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 1151 - 1175 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:783
  • end stage renal disease
  • Aliases:
    • end stage renal failure
    • end-stage kidney disease
Mus musculus (house mouse)
DOID:9246
  • cerebral amyloid angiopathy
  • Aliases:
    • Cerebral Hemorrhage, Hereditary, with Amyloidosis
    • Hereditary Cerebral Hemorrhage with Amyloidosis
Mus musculus (house mouse)
DOID:2747
  • glycogen storage disease
  • Aliases:
    • glycogenosis
Mus musculus (house mouse)
DOID:1289
  • neurodegenerative disease
  • Aliases:
    • degenerative disease
Mus musculus (house mouse)
DOID:384
  • Wolff-Parkinson-White syndrome
  • Aliases:
    • Anomalous A-V excitation
    • Wolff-Parkinson-White pattern
    • anomalous atrioventricular excitation
Mus musculus (house mouse)
DOID:0090101
  • lethal congenital glycogen storage disease of heart
  • Aliases:
    • fatal congenital hypertrophic cardiomyopathy due to GSD
    • fatal congenital hypertrophic cardiomyopathy due to glycogenosis
    • fatal congenital nonlysosomal cardiac glycogenosis
    • phosphorylase kinase deficiency of heart
Mus musculus (house mouse)
DOID:0110312
  • hypertrophic cardiomyopathy 6
  • Aliases:
    • CMH6
    • cardiomyopathy, familial hypertrophic 6
Mus musculus (house mouse)
DOID:10286
  • prostate carcinoma
  • Aliases:
    • cancer of prostate
    • carcinoma of prostate
Homo sapiens (human)
DOID:11119
  • Gilles de la Tourette syndrome
  • Aliases:
    • Guinon's disease
    • Psychogenic tics
    • Tourette syndrome
    • motor-verbal tic disorder
Mus musculus (house mouse)
DOID:0050571
  • congenital disorder of glycosylation type II
Mus musculus (house mouse)
DOID:6000
  • congestive heart failure
  • Aliases:
    • CHF
    • Cardiac Failure Congestive
    • Congestive heart disease
    • Weak heart
Mus musculus (house mouse)
DOID:1712
  • aortic valve stenosis
  • Aliases:
    • Aortic stenosis
    • Rheumatic aortic stenosis
    • rheumatic aortic valve stenosis
Mus musculus (house mouse)
DOID:0080240
  • non-syndromic X-linked intellectual disability 106
  • Aliases:
    • MRX106
    • X-linked mental retardation 106
Mus musculus (house mouse)
DOID:6419
  • tetralogy of Fallot
  • Aliases:
    • Ventricular septal defect with pulmonary stenosis or atresia, dextraposition of aorta, and hypertrophy of right ventricle
Mus musculus (house mouse)
DOID:7693
  • abdominal aortic aneurysm
  • Aliases:
    • AORTIC ANEURYSM, FAMILIAL ABDOMINAL 1
Mus musculus (house mouse)
DOID:14250
  • Down syndrome
  • Aliases:
    • Complete trisomy 21 syndrome
    • Down's syndrome
    • Down's syndrome - trisomy 21
    • Downs syndrome
    • G Trisomy
    • trisomy 21 syndrome
Mus musculus (house mouse)
DOID:9296
  • cleft lip
  • Aliases:
    • Labium leporinum
    • cheiloschisis
    • cleft lip, unilateral, complete
    • complete unilateral cleft lip
    • hare lip
Mus musculus (house mouse)
DOID:674
  • cleft palate
  • Aliases:
    • Palatoschisis
Mus musculus (house mouse)
DOID:0080016
  • spina bifida
Mus musculus (house mouse)
DOID:0080074
  • neural tube defect
Mus musculus (house mouse)
DOID:0080633
  • developmental cardiac valvular defect
Mus musculus (house mouse)
DOID:0081266
  • pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures
  • Aliases:
    • PAMDDFS
Homo sapiens (human)
DOID:13270
  • erythropoietic protoporphyria
  • Aliases:
    • EPP
    • Protoporphyria
Homo sapiens (human)
DOID:0111358
  • Floating-Harbor syndrome
  • Aliases:
    • FLHS
Homo sapiens (human)
DOID:0050737
  • autosomal recessive disease
Homo sapiens (human)

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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: December 9, 2024