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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 6651 - 6675 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0080325
  • tuberous sclerosis 2
Homo sapiens (human)
DOID:0050852
  • limb ischemia
Mus musculus (house mouse)
DOID:5176
  • renal Wilms' tumor
  • Aliases:
    • Nonanaplastic renal Wilm's tumor
    • Nonanaplastic renal Wilm's tumour
    • renal Wilms' tumour
Mus musculus (house mouse)
DOID:9206
  • Barrett's esophagus
  • Aliases:
    • Barrett esophagus
    • Barrett's esophagus with esophagitis
    • Barrett's oesophagus
    • Barrett's ulcer of esophagus
    • Barretts syndrome
    • ulcerative esophagitis
Danio rerio (zebrafish)
DOID:0081149
  • common variable immunodeficiency 6
Mus musculus (house mouse)
DOID:4051
  • alveolar rhabdomyosarcoma
  • Aliases:
    • alveolar childhood rhabdomyosarcoma
Homo sapiens (human)
DOID:418
  • systemic scleroderma
  • Aliases:
    • Scleroderma
    • Scleroderma syndrome
    • progressive systemic sclerosis
    • systemic sclerosis
Danio rerio (zebrafish)
DOID:0050430
  • multiple endocrine neoplasia type 2A
  • Aliases:
    • MEN2A
    • Sipple syndrome
    • multiple endocrine neoplasia II
Homo sapiens (human)
DOID:0080346
  • blepharocheilodontic syndrome 2
Homo sapiens (human)
DOID:0060825
  • Christianson syndrome
  • Aliases:
    • MRXSCH
    • X-linked Angelman-like syndrome
    • X-linked intellectual disability, South African type
    • X-linked intellectual disability-craniofacial dysmorphism-epilepsy-ophthalmoplegia-cerebellar atrophy syndrome
    • mental retardation, X-linked syndromic, Christianson type
    • mental retardation, microcephaly, epilepsy, and ataxia syndrome
Homo sapiens (human)
DOID:3829
  • pituitary adenoma
  • Aliases:
    • adenoma of the Pituitary gland
Caenorhabditis elegans
DOID:0070279
  • primary autosomal recessive microcephaly 14
  • Aliases:
    • MCPH14
Mus musculus (house mouse)
DOID:12120
  • pulmonary alveolar proteinosis
Rattus norvegicus (Norway rat)
DOID:0080586
  • Van Maldergem syndrome 2
Drosophila melanogaster (fruit fly)
DOID:3125
  • multiple endocrine neoplasia
  • Aliases:
    • Multiple endocrine adenomatosis
    • Multiple endocrine neoplasia syndrome
Homo sapiens (human)
DOID:0080097
  • myofibrillar myopathy 6
Mus musculus (house mouse)
DOID:4423
  • sea-blue histiocytosis
  • Aliases:
    • Sea-blue histiocyte syndrome
Homo sapiens (human)
DOID:0110525
  • autosomal recessive nonsyndromic deafness 77
  • Aliases:
    • DFNB77
    • autosomal recessive deafness 77
Homo sapiens (human)
DOID:0080739
  • Ehlers-Danlos syndrome spondylodysplastic type 3
Saccharomyces cerevisiae S288C
DOID:7475
  • diverticulitis
Rattus norvegicus (Norway rat)
DOID:12800
  • mucopolysaccharidosis VI
  • Aliases:
    • MPS VI - Maroteaux-Lamy syndrome
    • Maroteaux - Lamy syndrome
    • Maroteaux-Lamy syndrome
    • arylsulfatase B deficiency
    • deficiency of N-acetylgalactosamine-4-sulfatase
Rattus norvegicus (Norway rat)
DOID:8805
  • intermediate coronary syndrome
  • Aliases:
    • Angina at rest
    • Anginal chest pain at rest
    • Impending infarction
    • Preinfarction angina
    • Unstable angina
    • Worsening angina
Caenorhabditis elegans
DOID:7305
  • astroblastoma
Rattus norvegicus (Norway rat)
DOID:12798
  • mucopolysaccharidosis
Rattus norvegicus (Norway rat)
DOID:0070351
  • spinal muscular atrophy with lower extremity predominant 1
  • Aliases:
    • spinal muscular atrophy with lower extremity predominance 1
Rattus norvegicus (Norway rat)
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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