DiseaseID 4315
低凝血酶原血症
disease
MSH2017_2016_08_12:Absence or reduced levels of PROTHROMBIN in the blood.|CSP2006:absence or reduced levels of prothrombin in the blood.
Relationship Network
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Disease: 1Symptom: 7Target: 1Links: 8
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 4315
- Core Entity Id
- 60645
- Source Entity Count
- 1
- Preferred Name
- Hypoprothrombinemias
- Name Cn
- 低凝血酶原血症
- Name Pinyin
- Di Ning Xue Mei Yuan Xue Zheng
- Name En
- Hypoprothrombinemias
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
- Do Class
- genetic disease
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
- Hpo Class Name
- Do Class Name
- genetic disease
- Disease Definition
- MSH2017_2016_08_12:Absence or reduced levels of PROTHROMBIN in the blood.|CSP2006:absence or reduced levels of prothrombin in the blood.
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Hypoprothrombinemias
Role
preferred
Name
Hereditary Factor Ii Deficiency Disease
Role
preferred
Name
Inherited Factor Ii Deficiency
Role
preferred
Name
Prothrombin Deficiency, Congenital
Role
preferred
Name
DYSPROTHROMBINEMIA
Role
alias
Name
HYPOPROTHROMBINEMIA
Role
alias
Name
Prothrombin Deficiency
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS001501HBDIS006759HBDIS027821
Me Sh
D007020
Omim
613679
Umls
C0020640C0272317
Sym Map
SMDE03805SMDE09416SMDE09927
Do Class
DOID:630
Dis Ge Net
C0020640C0272317C4722227
Umls Sty
T047
Me Sh Class
C15C16
Tcmbank Disease
19279196924329
Itcmdb Generated
ITX-DISEASE-01BE1129712C
Attributes
Merged source attributes and domain-specific metadata.
Version
v1v2
Suppress
0
Do Class Name
genetic disease
Disease Type
disease
Do Disease Class
genetic disease
Umls Disease Type
Disease or Syndrome
Disease Definition
MSH2017_2016_08_12:Absence or reduced levels of PROTHROMBIN in the blood.|CSP2006:absence or reduced levels of prothrombin in the blood.NCI2016_02D:A very rare autosomal recessive inherited blood coagulation disorder characterized by deficiency of prothrombin, resulting in bleeding.
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Umls Semantic Type Name
Disease or Syndrome