Preferred Label : Rieger syndrome 2;
Obsolete resource : true;
Approved symbol HGNC : RIEG2;
Alias symbols HGNC : ARS;
Chromosome HGNC : 13q14;
Locus type HGNC : phenotype;
Origin ID : HGNC:10015;
UMLS CUI : C1419386;
Automatic exact mappings (from CISMeF team)
See also inter- (CISMeF)
Semantic type(s)