ZC3H14

Panel	Reviews	Mode of inheritance	Details
Amber ZC3H14 in Mendeliome Version 1.1902	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Mental retardation, autosomal recessive 56 OMIM# 617125
Amber ZC3H14 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 0.6063	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Expert list Phenotypes Mental retardation, autosomal recessive 56 OMIM# 617125

Panel

Reviews

Mode of inheritance

Details

Version 1.1902

review

BIALLELIC, autosomal or pseudoautosomal

Level 2: Neurology and neurodevelopmental disorders
Version 0.6063

review

BIALLELIC, autosomal or pseudoautosomal

2 panels