Recon progeroid syndrome - CISMeF

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CISMeF

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Recon progeroid syndromeOMIM Phenotype

Preferred Label : Recon progeroid syndrome;

Symbol : RECON;

Type : Phenotype, molecular basis known;

Prefixed ID : #620370;

Details

Origin ID

620370;

UMLS CUI

C5830504;

Genes related to phenotype
- Recq protein-like [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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10/05/2025

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