OMOP Concept 36716315
Agnathia, holoprosencephaly, situs inversus syndrome
StandardConditionSNOMED722283003Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Agnathia, holoprosencephaly, situs inversus syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 722283003 | Agnathia, holoprosencephaly, situs inversus syndrome | Non-standard |
Synonyms
Alternative names recorded for Agnathia, holoprosencephaly, situs inversus syndrome across source vocabularies.
- Agnathia, holoprosencephaly, situs inversus syndrome (disorder)
- síndrome de agnatia, holoprosencefalia y situs inversus
- síndrome de agnatia, holoprosencefalia y situs inversus (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(45)Roll up to these when you need a wider cohort.
- 1Congenital micrognathism
- 1Developmental hereditary disorder
- 1Hereditary disorder of musculoskeletal system
- 1Holoprosencephaly sequence
- 1Multiple malformation syndrome with facial defects as major feature
- 2Congenital anomaly of face
- 2Congenital anomaly of head
- 2Congenital anomaly of mandible
- 2Craniofacial microsomia
- 2Developmental disorder
- 2Disorder of musculoskeletal system
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Hypoplasia of mandibular bone
- 2Malformation sequence
- 2Multiple system malformation syndrome
- 3Congenital abnormality of skull and face bones
- 3Congenital anomaly of face bones
- 3Congenital anomaly of jaw
- 3Congenital malformation
- 3Congenital malformation syndrome
- 3Disease
- 3Disorder of body system
- 3Disorder of face
- 3Disorder of head
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