OMOP Concept 37117164
Revesz syndrome
StandardConditionSNOMED723512008Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Revesz syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C538371 | Revesz Debuse syndrome | Non-standard |
Synonyms
Alternative names recorded for Revesz syndrome across source vocabularies.
- disqueratosis congénita con retinopatía exudativa bilateral
- disqueratosis congénita con retinopatía exudativa bilateral (trastorno)
- Dyskeratosis congenita with bilateral exudative retinopathy
- Retinopathy, anaemia, central nervous system anomalies syndrome
- Retinopathy, anemia, central nervous system anomalies syndrome
- Revesz DeBuse syndrome
- Revesz syndrome (disorder)
- síndrome de Revesz
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(102)Roll up to these when you need a wider cohort.
- 1Autosomal dominant dyskeratosis congenita
- 1Constitutional aplastic anemia
- 1Hereditary disorder of the visual system
- 1Hereditary white blood cell disorder
- 1Inherited platelet disorder
- 1Retinal disorder
- 2Aplastic anemia
- 2Autosomal dominant hereditary disorder
- 2Congenital anemia
- 2Congenital anomaly of the hematopoietic system
- 2Congenital thrombocytopenia
- 2Disorder of vitreous body and/or retina
- 2Dyskeratosis congenita
- 2Hereditary disorder by system
- 2Hereditary disorder of cellular element of blood
- 2Hereditary disorder of immune system
- 2Platelet disorder
- 2Retina finding
- 2Visual system disorder
- 2White blood cell disorder
- 3Anemia
- 3Anemia due to decreased red cell production
- 3Autosomal hereditary disorder
- 3Bone marrow disorder
- 3Congenital disease
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