OMOP Concept 4266044
Hereditary lymphedema type I
StandardConditionSNOMED399889006Disorder
Maps from
2
Descendants
0
Valid from
31 Jul 2003
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Hereditary lymphedema type I via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 138762 | Hereditary lymphedema type I | Non-standard |
| Read | PH02.00 | Milroy's disease | Non-standard |
Synonyms
Alternative names recorded for Hereditary lymphedema type I across source vocabularies.
- Hereditary lymphedema type I (disorder)
- Hereditary lymphoedema type I
- linfedema hereditario tipo I
- linfedema hereditario tipo I (trastorno)
- Milroy lymphedema
- Milroy lymphoedema
- Nonne-Milroy lymphedema
- Nonne-Milroy lymphoedema
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(17)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Hereditary lymphedema
- 2Autosomal hereditary disorder
- 2Developmental hereditary disorder
- 2Primary lymphedema
- 3Developmental disorder
- 3Hereditary disease
- 3Lymphedema of limb
- 4Disease
- 4Disorder of limb
- 4Edema of extremity
- 4Genetic disease
- 4Lymphedema
- 5Clinical finding
- 5Disorder characterized by edema
- 5Edema
- 5Finding of limb structure
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