OMOP Concept 4250025
Metabolic disease of collagen
StandardConditionSNOMED73873008Disorder
Maps from
2
Descendants
60
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to Metabolic disease of collagen via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 134271 | Metabolic Disease of Collagen | Non-standard |
| Nebraska Lexicon | 73873008 | Metabolic disease of collagen | Non-standard |
Synonyms
Alternative names recorded for Metabolic disease of collagen across source vocabularies.
- enfermedad metabólica del colágeno
- enfermedad metabólica del colágeno (trastorno)
- Metabolic disease of collagen (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(4)Roll up to these when you need a wider cohort.
Narrower concepts
(60)Included automatically when you query with descendants.
- 1Collagen deficiency syndrome
- 1Cutis laxa
- 1Dermatosparaxis in cattle AND/OR sheep
- 1Ehlers-Danlos syndrome
- 1Gronblad-Strandberg syndrome
- 2Arthrochalasia Ehlers-Danlos syndrome
- 2Brittle cornea syndrome
- 2Cantu's syndrome
- 2Classical-like Ehlers-Danlos syndrome type 1
- 2Classical-like Ehlers-Danlos syndrome type 2
- 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
- 2Dermatosparaxis Ehlers-Danlos syndrome
- 2Drug-induced cutis laxa
- 2Ehlers-Danlos syndrome cardiac valvular type
- 2Ehlers-Danlos syndrome classic type
- 2Ehlers-Danlos syndrome, dysfibronectinemic
- 2Ehlers-Danlos syndrome kyphoscoliotic type
- 2Ehlers-Danlos syndrome musculocontractural type
- 2Hemolytic anemia with emphysema AND cutis laxa
- 2Hypermobile Ehlers-Danlos syndrome
- 2Inherited cutis laxa
- 2Myopathic Ehlers-Danlos syndrome
- 2Noninflammatory dermal elastolysis
- 2Periodontal Ehlers-Danlos syndrome
- 2Spondylodysplastic Ehlers-Danlos syndrome
- 2Vascular Ehlers-Danlos syndrome
- 2X-linked Ehlers-Danlos syndrome
- 3B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome
- 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
- 3Ehlers-Danlos syndrome classic type 2
- 3Ehlers-Danlos syndrome, hydroxylysine-deficient
- 3Ehlers-Danlos syndrome kyphoscoliotic and deafness type
- 3Ehlers-Danlos syndrome progeroid type
- 3Ehlers-Danlos syndrome spondylocheirodysplastic type
- 3Localized congenital cutis laxa
- 3Neonatal cutis laxa with marfanoid phenotype
- 3Post-inflammatory cutis laxa
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