ZNF407

Panel	Reviews	Mode of inheritance	Details
Amber ZNF407 in Mendeliome Version 1.1891	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes SIMHA syndrome, MIM# 619557 Global developmental delay Intellectual disability
Amber ZNF407 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 0.6063	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes SIMHA syndrome, MIM# 619557 Global developmental delay Intellectual disability

Panel

Reviews

Mode of inheritance

Details

Version 1.1891

review

BOTH monoallelic and biallelic, autosomal or pseudoautosomal

Level 2: Neurology and neurodevelopmental disorders
Version 0.6063

review

BOTH monoallelic and biallelic, autosomal or pseudoautosomal

2 panels