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Human Disease

autosomal recessive centronuclear myopathy

Term ID
DOID:0111216
Synonyms
  • AR-CNM
Definition
A centronuclear myopathy that has_material_basis_in autosomal recessive inheritance. https://www.ncbi.nlm.nih.gov/pubmed/30103348
References
  • GARD:12718
  • ORDO:169186
Ontology
Human Disease   ( DOID:0111216 )
Relationships
is a type of
has subtype
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Genes Involved
Zebrafish Models