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 5476 - 5500 of 7942 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism
DOID:2747
  • glycogen storage disease
  • Aliases:
    • glycogenosis
Danio rerio (zebrafish)
DOID:2747
  • glycogen storage disease
  • Aliases:
    • glycogenosis
Caenorhabditis elegans
DOID:2747
  • glycogen storage disease
  • Aliases:
    • glycogenosis
Xenopus tropicalis (tropical clawed frog)
DOID:2747
  • glycogen storage disease
  • Aliases:
    • glycogenosis
Homo sapiens (human)
DOID:2747
  • glycogen storage disease
  • Aliases:
    • glycogenosis
Saccharomyces cerevisiae S288C
DOID:2747
  • glycogen storage disease
  • Aliases:
    • glycogenosis
Mus musculus (house mouse)
DOID:2748
  • glycogen storage disease III
  • Aliases:
    • Glycogen storage disease 3
    • Glycogen storage disease, type III
    • amylo 1,6 glucosidase deficiency
    • deficiency of debranching enzyme
    • deficiency of dextrin
Saccharomyces cerevisiae S288C
DOID:2748
  • glycogen storage disease III
  • Aliases:
    • Glycogen storage disease 3
    • Glycogen storage disease, type III
    • amylo 1,6 glucosidase deficiency
    • deficiency of debranching enzyme
    • deficiency of dextrin
Homo sapiens (human)
DOID:2749
  • glycogen storage disease Ia
Mus musculus (house mouse)
DOID:2749
  • glycogen storage disease Ia
Homo sapiens (human)
DOID:2749
  • glycogen storage disease Ia
Rattus norvegicus (Norway rat)
DOID:2750
  • glycogen storage disease IV
  • Aliases:
    • Amylopectinosis
    • Branching-transferase deficiency glycogenosis
    • Glycogen storage disease 4
    • Glycogen storage disease, type IV
    • brancher deficiency glycogenosis
    • deficiency of 1,4-alpha-glucan branching enzyme
Homo sapiens (human)
DOID:2750
  • glycogen storage disease IV
  • Aliases:
    • Amylopectinosis
    • Branching-transferase deficiency glycogenosis
    • Glycogen storage disease 4
    • Glycogen storage disease, type IV
    • brancher deficiency glycogenosis
    • deficiency of 1,4-alpha-glucan branching enzyme
Mus musculus (house mouse)
DOID:2750
  • glycogen storage disease IV
  • Aliases:
    • Amylopectinosis
    • Branching-transferase deficiency glycogenosis
    • Glycogen storage disease 4
    • Glycogen storage disease, type IV
    • brancher deficiency glycogenosis
    • deficiency of 1,4-alpha-glucan branching enzyme
Saccharomyces cerevisiae S288C
DOID:2751
  • glycogen storage disease VIII
  • Aliases:
    • Glycogen storage disease 8
    • glycogen storage disease type VIII
    • glycogenosis type VIII
    • hepatic glycogen phosphorylase kinase deficiency
Homo sapiens (human)
DOID:2752
  • glycogen storage disease II
  • Aliases:
    • Generalized glycogenosis
    • Glycogen storage disease 2
    • Glycogen storage disease, type II
    • Glycogenosis, type 2
    • Lysosomal alpha-1,4-glucosidase deficiency
    • Pompe's disease
    • acid maltase deficiency
    • deficiency of glucoamylase
    • deficiency of maltase
    • glycogen storage disease type II
Mus musculus (house mouse)
DOID:2752
  • glycogen storage disease II
  • Aliases:
    • Generalized glycogenosis
    • Glycogen storage disease 2
    • Glycogen storage disease, type II
    • Glycogenosis, type 2
    • Lysosomal alpha-1,4-glucosidase deficiency
    • Pompe's disease
    • acid maltase deficiency
    • deficiency of glucoamylase
    • deficiency of maltase
    • glycogen storage disease type II
Rattus norvegicus (Norway rat)
DOID:2752
  • glycogen storage disease II
  • Aliases:
    • Generalized glycogenosis
    • Glycogen storage disease 2
    • Glycogen storage disease, type II
    • Glycogenosis, type 2
    • Lysosomal alpha-1,4-glucosidase deficiency
    • Pompe's disease
    • acid maltase deficiency
    • deficiency of glucoamylase
    • deficiency of maltase
    • glycogen storage disease type II
Homo sapiens (human)
DOID:2754
  • glycogen storage disease VI
  • Aliases:
    • Glycogen storage disease 6
    • Hers' disease
    • glycogen storage disease type VI
    • hepatic glycogen phosphorylase deficiency
    • hepatophosphorylase deficiency glycogenosis
Rattus norvegicus (Norway rat)
DOID:2754
  • glycogen storage disease VI
  • Aliases:
    • Glycogen storage disease 6
    • Hers' disease
    • glycogen storage disease type VI
    • hepatic glycogen phosphorylase deficiency
    • hepatophosphorylase deficiency glycogenosis
Saccharomyces cerevisiae S288C
DOID:2754
  • glycogen storage disease VI
  • Aliases:
    • Glycogen storage disease 6
    • Hers' disease
    • glycogen storage disease type VI
    • hepatic glycogen phosphorylase deficiency
    • hepatophosphorylase deficiency glycogenosis
Drosophila melanogaster (fruit fly)
DOID:2754
  • glycogen storage disease VI
  • Aliases:
    • Glycogen storage disease 6
    • Hers' disease
    • glycogen storage disease type VI
    • hepatic glycogen phosphorylase deficiency
    • hepatophosphorylase deficiency glycogenosis
Homo sapiens (human)
DOID:2754
  • glycogen storage disease VI
  • Aliases:
    • Glycogen storage disease 6
    • Hers' disease
    • glycogen storage disease type VI
    • hepatic glycogen phosphorylase deficiency
    • hepatophosphorylase deficiency glycogenosis
Mus musculus (house mouse)
DOID:2755
  • Mycobacterium avium complex disease
  • Aliases:
    • Infection due to Mycobacterium intracellulare
    • MAC disease
    • Mycobacterium Avium Infection
    • Mycobacterium avium Complex
Rattus norvegicus (Norway rat)
DOID:2755
  • Mycobacterium avium complex disease
  • Aliases:
    • Infection due to Mycobacterium intracellulare
    • MAC disease
    • Mycobacterium Avium Infection
    • Mycobacterium avium Complex
Homo sapiens (human)

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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