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 5276 - 5300 of 15957 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism Source
DOID:11650
  • bronchopulmonary dysplasia
  • Aliases:
    • Bronchopulmonary dysplasia of newborn
    • Chronic lung disease of prematurity
    • Neonatal chronic lung disease
    • Perinatal bronchopulmonary dysplasia
    • Respiratory insufficiency
    • neonatal chronic respiratory disease
Drosophila melanogaster (fruit fly)
DOID:3429
  • inclusion body myositis
Drosophila melanogaster (fruit fly)
DOID:0050453
  • lissencephaly
Drosophila melanogaster (fruit fly)
DOID:0050559
  • Fukuyama congenital muscular dystrophy
Drosophila melanogaster (fruit fly)
DOID:0110293
  • autosomal recessive limb-girdle muscular dystrophy type 2P
  • Aliases:
    • LGMD2P
    • MDDGC9
    • muscular dystrophy-dystroglycanopathy (limb-girdle) type C9
    • muscular dystrophy-dystroglycanopathy limb-girdle DAG1-related
Drosophila melanogaster (fruit fly)
DOID:0111232
  • congenital muscular dystrophy-dystroglycanopathy type A9
  • Aliases:
    • MDDGA9
    • Walker-Warburg syndrome or muscle-eye-brain disease DAG1-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A9
Drosophila melanogaster (fruit fly)
DOID:0110278
  • autosomal recessive limb-girdle muscular dystrophy type 2D
  • Aliases:
    • Alpha-sarcoglycanopathy
    • DMDA2
    • Duchenne-like autosomal recessive muscular dystrophy type 2
    • LGMD2D
    • muscular dystrophy, limb-girdle, type 2D
    • primary adhalinopathy
Drosophila melanogaster (fruit fly)
DOID:0050561
  • Lennox-Gastaut syndrome
  • Aliases:
    • Lennox syndrome
Mus musculus (house mouse)
DOID:0110170
  • Charcot-Marie-Tooth disease axonal type 2Q
  • Aliases:
    • CMT2Q
    • Charcot-Marie-Tooth neuropathy type 2Q
    • autosomal dominant Charcot-Marie-Tooth disease type 2Q
    • autosomal dominant axonal Charcot-Marie-Tooth disease type 2Q
Mus musculus (house mouse)
DOID:0111453
  • 2-aminoadipic 2-oxoadipic aciduria
  • Aliases:
    • AMOXAD
    • alpha-aminoadipic aciduria
Mus musculus (house mouse)
DOID:0110170
  • Charcot-Marie-Tooth disease axonal type 2Q
  • Aliases:
    • CMT2Q
    • Charcot-Marie-Tooth neuropathy type 2Q
    • autosomal dominant Charcot-Marie-Tooth disease type 2Q
    • autosomal dominant axonal Charcot-Marie-Tooth disease type 2Q
Rattus norvegicus (Norway rat)
DOID:0111453
  • 2-aminoadipic 2-oxoadipic aciduria
  • Aliases:
    • AMOXAD
    • alpha-aminoadipic aciduria
Rattus norvegicus (Norway rat)
DOID:4972
  • myelodysplastic/myeloproliferative neoplasm
  • Aliases:
    • Myeloproliferative/Myelodysplastic syndromes
    • myelodysplastic myeloproliferative cancer
Mus musculus (house mouse)
DOID:2729
  • dyskeratosis congenita
  • Aliases:
    • DKCD
Rattus norvegicus (Norway rat)
DOID:0070025
  • X-linked dyskeratosis congenita
  • Aliases:
    • DKCX
    • Zinsser-Cole-Engman syndrome
Rattus norvegicus (Norway rat)
DOID:2729
  • dyskeratosis congenita
  • Aliases:
    • DKCD
Mus musculus (house mouse)
DOID:0070025
  • X-linked dyskeratosis congenita
  • Aliases:
    • DKCX
    • Zinsser-Cole-Engman syndrome
Mus musculus (house mouse)
DOID:13714
  • anodontia
  • Aliases:
    • Complete absence of teeth
    • Developmental absence of tooth
    • Total anodontia of permanent and deciduous teeth
Mus musculus (house mouse)
DOID:3649
  • pyruvate decarboxylase deficiency
  • Aliases:
    • deficiency of pyruvic dehydrogenase
    • pyruvate dehydrogenase complex deficiency disease
    • pyruvate dehydrogenase deficiency
Mus musculus (house mouse)
DOID:3650
  • lactic acidosis
Mus musculus (house mouse)
DOID:3649
  • pyruvate decarboxylase deficiency
  • Aliases:
    • deficiency of pyruvic dehydrogenase
    • pyruvate dehydrogenase complex deficiency disease
    • pyruvate dehydrogenase deficiency
Rattus norvegicus (Norway rat)
DOID:3650
  • lactic acidosis
Rattus norvegicus (Norway rat)
DOID:14447
  • gonadal dysgenesis
  • Aliases:
    • Gonadal dysgenesis syndrome
Mus musculus (house mouse)
DOID:0014667
  • disease of metabolism
  • Aliases:
    • metabolic disease
Rattus norvegicus (Norway rat)
DOID:0060072
  • benign neoplasm
Mus musculus (house mouse)

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Last updated: December 9, 2024