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 6251 - 6275 of 7942 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism
DOID:0060180
  • colitis
Rattus norvegicus (Norway rat)
DOID:1907
  • malignant fibrous histiocytoma
  • Aliases:
    • Fibroxanthosarcoma
    • MFH
Rattus norvegicus (Norway rat)
DOID:10376
  • amblyopia
  • Aliases:
    • lazy eye
Rattus norvegicus (Norway rat)
DOID:10871
  • age related macular degeneration
  • Aliases:
    • Age Related Maculopathies
    • Age Related Maculopathy
    • Senile macular degeneration
    • Senile macular retinal degeneration
    • age-related macular degeneration
Rattus norvegicus (Norway rat)
DOID:263
  • kidney cancer
  • Aliases:
    • malignant neoplasm of kidney except pelvis
    • malignant tumour of kidney
    • renal cancer
Rattus norvegicus (Norway rat)
DOID:0080693
  • Noonan syndrome-like disorder with loose anagen hair 2
Mus musculus (house mouse)
DOID:0080693
  • Noonan syndrome-like disorder with loose anagen hair 2
Rattus norvegicus (Norway rat)
DOID:1289
  • neurodegenerative disease
  • Aliases:
    • degenerative disease
Mus musculus (house mouse)
DOID:384
  • Wolff-Parkinson-White syndrome
  • Aliases:
    • Anomalous A-V excitation
    • Wolff-Parkinson-White pattern
    • anomalous atrioventricular excitation
Mus musculus (house mouse)
DOID:0090101
  • lethal congenital glycogen storage disease of heart
  • Aliases:
    • fatal congenital hypertrophic cardiomyopathy due to GSD
    • fatal congenital hypertrophic cardiomyopathy due to glycogenosis
    • fatal congenital nonlysosomal cardiac glycogenosis
    • phosphorylase kinase deficiency of heart
Mus musculus (house mouse)
DOID:0110312
  • hypertrophic cardiomyopathy 6
  • Aliases:
    • CMH6
    • cardiomyopathy, familial hypertrophic 6
Mus musculus (house mouse)
DOID:3181
  • oligodendroglioma
  • Aliases:
    • oligodendroglial neoplasm
    • oligodendroglial tumor
Rattus norvegicus (Norway rat)
DOID:3181
  • oligodendroglioma
  • Aliases:
    • oligodendroglial neoplasm
    • oligodendroglial tumor
Mus musculus (house mouse)
DOID:0080208
  • metabolic dysfunction-associated steatotic liver disease
  • Aliases:
    • MAFLD
    • MASLD
    • NAFLD
    • metabolic dysfunction-associated fatty liver disease
    • metabolic dysfunction-related steatotic liver disease
    • metabolic-associated fatty liver disease
    • non-alcoholic fatty liver disease
    • nonalcoholic fatty liver disease
Drosophila melanogaster (fruit fly)
DOID:12365
  • malaria
  • Aliases:
    • induced malaria
Drosophila melanogaster (fruit fly)
DOID:0111077
  • pyruvate kinase deficiency of red cells
  • Aliases:
    • PK deficiency
    • hemolytic anemia due to red cell pyruvate kinase deficiency
    • pyruvate kinase deficiency of erythrocyte
Drosophila melanogaster (fruit fly)
DOID:1926
  • Gaucher's disease
  • Aliases:
    • Gaucher disease
    • acid beta-glucosidase deficiency
    • glocucerebrosidase deficiency
    • glucosylceramide beta-glucosidase deficiency
    • kerasin thesaurismosis
Drosophila melanogaster (fruit fly)
DOID:2754
  • glycogen storage disease VI
  • Aliases:
    • Glycogen storage disease 6
    • Hers' disease
    • glycogen storage disease type VI
    • hepatic glycogen phosphorylase deficiency
    • hepatophosphorylase deficiency glycogenosis
Mus musculus (house mouse)
DOID:2754
  • glycogen storage disease VI
  • Aliases:
    • Glycogen storage disease 6
    • Hers' disease
    • glycogen storage disease type VI
    • hepatic glycogen phosphorylase deficiency
    • hepatophosphorylase deficiency glycogenosis
Rattus norvegicus (Norway rat)
DOID:2746
  • glycogen storage disease V
  • Aliases:
    • Glycogen storage disease 5
    • Glycogen storage disease, type V
    • McArdle's disease
    • glycogen storage disease type V
    • myophosphorylase deficiency
Mus musculus (house mouse)
DOID:0090023
  • split hand-foot malformation 4
  • Aliases:
    • SHFM4
Homo sapiens (human)
DOID:0090022
  • split hand-foot malformation 5
  • Aliases:
    • SHFM5
Homo sapiens (human)
DOID:0090020
  • split hand-foot malformation
  • Aliases:
    • lobster-claw deformity
    • split-hand deformity
Homo sapiens (human)
DOID:0090025
  • split hand-foot malformation 3
  • Aliases:
    • SHFM3
    • chromosome 10q24 duplication syndrome
    • distal limb deficiencies with micrognathia
Homo sapiens (human)
DOID:0090026
  • split hand-foot malformation 6
  • Aliases:
    • SHFM6
Homo sapiens (human)

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Last updated: August 19, 2024