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 July 29, 2024
DisGeNET July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 6276 - 6300 of 7942 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism
DOID:2320
  • obstructive lung disease
  • Aliases:
    • respiratory airway obstruction
Homo sapiens (human)
DOID:2214
  • obsolete inherited blood coagulation disease
Homo sapiens (human)
DOID:1247
  • blood coagulation disease
  • Aliases:
    • coagulation protein disease
    • postpartum coagulation defect
    • postpartum coagulation defect with delivery
Homo sapiens (human)
DOID:1019
  • osteomyelitis
Homo sapiens (human)
DOID:0060868
  • leukoencephalopathy with vanishing white matter
  • Aliases:
    • CACH
    • CACH/VWM
    • childhood ataxia with central nervous system hypomyelination
    • vanishing white matter leukodystrophy
Homo sapiens (human)
DOID:0111340
  • dominant optic atrophy plus syndrome
  • Aliases:
    • DOA+
    • optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy
Homo sapiens (human)
DOID:0111442
  • optic atrophy 9
  • Aliases:
    • OPA9
Homo sapiens (human)
DOID:0050883
  • infantile cerebellar-retinal degeneration
Homo sapiens (human)
DOID:0111261
  • fumarase deficiency
  • Aliases:
    • FMRD
    • fumaric aciduria
Homo sapiens (human)
DOID:0111441
  • optic atrophy 1
  • Aliases:
    • OPA1
Homo sapiens (human)
DOID:0070329
  • mitochondrial DNA depletion syndrome
  • Aliases:
    • mtDNA depletion syndrome
Homo sapiens (human)
DOID:0111218
  • Friedreich ataxia 1
  • Aliases:
    • FA1
    • FRDA1
Homo sapiens (human)
DOID:12705
  • Friedreich ataxia
  • Aliases:
    • Friedreich's ataxia
    • Friedreich's tabes
Homo sapiens (human)
DOID:11661
  • blue color blindness
  • Aliases:
    • Tritan defect
    • Tritanopia
Homo sapiens (human)
DOID:13911
  • achromatopsia
  • Aliases:
    • ACHM
    • Monochromatism
Homo sapiens (human)
DOID:13399
  • color blindness
  • Aliases:
    • BLINDNESS COLOR
    • Colour blindness
    • Colour vision deficiency
Homo sapiens (human)
DOID:13912
  • acquired color blindness
  • Aliases:
    • acquired color vision deficiencies
    • acquired color vision deficiency
    • acquired colour blindness
    • acquired colour vision deficiencies
    • acquired colour vision deficiency
Homo sapiens (human)
DOID:13910
  • red color blindness
  • Aliases:
    • Protan defect
    • Protanopia
Homo sapiens (human)
DOID:5214
  • demyelinating polyneuropathy
  • Aliases:
    • peripheral demyelinating neuropathy
Homo sapiens (human)
DOID:14555
  • Foster-Kennedy syndrome
Homo sapiens (human)
DOID:1891
  • optic nerve disease
  • Aliases:
    • disorder of the second nerve
    • optic nerve disorder
    • optic neuropathy
Homo sapiens (human)
DOID:1393
  • visual pathway disease
Homo sapiens (human)
DOID:8501
  • fundus dystrophy
  • Aliases:
    • Retinal Dystrophy
Homo sapiens (human)
DOID:0110495
  • autosomal recessive nonsyndromic deafness 37
  • Aliases:
    • DFNB37
    • autosomal recessive deafness 37
Homo sapiens (human)
DOID:0110584
  • autosomal dominant nonsyndromic deafness 6
  • Aliases:
    • DFNA14
    • DFNA38
    • DFNA6
    • autosomal dominant deafness 14
    • autosomal dominant deafness 38
    • autosomal dominant deafness 6
Homo sapiens (human)

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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