OMOP Concept 4147430
Adams-Oliver syndrome
StandardConditionSNOMED34748004Disorder
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 Adams-Oliver syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 149456 | Adams-Oliver syndrome | Non-standard |
| MeSH | C538225 | Adams Oliver syndrome | Non-standard |
| Read | PKy0200 | Adams-Oliver syndrome | Non-standard |
Synonyms
Alternative names recorded for Adams-Oliver syndrome across source vocabularies.
- Adams-Oliver syndrome (disorder)
- Congenital absence of skin on scalp with limb-reduction anomaly
- síndrome de Adam - Oliver
- síndrome de Adam - Oliver (trastorno)
- Type 2 aplasia cutis
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(39)Roll up to these when you need a wider cohort.
- 1Aplasia cutis congenita
- 1Autosomal hereditary disorder
- 1Congenital anomaly of head
- 1Congenital anomaly of limb
- 1Developmental hereditary disorder
- 1Disorder of scalp
- 1Disorder of skin of head
- 1Hereditary disorder of the integument
- 1Multiple malformation syndrome with limb defect as major feature
- 2Aplasia of skin
- 2Congenital anomaly of skin
- 2Congenital malformation
- 2Developmental disorder
- 2Disorder of head
- 2Disorder of integument
- 2Disorder of limb
- 2Disorder of skin
- 2Disorder of skin AND/OR subcutaneous tissue of head
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Multiple system malformation syndrome
- 3Congenital anomaly of integument
- 3Congenital disease
- 3Congenital malformation syndrome
- 3Disease
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