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
DisGeNET
Glyco-Disease Genes Database (GDGDB)
Displaying entries 7526 - 7550 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism
DOID:0060473
  • Kabuki syndrome
  • Aliases:
    • KMS
    • Kabuki make up syndrome
    • Niikawa-Kuroki syndrome
Homo sapiens (human)
DOID:0080736
  • Ehlers-Danlos syndrome musculocontractural type 1
Mus musculus (house mouse)
DOID:0050156
  • idiopathic pulmonary fibrosis
  • Aliases:
    • FIBROCYSTIC PULMONARY DYSPLASIA
    • IDIOPATHIC PULMONARY FIBROSIS, FAMILIAL
    • cryptogenic fibrosing alveolitis
Drosophila melanogaster (fruit fly)
DOID:0080543
  • hyperprolinemia type 2
  • Aliases:
    • hyperprolinemia type II
Homo sapiens (human)
DOID:192
  • sex cord-gonadal stromal tumor
  • Aliases:
    • Sex Cord-Stromal neoplasm
    • Sex cord stromal tumour
    • Specialized gonadal neoplasm
    • Specialized gonadal tumor
    • Specialized gonadal tumour
    • sex cord-gonadal stromal tumour
Homo sapiens (human)
DOID:8577
  • ulcerative colitis
  • Aliases:
    • Left-sided ulcerative colitis
Mus musculus (house mouse)
DOID:4676
  • uremia
  • Aliases:
    • UREMIA OF renal ORIGIN
Mus musculus (house mouse)
DOID:3891
  • placental insufficiency
Homo sapiens (human)
DOID:906
  • peroxisomal disease
  • Aliases:
    • peroxisomal disorder
Drosophila melanogaster (fruit fly)
DOID:0110285
  • autosomal recessive limb-girdle muscular dystrophy type 2Q
  • Aliases:
    • LGMD2Q
    • autosomal recessive limb-girdle muscular dystrophy due to plectin deficiency
    • muscular dystrophy, limb-girdle, type 2Q
Homo sapiens (human)
DOID:4873
  • anterior horn cell disease
Homo sapiens (human)
DOID:4029
  • gastritis
  • Aliases:
    • Erosive Gastritis
    • Erosive gastropathy
    • acute gastric mucosal erosion
Homo sapiens (human)
DOID:0090059
  • enhanced S-cone syndrome
Homo sapiens (human)
DOID:0080038
  • pycnodysostosis
Homo sapiens (human)
DOID:10579
  • leukodystrophy
Homo sapiens (human)
DOID:4697
  • perineurioma
  • Aliases:
    • soft tissue Perineurioma
Homo sapiens (human)
DOID:3319
  • lymphangioleiomyomatosis
  • Aliases:
    • lung lymphangioleiomyomatosis
    • lymphangiomyomatosis
    • pulmonary lymphangioleiomyomatosis
Homo sapiens (human)
DOID:14500
  • fucosidosis
  • Aliases:
    • A-fucosidase deficiency
    • alpha fucosidase deficiency
Homo sapiens (human)
DOID:14264
  • benign neonatal seizures
  • Aliases:
    • benign familial neonatal seizures
    • benign neonatal convulsions
Rattus norvegicus (Norway rat)
DOID:12053
  • cryptococcosis
  • Aliases:
    • Busse-Buschke's disease
    • European cryptococcosis
    • cryptococcal infection
    • torula
    • torulosis
Drosophila melanogaster (fruit fly)
DOID:2366
  • West Nile fever
Homo sapiens (human)
DOID:5746
  • ovarian serous cystadenocarcinoma
  • Aliases:
    • serous cystadenoma
Homo sapiens (human)
DOID:0080547
  • metabolic dysfunction-associated steatohepatitis
  • Aliases:
    • MASH
    • NASH
    • non-alcoholic steatohepatitis
    • nonalcoholic steatohepatitis
Drosophila melanogaster (fruit fly)
DOID:12549
  • hepatitis A
  • Aliases:
    • Viral hepatitis, type A
Rattus norvegicus (Norway rat)
DOID:0110959
  • Gaucher's disease type III
  • Aliases:
    • GD III
    • Gaucher Disease, Chronic Neuronopathic Type
    • Gaucher Disease, Juvenile And Adult, Cerebral
    • Gaucher Disease, Subacute Neuronopathic Type
Caenorhabditis elegans

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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: August 19, 2024