Polycystic kidney, adult type

Preferred Label : Polycystic kidney, adult type;

Inclusion CIM-10 : Polycystic kidney, autosomal dominant;

Diag associé à un acte (%) : 86.5;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

Q612;

UMLS CUI

C0085413;

Currated CISMeF NLP mapping
- Autosomal Dominant Polycystic Kidney Disease [NCIt concept]
- Autosomal dominant polycystic kidney disease [ICD-11 Category]
- Autosomal dominant polycystic kidney disease [ORDO Disease]
- Autosomal dominant polycystic kidney disease (disorder) [SNOMED CT concept]
- Polycystic kidney disease 1 with or without polycystic liver disease [OMIM Phenotype]
- Polycystic kidney disease, adult type (disorder) [Inactive SNOMED CT concept]
- Polycystic kidney, adult type [ICD-10 Sub-category (who)]
- Polycystic kidney, autosomal dominant [MedDRA LLT]
- Polycystic kidney, autosomal dominant [ICD-9 code]
- autosomal dominant polycystic kidney disease [Disease (Nov.)]
- autosomal dominant polycystic kidney disease [DO Concept]
- polycystic kidney, autosomal dominant [MeSH concept]
- polycystic kidney, autosomal dominant [MeSH Descriptor]
Excluded by
- Renal dysplasia [ICD-10 Sub-category]
Orphanet concepts
- Autosomal dominant polycystic kidney disease [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal Dominant Polycystic Kidney Disease [NCIt concept]
- Autosomal dominant polycystic kidney disease (disorder) [SNOMED CT concept]
- Polycystic kidney disease, adult type (disorder) [Inactive SNOMED CT concept]
- Polycystic kidney, autosomal dominant [MedDRA LLT]
- Polycystic kidney, autosomal dominant [ICD-9 code]
- polycystic kidney disease, adult type [SNOMED Notion]
- polycystic kidney, autosomal dominant [MeSH Descriptor]
- polycystic kidney, autosomal dominant [MeSH concept]

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