Genomics England
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Genes and Entities
PRX
periaxin
OMIM:
605725
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Panel
Mode of inheritance
Details
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in
Hereditary neuropathy or pain disorder
R-numbers:
R78
Signed-off version 6.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Charcot-Marie-Tooth disease, type 4F, OMIM:614895, Dejerine-Sottas disease, OMIM:145900