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DO Term : centronuclear myopathy 5 [DOID:0111222] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  An autosomal recessive centronuclear myopathy characterized by severe neonatal hypotonia, respiratory insufficiency, and difficulty feeding that has_material_basis_in homozygous or compound heterozygous mutation in SPEG on 2q35.
  • synonyms:
  • 615959,
  • OMIM:615959,
  • CNM5
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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