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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 January 28, 2025
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 4301 - 4325 of 5716 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism Source
DOID:14219
  • renal tubular acidosis
Homo sapiens (human)
DOID:14219
  • renal tubular acidosis
Saccharomyces cerevisiae S288C
DOID:14221
  • abdominal obesity-metabolic syndrome 1
  • Aliases:
    • dysmetabolic syndrome X
    • metabolic syndrome X
Mus musculus (house mouse)
DOID:14221
  • abdominal obesity-metabolic syndrome 1
  • Aliases:
    • dysmetabolic syndrome X
    • metabolic syndrome X
Rattus norvegicus (Norway rat)
DOID:14227
  • azoospermia
Rattus norvegicus (Norway rat)
DOID:14227
  • azoospermia
Drosophila melanogaster (fruit fly)
DOID:14250
  • Down syndrome
  • Aliases:
    • Complete trisomy 21 syndrome
    • Down's syndrome
    • Down's syndrome - trisomy 21
    • Downs syndrome
    • G Trisomy
    • trisomy 21 syndrome
Caenorhabditis elegans
DOID:14250
  • Down syndrome
  • Aliases:
    • Complete trisomy 21 syndrome
    • Down's syndrome
    • Down's syndrome - trisomy 21
    • Downs syndrome
    • G Trisomy
    • trisomy 21 syndrome
Drosophila melanogaster (fruit fly)
DOID:14250
  • Down syndrome
  • Aliases:
    • Complete trisomy 21 syndrome
    • Down's syndrome
    • Down's syndrome - trisomy 21
    • Downs syndrome
    • G Trisomy
    • trisomy 21 syndrome
Homo sapiens (human)
DOID:14261
  • fragile X syndrome
  • Aliases:
    • FRAGILE X MENTAL RETARDATION SYNDROME
    • MARKER X SYNDROME
    • MARTIN-BELL SYNDROME
Homo sapiens (human)
DOID:14264
  • benign neonatal seizures
  • Aliases:
    • benign familial neonatal seizures
    • benign neonatal convulsions
Mus musculus (house mouse)
DOID:14264
  • benign neonatal seizures
  • Aliases:
    • benign familial neonatal seizures
    • benign neonatal convulsions
Homo sapiens (human)
DOID:14283
  • primary hypertrophic osteoarthropathy
  • Aliases:
    • Pachydermoperiostosis of nail
    • Pachydermoperiostosis syndrome
Homo sapiens (human)
DOID:14289
  • Ebstein anomaly
  • Aliases:
    • Ebstein's anomaly
    • Ebstein's anomaly of common atrioventricular valve
    • Ebstein's anomaly of right atrioventricular valve
    • Ebstein's anomaly of tricuspid valve
Mus musculus (house mouse)
DOID:14291
  • Noonan syndrome with multiple lentigines
  • Aliases:
    • Capute-Rimoin-Konigsmark-Esterly-Richardson syndrome
    • Generalized lentiginosis
    • Gorlin syndrome II
    • LEOPARD syndrome
    • Lentiginosis profusa syndrome
    • Moynahan syndrome
    • Multiple lentigines syndrome
    • Progressive cardiomyopathic lentiginosis
Mus musculus (house mouse)
DOID:1432
  • blindness
  • Aliases:
    • vision impairment
    • vision loss
    • visual impairment
Homo sapiens (human)
DOID:1432
  • blindness
  • Aliases:
    • vision impairment
    • vision loss
    • visual impairment
Mus musculus (house mouse)
DOID:14320
  • generalized anxiety disorder
Mus musculus (house mouse)
DOID:14320
  • generalized anxiety disorder
Drosophila melanogaster (fruit fly)
DOID:14320
  • generalized anxiety disorder
Homo sapiens (human)
DOID:14323
  • Marfan syndrome
  • Aliases:
    • Marfan's syndrome
Mus musculus (house mouse)
DOID:14323
  • Marfan syndrome
  • Aliases:
    • Marfan's syndrome
Homo sapiens (human)
DOID:14323
  • Marfan syndrome
  • Aliases:
    • Marfan's syndrome
Caenorhabditis elegans
DOID:14330
  • Parkinson's disease
  • Aliases:
    • Parkinson disease
    • paralysis agitans
Homo sapiens (human)
DOID:14330
  • Parkinson's disease
  • Aliases:
    • Parkinson disease
    • paralysis agitans
Caenorhabditis elegans
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Supported by JST NBDC Grant Number JPMJND2204

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

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Last updated: March 31, 2025