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DO Term : Leber congenital amaurosis 11 [DOID:0110216] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A Leber congenital amaurosis that has_material_basis_in mutation n the IMPDH1 gene on chromosome 7q31.3-q32.

synonyms:
LCA11,
OMIM:613837,
ICD10CM:H35.5,
MESH:C564140,
613837

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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