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 9126 - 9150 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0111196
  • X-linked distal spinal muscular atrophy 3
  • Aliases:
    • ATP7A-related distal motor neuropathy
    • DSMAX
    • SMAX3
    • X-linked dHMN3
    • X-linked dSMA3
    • X-linked distal hereditary motor neuropathy type 3
    • X-linked recessive distal spinal muscular atrophy
Homo sapiens (human)
DOID:5627
  • adenosquamous gallbladder carcinoma
  • Aliases:
    • Adenosquamous carcinoma of the gallbladder
Homo sapiens (human)
DOID:0060019
  • coronin-1A deficiency
Mus musculus (house mouse)
DOID:0110372
  • retinitis pigmentosa 4
  • Aliases:
    • RP4
Danio rerio (zebrafish)
DOID:10155
  • intestinal cancer
  • Aliases:
    • malignant intestinal tumors
    • malignant neoplasm of intestine
Danio rerio (zebrafish)
DOID:0112029
  • non-syndromic X-linked intellectual disability 50
  • Aliases:
    • MRX50
    • X-linked intellectual developmental disorder 50
    • X-linked mental retardation 50
    • XLID50
Drosophila melanogaster (fruit fly)
DOID:0110313
  • hypertrophic cardiomyopathy 7
  • Aliases:
    • CMH7
    • cardiomyopathy, familial hypertrophic 7
Mus musculus (house mouse)
DOID:4947
  • cholangiocarcinoma
  • Aliases:
    • adult primary Cholangiocarcinoma
    • adult primary cholangiocellular carcinoma
    • cholangiosarcoma
Danio rerio (zebrafish)
DOID:0060682
  • autosomal dominant nocturnal frontal lobe epilepsy 1
  • Aliases:
    • ENFL1
    • nocturnal frontal lobe epilepsy 1
Caenorhabditis elegans
DOID:0110644
  • long QT syndrome 1
  • Aliases:
    • LQT1
    • ventricular fibrillation with prolonged QT interval
Homo sapiens (human)
DOID:4258
  • Weissenbacher-Zweymuller syndrome
  • Aliases:
    • Piere-Robin syndrome
    • Pierre Robin Malformation
Saccharomyces cerevisiae S288C
DOID:12804
  • mucopolysaccharidosis IV
  • Aliases:
    • Mucopolysaccharidosis, MPS-IV
    • deficiency of N-acetylgalactosamine-6-sulphatase
    • deficiency of chondroitinsulphatase
    • galactosamine-6-sulfatase deficiency
Danio rerio (zebrafish)
DOID:0111153
  • congenital mirror movement disorder
  • Aliases:
    • familial congenital controlateral synkinesia
    • familial congenital mirror movements
    • hereditary congenital controlateral synkinesia
    • hereditary congenital mirror movements
    • isolated congenital controlateral synkinesia
    • isolated congenital mirror movements
Rattus norvegicus (Norway rat)
DOID:10595
  • Charcot-Marie-Tooth disease
  • Aliases:
    • CMT - Charcot-Marie-Tooth disease
Xenopus laevis (African clawed frog)
DOID:2152
  • ovary epithelial cancer
  • Aliases:
    • Ovarian Surface epithelial-Stromal tumor
Caenorhabditis elegans
DOID:769
  • neuroblastoma
Xenopus laevis (African clawed frog)
DOID:8354
  • complement component 3 deficiency
  • Aliases:
    • C3 deficiency
Homo sapiens (human)
DOID:9849
  • Meniere's disease
  • Aliases:
    • Meniere disease
    • Mnire's vertigo
    • Otogenic vertigo
Homo sapiens (human)
DOID:0110678
  • congenital myasthenic syndrome 4A
  • Aliases:
    • CMS Ia1
    • CMS1A1
    • CMS4A
    • congenital myasthenic syndrome 4A slow-channel
    • congenital myasthenic syndrometype Ia1
Xenopus laevis (African clawed frog)
DOID:0080954
  • arthrogryposis multiplex congenita
Drosophila melanogaster (fruit fly)
DOID:811
  • lipodystrophy
Homo sapiens (human)
DOID:11476
  • osteoporosis
Mus musculus (house mouse)
DOID:0110928
  • nemaline myopathy 2
  • Aliases:
    • NEM2
    • congenital myopathy 2
    • nemaline myopathy 2, autosomal recessive
Homo sapiens (human)
DOID:0111458
  • galactose epimerase deficiency
  • Aliases:
    • GALE deficiency
    • GALE-D
    • UDP-galactose-4-epimerase deficiency
    • epimerase deficiency galactosemia
    • galactosemia III
    • galactosemia type 3
    • uridine diphosphate galactose-4-epimerase deficiency
Mus musculus (house mouse)
DOID:0111844
  • X-linked intellectual developmental disorder 108
  • Aliases:
    • MRX108
Saccharomyces cerevisiae S288C

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Last updated: February 17, 2025