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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources October 9, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 13501 - 13525 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:0110482
  • autosomal recessive nonsyndromic deafness 24
  • Aliases:
    • DFNB24
    • autosomal recessive deafness 24
Homo sapiens (human)
DOID:0060322
  • mastoiditis
Homo sapiens (human)
DOID:0111992
  • immunodeficiency 53
  • Aliases:
    • IMD53
Homo sapiens (human)
DOID:10881
  • hand, foot and mouth disease
  • Aliases:
    • Vesicular stomatitis and exanthem
Homo sapiens (human)
DOID:0110556
  • autosomal dominant nonsyndromic deafness 27
  • Aliases:
    • DFNA27
    • autosomal dominant deafness 27
Homo sapiens (human)
DOID:0080280
  • gingival fibromatosis 5
Homo sapiens (human)
DOID:0050430
  • multiple endocrine neoplasia type 2A
  • Aliases:
    • MEN2A
    • Sipple syndrome
    • multiple endocrine neoplasia II
Homo sapiens (human)
DOID:0080204
  • renal hypoplasia
Homo sapiens (human)
DOID:10016
  • multiple endocrine neoplasia type 2B
  • Aliases:
    • MEN type IIB
    • MEN2B
    • Multiple endocrine neoplasia, type 3
    • Wagenmann-Froboese syndrome
    • mucosal neuroma syndrome
Homo sapiens (human)
DOID:0110394
  • retinitis pigmentosa 44
  • Aliases:
    • RP44
Homo sapiens (human)
DOID:12528
  • lesion of sciatic nerve
Homo sapiens (human)
DOID:0110317
  • hypertrophic cardiomyopathy 11
  • Aliases:
    • CMH11
    • cardiomyopathy familial hypertrophic 11
Homo sapiens (human)
DOID:0111562
  • overhydrated hereditary stomatocytosis
  • Aliases:
    • OHS
    • potassium sodium disorder of erythrocyte
    • stomatocytosisIOHST
Homo sapiens (human)
DOID:0050641
  • Rh deficiency syndrome
Homo sapiens (human)
DOID:0110862
  • congenital stationary night blindness autosomal dominant 1
  • Aliases:
    • CSNBAD1
    • rhodopsin-related congenital stationary night blindness
Homo sapiens (human)
DOID:0110372
  • retinitis pigmentosa 4
  • Aliases:
    • RP4
Homo sapiens (human)
DOID:0110713
  • Oguchi disease-2
  • Aliases:
    • CSNBO2
    • congenital stationary night blindness Oguchi type 2
Homo sapiens (human)
DOID:0070416
  • Luo-Schoch-Yamamoto syndrome
  • Aliases:
    • LUSYAM
Homo sapiens (human)
DOID:0111015
  • Newfoundland cone-rod dystrophy
  • Aliases:
    • NFRCD
Homo sapiens (human)
DOID:0050683
  • Bothnia retinal dystrophy
  • Aliases:
    • Vasterbotten dystrophy
Homo sapiens (human)
DOID:9286
  • priapism
  • Aliases:
    • Mentulagra
Rattus norvegicus (Norway rat)
DOID:0111907
  • thrombophilia due to thrombin defect
  • Aliases:
    • THPH1
    • prothrombin-related thrombophilia
    • thrombophilia due to factor 2 defect
Rattus norvegicus (Norway rat)
DOID:2211
  • factor XIII deficiency
  • Aliases:
    • Factor XIII deficiency disease
    • Hereditary factor XIII deficiency disease
    • deficiency, Laki-Lorand factor
Rattus norvegicus (Norway rat)
DOID:26
  • pancreas disease
Rattus norvegicus (Norway rat)
DOID:4897
  • bile duct carcinoma
Rattus norvegicus (Norway rat)
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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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

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Last updated: December 9, 2024