CDK6

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Amber CDK6 in Mendeliome Version 1.3512	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Victorian Clinical Genetics Services Victorian Clinical Genetics Services Phenotypes Microcephaly 12, primary, autosomal recessive, MIM#616080
Amber CDK6 in Microcephaly Level 2: Dysmorphic and congenital abnormality syndromes Version 1.357	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Microcephaly 12, primary, autosomal recessive, MIM#616080
Amber CDK6 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.410	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Genetic Health Queensland Phenotypes Microcephaly 12, primary, autosomal recessive, MIM#616080
Amber CDK6 in Fetal anomalies Version 1.465	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Microcephaly 12, primary, autosomal recessive, MIM#616080

4 panels