GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources July 29, 2024
DisGeNET July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 226 - 250 of 4621 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism
DOID:0050854
  • Muckle-Wells syndrome
  • Aliases:
    • MWS
    • neutrophilic urticaria
Homo sapiens (human)
DOID:0050855
  • renal fibrosis
Homo sapiens (human)
DOID:0050857
  • Perrault syndrome
Homo sapiens (human)
DOID:0050860
  • colorectal adenoma
Homo sapiens (human)
DOID:0050861
  • colorectal adenocarcinoma
Homo sapiens (human)
DOID:0050864
  • non-arteritic anterior ischemic optic neuropathy
  • Aliases:
    • non-arteritic anterior ischaemic optic neuropathy
    • nonarteritic anterior ischaemic optic neuropathy
    • nonarteritic anterior ischemic optic neuropathy
Homo sapiens (human)
DOID:0050865
  • tongue squamous cell carcinoma
Homo sapiens (human)
DOID:0050866
  • oral squamous cell carcinoma
  • Aliases:
    • mouth squamous cell carcinoma
Homo sapiens (human)
DOID:0050868
  • hepatocellular adenoma
Homo sapiens (human)
DOID:0050873
  • follicular lymphoma
Homo sapiens (human)
DOID:0050876
  • Caroli disease
Homo sapiens (human)
DOID:0050877
  • pancreatic agenesis
  • Aliases:
    • Agenesis of the dorsal pancreas
    • partial pancreatic agenesis
Homo sapiens (human)
DOID:0050879
  • fragile X-associated tremor/ataxia syndrome
  • Aliases:
    • FXTAS syndrome
Homo sapiens (human)
DOID:0050881
  • inclusion body myopathy with Paget disease of bone and frontotemporal dementia
  • Aliases:
    • IBMPFD
    • inclusion body myopathy with Paget's disease of bone and frontotemporal dementia
Homo sapiens (human)
DOID:0050882
  • spinocerebellar ataxia type 5
Homo sapiens (human)
DOID:0050883
  • infantile cerebellar-retinal degeneration
Homo sapiens (human)
DOID:0050884
  • triosephosphate isomerase deficiency
  • Aliases:
    • Triose phosphate-isomerase deficiency
Homo sapiens (human)
DOID:0050885
  • IMAGe syndrome
  • Aliases:
    • intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita, genital abnormalities
Homo sapiens (human)
DOID:0050886
  • Troyer syndrome
  • Aliases:
    • SPG20
    • autosomal recessive spastic paraplegia 20
    • autosomal recessive spastic paraplegia Troyer type
    • autosomal recessive spastic paraplegia type 20
    • childhood-onset spastic paraparesis with distal muscle wasting
    • hereditary spastic paraplegia 20
    • spastic paraplegia 20
    • spastic paraplegia type 20
Homo sapiens (human)
DOID:0050888
  • syndromic intellectual disability
Homo sapiens (human)
DOID:0050889
  • non-syndromic intellectual disability
Homo sapiens (human)
DOID:0050891
  • adrenal cortical adenoma
  • Aliases:
    • adrenocortical adenoma
Homo sapiens (human)
DOID:0050894
  • ameloblastoma
Homo sapiens (human)
DOID:0050902
  • medulloblastoma
  • Aliases:
    • CNS PNET
    • CPNET
    • Medulloblastoma, histologically defined
    • brain medulloblastoma
    • infratentorial primitive neuroectodermal tumor
    • localized primitive neuroectodermal tumor
Homo sapiens (human)
DOID:0050904
  • salivary gland carcinoma
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: August 19, 2024