ASCL1

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Amber ASCL1 in Central Hypoventilation Level 2: Neurology and neurodevelopmental disorders Version 1.6	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Central hypoventilation syndrome, congenital, MIM# 209880
Amber ASCL1 in Interstitial Lung Disease Level 2: Respiratory disorders Version 1.2	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Victorian Clinical Genetics Services Victorian Clinical Genetics Services Phenotypes Central hypoventilation syndrome, congenital, MIM# 209880
Amber ASCL1 in Mendeliome Version 1.3512	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Central hypoventilation syndrome, congenital, MIM# 209880
Red ASCL1 in Additional findings_Paediatric Level 2: Screening Version 0.278	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red BabySeq Category C gene Phenotypes Congenital central hypoventilation
Red ASCL1 in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.140	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources BabySeq Category C gene Expert Review Red Phenotypes Congenital central hypoventilation

5 panels