ZFIN Human Disease: autosomal recessive hyaline body myopathy

OBO ID: DOID:0111268

Term Name:	autosomal recessive hyaline body myopathy		Search Ontology:
Synonyms:	congenital myopathy 7B MSMB Myopathy, myosin storage, autosomal recessive
Definition:	A hyaline body myopathy that has_material_basis_in compound heterozygous or homozygous mutation in MYH7 on 14q11.2. https://www.ncbi.nlm.nih.gov/pubmed/17372140
References:	OMIM:255160
Ontology:	Human Disease ( DOID:0111268 )

Relationships

is a type of:	autosomal recessive disease hyaline body myopathy autosomal recessive 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 7B, myosin storage, autosomal recessive	255160

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None