OMOP Concept 4118020
Genitourinary congenital anomalies
StandardConditionSNOMED287085006Disorder
Maps from
3
Descendants
853
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
3 source codes normalize to Genitourinary congenital anomalies via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 119946 | Congenital anomaly of genital organs | Non-standard |
| CIEL | 139504 | Genitourinary Congenital Anomalies | Non-standard |
| MeSH | D014564 | Urogenital Abnormalities | Non-standard |
Synonyms
Alternative names recorded for Genitourinary congenital anomalies across source vocabularies.
- anomalías congénitas genitourinarias
- anomalías congénitas genitourinarias (trastorno)
- anomalía urogenital congénita
- Congenital genitourinary anomaly
- Congenital urogenital anomaly
- Genitourinary congenital anomalies (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(16)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of lower trunk
- 1Disorder of the genitourinary system
- 2Congenital abnormality of lower limb and pelvic girdle
- 2Congenital anomaly of trunk
- 2Disorder of abdominopelvic segment of trunk
- 2Disorder of body system
- 2Urogenital finding
- 3Congenital malformation
- 3Disease
- 3Disorder of trunk
- 3Finding of abdominopelvic segment of trunk
- 4Clinical finding
- 4Congenital disease
- 4Developmental disorder
- 4Finding of trunk structure
- 5Fetal and/or neonatal disorder
Narrower concepts
(853)Included automatically when you query with descendants.
- 12p21 microdeletion syndrome without cystinuria
- 1Acrofrontofacionasal dysostosis type 2
- 1Agenesis of corpus callosum and abnormal genitalia syndrome
- 1Autosomal recessive facio-digito-genital syndrome
- 1B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome
- 1BSG syndrome
- 1Cardiac urogenital syndrome
- 1Cardiomyopathy and renal anomaly syndrome
- 1Congenital anomaly of male urogenital tract
- 1Congenital female urogenital anomaly
- 1Congenital malformation of genital organs
- 1Congenital malformation of the urinary system
- 1DK phocomelia syndrome
- 1Exstrophy epispadias complex
- 1Hand-foot-genital syndrome
- 1Karandikar Maria Kamble syndrome
- 1Lethal hemolytic anemia and genital anomaly syndrome
- 1Prune belly syndrome
- 1RAB18 deficiency
- 1Spondylocostal dysostosis with anal atresia and genitourinary malformation syndrome
- 1STAR syndrome
- 1X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome
- 23-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency
- 246,XX disorder of sex development
- 246,XY disorder of sex development
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