OMOP Concept 37160959
Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome
StandardConditionSNOMED1172630000Disorder
Maps from
1
Descendants
0
Valid from
30 Sept 2021
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| ICD10CM | QA0.0102 | CACNA1A-related neurodevelopmental disorder | Non-standard |
Synonyms
Alternative names recorded for Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome across source vocabularies.
- Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome (disorder)
- síndrome de retraso del desarrollo global, anomalías neurooftálmicas, crisis convulsivas, discapacidad intelectual
- síndrome de retraso del desarrollo global, anomalías neurooftálmicas, crisis convulsivas, discapacidad intelectual (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(33)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Developmental hereditary disorder
- 1Global developmental delay
- 1Hereditary disorder of nervous system
- 1Intellectual disability
- 1Seizure disorder
- 2Autosomal hereditary disorder
- 2Behavior finding
- 2Developmental delay
- 2Developmental disorder
- 2Disorder of brain
- 2Disorder of nervous system
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Impaired cognition
- 2Intellectual ability - finding
- 2Neurodevelopmental disorder
- 2Seizure
- 3Cognitive function finding
- 3Disease
- 3Disorder of body system
- 3Disorder of head
- 3Disorder of the central nervous system
- 3Finding of brain
- 3Genetic disease
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