DiseaseID 11118

香豆素耐药

phenotype

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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: 1Herb: 10Symptom: 1Target: 19Links: 35
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Record Fields

Scalar fields from the final disease record.

Disease Id
11118
Core Entity Id
68415
Source Entity Count
1
Preferred Name
Coumarin Resistance
Name Cn
香豆素耐药
Name Pinyin
Xiang Dou Su Nai Yao
Name En
Coumarin Resistance
Name Latin
Bilingual Status
complete
Disease Type
phenotype
Umls Disease Type
Disease or Syndrome
Disgenet Type
phenotype
Mesh Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Do Class
Hpo Class
Mesh Class Name
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic 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
Coumarin Resistance
Role
preferred
Name
Coumarin Sensitivity
Role
preferred
Name
COUMARIN, POOR METABOLISM OF
Role
alias
Name
WARFARIN RESISTANCE
Role
alias
Name
WARFARIN SENSITIVITY
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS011067HBDIS019408
Omim
122700
Umls
C0750384C2608079C2675747
Sym Map
SMDE03195
Dis Ge Net
C0750384C2675747
Umls Sty
T047
Me Sh Class
C16C18
Etcm Disease
Coumarin Resistance
Tcmbank Disease
199228236
Itcmdb Generated
ITX-DISEASE-87393B7B741BITX-DISEASE-99253FF26DD9

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
Suppress
0
Page Title
Disease Coumarin Resistance Details page
Disease Type
phenotype
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Coumarin Resistance
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Blood diseases;Cardiovascular diseases
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Dis Ge Net Disease Type
phenotype
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Umls Semantic Type Name
Disease or Syndrome