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GlyCosmos Diseases

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

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

Displaying entries **1251 - 1275** of **4621** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism
DOID:4603	epidermolytic hyperkeratosis Aliases: Bullous ichthyosiform erythroderma Epidermolytic palmoplantar hyperkeratosis epidermolytic ichthyosis	ALOX12B STS	242 412	Homo sapiens (human)
DOID:1702	ichthyosis vulgaris Aliases: Dominant congenital ichthyosiform erythroderma	ALOX12B STS	242 412	Homo sapiens (human)
DOID:4535	hypotrichosis	ALOX12B GALNT3 GLB1 LSS PIGL PTGS2 SULT2B1 XYLT1	242 2591 2720 4047 5743 64131 6820 9487	Homo sapiens (human)
DOID:0060253	scapuloperoneal myopathy	ALOX5	240	Homo sapiens (human)
DOID:2123	tularemia	ALOX5	240	Homo sapiens (human)
DOID:0080821	exercise-induced bronchoconstriction Aliases: exercise-induced asthma	ALOX5	240	Homo sapiens (human)
DOID:10247	pleurisy	ALOX5 ICAM1 MTAP PIK3CG PLA2G10 PLA2G2A PLA2G6 PTGS2 TNF TPI1	240 3383 4507 5294 5320 5743 7124 7167 8398 8399	Homo sapiens (human)
DOID:13336	congenital toxoplasmosis Aliases: Toxoplasmosis - congen.	ALOX12 ENPP1	239 5167	Homo sapiens (human)
DOID:0050661	vitelliform macular dystrophy Aliases: Best disease Best macular dystrophy juvenile-onset vitelliform macular dystrophy	ALOX12 ALPP ATRNL1 PYGM RGN RPE	239 250 26033 5837 6120 9104	Homo sapiens (human)
DOID:8717	decubitus ulcer Aliases: Decubitus (pressure) ulcer Decubitus ulcer any site pressure sores pressure ulcer	ACSS2 CBR1 CHPT1 DHDDS PLA2G15 PTGS2	23659 55902 56994 5743 79947 873	Homo sapiens (human)
DOID:11044	gastroschisis	ACSS2 DSE ICAM1 PLA2G15 STS	23659 29940 3383 412 55902	Homo sapiens (human)
DOID:1858	McCune Albright syndrome Aliases: fibrous dysplasia of bone osteitis fibrosa disseminata polyostotic fibrous dysplasia	ACSS2 AMY1A AMY1B AMY1C APRT ENPP1 PLA2G15 SUCLG1	23659 276 277 278 353 5167 55902 8802	Homo sapiens (human)
DOID:0080288	spinocerebellar ataxia 46	PLD3	23646	Homo sapiens (human)
DOID:11219	conjunctival folliculosis Aliases: acute follicular conjunctivitis	PLD3	23646	Homo sapiens (human)
DOID:13014	shipyard eye Aliases: EKC Epidemic keratoconjunctivitis	PLD3	23646	Homo sapiens (human)
DOID:6195	conjunctivitis	ART4 CD14 IMPA1 LGALS1 MBL2 PLD3	23646 3612 3956 4153 420 929	Homo sapiens (human)
DOID:3073	brain glioblastoma multiforme Aliases: Glioblastoma multiforme of brain brain Glioblastoma	CLEC5A NCAM1	23601 4684	Homo sapiens (human)
DOID:2301	atrophy of prostate	AMACR	23600	Homo sapiens (human)
DOID:3025	acinar cell carcinoma Aliases: acinic cell carcinoma	AMACR LYZ NT5E PIK3CA PTEN	23600 4069 4907 5290 5728	Homo sapiens (human)
DOID:0111068	congenital bile acid synthesis defect 4 Aliases: CBAS4 intrahepatic cholestasis with defective conversion of trihydroxycoprostanic acid to cholic acid trihydroxycoprostanic acid in bile	AMACR HSD17B4	23600 3295	Homo sapiens (human)
DOID:0060602	alpha-methylacyl-CoA racemase deficiency Aliases: AMACR deficiency	AMACR HSD17B4	23600 3295	Homo sapiens (human)
DOID:906	peroxisomal disease Aliases: peroxisomal disorder	ACOX1 AMACR CAT DHRS11 HADH HSD17B4 HSD17B7	23600 3033 3295 51 51478 79154 847	Homo sapiens (human)
DOID:4889	lymph node tuberculosis Aliases: Tuberculous adenitis Tuberculous lymphadenopathy king's evil scrofula	SMUG1	23583	Homo sapiens (human)
DOID:7960	malignant spiradenoma Aliases: malignant eccrine spiradenoma	SMUG1	23583	Homo sapiens (human)
DOID:5292	mediastinum leiomyosarcoma Aliases: leiomyosarcoma of mediastinum	SMUG1	23583	Homo sapiens (human)

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