DiseaseID 16364
C1酯酶抑制物活性正常的遗传性血管性水肿
disease
SNOMEDCT_US_2016_09_01:Hereditary angioedema without abnormal C1 inhibitor levels or function. Found mostly in females in which symptoms may be triggered by pregnancy or estrogen-containing oral contraceptives. A few cas
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Disease: 1Symptom: 2Target: 1Links: 3
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 16364
- Core Entity Id
- 74429
- Source Entity Count
- 1
- Preferred Name
- Hereditary Angioedema With Normal C1 Esterase Inhibitor Activity
- Name Cn
- C1酯酶抑制物活性正常的遗传性血管性水肿
- Name Pinyin
- C1 Zhi Mei Yi Zhi Wu Huo Xing Zheng Chang De Yi Chuan Xing Xue Guan Xing Shui Zhong
- Name En
- Hereditary Angioedema With Normal C1 Esterase Inhibitor Activity
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Cardiovascular Diseases; Immune System Diseases; Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
- Do Class
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases; Cardiovascular Diseases
- Hpo Class Name
- Do Class Name
- Disease Definition
- SNOMEDCT_US_2016_09_01:Hereditary angioedema without abnormal C1 inhibitor levels or function. Found mostly in females in which symptoms may be triggered by pregnancy or estrogen-containing oral contraceptives. A few cases have been associated with gain of function mutations of coagulation factor XII
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Hereditary Angioedema With Normal C1 Esterase Inhibitor Activity
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS018617
Umls
C1960459
Sym Map
SMDE09407
Dis Ge Net
C1960459
Umls Sty
T047
Me Sh Class
C14C16C17C20
Tcmbank Disease
14030
Itcmdb Generated
ITX-DISEASE-449DA2474749
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disease Definition
SNOMEDCT_US_2016_09_01:Hereditary angioedema without abnormal C1 inhibitor levels or function. Found mostly in females in which symptoms may be triggered by pregnancy or estrogen-containing oral contraceptives. A few cases have been associated with gain of function mutations of coagulation factor XII
Me Sh Disease Class
Cardiovascular Diseases; Immune System Diseases; Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases; Cardiovascular Diseases
Umls Semantic Type Name
Disease or Syndrome