mental retardation, X-linked, syndromic 11

Preferred Label : mental retardation, X-linked, syndromic 11;

Obsolete resource : true;

Approved symbol HGNC : MRXS11;

Alias symbols HGNC : SMRXS;

Chromosome HGNC : Xq26-q27;

Locus type HGNC : phenotype;

Détails

Origin ID

HGNC:13865;

UMLS CUI

C1422242;

Automatic exact mappings (from CISMeF team)
- Intellectual developmental disorder, X-linked, syndromic, shashi type [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]

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