疾病ID:TCMBANKDI021852

疾病名:Properdin Deficiency, Type III

MeSH_Name:Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases

HPO_Name:-

UMLS_Name:Disease or Syndrome

DO_Name:-

疾病类型:disease

DisGeNET_Link:C1839456

MeSH_Link:C16; C20

HPO_Link:-

UMLS_Link:T047

DO_Link:-

HERB_ID:HBDIS015758