KCTD15

potassium channel tetramerization domain containing 15
OMIM: 615240, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel

No list KCTD15 in Mendeliome


Version 1.3470

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Literature
Phenotypes
  • frontonasal dysplasia, MONDO:0016643