DiseaseID 26811
凝血因子V和凝血因子Ⅷ联合缺乏症1
Factor V And Factor Viii, Combined Deficiency Of, 1
SNOMEDCT_US_2016_09_01:An inherited bleeding disorder caused by the reduction in activity and antigen levels of both factor V and factor VIII with manifestation of mild-to-moderate bleeding symptoms. Caused by mutations
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: 1Target: 2Links: 2
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 26811
- Core Entity Id
- 119379
- Source Entity Count
- 1
- Preferred Name
- Factor V And Factor Viii, Combined Deficiency Of, 1
- Name Cn
- 凝血因子V和凝血因子Ⅷ联合缺乏症1
- Name Pinyin
- Ning Xue Yin Zi V He Ning Xue Yin Zi Ⅷ Lian He Que Fa Zheng 1
- Name En
- Factor V And Factor Viii, Combined Deficiency Of, 1
- Name Latin
- Bilingual Status
- complete
- Disease Type
- Umls Disease Type
- Disgenet Type
- Mesh Class
- Do Class
- Hpo Class
- Mesh Class Name
- Hpo Class Name
- Do Class Name
- Disease Definition
- SNOMEDCT_US_2016_09_01:An inherited bleeding disorder caused by the reduction in activity and antigen levels of both factor V and factor VIII with manifestation of mild-to-moderate bleeding symptoms. Caused by mutations either in the LMAN1 gene (chromosome 18; q21) or in the MCFD2 gene (chromosome 2). Transmission is autosomal recessive.
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Factor V And Factor Viii, Combined Deficiency Of, 1
Role
preferred
Source
SymMap_v2
Preferred
Yes
Cross References
Trusted external identifiers retained for this final record.
Umls
C1856883
Sym Map
SMDE05103
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Disease Definition
SNOMEDCT_US_2016_09_01:An inherited bleeding disorder caused by the reduction in activity and antigen levels of both factor V and factor VIII with manifestation of mild-to-moderate bleeding symptoms. Caused by mutations either in the LMAN1 gene (chromosome 18; q21) or in the MCFD2 gene (chromosome 2). Transmission is autosomal recessive.