BDNF

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Red BDNF in Central Hypoventilation Level 2: Neurology and neurodevelopmental disorders Version 1.5	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Central hypoventilation syndrome, congenital, MIM#209880 Tags refuted
Red BDNF in Mendeliome Version 1.1891	review	Unknown	Sources Expert Review Red Victorian Clinical Genetics Services
Red BDNF in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 0.6063	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Genetic Health Queensland Phenotypes Central hypoventilation syndrome, congenital, MIM#209880
Red BDNF in Additional findings_Paediatric Level 2: Screening Version 0.278	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red BabySeq Category C gene Phenotypes Central hypoventilation syndrome
Red BDNF in BabyScreen+ newborn screening Level 2: Screening Version 1.113	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources BabySeq Category C gene Expert Review Red Phenotypes Central hypoventilation syndrome

5 panels