Search Ontology:
Human Disease

congenital structural myopathy

Term ID
DOID:422
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
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