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 1026 - 1050 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism
DOID:0050777
  • Joubert syndrome
  • Aliases:
    • JBTS
Homo sapiens (human)
DOID:0060270
  • pontocerebellar hypoplasia type 2D
Homo sapiens (human)
DOID:0090132
  • complex cortical dysplasia with other brain malformations 7
  • Aliases:
    • CDCBM7
    • polymicrogyria due to TUBB2B mutation
Homo sapiens (human)
DOID:0110096
  • short-rib thoracic dysplasia 14 with polydactyly
  • Aliases:
    • SRTD14
Homo sapiens (human)
DOID:0060277
  • pontocerebellar hypoplasia type 8
Homo sapiens (human)
DOID:0060278
  • pontocerebellar hypoplasia type 9
Homo sapiens (human)
DOID:4626
  • hydranencephaly
Homo sapiens (human)
DOID:0060276
  • pontocerebellar hypoplasia type 7
Homo sapiens (human)
DOID:0090137
  • complex cortical dysplasia with other brain malformations 1
  • Aliases:
    • CDCBM1
    • cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation
Homo sapiens (human)
DOID:0060807
  • syndromic X-linked intellectual disability Najm type
  • Aliases:
    • MICPCH
    • X-linked intellectual disability-microcephaly-pontocerebellar hypoplasia syndrome
    • mental retardation and microcephaly with pontine and cerebellar hypoplasia
Homo sapiens (human)
DOID:0090130
  • cortical dysplasia-focal epilepsy syndrome
  • Aliases:
    • CDFE syndrome
    • CDFES
    • PTHSL1
    • Pitt-Hopkins-like syndrome-1
Homo sapiens (human)
DOID:14447
  • gonadal dysgenesis
  • Aliases:
    • Gonadal dysgenesis syndrome
Homo sapiens (human)
DOID:3491
  • Turner syndrome
  • Aliases:
    • Bonnevie-Ullrich syndrome
    • Gonadal dysgenesis - Turner
    • Karyotype 45, X
    • Monosomy X
    • XO syndrome
    • monosomy X syndrome
Homo sapiens (human)
DOID:0111239
  • congenital muscular dystrophy-dystroglycanopathy type A10
  • Aliases:
    • MDDGA10
    • Walker-Warburg syndrome or muscle-eye-brain disease, TMEM5-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A10
Homo sapiens (human)
DOID:8469
  • influenza
  • Aliases:
    • Influenza with other manifestations
    • flu
    • influenza with non-respiratory manifestation
Homo sapiens (human)
DOID:13564
  • aspergillosis
  • Aliases:
    • Infection due to Aspergillus
Homo sapiens (human)
DOID:0060000
  • infective endocarditis
Homo sapiens (human)
DOID:4483
  • rhinitis
Homo sapiens (human)
DOID:5679
  • retinal disease
Homo sapiens (human)
DOID:9352
  • type 2 diabetes mellitus
  • Aliases:
    • NIDDM
    • insulin resistance
    • non-insulin-dependent diabetes mellitus
    • type 2 diabetes
    • type II diabetes mellitus
Mus musculus (house mouse)
DOID:9970
  • obesity
Mus musculus (house mouse)
DOID:9351
  • diabetes mellitus
  • Aliases:
    • diabetes
Mus musculus (house mouse)
DOID:11714
  • gestational diabetes
  • Aliases:
    • GDM
    • Gestational diabetes mellitus
    • Maternal gestational diabetes mellitus
Mus musculus (house mouse)
DOID:3393
  • coronary artery disease
  • Aliases:
    • CHD
    • Coronary disease
    • coronary arteriosclerosis
    • coronary heart disease
Mus musculus (house mouse)
DOID:9452
  • steatotic liver disease
  • Aliases:
    • Fatty change of liver
    • SLD
    • Steatosis of liver
    • alcoholic fatty liver
    • fatty liver disease
    • hepatic lipidosis
    • hepatic steatosis
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: August 19, 2024