Showing entry for Congenital absence of thymus



                               
General Disease Information
BXGD IdBXGD009825
Disease NameCongenital absence of thymus
Disease CUI IdC0685894
MeSH Codes C20  
Disease Class NameImmune System Diseases
Semantic TypeCongenital Abnormality
Human Phenotype Ontology Id HP:0000818   HP:0002715   HP:0001626  
Human Phenotype Ontology TermAbnormality of the endocrine system; Abnormality of the immune system; Abnormality of the cardiovascular system
Disease Ontology Id DOID:630   DOID:7  
Disease Ontology Class Namegenetic disease; disease of anatomical entity
Disorder Network disorder-protein-compound-food associations