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 2501 - 2525 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:8691
  • mycosis fungoides
  • Aliases:
    • mycosis fungoides lymphoma
Homo sapiens (human)
DOID:0050426
  • Stevens-Johnson syndrome
Homo sapiens (human)
DOID:11656
  • cicatricial pemphigoid
  • Aliases:
    • Cicatricial pemphigoid with ocular involvement
    • Ocular pemphigoid
    • benign mucous membrane pemphigoid
    • benign mucous membrane pemphigoid with ocular involvement
    • ocular pemphigus
Homo sapiens (human)
DOID:4251
  • conjunctival disease
Homo sapiens (human)
DOID:0060449
  • gelatinous drop-like corneal dystrophy
  • Aliases:
    • GDCD
    • corneal amyloidosis
    • primary familial amyloidosis of the cornea
    • subepithelial amyloidosis of the cornea
Homo sapiens (human)
DOID:4930
  • nasal cavity adenocarcinoma
  • Aliases:
    • adenocarcinoma of the nasal cavity
Homo sapiens (human)
DOID:5453
  • pulmonary venoocclusive disease
  • Aliases:
    • pulmonary veno-occlusive disease
Mus musculus (house mouse)
DOID:0060178
  • familial hemiplegic migraine
Mus musculus (house mouse)
DOID:863
  • nervous system disease
Mus musculus (house mouse)
DOID:0111558
  • Charcot-Marie-Tooth disease type 2DD
  • Aliases:
    • ATP1A1-related CMT2
    • ATP1A1-related autosomal dominant Charcot-Marie-Tooth disease type 2
    • CMT2DD
    • Charcot-Marie-Tooth disease, axonal, type 2DD
    • Charcot-Marie-Tooth neuropathy, type 2DD
Mus musculus (house mouse)
DOID:0050692
  • Brody myopathy
Mus musculus (house mouse)
DOID:14221
  • abdominal obesity-metabolic syndrome 1
  • Aliases:
    • dysmetabolic syndrome X
    • metabolic syndrome X
Mus musculus (house mouse)
DOID:2856
  • euthyroid sick syndrome
  • Aliases:
    • Sick-euthyroid syndrome
Mus musculus (house mouse)
DOID:2734
  • keratosis follicularis
  • Aliases:
    • DARIER-WHITE DISEASE
    • Darier's disease
Mus musculus (house mouse)
DOID:0050606
  • acrokeratosis verruciformis
  • Aliases:
    • Acrokeratosis verruciformis of Hopf
    • Hopf disease
Mus musculus (house mouse)
DOID:0050564
  • autosomal dominant nonsyndromic deafness
  • Aliases:
    • autosomal dominant deafness
Mus musculus (house mouse)
DOID:0110467
  • autosomal recessive nonsyndromic deafness 12
  • Aliases:
    • DFNB12
    • autosomal recessive deafness 12
Mus musculus (house mouse)
DOID:0050429
  • Hailey-Hailey disease
  • Aliases:
    • BENIGN CHRONIC PEMPHIGUS
    • Pemphigus, Benign Familial
Mus musculus (house mouse)
DOID:8929
  • atrophic gastritis
  • Aliases:
    • gastric atrophy
Mus musculus (house mouse)
DOID:0040090
  • autoimmune gastritis
Mus musculus (house mouse)
DOID:8725
  • vascular dementia
  • Aliases:
    • Multi Infarct Dementia
    • multifocal dementia
Mus musculus (house mouse)
DOID:0111498
  • combined oxidative phosphorylation deficiency 22
  • Aliases:
    • COXPD22
Mus musculus (house mouse)
DOID:0070461
  • mitochondrial complex V (ATP synthase) deficiency nuclear type 4A
  • Aliases:
    • MC5DN4A
Mus musculus (house mouse)
DOID:0070462
  • mitochondrial complex V (ATP synthase) deficiency nuclear type 4B
  • Aliases:
    • MC5DN4B
Mus musculus (house mouse)
DOID:0112275
  • developmental and epileptic encephalopathy 93
  • Aliases:
    • DEE93
    • IECEE3
    • infantile or early childhood epileptic encephalopathy 3
Mus musculus (house mouse)

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024