KAT6B, lysine acetyltransferase 6B, 23522

N. diseases: 208; N. variants: 27
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0005744
Disease: Blepharophimosis
Blepharophimosis
0.130 CausalMutation disease CLINVAR A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders. 26938784 2016
CUI: C0005744
Disease: Blepharophimosis
Blepharophimosis
0.130 GeneticVariation disease BEFREE KAT6B sequence variants have been identified previously in both patients with the Say-Barber-Biesecker type of blepharophimosis mental retardation syndromes (SBBS) and in the more severe genitopatellar syndrome (GPS). 25424711 2015
CUI: C0005744
Disease: Blepharophimosis
Blepharophimosis
0.130 GeneticVariation disease BEFREE Mutations of the histone acetyltransferase-encoding KAT6B gene cause the Say-Barber-Biesecker/Young-Simpson (SBBYS) type of blepharophimosis-"mental retardation" syndromes and the more severe genitopatellar syndrome. 26334766 2015
CUI: C0005744
Disease: Blepharophimosis
Blepharophimosis
0.130 GeneticVariation disease BEFREE An individual with blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) and additional features expands the phenotype associated with mutations in KAT6B. 24458743 2014
CUI: C0005744
Disease: Blepharophimosis
Blepharophimosis
0.130 GeneticVariation disease CLINVAR
CUI: C0005744
Disease: Blepharophimosis
Blepharophimosis
0.130 Biomarker disease HPO