| Disease ID | Source | Name | Description |
| 615731 | OMIM | Nemaline myopathy 9 (NEM9) | An autosomal recessive form of nemaline myopathy. Nemaline myopathies are muscular disorders characterized by muscle weakness of varying severity and onset, and abnormal thread-like or rod-shaped structures in muscle fibers on histologic examination. NEM9 phenotype is highly variable, ranging from death in infancy due to lack of antigravity movements, to slowly progressive distal muscle weakness with preserved ambulation later in childhood. The disease is caused by variants affecting the gene represented in this entry. |