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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 5001 - 5025 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0070398
  • hypomyelinating leukodystrophy 15
  • Aliases:
    • HLD15
Mus musculus (house mouse)
DOID:0110064
  • amelogenesis imperfecta type 1H
  • Aliases:
    • AI1H
    • amelogenesis imperfecta type IH
Rattus norvegicus (Norway rat)
DOID:0050451
  • Brugada syndrome
  • Aliases:
    • Bangungut
    • Brugada type idiopathic ventricular fibrillation
    • Dream disease
    • Pokkuri death syndrome
    • SUNDS
    • sudden unexplained nocturnal death syndrome
Homo sapiens (human)
DOID:3209
  • junctional epidermolysis bullosa
  • Aliases:
    • congenital junctional epidermolysis bullosa
Mus musculus (house mouse)
DOID:0111076
  • progressive familial heart block type IB
  • Aliases:
    • PFHB1B
Homo sapiens (human)
DOID:0080109
  • infantile myofibromatosis
  • Aliases:
    • lipofibromatosis
Mus musculus (house mouse)
DOID:0081179
  • autosomal recessive intellectual developmental disorder 3
Mus musculus (house mouse)
DOID:0081158
  • dilated cardiomyopathy 1MM
Rattus norvegicus (Norway rat)
DOID:0080762
  • autosomal recessive limb-girdle muscular dystrophy type 2Z
  • Aliases:
    • limb-girdle muscular dystrophy 21
Drosophila melanogaster (fruit fly)
DOID:8437
  • intestinal obstruction
Rattus norvegicus (Norway rat)
DOID:9120
  • amyloidosis
  • Aliases:
    • amyloid disease
Xenopus laevis (African clawed frog)
DOID:0111668
  • Kohlschutter-Tonz syndrome
  • Aliases:
    • KTZS
    • Kohlschutter's syndrome
    • amelocerebrohypohidrotic syndrome
    • epilepsy and yellow teeth
    • epilepsy dementia amelogenesis imperfecta
    • epilepsy-dementia-amelogenesis imperfecta syndrome
Homo sapiens (human)
DOID:3209
  • junctional epidermolysis bullosa
  • Aliases:
    • congenital junctional epidermolysis bullosa
Drosophila melanogaster (fruit fly)
DOID:4947
  • cholangiocarcinoma
  • Aliases:
    • adult primary Cholangiocarcinoma
    • adult primary cholangiocellular carcinoma
    • cholangiosarcoma
Caenorhabditis elegans
DOID:0081312
  • T-cell non-Hodgkin lymphoma
Danio rerio (zebrafish)
DOID:11984
  • hypertrophic cardiomyopathy
  • Aliases:
    • hypertrophic obstructive cardiomyopathy
Xenopus laevis (African clawed frog)
DOID:0110666
  • congenital myasthenic syndrome 3A
  • Aliases:
    • CMS3A
    • congenital myasthenic syndrome 3A, slow-channel
Homo sapiens (human)
DOID:0050560
  • Walker-Warburg syndrome
  • Aliases:
    • HARD syndrome
    • cerebroocular dysplasia-muscular dystrophy syndrome
Mus musculus (house mouse)
DOID:0060696
  • hyperekplexia 1
  • Aliases:
    • HKPX1
Mus musculus (house mouse)
DOID:0050636
  • familial visceral amyloidosis
  • Aliases:
    • AMYLOIDOSIS, FAMILIAL RENAL
    • German type amyloidosis
    • OSTERTAG TYPE AMYLOIDOSIS
    • systemic nonneuropathic amyloidosis
Mus musculus (house mouse)
DOID:8805
  • intermediate coronary syndrome
  • Aliases:
    • Angina at rest
    • Anginal chest pain at rest
    • Impending infarction
    • Preinfarction angina
    • Unstable angina
    • Worsening angina
Rattus norvegicus (Norway rat)
DOID:0112221
  • developmental and epileptic encephalopathy 87
  • Aliases:
    • DEE87
    • early infantile epileptic encephalopathy 87
Homo sapiens (human)
DOID:0081297
  • oculopharyngodistal myopathy 1
Homo sapiens (human)
DOID:3627
  • aortic aneurysm
  • Aliases:
    • ruptured aortic aneurysm
Homo sapiens (human)
DOID:0070303
  • multiple epiphyseal dysplasia 1
  • Aliases:
    • EDM1
    • MED1
    • multiple epiphyseal dysplasia COMP-related
    • polyepiphyseal dysplasia type 1
Drosophila melanogaster (fruit fly)
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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