Rieger syndrome 2

Preferred Label : Rieger syndrome 2;

Obsolete resource : true;

Approved symbol HGNC : RIEG2;

Alias symbols HGNC : ARS;

Chromosome HGNC : 13q14;

Locus type HGNC : phenotype;

Détails

Origin ID

HGNC:10015;

UMLS CUI

C1419386;

Automatic exact mappings (from CISMeF team)
- Al-raqad syndrome [OMIM Phenotype]
See also inter- (CISMeF)
- Axenfeld-rieger syndrome, type 2 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]

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