Genomics England
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Panels
Genes and Entities
WNK1
WNK lysine deficient protein kinase 1
OMIM:
605232
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Panel
Mode of inheritance
Details
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Hereditary neuropathy or pain disorder
R-numbers:
R78
Signed-off version 5.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Neuropathy, hereditary sensory and autonomic, type II, OMIM:201300