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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 13826 - 13850 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:6193
  • epithelioid sarcoma
  • Aliases:
    • epithelioid cell sarcoma
Homo sapiens (human)
DOID:5485
  • synovial sarcoma
Homo sapiens (human)
DOID:0111492
  • combined oxidative phosphorylation deficiency 32
  • Aliases:
    • COXPD32
Homo sapiens (human)
DOID:0112367
  • Coffin-Siris syndrome 8
  • Aliases:
    • CSS8
Homo sapiens (human)
DOID:4783
  • mesangial proliferative glomerulonephritis
Rattus norvegicus (Norway rat)
DOID:0112372
  • Coffin-Siris syndrome 11
  • Aliases:
    • CSS11
Homo sapiens (human)
DOID:0112368
  • Coffin-Siris syndrome 5
  • Aliases:
    • CSS5
Homo sapiens (human)
DOID:0050773
  • paraganglioma
  • Aliases:
    • chemodectoma
    • glomus body tumor
Mus musculus (house mouse)
DOID:0080533
  • Carney-Stratakis syndrome
Mus musculus (house mouse)
DOID:0081228
  • autosomal recessive intellectual developmental disorder 67
Mus musculus (house mouse)
DOID:0070111
  • Niemann-Pick disease type A
Homo sapiens (human)
DOID:0070112
  • Niemann-Pick disease type B
Homo sapiens (human)
DOID:0112086
  • nuclear type mitochondrial complex I deficiency 26
  • Aliases:
    • MC1DN26
Mus musculus (house mouse)
DOID:0110683
  • congenital myasthenic syndrome 18
  • Aliases:
    • CMS18
Homo sapiens (human)
DOID:3981
  • pantothenate kinase-associated neurodegeneration
  • Aliases:
    • Hallervorden-Spatz disease
    • Hallervorden-Spatz syndrome
    • NBIA1
    • Pigmentary pallidal degeneration
    • brain Iron Accumulation type I syndrome
    • neurodegeneration with brain iron accumulation 1
Homo sapiens (human)
DOID:0060895
  • Parkinson's disease 4
  • Aliases:
    • autosomal dominant Lewy body Parkinson disease 4
    • autosomal dominant Parkinson disease 4
    • autosomal dominant Parkinson's disease 4
Homo sapiens (human)
DOID:0060367
  • Parkinson's disease 1
  • Aliases:
    • autosomal dominant Parkinson disease 1
    • autosomal dominant Parkinson's disease 1
Homo sapiens (human)
DOID:2994
  • germ cell cancer
  • Aliases:
    • malignant tumor of the germ cell
Homo sapiens (human)
DOID:0111248
  • cerebrocostomandibular syndrome
  • Aliases:
    • CCM syndrome
    • CCMS
    • cerebro-costo-mandibular syndrome
    • rib gap defects with micrognathia
Homo sapiens (human)
DOID:0110708
  • hypotrichosis 11
  • Aliases:
    • Hypt11
Homo sapiens (human)
DOID:0080115
  • mitochondrial complex III deficiency nuclear type 6
Mus musculus (house mouse)
DOID:1060
  • Hartnup disease
  • Aliases:
    • Neutral 1 amino acid transport defect
    • deficiency of tryptophan oxygenase
    • neutral amino acid transport defect
Rattus norvegicus (Norway rat)
DOID:5113
  • nutritional deficiency disease
Homo sapiens (human)
DOID:0050809
  • mucopolysaccharidosis IX
Danio rerio (zebrafish)
DOID:3613
  • Canavan disease
  • Aliases:
    • ACY2 DEFICIENCY
    • AMINOACYLASE 2 DEFICIENCY
    • ASP DEFICIENCY
    • ASPA DEFICIENCY
    • ASPARTOACYLASE DEFICIENCY
    • CANAVAN-VAN BOGAERT-BERTRAND DISEASE
    • Spongy degeneration of central nervous system
Homo sapiens (human)
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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