NCAPD2

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Green NCAPD2 in Mendeliome Version 1.1902	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Microcephaly 21, primary, autosomal recessive OMIM #617983
Green NCAPD2 in Microcephaly Level 2: Dysmorphic and congenital abnormality syndromes Version 1.269	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Microcephaly 21, primary, autosomal recessive OMIM #617983
Green NCAPD2 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 0.6063	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes ?Microcephaly 21, primary, autosomal recessive OMIM #617983
Green NCAPD2 in Fetal anomalies Version 1.255	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert Review Phenotypes Microcephaly 21, primary, autosomal recessive OMIM #617983

4 panels