1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0110931 | nemaline myopathy 10 | A nemaline myopathy characterized by early-onset generalized muscle weakness and hypotonia with respiratory insufficiency and feeding difficulties that has_material_basis_in homozygous or compound heterozygous mutation in the LMOD3 gene on chromosome 3p14. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0081337 | congenital myopathy | A myopathy that is characterized by hypotonia and weakness, usually present from birth. |
