OMOP Concept 37110741
Cryptomicrotia brachydactyly syndrome
StandardConditionSNOMED725096002Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Cryptomicrotia brachydactyly syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C536219 | Cryptomicrotia brachydactyly syndrome | Non-standard |
Synonyms
Alternative names recorded for Cryptomicrotia brachydactyly syndrome across source vocabularies.
- Cryptomicrotia, brachydactyly, excess fingertip arch syndrome
- Cryptomicrotia brachydactyly syndrome (disorder)
- síndrome de criptomicrotia y braquidactilia
- síndrome de criptomicrotia y braquidactilia (trastorno)
- Tonoki Ohura Niikawa syndrome
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(62)Roll up to these when you need a wider cohort.
- 1Auditory system hereditary disorder
- 1Autosomal dominant hereditary disorder
- 1Brachymesophalangia
- 1Congenital abnormality of external ear
- 1Developmental hereditary disorder
- 1Hereditary disorder of musculoskeletal system
- 1Multiple malformation syndrome with limb defect as major feature
- 2Autosomal hereditary disorder
- 2Brachyphalangia
- 2Congenital malformation of ear
- 2Developmental disorder
- 2Disorder of auditory system
- 2Disorder of external ear
- 2Disorder of musculoskeletal system
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Multiple system malformation syndrome
- 3Abnormally short long bone
- 3Brachydactyly
- 3Congenital anomaly of head
- 3Congenital malformation syndrome
- 3Disease
- 3Disorder of body system
- 3Disorder of ear
- 3Ear and auditory finding
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