Potter sequence https://www.malacards.org/card/potters_syndrome Potter syndrome Potter's sequence NANDO:2200157 Editor note: check for subtypes, relationship to OMIM:263200 MONDO:0001558 ICD10CM:Q60.6 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:C40435 Potter's syndrome oligohydramnios sequence MEDGEN:472617 UMLS:C0178426 SCTID:41962002 DOID:12594 syndromic disease oligohydramnios bilateral renal agenesis