OMOP Concept 36714536
Xeroderma pigmentosum and Cockayne syndrome complex
StandardConditionSNOMED719819004Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Xeroderma pigmentosum and Cockayne syndrome complex via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 719819004 | Xeroderma pigmentosum and Cockayne syndrome complex | Non-standard |
Synonyms
Alternative names recorded for Xeroderma pigmentosum and Cockayne syndrome complex across source vocabularies.
- complejo de xerodermia pigmentosa y síndrome de Cockayne
- complejo de xerodermia pigmentosa y síndrome de Cockayne (trastorno)
- Xeroderma pigmentosum and Cockayne syndrome complex (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(44)Roll up to these when you need a wider cohort.
- 1Cockayne syndrome
- 1Xeroderma pigmentosum
- 2Autosomal recessive hereditary disorder
- 2Congenital anomaly of central nervous system
- 2Developmental hereditary disorder
- 2Genetic disorder of skin pigmentation
- 2Hereditary cancer-predisposing syndrome
- 2Hereditary disorder of nervous system
- 2Hereditary disorder of the integument
- 2Multiple malformation syndrome with senile-like appearance
- 2Skin deposits
- 2Xeroderma
- 3Autosomal hereditary disorder
- 3Congenital anomaly of nervous system
- 3Developmental disorder
- 3Disorder of integument
- 3Disorder of nervous system
- 3Disorder of skin
- 3Disorder of skin pigmentation
- 3Disorder of the central nervous system
- 3Finding of moistness of skin
- 3Genetic disease
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Multiple system malformation syndrome
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