GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources July 29, 2024
DisGeNET July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 4576 - 4600 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism
DOID:0110218
  • Brugada syndrome 1
  • Aliases:
    • BRGDA1
Homo sapiens (human)
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:0110226
  • Brugada syndrome 9
  • Aliases:
    • BRGDA9
Homo sapiens (human)
DOID:0110219
  • Brugada syndrome 2
  • Aliases:
    • BRGDA2
Homo sapiens (human)
DOID:0110387
  • retinitis pigmentosa 9
  • Aliases:
    • RP9
Homo sapiens (human)
DOID:0080322
  • polycystic kidney disease
Homo sapiens (human)
DOID:0050770
  • polycystic liver disease
  • Aliases:
    • congenital cystic liver disease
    • congenital hepatic cyst
    • fibrocystic liver disease
Homo sapiens (human)
DOID:0110859
  • polycystic kidney disease 2
  • Aliases:
    • Apkd2
    • Pkd2
    • Polycystic Kidney Disease, Adult, Type II
Homo sapiens (human)
DOID:0050120
  • hemophagocytic lymphohistiocytosis
  • Aliases:
    • haemophagocytic syndrome
Homo sapiens (human)
DOID:8691
  • mycosis fungoides
  • Aliases:
    • mycosis fungoides lymphoma
Homo sapiens (human)
DOID:0080468
  • developmental and epileptic encephalopathy 1
  • Aliases:
    • DEE1
    • X-linked infantile spasm syndrome 1
    • early infantile epileptic encephalopathy 1
Homo sapiens (human)
DOID:0060551
  • poikiloderma with neutropenia
  • Aliases:
    • poikiloderma with neutropenia, Clericuzio type
Homo sapiens (human)
DOID:0080459
  • developmental and epileptic encephalopathy 12
  • Aliases:
    • DEE12
    • early infantile epileptic encephalopathy 12
Homo sapiens (human)
DOID:8838
  • Hodgkin's lymphoma, nodular sclerosis
  • Aliases:
    • Classical Hodgkin lymphoma, nodular sclerosis
Homo sapiens (human)
DOID:0060178
  • familial hemiplegic migraine
Mus musculus (house mouse)
DOID:863
  • nervous system disease
Mus musculus (house mouse)
DOID:0050635
  • alternating hemiplegia of childhood
  • Aliases:
    • AHC
Mus musculus (house mouse)
DOID:0070385
  • developmental and epileptic encephalopathy 99
  • Aliases:
    • DEE99
    • early infantile epileptic encephalopathy 99
Mus musculus (house mouse)
DOID:0090056
  • dystonia 12
Mus musculus (house mouse)
DOID:0060462
  • Desbuquois dysplasia
  • Aliases:
    • Desbuquois syndrome
    • micromelic dwarfism with vertebral and metaphyseal abnormalities and advanced carpotarsal ossification
Mus musculus (house mouse)
DOID:0060653
  • lethal congenital contracture syndrome 3
  • Aliases:
    • Israeli Bedouin type B multiple contracture syndrome
Homo sapiens (human)
DOID:13133
  • HELLP syndrome
Homo sapiens (human)
DOID:7365
  • Kimura disease
  • Aliases:
    • Kimura's disease
Homo sapiens (human)
DOID:0111157
  • Castleman disease
  • Aliases:
    • angiofollicular lymph hyperplasia
    • angiofollicular lymph node hyperplasia
    • giant lymph node hyperplasia
    • lymphoid hamartoma
Homo sapiens (human)
DOID:0060451
  • Meesmann corneal dystrophy
  • Aliases:
    • MECD
    • Stocker-Holt dystrophy
    • juvenile hereditary epithelial dystrophy
Homo sapiens (human)

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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: August 19, 2024