OMOP Concept 37312387
Alopecia, epilepsy, intellectual disability syndrome Moynahan type
StandardConditionSNOMED788417006Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2020
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to Alopecia, epilepsy, intellectual disability syndrome Moynahan type via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 133833 | Moynahan's Syndrome | Non-standard |
| MeSH | C537052 | Alopecia epilepsy oligophrenia syndrome of Moynahan | Non-standard |
Synonyms
Alternative names recorded for Alopecia, epilepsy, intellectual disability syndrome Moynahan type across source vocabularies.
- Alopecia, epilepsy, intellectual disability syndrome Moynahan type (disorder)
- Moynahan syndrome
- síndrome de alopecia, epilepsia y discapacidad intelectual tipo Moynahan
- síndrome de alopecia, epilepsia y discapacidad intelectual tipo Moynahan (trastorno)
- síndrome de Moynahan
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(58)Roll up to these when you need a wider cohort.
- 1Abnormal nervous system function
- 1Autosomal recessive hereditary disorder
- 1Congenital alopecia
- 1Developmental hereditary disorder
- 1Epilepsy
- 1Genetic intellectual disability
- 1Hereditary disorder of nervous system
- 1Hereditary disorder of the integument
- 2Alopecia
- 2Autosomal hereditary disorder
- 2Congenital anomaly of hair
- 2Developmental disorder
- 2Disorder of integument
- 2Disorder of nervous system
- 2Functional finding
- 2Genetic disease
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Intellectual disability
- 2Neurological finding
- 2OMOP Seizure 1
- 2Seizure disorder
- 3Abnormal behavior
- 3Clinical finding
- 3Congenital anomaly of skin
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