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 3201 - 3225 of 7942 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism
DOID:1459
  • hypothyroidism
  • Aliases:
    • Thyroid deficiency
    • Thyroid insufficiency
Caenorhabditis elegans
DOID:1459
  • hypothyroidism
  • Aliases:
    • Thyroid deficiency
    • Thyroid insufficiency
Rattus norvegicus (Norway rat)
DOID:1459
  • hypothyroidism
  • Aliases:
    • Thyroid deficiency
    • Thyroid insufficiency
Xenopus tropicalis (tropical clawed frog)
DOID:1459
  • hypothyroidism
  • Aliases:
    • Thyroid deficiency
    • Thyroid insufficiency
Saccharomyces cerevisiae S288C
DOID:14566
  • disease of cellular proliferation
  • Aliases:
    • cell process disease
    • neoplasm
Rattus norvegicus (Norway rat)
DOID:14566
  • disease of cellular proliferation
  • Aliases:
    • cell process disease
    • neoplasm
Homo sapiens (human)
DOID:14566
  • disease of cellular proliferation
  • Aliases:
    • cell process disease
    • neoplasm
Mus musculus (house mouse)
DOID:14557
  • primary pulmonary hypertension
  • Aliases:
    • Idiopathic pulmonary arterial hypertension
Homo sapiens (human)
DOID:14555
  • Foster-Kennedy syndrome
Homo sapiens (human)
DOID:14550
  • root resorption
Homo sapiens (human)
DOID:14550
  • root resorption
Mus musculus (house mouse)
DOID:14550
  • root resorption
Rattus norvegicus (Norway rat)
DOID:1455
  • geographic tongue
  • Aliases:
    • Glossitis areata exfoliativa
    • Pityriasis linguae
    • benign migratory glossitis
Homo sapiens (human)
DOID:14525
  • Reye syndrome
  • Aliases:
    • Reye's syndrome
Homo sapiens (human)
DOID:14524
  • senile degeneration of brain
  • Aliases:
    • Senile brain degen.
Homo sapiens (human)
DOID:14515
  • WAGR syndrome
  • Aliases:
    • 11p partial monosomy syndrome
    • Wilms tumor-Aniridia-Genitourinary Anomalies-Mental Retardation syndrome
    • chromosome 11p13 deletion syndrome
Homo sapiens (human)
DOID:14504
  • Niemann-Pick disease
  • Aliases:
    • Sphingomyelinase Deficiency Disease
    • lipoid histiocytosis
    • sphingomyelin lipidosis
Mus musculus (house mouse)
DOID:14504
  • Niemann-Pick disease
  • Aliases:
    • Sphingomyelinase Deficiency Disease
    • lipoid histiocytosis
    • sphingomyelin lipidosis
Caenorhabditis elegans
DOID:14504
  • Niemann-Pick disease
  • Aliases:
    • Sphingomyelinase Deficiency Disease
    • lipoid histiocytosis
    • sphingomyelin lipidosis
Homo sapiens (human)
DOID:14503
  • neuronal ceroid lipofuscinosis
  • Aliases:
    • hereditary ceroid lipofuscinosis
Homo sapiens (human)
DOID:14502
  • cholesterol ester storage disease
  • Aliases:
    • CESD
    • partial LAL deficiency
    • partial LIPA deficiency
    • partial cholesterol ester hydrolase deficiency
    • partial lysosomal acid lipase deficiency
Homo sapiens (human)
DOID:14502
  • cholesterol ester storage disease
  • Aliases:
    • CESD
    • partial LAL deficiency
    • partial LIPA deficiency
    • partial cholesterol ester hydrolase deficiency
    • partial lysosomal acid lipase deficiency
Mus musculus (house mouse)
DOID:14501
  • Sjogren-Larsson syndrome
  • Aliases:
    • FALDH deficiency
    • SLS
    • Sjogren Larsson syndrome
    • Sjogren-Larsson's syndrome
    • fatty acid alcohol oxidoreductase deficiency
Homo sapiens (human)
DOID:14500
  • fucosidosis
  • Aliases:
    • A-fucosidase deficiency
    • alpha fucosidase deficiency
Caenorhabditis elegans
DOID:14500
  • fucosidosis
  • Aliases:
    • A-fucosidase deficiency
    • alpha fucosidase deficiency
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