OMOP Concept 36717562
Matthew Wood syndrome
StandardConditionSNOMED722458000Disorder
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 Matthew Wood syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C537768 | Anophthalmia with pulmonary hypoplasia | Non-standard |
| Nebraska Lexicon | 722458000 | Anophthalmia with pulmonary hypoplasia syndrome | Non-standard |
Synonyms
Alternative names recorded for Matthew Wood syndrome across source vocabularies.
- Anophthalmia with pulmonary hypoplasia syndrome
- Matthew Wood syndrome (disorder)
- síndrome de anoftalmía con hipoplasia pulmonar
- síndrome de Matthew Wood
- síndrome de Matthew Wood (trastorno)
- Syndromic microphthalmia type 9
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(48)Roll up to these when you need a wider cohort.
- 1Autosomal hereditary disorder
- 1Congenital anomaly of eye
- 1Congenital anomaly of lung
- 1Developmental hereditary disorder
- 1Hereditary disorder of the visual system
- 1Multiple system malformation syndrome
- 2Anomaly of eye
- 2Congenital anomaly of head
- 2Congenital anomaly of lower respiratory system
- 2Congenital anomaly of thorax
- 2Congenital anomaly of visual system
- 2Congenital malformation syndrome
- 2Developmental disorder
- 2Disorder of lung
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Visual system disorder
- 3Congenital anomaly of upper trunk
- 3Congenital malformation
- 3Congenital malformation of the respiratory system
- 3Disease
- 3Disorder of body system
- 3Disorder of eye
- 3Disorder of head
- 3Disorder of lower respiratory system
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