OMOP Concept 36716045
Microphthalmia with linear skin defect syndrome
StandardConditionSNOMED721879006Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Microphthalmia with linear skin defect syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C537466 | Microphthalmia, syndromic 7 | Non-standard |
| Nebraska Lexicon | 721879006 | Microphthalmia with linear skin defect syndrome | Non-standard |
Synonyms
Alternative names recorded for Microphthalmia with linear skin defect syndrome across source vocabularies.
- Microphthalmia with linear skin defect syndrome (disorder)
- MIDAS syndrome
- MIDAS syndrome (microphthalmia, dermal aplasia, sclerocornea) syndrome
- síndrome de microftalmía con defecto cutáneo lineal
- síndrome de microftalmía con defecto cutáneo lineal (trastorno)
- síndrome MIDAS
- Syndromic microphthalmia type 7
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(41)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of skin
- 1Developmental hereditary disorder
- 1Hereditary disorder of the integument
- 1Hereditary disorder of the visual system
- 1Microphthalmos
- 1X-linked dominant hereditary disease
- 2Congenital anomaly of eye
- 2Congenital anomaly of integument
- 2Developmental disorder
- 2Disorder of integument
- 2Disorder of skin
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Visual system disorder
- 2X-linked hereditary disease
- 3Anomaly of eye
- 3Congenital anomaly of head
- 3Congenital anomaly of visual system
- 3Congenital malformation
- 3Disease
- 3Disorder involving the integument of fetus OR newborn
- 3Disorder of body system
- 3Disorder of skin and/or subcutaneous tissue
- 3Eye / vision finding
- 3Genetic disease
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