KCTD19:Ensemblv90

potassium channel tetramerization domain containing 19
ClinGen, DECIPHER

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Green KCTD19 in Mendeliome


Version 1.3802

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
  • Literature
Phenotypes
  • Infertility disorder, MONDO:0005047, KCTD19-related