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DO Term : Leber congenital amaurosis 9 [DOID:0110005] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A Leber congenital amaurosis that has_material_basis_in mutation in the NMNAT1 gene on chromosome 1p36.

synonyms:
LCA9,
608553,
ICD10CM:H35.5,
OMIM:608553

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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