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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 2526 - 2550 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0110665
  • congenital myasthenic syndrome 3B
  • Aliases:
    • CMS3B
    • congenital myasthenic syndrome 3B, fast-channel
Homo sapiens (human)
DOID:4492
  • avian influenza
  • Aliases:
    • avian flu
    • bird flu
Rattus norvegicus (Norway rat)
DOID:6088
  • acute stress disorder
  • Aliases:
    • traumatic stress disorder
Homo sapiens (human)
DOID:0111675
  • neurooculocardiogenitourinary syndrome
  • Aliases:
    • NOCGUS
Homo sapiens (human)
DOID:1229
  • paranoid schizophrenia
  • Aliases:
    • Paranoid type schizophrenia
    • Paraphrenia - late
    • Paraphrenic schizophrenia
    • chronic paranoid schizophrenia
    • paranoid type schizophrenia subchronic state
Mus musculus (house mouse)
DOID:0070216
  • familial hyperinsulinemic hypoglycemia 3
  • Aliases:
    • HHF3
    • hyperinsulinemic hypoglycemia due to glucokinase deficiency
    • hyperinsulinism due to glucokinase deficiency
Saccharomyces cerevisiae S288C
DOID:3119
  • gastrointestinal system cancer
  • Aliases:
    • GI tumor
    • digestive system cancer
    • gastrointestinal tract cancer
Mus musculus (house mouse)
DOID:576
  • proteinuria
Caenorhabditis elegans
DOID:0050951
  • hereditary ataxia
Rattus norvegicus (Norway rat)
DOID:0110678
  • congenital myasthenic syndrome 4A
  • Aliases:
    • CMS Ia1
    • CMS1A1
    • CMS4A
    • congenital myasthenic syndrome 4A slow-channel
    • congenital myasthenic syndrometype Ia1
Mus musculus (house mouse)
DOID:0080420
  • developmental and epileptic encephalopathy 62
  • Aliases:
    • DEE62
    • early infantile epileptic encephalopathy 62
Homo sapiens (human)
DOID:0112332
  • pontocerebellar hypoplasia type 13
  • Aliases:
    • PCH13
Homo sapiens (human)
DOID:14705
  • Pfeiffer syndrome
  • Aliases:
    • acrocephalosyndactylia type V
Rattus norvegicus (Norway rat)
DOID:999
  • hypereosinophilic syndrome
  • Aliases:
    • Eosinophilic leukocytosis
    • eosinophilia
Drosophila melanogaster (fruit fly)
DOID:0110660
  • congenital myasthenic syndrome 12
  • Aliases:
    • CMS12
    • congenital myasthenia 12 with tubular aggregates
Homo sapiens (human)
DOID:9281
  • phenylketonuria
  • Aliases:
    • Folling's disease
    • PKU
    • maternal phenylketonuria
    • phenylalaninemia
Saccharomyces cerevisiae S288C
DOID:1389
  • polyneuropathy
Mus musculus (house mouse)
DOID:0080325
  • tuberous sclerosis 2
Rattus norvegicus (Norway rat)
DOID:0060327
  • omphalocele
  • Aliases:
    • omphalocoele
Rattus norvegicus (Norway rat)
DOID:0050545
  • visceral heterotaxy
  • Aliases:
    • heterotaxia
    • situs ambiguus
Mus musculus (house mouse)
DOID:0081119
  • benign familial infantile seizures 6
  • Aliases:
    • Autosomal dominant nocturnal frontal lobe epilepsy
    • Benign Familial Infantile Seizures, 6
    • nocturnal frontal lobe epilepsy-4
Drosophila melanogaster (fruit fly)
DOID:0070063
  • autosomal dominant intellectual developmental disorder 33
  • Aliases:
    • MRD33
    • autosomal dominant mental retardation 33
    • autosomal dominant non-syndromic intellectual disability 33
Homo sapiens (human)
DOID:0081424
  • familial focal epilepsy with variable foci 4
Homo sapiens (human)
DOID:0060224
  • atrial fibrillation
  • Aliases:
    • A-fib
    • AFib
Rattus norvegicus (Norway rat)
DOID:0111837
  • congenital nongoitrous hypothyroidism 8
  • Aliases:
    • CHNG8
Mus musculus (house mouse)
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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