Dyskeratosis congenita, digenic - CISMeF

" /> Dyskeratosis congenita, digenic - CISMeF

CISMeF

chu

Dyskeratosis congenita, digenicOMIM Phenotype

Preferred Label : Dyskeratosis congenita, digenic;

Symbol : DKCD;

Type : Phenotype, molecular basis known;

Prefixed ID : #620040;

Details

Origin ID

620040;

UMLS CUI

C5774217;

Genes related to phenotype
- Thymidylate synthetase [OMIM gene]
ORDO concept(s)
- Dyskeratosis congenita [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients

Nous contacter.
06/05/2025

© Rouen University Hospital. Any partial or total use of this material must mention the source.