congenital myopathy 26 Disease Ontology Browser

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congenital myopathy 26 (DOID:0061257)
Alliance: disease page
Alt IDs: OMIM:621225
Definition: A congenital myopathy characterized by limb muscle weakness and mild motor delay apparent from infancy that has_material_basis_in heterozygous mutation in the TUBA4A gene on chromosome 2q35.

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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