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 6626 - 6650 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:0080555
  • congenital disorder of glycosylation Ic
  • Aliases:
    • congenital disorder of glycosylation 1c
Homo sapiens (human)
DOID:1510
  • personality disorder
  • Aliases:
    • character disorder
Homo sapiens (human)
DOID:0050809
  • mucopolysaccharidosis IX
Homo sapiens (human)
DOID:0060412
  • chromosome 1q41-q42 deletion syndrome
  • Aliases:
    • 1q41-q42 microdeletion syndrome
    • 1q41q42 microdeletion syndrome
Homo sapiens (human)
DOID:0050888
  • syndromic intellectual disability
Homo sapiens (human)
DOID:0070161
  • hereditary sensory and autonomic neuropathy type 2
  • Aliases:
    • HSAN2
    • hereditary sensory and autonomic neuropathy type II
Homo sapiens (human)
DOID:9487
  • Meckel's diverticulum
  • Aliases:
    • Meckel Diverticulum
    • Persistent vitelline duct
Homo sapiens (human)
DOID:0110474
  • autosomal recessive nonsyndromic deafness 18B
  • Aliases:
    • DFNB18B
    • autosomal recessive deafness 18B
Homo sapiens (human)
DOID:6496
  • obsolete extraskeletal myxoid chondrosarcoma
Homo sapiens (human)
DOID:178
  • vascular disease
  • Aliases:
    • vascular tissue disease
Homo sapiens (human)
DOID:1441
  • autosomal dominant cerebellar ataxia
  • Aliases:
    • spinocerebellar ataxia
Homo sapiens (human)
DOID:2723
  • dermatitis
  • Aliases:
    • eczema
    • skin inflammation
Homo sapiens (human)
DOID:0080721
  • calvarial doughnut lesions with bone fragility
Homo sapiens (human)
DOID:5884
  • benign intermediate mesothelioma
  • Aliases:
    • Well-differentiated Papillary tumor of Mesothelium
Homo sapiens (human)
DOID:4959
  • epidermolysis bullosa dystrophica
  • Aliases:
    • Dystrophic epidermolysis bullosa
Homo sapiens (human)
DOID:4896
  • bile duct adenocarcinoma
Homo sapiens (human)
DOID:3852
  • Peutz-Jeghers syndrome
  • Aliases:
    • Colonic hamartomatous polyp
    • Peutz Jeghers colon polyp
    • Peutz Jeghers polyp
    • Peutz-Jeghers polyp of small Intestine
    • gastric Peutz-Jeghers polyp
    • peutz-jeghers small bowel hamartoma
Homo sapiens (human)
DOID:8689
  • anorexia nervosa
Homo sapiens (human)
DOID:8622
  • measles
  • Aliases:
    • morbilli
Homo sapiens (human)
DOID:0110861
  • autosomal recessive polycystic kidney disease
  • Aliases:
    • Arpkd
    • Pkhd1
    • Polycystic Kidney Disease, Infantile, Type I
    • Polycystic Kidney and Hepatic Disease 1
Homo sapiens (human)
DOID:0060856
  • right atrial isomerism
  • Aliases:
    • Ivemark syndrome
    • asplenia with cardiovascular anomalies
Homo sapiens (human)
DOID:11155
  • hypohidrosis
  • Aliases:
    • Oligohidrosis
Homo sapiens (human)
DOID:4232
  • extraosseous Ewing sarcoma
  • Aliases:
    • extraosseous Ewing's sarcoma
    • extraosseous Ewing's sarcoma/peripheral primitive neuroectodermal tumor
    • extraskeletal Ewing sarcom
Homo sapiens (human)
DOID:767
  • muscular atrophy
  • Aliases:
    • Amyotrophia
    • Muscle wasting
    • Wasting - muscle
Homo sapiens (human)
DOID:3068
  • glioblastoma
  • Aliases:
    • GBM
    • adult glioblastoma multiforme
    • glioblastoma multiforme
    • grade IV adult Astrocytic tumor
    • primary glioblastoma multiforme
    • spongioblastoma multiforme
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