glycogen storage disease XI Disease Ontology Browser

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glycogen storage disease XI (DOID:0061286)
Alliance: disease page
Synonyms: lactate dehydrogenase A deficiency
Alt IDs: OMIM:612933
Definition: A glycogen storage disease that has_material_basis_in homozygous mutation in the LDHA gene, which encodes lactate dehydrogenase, on chromosome 11p15.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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