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DO Term : autosomal recessive hyaline body myopathy [DOID:0111268] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hyaline body myopathy that has_material_basis_in compound heterozygous or homozygous mutation in MYH7 on 14q11.2.

synonyms:
OMIM:255160,
255160,
Myopathy, myosin storage, autosomal recessive,
MSMB,
congenital myopathy 7B

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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