Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9785
Gene Symbol: DHX38
DHX38
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa
0.520 GermlineCausalMutation ORPHANET We identified a second deleterious DHX38 variant that segregates with arRP in two families, providing additional evidence that DHX38 is involved in RP etiology. 30208423

2018