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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 8826 - 8850 of 15957 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism Source
DOID:0110552
  • autosomal dominant nonsyndromic deafness 22
  • Aliases:
    • DFNA22
    • autosomal dominant deafness 22
Homo sapiens (human)
DOID:0110477
  • autosomal recessive nonsyndromic deafness 2
  • Aliases:
    • DFNB2
    • autosomal recessive deafness 2
Homo sapiens (human)
DOID:0110543
  • autosomal dominant nonsyndromic deafness 11
  • Aliases:
    • DFNA11
    • autosomal dominant deafness 11
Homo sapiens (human)
DOID:0110826
  • Usher syndrome type 1
  • Aliases:
    • US1
    • USH1
Homo sapiens (human)
DOID:14159
  • obstructive hydrocephalus
Homo sapiens (human)
DOID:1068
  • juvenile glaucoma
  • Aliases:
    • Glaucoma of childhood
Homo sapiens (human)
DOID:0110445
  • dilated cardiomyopathy 1KK
  • Aliases:
    • CMD1KK
Homo sapiens (human)
DOID:0110933
  • nemaline myopathy 11
  • Aliases:
    • NEM11
    • nemaline myopathy 11, autosomal recessive
Homo sapiens (human)
DOID:3044
  • food allergy
  • Aliases:
    • food hypersensitivity
Rattus norvegicus (Norway rat)
DOID:0110820
  • hereditary spastic paraplegia 75
  • Aliases:
    • SPG75
    • autosomal recessive spastic paraplegia 75
    • autosomal recessive spastic paraplegia type 75
Mus musculus (house mouse)
DOID:573
  • nerve compression syndrome
  • Aliases:
    • Compression neuropathy
    • entrapment neuropathy
    • peripheral nerve entrapment syndrome
Mus musculus (house mouse)
DOID:0110820
  • hereditary spastic paraplegia 75
  • Aliases:
    • SPG75
    • autosomal recessive spastic paraplegia 75
    • autosomal recessive spastic paraplegia type 75
Rattus norvegicus (Norway rat)
DOID:573
  • nerve compression syndrome
  • Aliases:
    • Compression neuropathy
    • entrapment neuropathy
    • peripheral nerve entrapment syndrome
Rattus norvegicus (Norway rat)
DOID:0080319
  • X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia
  • Aliases:
    • XMEN
Rattus norvegicus (Norway rat)
DOID:0111839
  • congenital disorder of glycosylation Icc
  • Aliases:
    • congenital disorder of glycosylation type Icc
Rattus norvegicus (Norway rat)
DOID:0080319
  • X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia
  • Aliases:
    • XMEN
Mus musculus (house mouse)
DOID:0111839
  • congenital disorder of glycosylation Icc
  • Aliases:
    • congenital disorder of glycosylation type Icc
Mus musculus (house mouse)
DOID:9266
  • cystinuria
Drosophila melanogaster (fruit fly)
DOID:0081097
  • Rafiq syndrome
  • Aliases:
    • MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15
Mus musculus (house mouse)
DOID:0081097
  • Rafiq syndrome
  • Aliases:
    • MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15
Rattus norvegicus (Norway rat)
DOID:1338
  • congenital dyserythropoietic anemia
  • Aliases:
    • congenital dyshaematopoietic anaemia
Rattus norvegicus (Norway rat)
DOID:3413
  • alpha-mannosidosis
  • Aliases:
    • Alpha-D-mannosidosis
    • alpha-mannosidase deficiency
    • deficiency of alpha-mannosidase
Mus musculus (house mouse)
DOID:3633
  • beta-mannosidosis
  • Aliases:
    • Beta-D-mannosidosis
    • beta-mannosidase deficiency
    • lysosomal beta-mannosidase deficiency
Mus musculus (house mouse)
DOID:3633
  • beta-mannosidosis
  • Aliases:
    • Beta-D-mannosidosis
    • beta-mannosidase deficiency
    • lysosomal beta-mannosidase deficiency
Rattus norvegicus (Norway rat)
DOID:0050454
  • periventricular nodular heterotopia
  • Aliases:
    • periventricular heterotopia
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