OMOP Concept 36714981
Acrofacial dysostosis Rodriguez type
StandardConditionSNOMED720430002Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Acrofacial dysostosis Rodriguez type via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C538183 | Acrofacial dysostosis Rodriguez type | Non-standard |
| Nebraska Lexicon | 720430002 | Acrofacial dysostosis Rodriguez type | Non-standard |
Synonyms
Alternative names recorded for Acrofacial dysostosis Rodriguez type across source vocabularies.
- Acrofacial dysostosis Rodriguez type (disorder)
- disostosis acrofacial tipo Rodriguez
- disostosis acrofacial tipo Rodriguez (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(49)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Congenital anomaly of face bones
- 1Congenital dysplasia of limb
- 1Developmental hereditary disorder
- 1Dysostosis
- 1Hereditary disorder of musculoskeletal system
- 1Lesion of face
- 1Longitudinal deficiency of limb
- 1Multiple malformation syndrome with facial-limb defects as major feature
- 2Autosomal hereditary disorder
- 2Congenital abnormality of skull and face bones
- 2Congenital anomaly of face
- 2Congenital anomaly of limb
- 2Congenital anomaly of skeletal bone
- 2Congenital deformity
- 2Deformity of limb
- 2Developmental disorder
- 2Disorder of face
- 2Disorder of facial bone
- 2Disorder of musculoskeletal system
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Multiple malformation syndrome with facial defects as major feature
- 2Multiple malformation syndrome with limb defect as major feature
- 2Skeletal dysplasia
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