DiseaseID 919
良性复发性肝内胆汁淤积1型
disease
NCI2016_02D:A genetic syndrome affecting infants and children. It is characterized by chronic intrahepatic cholestasis usually progressing to cirrhosis within the first ten years of life.
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Formula: 6Herb: 4Symptom: 5Target: 23Links: 39
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 919
- Core Entity Id
- 1037
- Source Entity Count
- 1
- Preferred Name
- Cholestasis, Benign Recurrent Intrahepatic 1
- Name Cn
- 良性复发性肝内胆汁淤积1型
- Name Pinyin
- Liang Xing Fu Fa Xing Gan Nei Dan Zhi Yu Ji 1 Xing
- Name En
- Cholestasis, Benign Recurrent Intrahepatic 1
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Digestive System Diseases
- Do Class
- disease of anatomical entity; genetic disease
- Hpo Class
- Mesh Class Name
- Digestive System Diseases
- Hpo Class Name
- Do Class Name
- genetic disease; disease of anatomical entity
- Disease Definition
- NCI2016_02D:A genetic syndrome affecting infants and children. It is characterized by chronic intrahepatic cholestasis usually progressing to cirrhosis within the first ten years of life.
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Cholestasis, Benign Recurrent Intrahepatic 1
Role
preferred
Name
Cholestasis, Benign Recurrent Intrahepatic, 1
Role
preferred
Name
Cholestasis, Progressive Familial Intrahepatic, 1
Role
preferred
Name
Cholestasis, Progressive Familial Intrahepatic 1
Role
preferred
Name
BRIC1
Role
alias
Name
BYLER DISEASE
Role
alias
Name
Benign Recurrent Intrahepatic Cholestasis 1
Role
alias
Name
PFIC1
Role
alias
Name
Progressive Familial Intrahepatic Cholestasis 1
Role
alias
Name
SUMMERSKILL SYNDROME
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS027335HBDIS027336
Omim
211600243300
Umls
C0268312
Sym Map
SMDE03088SMDE03127
Do Class
DOID:630DOID:7
Dis Ge Net
C4551898C4551899
Umls Sty
T047
Me Sh Class
C06
Etcm Disease
Cholestasis, Benign Recurrent Intrahepatic, 1Cholestasis, Progressive Familial Intrahepatic, 1
Tcmbank Disease
1314928091
Itcmdb Generated
ITX-DISEASE-813563497CC1ITX-DISEASE-DCF319190850
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
01
Page Title
Disease Cholestasis, Benign Recurrent Intrahepatic, 1 Details pageDisease Cholestasis, Progressive Familial Intrahepatic, 1 Details page
Do Class Name
genetic disease; disease of anatomical entity
Disease Type
disease
Link Disease Id
3088.0
Do Disease Class
disease of anatomical entity; genetic disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Cholestasis, Benign Recurrent Intrahepatic, 1
Global Category
Cancer diseases;Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Gastrointestinal Diseases;Liver diseases
Disease Name
Cholestasis, Progressive Familial Intrahepatic, 1
Global Category
Cancer diseases;Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Gastrointestinal Diseases;Liver diseases
Disease Definition
NCI2016_02D:A genetic syndrome affecting infants and children. It is characterized by chronic intrahepatic cholestasis usually progressing to cirrhosis within the first ten years of life.
Me Sh Disease Class
Digestive System Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Digestive System Diseases
Umls Semantic Type Name
Disease or Syndrome