CCNO

Panel	Reviews	Mode of inheritance	Details
Filter panels 6 panels
Green CCNO in Ciliary Dyskinesia Level 2: Respiratory disorders Version 1.47	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Ciliary dyskinesia, primary, 29, MIM# 615872
Red CCNO in Heterotaxy Level 2: Dysmorphic and congenital abnormality syndromes Version 1.36	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Ciliary dyskinesia, primary, 29, MIM# 615872
Green CCNO in Mendeliome Version 1.2374	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Ciliary dyskinesia, primary, 29, MIM# 615872
Green CCNO in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 0.109	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Ciliary diskinesia, primary, 29, 615872 (3)
Red CCNO in Fetal anomalies Version 1.314	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Genomics England PanelApp Phenotypes Ciliary dyskinesia, primary, 29 615872
Green CCNO in Prepair 1000+ Level 2: Screening Version 1.1586	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Ciliary diskinesia, primary, 29, MIM#615872

6 panels