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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 12176 - 12200 of 15957 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism Source
DOID:0060752
  • familial temporal lobe epilepsy 5
  • Aliases:
    • ETL5
Homo sapiens (human)
DOID:0111308
  • familial febrile seizures 11
  • Aliases:
    • FEB11
    • familial febrile convulsions 11
Homo sapiens (human)
DOID:12119
  • hemosiderosis
  • Aliases:
    • haemosiderosis
Homo sapiens (human)
DOID:0050711
  • aceruloplasminemia
Homo sapiens (human)
DOID:0070485
  • mitochondrial complex IV deficiency nuclear type 23
  • Aliases:
    • MC4DN23
Homo sapiens (human)
DOID:3762
  • cytochrome-c oxidase deficiency disease
  • Aliases:
    • MITOCHONDRIAL COMPLEX IV DEFICIENCY
Homo sapiens (human)
DOID:3762
  • cytochrome-c oxidase deficiency disease
  • Aliases:
    • MITOCHONDRIAL COMPLEX IV DEFICIENCY
Rattus norvegicus (Norway rat)
DOID:3762
  • cytochrome-c oxidase deficiency disease
  • Aliases:
    • MITOCHONDRIAL COMPLEX IV DEFICIENCY
Mus musculus (house mouse)
DOID:0060019
  • coronin-1A deficiency
Homo sapiens (human)
DOID:0090014
  • severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive
  • Aliases:
    • autosomal recessive T cell-negative, B-cell positive, NK cell-positive SCID
Homo sapiens (human)
DOID:0070242
  • primary coenzyme Q10 deficiency 5
  • Aliases:
    • COQ10D5
    • coenzyme Q10 deficiency, primary, 5
    • encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome
Homo sapiens (human)
DOID:0070243
  • primary coenzyme Q10 deficiency 6
  • Aliases:
    • COQ10D6
    • coenzyme Q10 deficiency, primary, 6
    • familial steroid-resistant nephrotic syndrome with sensorineural deafness
Homo sapiens (human)
DOID:3204
  • schwannomatosis
  • Aliases:
    • SWN
    • neurilemmomatosis
    • neurinomatosis
Homo sapiens (human)
DOID:0070238
  • primary coenzyme Q10 deficiency 1
  • Aliases:
    • COQ10D1
    • CoQ deficiency 1
    • CoQ10 deficiency, primary, 1
    • coenzyme Q deficiency 1
    • ubiquinone deficiency 1
Homo sapiens (human)
DOID:0050730
  • coenzyme Q10 deficiency disease
  • Aliases:
    • COENZYME Q10 DEFICIENCY, PRIMARY
Homo sapiens (human)
DOID:0111962
  • combined immunodeficiency
Homo sapiens (human)
DOID:2344
  • polyclonal hypergammaglobulinemia
Homo sapiens (human)
DOID:0070281
  • primary autosomal recessive microcephaly 19
  • Aliases:
    • MCPH19
Homo sapiens (human)
DOID:0081242
  • autoimmune interstitial lung, joint, and kidney disease
  • Aliases:
    • Autoimmune interstitial lung disease-arthritis syndrome
    • COPA syndrome
Homo sapiens (human)
DOID:12129
  • bulimia nervosa
  • Aliases:
    • hyperorexia nervosa
Homo sapiens (human)
DOID:12401
  • intermittent explosive disorder
  • Aliases:
    • explosive personality disorder
Homo sapiens (human)
DOID:13078
  • eumycotic mycetoma
  • Aliases:
    • Madura foot
    • Maduromycosis, mycotic
    • Mycotic mycetoma
    • eumycetoma
    • maduromycosis
Homo sapiens (human)
DOID:12399
  • pathological gambling
  • Aliases:
    • Compulsive gambling
Homo sapiens (human)
DOID:9828
  • neonatal abstinence syndrome
  • Aliases:
    • Drug withdrawal syndrome in newborn
Homo sapiens (human)
DOID:0080047
  • pseudoachondroplasia
  • Aliases:
    • SPONDYLOEPIPHYSEAL DYSPLASIA, PSEUDOACHONDROPLASTIC
    • pseudoachondroplastic dysplasia
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