OMOP Concept 36715416
Deafness and intellectual disability Martin Probst type syndrome
StandardConditionSNOMED721087008Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to Deafness and intellectual disability Martin Probst type syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C564495 | Martin-Probst Deafness-Mental Retardation Syndrome | Non-standard |
| Nebraska Lexicon | 721087008 | Deafness and intellectual disability Martin Probst type syndrome | Non-standard |
Synonyms
Alternative names recorded for Deafness and intellectual disability Martin Probst type syndrome across source vocabularies.
- Deafness and intellectual disability Martin Probst type syndrome (disorder)
- Martin Probst syndrome
- síndrome de Martin Probst
- síndrome de sordera y discapacidad intelectual, tipo Martin Probst
- síndrome de sordera y discapacidad intelectual, tipo Martin Probst (trastorno)
- X-linked deafness and intellectual disability syndrome
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(47)Roll up to these when you need a wider cohort.
- 1Bilateral hearing loss
- 1Congenital sensorineural hearing loss
- 1Developmental hereditary disorder
- 1Hearing loss associated with syndrome
- 1Intellectual disability
- 1Multiple malformation syndrome with facial defects as major feature
- 1X-linked recessive hereditary disease
- 1X-linked sensorineural hearing loss
- 2Auditory system hereditary disorder
- 2Behavior finding
- 2Congenital anomaly of face
- 2Congenital hearing disorder
- 2Developmental disorder
- 2Hearing loss
- 2Hearing loss of left ear
- 2Hearing loss of right ear
- 2Hereditary disease
- 2Impaired cognition
- 2Intellectual ability - finding
- 2Multiple system malformation syndrome
- 2Neurodevelopmental disorder
- 2Sensorineural hearing loss
- 2X-linked hereditary disease
- 3Cognitive function finding
- 3Congenital anomaly of head
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