Showing entry for LEBER CONGENITAL AMAUROSIS 13

General Disease Information
BXGD Id	BXGD017277
Disease Name	LEBER CONGENITAL AMAUROSIS 13
Disease CUI Id	C2675186
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