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 2876 - 2900 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:0110455
  • dilated cardiomyopathy 1U
  • Aliases:
    • CMD1U
Homo sapiens (human)
DOID:0110312
  • hypertrophic cardiomyopathy 6
  • Aliases:
    • CMH6
    • cardiomyopathy, familial hypertrophic 6
Homo sapiens (human)
DOID:8986
  • narcolepsy
  • Aliases:
    • Narcolepsy, without cataplexy
    • paroxysmal sleep
Homo sapiens (human)
DOID:230
  • lateral sclerosis
  • Aliases:
    • adult-onset primary lateral sclerosis
    • primary lateral sclerosis
Homo sapiens (human)
DOID:9395
  • croup
  • Aliases:
    • Croup syndrome
    • Laryngotracheobronchitis
    • acute Obstructive Laryngitis
    • acute laryngotracheobronchitis
Homo sapiens (human)
DOID:0110916
  • hereditary spherocytosis type 1
  • Aliases:
    • HS1
    • SPH1
    • hereditary spherocytosis 1
Homo sapiens (human)
DOID:0080141
  • mosaic variegated aneuploidy syndrome 1
Homo sapiens (human)
DOID:11201
  • parathyroid gland disease
  • Aliases:
    • disease of parathyroid glands
Homo sapiens (human)
DOID:0110128
  • Bardet-Biedl syndrome 6
  • Aliases:
    • BBS6
Homo sapiens (human)
DOID:8503
  • impetigo herpetiformis
Homo sapiens (human)
DOID:9256
  • colorectal cancer
Homo sapiens (human)
DOID:0090104
  • Huntington's disease-like 2
  • Aliases:
    • HDL2
    • Huntington disease-like 2
Homo sapiens (human)
DOID:3687
  • MELAS syndrome
  • Aliases:
    • MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES
Homo sapiens (human)
DOID:0110815
  • hereditary spastic paraplegia 64
  • Aliases:
    • SPG64
    • autosomal recessive spastic paraplegia 64
    • autosomal recessive spastic paraplegia type 64
Homo sapiens (human)
DOID:10481
  • diaphragm disease
Homo sapiens (human)
DOID:0050955
  • spinocerebellar ataxia type 2
Homo sapiens (human)
DOID:11212
  • hydrophthalmos
Homo sapiens (human)
DOID:0110471
  • autosomal recessive nonsyndromic deafness 16
  • Aliases:
    • DFNB16
    • autosomal recessive deafness 16
Homo sapiens (human)
DOID:0110521
  • autosomal recessive nonsyndromic deafness 70
  • Aliases:
    • DFNB70
    • autosomal recessive deafness 70
Homo sapiens (human)
DOID:2691
  • myoma
  • Aliases:
    • benign neoplasm of the Muscle
Homo sapiens (human)
DOID:9931
  • Waterhouse-Friderichsen syndrome
  • Aliases:
    • Meningococcal hemorrhagic adrenalitis
Homo sapiens (human)
DOID:11200
  • T cell deficiency
  • Aliases:
    • T cell immunodeficiency
    • T lymphocyte deficiency
    • T lymphocyte immunodeficiency
Homo sapiens (human)
DOID:0060875
  • isolated growth hormone deficiency type III
  • Aliases:
    • Fleisher syndrome
    • IGHD III
    • X-linked IGHD
    • X-linked agammaglobulinemia and isolated growth hormone deficiency
    • X-linked hypogammaglobulinemia and isolated growth hormone deficiency
    • X-linked isolated growth hormone deficiency
    • congenital IGHD type III
    • congenital isolated GH deficiency type III
    • congenital isolated growth hormone deficiency type III
    • growth hormone deficiency with hypogammaglobulinemia
Homo sapiens (human)
DOID:5403
  • microcystic adenoma
Homo sapiens (human)
DOID:403
  • mouth disease
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