NODAL

nodal growth differentiation factor
OMIM: 601265, Gene2Phenotype

8 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 8 panels
Amber NODAL in Congenital Heart Defect Level 2: Cardiovascular disorders Version 0.418	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Heterotaxy, visceral, 5 (MIM#270100) Tags disputed
Red NODAL in Ciliopathies Level 2: Dysmorphic and congenital abnormality syndromes Version 1.54	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Heterotaxy, visceral, 5 (MIM#270100) Tags disputed
Amber NODAL in Heterotaxy Level 2: Dysmorphic and congenital abnormality syndromes Version 1.32	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Expert Review Phenotypes Heterotaxy, visceral, 5 (MIM#270100) Tags disputed
Red NODAL in Holoprosencephaly and septo-optic dysplasia Level 2: Neurology and neurodevelopmental disorders Version 1.16	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Heterotaxy, visceral, 5 (MIM#270100) Tags disputed
Amber NODAL in Mendeliome Version 1.1891	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Heterotaxy, visceral, 5 (MIM#270100) Tags disputed
Red NODAL in Skeletal dysplasia Level 3: Skeletal dysplasias Level 2: Skeletal disorders Version 0.285	review	Not set	Sources Expert Review Red Emory Genetics Laboratory Victorian Clinical Genetics Services
Red NODAL in Pituitary hormone deficiency Level 2: Endocrine disorders Version 0.34	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Red Genomics England PanelApp Phenotypes Holoprosencephaly Heterotaxy, visceral, 5 (270100)
Amber NODAL in Fetal anomalies Version 1.255	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Genomics England PanelApp Expert Review Victorian Clinical Genetics Services Phenotypes Heterotaxy, visceral, 5 (MIM#270100)