Renpenning syndrome 2

Preferred Label : Renpenning syndrome 2;

Obsolete resource : true;

Approved symbol HGNC : RENS2;

Name synonyms HGNC : Renpenning-like syndrome;

Alias symbols HGNC : MRXS9;

Chromosome HGNC : Xq12-q21.31;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:9961;

UMLS CUI

C1419341;

Automatic exact mappings (from CISMeF team)
- Intellectual developmental disorder, X-linked, syndromic 9 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]

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