Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10472
Gene Symbol: ZBTB18
ZBTB18
CUI: C3808184
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 22
MENTAL RETARDATION, AUTOSOMAL DOMINANT 22 		0.600 Biomarker GENOMICS_ENGLAND Identification of novel genetic causes of Rett syndrome-like phenotypes. 26740508

2016
Entrez Id: 10472
Gene Symbol: ZBTB18
ZBTB18
CUI: C3808184
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 22
MENTAL RETARDATION, AUTOSOMAL DOMINANT 22 		0.600 Biomarker GENOMICS_ENGLAND Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data. 25529582

2015
Entrez Id: 10472
Gene Symbol: ZBTB18
ZBTB18
CUI: C3808184
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 22
MENTAL RETARDATION, AUTOSOMAL DOMINANT 22 		0.600 CausalMutation CLINVAR

Entrez Id: 10472
Gene Symbol: ZBTB18
ZBTB18
CUI: C3808184
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 22
MENTAL RETARDATION, AUTOSOMAL DOMINANT 22 		0.600 Biomarker CTD_human

Entrez Id: 10472
Gene Symbol: ZBTB18
ZBTB18
CUI: C3808184
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 22
MENTAL RETARDATION, AUTOSOMAL DOMINANT 22 		0.600 GeneticVariation CLINVAR