Potter sequence
MONDO:0001558Mondo
Findings
No curated finding names Potter sequence yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
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.
Definition from the Mondo Disease Ontology (MONDO:0001558), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
Other names
4 names
Resolves to: Potter sequence
- Also called
- oligohydramnios sequencePotter syndromePotter's sequencePotter's syndrome