DiseaseID 3979
遗传性因子XIII缺乏症
disease
HPO2016_07_04:Deficiency of factor XIII subunit A, leading to a reduced factor XIII activity. Activated Factor XIII cross-links fibrin polymers solidifying the clot. []
Relationship Network
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Disease: 1Herb: 1Symptom: 2Target: 19Links: 27
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 3979
- Core Entity Id
- 60257
- Source Entity Count
- 1
- Preferred Name
- Hereditary Factor Xiii Deficiency
- Name Cn
- 遗传性因子XIII缺乏症
- Name Pinyin
- Yi Chuan Xing Yin Zi Xiii Que Fa Zheng
- Name En
- Hereditary Factor Xiii 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
- HPO2016_07_04:Deficiency of factor XIII subunit A, leading to a reduced factor XIII activity. Activated Factor XIII cross-links fibrin polymers solidifying the clot. []
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Hereditary Factor Xiii Deficiency
Role
preferred
Name
Factor Xiii, A Subunit, Deficiency Of
Role
preferred
Name
Factor Xiii, B Subunit, Deficiency Of
Role
preferred
Name
Factor Xiii Deficiency
Role
alias
Name
Factor Xiii Subunit A Deficiency
Role
alias
Name
Factor Xiii Subunit B Deficiency
Role
alias
Name
Reduced Factor Xiii, Subunit A
Role
alias
Name
Reduced Factor Xiii, Subunit B
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0040233HP:0040234
Herb
HBDIS001034HBDIS019872HBDIS019874
Me Sh
D005177
Omim
613225613235
Umls
C2750481C2750514
Sym Map
SMDE02521SMDE03238
Do Class
DOID:630DOID:7
Dis Ge Net
C0015530C2750481C2750514
Umls Sty
T033T047
Hpo Class
HP:0001871
Me Sh Class
C15C16
Etcm Disease
Factor Xiii, B Subunit, Deficiency ofFactor Xiii, a Subunit, Deficiency of
Tcmbank Disease
13444292373592
Itcmdb Generated
ITX-DISEASE-304489C84B5BITX-DISEASE-D789B90B6908
Attributes
Merged source attributes and domain-specific metadata.
Version
v1v1,v2
Suppress
0
Page Title
Disease Factor Xiii, B Subunit, Deficiency of Details pageDisease Factor Xiii, a Subunit, Deficiency of Details page
Do Class Name
genetic disease; disease of anatomical entity
Disease Type
disease
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 Xiii, B Subunit, Deficiency of
Global Category
Genetic diseases
Anatomical Category
Blood diseases
Disease Name
Factor Xiii, a Subunit, Deficiency of
Global Category
Genetic diseases
Anatomical Category
Blood diseases
Disease Definition
HPO2016_07_04:Deficiency of factor XIII subunit A, leading to a reduced factor XIII activity. Activated Factor XIII cross-links fibrin polymers solidifying the clot. []HPO2016_07_04:Deficiency of factor XIII subunit B, leading to a reduced factor XIII activity. Activated Factor XIII cross-links fibrin polymers solidifying the clot. []
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 SyndromeFinding