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 11001 - 11025 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲ Source
DOID:573
  • nerve compression syndrome
  • Aliases:
    • Compression neuropathy
    • entrapment neuropathy
    • peripheral nerve entrapment syndrome
Mus musculus (house mouse)
DOID:9155
  • mucocutaneous leishmaniasis
  • Aliases:
    • American cutaneous leishmaniasis
    • American mucocutaneous leishmaniasis
    • Cutaneous leishmaniasis, American
    • Mucocutaneous leishmaniasis, American
    • New World cutaneous leishmaniasis
Mus musculus (house mouse)
DOID:4989
  • pancreatitis
Mus musculus (house mouse)
DOID:0050758
  • metabolic acidosis
Mus musculus (house mouse)
DOID:1060
  • Hartnup disease
  • Aliases:
    • Neutral 1 amino acid transport defect
    • deficiency of tryptophan oxygenase
    • neutral amino acid transport defect
Mus musculus (house mouse)
DOID:13375
  • temporal arteritis
  • Aliases:
    • Horton's disease
    • giant cell arteritis
Mus musculus (house mouse)
DOID:0080130
  • mitochondrial DNA depletion syndrome 12a
Mus musculus (house mouse)
DOID:10907
  • microcephaly
  • Aliases:
    • Microcephalus
    • microencephaly
Mus musculus (house mouse)
DOID:0080694
  • Galloway-Mowat syndrome
Mus musculus (house mouse)
DOID:0090127
  • camptodactyly-arthropathy-coxa vara-pericarditis syndrome
  • Aliases:
    • CACP
    • CACP syndrome
    • CAP syndrome
    • Jacobs syndrome
    • PAC syndrome
    • arthropathy-camptodactyly syndrome
    • camptodactyly-arthropathy-pericarditis syndrome
    • congenital familial hypertrophic synovitis
    • familial fibrosing serositis
    • pericarditis-arthropathy-camptodactyly syndrome
Mus musculus (house mouse)
DOID:263
  • kidney cancer
  • Aliases:
    • malignant neoplasm of kidney except pelvis
    • malignant tumour of kidney
    • renal cancer
Mus musculus (house mouse)
DOID:2590
  • familial nephrotic syndrome
  • Aliases:
    • Congenital nephrotic syndrome
Mus musculus (house mouse)
DOID:811
  • lipodystrophy
Mus musculus (house mouse)
DOID:1574
  • alcohol use disorder
  • Aliases:
    • Ethanol abuse
    • alcohol abuse
Mus musculus (house mouse)
DOID:1579
  • respiratory system disease
Mus musculus (house mouse)
DOID:13711
  • dental fluorosis
  • Aliases:
    • Intrinsic enamel discolouration of fluorosis
    • Mottled teeth
    • Mottling of enamel
Mus musculus (house mouse)
DOID:0050752
  • amyotrophic lateral sclerosis type 8
  • Aliases:
    • ALS8
    • amyotrophic lateral sclerosis 8
Mus musculus (house mouse)
DOID:0070111
  • Niemann-Pick disease type A
Mus musculus (house mouse)
DOID:12732
  • intermediate uveitis
  • Aliases:
    • chronic cyclitis
    • peripheral uveoretinitis
Mus musculus (house mouse)
DOID:0111633
  • congenital sucrase-isomaltase deficiency
  • Aliases:
    • CSID
    • SI deficiency
    • congenital sucrase-isomaltose malabsorption
    • congenital sucrose intolerance
    • disaccharide intolerance
Mus musculus (house mouse)
DOID:0080500
  • ovarian dysgenesis 8
Mus musculus (house mouse)
DOID:0110291
  • Leber congenital amaurosis 10
  • Aliases:
    • LCA10
Mus musculus (house mouse)
DOID:9281
  • phenylketonuria
  • Aliases:
    • Folling's disease
    • PKU
    • maternal phenylketonuria
    • phenylalaninemia
Mus musculus (house mouse)
DOID:0110704
  • hypotrichosis 7
  • Aliases:
    • Hypt7
    • Lah2
    • hypotrichosis, localized, autosomal recessive 2
    • total Mari type hypotrichosis,
Mus musculus (house mouse)
DOID:0110149
  • Charcot-Marie-Tooth disease type 1F
  • Aliases:
    • CMT1F
    • Charcot-Marie-Tooth neuropathy type 1F
Mus musculus (house mouse)

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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