Genomics England
GMS Panels
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Genes and Entities
SEPT9
septin 9
OMIM:
604061
See this entity in PanelApp
Panel
Mode of inheritance
Details
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in
Hereditary neuropathy or pain disorder
R-numbers:
R78
Signed-off version 4.11
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Amyotrophy, hereditary neuralgic, Neuralgic amyotrophy