疾病ID:TCMBANKDI004388

疾病名:Dysfibrinogenemia, Congenital

MeSH_Name:Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases

HPO_Name:-

UMLS_Name:Disease or Syndrome

DO_Name:genetic disease; disease of anatomical entity

疾病类型:disease

DisGeNET_Link:C0272350

MeSH_Link:C16; C15

HPO_Link:-

UMLS_Link:T047

DO_Link:DOID:630; DOID:7

HERB_ID:-