VANGL1

Panel	Reviews	Mode of inheritance	Details
Red VANGL1 in Mendeliome Version 1.1902	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Caudal regression syndrome, MIM# 600145 {Neural tube defects, susceptibility to} 182940
Red VANGL1 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 Expert list Phenotypes Caudal regression syndrome, OMIM #600145 {Neural tube defects, susceptibility to}, OMIM #182940

Panel

Reviews

Mode of inheritance

Details

Version 1.1902

review

MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

Level 2: Neurology and neurodevelopmental disorders
Version 0.6063

review

MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

2 panels