congenital cystic kidney disease

Preferred Label : congenital cystic kidney disease;

Synonyme SNOMED : Polykystome rénal; Rein en éponge; Polykystose rénale; Rein polykystique;

Details

Origin ID

D4-71300;

UMLS CUI

C0311245;

Automatic exact mappings (from CISMeF team)
- Hereditary or congenital cystic or dysplastic kidney disease, inheritance unknown [Vue CIM-11]
- Medullary cystic kidney [ICD-10 Sub-category (who)]
- Medullary sponge kidney [ORDO Disease]
- Medullary sponge kidney [MedDRA LLT]
- Polycystic kidney, unspecified [ICD-10 Sub-category (who)]
- kidney, polycystic [MeSH concept]
- medullary sponge kidney [MeSH Descriptor]
- medullary sponge kidney [MeSH concept]
Currated CISMeF NLP mapping
- Congenital cystic kidney disease [MedDRA Preferred Term]
- Congenital cystic kidney disease (disorder) [SNOMED CT concept]
- Cystic kidney disease [ICD-9 code]
- polycystic kidney diseases [MeSH concept]
- polycystic kidney diseases [MeSH Descriptor]
ICD-10 exact mapping(s)
- Polycystic kidney, unspecified [ICD-10 Sub-category (who)]
Manual NTBT mappings (CISMeF)
- Non-syndromic renal or urinary tract malformation [ORDO Disease]
Metaterm(s)
- nephrology [CISMeF Metaterm]
- pediatrics [CISMeF Metaterm]
- urology [CISMeF Metaterm]
Référence SNOMED
- congenital cavitation, nos [SNOMED Notion]
- kidney, nos [SNOMED Notion]
SNOMED CT concept
- Congenital cystic kidney disease (disorder) [SNOMED CT concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital cystic kidney disease [MedDRA Preferred Term]
- Congenital cystic kidney disease (disorder) [SNOMED CT concept]
- Cystic kidney disease [ICD-9 code]
- Cystic kidney disease, unspecified [ICD-9 code]
- Meckel syndrome [DO Concept]

Keyword's position in hierarchy(ies) :

Main resources

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