DiseaseID 14040

尿激肽释放酶活性降低

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: 1Target: 2Links: 2
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Record Fields

Scalar fields from the final disease record.

Disease Id
14040
Core Entity Id
71769
Source Entity Count
1
Preferred Name
Kallikrein, Decreased Urinary Activity Of
Name Cn
尿激肽释放酶活性降低
Name Pinyin
Niao Ji Tai Shi Fang Mei Huo Xing Jiang Di
Name En
Kallikrein, Decreased Urinary Activity Of
Name Latin
Bilingual Status
complete
Disease Type
phenotype
Umls Disease Type
Finding
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
Suppressed

Names

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

Name
Kallikrein, Decreased Urinary Activity Of
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS015347
Omim
615953
Dis Ge Net
C1835808
Umls Sty
T033
Me Sh Class
C16C18
Tcmbank Disease
31060

Attributes

Merged source attributes and domain-specific metadata.

Disease Type
phenotype
Umls Disease Type
Finding
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
Finding