PCDH19, protocadherin 19, 57526

N. diseases: 93; N. variants: 48
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0009241
Disease: Cognition Disorders
Cognition Disorders
0.010 GeneticVariation group BEFREE Autism features and various degrees of cognitive deficit are reported in patients with PCDH-19 mutations and epilepsy. 27179713 2016