Genomics England
GMS Panels
Panels
Genes and Entities
STRC
stereocilin
OMIM:
606440
See this entity in PanelApp
Panel
Mode of inheritance
Details
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in
Monogenic hearing loss
Component of the following Super Panels:
- Paediatric disorders
R-numbers:
R67
Signed-off version 4.42
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Deafness, autosomal recessive 16, 603720