| Metadata | |
|---|---|
| ID | DOID:0110932 |
| Name | nemaline myopathy 4 |
| 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 |
| Xrefs | |
| Synonyms |
CAP myopathy 2 [EXACT] NEM4 [EXACT] nemaline myopathy 4, autosomal dominant [EXACT] |
| Parent Relationships |
is_a nemaline myopathy |