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 3651 - 3675 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:297
  • pleomorphic adenoma carcinoma
  • Aliases:
    • carcinoma ex pleomorphic adenoma
    • carcinoma in pleomorphic adenoma
Homo sapiens (human)
DOID:14323
  • Marfan syndrome
  • Aliases:
    • Marfan's syndrome
Homo sapiens (human)
DOID:0080502
  • GM1 gangliosidosis type 1
Homo sapiens (human)
DOID:0110786
  • hereditary spastic paraplegia 35
  • Aliases:
    • FAHN
    • SPG35
    • autosomal recessive spastic paraplegia 35
    • autosomal recessive spastic paraplegia type 35
    • fatty acid hydroxylase-associated neurodegeneration
    • leukodystrophy, dysmyelinating and spastic paraparesis with or without dystonia
Homo sapiens (human)
DOID:0110047
  • Alzheimer's disease 14
  • Aliases:
    • AD14
    • Alzheimer disease 14
    • Alzheimer's disease 14, late onset
Homo sapiens (human)
DOID:0050175
  • tick-borne encephalitis
  • Aliases:
    • Central European encephalitis
    • Far Eastern TBE
    • Russian spring-summer encephalitis
    • Siberian tick-borne encephalitis
    • Taiga encephalitis
    • Western European tick-borne encephalitis
    • west-Siberian encephalitis
Homo sapiens (human)
DOID:0050980
  • spinocerebellar ataxia type 31
Homo sapiens (human)
DOID:12594
  • Potter's syndrome
  • Aliases:
    • Potter sequence
    • Potter syndrome
Homo sapiens (human)
DOID:0110425
  • dilated cardiomyopathy 1A
  • Aliases:
    • CDCD1
    • dilated cardiomyopathy with conduction defect 1
    • familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Homo sapiens (human)
DOID:0050328
  • congenital hypothyroidism
Homo sapiens (human)
DOID:782
  • renal infectious disease
Homo sapiens (human)
DOID:0110465
  • autosomal recessive nonsyndromic deafness 104
  • Aliases:
    • DFNB104
    • autosomal recessive deafness 104
Homo sapiens (human)
DOID:2339
  • Crouzon syndrome
  • Aliases:
    • Craniofacial Dysostosis
Homo sapiens (human)
DOID:116
  • pericardium cancer
  • Aliases:
    • Pericardial tumor
    • malignant neoplasm of pericardium
    • malignant tumor of Pericardium
Homo sapiens (human)
DOID:7566
  • eccrine porocarcinoma
  • Aliases:
    • Eccrine porocarcinoma of skin
    • Porocarcinoma
    • malignant Eccrine Poroma
Homo sapiens (human)
DOID:1270
  • hereditary hemorrhagic telangiectasia
  • Aliases:
    • Osler hemorrhagic telangiectasia syndrome
    • Osler-Weber-Rendu disease
    • Rendu-Osler-Weber disease
Homo sapiens (human)
DOID:1563
  • dermatomycosis
Homo sapiens (human)
DOID:0080195
  • Marinesco-Sjogren syndrome
  • Aliases:
    • Garland-Moorhouse syndrome
    • Marinesco-Garland syndrome
    • Oligophrenic cerebellolenticular degeneration
    • hereditary oligophrenic cerebello-lental degeneration
Homo sapiens (human)
DOID:4325
  • Ebola hemorrhagic fever
  • Aliases:
    • Ebola virus disease
Homo sapiens (human)
DOID:5241
  • hemangioblastoma
  • Aliases:
    • Capillary Hemangioblastoma
Homo sapiens (human)
DOID:13711
  • dental fluorosis
  • Aliases:
    • Intrinsic enamel discolouration of fluorosis
    • Mottled teeth
    • Mottling of enamel
Homo sapiens (human)
DOID:9432
  • renal glycosuria
  • Aliases:
    • renal diabetes
Homo sapiens (human)
DOID:2495
  • senile angioma
  • Aliases:
    • Senile hemangioma
    • Senile naevus of skin
Homo sapiens (human)
DOID:530
  • eyelid disease
Homo sapiens (human)
DOID:0060158
  • acquired metabolic disease
Homo sapiens (human)

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024