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 13526 - 13550 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism Source
DOID:4449
  • macular retinal edema
  • Aliases:
    • macular edema
    • macular oedema
    • macular retinal oedema
Mus musculus (house mouse)
DOID:3145
  • hyperlipoproteinemia type III
  • Aliases:
    • Remnant hyperlipidemia
    • carbohydrate induced hyperlipemia
    • familial hypercholesterolaemia with hyperlipaemia
    • familial type 3 hyperlipoproteinemia
Mus musculus (house mouse)
DOID:0111370
  • apolipoprotein C-III deficiency
  • Aliases:
    • HALP2
    • hyperalphalipoproteinemia 2
Mus musculus (house mouse)
DOID:2972
  • renal artery obstruction
Mus musculus (house mouse)
DOID:11266
  • Hantavirus hemorrhagic fever with renal syndrome
  • Aliases:
    • HFRS
    • Hemorrhagic fever, Russian
    • Hemorrhagic nephrosonephritis
    • Puumala virus nephropathy
Mus musculus (house mouse)
DOID:2154
  • nephroblastoma
  • Aliases:
    • adult nephroblastoma
Mus musculus (house mouse)
DOID:0111312
  • idiopathic generalized epilepsy 11
  • Aliases:
    • EIG11
Homo sapiens (human)
DOID:10579
  • leukodystrophy
Homo sapiens (human)
DOID:446
  • primary hyperaldosteronism
  • Aliases:
    • Cushing syndrome
    • Cushing's syndrome
    • hyperaldosteronism
Homo sapiens (human)
DOID:0080348
  • Alzheimer's disease 1
  • Aliases:
    • Alzheimer's disease 1, early onset
Mus musculus (house mouse)
DOID:11044
  • gastroschisis
Homo sapiens (human)
DOID:13809
  • familial combined hyperlipidemia
  • Aliases:
    • familial multiple lipoprotein-type hyperlipidemia
    • hyperbetalipoproteinemia with prebetalipoproteinemia
    • mixed hyperlipidaemia
    • type IIb hyperlipoproteinemia
Homo sapiens (human)
DOID:10908
  • hydrocephalus
  • Aliases:
    • hydrocephalus, X-linked
    • hydrocephalus, nonsyndromic, autosomal recessive
Homo sapiens (human)
DOID:3328
  • temporal lobe epilepsy
  • Aliases:
    • epilepsy, temporal lobe
Homo sapiens (human)
DOID:0081361
  • spastic quadriplegic cerebral palsy 3
  • Aliases:
    • CPSQ3
Homo sapiens (human)
DOID:0110839
  • Usher syndrome type 2C
  • Aliases:
    • USH2C
    • Usher syndrome IIC
    • Usher syndrome type IIC
Rattus norvegicus (Norway rat)
DOID:2355
  • anemia
  • Aliases:
    • anaemia
Rattus norvegicus (Norway rat)
DOID:0111222
  • centronuclear myopathy 5
  • Aliases:
    • CNM5
Mus musculus (house mouse)
DOID:0080448
  • developmental and epileptic encephalopathy 48
  • Aliases:
    • DEE48
    • early infantile epileptic encephalopathy 48
Mus musculus (house mouse)
DOID:2223
  • platelet storage pool deficiency
  • Aliases:
    • Dense body defect
    • Platelet dense granule deficiency
    • Platelet storage pool defect
Mus musculus (house mouse)
DOID:0060540
  • Hermansky-Pudlak syndrome 2
Mus musculus (house mouse)
DOID:3753
  • Hermansky-Pudlak syndrome
Mus musculus (house mouse)
DOID:1227
  • neutropenia
Mus musculus (house mouse)
DOID:3082
  • interstitial lung disease
  • Aliases:
    • ILD
Mus musculus (house mouse)
DOID:0060307
  • autosomal dominant intellectual developmental disorder
  • Aliases:
    • autosomal dominant mental retardation
    • autosomal dominant non-syndromic mental retardation
Mus musculus (house mouse)

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.1.0

Last updated: December 9, 2024