DiseaseID 3697
多囊肾病5型
disease
Autosomal recessive polycystic kidney disease (ARPKD) is an inherited disorder characterised by the development of cysts affecting the collecting ducts. It is frequently associated with hepatic involv
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Disease: 1Symptom: 2Target: 12Links: 14
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 3697
- Core Entity Id
- 59934
- Source Entity Count
- 1
- Preferred Name
- Polycystic Kidney Disease 5
- Name Cn
- 多囊肾病5型
- Name Pinyin
- Duo Nang Shen Bing 5 Xing
- Name En
- Polycystic Kidney Disease 5
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Digestive System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Pathological Conditions, Signs and SymptomsMale Urogenital Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications
- Do Class
- disease of anatomical entity; genetic disease
- Hpo Class
- Abnormality of the digestive system
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital DiseasesPathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases
- Hpo Class Name
- Abnormality of the digestive system
- Do Class Name
- genetic disease; disease of anatomical entity
- Disease Definition
- Autosomal recessive polycystic kidney disease (ARPKD) is an inherited disorder characterised by the development of cysts affecting the collecting ducts. It is frequently associated with hepatic involv
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Polycystic Kidney Disease 5
Role
preferred
Name
Autosomal Recessive Polycystic Kidney Disease
Role
preferred
Name
Hepatic Fibrosis, Congenital
Role
preferred
Name
Congenital Hepatic Fibrosis
Role
alias
Name
Excessive Buildup of Connective Tissue And Scarring of Liver At Birth
Role
alias
Name
Polycystic Kidney Disease 4
Role
alias
Name
Polycystic Kidney Disease 4 With Or Without Polycystic Liver Disease
Role
alias
Name
Polycystic Kidney Disease, Autosomal Recessive
Role
alias
Name
Polycystic Kidney, Autosomal Recessive
Role
alias
Name
Polycystic Kidney, Infantile Type
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0002612
Herb
HBDIS000643HBDIS003302HBDIS030024
Me Sh
D017044
Omim
263200617610
Umls
C0085548
Icd10
Q61.1
Med Dra
10036047
Sym Map
SMDE00280
Do Class
DOID:630DOID:7
Dis Ge Net
C0009714C0085548C4539903
Orphanet
731
Umls Sty
T047
Hpo Class
HP:0025031
Me Sh Class
C06C12C13C16C23
Tcmbank Disease
2732229813
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Do Class Name
genetic disease; disease of anatomical entity
Disease Type
disease
Hpo Class Name
Abnormality of the digestive system
Do Disease Class
disease of anatomical entity; genetic disease
Hpo Disease Class
Abnormality of the digestive system
Umls Disease Type
Disease or Syndrome
Disease Definition
Autosomal recessive polycystic kidney disease (ARPKD) is an inherited disorder characterised by the development of cysts affecting the collecting ducts. It is frequently associated with hepatic involv
Me Sh Disease Class
Digestive System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Pathological Conditions, Signs and SymptomsMale Urogenital Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital DiseasesPathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases
Umls Semantic Type Name
Disease or Syndrome