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 6076 - 6100 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:1094
  • attention deficit hyperactivity disorder
  • Aliases:
    • ADHD
    • attention deficit disorder
    • hyperkinetic disorder
Mus musculus (house mouse)
DOID:0050700
  • cardiomyopathy
  • Aliases:
    • Cardiomyopathies
Mus musculus (house mouse)
DOID:1508
  • candidiasis
  • Aliases:
    • Disseminated candidiasis
    • systemic candidiasis
Mus musculus (house mouse)
DOID:1749
  • squamous cell carcinoma
  • Aliases:
    • epidermoid carcinoma
    • malignant squamous cell tumor
    • squamous carcinoma
    • squamous cell Epithelioma
    • squamous cell cancer
Mus musculus (house mouse)
DOID:9282
  • ocular hypertension
Mus musculus (house mouse)
DOID:594
  • panic disorder
  • Aliases:
    • panic anxiety syndrome
Mus musculus (house mouse)
DOID:0111453
  • 2-aminoadipic 2-oxoadipic aciduria
  • Aliases:
    • AMOXAD
    • alpha-aminoadipic aciduria
Mus musculus (house mouse)
DOID:1074
  • kidney failure
  • Aliases:
    • renal failure
Mus musculus (house mouse)
DOID:12053
  • cryptococcosis
  • Aliases:
    • Busse-Buschke's disease
    • European cryptococcosis
    • cryptococcal infection
    • torula
    • torulosis
Mus musculus (house mouse)
DOID:7147
  • ankylosing spondylitis
  • Aliases:
    • Bekhterev syndrome
    • Bekhterev's disease
    • Marie-Strumpell disease
Mus musculus (house mouse)
DOID:0111230
  • congenital muscular dystrophy-dystroglycanopathy type A11
  • Aliases:
    • MDDGA11
    • Walker-Warburg syndrome or muscle-eye-brain disease B3GALNT2-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A11
Mus musculus (house mouse)
DOID:0080217
  • lysosomal acid lipase deficiency
  • Aliases:
    • LAL deficiency
    • LAL-D
Mus musculus (house mouse)
DOID:0110474
  • autosomal recessive nonsyndromic deafness 18B
  • Aliases:
    • DFNB18B
    • autosomal recessive deafness 18B
Mus musculus (house mouse)
DOID:12401
  • intermittent explosive disorder
  • Aliases:
    • explosive personality disorder
Mus musculus (house mouse)
DOID:3659
  • sialuria
Mus musculus (house mouse)
DOID:0111630
  • familial erythrocytosis 8
  • Aliases:
    • BPGM deficiency
    • DPGM deficiency
    • ECYT8
    • bisphosphoglycerate mutase deficiency
    • bisphosphoglyceromutase deficiency
    • diphosphoglycerate mutase deficiency of erythrocyte
    • hemolytic anemia due to diphosphoglycerate mutase deficiency
Mus musculus (house mouse)
DOID:0060887
  • ossification of the posterior longitudinal ligament of spine
  • Aliases:
    • OPLL
Mus musculus (house mouse)
DOID:3892
  • insulinoma
  • Aliases:
    • Insulin-Producing tumor of Islet cells
    • Islet cell adenoma
Mus musculus (house mouse)
DOID:1577
  • limited scleroderma
  • Aliases:
    • Limited cutaneous systemic sclerosis
    • systemic sclerosis, limited
Mus musculus (house mouse)
DOID:0080899
  • lung pleomorphic carcinoma
Mus musculus (house mouse)
DOID:0112198
  • spondyloepimetaphyseal dysplasia with joint laxity type 1
  • Aliases:
    • SEMDJL1
    • spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures
Mus musculus (house mouse)
DOID:11758
  • iron deficiency anemia
Mus musculus (house mouse)
DOID:1520
  • colon carcinoma
  • Aliases:
    • Colonic carcinoma
    • carcinoma of colon
Mus musculus (house mouse)
DOID:12732
  • intermediate uveitis
  • Aliases:
    • chronic cyclitis
    • peripheral uveoretinitis
Mus musculus (house mouse)
DOID:28
  • endocrine system disease
Mus musculus (house mouse)

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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