Search Ontology:
Human Disease
nemaline myopathy 2
- Term ID
- DOID:0110928
- Synonyms
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- congenital myopathy 2
- NEM2
- nemaline myopathy 2, autosomal recessive
- Definition
- A nemaline myopathy that has_material_basis_in homozygous or compound heterozygous mutation in the NEB gene on chromosome 2q23. (2)
- References
- Ontology
- Human Disease ( DOID:0110928 )
- is a type of
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