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 January 28, 2025
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 176 - 200 of 5716 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism Source
DOID:0111442
  • optic atrophy 9
  • Aliases:
    • OPA9
Homo sapiens (human)
DOID:0050883
  • infantile cerebellar-retinal degeneration
Homo sapiens (human)
DOID:0070516
  • Mitchell syndrome
Drosophila melanogaster (fruit fly)
DOID:0070516
  • Mitchell syndrome
Homo sapiens (human)
DOID:0050797
  • peroxisomal acyl-CoA oxidase deficiency
  • Aliases:
    • Peroxisomal acyl-coenzyme A oxidase
Homo sapiens (human)
DOID:0111067
  • congenital bile acid synthesis defect 6
  • Aliases:
    • CBAS6
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
Homo sapiens (human)
DOID:0080953
  • amelogenesis imperfecta type 1J
  • Aliases:
    • Amelogenesis imperfecta, type IJ
Homo sapiens (human)
DOID:0112295
  • spondylometaphyseal dysplasia
Homo sapiens (human)
DOID:0070586
  • spermatogenic failure 87
  • Aliases:
    • SPGF87
Homo sapiens (human)
DOID:0111263
  • combined malonic and methylmalonic acidemia
  • Aliases:
    • CMAMMA
    • combined malonic and methylmalonic aciduria
Homo sapiens (human)
DOID:1059
  • intellectual disability
Homo sapiens (human)
DOID:0112050
  • non-syndromic X-linked intellectual disability 63
  • Aliases:
    • ACSL4-related intellectual disability
    • MRX63
    • MRX68
    • X-linked mental retardation 63
    • X-linked mental retardation 68
Homo sapiens (human)
DOID:0060774
  • congenital diarrhea
Homo sapiens (human)
DOID:0050567
  • orofacial cleft
Homo sapiens (human)
DOID:0081340
  • congenital myopathy 2C
Homo sapiens (human)
DOID:0110927
  • nemaline myopathy 3
  • Aliases:
    • NEM3
    • congenital myopathy 2A
    • nemaline myopathy 3, autosomal dominant or recessive
Homo sapiens (human)
DOID:0081339
  • congenital myopathy 2B
Homo sapiens (human)
DOID:13099
  • Moyamoya disease
  • Aliases:
    • progressive intracranial arterial occlusion
Homo sapiens (human)
DOID:14004
  • thoracic aortic aneurysm
Homo sapiens (human)
DOID:1588
  • thrombocytopenia
Homo sapiens (human)
DOID:0081112
  • Baraitser-Winter syndrome 1
Homo sapiens (human)
DOID:0110456
  • dilated cardiomyopathy 1R
  • Aliases:
    • CMD1R
Homo sapiens (human)
DOID:0110317
  • hypertrophic cardiomyopathy 11
  • Aliases:
    • CMH11
    • cardiomyopathy familial hypertrophic 11
Homo sapiens (human)
DOID:0110110
  • atrial heart septal defect 5
  • Aliases:
    • ASD5
    • atrial septal defect 5
Homo sapiens (human)

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Last updated: April 7, 2025