Search Ontology:
Human Disease

nemaline myopathy 3

Term ID
DOID:0110927
Synonyms
  • congenital myopathy 2A
  • NEM3
  • nemaline myopathy 3, autosomal dominant or recessive
Definition
A nemaline myopathy that has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation in the ACTA1 gene on chromosome 1q42. (2)
References
Ontology
Human Disease   ( DOID:0110927 )
Relationships
is a type of
inverse disjoint_from
Other Pages
Genes Involved
Zebrafish Models