OBO ID: DOID:0110933
Term Name: nemaline myopathy 11 Search Ontology:
Synonyms:
  • NEM11
  • nemaline myopathy 11, autosomal recessive
Definition: A nemaline myopathy characterized by onset of slowly progressive muscle weakness in the first decade of life that has_material_basis_in homozygous or compound heterozygous mutation in the MYPN gene on chromosome 10q21. https://www.ncbi.nlm.nih.gov/pubmed/28017374
References:
Ontology: Human Disease   ( DOID:0110933 )
Relationships
is a type of:
OTHER nemaline myopathy 11 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MYPN Congenital myopathy 24 617336
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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