oligohydramnios sequence

Preferred Label : oligohydramnios sequence;

Origin ID

D4-01551;

UMLS CUI

C0178426;

Automatic exact mappings (from CISMeF team)
- Potter syndrome [PASCAL descriptor]
- Potter syndrome [ICD-11 More detail]
Currated CISMeF NLP mapping
- Oligohydramnios sequence (disorder) [SNOMED CT concept]
- Potter Syndrome [NCIt concept]
- Potter's syndrome [ICD-10 Sub-category]
- Potter's syndrome [MedDRA Preferred Term]
- Potters syndrome [ICD-10 Sub-category (who)]
ICD-10 exact mapping(s)
- Potters syndrome [ICD-10 Sub-category (who)]
Metaterm(s)
- pediatrics [CISMeF Metaterm]
Référence SNOMED
- both kidneys [SNOMED Notion]
- congenital absence, nos [SNOMED Notion]
SNOMED CT concept
- Oligohydramnios sequence (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Oligohydramnios sequence (disorder) [SNOMED CT concept]
- Potter Syndrome [NCIt concept]
- Potter's syndrome [MedDRA Preferred Term]
- Potter's syndrome [ICD-10 Sub-category]
- Potter's syndrome [DO Concept]