Showing entry for Night blindness, congenital stationary, type 1



                               
General Disease Information
BXGD IdBXGD019030
Disease NameNight blindness, congenital stationary, type 1
Disease CUI IdC3501847
MeSH Codes C16   C11  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id   
Disease Ontology Class Name
Disorder Network disorder-protein-compound-food associations