OMOP Concept 4313273
Congenital melanosis
StandardConditionSNOMED86042009Disorder
Maps from
1
Descendants
15
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Congenital melanosis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 143826 | Congenital Melanosis | Non-standard |
Synonyms
Alternative names recorded for Congenital melanosis across source vocabularies.
- Congenital melanosis (disorder)
- melanosis congénita
- melanosis congénita (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(6)Roll up to these when you need a wider cohort.
Narrower concepts
(15)Included automatically when you query with descendants.
- 1Acromelanosis
- 1Arterial dissection and lentiginosis syndrome
- 1Centrofacial lentiginosis syndrome
- 1Congenital melanosis of sclera
- 1Dermal melanocytic hamartoma
- 1Familial generalized lentiginosis
- 1Hereditary benign acanthosis nigricans
- 1Hereditary benign acanthosis nigricans with insulin resistance
- 1Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome
- 1Ocular melanosis
- 1Peutz-Jeghers syndrome
- 2Congenital ocular melanocytosis of left eye
- 2Congenital ocular melanocytosis of right eye
- 2Peutz-Jeghers polyps of small bowel
- 3Bilateral congenital ocular melanocytosis of eyes
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