OMOP Concept 4195318
Xeroderma pigmentosum
StandardConditionSNOMED44600005Disorder
Maps from
12
Descendants
10
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
12 source codes normalize to Xeroderma pigmentosum via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 122802 | Xeroderma pigmentosum | Non-standard |
| CIEL | 130204 | Pigmented Xerodermoid | Non-standard |
| CIM10 | Q82.1 | Xeroderma pigmentosum | Non-standard |
| ICD10 | Q82.1 | Xeroderma pigmentosum | Non-standard |
| ICD10CM | Q82.1 | Xeroderma pigmentosum | Non-standard |
| ICD10CN | Q82.1 | Xeroderma pigmentosum | Non-standard |
| ICD10CN | Q82.100 | Xeroderma pigmentosum | Non-standard |
| ICD10GM | Q82.1 | Xeroderma pigmentosum | Non-standard |
| KCD7 | Q82.1 | Xeroderma pigmentosum | Non-standard |
| MeSH | D014983 | Xeroderma Pigmentosum | Non-standard |
| Read | PH32200 | Xeroderma pigmentosum | Non-standard |
| Read | PH32211 | Kaposi's xeroderma pigmentosum | Non-standard |
Synonyms
Alternative names recorded for Xeroderma pigmentosum across source vocabularies.
- angioma pigmentoso atrófico
- Angioma pigmentosum atrophicum
- atrodermia pigmentosa
- Atrophoderma pigmentosum
- dermatosis de Kaposi
- epiteliomatosis pigmentada
- Kaposi dermatosis
- Melanosis lenticularis progressiva
- melanosis lenticular progresiva
- Pigmented epitheliomatosis
- Xeroderma of Kaposi
- xeroderma pigmentaria
- Xeroderma pigmentosum (disorder)
- xerodermia de Kaposi
- xerodermia pigmentosa
- xerodermia pigmentosa (trastorno)
- XP - Xeroderma pigmentosum
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(30)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Developmental hereditary disorder
- 1Genetic disorder of skin pigmentation
- 1Hereditary cancer-predisposing syndrome
- 1Hereditary disorder of the integument
- 1Skin deposits
- 1Xeroderma
- 2Autosomal hereditary disorder
- 2Developmental disorder
- 2Disorder of integument
- 2Disorder of skin
- 2Disorder of skin pigmentation
- 2Finding of moistness of skin
- 2Genetic disease
- 2Hereditary disease
- 2Hereditary disorder by system
- 3Disease
- 3Disorder of body system
- 3Disorder of pigmentation
- 3Disorder of skin and/or subcutaneous tissue
- 3Integumentary system finding
- 3Skin finding
- 3Skin lesion
- 4Clinical finding
- 4Disorder of soft tissue
Showing 25 of 30. Retrieve the full set via the API.
Narrower concepts
(10)Included automatically when you query with descendants.
- 1Non-neurologic xeroderma pigmentosum
- 1Xeroderma pigmentosum and Cockayne syndrome complex
- 1Xeroderma pigmentosum, group A
- 1Xeroderma pigmentosum, group B
- 1Xeroderma pigmentosum, group C
- 1Xeroderma pigmentosum, group D
- 1Xeroderma pigmentosum, group E
- 1Xeroderma pigmentosum, group F
- 1Xeroderma pigmentosum, group G
- 1Xeroderma pigmentosum, variant form
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