Showing entry for Hypoplasia of optic disc



                               
General Disease Information
BXGD IdBXGD012251
Disease NameHypoplasia of optic disc
Disease CUI IdC1298695
MeSH Codes C16   C11   C10  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases
Semantic TypeCongenital Abnormality
Human Phenotype Ontology Id HP:0000478  
Human Phenotype Ontology TermAbnormality of the eye
Disease Ontology Id   
Disease Ontology Class Name
Disorder Network disorder-protein-compound-food associations