CDK9:Ensemblv90

cyclin dependent kinase 9
OMIM: 603251, ClinGen, DECIPHER

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green CDK9 in Mendeliome Version 1.3802	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome MONDO:0015160 CHARGE-like syndrome with retinal dystrophy
Amber CDK9 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.508	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome MONDO:0015160 CHARGE-like syndrome with retinal dystrophy
Green CDK9 in Syndromic Retinopathy Level 2: Ophthalmological disorders Version 0.235 Component of the following Super Panels: Retinal Disorders Superpanel	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome MONDO:0015160 CHARGE-like syndrome with retinal dystrophy
Amber CDK9 in Fetal anomalies Version 1.482	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome MONDO:0015160 CHARGE-like syndrome with retinal dystrophy
Green CDK9 in Syndromic Retinopathy Level 2: Ophthalmological disorders Version 1.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Literature Expert Review Green Phenotypes multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome MONDO:0015160 CHARGE-like syndrome with retinal dystrophy