KCTD19

potassium channel tetramerization domain containing 19
OMIM: 619943, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Green KCTD19 in Mendeliome


Version 2.0

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

Green KCTD19 in Infertility and Recurrent Pregnancy Loss


Version 2.0

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