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DO Term : myofibrillar myopathy 2 [DOID:0080093] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A myofibrillar myopathy that has_material_basis_in heterozygous mutation in the alpha-B-crystallin gene on chromosome 11q23.

synonyms:
alpha-b crystallinopathy,
OMIM:608810,
608810,
ORDO:399058

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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