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 1626 - 1650 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism
DOID:0060449
  • gelatinous drop-like corneal dystrophy
  • Aliases:
    • GDCD
    • corneal amyloidosis
    • primary familial amyloidosis of the cornea
    • subepithelial amyloidosis of the cornea
Homo sapiens (human)
DOID:9351
  • diabetes mellitus
  • Aliases:
    • diabetes
Drosophila melanogaster (fruit fly)
DOID:0050563
  • nonsyndromic deafness
  • Aliases:
    • nonsyndromic hearing loss
    • nonsyndromic hereditary hearing loss
Rattus norvegicus (Norway rat)
DOID:14227
  • azoospermia
Danio rerio (zebrafish)
DOID:9402
  • epididymitis
Mus musculus (house mouse)
DOID:10930
  • borderline personality disorder
Homo sapiens (human)
DOID:303
  • substance-related disorder
Mus musculus (house mouse)
DOID:576
  • proteinuria
Caenorhabditis elegans
DOID:850
  • lung disease
Rattus norvegicus (Norway rat)
DOID:0060470
  • salt and pepper syndrome
  • Aliases:
    • salt & pepper syndrome
    • salt-and-pepper syndrome
Mus musculus (house mouse)
DOID:0050809
  • mucopolysaccharidosis IX
Mus musculus (house mouse)
DOID:12170
  • radial nerve lesion
  • Aliases:
    • Lesion of radial nerve
    • Radial nerve lesions
Homo sapiens (human)
DOID:13087
  • Lown-Ganong-Levine syndrome
  • Aliases:
    • atrial tachyarrhythmia with short PR interval
    • syndrome of short P-R interval, normal QRS complexes, and supraventricular tachycardias
Homo sapiens (human)
DOID:0060050
  • autoimmune disease of blood
Drosophila melanogaster (fruit fly)
DOID:14175
  • von Hippel-Lindau disease
  • Aliases:
    • Hippel Lindau syndrome
    • von Hippel-Lindau syndrome
Homo sapiens (human)
DOID:0111235
  • congenital muscular dystrophy-dystroglycanopathy type A12
  • Aliases:
    • MDDGA12
    • Walker-Warburg syndrome or muscle-eye-brain disease POMK-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A12
Homo sapiens (human)
DOID:11476
  • osteoporosis
Homo sapiens (human)
DOID:4176
  • blood group incompatibility
Homo sapiens (human)
DOID:10024
  • migraine with aura
  • Aliases:
    • classic migraine
Rattus norvegicus (Norway rat)
DOID:0110536
  • autosomal recessive nonsyndromic deafness 91
  • Aliases:
    • DFNB91
    • autosomal recessive deafness 91
Homo sapiens (human)
DOID:2129
  • atypical teratoid rhabdoid tumor
  • Aliases:
    • Atypical teratoid/rhabdoid tumor
    • Atypical teratoid/rhabdoid tumour
    • Rhabdoid tumor of the CNS
    • Rhabdoid tumour of the CNS
    • atypical teratoid rhabdoid tumour
Homo sapiens (human)
DOID:3596
  • placental site trophoblastic tumor
  • Aliases:
    • Placental-Site Gestational Trophoblastic neoplasm
    • placental site trophoblastic tumour
Drosophila melanogaster (fruit fly)
DOID:3946
  • pituitary-dependent Cushing's disease
  • Aliases:
    • Overproduction of ACTH
    • pituitary-dependent Cushing disease
Homo sapiens (human)
DOID:0080354
  • Phelan-McDermid syndrome
  • Aliases:
    • 22q13.3 deletion syndrome
    • monosomy 22q13 syndrome
Homo sapiens (human)
DOID:4608
  • common bile duct neoplasm
  • Aliases:
    • neoplasm of common bile duct
Mus musculus (house mouse)

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: August 19, 2024