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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 **4301 - 4325** of **7942** in total

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Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism
DOID:10652	Alzheimer's disease Aliases: Alzheimer disease Alzheimers dementia	ENO1 ENO2 ERR1 ERR2 ERR3 GTT2 TDH1 TDH2 TDH3	850666 853106 853169 853395 853465 854575 855373 855848 856579	Saccharomyces cerevisiae S288C
DOID:11832	visual epilepsy Aliases: epilepsy, visual	ENO1 ENO2 ERR1 ERR2 ERR3 KAR2	853169 853418 854575 855373 855848 856579	Saccharomyces cerevisiae S288C
DOID:14115	toxic shock syndrome Aliases: TSS toxic shock	ENO1 ENO2 ERR1 ERR2 ERR3	853169 854575 855373 855848 856579	Saccharomyces cerevisiae S288C
DOID:1712	aortic valve stenosis Aliases: Aortic stenosis Rheumatic aortic stenosis rheumatic aortic valve stenosis	ENO1 ENO2 ERR1 ERR2 ERR3	853169 854575 855373 855848 856579	Saccharomyces cerevisiae S288C
DOID:0080855	Parkinsonism	ENO1 ENO2 ERR1 ERR2 ERR3	853169 854575 855373 855848 856579	Saccharomyces cerevisiae S288C
DOID:10283	prostate cancer Aliases: NGP - new growth of prostate hereditary prostate cancer malignant tumor of the prostate prostate cancer, familial prostate neoplasm prostatic cancer prostatic neoplasm tumor of the prostate	ENO1 ENO2 GCY1 OGG1 OST3 YPR1	851974 853169 854252 854287 854942 856579	Saccharomyces cerevisiae S288C
DOID:11054	urinary bladder cancer Aliases: bladder cancer tumor of the bladder	ENO1 ENO2 HXK1 RHO1	850614 853169 856294 856579	Saccharomyces cerevisiae S288C
DOID:3459	breast carcinoma Aliases: Mammary carcinoma carcinoma of breast	ENO1 ENO2 RHO1	853169 856294 856579	Saccharomyces cerevisiae S288C
DOID:12783	migraine without aura Aliases: common migraine	ENO1 ENO2	853169 856579	Saccharomyces cerevisiae S288C
DOID:1800	neuroendocrine carcinoma	ENO1 ENO2	853169 856579	Saccharomyces cerevisiae S288C
DOID:936	brain disease Aliases: encephalopathy	ENO1 ENO2	853169 856579	Saccharomyces cerevisiae S288C
DOID:11459	pseudotumor cerebri Aliases: benign intracranial hypertension idiopathic intracranial hypertension	ENO2 GLB1 L1CAM PARP4 PIK3CA PTEN SDHB SDHC	143 2026 2720 3897 5290 5728 6390 6391	Homo sapiens (human)
DOID:9428	intracranial hypertension Aliases: Raised intracranial pressure	ENO2 GLB1 L1CAM PARP4 PIK3CA PTEN SDHB SDHC	143 2026 2720 3897 5290 5728 6390 6391	Homo sapiens (human)
DOID:3093	nervous system cancer Aliases: malignant neoplasm of nervous system neoplasm of nervous system nervous system neoplasm neural neoplasm neural tumor tumor of the nervous system	ENO2 IDH1 L2HGDH MUTYH NEU1 PTEN	2026 3417 4595 4758 5728 79944	Homo sapiens (human)
DOID:2685	ossifying fibromyxoid tumor Aliases: Ossifying Fibromyxoma ossifying fibromyxoid tumour	ENO2	2026	Homo sapiens (human)
DOID:0060551	poikiloderma with neutropenia Aliases: poikiloderma with neutropenia, Clericuzio type	ENOSF1 GPX1 GPX3 MAG PLCB1	23236 2876 2878 4099 55556	Homo sapiens (human)
DOID:14679	VACTERL association	ENOSF1 IL18R1 OGG1 PIK3CA PTEN	4968 5290 55556 5728 8809	Homo sapiens (human)
DOID:0060468	Holt-Oram syndrome Aliases: atrio-digital syndrome atriodigital dysplasia heart-hand syndrome	ENOSF1 IL18R1 OGG1 PIK3CA	4968 5290 55556 8809	Homo sapiens (human)
DOID:14699	thrombocytopenia-absent radius syndrome Aliases: Radial aplasia-thrombocytopenia syndrome Thrombocytopenia with absent radii (TAR) syndrome	ENOSF1 IL18R1 OGG1 PIK3CA	4968 5290 55556 8809	Homo sapiens (human)
DOID:2926	Klippel-Trenaunay syndrome Aliases: Haemangiectatic hypertrophy Klippel-Trenaunay-Weber syndrome angioosteohypertrophy syndrome	ENOSF1 IL18R1 OGG1 PIK3CA	4968 5290 55556 8809	Homo sapiens (human)
DOID:1933	Rubinstein-Taybi syndrome Aliases: Broad Thumb-Hallux syndrome Rubinstein syndrome proximal chromosome 16p13.3 deletion syndrome	ENOSF1 IL18R1 OGG1 PIK3CA	4968 5290 55556 8809	Homo sapiens (human)
DOID:9467	nail-patella syndrome Aliases: Fong disease Turner-Kiser syndrome hereditary onychoostedysplasia iliac horn syndrome nail patella syndrome	ENOSF1 IL18R1 OGG1 PIK3CA	4968 5290 55556 8809	Homo sapiens (human)
DOID:0090024	split hand-foot malformation 1 with sensorineural hearing loss Aliases: SHFM1D congenital deafness with split hands and feet	ENOSF1 IL18R1 OGG1 PIK3CA	4968 5290 55556 8809	Homo sapiens (human)
DOID:0060861	microphthalmia with limb anomalies Aliases: MLA OAS Waardenburg anophthalmia syndrome anophthalmia-syndactyly syndrome ophthalmoacromelic syndrome	ENOSF1 IL18R1 OGG1 PIK3CA	4968 5290 55556 8809	Homo sapiens (human)
DOID:0050949	autosomal recessive hypophosphatemic rickets	ENPP1 GALNT3 IDUA	2591 3425 5167	Homo sapiens (human)

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