1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0081375 | nemaline myopathy 5C | A nemaline myopathy that has_material_basis_in autosomal dominant inheritance of a homozygous or compound heterozygous mutation in the TNNT1 gene on chromosome 19q13. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:17 | musculoskeletal system disease | A disease of anatomical entity that occurs in the muscular and/or skeletal system. |
