3CB PIK3CD PIK3CG SELP SLC17A5 SLC27A5 SLC35A1 SLC35A2 SLC37A4 TMTC3 TNFRSF10C UGGT1 UGT1A10 UGT1A1 UGT1A3 UGT1A4 UGT1A5 UGT1A6 UGT1A7 UGT1A8 UGT1A9 UMPS	10135 10559 1056 10998 142 1545 1555 1557 1558 1559 1577 160418 1636 175 2215 2271 2538 2542 25839 26503 27087 28 3161 3425 4153 4594 4684 5095 5096 51302 5238 5290 5291 5293 5294 54575 54576 54577 54578 54579 54600 54657 54658 54659 56886 56994 57126 6403 7355 7372 79947 83666 8794 92579 945 9663	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET
DOID:593	agoraphobia Aliases: Fear of open spaces	ACE GAD1	1636 2571	Homo sapiens (human)	DisGeNET
DOID:4090	agnosia Aliases: Dyspraxia Dyspraxia syndrome	ACADSB ACAT1 ACE AGK AGRN ALDH2 ALDH5A1 ALG13 ALG14 ALG2 ARSA ASAH1 ATP6AP2 ATP6V0A2 ATP6V1A B3GALNT2 B3GAT1 CACNA2D2 CAT CHAT CHI3L1 CHKB CHST14 CHST3 CLN5 COG4 COG5 COMT CRPPA CYP19A1 CYP27B1 CYP2B6 CYP2C9 CYP2R1 CYP2U1 CYP3A4 CYP3A5 DAG1 DGKK DPAGT1 EPM2A EXT2 EXTL3 FASN FCGR3B FKRP FKTN GAD2 GALT GBA1 GCK GFPT1 GMDS GMPPB GPAA1 GPX1 GPX3 HACD1 HADH HADHA HADHB HGSNAT HIBCH HPRT1 INPP5K LARGE1 LGALS1 LMAN2L MAN1B1 MBOAT7 MDH2 MGLL MTMR14 MTMR2 NDST1 PGAP1 PIGC PIK3CA PLA2G6 PLCB4 PNP PNPLA2 POMGNT1 POMK POMT1 POMT2 PRNP PRPS1 PSAP PTEN PTGS2 RPIA SDHA SDHB SDHD SLC35G1 SRD5A3 ST3GAL3 ST3GAL5 TECR TUSC3 UGT2B7	10159 10466 10585 1103 1116 1120 11253 113189 11343 113612 120227 1203 1312 138050 139189 148789 1555 1559 1576 1577 1588 159371 1594 1605 1636 1798 199857 2132 2137 217 2194 2215 2218 22934 23545 2572 25839 2592 26275 2629 2645 2673 27087 2762 2876 2878 29925 29954 3030 3032 3033 3251 3340 36 375790 38 3956 410 4191 427 4860 51763 523 5279 5290 5332 55624 55750 5621 5631 5660 57104 5728 5743 6389 6390 6392 64419 6487 729920 7364 79143 79147 7915 7957 79644 79868 7991 80055 81562 8398 84197 847 85365 8733 8869 8898 9200 9215 9254 9469 9524	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET
DOID:4971	myelofibrosis Aliases: Agnogenic myeloid metaplasia Aleukemic myelosis Megakaryocytic myelosclerosis bone Marrow Fibrosis myelosclerosis primary myelofibrosis	ACE AKR1C4 ALPI ALPP CALR CAT CD177 CEACAM5 CEACAM6 CHI3L1 CHIT1 FREM1 G6PD IDH1 IDH2 IL18R1 LDHA LDHB LGALS1 LGALS3 PIK3CA PIK3CB PIK3CD PIK3CG PRG2 SELP SOAT1 STS TBXAS1 TP53	1048 1109 1116 1118 158326 1636 248 250 2539 3417 3418 3939 3945 3956 3958 412 4680 5290 5291 5293 5294 5553 57126 6403 6646 6916 7157 811 847 8809	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:11476	osteoporosis	ABO ACE ACHE AGPAT2 AKR1A1 AKR1B1 AKR1C4 AKR1D1 ALDH2 ALDH7A1 ALOX12 ALOX15 ALPL ALPP ARSA ASAH1 ATRNL1 B3GALT6 B3GAT3 CAT CD14 CD38 CD44 CHST3 CLC COMT CPT1A CYP11A1 CYP11B1 CYP17A1 CYP19A1 CYP1A1 CYP1B1 CYP24A1 CYP27A1 CYP27B1 CYP2B6 CYP3A4 DDOST DGCR2 DPEP1 ENO1 ENPP1 EXT1 FASN FDPS G6PC1 GALNS GALNT3 GALT GAPDH GK GLB1 GLO1 GPAA1 GPC6 GPD2 GPLD1 GPNMB GPX1 HJV HPGDS HPRT1 HPSE HS6ST1 HSD11B1 HSD11B2 HSD17B1 HSD17B2 HSD17B4 HSD3B2 HSD3B7 HSPG2 ICAM1 IDH2 IDUA IGF2 INPP4B IRS2 ITLN1 