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DO Term : nemaline myopathy 4 [DOID:0110932] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A nemaline myopathy that has_material_basis_in heterozygous mutation in the TPM2 gene on chromosome 9p13.

synonyms:
NEM4,
609285,
nemaline myopathy 4, autosomal dominant,
CAP myopathy 2,
OMIM:609285,
MESH:C538351

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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