Showing entry for Night blindness, congenital stationary

General Disease Information
BXGD Id	BXGD007263
Disease Name	Night blindness, congenital stationary
Disease CUI Id	C0339535
MeSH Codes	C16   C11
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
Semantic Type	Congenital Abnormality
Human Phenotype Ontology Id	HP:0000478
Human Phenotype Ontology Term	Abnormality of the eye
Disease Ontology Id	DOID:7
Disease Ontology Class Name	disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations