OMOP Concept 36714682
Microphthalmia with brain atrophy syndrome
StandardConditionSNOMED720010009Disorder
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 brain atrophy syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C566985 | Microphthalmia, Syndromic 10 | Non-standard |
| Nebraska Lexicon | 720010009 | Microphthalmia with brain atrophy syndrome | Non-standard |
Synonyms
Alternative names recorded for Microphthalmia with brain atrophy syndrome across source vocabularies.
- microftalmía con síndrome de atrofia encefálica
- microftalmía con síndrome de atrofia encefálica (trastorno)
- microftalmía sindrómica tipo 10
- Microphthalmia with brain atrophy syndrome (disorder)
- MOBA syndrome
- Syndromic microphthalmia type 10
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.
- 1Autosomal recessive hereditary disorder
- 1Chronic brain syndrome
- 1Chronic disease of musculoskeletal system
- 1Congenital blindness
- 1Degenerative brain disorder
- 1Developmental hereditary disorder
- 1Disorder of skeletal muscle
- 1Hereditary degenerative disease of central nervous system
- 1Hereditary disorder of musculoskeletal system
- 1Hereditary disorder of the visual system
- 1Microphthalmos
- 1Seizure disorder
- 1Severe intellectual disability
- 1Spasticity
- 2Autosomal hereditary disorder
- 2Blindness AND/OR vision impairment level
- 2Chronic disease
- 2Chronic nervous system disorder
- 2Congenital anomaly of eye
- 2Congenital anomaly of visual system
- 2Degenerative disease of the central nervous system
- 2Developmental disorder
- 2Disorder of brain
- 2Disorder of muscle
- 2Disorder of musculoskeletal system
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