OMOP Concept 37471508
Genetic disease of glomerulus
StandardConditionSNOMED1367653005Disorder
Maps from
0
Descendants
48
Valid from
1 Jul 2025
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for Genetic disease of glomerulus across source vocabularies.
- enfermedad genética de glomérulo
- enfermedad genética de glomérulo (trastorno)
- Genetic disease of glomerulus (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(22)Roll up to these when you need a wider cohort.
- 1Genetic disease
- 1Glomerular disease
- 2Disease
- 2Disorder of renal parenchyma
- 3Clinical finding
- 3Kidney disease
- 4Disorder of kidney and/or ureter
- 4Disorder of retroperitoneum
- 4Kidney finding
- 5Abdominal organ finding
- 5Disorder of abdomen
- 5Disorder of urinary system
- 5Urinary system finding
- 6Disorder of abdominopelvic segment of trunk
- 6Disorder of the genitourinary system
- 6Finding of abdomen
- 6Urogenital finding
- 6Viscus structure finding
- 7Disorder of body system
- 7Disorder of trunk
- 7Finding of abdominopelvic segment of trunk
- 8Finding of trunk structure
Narrower concepts
(48)Included automatically when you query with descendants.
- 1Autosomal dominant intermediate Charcot-Marie-Tooth disease type E
- 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
- 1Diffuse mesangial sclerosis with ocular abnormalities
- 1Drash syndrome
- 1Familial hematuria
- 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
- 1Hereditary diffuse crescentic glomerulonephritis
- 1Hereditary focal and segmental glomerular lesions
- 1Hereditary minor glomerular abnormality
- 1Hereditary nephritis
- 1Hereditary podocytopathy
- 1Hypotrichosis, lymphedema, telangiectasia, renal defect syndrome
- 1LAMB2-related infantile-onset nephrotic syndrome
- 1Lipoprotein glomerulopathy
- 1Non-progressive hereditary glomerulonephritis
- 1Pierson syndrome
- 1Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations
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