OBO ID: DOID:0111220
Term Name: centronuclear myopathy 2 Search Ontology:
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 centronuclear myopathy 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
BIN1 Centronuclear myopathy 2 255200
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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