Genomics England
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Panels
Genes and Entities
CLDN10
claudin 10
OMIM:
617579
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Panel
Mode of inheritance
Details
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in
Renal tubulopathies
R-numbers:
R198
Signed-off version 4.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Hypokalemic-alkalotic salt-losing tubulopathy, HELIX syndrome, OMIM:617671