Showing entry for Congenital dyserythropoietic anemia, type I



                               
General Disease Information
BXGD IdBXGD006281
Disease NameCongenital dyserythropoietic anemia, type I
Disease CUI IdC0271933
MeSH Codes C16   C15  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic 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