You are using an outdated browser. Please upgrade your browser to improve your experience.

Potter sequence

Disease Summary
Associated Targets (0)

Explore Associated Targets
Mondo Description 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.
Mondo Term and Equivalent IDs
MONDO:0001558:  Potter sequence
GARD:0004462: 
ICD10:Q60.6: 
NCIT:C40435: 
SCTID:41962002: 
UMLS:C0178426: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found