Showing entry for Congenital absence of part of brain



                               
General Disease Information
BXGD IdBXGD005673
Disease NameCongenital absence of part of brain
Disease CUI IdC0266461
MeSH Codes C16  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities
Semantic TypeCongenital Abnormality
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id DOID:630   DOID:7   DOID:225   DOID:150   DOID:0080015  
Disease Ontology Class Namegenetic disease; disease of anatomical entity; syndrome; disease of mental health; physical disorder
Disorder Network disorder-protein-compound-food associations