OMOP Concept 45757752
Hereditary nephropathy
StandardConditionSNOMED367591000119105Disorder
Maps from
33
Descendants
168
Valid from
31 Jan 2015
Valid to
31 Dec 2099
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Source codes that map to this concept
33 source codes normalize to Hereditary nephropathy via the OMOP "Maps to" relationship.
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
(168)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
- 1Diffuse mesangial sclerosis with ocular abnormalities
- 1Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis
- 1Drash syndrome
- 1Dysmorphic sialidosis with renal involvement
- 1EGF-related primary hypomagnesemia with intellectual disability
- 1Enamel-renal syndrome
- 1Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome
- 1Fabry's disease
- 1Faciocardiorenal syndrome
- 1Familial amyloid nephropathy with urticaria AND deafness
- 1Familial arthrogryposis-cholestatic hepatorenal syndrome
- 1Familial hypokalemic alkalosis, Gullner type
- 1Familial juvenile hyperuricemic nephropathy
- 1Familial papillary thyroid carcinoma with renal papillary neoplasia syndrome
- 1Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis
- 1Familial renal cell carcinoma
- 1Familial renal iminoglycinuria
- 1Familial steroid-resistant nephrotic syndrome with adrenal insufficiency
- 1Familial steroid-resistant nephrotic syndrome with sensorineural deafness
- 1Fibronectin glomerulopathy
- 1Galloway Mowat syndrome
- 1Genetic steroid-resistant nephrotic syndrome
- 1Gitelman syndrome
- 1Glycogenosis with glucoaminophosphaturia
- 1HELIX syndrome
- 1Hereditary diffuse crescentic glomerulonephritis
- 1Hereditary focal and segmental glomerular lesions
- 1Hereditary minor glomerular abnormality
- 1Hereditary nephritis
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