OMOP Concept 4326230
Dyskeratosis congenita
StandardConditionSNOMED74911008Disorder
Maps from
5
Descendants
5
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
5 source codes normalize to Dyskeratosis congenita via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 141626 | Dyskeratosis congenita | Non-standard |
| MeSH | D019871 | Dyskeratosis Congenita | Non-standard |
| Read | PH33700 | Dyskeratosis congenita | Non-standard |
| Read | PH33711 | Zinsser-Cole-Engman syndrome | Non-standard |
| Read | PH33712 | Cole-Engman-Zinsser syndrome | Non-standard |
Synonyms
Alternative names recorded for Dyskeratosis congenita across source vocabularies.
- Cole-Engmann-Zinsser syndrome
- Cole-Engman-Zinsser syndrome
- Congenital dyskeratosis
- disqueratosis congénita
- disqueratosis congénita (trastorno)
- DKC - Dyskeratosis congenita
- Dyskeratosis congenita (disorder)
- síndrome de Zinsser - Cole - Engman
- Zinsser-Cole-Engmann syndrome
- Zinsser-Cole-Engman syndrome
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(32)Roll up to these when you need a wider cohort.
- 1Developmental hereditary disorder
- 1Ectodermal dysplasia
- 1Hereditary cancer-predisposing syndrome
- 1Hereditary disorder of the integument
- 1Skin lesion
- 2Congenital ectodermal defect
- 2Developmental disorder
- 2Disorder of integument
- 2Disorder of skin
- 2Genodermatosis
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Lesion of skin and/or skin-associated mucous membrane
- 2Lesion of soft tissue
- 3Congenital anomaly of skin
- 3Congenital malformation
- 3Disease
- 3Disorder of body system
- 3Disorder of embryonic structure
- 3Disorder of skin and/or subcutaneous tissue
- 3Disorder of soft tissue
- 3Genetic disease
- 3Integumentary system finding
- 3Skin finding
- 3Skin or mucosa lesion
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Narrower concepts
(5)Included automatically when you query with descendants.
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