Showing entry for Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant



                               
General Disease Information
BXGD IdBXGD017516
Disease NameAutoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant
Disease CUI IdC2717884
MeSH Codes C16   C20   C15  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id   
Disease Ontology Class Name
Disorder Network disorder-protein-compound-food associations