OMOP Concept 600509
Microlissencephaly
StandardConditionSNOMED1003374009Disorder
Maps from
1
Descendants
1
Valid from
31 Jan 2021
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to Microlissencephaly via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| HPO | HP_0045028 | Microlissencephaly | Non-standard |
Synonyms
Alternative names recorded for Microlissencephaly across source vocabularies.
- microlisencefalia
- microlisencefalia (trastorno)
- Microlissencephaly (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(21)Roll up to these when you need a wider cohort.
- 1Congenital microencephaly
- 1Lissencephaly
- 2Congenital anomaly of brain
- 2Disorder of neuronal migration and differentiation
- 3Congenital anomaly of central nervous system
- 3Congenital anomaly of head
- 3Disorder of brain
- 4Congenital anomaly of nervous system
- 4Congenital malformation
- 4Disorder of head
- 4Disorder of the central nervous system
- 4Finding of brain
- 5Central nervous system finding
- 5Congenital disease
- 5Developmental disorder
- 5Disease
- 5Disorder of nervous system
- 5Head finding
- 6Clinical finding
- 6Disorder of body system
- 6Disorder of fetus and/or newborn
Narrower concepts
(1)Included automatically when you query with descendants.
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