C21orf59

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Green C21orf59 in Ciliary Dyskinesia Level 2: Respiratory disorders Version 1.63	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Ciliary dyskinesia, primary, 26, MIM# 615500 Tags founder new gene name
Green C21orf59 in Heterotaxy Level 2: Dysmorphic and congenital abnormality syndromes Version 1.44	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Ciliary dyskinesia, primary, 26, MIM# 615500 Tags founder new gene name
Green C21orf59 in Mendeliome Version 1.3499	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Ciliary dyskinesia, primary, 26, MIM# 615500 Tags founder new gene name
Green C21orf59 in Fetal anomalies Version 1.465	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Victorian Clinical Genetics Services Phenotypes Primary ciliary dyskinesia 26, MONDO:0014211 Ciliary dyskinesia, primary, 26, OMIM:615500 Tags founder new gene name

4 panels