Gene: PTCH1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5727
Gene Symbol: PTCH1
PTCH1 		0.110 GeneticVariation disease BEFREE Haploinsufficiency of PTCH causes the BCNS syndrome and mutations in ROR2 have been found in an autosomal recessive Robinow syndrome and a dominantly inherited brachydactyly type 1B. 17632781 2007
Entrez Id: 5727
Gene Symbol: PTCH1
PTCH1 		0.110 Biomarker disease HPO
Entrez Id: 5727
Gene Symbol: PTCH1
PTCH1 		0.110 CausalMutation disease CLINVAR