NME8

Panel	Reviews	Mode of inheritance	Details
Filter panels 6 panels
Red NME8 in Ciliary Dyskinesia Level 2: Respiratory disorders Version 1.77	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Ciliary dyskinesia, primary, 6, MIM# 610852 Tags disputed
Red NME8 in Heterotaxy Level 2: Dysmorphic and congenital abnormality syndromes Version 1.45	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Ciliary dyskinesia, primary, 6, MIM# 610852 Tags disputed
Red NME8 in Mendeliome Version 1.4851	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Ciliary dyskinesia, primary, 6, MIM# 610852 primary ciliary dyskinesia MONDO:0016575 Tags disputed
Red NME8 in Skeletal dysplasia Level 3: Skeletal dysplasias Level 2: Skeletal disorders Version 0.444	1 review	Not set	Sources Emory Genetics Laboratory
Red NME8 in Additional findings_Paediatric Level 2: Screening Version 0.280	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red BabySeq Category C gene Phenotypes Ciliary dyskinesia, primary
Red NME8 in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.148	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources BabySeq Category C gene Expert Review Red Phenotypes Ciliary dyskinesia, primary

6 panels