Showing entry for Nonnuclear polymorphic congenital cataract

General Disease Information
BXGD Id	BXGD019969
Disease Name	Nonnuclear polymorphic congenital cataract
Disease CUI Id	C3888391
MeSH Codes
Disease Class Name
Semantic Type	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