OMOP Concept 36716051
Scalp, ear, nipple syndrome
StandardConditionSNOMED721888002Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Scalp, ear, nipple syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C536623 | Scalp ear nipple syndrome | Non-standard |
Synonyms
Alternative names recorded for Scalp, ear, nipple syndrome across source vocabularies.
- Finlay Marks syndrome
- Scalp, ear, nipple syndrome (disorder)
- síndrome de cuero cabelludo, oído y pezón
- síndrome de cuero cabelludo, oído y pezón (trastorno)
- síndrome de Finlay Marks
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(71)Roll up to these when you need a wider cohort.
- 1Aplasia of skin
- 1Auditory system hereditary disorder
- 1Autosomal dominant hereditary disorder
- 1Congenital abnormality of external ear
- 1Congenital absence of nipple
- 1Developmental hereditary disorder
- 1Disorder of pinna
- 1Disorder of scalp
- 1Disorder of skin of head
- 1Ectodermal dysplasia
- 1Hereditary disorder of the integument
- 2Autosomal hereditary disorder
- 2Congenital abnormality of nipple
- 2Congenital absence of breast
- 2Congenital ectodermal defect
- 2Congenital malformation of ear
- 2Developmental disorder
- 2Disorder of auditory system
- 2Disorder of external ear
- 2Disorder of head
- 2Disorder of integument
- 2Disorder of skin
- 2Disorder of skin AND/OR subcutaneous tissue of head
- 2Genodermatosis
- 2Hereditary disease
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