Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
Click a node to open it in a new tab
Disease: 1Formula: 5Herb: 1Symptom: 1Target: 17Links: 31
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 7577
- Core Entity Id
- 64394
- Source Entity Count
- 1
- Preferred Name
- Enterokinase Deficiency
- Name Cn
- 肠激酶缺乏症
- Name Pinyin
- Chang Ji Mei Que Fa Zheng
- Name En
- Enterokinase Deficiency
- 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; 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,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Enterokinase Deficiency
Role
preferred
Name
ENTEROPEPTIDASE DEFICIENCY
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS006305
Omim
226200
Umls
C0268416
Sym Map
SMDE03530
Dis Ge Net
C0268416
Umls Sty
T047
Me Sh Class
C16C18
Etcm Disease
Enterokinase Deficiency
Tcmbank Disease
27995
Itcmdb Generated
ITX-DISEASE-E5BFC8276AFA
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Page Title
Disease Enterokinase Deficiency Details page
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Enterokinase Deficiency
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Endocrine diseases;Gastrointestinal Diseases
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Umls Semantic Type Name
Disease or Syndrome