DiseaseID 3465
出血倾向
group
MSH2017_2016_08_12:Hemorrhagic and thrombotic disorders that occur as a consequence of inherited abnormalities in blood coagulation.
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Disease: 1Symptom: 12Target: 12Links: 24
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 3465
- Core Entity Id
- 59672
- Source Entity Count
- 1
- Preferred Name
- Bleeding Tendency
- Name Cn
- 出血倾向
- Name Pinyin
- Chu Xie Qing Xiang
- Name En
- Bleeding Tendency
- Name Latin
- Bilingual Status
- complete
- Disease Type
- group
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- group
- Mesh Class
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic DiseasesHemic and Lymphatic Diseases
- Do Class
- disease of anatomical entitydisease of anatomical entity; genetic disease
- Hpo Class
- Abnormality of blood and blood-forming tissues
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic DiseasesHemic and Lymphatic Diseases
- Hpo Class Name
- Abnormality of blood and blood-forming tissues
- Do Class Name
- disease of anatomical entitygenetic disease; disease of anatomical entity
- Disease Definition
- MSH2017_2016_08_12:Hemorrhagic and thrombotic disorders that occur as a consequence of inherited abnormalities in blood coagulation.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Bleeding Tendency
Role
preferred
Name
Blood Coagulation Disorders, Inherited
Role
preferred
Name
Hemorrhagic Disorders
Role
preferred
Name
Abnormality Of Coagulation
Role
preferred
Name
Blood Coagulation Disorders
Role
preferred
Name
Abnormal Bleeding
Role
alias
Name
Abnormal Blood Clotting
Role
alias
Name
Abnormal Blood Coagulation Studies
Role
alias
Name
Abnormality of The Coagulation Cascade
Role
alias
Name
Bleeding Diathesis
Role
alias
Name
Blood Coagulation Disease
Role
alias
Name
Blood Coagulation Disorder
Role
alias
Name
Coagulation Abnormalities
Role
alias
Name
Coagulation Abnormality
Role
alias
Name
Coagulation Defect, Unspecified
Role
alias
Name
Coagulopathy
Role
alias
Name
Haemorrhagic Condition, Unspecified
Role
alias
Name
Haemorrhagic Disorders
Role
alias
Name
Hemorrhagic Diathesis
Role
alias
Name
Hemorrhagic Disease
Role
alias
Name
Inherited Blood Coagulation Disease
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0001892HP:0001928HP:0003256
Herb
HBDIS000350HBDIS001319HBDIS011851HBDIS014300HBDIS016356
Me Sh
D001778D006474D025861
Umls
C0005779C0019087C0852077
Icd10
D68.9D69.9
Sym Map
SMDE06497SMDE06498SMDE09344
Do Class
DOID:630DOID:7
Dis Ge Net
C0005779C0019087C0852077C1458140C1846821
Umls Sty
T033T046T047
Hpo Class
HP:0001871
Me Sh Class
C15C16
Tcmbank Disease
1827020137229353134558776558
Itcmdb Generated
ITX-DISEASE-2CCFD46002F5
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Do Class Name
disease of anatomical entitygenetic disease; disease of anatomical entity
Disease Type
groupphenotype
Hpo Class Name
Abnormality of blood and blood-forming tissues
Do Disease Class
disease of anatomical entitydisease of anatomical entity; genetic disease
Hpo Disease Class
Abnormality of blood and blood-forming tissues
Umls Disease Type
Disease or SyndromeFindingPathologic Function
Disease Definition
MSH2017_2016_08_12:Hemorrhagic and thrombotic disorders that occur as a consequence of inherited abnormalities in blood coagulation.MSH2017_2016_08_12:Spontaneous or near spontaneous bleeding caused by a defect in clotting mechanisms (BLOOD COAGULATION DISORDERS) or another abnormality causing a structural flaw in the blood vessels (HEMOSTATIC DISORDERS).|CSP2006:spontaneous or near spontaneous bleeding caused by a defect in clotting mechanisms (blood coagulation disorders) or another abnormality causing a structural flaw in the blood vessels (vascular hemostatic disorders).SNOMEDCT_US_2016_09_01:Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system|NCI2016_NICHD_1602D:A condition of abnormal blood clotting or bleeding.|NCI2016_02D:A condition in which there is a deviation from or interruption of the normal coagulation properties of the blood.|MSH2017_2016_08_12:Hemorrhagic and thrombotic disorders that occur as a consequence of abnormalities in blood coagulation due to a variety of factors such as COAGULATION PROTEIN DISORDERS; BLOOD PLATELET DISORDERS; BLOOD PROTEIN DISORDERS or nutritional conditions.|HPO2016_07_04:An abnormality of the coagulation cascade, which is comprised of the contact activation pathway (also known as the intrinsic pathway) and the tissue factor pathway (also known as the extrinsic pathway) as well as cofactors and regulators. [HPO:probinson]|CSP2006:condition in which there is a deviation from or interruption of the normal coagulation properties of the blood.
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic DiseasesHemic and Lymphatic Diseases
Dis Ge Net Disease Type
groupphenotype
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic DiseasesHemic and Lymphatic Diseases
Umls Semantic Type Name
Disease or SyndromeFindingPathologic Function