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Metadata
ID	DOID:0110005
Name	Leber congenital amaurosis 9
Definition	A Leber congenital amaurosis that has_material_basis_in mutation in the NMNAT1 gene on chromosome 1p36. https://www.ncbi.nlm.nih.gov/pubmed/22842230
Xrefs	ICD10CM:H35.5 MIM:608553
Synonyms	LCA9 [EXACT]
Parent Relationships	is_a Leber congenital amaurosis is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance disease has basis in some Abnormality of prenatal development or birth