SMAP1, small ArfGAP 1, 60682

N. diseases: 5; N. variants: 1
Disease: Retinitis Pigmentosa 25 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1864446
Disease: Retinitis Pigmentosa 25
Retinitis Pigmentosa 25 		0.010 Biomarker disease BEFREE The absence of pathogenic mutations after molecular analysis argues against the implication of ELOVL5, SMAP1 and GLULD1 in the development of RP25 phenotype. 16273301 2005