OMOP Concept 45765422
PPM-X syndrome
StandardConditionSNOMED702356009Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2014
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to PPM-X syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C563139 | Mental Retardation, X-Linked 16 | Non-standard |
Synonyms
Alternative names recorded for PPM-X syndrome across source vocabularies.
- Lindsay Burn syndrome
- PPMX - Mental retardation with psychosis, pyramidal signs, and macroorchidism
- retardo mental con psicosis, signos piramidales y macroorquidia
- retraso mental sindrómico ligado al cromosoma X, 13
- síndrome de discapacidad intelectual, psicosis y macroorquidia ligado al cromosoma X, 13
- síndrome de discapacidad intelectual, psicosis y macroorquidia ligado al cromosoma X, 13 (trastorno)
- X-linked intellectual disability-psychosis-macroorchidism syndrome
- X-linked intellectual disability-psychosis-macroorchidism syndrome (disorder)
- X-linked mental retardation, syndromic 13
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(29)Roll up to these when you need a wider cohort.
- 1Developmental hereditary disorder
- 1Disorder of the central nervous system
- 1Genetic intellectual disability
- 1Hereditary disorder of nervous system
- 1MECP2 related disorder
- 1Neurodevelopmental delay
- 1X-linked dominant hereditary disease
- 2Central nervous system finding
- 2Developmental delay
- 2Developmental disorder
- 2Disorder of nervous system
- 2Genetic disease
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Intellectual disability
- 2Neurodevelopmental disorder
- 2X-linked hereditary disease
- 3Abnormal behavior
- 3Clinical finding
- 3Disease
- 3Disorder of body system
- 3Impaired cognition
- 3Intellectual ability - finding
- 3Sex-linked hereditary disorder
- 4Behavior finding
Showing 25 of 29. Retrieve the full set via the API.
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