OBO ID: DOID:0110932
Term Name: nemaline myopathy 4 Search Ontology:
Synonyms:
  • CAP myopathy 2
  • NEM4
  • nemaline myopathy 4, autosomal dominant
Definition: A nemaline myopathy that has_material_basis_in heterozygous mutation in the TPM2 gene on chromosome 9p13. https://www.ncbi.nlm.nih.gov/pubmed/11738357
References:
Ontology: Human Disease   ( DOID:0110932 )
Relationships
is a type of:
OTHER nemaline myopathy 4 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TPM2 Congenital myopathy 23 609285
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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