Showing entry for Maternal hyperphenylalaninemia


　 　 　 　 　 　 　 　 　 　 　 　 　 　 　 　
General Disease Information
BXGD IdBXGD020870
Disease NameMaternal hyperphenylalaninemia
Disease CUI IdC4022014
MeSH Codes   
Disease Class Name
Semantic TypeFinding
Human Phenotype Ontology Id HP:0001939   HP:0001197  
Human Phenotype Ontology TermAbnormality of metabolism/homeostasis; Abnormality of prenatal development or birth
Disease Ontology Id   
Disease Ontology Class Name
Disorder Network disorder-protein-compound-food associations