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DO Term : congenital structural myopathy [DOID:422] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A myopathy that is characterized by hypotonia, muscle weakness, and delayed development of motor skills.

synonyms:
MESH:D020914,
UMLS_CUI:C0752282,
NCI:C84648

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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