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 1401 - 1425 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism
DOID:0111157
  • Castleman disease
  • Aliases:
    • angiofollicular lymph hyperplasia
    • angiofollicular lymph node hyperplasia
    • giant lymph node hyperplasia
    • lymphoid hamartoma
Homo sapiens (human)
DOID:7365
  • Kimura disease
  • Aliases:
    • Kimura's disease
Homo sapiens (human)
DOID:13133
  • HELLP syndrome
Homo sapiens (human)
DOID:0060653
  • lethal congenital contracture syndrome 3
  • Aliases:
    • Israeli Bedouin type B multiple contracture syndrome
Homo sapiens (human)
DOID:8838
  • Hodgkin's lymphoma, nodular sclerosis
  • Aliases:
    • Classical Hodgkin lymphoma, nodular sclerosis
Homo sapiens (human)
DOID:0080459
  • developmental and epileptic encephalopathy 12
  • Aliases:
    • DEE12
    • early infantile epileptic encephalopathy 12
Homo sapiens (human)
DOID:0060551
  • poikiloderma with neutropenia
  • Aliases:
    • poikiloderma with neutropenia, Clericuzio type
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:8691
  • mycosis fungoides
  • Aliases:
    • mycosis fungoides lymphoma
Homo sapiens (human)
DOID:0050120
  • hemophagocytic lymphohistiocytosis
  • Aliases:
    • haemophagocytic syndrome
Homo sapiens (human)
DOID:0110859
  • polycystic kidney disease 2
  • Aliases:
    • Apkd2
    • Pkd2
    • Polycystic Kidney Disease, Adult, Type II
Homo sapiens (human)
DOID:0050770
  • polycystic liver disease
  • Aliases:
    • congenital cystic liver disease
    • congenital hepatic cyst
    • fibrocystic liver disease
Homo sapiens (human)
DOID:0080322
  • polycystic kidney disease
Homo sapiens (human)
DOID:0110387
  • retinitis pigmentosa 9
  • Aliases:
    • RP9
Homo sapiens (human)
DOID:0110219
  • Brugada syndrome 2
  • Aliases:
    • BRGDA2
Homo sapiens (human)
DOID:0110218
  • Brugada syndrome 1
  • Aliases:
    • BRGDA1
Homo sapiens (human)
DOID:0110224
  • Brugada syndrome 7
  • Aliases:
    • BRGDA7
Homo sapiens (human)
DOID:0110220
  • Brugada syndrome 3
  • Aliases:
    • BRGDA3
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:0110223
  • Brugada syndrome 6
  • Aliases:
    • BRGDA6
Homo sapiens (human)
DOID:0110225
  • Brugada syndrome 8
  • Aliases:
    • BRGDA8
Homo sapiens (human)
DOID:0110222
  • Brugada syndrome 5
  • Aliases:
    • BRGDA5
Homo sapiens (human)
DOID:0110221
  • Brugada syndrome 4
  • Aliases:
    • BRGDA4
Homo sapiens (human)
DOID:0110226
  • Brugada syndrome 9
  • Aliases:
    • BRGDA9
Homo sapiens (human)
DOID:0060465
  • fibrochondrogenesis
Homo sapiens (human)

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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