PTCHD3

patched domain containing 3
OMIM: 611791, ClinGen, DECIPHER

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red PTCHD3 in Mendeliome


Version 1.4902

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Nevoid basal cell carcinoma syndrome, MONDO:0007187