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 )
Relationships
is a type of:
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
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