C5399872_SNOMEDCT_US | Knowledge4COVID-19

Property	Value
?:definition	A rare genetic muscular dystrophy disease with characteristics of the co-occurrence of late onset scapular and peroneal muscle weakness, principally manifesting with distal lower limb and proximal upper limb weakness and scapular winging. Caused by mutation in the FHL1 gene.
?:hasCUIAnnotation	<https://research.tib.eu/covid-19/entity/C5399872>
?:hasGeneratedBy	<https://research.tib.eu/covid-19/SourceName/SNOMEDCT_US>
?:type	<https://research.tib.eu/covid-19/vocab/AnnotationDefinition>

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