Terminology Service for NFDI4Health
nemaline myopathy 4
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http://purl.obolibrary.org/obo/DOID_0110932
A nemaline myopathy that has_material_basis_in heterozygous mutation in the TPM2 gene on chromosome 9p13. [ http://purl.obolibrary.org/obo/ECO_0007645 ]
Term info
Label
nemaline myopathy 4
Synonyms
- NEM4
- nemaline myopathy 4, autosomal dominant
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disease_ontology
id
DOID:0110932