Autosomal recessive hereditary disorder	Developmental hereditary disorder	Hereditary nephropathy	Left renal agenesis	Right renal agenesis
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Oligohydramnios sequence (disorder)
	Oligohydramnios sequence
	BRA - Bilateral renal agenesis Potter's anomaly of the kidney Bilateral congenital absence of kidneys Potter syndrome Renofacial syndrome Renal agenesis syndrome Congenital absence of kidneys syndrome
	Potter-syndroom
	syndroom van Potter renofaciale dysplasie
	syndroom van Potter
	Zeldzame aangeboren aandoening met als voornaamste kenmerken afwezigheid van nierweefsel en ernstige misvorming van de nieren, karakteristieke gelaatskenmerken en niet goed ontwikkelde longen.

Id	41962002
Status	Primitive

Associated morphology	Agenesis
Finding site	Entire right kidney
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Agenesis
Finding site	Entire left kidney
Occurrence	Congenital
Pathological process	Pathological developmental process

PALGA thesaurus simple reference set for pathology

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	Q60.6
Rule	TRUE
Advice	ALWAYS Q60.6
Correlation	SNOMED CT source code to target map code correlation not specified

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Oligohydramnios sequence in pregnancy