OMOP Concept 35623052
Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
StandardConditionSNOMED765331004Disorder
Maps from
2
Descendants
0
Valid from
31 Jul 2018
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
2 source codes normalize to Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C536328 | Polycystic kidneys, severe infantile with tuberous sclerosis | Non-standard |
| Nebraska Lexicon | 765331004 | Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis | Non-standard |
Synonyms
Alternative names recorded for Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis across source vocabularies.
- Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis (disorder)
- enfermedad renal poliquística autosómica dominante tipo 1 con esclerosis tuberosa
- enfermedad renal poliquística autosómica dominante tipo 1 con esclerosis tuberosa (trastorno)
- Tuberous sclerosis, polycystic kidney disease contiguous gene syndrome
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(87)Roll up to these when you need a wider cohort.
- 1Autosomal dominant polycystic kidney disease
- 1Congenital anomaly of skin
- 1Congenital anomaly of the kidney
- 1Developmental hereditary disorder
- 1Tuberous sclerosis syndrome
- 2Autosomal dominant hereditary disorder
- 2Congenital anomaly of abdomen
- 2Congenital anomaly of integument
- 2Congenital malformation of the urinary system
- 2Developmental disorder
- 2Disorder of skin
- 2Disorder of the central nervous system
- 2Hereditary cancer-predisposing syndrome
- 2Hereditary disease
- 2Hereditary disorder of nervous system
- 2Hereditary disorder of the integument
- 2Hereditary nephropathy
- 2Kidney disease
- 2Multiple congenital cysts of kidney
- 2Neurocutaneous syndrome
- 3Autosomal hereditary disorder
- 3Central nervous system finding
- 3Congenital anomaly of lower trunk
- 3Congenital disease
- 3Congenital malformation
Get this concept via the API
Resolve Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis - 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/35623052?include_relationships=true" \
-H "Authorization: Bearer $OMOPHUB_API_KEY"Get your free API key3,000 calls/month free · no credit card