OBO ID: DOID:422
Term Name: congenital structural myopathy Search Ontology:
Synonyms:
Definition: A myopathy that is characterized by hypotonia, muscle weakness, and delayed development of motor skills. https://pubmed.ncbi.nlm.nih.gov/23897157/
References:
Ontology: Human Disease   ( DOID:422 )
Relationships
is a type of:
has subtype:
OTHER congenital structural myopathy PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS (1)
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