Jacobsen syndrome

Preferred Label : Jacobsen syndrome;

Obsolete resource : true;

Approved symbol HGNC : JBS;

Chromosome HGNC : 11q24.1;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:6194;

UMLS CUI

C1416527;

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

Keyword's position in hierarchy(ies) :

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