OMOP Concept 4263213
Von Hippel-Lindau syndrome
StandardConditionSNOMED46659004Disorder
Maps from
5
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
5 source codes normalize to Von Hippel-Lindau syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 122979 | Von Hippel-Lindau syndrome | Non-standard |
| ICD10CM | Q85.83 | Von Hippel-Lindau syndrome | Non-standard |
| MeSH | D006623 | von Hippel-Lindau Disease | Non-standard |
| Read | PK62.00 | Von Hippel-Lindau syndrome | Non-standard |
| Read | PK62.11 | Lindau's disease | Non-standard |
Synonyms
Alternative names recorded for Von Hippel-Lindau syndrome across source vocabularies.
- angiomatosis cerebelorretiniana familiar
- angiomatosis cerebrorretiniana
- Cerebroretinal angiomatosis
- enfermedad de Lindau
- Familial cerebello-retinal angiomatosis
- Lindau' disease
- Lindau's disease
- síndrome de Von Hippel - Lindau
- síndrome de Von Hippel - Lindau (trastorno)
- VHL (Von Hippel-Lindau) syndrome
- Von Hippel-Lindau syndrome (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(38)Roll up to these when you need a wider cohort.
- 1Hereditary cancer-predisposing syndrome
- 1Hereditary disorder of nervous system
- 1Hereditary disorder of the integument
- 1Neurocutaneous syndrome
- 2Congenital disease
- 2Disorder of integument
- 2Disorder of nervous system
- 2Fetal and/or neonatal disorder of integument
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Neoplasm of nervous system
- 2Neoplasm of skin
- 3Disorder of body system
- 3Fetal and/or neonatal disorder
- 3Genetic disease
- 3Integumentary system finding
- 3Mass of skin
- 3Neoplasm of integumentary system
- 3Neoplasm of soft tissue
- 3Neoplastic disease
- 3Skin lesion
- 3Space-occupying lesion of nervous system
- 4Clinical finding
- 4Disease
- 4Disorder of skin
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