OMOP Concept 36716264
Severe X-linked intellectual disability Gustavson type
StandardConditionSNOMED722213009Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Severe X-linked intellectual disability Gustavson type via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 722213009 | Severe X-linked intellectual disability Gustavson type | Non-standard |
Synonyms
Alternative names recorded for Severe X-linked intellectual disability Gustavson type across source vocabularies.
- discapacidad intelectual severa ligada al cromosoma X, tipo Gustavson
- discapacidad intelectual severa ligada al cromosoma X, tipo Gustavson (trastorno)
- Severe X-linked intellectual disability Gustavson type (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(67)Roll up to these when you need a wider cohort.
- 1Auditory system hereditary disorder
- 1Congenital anomaly of optic nerve
- 1Congenital atrophy of optic nerve
- 1Congenital degeneration of nervous system
- 1Congenital hearing disorder
- 1Congenital microcephaly
- 1Developmental hereditary disorder
- 1Hearing loss associated with syndrome
- 1Hereditary degenerative disease of central nervous system
- 1Inherited optic neuropathy
- 1Intellectual disability
- 1Multiple malformation syndrome with facial defects as major feature
- 1X-linked recessive hereditary disease
- 2Behavior finding
- 2Congenital anomaly of central nervous system
- 2Congenital anomaly of face
- 2Congenital anomaly of head
- 2Congenital anomaly of nervous system
- 2Congenital anomaly of visual system
- 2Congenital disease
- 2Degenerative disease of the central nervous system
- 2Degenerative disorder
- 2Developmental disorder
- 2Disorder of auditory system
- 2Disorder of optic nerve
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