KL LCT LEP LEPR LGALS8 LRP5 MAPK14 MBL2 MGLL MMP17 NAMPT NDUFAB1 NGLY1 OXCT1 PCCA PCCB PCNA PGLS PIGT PIK3CA PIK3CB PIK3CD PIK3CG PIP5K1B PKM PLCG2 PMM2 PNP PRKAA2 PTEN SGMS2 SIGLEC15 SIRT2 SIRT6 SLC26A2 SLC37A4 SMPD1 SMUG1 SOAT1 ST3GAL4 TM7SF2 TMEM165 TPI1 UGT2B17 UMOD VCAM1 XXYLT1 XYLT2	10082 10135 10327 10457 10555 10855 1109 11343 1178 126792 1312 1374 1432 148738 152002 1543 1545 1555 1576 1583 1584 1586 1588 1591 1593 1594 1636 1650 166929 1800 1836 2023 2131 217 2194 2224 22933 231 23583 239 246 249 250 2538 2542 25796 2588 2591 2592 2597 26033 26229 2710 2720 27306 2739 28 2820 2822 284266 2876 3251 3284 3290 3291 3292 3294 3295 3339 3383 3418 3425 3481 3938 3952 3953 3964 4041 410 4153 427 43 4326 4706 4860 501 5019 5095 5096 5111 51548 51604 5167 5290 5291 5293 5294 5315 5336 5373 55600 5563 55768 55858 5728 64132 6484 6609 6646 6718 7108 7167 7367 7369 7412 80270 8395 847 8660 8733 8821 929 9365 9394 9469 952 960 9993	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:2583	agammaglobulinemia Aliases: IGHM hypogammaglobulinemia mu heavy chain deficiency	ABO AGPS CD55 FCER2 IDS MOGS NT5E PIK3CD PNP SLC17A5	1604 2208 26503 28 3423 4860 4907 5293 7841 8540	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:2215	factor VII deficiency Aliases: deficiency, stable	LMAN1 MCFD2 NGLY1 PC	3998 5091 55768 90411	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:2236	congenital afibrinogenemia Aliases: Factor I deficiency Fibrinogen deficiency	LMAN1 MCFD2 NGLY1 PC	3998 5091 55768 90411	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:2216	factor V deficiency Aliases: Hereditary hypoproaccelerinaemia Labile factor deficiency Proaccelerin deficiency deficiency, labile	LMAN1 MCFD2 NGLY1 PC	3998 5091 55768 90411	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:3324	mood disorder Aliases: episodic mood disorder	ABAT ABO ACE CAT CD44 COMT CRYL1 CYP19A1 DGKG DGKH GAD1 GAD2 GLO1 GLUL HPGDS HSD11B2 IMPA2 KL LDHA NCAM1 PAFAH1B1 PDIA3 PFKFB3 PFKL PGD PGM1 PIK3CA PIK3CB PIK3CD PIK3CG PLA2G4A PLB1 PLCB1 PLCB4 PNPLA3 PRNP PTGS1 PTGS2 SIRT2 SOAT1 ST8SIA2 STS TM7SF2	1312 151056 1588 1608 160851 1636 18 22933 23236 2571 2572 27306 2739 2752 28 2923 3291 3613 3939 412 4684 5048 51084 5209 5211 5226 5236 5290 5291 5293 5294 5321 5332 5621 5742 5743 6646 7108 80339 8128 847 9365 960	Homo sapiens (human)	DisGeNET DisGeNET
DOID:3312	bipolar disorder Aliases: Manic Bipolar Affective disorder Manic Depressive disorder Manic bipolar I disorder bipolar depression bipolar disorder manic phase manic depression manic disorder mixed bipolar disorder	ABO ACACA ACADS ACE ACHE ACO1 ACO2 ACSL4 ADIPOQ AKR1C4 AKT1 ALDH2 ALOX12 CALR CAT CDH13 CDS1 CEACAM5 CHI3L1 CLEC10A CNTN4 CNTN5 CNTN6 COMT CS CYP19A1 DGCR2 DGKB DGKH EHHADH ETNPPL FADS1 FADS2 FUT3 G6PD GAD1 GAD2 GALC GFRA2 GLO1 GLT8D1 GPX3 GSK3B HPGDS HPSE HSD3B2 HSPG2 IDH1 IDH2 IDH3A IDH3B IL18R1 IL1R1 IMPA1 IMPA2 INPP1 KL L1CAM LDHA LMAN2L MACROD1 MACROD2 