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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 9201 - 9225 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism Source
DOID:0080909
  • castration-resistant prostate carcinoma
Mus musculus (house mouse)
DOID:0080836
  • growth hormone insensitivity syndrome with immune dysregulation 1
Mus musculus (house mouse)
DOID:3261
  • hyper IgE recurrent infection syndrome 1
  • Aliases:
    • Job syndrome
    • Job's syndrome
    • hyperimmunoglobulin E syndrome
Mus musculus (house mouse)
DOID:9997
  • peripartum cardiomyopathy
  • Aliases:
    • antepartum peripartum cardiomyopathy
    • postpartum peripartum cardiomyopathy
Mus musculus (house mouse)
DOID:9953
  • acute biphenotypic leukemia
  • Aliases:
    • mixed phenotype acute leukemia
Mus musculus (house mouse)
DOID:0110289
  • autosomal recessive limb-girdle muscular dystrophy type 2Y
  • Aliases:
    • LGMD2Y
    • autosomal recessive muscular dystrophy due to LAP1B deficiency
    • autosomal recessive muscular dystrophy due to Torsin-1A-interacting protein 1 deficiency
    • muscular dystrophy with progressive weakness, distal contractures and rigid spine
    • muscular dystrophy, limb-girdle, type 2Y
Mus musculus (house mouse)
DOID:0080563
  • congenital disorder of glycosylation Ik
  • Aliases:
    • congenital disorder of glycosylation 1k
Mus musculus (house mouse)
DOID:3125
  • multiple endocrine neoplasia
  • Aliases:
    • Multiple endocrine adenomatosis
    • Multiple endocrine neoplasia syndrome
Mus musculus (house mouse)
DOID:0111693
  • familial adult myoclonic epilepsy 4
  • Aliases:
    • FAME4
    • FCMTE4
    • familial cortical myoclonic tremor and epilepsy 4
Mus musculus (house mouse)
DOID:8557
  • oropharynx cancer
  • Aliases:
    • Oropharyngeal carcinoma
    • malignant Oropharyngeal tumor
    • malignant tumor of oropharynx
    • malignant tumour of mesopharynx
    • oropharyngeal cancer
Homo sapiens (human)
DOID:0070417
  • neurodevelopmental disorder with speech impairment and dysmorphic facies
  • Aliases:
    • NEDSID
Mus musculus (house mouse)
DOID:0112263
  • hypoinsulinemic hypoglycemia with hemihypertrophy
  • Aliases:
    • HIHGHH
    • hypoinsulinemic hypoglycemia and body hemihypertrophy
Homo sapiens (human)
DOID:0080567
  • congenital disorder of glycosylation Ip
  • Aliases:
    • congenital disorder of glycosylation 1p
Mus musculus (house mouse)
DOID:0060966
  • dystonia 22, juvenile-onset
Mus musculus (house mouse)
DOID:0060967
  • dystonia 22, adult-onset
Mus musculus (house mouse)
DOID:218
  • ascending colon cancer
  • Aliases:
    • Ca ascending colon
    • malignant neoplasm of right colon
    • malignant tumor of ascending colon
Mus musculus (house mouse)
DOID:0050869
  • villous adenoma
Mus musculus (house mouse)
DOID:0070162
  • hereditary sensory and autonomic neuropathy type 1
  • Aliases:
    • HSAN1
    • hereditary sensory and autonomic neuropathy type I
Mus musculus (house mouse)
DOID:0070157
  • hereditary sensory and autonomic neuropathy type 1C
  • Aliases:
    • HSAN1C
    • hereditary sensory and autonomic neuropathy type IC
Mus musculus (house mouse)
DOID:0111675
  • neurooculocardiogenitourinary syndrome
  • Aliases:
    • NOCGUS
Mus musculus (house mouse)
DOID:640
  • encephalomyelitis
  • Aliases:
    • Encephalitis &/or myelitis
Mus musculus (house mouse)
DOID:0050882
  • spinocerebellar ataxia type 5
Mus musculus (house mouse)
DOID:0080908
  • Cockayne syndrome B
  • Aliases:
    • Cockayne syndrome 2
    • Cockayne syndrome type II
Homo sapiens (human)
DOID:0080868
  • primary ovarian insufficiency 11
Homo sapiens (human)
DOID:0080911
  • cerebrooculofacioskeletal syndrome 1
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: December 9, 2024