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Disease Ontology Browser
Leber congenital amaurosis 13 (DOID:0110330)
Synonyms: LCA13
Alt IDs: OMIM:612712, ICD10CM:H35.5, ORDO:65
Definition: A Leber congenital amaurosis thatis characterized by mild or absent hyperopia, transient improvement of visual acuity, and eventual macular atrophy with severe disease progression and has_material_basis_in mutation in the RDH12 gene on chromosome 14q23.3.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
03/21/2017
MGI 6.08
The Jackson Laboratory