MBL2 MDGA1 ME2 MGAT4A MPPE1 MRC1 NCAM1 NCAN NPL NTNG1 PARP10 PARP9 PC PFKFB3 PFKL PGAM1 PGAP3 PGP PI4K2B PIK3C3 PIK3CA PIK3CB PIK3CD PIK3CG PIP4K2A PIP4K2C PLA2G10 PLA2G1B PLA2G2A PLA2G4A PLA2G6 PLB1 PLCB1 PLCB4 PLCG1 PNPLA3 POGLUT2 PRNP PTGDS PTGS1 PTGS2 RBKS RPN2 SCD SDHC SIGLEC7 SLC35F4 SMPD1 SMUG1 SPTLC1 SRD5A1 ST3GAL1 ST3GAL3 ST8SIA2 STT3A SYNJ1 TMTC1 TPI1 UXS1	1012 1040 10462 1048 10558 10855 1109 1116 11320 1312 140733 1431 1463 151056 152330 1588 1607 160851 1636 1962 207 217 2182 22854 23236 23583 239 2525 2539 2571 2572 2581 266727 2675 27036 27255 27306 2739 28 283871 2878 28992 2932 31 3284 3339 3417 3418 341880 3419 3420 35 3554 3612 3613 3628 3703 3897 3939 3992 4153 4200 43 4360 4684 48 50 5091 5209 5211 5223 5289 5290 5291 5293 5294 5305 5319 5320 5321 5332 5335 53942 55300 55830 5621 5730 5742 5743 6185 6319 6391 64080 6482 64850 6487 65258 6609 6715 7167 79070 79837 80146 80339 80896 811 8128 81562 83666 83857 8398 8399 847 84875 8809 8867 93210 9365 9370 9415 9993	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:0050811	congenital adrenal hyperplasia Aliases: adrenal hyperplasia 1 congenital lipoid adrenal hyperplasia lipoid CAH	ACADVL CFC1 CHST3 CYP11A1 CYP11B1 CYP11B2 CYP17A1 CYP19A1 CYP21A2 CYP2B6 CYP2C19 CYP4F3 FH GLO1 GML HADHA HSD11B2 HSD17B1 HSD17B3 HSD17B6 HSD3B1 HSD3B2 IDS MDH2 OTOA SDHB	146183 1555 1557 1583 1584 1585 1586 1588 1589 2271 2739 2765 3030 3283 3284 3291 3292 3293 3423 37 4051 4191 55997 6390 8630 9469	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:3953	adrenal gland cancer Aliases: adrenal cancer adrenal neoplasm malignant Adrenal tumor malignant neoplasm of adrenal gland neoplasm of adrenal gland tumor of the Adrenal gland	ACACA ACE ACO1 APRT CAT CD44 CHGA CHST3 CNTN4 COMT CS CYP11B1 CYP11B2 CYP17A1 CYP19A1 CYP21A2 CYP4F3 DGCR2 DHCR24 DHRS11 DLST FH G6PD GUSB HPSE HSD11B1 HSD17B7 IDH1 IDH2 L1CAM LGALS3 MDH2 PARP1 PIK3CA PIK3CB PIK3CD PIK3CG PKD2 PTEN PTGS2 SDHA SDHB SDHC SDHD SLC33A1 SMPD1 SMUG1 SORD	10855 1113 1312 142 1431 152330 1584 1585 1586 1588 1589 1636 1718 1743 2271 23583 2539 2990 31 3290 3417 3418 353 3897 3958 4051 4191 48 51478 5290 5291 5293 5294 5311 5728 5743 6389 6390 6391 6392 6609 6652 79154 847 9197 9469 960 9993	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:3947	adrenal gland hyperfunction Aliases: Adrenocortical hyperfunction hyperadrenalism hypercortisolism	ACAT1 ACE AKR1B1 APRT CYP11B1 CYP11B2 CYP17A1 CYP19A1 CYP3A4 CYP4F3 FASN FH HSD11B1 HSD11B2 HSD3B1 HSD3B2 SMUG1	1576 1584 1585 1586 1588 1636 2194 2271 231 23583 3283 3284 3290 3291 353 38 4051	Homo sapiens (human)	DisGeNET DisGeNET
DOID:12252	obsolete Cushing's syndrome	ACAT1 ACE AKR1B1 APRT CYP11B1 CYP11B2 CYP17A1 CYP19A1 CYP3A4 CYP4F3 FASN FH HSD11B1 HSD11B2 HSD3B1 HSD3B2 SMUG1	1576 1584 1585 1586 1588 1636 2194 2271 231 23583 3283 3284 3290 3291 353 38 4051	Homo sapiens (human)	DisGeNET DisGeNET

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