Showing entry for Cataract, congenital, cerulean type 1

General Disease Information
BXGD Id	BXGD007685
Disease Name	Cataract, congenital, cerulean type 1
Disease CUI Id	C0344523
MeSH Codes	C11
Disease Class Name	Eye Diseases
Semantic Type	Congenital Abnormality
Human Phenotype Ontology Id	HP:0000478
Human Phenotype Ontology Term	Abnormality of the eye
Disease Ontology Id	DOID:630   DOID:7
Disease Ontology Class Name	genetic disease; disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations