DiseaseID 3977
因子X缺乏症
disease
MSH2017_2016_08_12:Blood coagulation disorder usually inherited as an autosomal recessive trait, though it can be acquired. It is characterized by defective activity in both the intrinsic and extrinsic pathways, impaired
Relationship Network
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Disease: 1Formula: 21Herb: 4Symptom: 4Target: 16Links: 53
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 3977
- Core Entity Id
- 60255
- Source Entity Count
- 1
- Preferred Name
- Factor X Deficiency
- Name Cn
- 因子X缺乏症
- Name Pinyin
- Yin Zi X Que Fa Zheng
- Name En
- Factor X Deficiency
- 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
- disease 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 Diseases
- Hpo Class Name
- Abnormality of blood and blood-forming tissues
- Do Class Name
- genetic disease; disease of anatomical entity
- Disease Definition
- MSH2017_2016_08_12:Blood coagulation disorder usually inherited as an autosomal recessive trait, though it can be acquired. It is characterized by defective activity in both the intrinsic and extrinsic pathways, impaired thromboplastin time, and impaired prothrombin consumption.
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Factor X Deficiency
Role
preferred
Name
Reduced Factor X Activity
Role
preferred
Name
Decreased Factor X Activity
Role
alias
Name
F10 DEFICIENCY
Role
alias
Name
STUART-PROWER FACTOR DEFICIENCY
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0008321
Herb
HBDIS001031HBDIS024656
Me Sh
D005171
Omim
227600
Umls
C0015519
Sym Map
SMDE02623
Do Class
DOID:630DOID:7
Dis Ge Net
C0015519C4024702
Umls Sty
T033T047
Hpo Class
HP:0001871
Me Sh Class
C15C16
Etcm Disease
Factor X Deficiency
Tcmbank Disease
200222194629433
Itcmdb Generated
ITX-DISEASE-320B4C153836ITX-DISEASE-C247294C54EB
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Page Title
Disease Factor X Deficiency Details page
Do Class Name
genetic disease; disease of anatomical entity
Disease Type
diseasephenotype
Hpo Class Name
Abnormality of blood and blood-forming tissues
Do Disease Class
disease of anatomical entity; genetic disease
Hpo Disease Class
Abnormality of blood and blood-forming tissues
Umls Disease Type
Disease or SyndromeFinding
Basic Information
Disease Name
Factor X Deficiency
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Blood diseases
Disease Definition
MSH2017_2016_08_12:Blood coagulation disorder usually inherited as an autosomal recessive trait, though it can be acquired. It is characterized by defective activity in both the intrinsic and extrinsic pathways, impaired thromboplastin time, and impaired prothrombin consumption.
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Dis Ge Net Disease Type
diseasephenotype
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Umls Semantic Type Name
Disease or SyndromeFinding