Disorders

NMNAT1-Related Leber Congenital Amaurosis

Synonym(s): LCA9 Leber Congenital Amaurosis, Leber Congenital Amaurosis 9

Gene	Locus	Protein
NMNAT1	1p36.22

Laboratory	Test Method	Prenatal	Carrier *
Oregon Health and Science University, Casey Eye Institute Molecular Diagnostic Laboratory - Portland, OR, USA

^* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.