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nemaline myopathy 2

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description An autosomal recessive inherited myopathy caused by mutations in the NEB gene. It is characterized by generalized hypotonia and skeletal muscle weakness.
Uniprot Description A 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.
Mondo Term and Equivalent IDs
MONDO:0009725:  nemaline myopathy 2
MESH:C538349: 
NCIT:C118784: 
UMLS:C1850569: 
UMLS:CN187052: