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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 9076 - 9100 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0080301
  • atypical hemolytic-uremic syndrome
Caenorhabditis elegans
DOID:206
  • hereditary multiple exostoses
  • Aliases:
    • Multiple congenital exostosis
    • Multiple exostosis syndromes
    • Osteochondromatosis syndrome
    • hereditary multiple exostoses 1
    • hereditary multiple exostoses 2
    • hereditary multiple exostoses 3
    • multiple ostechondromas
Homo sapiens (human)
DOID:14250
  • Down syndrome
  • Aliases:
    • Complete trisomy 21 syndrome
    • Down's syndrome
    • Down's syndrome - trisomy 21
    • Downs syndrome
    • G Trisomy
    • trisomy 21 syndrome
Drosophila melanogaster (fruit fly)
DOID:0050904
  • salivary gland carcinoma
Caenorhabditis elegans
DOID:0111252
  • vestibular schwannomatosis
  • Aliases:
    • ACN
    • BANF
    • NF2
    • NF2-related schwannomatosis
    • SWN3
    • SWNV
    • acoustic neurofibromatosis
    • bilateral acoustic neurinoma
    • bilateral acoustic neurofibromatosis
    • bilateral acoustic schwannomas
    • central neurofibromatosis
    • familial acoustic neuromas
    • neurofibromatosis 2
    • neurofibromatosis type II
    • schwannomatosis 3
Mus musculus (house mouse)
DOID:0111007
  • X-linked cone-rod dystrophy 3
  • Aliases:
    • CORDX3
Rattus norvegicus (Norway rat)
DOID:9471
  • meningitis
Rattus norvegicus (Norway rat)
DOID:319
  • spinal cord disease
Homo sapiens (human)
DOID:0081319
  • multiple synostoses syndrome 3
Xenopus laevis (African clawed frog)
DOID:0080070
  • mucolipidosis II alpha/beta
  • Aliases:
    • I-cell disease
    • inclusion-cell disease
    • mucolipidosis II
Danio rerio (zebrafish)
DOID:0060780
  • congenital diarrhea 6
  • Aliases:
    • chronic diarrhea due to guanylate cyclase 2C overactivity
    • chronic diarrhoea due to guanylate cyclase 2C overactivity
    • congenital diarrhoea 6
Rattus norvegicus (Norway rat)
DOID:0040094
  • autoimmune glomerulonephritis
Mus musculus (house mouse)
DOID:0110959
  • Gaucher's disease type III
  • Aliases:
    • GD III
    • Gaucher Disease, Chronic Neuronopathic Type
    • Gaucher Disease, Juvenile And Adult, Cerebral
    • Gaucher Disease, Subacute Neuronopathic Type
Mus musculus (house mouse)
DOID:0090016
  • chromosome 5q deletion syndrome
  • Aliases:
    • 5q- syndrome, refractory macrocytic anemia due to 5q deletion
    • myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
Homo sapiens (human)
DOID:0050580
  • hereditary lymphedema
Rattus norvegicus (Norway rat)
DOID:3393
  • coronary artery disease
  • Aliases:
    • CHD
    • Coronary disease
    • coronary arteriosclerosis
    • coronary heart disease
Drosophila melanogaster (fruit fly)
DOID:0050770
  • polycystic liver disease
  • Aliases:
    • congenital cystic liver disease
    • congenital hepatic cyst
    • fibrocystic liver disease
Homo sapiens (human)
DOID:0111773
  • 46,XY sex reversal 8
  • Aliases:
    • SRXY8
    • TDD
    • male pseudohermaphroditism due to deficiency of testicular 17,20-desmolase
Homo sapiens (human)
DOID:6255
  • growth hormone secreting pituitary adenoma
  • Aliases:
    • Growth Hormone Producing adenoma of the Pituitary
    • Somatotroph adenoma
    • growth hormone secreting adenoma of pituitary
Homo sapiens (human)
DOID:0081317
  • multiple synostoses syndrome 1
Xenopus laevis (African clawed frog)
DOID:0090127
  • camptodactyly-arthropathy-coxa vara-pericarditis syndrome
  • Aliases:
    • CACP
    • CACP syndrome
    • CAP syndrome
    • Jacobs syndrome
    • PAC syndrome
    • arthropathy-camptodactyly syndrome
    • camptodactyly-arthropathy-pericarditis syndrome
    • congenital familial hypertrophic synovitis
    • familial fibrosing serositis
    • pericarditis-arthropathy-camptodactyly syndrome
Homo sapiens (human)
DOID:0060180
  • colitis
Caenorhabditis elegans
DOID:12803
  • Sly syndrome
  • Aliases:
    • MPS VII - Sly syndrome
    • beta-glucuronidase deficiency
    • deficiency of beta-glucuronidase
    • mucopolysaccharidosis VII
Caenorhabditis elegans
DOID:0110298
  • autosomal recessive limb-girdle muscular dystrophy type 2N
  • Aliases:
    • LGMD2N
    • muscular dystrophy-dystroglycanopathy (limb-girdle) type C 2
    • muscular dystrophy-dystroglycanopathy limb-girdle POMT2-related
Mus musculus (house mouse)
DOID:14731
  • Weaver syndrome
  • Aliases:
    • WEAVER-LIKE SYNDROME
    • Weaver-Williams syndrome
Homo sapiens (human)
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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