Revesz syndrome (Q7318329)
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dyskeratosis congenita that has material basis in an X-linked recessive mutation of TINF2 on chromosome 14q12
- exudative retinopathy with bone marrow failure
- DKCA5
- Dyskeratosis Congenita, Autosomal Dominant 5
- Retinopathy-anemia-central nervous system anomalies syndrome
- REVESZ SYNDROME
- Revesz-DeBuse syndrome
- Dyskeratosis congenita with bilateral exudative retinopathy
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Revesz syndrome |
dyskeratosis congenita that has material basis in an X-linked recessive mutation of TINF2 on chromosome 14q12 |
|
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Sitelinks
Wikipedia(6 entries)
- dewiki Revesz-Syndrom
- enwiki Revesz syndrome
- eswiki Síndrome de Revesz
- fawiki سندرم ریوز
- plwiki Zespół Revesza
- trwiki Revesz sendromu