Prieto X-linked mental retardation syndrome

Preferred Label : Prieto X-linked mental retardation syndrome;

Obsolete resource : true;

Approved symbol HGNC : PRS;

Chromosome HGNC : Xp21-p11;

Locus type HGNC : phenotype;

Détails

Origin ID

HGNC:9471;

UMLS CUI

C1418963;

Automatic exact mappings (from CISMeF team)
- Prieto syndrome [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]

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