OMOP Concept 36713766
Lissencephaly type 3 familial fetal akinesia sequence syndrome
StandardConditionSNOMED718719001Disorder
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 Lissencephaly type 3 familial fetal akinesia sequence syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 718719001 | Lissencephaly type 3 familial foetal akinesia sequence syndrome | Non-standard |
Synonyms
Alternative names recorded for Lissencephaly type 3 familial fetal akinesia sequence syndrome across source vocabularies.
- Lissencephaly type 3 familial fetal akinesia sequence syndrome (disorder)
- Lissencephaly type 3 familial foetal akinesia sequence syndrome
- síndrome de lisencefalia tipo 3 familiar con secuencia de acinesia fetal
- síndrome de lisencefalia tipo 3 familiar con secuencia de acinesia fetal (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(29)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Developmental hereditary disorder
- 1Hereditary disorder of nervous system
- 1Microlissencephaly
- 2Autosomal hereditary disorder
- 2Congenital microencephaly
- 2Developmental disorder
- 2Disorder of nervous system
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Lissencephaly
- 3Congenital anomaly of brain
- 3Disease
- 3Disorder of body system
- 3Disorder of neuronal migration and differentiation
- 3Genetic disease
- 4Clinical finding
- 4Congenital anomaly of central nervous system
- 4Congenital anomaly of head
- 4Disorder of brain
- 5Congenital anomaly of nervous system
- 5Congenital malformation
- 5Disorder of head
- 5Disorder of the central nervous system
- 5Finding of brain
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