OMOP Concept 201675
Polycystic kidney disease, infantile type
StandardConditionSNOMED28770003Disorder
Maps from
16
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
16 source codes normalize to Polycystic kidney disease, infantile type via the OMOP "Maps to" relationship.
Synonyms
Alternative names recorded for Polycystic kidney disease, infantile type across source vocabularies.
- ARPKD - Autosomal recessive polycystic kidney disease
- Autosomal recessive infantile polycystic kidney disease
- Autosomal recessive polycystic kidney disease
- enfermedad poliquística del riñón, tipo infantil
- enfermedad renal poliquística, forma autosómica recesiva
- Infantile polycystic kidney disease
- IPKD - Infantile polycystic kidney disease
- poliquistosis renal, tipo infantil
- poliquistosis renal, tipo infantil (trastorno)
- Polycystic kidney disease, infantile type (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(53)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Congenital anomaly of the kidney
- 1Developmental hereditary disorder
- 1Hereditary nephropathy
- 1Multiple congenital cysts of kidney
- 2Autosomal hereditary disorder
- 2Congenital anomaly of abdomen
- 2Congenital malformation of the urinary system
- 2Congenital renal cyst
- 2Developmental disorder
- 2Hereditary disease
- 2Hereditary disorder of the urinary system
- 2Kidney disease
- 3Congenital anomaly of lower trunk
- 3Congenital disease
- 3Cyst of kidney
- 3Disease
- 3Disorder of abdomen
- 3Disorder of kidney and/or ureter
- 3Disorder of retroperitoneum
- 3Disorder of urinary system
- 3Genetic disease
- 3Genitourinary congenital anomalies
- 3Hereditary disorder by system
- 3Kidney finding
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