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 3251 - 3275 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:0050879
  • fragile X-associated tremor/ataxia syndrome
  • Aliases:
    • FXTAS syndrome
Homo sapiens (human)
DOID:2450
  • central retinal vein occlusion
Homo sapiens (human)
DOID:6084
  • childhood ovarian germ cell tumor
  • Aliases:
    • paediatric Ovarian germ cell neoplasm
    • paediatric ovarian germ cell tumour
    • pediatric Ovarian germ cell neoplasm
    • pediatric ovarian germ cell tumor
Homo sapiens (human)
DOID:0080525
  • differentiated thyroid gland carcinoma
Homo sapiens (human)
DOID:0060580
  • Noonan syndrome 2
  • Aliases:
    • NS2
Homo sapiens (human)
DOID:0050909
  • extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue
  • Aliases:
    • MALT lymphoma
    • MALT lymphoma of the dura
    • mucosa-associated lymphoid tissue lymphoma
Homo sapiens (human)
DOID:10328
  • siderosis
  • Aliases:
    • pulmonary siderosis
Homo sapiens (human)
DOID:2722
  • acrodermatitis
Homo sapiens (human)
DOID:0111633
  • congenital sucrase-isomaltase deficiency
  • Aliases:
    • CSID
    • SI deficiency
    • congenital sucrase-isomaltose malabsorption
    • congenital sucrose intolerance
    • disaccharide intolerance
Homo sapiens (human)
DOID:0110479
  • autosomal recessive nonsyndromic deafness 21
  • Aliases:
    • DFNB21
    • autosomal recessive deafness 21
Homo sapiens (human)
DOID:0080369
  • ovarian sex-cord stromal tumor
Homo sapiens (human)
DOID:5660
  • lymphoepithelioma-like carcinoma
  • Aliases:
    • Nasopharyngeal type Undifferentiated carcinoma
    • lymphoepithelial carcinoma
Homo sapiens (human)
DOID:0110448
  • dilated cardiomyopathy 1HH
  • Aliases:
    • CMD1HH
Homo sapiens (human)
DOID:11486
  • Horner's syndrome
  • Aliases:
    • Bernard Horner syndrome
    • Horner syndrome
    • cervical sympathetic paralysis
Homo sapiens (human)
DOID:1686
  • glaucoma
Homo sapiens (human)
DOID:0050861
  • colorectal adenocarcinoma
Homo sapiens (human)
DOID:0110444
  • dilated cardiomyopathy 1X
  • Aliases:
    • CMD1X
    • dilated cardiomyopathy with mild or no proximal muscle weakness
Homo sapiens (human)
DOID:0070124
  • congenital nongoitrous hypothyroidism 2
  • Aliases:
    • CHNG2
    • congenital hypothyroidism due to thyroid dysgenesis or hypoplasia
Homo sapiens (human)
DOID:0080070
  • mucolipidosis II alpha/beta
  • Aliases:
    • I-cell disease
    • inclusion-cell disease
    • mucolipidosis II
Homo sapiens (human)
DOID:0080502
  • GM1 gangliosidosis type 1
Homo sapiens (human)
DOID:0050545
  • visceral heterotaxy
  • Aliases:
    • heterotaxia
    • situs ambiguus
Homo sapiens (human)
DOID:0111261
  • fumarase deficiency
  • Aliases:
    • FMRD
    • fumaric aciduria
Homo sapiens (human)
DOID:0050757
  • deafness-dystonia-optic neuronopathy syndrome
  • Aliases:
    • Deafness Dystonia Optic Atrophy Syndrome
    • Deafness Dystonia Optic Neuronopathy Syndrome
    • Dystonia Deafness Syndrome
    • Jensen syndrome
    • Mohr-Tranebjaerg syndrome
    • deafness dystonia syndrome
Homo sapiens (human)
DOID:0060745
  • Doyne honeycomb retinal dystrophy
  • Aliases:
    • DHRD
    • Doyne honeycomb degeneration of retina
Homo sapiens (human)
DOID:0110592
  • autosomal dominant nonsyndromic deafness 70
  • Aliases:
    • DFNA70
    • autosomal dominant deafness 70
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