KCTD1

potassium channel tetramerization domain containing 1
OMIM: 613420
PanelMode of inheritanceDetails
2 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 2.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
SCALP-EAR-NIPPLE SYNDROME
R-numbers: R21
Signed-off version 1.92
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
SCALP-EAR-NIPPLE SYNDROME