OMOP Concept 45765425
Congenital deafness with labyrinthine aplasia, microtia and microdontia
StandardConditionSNOMED702360007Disorder
Maps from
2
Descendants
0
Valid from
31 Jul 2014
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Congenital deafness with labyrinthine aplasia, microtia and microdontia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C565195 | Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia | Non-standard |
| Nebraska Lexicon | 702360007 | Congenital deafness with labyrinthine aplasia, microtia and microdontia | Non-standard |
Synonyms
Alternative names recorded for Congenital deafness with labyrinthine aplasia, microtia and microdontia across source vocabularies.
- Congenital deafness with inner ear agenesis, microtia, and microdontia
- Congenital deafness with labyrinthine aplasia, microtia and microdontia (disorder)
- LAMM syndrome
- síndrome LAMM
- sordera congénita con agenesia de oído interno, microtia y microdoncia
- sordera congénita con aplasia laberíntica, microtia y microdoncia
- sordera congénita con aplasia laberíntica, microtia y microdoncia (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(71)Roll up to these when you need a wider cohort.
- 1Auditory system hereditary disorder
- 1Autosomal recessive hereditary disorder
- 1Congenital anomaly of ear with impairment of hearing
- 1Congenital anomaly of inner ear
- 1Congenital anomaly of tooth
- 1Congenital deafness
- 1Decreased hearing
- 1Developmental hereditary disorder
- 1Hearing loss associated with syndrome
- 1Hereditary disorder of tooth
- 1Microdontia
- 1Microtia
- 1Multiple system malformation syndrome
- 2Autosomal hereditary disorder
- 2Complete deafness
- 2Congenital abnormality of external ear
- 2Congenital abnormality of oral cavity
- 2Congenital anomaly of digestive organ
- 2Congenital anomaly of jaw
- 2Congenital hearing disorder
- 2Congenital malformation of ear
- 2Congenital malformation syndrome
- 2Decline in functional status
- 2Developmental disorder
- 2Digestive system hereditary disorder
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