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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 **4826 - 4850** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism
DOID:4404	occupational dermatitis Aliases: Occupational allergic contact dermatitis Occupational eczema	AKR1B10 AKR1C2 CD44 CYP1A1 CYP1B1 G6PD GLB1 UGT1A1 UGT1A6	1543 1545 1646 2539 2720 54578 54658 57016 960	Homo sapiens (human)
DOID:2773	contact dermatitis Aliases: Contact dermatitis/eczema Contact eczema Dermatitis, venenata dermatitis venenata	AKR1B10 AKR1C2 CD44 CYP1A1 CYP1B1 G6PD GLB1 UGT1A1 UGT1A6	1543 1545 1646 2539 2720 54578 54658 57016 960	Homo sapiens (human)
DOID:2712	phimosis Aliases: Tight foreskin Tight frenulum	CYP1A1 CYP1B1 CYP27B1 SRD5A2	1543 1545 1594 6716	Homo sapiens (human)
DOID:0050448	white sponge nevus Aliases: hereditary mucosal leukokeratosis white sponge nevus of Cannon	ALDH2 CYP1A1 CYP1B1 CYP2E1 HPGDS LGALS1 LYZ OGG1 PTGS2	1543 1545 1571 217 27306 3956 4069 4968 5743	Homo sapiens (human)
DOID:9655	oral mucosa leukoplakia	ALDH2 CYP1A1 CYP1B1 CYP2E1 HPGDS LGALS1 LYZ OGG1 PTGS2 TP53	1543 1545 1571 217 27306 3956 4069 4968 5743 7157	Homo sapiens (human)
DOID:750	peptic ulcer disease Aliases: acute peptic ulcer with hemorrhage acute peptic ulcer with hemorrhage and perforation acute peptic ulcer without hemorrhage and without perforation	A4GNT ABO ACE CD14 CYP1A1 CYP1A2 CYP2C19 CYP2C8 CYP2C9 CYP2E1 FUT4 GGT1 LDHA PTGS1 PTGS2 SI	1543 1544 1557 1558 1559 1571 1636 2526 2678 28 3939 51146 5742 5743 6476 929	Homo sapiens (human)
DOID:229	female reproductive system disease	CYP19A1 CYP1A1 CYP1A2 CYP2B6 LGALS9	1543 1544 1555 1588 3965	Homo sapiens (human)
DOID:0050689	brachydactyly-syndactyly syndrome	MBOAT1	154141	Homo sapiens (human)
DOID:10908	hydrocephalus Aliases: hydrocephalus, X-linked hydrocephalus, nonsyndromic, autosomal recessive	Hmgb1 Pomk Ppara	15289 19013 74653	Mus musculus (house mouse)
DOID:234	colon adenocarcinoma Aliases: Colonic adenocarcinoma adenocarcinoma of colon	Hmgb1 Pik3ca	15289 18706	Mus musculus (house mouse)
DOID:3526	cerebral infarction Aliases: CVA - Cerebral infarction Cerebral infarct	Hmgb1 Pdx1 Rbp4 Tnf	15289 18609 19662 21926	Mus musculus (house mouse)
DOID:13603	obstructive jaundice Aliases: Cholestatic Jaundice Cholestatic jaundice syndrome Obstructive hyperbilirubinemia	Hmgb1 Pcna Ucp2	15289 18538 22228	Mus musculus (house mouse)
DOID:11446	sciatic neuropathy	Gsk3b Hmgb1 Kcnj11 Pcna Ppargc1a Tlr4 Tnf	15289 16514 18538 19017 21898 21926 56637	Mus musculus (house mouse)
DOID:0050948	autosomal dominant hypophosphatemic rickets	ENPP1 GALNT8 KLB	152831 26290 5167	Homo sapiens (human)
DOID:1100	ovarian disease	CYP19A1 KLB	152831 1588	Homo sapiens (human)
DOID:0110741	type 1 diabetes mellitus 2 Aliases: IDDM2 Insulin-Dependent Diabetes Mellitus 2	Hk2 Ins1 Ins2	15277 16333 16334	Mus musculus (house mouse)
DOID:0110196	Charcot-Marie-Tooth disease type 4G Aliases: CMT4G Charcot-Marie-Tooth neuropathy type 4G HMSNR autosomal recessive Charcot-Marie-Tooth disease type 4G hereditary motor and sensory neuropathy Russe type	Hk1	15275	Mus musculus (house mouse)
DOID:10923	sickle cell anemia Aliases: Hb SC disease Hb-S/Hb-C disease Hb-SS disease without crisis Hemoglobin S disease without crisis Sickle-cell/Hb-C disease without crisis drepanocytosis haemoglobin SC disease hemoglobin SC disease sickle cell anaemia	Hk1 Pgf Tnf	15275 18654 21926	Mus musculus (house mouse)
DOID:10584	retinitis pigmentosa Aliases: pericentral pigmentary retinopathy	Hk1 Hkdc1 Kl Pomgnt1	15275 16591 216019 68273	Mus musculus (house mouse)
DOID:0080029	autosomal recessive spinocerebellar ataxia 16 Aliases: SCAR16	CNTN4 SUMF1	152330 285362	Homo sapiens (human)
DOID:3211	lysosomal storage disease Aliases: disorder of lysosomal enzyme inborn lysosomal enzyme disorder lysosomal storage metabolism disorder	Hexb	15212	Mus musculus (house mouse)
DOID:3323	Sandhoff disease Aliases: Sandhoff Jatzkewitz disease	Hexb	15212	Mus musculus (house mouse)
DOID:12377	spinal muscular atrophy	Hexb	15212	Mus musculus (house mouse)
DOID:3320	Tay-Sachs disease Aliases: GM2 gangliosidosis, type 1 hexosaminidase A deficiency	Hexa	15211	Mus musculus (house mouse)
DOID:9409	diabetes insipidus	Has2	15117	Mus musculus (house mouse)

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