OBO ID: DOID:0081337 |
Term Name: | congenital myopathy | Search Ontology: | |
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Definition: | A myopathy that is characterized by hypotonia and weakness, usually present from birth. https://ijponline.biomedcentral.com/articles/10.1186/s13052-017-0419-z | ||
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Ontology: | Human Disease ( DOID:0081337 ) |
OTHER congenital myopathy PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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