CDK6

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Amber CDK6 in Mendeliome Version 1.1891	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 1.269	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 0.6063	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 1.255	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Microcephaly 12, primary, autosomal recessive, MIM#616080

4 panels