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 1201 - 1225 of 4621 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism
DOID:0111232
  • congenital muscular dystrophy-dystroglycanopathy type A9
  • Aliases:
    • MDDGA9
    • Walker-Warburg syndrome or muscle-eye-brain disease DAG1-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A9
Homo sapiens (human)
DOID:9537
  • Lassa fever
Homo sapiens (human)
DOID:767
  • muscular atrophy
  • Aliases:
    • Amyotrophia
    • Muscle wasting
    • Wasting - muscle
Homo sapiens (human)
DOID:0112374
  • muscular dystrophy-dystroglycanopathy
  • Aliases:
    • MDDG
Homo sapiens (human)
DOID:0050629
  • Aicardi-Goutieres syndrome
  • Aliases:
    • AGS
    • Cree encephalitis
Homo sapiens (human)
DOID:0111070
  • congenital bile acid synthesis defect 3
  • Aliases:
    • CBAS3
    • oxysterol 7-alpha-hydroxylase deficiency
Homo sapiens (human)
DOID:0050242
  • primary amebic meningoencephalitis
  • Aliases:
    • Naegleria fowleri infection
Homo sapiens (human)
DOID:0080159
  • Cryptococcal meningitis
Homo sapiens (human)
DOID:2789
  • parasitic protozoa infectious disease
  • Aliases:
    • mastigophora infectious disease
    • sarcomastigophora infectious disease
Homo sapiens (human)
DOID:0111459
  • classic galactosemia
  • Aliases:
    • GALT deficiency
    • galactose-1-phosphate uridyltransferase deficiency
    • galactosemia type 1
Homo sapiens (human)
DOID:11367
  • congenital aphakia
  • Aliases:
    • APHAKIA, CONGENITAL PRIMARY
    • Congenital absence of lens
Homo sapiens (human)
DOID:13767
  • clonorchiasis
  • Aliases:
    • Oriental liver fluke disease
Homo sapiens (human)
DOID:0110078
  • Leber congenital amaurosis 1
  • Aliases:
    • LCA1
    • amaurosis congenita of Leber I
Homo sapiens (human)
DOID:0080887
  • vitamin D-dependent rickets type 1B
Homo sapiens (human)
DOID:0070172
  • spermatogenic failure 15
  • Aliases:
    • SPGF15
Homo sapiens (human)
DOID:0050868
  • hepatocellular adenoma
Homo sapiens (human)
DOID:2044
  • drug-induced hepatitis
  • Aliases:
    • Drug-induced chronic hepatitis
Homo sapiens (human)
DOID:0060479
  • Shwachman-Diamond syndrome
  • Aliases:
    • Shwachman syndrome
    • Shwachman-Bodian-Diamond syndrome
    • Shwachman-Diamond type metaphyseal dysplasia
    • pancreatic insufficiency and bone marrow dysfunction
Homo sapiens (human)
DOID:0080665
  • warfarin resistance
Homo sapiens (human)
DOID:11249
  • vitamin K deficiency bleeding
  • Aliases:
    • deficiency of vitamin K
    • vitamin K deficiency
    • vitamin K deficiency hemorrhagic disease
Homo sapiens (human)
DOID:10481
  • diaphragm disease
Homo sapiens (human)
DOID:4661
  • multiple chemical sensitivity
  • Aliases:
    • 20th century disease
    • chemical AIDS
    • environmental illness
    • idiopathic environmental illness
    • total allergy syndrome
Homo sapiens (human)
DOID:0050073
  • invasive aspergillosis
Homo sapiens (human)
DOID:2275
  • pharyngitis
  • Aliases:
    • Inflamed throat
    • Persistent sore throat
    • Pharyngeal disorder
    • Pharyngitis - acute
    • Sore throat - chronic
    • acute pharyngitis
    • acute sore throat
    • chronic pharyn/nasopharyngitis
    • chronic pharyngitis
    • chronic pharyngitis and nasopharyngitis
    • chronic sore throat
Homo sapiens (human)
DOID:3133
  • acute porphyria
  • Aliases:
    • hepatic porphyria
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: August 19, 2024