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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources January 28, 2025
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 4351 - 4375 of 5716 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism Source
DOID:14500
  • fucosidosis
  • Aliases:
    • A-fucosidase deficiency
    • alpha fucosidase deficiency
Homo sapiens (human)
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: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:14503
  • neuronal ceroid lipofuscinosis
  • Aliases:
    • hereditary ceroid lipofuscinosis
Drosophila melanogaster (fruit fly)
DOID:14503
  • neuronal ceroid lipofuscinosis
  • Aliases:
    • hereditary ceroid lipofuscinosis
Mus musculus (house mouse)
DOID:14503
  • neuronal ceroid lipofuscinosis
  • Aliases:
    • hereditary ceroid lipofuscinosis
Homo sapiens (human)
DOID:14503
  • neuronal ceroid lipofuscinosis
  • Aliases:
    • hereditary ceroid lipofuscinosis
Caenorhabditis elegans
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
Saccharomyces cerevisiae S288C
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
Homo sapiens (human)
DOID:14557
  • primary pulmonary hypertension
  • Aliases:
    • Idiopathic pulmonary arterial hypertension
Homo sapiens (human)
DOID:14557
  • primary pulmonary hypertension
  • Aliases:
    • Idiopathic pulmonary arterial hypertension
Mus musculus (house mouse)
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
Rattus norvegicus (Norway rat)
DOID:1459
  • hypothyroidism
  • Aliases:
    • Thyroid deficiency
    • Thyroid insufficiency
Rattus norvegicus (Norway rat)
DOID:1459
  • hypothyroidism
  • Aliases:
    • Thyroid deficiency
    • Thyroid insufficiency
Homo sapiens (human)
DOID:14654
  • prostatitis
Homo sapiens (human)
DOID:14669
  • acrodysostosis
Homo sapiens (human)
DOID:14671
  • multiple intestinal atresia
  • Aliases:
    • GIDID
    • Multiple gastrointestinal atresias
    • familial intestinal polyatresia syndrome
    • gastrointestinal defects and immunodeficiency syndrome
Homo sapiens (human)
DOID:14679
  • VACTERL association
Mus musculus (house mouse)
DOID:14681
  • Silver-Russell syndrome
  • Aliases:
    • Silver Russell Dwarfism
Homo sapiens (human)
DOID:14686
  • Axenfeld-Rieger syndrome
  • Aliases:
    • Anomaly, Rieger's
    • Axenfeld syndrome
    • RGS - Rieger syndrome
    • Rieger's anomaly
Homo sapiens (human)
DOID:14687
  • diastrophic dysplasia
Homo sapiens (human)
DOID:14687
  • diastrophic dysplasia
Mus musculus (house mouse)
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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: March 31, 2025