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Potter sequence

^ http://purl.obolibrary.org/obo/MONDO_0001558

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. [ NCIT:P378 ]

Term info

database cross reference
  • SCTID:41962002 (MONDO:equivalentTo)
  • UMLS:C0178426 (MONDO:equivalentTo)
  • DOID:12594 (MONDO:equivalentTo)
  • GARD:0004462 (MONDO:equivalentTo)
  • NCIT:C40435 (MONDO:equivalentTo)
  • ICD10CM:Q60.6 (MONDO:equivalentTo)
Subsets

gard_rare

comment

Editor note: check for subtypes, relationship to OMIM:263200

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.

exactMatch

http://identifiers.org/snomedct/41962002, http://purl.obolibrary.org/obo/DOID_12594, http://purl.obolibrary.org/obo/NCIT_C40435, http://purl.bioontology.org/ontology/ICD10CM/Q60.6, http://linkedlifedata.com/resource/umls/id/C0178426

has exact synonym

oligohydramnios sequence, Potter's sequence, Potter's syndrome, Potter syndrome

id

MONDO:0001558