DiseaseID 16993

蛋白C缺乏所致血栓形成倾向,常染色体隐性遗传

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: 1Symptom: 3Target: 2Links: 5
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Record Fields

Scalar fields from the final disease record.

Disease Id
16993
Core Entity Id
75150
Source Entity Count
1
Preferred Name
Thrombophilia Due To Protein C Deficiency, Autosomal Recessive
Name Cn
蛋白C缺乏所致血栓形成倾向,常染色体隐性遗传
Name Pinyin
Dan Bai C Que Fa Suo Zhi Xue Shuan Xing Cheng Qing Xiang , Chang Ran Se Ti Yin Xing Yi Chuan
Name En
Thrombophilia Due To Protein C Deficiency, Autosomal Recessive
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
Version
v1,v2
Suppressed
No

Names

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

Name
Thrombophilia Due To Protein C Deficiency, Autosomal Recessive
Role
preferred
Name
Thrombophilia, Hereditary, Due To Protein C Deficiency, Autosomal Recessive
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS019457
Omim
612304
Umls
C2676759
Sym Map
SMDE02724
Dis Ge Net
C2676759
Umls Sty
T047
Me Sh Class
C15C16
Tcmbank Disease
26692

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0
Disease Type
disease
Umls Disease Type
Disease or Syndrome
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