ZFIN Human Disease: autosomal dominant hyaline body myopathy

OBO ID: DOID:0111269

Term Name:	autosomal dominant hyaline body myopathy		Search Ontology:
Synonyms:	congenital myopathy 7A MSMA myopathy with lysis of type I myofibrils Myopathy, myosin storage, autosomal dominant
Definition:	A hyaline body myopathy that has_material_basis_in heterozygous mutation in MYH7 on 14q11.2. https://www.ncbi.nlm.nih.gov/pubmed/16684601
References:	OMIM:608358
Ontology:	Human Disease ( DOID:0111269 )

Relationships

is a type of:	autosomal dominant disease hyaline body myopathy autosomal dominant disease hyaline body myopathy Show first 5 Terms

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Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
MYH7	myh7	Congenital myopathy 7A, myosin storage, autosomal dominant	608358

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None