01
Diseases
Polycystic Kidney, Autosomal Dominant
polycystic kidney, autosomal dominant
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 8
Basic Information
Grouped by core information, identifiers, and descriptions.
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Core Information
- Disease Name
- Polycystic Kidney, Autosomal Dominant
- Standard Disease Name
- polycystic kidney, autosomal dominant
- MeSH Tree
- No data
- ICD-10
- Q61.2
Identifiers
- DO ID
- No data
- MeSH ID
- D016891
- OMIM ID
- 173900
- UMLS ID
- C0085413
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_NICHD_1602D:Polycystic kidney disease inherited in an autosomal dominant pattern.|NCI2016_02D:Polycystic kidney disease inherited in an autosomal dominant pattern. Symptoms usually appear at middle age and include abdominal pain, hematuria and high blood pressure. Patients may develop brain aneurysms and liver cysts.|MSH2017_2016_08_12:Kidney disorders with autosomal dominant inheritance and characterized by multiple CYSTS in both KIDNEYS with progressive deterioration of renal function.
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Related Targets
target disease8 Targets