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DO Term : Leber congenital amaurosis 8 [DOID:0110079] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A Leber congenital amaurosis that is characterized by night blindness and thick unlaminated retinas and has_material_basis_in mutation in the CRB1 gene on chromosome 1q31-q32.

synonyms:
613835,
ICD10CM:H35.5,
LCA8,
OMIM:613835

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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