OMOP Concept 37205090
Autosomal recessive cutis laxa type 2A
StandardConditionSNOMED784381008Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2019
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Autosomal recessive cutis laxa type 2A via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C562632 | Cutis Laxa, Autosomal Recessive, Type IIA | Non-standard |
Synonyms
Alternative names recorded for Autosomal recessive cutis laxa type 2A across source vocabularies.
- ARCL2A - autosomal recessive cutis laxa type 2A
- Autosomal recessive cutis laxa type 2A (disorder)
- piel laxa autosómica recesiva tipo 2A
- piel laxa autosómica recesiva tipo 2A (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(57)Roll up to these when you need a wider cohort.
- 1Cutis laxa, recessive, type II
- 1Dysplasia with decreased bone density
- 1Fetal and/or neonatal disorder of integument
- 1Hereditary disorder of musculoskeletal system
- 1Metabolic bone disease
- 1Musculoskeletal and connective tissue disorder
- 2Bone density below reference range
- 2Congenital anomaly of skeletal bone
- 2Cutis laxa, autosomal recessive
- 2Disorder of bone
- 2Disorder of connective tissue
- 2Disorder of integument
- 2Disorder of musculoskeletal system
- 2Fetal and/or neonatal disorder
- 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
- 3Disease
- 3Disorder of body system
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