Showing entry for LEBER CONGENITAL AMAUROSIS 6 (disorder)

General Disease Information
BXGD Id	BXGD015390
Disease Name	LEBER CONGENITAL AMAUROSIS 6 (disorder)
Disease CUI Id	C1854260
MeSH Codes	C11
Disease Class Name	Eye Diseases
Semantic Type	Disease or Syndrome; Congenital Abnormality
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