OMOP Concept 4108905
Congenital malformation of the urinary system
StandardConditionSNOMED253859003Disorder
Maps from
30
Descendants
301
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
30 source codes normalize to Congenital malformation of the urinary system via the OMOP "Maps to" relationship.
Synonyms
Alternative names recorded for Congenital malformation of the urinary system across source vocabularies.
- anomalía congénita del sistema urinario
- Congenital abnormality of urinary system
- Congenital anomaly of the urinary system
- Congenital malformation of the urinary system (disorder)
- malformación congénita del sistema urinario
- malformación congénita del sistema urinario (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(19)Roll up to these when you need a wider cohort.
- 1Disorder of urinary system
- 1Genitourinary congenital anomalies
- 2Congenital anomaly of lower trunk
- 2Disorder of the genitourinary system
- 2Urinary system finding
- 3Congenital abnormality of lower limb and pelvic girdle
- 3Congenital anomaly of trunk
- 3Disorder of abdominopelvic segment of trunk
- 3Disorder of body system
- 3Urogenital finding
- 4Congenital malformation
- 4Disease
- 4Disorder of trunk
- 4Finding of abdominopelvic segment of trunk
- 5Clinical finding
- 5Congenital disease
- 5Developmental disorder
- 5Finding of trunk structure
- 6Disorder of fetus and/or newborn
Narrower concepts
(301)Included automatically when you query with descendants.
- 1Cholestasis with pigmentary retinopathy and cleft palate syndrome
- 1Congenital anomaly of the kidney
- 1Congenital anomaly of the urinary tract proper
- 1Hydrocephalus, blue sclera, nephropathy syndrome
- 1Malformation of urachus
- 1Split hand, obstructive uropathy, spina bifida, diaphragmatic defect syndrome
- 215q overgrowth syndrome
- 2Accessory kidney
- 2Acrorenal mandibular syndrome
- 2Acrorenal syndrome
- 2Acrorenoocular syndrome
- 2Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome
- 2Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
- 2Boichis syndrome
- 2Congenital abnormal shape of kidney
- 2Congenital absence of renal papilla
- 2Congenital anomaly of renal pelvis
- 2Congenital anomaly of ureter
- 2Congenital anomaly of urethra
- 2Congenital anomaly of urinary bladder
- 2Congenital calculus of kidney
- 2Congenital calyceal diverticulum
- 2Congenital duplication of renal collecting system
- 2Congenital enlarged kidney
- 2Congenital fistula between uterus and urinary tract
- 2Congenital fistula of urachus
- 2Congenital fusion of kidneys
- 2Congenital gastrointestinal-urinary tract fistula
- 2Congenital hydrocalicosis
- 2Congenital hydronephrosis
- 2Congenital hyperplasia of kidney
- 2Congenital hypoplasia of kidney
- 2Congenital lobulation of kidney
- 2Congenital malposition of kidney
- 2Congenital nephrotic syndrome
- 2Congenital renal failure
- 2Congenital single renal cyst
- 2Congenital vertebral, cardiac, renal anomalies syndrome
- 2Crome syndrome
- 2Cystic hamartoma of lung and kidney
- 2Diffuse hyperplastic perilobular nephroblastomatosis
- 2Double uterus, hemivagina, renal agenesis syndrome
- 2Drash syndrome
- 2Ectopic kidney
- 2Hepatic fibrosis, renal cyst, intellectual disability syndrome
- 2Infection of urachal remnant
- 2Infundibulopelvic stenosis multicystic kidney syndrome
- 2Inherited renal tubule insufficiency with cholestatic jaundice
- 2Lowe Kohn Cohen syndrome
- 2Lowe syndrome
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