OMOP Concept 4178955
Hereditary disorder of the urinary system
StandardConditionSNOMED363338001Disorder
Maps from
1
Descendants
184
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Hereditary disorder of the urinary system via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 363338001 | Hereditary disorder of the urinary system | Non-standard |
Synonyms
Alternative names recorded for Hereditary disorder of the urinary system across source vocabularies.
- Hereditary disorder of the urinary system (disorder)
- trastorno hereditario del tracto urinario
- trastorno hereditario de vías urinarias
- trastorno hereditario de vías urinarias (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(14)Roll up to these when you need a wider cohort.
- 1Disorder of urinary system
- 1Hereditary disorder by system
- 2Disorder of body system
- 2Disorder of the genitourinary system
- 2Hereditary disease
- 2Urinary system finding
- 3Disease
- 3Disorder of abdominopelvic segment of trunk
- 3Genetic disease
- 3Urogenital finding
- 4Clinical finding
- 4Disorder of trunk
- 4Finding of abdominopelvic segment of trunk
- 5Finding of trunk structure
Narrower concepts
(184)Included automatically when you query with descendants.
- 13-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency
- 1Familial penile hypospadias
- 1Familial vesicoureteral reflux
- 1Goldblatt Wallis syndrome
- 1Hereditary hollow viscus myopathy
- 1Hereditary hypophosphatemic rickets with hypercalciuria
- 1Hereditary nephropathy
- 1Hereditary vasopressin resistance
- 1Megacystis, microcolon, hypoperistalsis syndrome
- 1Opitz-Frias syndrome
- 1Schmitt Gillenwater Kelly syndrome
- 1Split hand, obstructive uropathy, spina bifida, diaphragmatic defect syndrome
- 2Acrorenal mandibular syndrome
- 2Acrorenal syndrome
- 2Acrorenoocular syndrome
- 2Aniridia, renal agenesis, psychomotor retardation syndrome
- 2Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome
- 2Autosomal dominant intermediate Charcot-Marie-Tooth disease type E
- 2Autosomal dominant polycystic kidney disease
- 2Autosomal dominant progressive nephropathy with hypertension
- 2Autosomal dominant tubulointerstitial kidney disease
- 2Autosomal hereditary vasopressin resistance
- 2Bartter syndrome
- 2Cerebral ventriculomegaly, cystic kidney disease
- 2Congenital nephrotic syndrome
- 2Congenital nephrotic syndrome due to congenital infection
- 2Congenital nephrotic syndrome due to diffuse mesangial sclerosis
- 2Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome
- 2Congenital nephrotic syndrome with focal glomerulosclerosis
- 2Congenital neutropenia, myelofibrosis, nephromegaly syndrome
- 2Congenital vertebral, cardiac, renal anomalies syndrome
- 2Crome syndrome
- 2Cystinuria, type 1
- 2Dent's disease
- 2Diffuse mesangial sclerosis with ocular abnormalities
- 2Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis
- 2Drash syndrome
- 2Dysmorphic sialidosis with renal involvement
- 2EGF-related primary hypomagnesemia with intellectual disability
- 2Enamel-renal syndrome
- 2Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome
- 2Fabry's disease
- 2Faciocardiorenal syndrome
- 2Familial amyloid nephropathy with urticaria AND deafness
- 2Familial arthrogryposis-cholestatic hepatorenal syndrome
- 2Familial hypokalemic alkalosis, Gullner type
- 2Familial juvenile hyperuricemic nephropathy
- 2Familial papillary thyroid carcinoma with renal papillary neoplasia syndrome
- 2Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis
- 2Familial renal cell carcinoma
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