Showing entry for Congenital chloride diarrhea



                               
General Disease Information
BXGD IdBXGD005764
Disease NameCongenital chloride diarrhea
Disease CUI IdC0267662
MeSH Codes C23   C16   C18  
Disease Class NamePathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id DOID:630   DOID:7  
Disease Ontology Class Namegenetic disease; disease of anatomical entity
Disorder Network disorder-protein-compound-food associations