NCAPD3

Panel	Reviews	Mode of inheritance	Details
Amber NCAPD3 in Mendeliome Version 1.1902	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Microcephaly 22, primary, autosomal recessive, MIM# 617984
Amber NCAPD3 in Microcephaly Level 2: Dysmorphic and congenital abnormality syndromes Version 1.269	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Microcephaly 22, primary, autosomal recessive, MIM# 617984

Panel

Reviews

Mode of inheritance

Details

Version 1.1902

review

BIALLELIC, autosomal or pseudoautosomal

Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.269

review

BIALLELIC, autosomal or pseudoautosomal

2 panels