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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 5301 - 5325 of 15957 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism Source
DOID:0060227
  • Adams-Oliver syndrome
  • Aliases:
    • Adams Oliver syndrome
Rattus norvegicus (Norway rat)
DOID:264
  • hemangiopericytoma
  • Aliases:
    • Haemangiopericytic meningioma
    • hemangiopericytoma, malignant
    • malignant hemangiopericytoma
Rattus norvegicus (Norway rat)
DOID:799
  • varicose veins
  • Aliases:
    • Varix
    • Venous ectasia
    • Venous varices
    • varices
Rattus norvegicus (Norway rat)
DOID:4556
  • lung large cell carcinoma
  • Aliases:
    • large cell carcinoma of lung
    • large cell lung carcinoma
Rattus norvegicus (Norway rat)
DOID:799
  • varicose veins
  • Aliases:
    • Varix
    • Venous ectasia
    • Venous varices
    • varices
Mus musculus (house mouse)
DOID:264
  • hemangiopericytoma
  • Aliases:
    • Haemangiopericytic meningioma
    • hemangiopericytoma, malignant
    • malignant hemangiopericytoma
Mus musculus (house mouse)
DOID:0050773
  • paraganglioma
  • Aliases:
    • chemodectoma
    • glomus body tumor
Mus musculus (house mouse)
DOID:0110461
  • X-linked dilated cardiomyopathy
  • Aliases:
    • CMD3B
    • DMD-related dilated cardiomyopathy
Mus musculus (house mouse)
DOID:9883
  • Becker muscular dystrophy
  • Aliases:
    • Benign pseudohypertrophic muscular dystrophy
    • benign congenital myopathy
Mus musculus (house mouse)
DOID:0081164
  • dilated cardiomyopathy 3B
Mus musculus (house mouse)
DOID:0050949
  • autosomal recessive hypophosphatemic rickets
Mus musculus (house mouse)
DOID:0112217
  • developmental and epileptic encephalopathy 81
  • Aliases:
    • DEE81
    • early infantile epileptic encephalopathy 81
Mus musculus (house mouse)
DOID:0080267
  • autosomal dominant nonsyndromic deafness 71
Mus musculus (house mouse)
DOID:0110612
  • primary ciliary dyskinesia 10
  • Aliases:
    • CILD10
    • primary ciliary dyskinesia 10 with or without situs inversus
Mus musculus (house mouse)
DOID:0050144
  • Kartagener syndrome
  • Aliases:
    • Kartagener's syndrome
Mus musculus (house mouse)
DOID:0110605
  • primary ciliary dyskinesia 7
  • Aliases:
    • CILD7
    • primary ciliary dyskinesia 7 with or without situs inversus
Mus musculus (house mouse)
DOID:0110599
  • primary ciliary dyskinesia 3
  • Aliases:
    • CILD3
    • primary ciliary dyskinesia 3 with or without situs inversus
Mus musculus (house mouse)
DOID:0110594
  • primary ciliary dyskinesia 1
  • Aliases:
    • CILD1
    • primary ciliary dyskinesia 1 with or without situs inversus
Mus musculus (house mouse)
DOID:0060891
  • Parkinson's disease 19A
  • Aliases:
    • juvenile onset Parkinson disease 19A
    • juvenile onset Parkinson's disease 19A
Mus musculus (house mouse)
DOID:0111223
  • centronuclear myopathy 1
  • Aliases:
    • CNM1
Mus musculus (house mouse)
DOID:11252
  • microcytic anemia
Mus musculus (house mouse)
DOID:0110197
  • Charcot-Marie-Tooth disease dominant intermediate B
  • Aliases:
    • CMTDI1
    • CMTDIB
    • Charcot-Marie-Tooth neuropathy dominant intermediate B
    • DI-CMTB
Mus musculus (house mouse)
DOID:1827
  • idiopathic generalized epilepsy
  • Aliases:
    • Generalised epilepsy
Mus musculus (house mouse)
DOID:0070376
  • developmental and epileptic encephalopathy 31B
  • Aliases:
    • DEE31B
Mus musculus (house mouse)
DOID:0080437
  • developmental and epileptic encephalopathy 31A
  • Aliases:
    • DEE31
    • DEE31A
    • developmental and epileptic encephalopathy 31
    • early infantile epileptic encephalopathy 31
Mus musculus (house mouse)
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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