OMOP Concept 605204
X-linked complicated corpus callosum dysgenesis
StandardConditionSNOMED1010630006Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2021
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to X-linked complicated corpus callosum dysgenesis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C564115 | Corpus Callosum, Partial Agenesis of, X-Linked | Non-standard |
Synonyms
Alternative names recorded for X-linked complicated corpus callosum dysgenesis across source vocabularies.
- disgenesia del cuerpo calloso compleja ligada al cromosoma X
- disgenesia del cuerpo calloso compleja ligada al cromosoma X (trastorno)
- X-linked complicated corpus callosum dysgenesis (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(49)Roll up to these when you need a wider cohort.
- 1L1 syndrome
- 2Congenital hydrocephalus
- 2Developmental hereditary disorder
- 2Hereditary disorder of nervous system
- 2Hypoplasia of corpus callosum
- 2Intellectual disability
- 2Multiple malformation syndrome with limb defect as major feature
- 2X-linked recessive hereditary disease
- 3Behavior finding
- 3Congenital anomaly of brain
- 3Congenital hypoplasia of cerebrum
- 3Congenital malformation of corpus callosum
- 3Developmental disorder
- 3Disorder of nervous system
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Hydrocephalus
- 3Impaired cognition
- 3Intellectual ability - finding
- 3Multiple system malformation syndrome
- 3Neurodevelopmental disorder
- 3X-linked hereditary disease
- 4Cognitive function finding
- 4Congenital anomaly of central nervous system
- 4Congenital anomaly of cerebrum
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