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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 10326 - 10350 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism Source
DOID:0060643
  • primary sclerosing cholangitis
Caenorhabditis elegans
DOID:635
  • acquired immunodeficiency syndrome
  • Aliases:
    • AIDS
    • acquired Immune deficiency
Caenorhabditis elegans
DOID:0070222
  • progressive familial intrahepatic cholestasis 2
  • Aliases:
    • BSEP deficiency
    • PFIC2
Caenorhabditis elegans
DOID:2917
  • cryoglobulinemia
  • Aliases:
    • Cryoimmunoglobulinaemia
Caenorhabditis elegans
DOID:0080797
  • nasal type extranodal NK/T-cell lymphoma
Caenorhabditis elegans
DOID:2559
  • opiate dependence
  • Aliases:
    • Opioid type dependence
Caenorhabditis elegans
DOID:3008
  • invasive ductal carcinoma
  • Aliases:
    • Infiltrating ductal carcinoma of breast
    • Invasive ductal carcinoma, NST
    • ductal adenocarcinoma
Caenorhabditis elegans
DOID:2987
  • familial mediterranean fever
  • Aliases:
    • FMF
    • benign paroxysmal peritonitis
Caenorhabditis elegans
DOID:0050848
  • obstructive sleep apnea
  • Aliases:
    • obstructive sleep apnea syndrome
Caenorhabditis elegans
DOID:10159
  • osteonecrosis
  • Aliases:
    • Avascular necrosis of bone
    • aseptic necrosis
    • bone necrosis
Caenorhabditis elegans
DOID:0110813
  • hereditary spastic paraplegia 62
  • Aliases:
    • SPG62
    • autosomal recessive spastic paraplegia 62
    • autosomal recessive spastic paraplegia type 62
Caenorhabditis elegans
DOID:0110771
  • hereditary spastic paraplegia 18
  • Aliases:
    • IDMDC
    • SPG18
    • autosomal recessive spastic paraplegia 18
    • autosomal recessive spastic paraplegia type 18
    • intellectual disability, motor dysfunction and joint contractures
Caenorhabditis elegans
DOID:0060488
  • Pitt-Hopkins syndrome
Caenorhabditis elegans
DOID:13365
  • reading disorder
Caenorhabditis elegans
DOID:0060308
  • autosomal recessive intellectual developmental disorder
  • Aliases:
    • autosomal recessive mental retardation
    • autosomal recessive non-syndromic mental retardation
Caenorhabditis elegans
DOID:11257
  • social phobia
Caenorhabditis elegans
DOID:4189
  • mutism
Caenorhabditis elegans
DOID:0090130
  • cortical dysplasia-focal epilepsy syndrome
  • Aliases:
    • CDFE syndrome
    • CDFES
    • PTHSL1
    • Pitt-Hopkins-like syndrome-1
Caenorhabditis elegans
DOID:4186
  • articulation disorder
  • Aliases:
    • Articulation impairment
    • Phonological disorder
Caenorhabditis elegans
DOID:0060244
  • specific language impairment
Caenorhabditis elegans
DOID:0060558
  • lethal congenital contracture syndrome
Caenorhabditis elegans
DOID:0060777
  • congenital secretory sodium diarrhea 8
  • Aliases:
    • DIAR8
Caenorhabditis elegans
DOID:0111729
  • familial episodic pain syndrome 1
  • Aliases:
    • FEPS1
Caenorhabditis elegans
DOID:0070355
  • overactive bladder syndrome
  • Aliases:
    • OAB
    • overactive bladder
    • urge syndrome
    • urgency-frequency syndrome
Caenorhabditis elegans
DOID:3371
  • chondrosarcoma
  • Aliases:
    • Cartilaginous cancer
    • chondrosarcoma of bone
    • primary chondrosarcoma of the bone
Caenorhabditis elegans
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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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

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Last updated: December 9, 2024