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 651 - 675 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism
DOID:0050625
  • biliary tract benign neoplasm
  • Aliases:
    • extrahepatic bile duct neoplasm
    • neoplasm of extrahepatic bile ducts
    • tumor of the extrahepatic bile duct
Mus musculus (house mouse)
DOID:0080664
  • diaphyseal medullary stenosis with malignant fibrous histiocytoma
  • Aliases:
    • Hardcastle syndrome
    • bone dysplasia-medullary fibrosarcoma syndrome
    • diaphyseal medullary stenosis-malignant fibrous histiocytoma syndrome
Mus musculus (house mouse)
DOID:4608
  • common bile duct neoplasm
  • Aliases:
    • neoplasm of common bile duct
Mus musculus (house mouse)
DOID:0111630
  • familial erythrocytosis 8
  • Aliases:
    • BPGM deficiency
    • DPGM deficiency
    • ECYT8
    • bisphosphoglycerate mutase deficiency
    • bisphosphoglyceromutase deficiency
    • diphosphoglycerate mutase deficiency of erythrocyte
    • hemolytic anemia due to diphosphoglycerate mutase deficiency
Homo sapiens (human)
DOID:0110658
  • congenital myasthenic syndrome 15
  • Aliases:
    • CMS15
    • congenital myasthenic syndrome 15 without tubular aggregates
Mus musculus (house mouse)
DOID:0081427
  • autosomal recessive distal hereditary motor neuronopathy 8
  • Aliases:
    • SORDD
    • sorbitol dehydrogenase deficiency with peripheral neuropathy
Homo sapiens (human)
DOID:0081376
  • obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy
Homo sapiens (human)
DOID:8553
  • pyoderma gangrenosum
Homo sapiens (human)
DOID:0050169
  • cutaneous lupus erythematosus
Homo sapiens (human)
DOID:10579
  • leukodystrophy
Mus musculus (house mouse)
DOID:990
  • congenital heart block
Homo sapiens (human)
DOID:0111619
  • combined D-2- and L-2-hydroxyglutaric aciduria
  • Aliases:
    • D,L-2-HGA
    • D,L-2-hydroxyglutaric acidemia
    • D,L-2-hydroxyglutaric aciduria
    • combined D,L-2-hydroxyglutaric aciduria
    • combined D-2-hydroxyglutaric acidemia and L-2-hydroxyglutaric acidemia
    • combined D-2-hydroxyglutaric aciduria and L-2-hydroxyglutaric aciduria
Homo sapiens (human)
DOID:0050157
  • cryptogenic organizing pneumonia
  • Aliases:
    • BOOP
    • Cryptogenic organising pneumonitis
    • Cryptogenic organizing pneumonitis
    • bronchiolitis obliterans organising pneumonia
    • bronchiolitis obliterans organizing pneumonia
    • cryptogenic organising pneumonia
    • idiopathic bronchiolitis obliterans with organising pneumonia
    • idiopathic bronchiolitis obliterans with organizing pneumonia
Homo sapiens (human)
DOID:96
  • staphyloenterotoxemia
  • Aliases:
    • Staphylococcal food poisoning
    • Staphylococcal toxaemia due to food
    • staphyloenterotoxicosis
Homo sapiens (human)
DOID:0080899
  • lung pleomorphic carcinoma
Homo sapiens (human)
DOID:0060858
  • hypotonia-cystinuria syndrome
  • Aliases:
    • cystinuria with mitochondrial disease
Homo sapiens (human)
DOID:0080587
  • congenital myasthenic syndrome 22
Homo sapiens (human)
DOID:11721
  • glycogen storage disease VII
  • Aliases:
    • Glycogen storage disease 7
    • Glycogen storage disease, type VII
    • Muscle phosphofructokinase deficiency
    • glycogen storage disease type VII
    • phosphofructokinase myopathy
Rattus norvegicus (Norway rat)
DOID:10486
  • intestinal atresia
Homo sapiens (human)
DOID:0111313
  • idiopathic generalized epilepsy 12
  • Aliases:
    • EIG12
Homo sapiens (human)
DOID:0090044
  • dystonia 9
Homo sapiens (human)
DOID:0060050
  • autoimmune disease of blood
Rattus norvegicus (Norway rat)
DOID:0080414
  • developmental and epileptic encephalopathy 15
  • Aliases:
    • DEE15
    • early infantile epileptic encephalopathy 15
Homo sapiens (human)
DOID:0081180
  • autosomal recessive intellectual developmental disorder 12
Homo sapiens (human)
DOID:0070311
  • oligoasthenoteratozoospermia
  • Aliases:
    • OAT
    • oligoasthenoteratospermia
Homo sapiens (human)

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Last updated: August 19, 2024