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 776 - 800 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism
DOID:13208
  • background diabetic retinopathy
  • Aliases:
    • Non proliferative diabetic retinopathy
    • Non-Proliferative Diabetic Retinopathy
Homo sapiens (human)
DOID:1492
  • obsolete eye and adnexa disease
Homo sapiens (human)
DOID:11994
  • atrophy of testis
Homo sapiens (human)
DOID:2272
  • vulvovaginal candidiasis
  • Aliases:
    • Candidal cervix
    • Candidal vulvovaginitis
    • Candidiasis of vulva and vagina
    • Monilial vulvovaginitis
Homo sapiens (human)
DOID:13724
  • scurvy
Homo sapiens (human)
DOID:5509
  • childhood ependymoma
Homo sapiens (human)
DOID:6271
  • gastric cardia adenocarcinoma
  • Aliases:
    • adenocarcinoma of Cardia of stomach
Homo sapiens (human)
DOID:10908
  • hydrocephalus
  • Aliases:
    • hydrocephalus, X-linked
    • hydrocephalus, nonsyndromic, autosomal recessive
Homo sapiens (human)
DOID:0050560
  • Walker-Warburg syndrome
  • Aliases:
    • HARD syndrome
    • cerebroocular dysplasia-muscular dystrophy syndrome
Homo sapiens (human)
DOID:0111237
  • congenital muscular dystrophy-dystroglycanopathy type A1
  • Aliases:
    • MDDGA1
    • Walker-Warburg syndrome or muscle-eye-brain disease, POMT1-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A1
Homo sapiens (human)
DOID:1686
  • glaucoma
Homo sapiens (human)
DOID:83
  • cataract
Homo sapiens (human)
DOID:0060287
  • cornea plana
  • Aliases:
    • flat cornea
Homo sapiens (human)
DOID:0060673
  • Peters anomaly
Homo sapiens (human)
DOID:1573
  • communicating hydrocephalus
Homo sapiens (human)
DOID:14159
  • obstructive hydrocephalus
Homo sapiens (human)
DOID:14524
  • senile degeneration of brain
  • Aliases:
    • Senile brain degen.
Homo sapiens (human)
DOID:2785
  • Dandy-Walker syndrome
  • Aliases:
    • Atresia of foramina of Magendie and Luschka
Homo sapiens (human)
DOID:8501
  • fundus dystrophy
  • Aliases:
    • Retinal Dystrophy
Homo sapiens (human)
DOID:5327
  • retinal detachment
Homo sapiens (human)
DOID:11723
  • Duchenne muscular dystrophy
  • Aliases:
    • Muscular dystrophy, Duchenne
Homo sapiens (human)
DOID:0050557
  • congenital muscular dystrophy
Homo sapiens (human)
DOID:0060255
  • rippling muscle disease 2
  • Aliases:
    • autosomal dominant limb-girdle muscular dystrophy type 1C
Homo sapiens (human)
DOID:0080092
  • myofibrillar myopathy 1
  • Aliases:
    • autosomal recessive limb-girdle muscular dystrophy type 2R
    • desminopathy
Homo sapiens (human)
DOID:0070247
  • autosomal dominant Emery-Dreifuss muscular dystrophy 2
  • Aliases:
    • EDMD2
    • EMD2
    • Emery-Dreifuss muscular dystrophy 2, autosomal dominant
    • Emery-Dreifuss muscular dystrophy, autosomal dominant
    • Hauptmann-Thannhauser muscular dystrophy
    • autosomal dominant limb-girdle muscular dystrophy type 1B
    • muscular dystrophy with early contractures and cardiomyopathy, autosomal dominant
    • scapuloilioperoneal atrophy with cardiopathy
Homo sapiens (human)

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: August 19, 2024