Potter Syndrome

Preferred Label : Potter Syndrome;

NCIt related terms : Potter's Sequence; Oligohydramnios Sequence;

NCIt definition : A rare, lethal congenital malformation characterized by bilateral renal agenesis and the absence or decreased volume of amniotic fluid (oligohydramnios). The presence of oligohydramnios gives rise to congenital anomalies that include hypoplastic lungs, lower extremities abnormalities, and characteristic facial features (low-set ears, widely separated eyes, nose flattening, and receding chin). Newborn infants usually die of respiratory failure.;

NCI Metathesaurus CUI : CL524121;

Détails

Origin ID

C40435;

UMLS CUI

C0178426;

Automatic exact mappings (from CISMeF team)
- Potter syndrome [PASCAL descriptor]
- Potter syndrome [ICD-11 More detail]
- Potter's syndrome [DO Concept]
Currated CISMeF NLP mapping
- Oligohydramnios sequence (disorder) [SNOMED CT concept]
- Potter's syndrome [ICD-10 Sub-category]
- Potter's syndrome [MedDRA Preferred Term]
- Potters syndrome [ICD-10 Sub-category (who)]
- bilateral renal agenesis [Disease (Nov.)]
- hereditary renal agenesis [MeSH Supplementary Concept]
- oligohydramnios sequence [SNOMED Notion]
DO Cross reference
- Potter's syndrome [DO Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Oligohydramnios sequence (disorder) [SNOMED CT concept]
- Potter's syndrome [ICD-10 Sub-category]
- Potter's syndrome [MedDRA Preferred Term]
- Potter's syndrome [DO Concept]
- oligohydramnios sequence [SNOMED Notion]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Neonatal Research Network Terminology [NCIt concept]
may_be_associated_disease_of_disease
- Juvenile Bilateral Ovarian Granulosa Cell Tumor [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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