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 5101 - 5125 of 7942 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism
DOID:0111103
  • maturity-onset diabetes of the young type 4
  • Aliases:
    • MODY type 4
    • MODY4
Mus musculus (house mouse)
DOID:0111103
  • maturity-onset diabetes of the young type 4
  • Aliases:
    • MODY type 4
    • MODY4
Homo sapiens (human)
DOID:0111103
  • maturity-onset diabetes of the young type 4
  • Aliases:
    • MODY type 4
    • MODY4
Rattus norvegicus (Norway rat)
DOID:0111102
  • maturity-onset diabetes of the young type 3
  • Aliases:
    • MODY type 3
    • MODY3
Homo sapiens (human)
DOID:0111100
  • maturity-onset diabetes of the young type 2
  • Aliases:
    • MODY glucokinase-related
    • MODY type 2
    • MODY2
Mus musculus (house mouse)
DOID:0111100
  • maturity-onset diabetes of the young type 2
  • Aliases:
    • MODY glucokinase-related
    • MODY type 2
    • MODY2
Homo sapiens (human)
DOID:0111100
  • maturity-onset diabetes of the young type 2
  • Aliases:
    • MODY glucokinase-related
    • MODY type 2
    • MODY2
Drosophila melanogaster (fruit fly)
DOID:0111100
  • maturity-onset diabetes of the young type 2
  • Aliases:
    • MODY glucokinase-related
    • MODY type 2
    • MODY2
Rattus norvegicus (Norway rat)
DOID:0111100
  • maturity-onset diabetes of the young type 2
  • Aliases:
    • MODY glucokinase-related
    • MODY type 2
    • MODY2
Saccharomyces cerevisiae S288C
DOID:0111095
  • Fanconi anemia complementation group A
  • Aliases:
    • FANCA
Homo sapiens (human)
DOID:0111087
  • Fanconi anemia complementation group C
  • Aliases:
    • FA3
    • FACC
    • FANCC
    • Fanconi pancytopenia type 3
Homo sapiens (human)
DOID:0111083
  • Fanconi anemia complementation group D2
  • Aliases:
    • FA4
    • FAD2
    • FANCD2
    • Fanconi pancytopenia type 4
Homo sapiens (human)
DOID:0111078
  • tibial muscular dystrophy
  • Aliases:
    • Finnish tibial muscular dystrophy
    • TMD
    • Tardive tibial muscular dystrophy
    • Udd myopathy
    • Udd type distal myopathy
    • distal titinopathy
Homo sapiens (human)
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
Rattus norvegicus (Norway rat)
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
Homo sapiens (human)
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:0111077
  • pyruvate kinase deficiency of red cells
  • Aliases:
    • PK deficiency
    • hemolytic anemia due to red cell pyruvate kinase deficiency
    • pyruvate kinase deficiency of erythrocyte
Saccharomyces cerevisiae S288C
DOID:0111071
  • congenital bile acid synthesis defect 1
  • Aliases:
    • CBAS1
Homo sapiens (human)
DOID:0111070
  • congenital bile acid synthesis defect 3
  • Aliases:
    • CBAS3
    • oxysterol 7-alpha-hydroxylase deficiency
Homo sapiens (human)
DOID:0111069
  • congenital bile acid synthesis defect 2
  • Aliases:
    • CBAS2
    • cholestasis with delta(4)-3-oxosteroid 5-beta-reductase deficiency
Saccharomyces cerevisiae S288C
DOID:0111069
  • congenital bile acid synthesis defect 2
  • Aliases:
    • CBAS2
    • cholestasis with delta(4)-3-oxosteroid 5-beta-reductase deficiency
Homo sapiens (human)
DOID:0111068
  • congenital bile acid synthesis defect 4
  • Aliases:
    • CBAS4
    • intrahepatic cholestasis with defective conversion of trihydroxycoprostanic acid to cholic acid
    • trihydroxycoprostanic acid in bile
Homo sapiens (human)
DOID:0111067
  • congenital bile acid synthesis defect 6
  • Aliases:
    • CBAS6
Homo sapiens (human)
DOID:0111064
  • autosomal recessive distal hereditary motor neuronopathy 1
  • Aliases:
    • DSMA1
    • SIANRF
    • SMARD1
    • autosomal recessive distal spinal muscular atrophy 1
    • autosomal recessive spinal muscular atrophy with respiratory distress
    • dHMN6
    • diaphragmatic spinal muscular atrophy
    • distal hereditary motor neuropathy type 6
    • distal spinal muscular atrophy 1
    • distal-HMN type 6
    • severe infantile axonal neuropathy with respiratory failure type 1
    • spinal muscular atrophy with respiratory distress type 1
Homo sapiens (human)
DOID:0111063
  • hyperphosphatemic familial tumoral calcinosis
  • Aliases:
    • HFTC
    • HHS
    • PHPTC
    • cortical hyperostosis with hyperphosphatemia
    • familial Teutschlaender disease
    • familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome
    • hypercalcemic tumoral calcinosis
    • hyperostosis with hyperphosphatemia
    • hyperphosphatemia hyperostosis
    • hyperphosphatemia hyperostosis syndrome
    • hyperphosphatemia tumoral calcinosis
    • lipocalcinogranulomatosis
    • morbus Teutschlaender
    • primary hyperphosphatemic tumoral calcinosis
    • tumoral calcinosis with hyperphosphatemia
Mus musculus (house mouse)

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024