Source: UNIPROT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 64421
Gene Symbol: DCLRE1C
DCLRE1C
CUI: C2700553
Disease: Omenn Syndrome
Omenn Syndrome 		0.750 GeneticVariation UNIPROT We report on a first patient with clinical and immunologic features of OS caused by hypomorphic ARTEMIS mutations. 15731174

2005