OMOP Concept 4281660
Acrodysostosis
StandardConditionSNOMED66758006Disorder
Maps from
3
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
3 source codes normalize to Acrodysostosis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 149961 | Acrodysostosis | Non-standard |
| MeSH | C538179 | Acrodysostosis | Non-standard |
| Read | PG5F.00 | Acrodysostosis | Non-standard |
Synonyms
Alternative names recorded for Acrodysostosis across source vocabularies.
- acrodisostosis
- acrodisostosis (trastorno)
- Acrodysostosis (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(63)Roll up to these when you need a wider cohort.
- 1Acromesomelic dysplasia syndrome
- 1Autosomal dominant hereditary disorder
- 1Congenital deformity of hand
- 1Congenital dysplasia of lower limb
- 1Congenital undergrowth of partial lower limb
- 1Developmental hereditary disorder
- 1Dysostosis
- 1Hereditary disorder of musculoskeletal system
- 1Longitudinal deficiency of foot
- 1Longitudinal deficiency of part of upper limb
- 2Autosomal hereditary disorder
- 2Congenital anomaly of hand
- 2Congenital anomaly of lower limb
- 2Congenital anomaly of skeletal bone
- 2Congenital deformity of foot
- 2Congenital deformity of lower limb
- 2Congenital deformity of upper limb
- 2Congenital dysplasia of limb
- 2Deformity of hand
- 2Developmental disorder
- 2Disorder of musculoskeletal system
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Lesion of bone
- 2Longitudinal deficiency of part of limb
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