KCTD1

potassium channel tetramerization domain containing 1
OMIM: 613420
PanelMode of inheritanceDetails
1 panel
R-numbers: R21, R412
Signed-off version 7.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
SCALP-EAR-NIPPLE SYNDROME