CEP19

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Red CEP19 in Bardet Biedl syndrome Level 2: Dysmorphic and congenital abnormality syndromes Version 1.10 Component of the following Super Panels: Retinal Disorders Superpanel	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Expert list Phenotypes Bardet Biedl syndrome
Red CEP19 in Ciliopathies Level 2: Dysmorphic and congenital abnormality syndromes Version 1.54	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Expert list Phenotypes Bardet-Biedl syndorme
Amber CEP19 in Mendeliome Version 1.1902	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Literature Phenotypes Morbid obesity and spermatogenic failure MIM#615703 Bardet-Biedl syndorme
Amber CEP19 in Severe early-onset obesity Level 2: Endocrine disorders Version 1.10	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Genomics England PanelApp Expert list Phenotypes Morbid obesity and spermatogenic failure, OMIM:615703 Bardet Biedl syndrome

4 panels