OMOP Concept 36713440
Alport syndrome autosomal dominant
StandardConditionSNOMED717766000Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
OMOP concepts
Concept Lookup Tool
Search 11M+ concepts across SNOMED, RxNorm, ICD-10 & LOINC.
Source codes that map to this concept
1 source code normalizes to Alport syndrome autosomal dominant via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 717766000 | Alport syndrome autosomal dominant | Non-standard |
Synonyms
Alternative names recorded for Alport syndrome autosomal dominant across source vocabularies.
- Alport syndrome autosomal dominant (disorder)
- síndrome de Alport autosómico dominante
- síndrome de Alport autosómico dominante (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(45)Roll up to these when you need a wider cohort.
- 1Alport syndrome
- 1Autosomal dominant hereditary disorder
- 2Auditory system hereditary disorder
- 2Autosomal hereditary disorder
- 2Hereditary nephritis
- 2Sensorineural hearing loss
- 3Disorder of auditory system
- 3Glomerulonephritis
- 3Hearing loss
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Hereditary nephropathy
- 4Disorder of body system
- 4Ear and auditory finding
- 4Genetic disease
- 4Glomerular disease
- 4Hearing disorder
- 4Hereditary disorder of the urinary system
- 4Kidney disease
- 4Nephritis
- 5Clinical finding
- 5Disease
- 5Disorder of kidney and/or ureter
- 5Disorder of renal parenchyma
- 5Disorder of retroperitoneum
Get this concept via the API
Resolve Alport syndrome autosomal dominant - and every code that maps to it - over HTTPS, against the current vocabulary release. No downloads, no local database.
curl "https://api.omophub.com/v1/concepts/36713440?include_relationships=true" \
-H "Authorization: Bearer $OMOPHUB_API_KEY"Get your free API key3,000 calls/month free · no credit card