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Human Disease

centronuclear myopathy 2

Term ID
DOID:0111220
Synonyms
  • CNM2
Definition
An autosomal recessive centronuclear myopathy that has_material_basis_in homozygous or compound heterozygous mutation in BIN1 on 2q14.3. https://www.ncbi.nlm.nih.gov/pubmed/17676042
References
Ontology
Human Disease   ( DOID:0111220 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models