Genomics England
GMS Panels
Panels
Genes and Entities
KY
kyphoscoliosis peptidase
OMIM:
605739
See this entity in PanelApp
Panel
Mode of inheritance
Details
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Congenital myopathy
Component of the following Super Panels:
- Hypotonic infant
- Other rare neuromuscular disorders
R-numbers:
R81
Signed-off version 5.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Myopathy, myofibrillar, 7, OMIM:617114