Showing entry for Leber Congenital Amaurosis 14

General Disease Information
BXGD Id	BXGD017643
Disease Name	Leber Congenital Amaurosis 14
Disease CUI Id	C2750063
MeSH Codes	C16   C11
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; 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