OMOP Concept 45765499
FOXG1 syndrome
StandardConditionSNOMED702450004Disorder
Maps from
2
Descendants
0
Valid from
31 Jul 2014
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to FOXG1 syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| ICD10CM | QA0.0151 | FOXG1 syndrome | Non-standard |
| Nebraska Lexicon | 702450004 | Congenital variant of Rett syndrome | Non-standard |
Synonyms
Alternative names recorded for FOXG1 syndrome across source vocabularies.
- FOXG1 syndrome (disorder)
- síndrome FOXG1
- síndrome FOXG1 (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(30)Roll up to these when you need a wider cohort.
- 1Autism spectrum disorder
- 1Autosomal dominant hereditary disorder
- 1Congenital anomaly of brain
- 1Developmental hereditary disorder
- 1Hereditary disorder of nervous system
- 2Autosomal hereditary disorder
- 2Congenital anomaly of central nervous system
- 2Congenital anomaly of head
- 2Developmental disorder
- 2Disorder of brain
- 2Disorder of nervous system
- 2Disorder of psychological development
- 2Hereditary disease
- 2Hereditary disorder by system
- 3Congenital anomaly of nervous system
- 3Congenital malformation
- 3Developmental mental disorder
- 3Disease
- 3Disorder of body system
- 3Disorder of head
- 3Disorder of the central nervous system
- 3Finding of brain
- 3Genetic disease
- 4Central nervous system finding
- 4Clinical finding
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