OMOP Concept 4242416
Cutis laxa
StandardConditionSNOMED58588007Disorder
Maps from
5
Descendants
33
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
5 source codes normalize to Cutis laxa via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 119718 | Cutis laxa | Non-standard |
| HPO | HP_0000973 | Cutis laxa | Non-standard |
| MeSH | C531660 | Generalized elastolysis | Non-standard |
| MeSH | D003483 | Cutis Laxa | Non-standard |
| Nebraska Lexicon | 58588007 | Generalized dermatochalasis | Non-standard |
Synonyms
Alternative names recorded for Cutis laxa across source vocabularies.
- chalazodermia
- Chalazodermia
- cutis laxa
- Cutis laxa (disorder)
- cutis laxo
- cutis laxo (trastorno)
- dermatólisis
- Dermatolysis
- dermatomegalia
- Dermatomegaly
- elastólisis primaria
- Generalised elastolysis
- Generalised elastorrhexis
- Generalized elastolysis
- Generalized elastorrhexis
- Primary elastolysis
- Systematised elastorrhexis
- Systematized elastorrhexis
- Systemic elastorrhexis
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(15)Roll up to these when you need a wider cohort.
- 1Collagen and elastic tissue disorders affecting skin
- 1Metabolic disease of collagen
- 2Disorder of connective tissue
- 2Disorder of skin
- 2Metabolic disease
- 3Disease
- 3Disorder of skin and/or subcutaneous tissue
- 3Skin finding
- 4Clinical finding
- 4Disorder of integument
- 4Disorder of soft tissue
- 4General finding of soft tissue
- 4Integumentary system finding
- 4Skin AND/OR mucosa finding
- 5Disorder of body system
Narrower concepts
(33)Included automatically when you query with descendants.
- 1Cantu's syndrome
- 1Craniofaciofrontodigital syndrome
- 1Cutis laxa, acquired type
- 1Cutis laxa of lower eyelid
- 1Cutis laxa of upper eyelid
- 1Cutis laxa secondary to inherited disorder of connective tissue
- 1Cutis laxa senilis
- 1Cutis laxa with osteodystrophy
- 1Drug-induced cutis laxa
- 1Hemolytic anemia with emphysema AND cutis laxa
- 1Inherited cutis laxa
- 1Noninflammatory dermal elastolysis
- 2Cutis laxa, autosomal dominant
- 2Cutis laxa, autosomal recessive
- 2Cutis laxa following hypersensitivity reaction
- 2Cutis laxa following urticaria-angioedema
- 2Cutis laxa of bilateral lower eyelid
- 2Cutis laxa of bilateral upper eyelid
- 2Cutis laxa with complement deficiency
- 2Cutis laxa, x-linked
- 2Localized congenital cutis laxa
- 2Neonatal cutis laxa with marfanoid phenotype
- 2Post-inflammatory cutis laxa
- 2SCARF syndrome
- 3Cutis laxa, recessive, type I
- 3Cutis laxa, recessive, type II
- 3Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies
- 3de Barsey syndrome
- 3MACS syndrome
- 4ALDH18A1-related de Barsy syndrome
- 4Autosomal recessive cutis laxa type 2A
- 4Autosomal recessive cutis laxa type 2B
- 4Pyrroline-5-carboxylate reductase 1 related de Barsy syndrome
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