Disease association ontology term - MONDO:0012239 - congenital myopathy 4B, autosomal recessive
Term summary
- ID
- MONDO:0012239
- Name
- congenital myopathy 4B, autosomal recessive
- Ontology or CV name
- Disease association
- Definition
- Any congenital myopathy in which the cause of the disease is a mutation in the TPM3 gene.
