Showing entry for Congenital pontocerebellar hypoplasia



                               
General Disease Information
BXGD IdBXGD005677
Disease NameCongenital pontocerebellar hypoplasia
Disease CUI IdC0266468
MeSH Codes C10  
Disease Class NameNervous System Diseases
Semantic TypeCongenital Abnormality
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id DOID:7  
Disease Ontology Class Namedisease of anatomical entity
Disorder Network disorder-protein-compound-food associations