OBO ID: DOID:0080098
Term Name: myofibrillar myopathy 7 Search Ontology:
Synonyms:
Definition: A myofibrillar myopathy that has_material_basis_in homozygous mutation in the KY gene on chromosome 3q22. https://www.omim.org/entry/617114
References:
Ontology: Human Disease   (DOID:0080098)
OTHER myofibrillar myopathy 7 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
KY Myopathy, myofibrillar, 7 617114
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None