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 651 - 675 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:1858
  • McCune Albright syndrome
  • Aliases:
    • fibrous dysplasia of bone
    • osteitis fibrosa disseminata
    • polyostotic fibrous dysplasia
Homo sapiens (human)
DOID:13709
  • premature ejaculation
Homo sapiens (human)
DOID:0090126
  • branched-chain keto acid dehydrogenase kinase deficiency
  • Aliases:
    • BCKDK deficiency
    • BCKDKD
    • autism-epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency
Homo sapiens (human)
DOID:2073
  • perinatal intestinal perforation
Homo sapiens (human)
DOID:1561
  • cognitive disorder
  • Aliases:
    • cognitive disease
Homo sapiens (human)
DOID:0050598
  • extrapulmonary tuberculosis
Homo sapiens (human)
DOID:11077
  • brucellosis
  • Aliases:
    • Maltese fever
    • undulant fever
Homo sapiens (human)
DOID:4450
  • renal cell carcinoma
  • Aliases:
    • RCC
    • adenocarcinoma of kidney
    • hypernephroma
Homo sapiens (human)
DOID:0080367
  • chronic eosinophilic leukemia
Homo sapiens (human)
DOID:0050886
  • Troyer syndrome
  • Aliases:
    • SPG20
    • autosomal recessive spastic paraplegia 20
    • autosomal recessive spastic paraplegia Troyer type
    • autosomal recessive spastic paraplegia type 20
    • childhood-onset spastic paraparesis with distal muscle wasting
    • hereditary spastic paraplegia 20
    • spastic paraplegia 20
    • spastic paraplegia type 20
Homo sapiens (human)
DOID:7007
  • childhood cerebral astrocytoma
  • Aliases:
    • pediatric astrocytoma of Cerebrum
Homo sapiens (human)
DOID:3770
  • pulmonary fibrosis
  • Aliases:
    • Fibrosis of lung
Homo sapiens (human)
DOID:0110725
  • neuronal ceroid lipofuscinosis 10
  • Aliases:
    • CLN10
    • Cathepsin D deficiency
    • neuronal ceroid lipofuscinosis cathepsin D-deficient
    • neuronal ceroid lipofuscinosis due to cathepsin D deficiency
Homo sapiens (human)
DOID:0050632
  • oculocutaneous albinism
Homo sapiens (human)
DOID:9767
  • myocardial stunning
Homo sapiens (human)
DOID:9246
  • cerebral amyloid angiopathy
  • Aliases:
    • Cerebral Hemorrhage, Hereditary, with Amyloidosis
    • Hereditary Cerebral Hemorrhage with Amyloidosis
Homo sapiens (human)
DOID:3451
  • skin carcinoma
  • Aliases:
    • carcinoma of skin
Homo sapiens (human)
DOID:4997
  • Camurati-Engelmann disease
  • Aliases:
    • Diaphyseal dysplasia
    • Engelman's disease
    • progressive diaphyseal dysplasia
Homo sapiens (human)
DOID:3683
  • lung benign neoplasm
  • Aliases:
    • tumor of the lung
Homo sapiens (human)
DOID:10371
  • yaws
  • Aliases:
    • Bouba
    • frambesia
    • frambesia tropica
    • frambosie
    • polypapilloma tropicum
    • thymosis
Homo sapiens (human)
DOID:11121
  • pulpitis
  • Aliases:
    • pulp stones
Homo sapiens (human)
DOID:0060688
  • arteriovenous malformations of the brain
  • Aliases:
    • cerebral arteriovenous malformation
    • intracranial arteriovenous malformation
Homo sapiens (human)
DOID:11446
  • sciatic neuropathy
Homo sapiens (human)
DOID:13366
  • Stiff-Person syndrome
  • Aliases:
    • Stiff-man syndrome
    • stiff man syndrome
Homo sapiens (human)
DOID:0070127
  • congenital nongoitrous hypothyroidism 3
  • Aliases:
    • CHNG3
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