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 2226 - 2250 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism
DOID:2825
  • nose disease
  • Aliases:
    • disorder of the nose
    • nasal disorder
Homo sapiens (human)
DOID:1184
  • nephrotic syndrome
Mus musculus (house mouse)
DOID:2945
  • severe acute respiratory syndrome
  • Aliases:
    • SARS
    • SARS-CoV infection
Xenopus tropicalis (tropical clawed frog)
DOID:0110446
  • dilated cardiomyopathy 1W
  • Aliases:
    • CMD1W
Homo sapiens (human)
DOID:0060405
  • chromosome 17q23.1-q23.2 deletion syndrome
  • Aliases:
    • 17q23.1-q23.2 microdeletion syndrome
    • 17q23.1q23.2 microdeletion syndrome
Homo sapiens (human)
DOID:3323
  • Sandhoff disease
  • Aliases:
    • Sandhoff Jatzkewitz disease
Rattus norvegicus (Norway rat)
DOID:2051
  • maxillary sinusitis
Homo sapiens (human)
DOID:8466
  • retinal degeneration
  • Aliases:
    • degeneration of retina
Caenorhabditis elegans
DOID:8692
  • myeloid leukemia
  • Aliases:
    • Non-Lymphocytic Leukemia
    • leukaemia myelogenous
    • leukemia myelogenous
    • myeloid granulocytic leukaemia
    • myeloid granulocytic leukemia
    • myeloid leukaemia
Xenopus tropicalis (tropical clawed frog)
DOID:0050427
  • xeroderma pigmentosum
Homo sapiens (human)
DOID:5844
  • myocardial infarction
  • Aliases:
    • Myocardial infarct
    • heart attack
Drosophila melanogaster (fruit fly)
DOID:0110789
  • hereditary spastic paraplegia 38
  • Aliases:
    • SPG38
    • autosomal dominant spastic paraplegia 38
    • autosomal dominant spastic paraplegia type 38
Homo sapiens (human)
DOID:0110187
  • Charcot-Marie-Tooth disease type 4K
  • Aliases:
    • CMT4K
    • SURF1-related CMT4
    • SURF1-related Charcot-Marie-Tooth disease type 4
    • SURF1-related severe demyelinating Charcot-Marie-Tooth disease
    • autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4K
    • autosomal recessive demyelinating Charcot-Marie-Tooth neuropathy type 4K
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:0080108
  • myoglobinuria
Saccharomyces cerevisiae S288C
DOID:11823
  • hepatorenal syndrome
Homo sapiens (human)
DOID:14183
  • alcoholic neuropathy
  • Aliases:
    • Alcohol-related polyneuropathy
    • Alcoholic polyneuropathy
Rattus norvegicus (Norway rat)
DOID:1443
  • cerebral degeneration
  • Aliases:
    • Brain degeneration
Homo sapiens (human)
DOID:9598
  • fasciitis
Homo sapiens (human)
DOID:171
  • neuroectodermal tumor
  • Aliases:
    • primitive Neuroectodermal neoplasm
Homo sapiens (human)
DOID:0081134
  • 3-methylglutaconic aciduria type 7b
Saccharomyces cerevisiae S288C
DOID:11339
  • pneumocystosis
  • Aliases:
    • Pneumocystis carinii pneumonia
    • Pneumocystis jirovecii pneumonia
    • Pneumocystis pneumonia
    • Pneumocystosis pneumonia
    • pulmonary pneumocystosis
Homo sapiens (human)
DOID:0080557
  • congenital disorder of glycosylation Ie
  • Aliases:
    • congenital disorder of glycosylation 1e
Homo sapiens (human)
DOID:0080567
  • congenital disorder of glycosylation Ip
  • Aliases:
    • congenital disorder of glycosylation 1p
Drosophila melanogaster (fruit fly)
DOID:12053
  • cryptococcosis
  • Aliases:
    • Busse-Buschke's disease
    • European cryptococcosis
    • cryptococcal infection
    • torula
    • torulosis
Rattus norvegicus (Norway rat)

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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