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Human Disease

nemaline myopathy 4

Term ID
DOID:0110932
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
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Genes Involved
Zebrafish Models