Showing entry for LEBER CONGENITAL AMAUROSIS 12 (disorder)

General Disease Information
BXGD Id	BXGD015745
Disease Name	LEBER CONGENITAL AMAUROSIS 12 (disorder)
Disease CUI Id	C1857743
MeSH Codes	C11
Disease Class Name	Eye Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:630   DOID:7
Disease Ontology Class Name	genetic disease; disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations