DiseaseID 7860
遗传性因子X缺乏症
disease
NCI2016_02D:A rare autosomal recessive inherited blood coagulation disorder characterized by deficiency of factor X, resulting in bleeding.
Relationship Network
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Disease: 1Symptom: 3Target: 12Links: 15
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 7860
- Core Entity Id
- 64727
- Source Entity Count
- 1
- Preferred Name
- Hereditary Factor X Deficiency Disease
- Name Cn
- 遗传性因子X缺乏症
- Name Pinyin
- Yi Chuan Xing Yin Zi X Que Fa Zheng
- Name En
- Hereditary Factor X Deficiency Disease
- 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
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
- Hpo Class Name
- Do Class Name
- Disease Definition
- NCI2016_02D:A rare autosomal recessive inherited blood coagulation disorder characterized by deficiency of factor X, resulting in bleeding.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Hereditary Factor X Deficiency Disease
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS006764
Umls
C0272327
Sym Map
SMDE09417
Dis Ge Net
C0272327
Umls Sty
T047
Me Sh Class
C15C16
Tcmbank Disease
20576
Itcmdb Generated
ITX-DISEASE-5236812C31FD
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disease Definition
NCI2016_02D:A rare autosomal recessive inherited blood coagulation disorder characterized by deficiency of factor X, 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