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 851 - 875 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:0090041
  • torsion dystonia 4
Homo sapiens (human)
DOID:0060798
  • hypomyelinating leukodystrophy 6
  • Aliases:
    • H-ABC
    • HABC
    • HLD6
    • hypomyelinating leukodystrophy with atrophy of the basal ganglia and cerebellum
    • hypomyelination with atrophy of basal ganglia and cerebellum
Homo sapiens (human)
DOID:0112240
  • Leber congenital amaurosis with early-onset deafness
  • Aliases:
    • LCAEOD
Homo sapiens (human)
DOID:5679
  • retinal disease
Homo sapiens (human)
DOID:14447
  • gonadal dysgenesis
  • Aliases:
    • Gonadal dysgenesis syndrome
Homo sapiens (human)
DOID:2476
  • hereditary spastic paraplegia
  • Aliases:
    • French settlement disease
    • Strumpell-Lorrain disease
    • familial spastic paraplegia
    • hereditary spastic paraparesis
Mus musculus (house mouse)
DOID:0112202
  • developmental and epileptic encephalopathy
Mus musculus (house mouse)
DOID:854
  • collagen disease
  • Aliases:
    • collagen disorder
Mus musculus (house mouse)
DOID:11252
  • microcytic anemia
Mus musculus (house mouse)
DOID:0111223
  • centronuclear myopathy 1
  • Aliases:
    • CNM1
Mus musculus (house mouse)
DOID:0110197
  • Charcot-Marie-Tooth disease dominant intermediate B
  • Aliases:
    • CMTDI1
    • CMTDIB
    • Charcot-Marie-Tooth neuropathy dominant intermediate B
    • DI-CMTB
Mus musculus (house mouse)
DOID:0070205
  • familial partial lipodystrophy type 4
  • Aliases:
    • FPLD4
    • PLIN1-related FPLD
    • PLIN1-related familial partial lipodystrophy
    • familial partial lipodystrophy associated with PLIN1 mutations
Mus musculus (house mouse)
DOID:0110186
  • Charcot-Marie-Tooth disease type 4D
  • Aliases:
    • CMT4D
    • Charcot-Marie-Tooth neuropathy type 4D
    • HMSN Lom type
    • HMSN-Lom
    • HMSN4D
    • HMSNL
    • autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4D
    • hereditary motor and sensory neuropathy LOM type
Homo sapiens (human)
DOID:0080326
  • familial hypertrophic cardiomyopathy
Homo sapiens (human)
DOID:0060610
  • megacystis-microcolon-intestinal hypoperistalsis syndrome
  • Aliases:
    • Berdon syndrome
    • Megacystis microcolon intestinal hypoperistalsis syndrome
    • megacystis-microcolon-intestinal hypoperistalsis syndrome, MMIH
    • visceral myopathy
Homo sapiens (human)
DOID:10763
  • hypertension
  • Aliases:
    • HTN
    • hyperpiesia
    • vascular hypertensive disorder
Mus musculus (house mouse)
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:3393
  • coronary artery disease
  • Aliases:
    • CHD
    • Coronary disease
    • coronary arteriosclerosis
    • coronary heart disease
Mus musculus (house mouse)
DOID:9351
  • diabetes mellitus
  • Aliases:
    • diabetes
Mus musculus (house mouse)
DOID:2018
  • hyperinsulinism
  • Aliases:
    • hyperinsulinemia
Mus musculus (house mouse)
DOID:11714
  • gestational diabetes
  • Aliases:
    • GDM
    • Gestational diabetes mellitus
    • Maternal gestational diabetes mellitus
Mus musculus (house mouse)
DOID:4195
  • hyperglycemia
Mus musculus (house mouse)
DOID:9993
  • hypoglycemia
  • Aliases:
    • Hypoglycaemia
Mus musculus (house mouse)
DOID:4194
  • glucose metabolism disease
  • Aliases:
    • disorder of glucose metabolism
Mus musculus (house mouse)
DOID:0060639
  • permanent neonatal diabetes mellitus
  • Aliases:
    • PDMI
    • PNDM
    • permanent diabetes mellitus of infancy
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: December 9, 2024