OMOP Concept 4111183
Craniofacial microsomia
StandardConditionSNOMED254026007Disorder
Maps from
1
Descendants
43
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Craniofacial microsomia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 254026007 | Craniofacial microsomia | Non-standard |
Synonyms
Alternative names recorded for Craniofacial microsomia across source vocabularies.
- Craniofacial microsomia (disorder)
- microsomía craneofacial
- microsomía craneofacial (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(19)Roll up to these when you need a wider cohort.
- 1Congenital abnormality of skull and face bones
- 2Congenital anomaly of head
- 2Congenital anomaly of skeletal bone
- 3Congenital anomaly of musculoskeletal system
- 3Congenital malformation
- 3Disorder of bone development
- 3Disorder of head
- 4Congenital disease
- 4Developmental disorder
- 4Disease
- 4Disorder of bone
- 4Disorder of musculoskeletal system
- 4Head finding
- 5Bone finding
- 5Clinical finding
- 5Disorder of body system
- 5Disorder of fetus and/or newborn
- 5Disorder of skeletal system
- 5Musculoskeletal finding
Narrower concepts
(43)Included automatically when you query with descendants.
- 1Acrorenal mandibular syndrome
- 1Antley-Bixler syndrome
- 1Bilateral craniofacial microsomia
- 1Congenital alveolar hypoplasia of mandible
- 1Congenital hypoplasia of alisphenoid bone
- 1Congenital hypoplasia of basioccipital bone
- 1Congenital hypoplasia of exoccipital bone
- 1Congenital hypoplasia of frontal bone
- 1Congenital hypoplasia of interparietal bone
- 1Congenital hypoplasia of lacrimal bone
- 1Congenital hypoplasia of nasal bone
- 1Congenital hypoplasia of palatine bone
- 1Congenital hypoplasia of parietal bone
- 1Congenital hypoplasia of squamosal bone
- 1Congenital hypoplasia of zygomatic bone
- 1Congenital maxillary hypoplasia
- 1Congenital micrognathism
- 1Goldenhar syndrome
- 1Hemifacial microsomia
- 1Non-eruption of teeth, maxillary hypoplasia, genu valgum syndrome
- 2Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome
- 2Agnathia, holoprosencephaly, situs inversus syndrome
- 2Cerebro-costo-mandibular syndrome
- 2Congenital alveolar hypoplasia of maxilla
- 2Congenital horizontal mandibular hypoplasia
- 2Congenital hypoplasia of left zygomatic bone
- 2Congenital hypoplasia of right zygomatic bone
- 2Congenital hypoplasia of vomer
- 2Congenital transverse mandibular hypoplasia
- 2Congenital transverse maxillary hypoplasia
- 2Congenital vertical mandibular hypoplasia
- 2Congenital vertical maxillary hypoplasia
- 2Distal limb deficiency with micrognathia syndrome
- 2Hemifacial microsomia with radial defect syndrome
- 2Joint contracture, webbed neck, micrognathia, hypoplastic nipple syndrome
- 2Mandibular hypoplasia, deafness, progeroid syndrome
- 2Metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome
- 2Oculo-auriculo-vertebral spectrum
- 2SATB2-associated syndrome
- 2Short stature, auditory canal atresia, mandibular hypoplasia, skeletal anomalies syndrome
- 2Splenogonadal fusion, limb defect, micrognathia syndrome
- 2Thickened earlobe with conductive deafness syndrome
- 3Congenital hypoplasia of bilateral zygomatic bones
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