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 701 - 725 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲ Source
DOID:11714
  • gestational diabetes
  • Aliases:
    • GDM
    • Gestational diabetes mellitus
    • Maternal gestational diabetes mellitus
Caenorhabditis elegans
DOID:2560
  • morphine dependence
Caenorhabditis elegans
DOID:2512
  • nevoid basal cell carcinoma syndrome
  • Aliases:
    • Gorlin syndrome
    • NBCCS
    • basal cell nevus syndrome
Caenorhabditis elegans
DOID:0111404
  • Jalili syndrome
  • Aliases:
    • Cone rod dystrophy-amelogenesis imperfecta syndrome
    • cone-rod dystrophy and amelogenesis imperfecta
Caenorhabditis elegans
DOID:0060850
  • annular pancreas
Caenorhabditis elegans
DOID:10376
  • amblyopia
  • Aliases:
    • lazy eye
Caenorhabditis elegans
DOID:13809
  • familial combined hyperlipidemia
  • Aliases:
    • familial multiple lipoprotein-type hyperlipidemia
    • hyperbetalipoproteinemia with prebetalipoproteinemia
    • mixed hyperlipidaemia
    • type IIb hyperlipoproteinemia
Caenorhabditis elegans
DOID:0080520
  • Tn polyagglutination syndrome
  • Aliases:
    • galactosyltransferase deficiency
Caenorhabditis elegans
DOID:0050563
  • nonsyndromic deafness
  • Aliases:
    • nonsyndromic hearing loss
    • nonsyndromic hereditary hearing loss
Caenorhabditis elegans
DOID:0112379
  • muscular dystrophy-dystroglycanopathy type B4
  • Aliases:
    • MDDGB4
    • congenital muscular dystrophy FKTN-related
Caenorhabditis elegans
DOID:0112198
  • spondyloepimetaphyseal dysplasia with joint laxity type 1
  • Aliases:
    • SEMDJL1
    • spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures
Caenorhabditis elegans
DOID:0081182
  • autosomal recessive intellectual developmental disorder 6
Caenorhabditis elegans
DOID:2378
  • relapsing-remitting multiple sclerosis
  • Aliases:
    • RRMS
    • Relapsing-remitting MS
Caenorhabditis elegans
DOID:0112171
  • wrinkly skin syndrome
  • Aliases:
    • WSS
Caenorhabditis elegans
DOID:0110727
  • neuronal ceroid lipofuscinosis 13
  • Aliases:
    • CLN13
    • neuronal ceroid lipofuscinosis 13 Kufs type
Caenorhabditis elegans
DOID:12678
  • hypercalcemia
Caenorhabditis elegans
DOID:0110875
  • holoprosencephaly 3
  • Aliases:
    • HLP3
    • HPE3
Caenorhabditis elegans
DOID:3602
  • toxic encephalopathy
  • Aliases:
    • neurotoxicity
    • neurotoxicity syndrome
Caenorhabditis elegans
DOID:11132
  • prostatic hypertrophy
Caenorhabditis elegans
DOID:1928
  • Williams-Beuren syndrome
  • Aliases:
    • Fanconi Schlesinger syndrome
    • WBS
Caenorhabditis elegans
DOID:0050869
  • villous adenoma
Caenorhabditis elegans
DOID:0060676
  • catecholaminergic polymorphic ventricular tachycardia 2
  • Aliases:
    • CVPT2
Caenorhabditis elegans
DOID:2043
  • hepatitis B
  • Aliases:
    • chronic hepatitis B
    • hepatitis B infection
Caenorhabditis elegans
DOID:12241
  • beta thalassemia
Caenorhabditis elegans
DOID:0050579
  • glycogen storage disease XV
  • Aliases:
    • Glycogen storage disease 15
    • Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency
    • glycogen storage disease type XV
Caenorhabditis elegans

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Last updated: December 9, 2024