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 1226 - 1250 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:1687
  • neovascular glaucoma
  • Aliases:
    • secondary angle-closure glaucoma with rubeosis
Rattus norvegicus (Norway rat)
DOID:9164
  • achalasia
  • Aliases:
    • Lack of reflex relaxation of lower oesophageal sphincter
    • achalasia of cardia
    • achalasia of esophagus
    • cardiospasm
    • esophageal achalasia
    • hypertensive lower esophageal sphincter
Caenorhabditis elegans
DOID:3083
  • chronic obstructive pulmonary disease
  • Aliases:
    • COLD
    • COPD
    • chronic obstructive airway disease
    • chronic obstructive lung disease
Homo sapiens (human)
DOID:934
  • viral infectious disease
  • Aliases:
    • Viral Infection
    • Viral disease
    • virus infection
Homo sapiens (human)
DOID:10283
  • prostate cancer
  • Aliases:
    • NGP - new growth of prostate
    • hereditary prostate cancer
    • malignant tumor of the prostate
    • prostate cancer, familial
    • prostate neoplasm
    • prostatic cancer
    • prostatic neoplasm
    • tumor of the prostate
Drosophila melanogaster (fruit fly)
DOID:9280
  • carbamoyl phosphate synthetase I deficiency disease
  • Aliases:
    • CPS I deficiency
Homo sapiens (human)
DOID:0050814
  • temtamy preaxial brachydactyly syndrome
  • Aliases:
    • PREAXIAL BRACHYDACTYLY SYNDROME, TEMTAMY TYPE
Xenopus tropicalis (tropical clawed frog)
DOID:0050746
  • mantle cell lymphoma
Homo sapiens (human)
DOID:9498
  • pulmonary eosinophilia
Mus musculus (house mouse)
DOID:5723
  • optic atrophy
  • Aliases:
    • atrophy of optic disc
Homo sapiens (human)
DOID:0111973
  • immunodeficiency 17
  • Aliases:
    • CD3-gamma deficiency
    • IMD17
    • SCID-like immunodeficiency, T cell-partial, B cell-positive, NK cell-positive
    • immunodeficiency 17, CD3 gamma deficient
Mus musculus (house mouse)
DOID:0111272
  • occipital horn syndrome
  • Aliases:
    • EDS IX
    • Ehlers-Danlos syndrome type 9
    • Ehlers-Danlos syndrome type IX
    • X-linked cutis laxa
Rattus norvegicus (Norway rat)
DOID:0111261
  • fumarase deficiency
  • Aliases:
    • FMRD
    • fumaric aciduria
Mus musculus (house mouse)
DOID:0081350
  • congenital myopathy 18
Mus musculus (house mouse)
DOID:13910
  • red color blindness
  • Aliases:
    • Protan defect
    • Protanopia
Mus musculus (house mouse)
DOID:3211
  • lysosomal storage disease
  • Aliases:
    • disorder of lysosomal enzyme
    • inborn lysosomal enzyme disorder
    • lysosomal storage metabolism disorder
Caenorhabditis elegans
DOID:4926
  • bronchiolo-alveolar adenocarcinoma
  • Aliases:
    • Bronchioalveolar lung carcinoma
    • Bronchioloalveolar carcinoma
    • Minimally Invasive Lung Adenocarcinoma
Homo sapiens (human)
DOID:0111527
  • spinal muscular atrophy with progressive myoclonic epilepsy
  • Aliases:
    • Jankovic-Rivera syndrome
    • SMA-PME
    • SMAPME
    • hereditary myoclonus-progressive distal muscular atrophy syndrome
Caenorhabditis elegans
DOID:2361
  • macrocytic anemia
  • Aliases:
    • ANEMIA MACROCYTIC
    • Macrocytic anaemia
Caenorhabditis elegans
DOID:0081440
  • Peroxisome biogenesis disorder 10B
Homo sapiens (human)
DOID:0050873
  • follicular lymphoma
Mus musculus (house mouse)
DOID:0070501
  • mitochondrial complex IV deficiency nuclear type 16
  • Aliases:
    • MC4DN16
Rattus norvegicus (Norway rat)
DOID:2256
  • osteochondrodysplasia
  • Aliases:
    • Cartilage Development disorder
    • Congenital anomaly of cartilage
    • Osteochondrodysplasia syndrome
    • chondrodystrophy
    • skeletal dysplasia
Rattus norvegicus (Norway rat)
DOID:0110919
  • hereditary spherocytosis type 4
  • Aliases:
    • HS4
    • SPH4
    • hereditary spherocytosis 4
Mus musculus (house mouse)
DOID:0080419
  • developmental and epileptic encephalopathy 50
  • Aliases:
    • CDG syndrome type Iz
    • CDG-Iz
    • Carbohydrate deficient glycoprotein syndrome type Iz
    • Congenital disorder of glycosylation type 1z
    • DEE50
    • early infantile epileptic encephalopathy 50
Mus musculus (house mouse)

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Last updated: December 9, 2024