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: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.040 AlteredExpression disease BEFREE Consistent with the autism observed in EFMR females, we found Pcdh19 heterozygous KO female mice (with mosaic expression of PCDH19) show defects in sociability in the 3-chamber test. 31747920 2019
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.040 Biomarker disease BEFREE Protocadherin 19 (PCDH19) female limited epilepsy (PCDH19-FE; also known as epilepsy and mental retardation limited to females, EFMR; MIM300088) is an infantile onset epilepsy syndrome with or without intellectual disability (ID) and autism. 26123493 2015
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.040 Biomarker disease BEFREE For example, CDH15 and PCDH19 are associated with cognitive impairment; CDH5, CDH8, CDH9, CDH10, CDH13, CDH15, PCDH10, PCDH19 and PCDHb4 with autism; CDH7, CDH12, CDH18, PCDH12 and FAT with bipolar disease and schizophrenia; and CDH11, CDH12 and CDH13 with methamphetamine and alcohol dependency. 22765916 2012
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.040 Biomarker disease LHGDN Autism spectrum disorders associated with X chromosome markers in French-Canadian males. 16261168 2006