OMOP Concept 45757752
Hereditary nephropathy
StandardConditionSNOMED367591000119105Disorder
Maps from
32
Descendants
173
Valid from
31 Jan 2015
Valid to
31 Dec 2099
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Source codes that map to this concept
32 source codes normalize to Hereditary nephropathy via the OMOP "Maps to" relationship.
Showing 25 of 32 source codes. Retrieve the full set via the API.
Synonyms
Alternative names recorded for Hereditary nephropathy across source vocabularies.
- Hereditary disorder of kidney
- Hereditary nephropathy (disorder)
- Inherited renal disease
- nefropatía hereditaria
- nefropatía hereditaria (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(23)Roll up to these when you need a wider cohort.
- 1Hereditary disorder of the urinary system
- 1Kidney disease
- 2Disorder of kidney and/or ureter
- 2Disorder of retroperitoneum
- 2Disorder of urinary system
- 2Hereditary disorder by system
- 2Kidney finding
- 3Abdominal organ finding
- 3Disorder of abdomen
- 3Disorder of body system
- 3Disorder of the genitourinary system
- 3Hereditary disease
- 3Urinary system finding
- 4Disease
- 4Disorder of abdominopelvic segment of trunk
- 4Finding of abdomen
- 4Genetic disease
- 4Urogenital finding
- 4Viscus structure finding
- 5Clinical finding
- 5Disorder of trunk
- 5Finding of abdominopelvic segment of trunk
- 6Finding of trunk structure
Narrower concepts
(173)Included automatically when you query with descendants.
- 1Acrorenal mandibular syndrome
- 1Acrorenal syndrome
- 1Acrorenoocular syndrome
- 1Aniridia, renal agenesis, psychomotor retardation syndrome
- 1Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome
- 1Autosomal dominant intermediate Charcot-Marie-Tooth disease type E
- 1Autosomal dominant polycystic kidney disease
- 1Autosomal dominant progressive nephropathy with hypertension
- 1Autosomal dominant tubulointerstitial kidney disease
- 1Bartter syndrome
- 1Cerebral ventriculomegaly, cystic kidney disease
- 1Congenital nephrotic syndrome
- 1Congenital nephrotic syndrome due to congenital infection
- 1Congenital nephrotic syndrome due to diffuse mesangial sclerosis
- 1Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome
- 1Congenital nephrotic syndrome with focal glomerulosclerosis
- 1Congenital neutropenia, myelofibrosis, nephromegaly syndrome
- 1Congenital vertebral, cardiac, renal anomalies syndrome
- 1Crome syndrome
- 1Cystinuria, type 1
- 1Dent's disease
- 1Dibasic amino aciduria type 1
- 1Diffuse mesangial sclerosis with ocular abnormalities
- 1Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis
- 1Drash syndrome
Showing 25 of 173. Retrieve the full set via the API.
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