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DOID:0080093 - myofibrillar myopathy 2
Disease Ontology Definition:A myofibrillar myopathy that has_material_basis_in heterozygous mutation in the alpha-B-crystallin gene on chromosome 11q23.
Synonyms: alpha-b crystallinopathy,
Xenbase Genes : cryab
MONDO:0012130 - myofibrillar myopathy 2 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee