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 5651 - 5675 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism
DOID:0080490
  • mucolipidosis type IV
Homo sapiens (human)
DOID:2565
  • macular corneal dystrophy
  • Aliases:
    • Fehr corneal dystrophy
    • MACULAR DYSTROPHY, CORNEAL, 1
Rattus norvegicus (Norway rat)
DOID:0090016
  • chromosome 5q deletion syndrome
  • Aliases:
    • 5q- syndrome, refractory macrocytic anemia due to 5q deletion
    • myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
Homo sapiens (human)
DOID:780
  • placenta disease
Homo sapiens (human)
DOID:496
  • spindle cell hemangioma
  • Aliases:
    • SCH
Homo sapiens (human)
DOID:0111052
  • Scott syndrome
  • Aliases:
    • BDPLT7
    • SCTS
    • bleeding abnormality due to deficiency of platelet biding of factor X
    • familial prothrombin consumption inhibitor
    • familial prothrombin conversion defect
    • platelet-type bleeding disorder 7
    • prothrombin consumption deficiency
Homo sapiens (human)
DOID:0050598
  • extrapulmonary tuberculosis
Homo sapiens (human)
DOID:0110635
  • muscular dystrophy-dystroglycanopathy type B5
  • Aliases:
    • FKRP-related congenital muscular dystrophy
    • MDC1C
    • MDDGB5
    • congenital muscular dystrophy 1C
    • muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5
    • muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type B, 5
Rattus norvegicus (Norway rat)
DOID:0110299
  • autosomal recessive limb-girdle muscular dystrophy type 2I
  • Aliases:
    • LGMD2I
    • Limb-girdle muscular dystrophy due to FKRP deficiency
    • MDDGC5
    • muscular dystrophy limb-girdle type 2I
    • muscular dystrophy-dystroglycanopathy (limb-girdle) type C 5
    • muscular dystrophy-dystroglycanopathy limb-girdle FRKP-related
Rattus norvegicus (Norway rat)
DOID:0111241
  • congenital muscular dystrophy-dystroglycanopathy type A5
  • Aliases:
    • MDDGA5
    • Walker-Warburg syndrome or muscle-eye-brain disease, FKRP-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5
Rattus norvegicus (Norway rat)
DOID:11724
  • limb-girdle muscular dystrophy
  • Aliases:
    • Erb's muscular dystrophy
    • Leyden-Mbius muscular dystrophy
    • limb girdle muscular dystrophy
Rattus norvegicus (Norway rat)
DOID:0050731
  • vitamin B12 deficiency
  • Aliases:
    • cobalamin deficiency
    • hypocobalaminemia
Rattus norvegicus (Norway rat)
DOID:0111061
  • familial hypobetalipoproteinemia 2
  • Aliases:
    • FHBL2
    • combined familial hypolipidemia
Mus musculus (house mouse)
DOID:14250
  • Down syndrome
  • Aliases:
    • Complete trisomy 21 syndrome
    • Down's syndrome
    • Down's syndrome - trisomy 21
    • Downs syndrome
    • G Trisomy
    • trisomy 21 syndrome
Rattus norvegicus (Norway rat)
DOID:5468
  • biliary papillomatosis
  • Aliases:
    • bile duct papillomatosis
Homo sapiens (human)
DOID:4682
  • extrahepatic bile duct carcinoma
  • Aliases:
    • carcinoma of extrahepatic bile duct
    • extrahepatic bile duct cancer
Homo sapiens (human)
DOID:4877
  • breast adenoid cystic carcinoma
  • Aliases:
    • Mammary Adenocystic carcinoma
Homo sapiens (human)
DOID:1252
  • trichuriasis
  • Aliases:
    • Infection by Trichuris trichura
    • Trichuriasis infection
    • Whipworm disease
    • trichuris trichiura infection
Homo sapiens (human)
DOID:2433
  • epidermal appendage tumor
  • Aliases:
    • neoplasm of skin with adnexal differentiation
    • neoplasm of the skin Appendage
    • skin appendage tumour
Homo sapiens (human)
DOID:0110274
  • autosomal recessive limb-girdle muscular dystrophy
Drosophila melanogaster (fruit fly)
DOID:9884
  • muscular dystrophy
Drosophila melanogaster (fruit fly)
DOID:0112374
  • muscular dystrophy-dystroglycanopathy
  • Aliases:
    • MDDG
Drosophila melanogaster (fruit fly)
DOID:0050453
  • lissencephaly
Drosophila melanogaster (fruit fly)
DOID:0050560
  • Walker-Warburg syndrome
  • Aliases:
    • HARD syndrome
    • cerebroocular dysplasia-muscular dystrophy syndrome
Drosophila melanogaster (fruit fly)
DOID:0112380
  • muscular dystrophy-dystroglycanopathy type B2
  • Aliases:
    • MDDGB2
    • congenital muscular dystrophy POMT2-related
Drosophila melanogaster (fruit fly)

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Last updated: August 19, 2024