DiseaseID 170
凝血因子XI缺乏症
disease
NCI2016_02D:A rare inherited bleeding disorder caused by deficiency of coagulation factor XI. It may be asymptomatic or manifest with bleeding.|MSH2017_2016_08_12:A hereditary deficiency of blood coagulation factor XI (a
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
Click a node to open it in a new tab
Disease: 1Formula: 4Symptom: 5Target: 18Links: 33
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 170
- Core Entity Id
- 193
- Source Entity Count
- 1
- Preferred Name
- Factor Xi Deficiency
- Name Cn
- 凝血因子XI缺乏症
- Name Pinyin
- Ning Xue Yin Zi Xi Que Fa Zheng
- Name En
- Factor XI Deficiency
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Do Class
- Hpo Class
- Mesh Class Name
- Hpo Class Name
- Do Class Name
- Disease Definition
- NCI2016_02D:A rare inherited bleeding disorder caused by deficiency of coagulation factor XI. It may be asymptomatic or manifest with bleeding.|MSH2017_2016_08_12:A hereditary deficiency of blood coagulation factor XI (also known as plasma thromboplastin antecedent or PTA or antihemophilic factor C) resulting in a systemic blood-clotting defect called hemophilia C or Rosenthal's syndrome, that may resemble classical hemophilia.|HPO2016_07_04:Decreased activity of coagulation factor XI. Factor XI, also known as plasma thromboplastin antecedent, is a serine proteinase that activates factor IX. [HPO:probinson]
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Factor Xi Deficiency
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS026466
Umls
C0015523
Sym Map
SMDE02497
Dis Ge Net
C4321502
Umls Sty
T047
Etcm Disease
Factor Xi Deficiency
Tcmbank Disease
5776
Itcmdb Generated
ITX-DISEASE-58AA9F3A2DFD
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Page Title
Disease Factor Xi Deficiency Details page
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Factor Xi Deficiency
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Blood diseases;Immune diseases
Disease Definition
NCI2016_02D:A rare inherited bleeding disorder caused by deficiency of coagulation factor XI. It may be asymptomatic or manifest with bleeding.|MSH2017_2016_08_12:A hereditary deficiency of blood coagulation factor XI (also known as plasma thromboplastin antecedent or PTA or antihemophilic factor C) resulting in a systemic blood-clotting defect called hemophilia C or Rosenthal's syndrome, that may resemble classical hemophilia.|HPO2016_07_04:Decreased activity of coagulation factor XI. Factor XI, also known as plasma thromboplastin antecedent, is a serine proteinase that activates factor IX. [HPO:probinson]
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Disease or Syndrome