Search Ontology:
Human Disease

centronuclear myopathy 4

Term ID
DOID:0111224
Synonyms
  • CNM4
Definition
An autosomal dominant centronuclear myopathy that has_material_basis_in heterozygous mutation in CCDC78 on 16p13.3. https://www.ncbi.nlm.nih.gov/pubmed/22818856
References
Ontology
Human Disease   ( DOID:0111224 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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