OMOP Concept 4102522
Alobar holoprosencephaly
StandardConditionSNOMED253137003Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to Alobar holoprosencephaly via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 149063 | Alobar holoprosencephaly | Non-standard |
| HPO | HP_0006988 | Alobar holoprosencephaly | Non-standard |
Synonyms
Alternative names recorded for Alobar holoprosencephaly across source vocabularies.
- Alobar holoprosencephaly (disorder)
- holoprosencefalia alobar
- holoprosencefalia alobular
- holoprosencefalia alobular (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(22)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of cerebrum
- 1Holoprosencephaly sequence
- 2Congenital anomaly of brain
- 2Congenital anomaly of head
- 2Malformation sequence
- 3Congenital anomaly of central nervous system
- 3Congenital malformation
- 3Congenital malformation syndrome
- 3Disorder of brain
- 3Disorder of head
- 4Congenital anomaly of nervous system
- 4Congenital disease
- 4Developmental disorder
- 4Disease
- 4Disorder of the central nervous system
- 4Finding of brain
- 4Head finding
- 5Central nervous system finding
- 5Clinical finding
- 5Disorder of nervous system
- 5Fetal and/or neonatal disorder
- 6Disorder of body system
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