OMOP Concept 4032906
Collagen and elastic tissue disorders affecting skin
StandardConditionSNOMED238846003Disorder
Maps from
1
Descendants
39
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Collagen and elastic tissue disorders affecting skin via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 238846003 | Collagen and elastic tissue disorders affecting skin | Non-standard |
Synonyms
Alternative names recorded for Collagen and elastic tissue disorders affecting skin across source vocabularies.
- Collagen and elastic tissue disorders affecting skin (disorder)
- enfermedad del colágeno y tejido elástico
- trastorno del colágeno y del tejido elástico que afecta la piel
- trastorno del colágeno y del tejido elástico que afecta la piel (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(11)Roll up to these when you need a wider cohort.
Narrower concepts
(39)Included automatically when you query with descendants.
- 1Body skin hyperlaxity due to vitamin K dependent coagulation factor deficiency
- 1Confetti-like atrophic macular lesions of skin
- 1Cutis laxa
- 1Extensive congenital erosions, vesicles and reticulate scarring
- 1Menkes kinky-hair syndrome
- 1Papular elastorrhexis
- 2Cantu's syndrome
- 2Craniofaciofrontodigital syndrome
- 2Cutis laxa, acquired type
- 2Cutis laxa of lower eyelid
- 2Cutis laxa of upper eyelid
- 2Cutis laxa secondary to inherited disorder of connective tissue
- 2Cutis laxa senilis
- 2Cutis laxa with osteodystrophy
- 2Drug-induced cutis laxa
- 2Hemolytic anemia with emphysema AND cutis laxa
- 2Inherited cutis laxa
- 2Noninflammatory dermal elastolysis
- 3Cutis laxa, autosomal dominant
- 3Cutis laxa, autosomal recessive
- 3Cutis laxa following hypersensitivity reaction
- 3Cutis laxa following urticaria-angioedema
- 3Cutis laxa of bilateral lower eyelid
- 3Cutis laxa of bilateral upper eyelid
- 3Cutis laxa with complement deficiency
- 3Cutis laxa, x-linked
- 3Localized congenital cutis laxa
- 3Neonatal cutis laxa with marfanoid phenotype
- 3Post-inflammatory cutis laxa
- 3SCARF syndrome
- 4Cutis laxa, recessive, type I
- 4Cutis laxa, recessive, type II
- 4Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies
- 4de Barsey syndrome
- 4MACS syndrome
- 5ALDH18A1-related de Barsy syndrome
- 5Autosomal recessive cutis laxa type 2A
- 5Autosomal recessive cutis laxa type 2B
- 5Pyrroline-5-carboxylate reductase 1 related de Barsy syndrome
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