OMOP Concept 36680612
Autosomal recessive cutis laxa type 2B
StandardConditionSNOMED778068007Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2019
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to Autosomal recessive cutis laxa type 2B via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C567855 | Cutis Laxa, Autosomal Recessive, Type IIB | Non-standard |
Synonyms
Alternative names recorded for Autosomal recessive cutis laxa type 2B across source vocabularies.
- ARCL2B - autosomal recessive cutis laxa type 2B
- Autosomal recessive cutis laxa type 2B (disorder)
- Autosomal recessive cutis laxa type 2 progeroid type
- cutis laxa autosómica recesiva tipo 2B
- cutis laxa autosómica recesiva tipo 2B (trastorno)
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.
- 1Congenital anomaly of skin
- 1Cutis laxa, recessive, type II
- 1Disorder of proline AND/OR hydroxyproline metabolism
- 1Dysplasia with decreased bone density
- 1Hereditary disorder of musculoskeletal system
- 1Metabolic bone disease
- 1Musculoskeletal and connective tissue disorder
- 2Bone density below reference range
- 2Congenital anomaly of integument
- 2Congenital anomaly of skeletal bone
- 2Cutis laxa, autosomal recessive
- 2Disorder of amino acid and organic acid metabolism
- 2Disorder of bone
- 2Disorder of connective tissue
- 2Disorder of musculoskeletal system
- 2Disorder of skin
- 2Hereditary disorder by system
- 2Lesion of bone
- 2Metabolic disease
- 2Skeletal dysplasia
- 3Autosomal recessive hereditary disorder
- 3Bone densimetry abnormal
- 3Bone density finding
- 3Bone finding
- 3Congenital anomaly of musculoskeletal system
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