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 576 - 600 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism Source
DOID:2917
  • cryoglobulinemia
  • Aliases:
    • Cryoimmunoglobulinaemia
Saccharomyces cerevisiae S288C
DOID:0070232
  • benign recurrent intrahepatic cholestasis 2
  • Aliases:
    • BRIC type 2
    • BRIC2
Saccharomyces cerevisiae S288C
DOID:1849
  • cannabis dependence
Saccharomyces cerevisiae S288C
DOID:9976
  • heroin dependence
Saccharomyces cerevisiae S288C
DOID:3328
  • temporal lobe epilepsy
  • Aliases:
    • epilepsy, temporal lobe
Saccharomyces cerevisiae S288C
DOID:0060750
  • familial temporal lobe epilepsy 3
  • Aliases:
    • FMTLE
    • familial mesial temporal lobe epilepsy
Saccharomyces cerevisiae S288C
DOID:0050848
  • obstructive sleep apnea
  • Aliases:
    • obstructive sleep apnea syndrome
Saccharomyces cerevisiae S288C
DOID:13413
  • hepatic encephalopathy
  • Aliases:
    • Portal-systemic encephalopathy
Saccharomyces cerevisiae S288C
DOID:12365
  • malaria
  • Aliases:
    • induced malaria
Saccharomyces cerevisiae S288C
DOID:0060643
  • primary sclerosing cholangitis
Saccharomyces cerevisiae S288C
DOID:0080561
  • congenital disorder of glycosylation Ii
  • Aliases:
    • congenital disorder of glycosylation 1i
Homo sapiens (human)
DOID:0110669
  • congenital myasthenic syndrome 14
  • Aliases:
    • CMS14
    • CMSTA3
    • congenital myasthenic syndrome 14, with tubular aggregates
    • congenital myasthenic syndrome with tubular aggregates 3
Homo sapiens (human)
DOID:0050588
  • muscular dystrophy-dystroglycanopathy type B1
  • Aliases:
    • CMD due to dystroglycanopathy
    • Muscular dystrophy-dystroglycanopathy congenital with impaired intellectual development B1
Saccharomyces cerevisiae S288C
DOID:0110297
  • autosomal recessive limb-girdle muscular dystrophy type 2K
  • Aliases:
    • LGMD2K
    • MDDGC1
    • limb-girdle muscular dystrophy-intellectual disability syndrome
    • muscular dystrophy limb-girdle type 2K
    • muscular dystrophy-dystroglycanopathy (limb-girdle) type C 1
Saccharomyces cerevisiae S288C
DOID:9296
  • cleft lip
  • Aliases:
    • Labium leporinum
    • cheiloschisis
    • cleft lip, unilateral, complete
    • complete unilateral cleft lip
    • hare lip
Saccharomyces cerevisiae S288C
DOID:0111237
  • congenital muscular dystrophy-dystroglycanopathy type A1
  • Aliases:
    • MDDGA1
    • Walker-Warburg syndrome or muscle-eye-brain disease, POMT1-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A1
Saccharomyces cerevisiae S288C
DOID:0081421
  • familial focal epilepsy with variable foci 1
Saccharomyces cerevisiae S288C
DOID:0081423
  • familial focal epilepsy with variable foci 3
Saccharomyces cerevisiae S288C
DOID:2234
  • focal epilepsy
  • Aliases:
    • localisation-related epilepsy
    • partial epilepsy
Saccharomyces cerevisiae S288C
DOID:0112202
  • developmental and epileptic encephalopathy
Saccharomyces cerevisiae S288C
DOID:0081097
  • Rafiq syndrome
  • Aliases:
    • MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15
Saccharomyces cerevisiae S288C
DOID:0111030
  • hemochromatosis type 3
  • Aliases:
    • HFE3
    • TFR2-related hemochromatosis
    • hemochromatosis due to defect in transferrin receptor 2
Saccharomyces cerevisiae S288C
DOID:3702
  • cervical adenocarcinoma
  • Aliases:
    • adenocarcinoma cervix uteri
    • adenocarcinoma of cervix
    • adenocarcinoma of the uterine Cervix
Saccharomyces cerevisiae S288C
DOID:374
  • nutrition disease
  • Aliases:
    • Nutritional disorder
Saccharomyces cerevisiae S288C
DOID:2352
  • hemochromatosis
  • Aliases:
    • Haemochromatosis
    • diabetes bronze
    • iron storage disorder
Saccharomyces cerevisiae S288C

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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