KCTD15

potassium channel tetramerization domain containing 15
OMIM: 615240, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber KCTD15 in Frontonasal dysplasia


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.3

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

Amber KCTD15 in Mendeliome


Version 1.3795

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