Adult solid tumours for rare diseaseGene: PTCH1
Created: 5 Jul 2017, 12:19 p.m.
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Gorlin syndrome, BCC
5th March 2018 - promoted to version 1 after expert review and internal clinical review.
PTCH1 was added to Adult solid tumours for rare disease panel. Sources: Expert Review Green,Expert list
PTCH1 was created by Ellen McDonagh