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An Entity of Type : owl:Class, within Data Space : linked.opendata.cz associated with source document(s)

AttributesValues
rdf:type
rdfs:label
  • Potter Syndrome
rdfs:subClassOf
Has_NICHD_Parent
Concept_In_Subset
Semantic_Type
  • Disease or Syndrome
Preferred_Name
  • Potter Syndrome
UMLS_CUI
  • C1609433
Contributing_Source
  • NICHD
Legacy_Concept_Name
  • Potter_Syndrome
FULL_SYN
  • Potter SyndromePTNCI
  • Oligohydramnios SequencePTNICHD
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
code
  • C40435
is someValuesFrom of
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