OMOP Concept 4241225
Cutis laxa, x-linked
StandardConditionSNOMED59399004Disorder
Maps from
2
Descendants
0
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 Cutis laxa, x-linked via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 143056 | Cutis laxa, X-linked | Non-standard |
| MeSH | C537860 | Occipital horn syndrome | Non-standard |
Synonyms
Alternative names recorded for Cutis laxa, x-linked across source vocabularies.
- cutis laxa, ligado al cromosoma X
- cutis laxa, ligado al cromosoma X (trastorno)
- Cutis laxa, x-linked (disorder)
- Ehlers-Danlos syndrome, mental retardation type
- Ehlers-Danlos syndrome, occipital horn type
- Ehlers-Danlos syndrome, type 9
- Ehlers-Danlos syndrome type 9 X-linked
- Ehlers-Danlos syndrome, x-linked skeletal type
- Occipital horn syndrome
- piel hiperelástica, ligada al cromosoma X
- síndrome de Ehlers-Danlos, tipo 9
- síndrome de Ehlers-Danlos, tipo cuerno occipital
- síndrome de Ehlers-Danlos, tipo esquelético ligado al cromosoma X
- síndrome de Ehlers-Danlos, tipo retraso mental
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(50)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of skeletal bone
- 1Congenital anomaly of skin
- 1Disorder of copper metabolism
- 1Hereditary disorder of musculoskeletal system
- 1Inherited cutis laxa
- 1Lesion of bone
- 1Metabolic bone disease
- 1Musculoskeletal and connective tissue disorder
- 1Skeletal dysplasia
- 1X-linked recessive hereditary disease
- 2Congenital anomaly of integument
- 2Congenital anomaly of musculoskeletal system
- 2Congenital connective tissue disorder
- 2Connective tissue hereditary disorder
- 2Cutis laxa
- 2Developmental hereditary disorder
- 2Disorder of bone
- 2Disorder of bone development
- 2Disorder of connective tissue
- 2Disorder of mineral metabolism
- 2Disorder of musculoskeletal system
- 2Disorder of skin
- 2Hereditary disorder by system
- 2Hereditary disorder of the integument
- 2Metabolic disease
Showing 25 of 50. Retrieve the full set via the API.
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