DiseaseID 17192

X连锁易栓症,因子IX缺陷所致

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: 1Links: 1
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Record Fields

Scalar fields from the final disease record.

Disease Id
17192
Core Entity Id
75380
Source Entity Count
1
Preferred Name
Thrombophilia, X-Linked, Due To Factor Ix Defect
Name Cn
X连锁易栓症,因子IX缺陷所致
Name Pinyin
X Lian Suo Yi Shuan Zheng , Yin Zi Ix Que Xian Suo Zhi
Name En
Thrombophilia, X-Linked, Due To Factor Ix Defect
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
Suppressed
No

Names

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

Name
Thrombophilia, X-Linked, Due To Factor Ix Defect
Role
preferred
Name
DEEP VENOUS THROMBOSIS, PROTECTION AGAINST
Role
alias
Name
THPH8
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS019789
Omim
300807
Umls
C2749016C3275410
Sym Map
SMDE01360
Dis Ge Net
C2749016
Umls Sty
T047
Me Sh Class
C15C16
Tcmbank Disease
3256

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
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