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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 5926 - 5950 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism Source
DOID:0050801
  • androgenic alopecia
  • Aliases:
    • alopecia androgenetica, male pattern baldness
    • androgenetic alopecia
Homo sapiens (human)
DOID:1229
  • paranoid schizophrenia
  • Aliases:
    • Paranoid type schizophrenia
    • Paraphrenia - late
    • Paraphrenic schizophrenia
    • chronic paranoid schizophrenia
    • paranoid type schizophrenia subchronic state
Homo sapiens (human)
DOID:778
  • delusional disorder
Homo sapiens (human)
DOID:2907
  • Goldenhar syndrome
  • Aliases:
    • Facio-auriculo-vertebral spectrum
    • First AND second branchial arch syndrome
    • First arch syndrome
    • HEMIFACIAL MICROSOMIA
    • OAV (oculoauriculovertebral) dysplasia
    • Otomandibular dysostosis
Homo sapiens (human)
DOID:0111238
  • congenital muscular dystrophy-dystroglycanopathy type A13
  • Aliases:
    • MDDGA13
    • Walker-Warburg syndrome or muscle-eye-brain disease, B3GNT1-related
    • Walker-Warburg syndrome or muscle-eye-brain disease, B4GNT1-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A13
Homo sapiens (human)
DOID:0060668
  • anencephaly
Homo sapiens (human)
DOID:4160
  • differentiating neuroblastoma
Homo sapiens (human)
DOID:0110671
  • congenital myasthenic syndrome 6
  • Aliases:
    • CMS Ia2
    • CMS1A2
    • CMS6
    • CMSEA
    • FIM
    • FIMG2
    • congenital myasthenic syndrome 6, presynaptic
    • congenital myasthenic syndrome type Ia2
    • congenital presynaptic myasthenic syndrome associated with episodic apnea
    • familial infantile myasthenia
    • familial infantile myasthenia gravis 2
Homo sapiens (human)
DOID:0110672
  • congenital myasthenic syndrome 21
  • Aliases:
    • CMS21
    • congenital myasthenic syndrome 21, presynaptic
Homo sapiens (human)
DOID:14784
  • olivopontocerebellar atrophy
  • Aliases:
    • Dejerine-Thomas syndrome
    • Thomas' syndrome
    • WADIA-SWAMI SYNDROME
Homo sapiens (human)
DOID:9786
  • bulbar polio
  • Aliases:
    • bulbar poliomyelitis
Homo sapiens (human)
DOID:4953
  • poliomyelitis
Homo sapiens (human)
DOID:11914
  • gastroparesis
  • Aliases:
    • Gastroparalysis
    • Gastroparesis syndrome
    • gastric atonia
Homo sapiens (human)
DOID:2382
  • kernicterus
  • Aliases:
    • bilirubin encephalopathy
Homo sapiens (human)
DOID:12043
  • kernicterus due to isoimmunization
Homo sapiens (human)
DOID:1206
  • Rett syndrome
  • Aliases:
    • Rett's disorder
    • cerebroatrophic hyperammonemia
Homo sapiens (human)
DOID:0050214
  • Lambert-Eaton myasthenic syndrome
  • Aliases:
    • Eaton-Lambert syndrome
    • LEMS
    • Lambert-Eaton syndrome
Homo sapiens (human)
DOID:3635
  • congenital myasthenic syndrome
Homo sapiens (human)
DOID:9840
  • esotropia
  • Aliases:
    • Convergence in manifest squint
    • Internal Strabismus
    • crossed eyes
Homo sapiens (human)
DOID:10293
  • monocular esotropia
Homo sapiens (human)
DOID:3240
  • aspiration pneumonitis
  • Aliases:
    • Chemical pneumonitis
    • Mendelson's Syndrome
Homo sapiens (human)
DOID:0050152
  • aspiration pneumonia
Homo sapiens (human)
DOID:12155
  • lymphocytic choriomeningitis
  • Aliases:
    • LCM
    • Lymphocytic choriomeningitis virus encephalomyelitis
    • Lymphocytic meningitis
    • Lymphocytic meningoencephalitis
Homo sapiens (human)
DOID:8457
  • pellagra
  • Aliases:
    • Niacin deficiency
    • Niacin-tryptophan deficiency
Homo sapiens (human)
DOID:0070318
  • dry beriberi
Homo sapiens (human)
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Last updated: August 19, 2024