DiseaseID 17739

补体C1S缺乏症

disease

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Relationship Network

Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.

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Disease: 1Target: 2Links: 2
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Record Fields

Scalar fields from the final disease record.

Disease Id
17739
Core Entity Id
76024
Source Entity Count
1
Preferred Name
Complement Component C1S Deficiency
Name Cn
补体C1S缺乏症
Name Pinyin
Bu Ti C1s Que Fa Zheng
Name En
Complement Component C1S Deficiency
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Immune System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Do Class
Hpo Class
Mesh Class Name
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases
Hpo Class Name
Do Class Name
Disease Definition
Version
v1
Suppressed
No

Names

Preferred names, aliases, and source labels retained in the final schema.

Name
Complement Component C1S Deficiency
Role
preferred
Name
C1SD
Role
alias
Name
C1s DEFICIENCY
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS020759
Omim
613783
Umls
C3151078
Sym Map
SMDE02035
Dis Ge Net
C3151078
Umls Sty
T047
Me Sh Class
C16C20
Tcmbank Disease
3743

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
Suppress
0
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Me Sh Disease Class
Immune System 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; Immune System Diseases
Umls Semantic Type Name
Disease or Syndrome