DDHD2, DDHD domain containing 2, 23259

N. diseases: 37; N. variants: 11
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0037772
Disease: Spastic Paraplegia
Spastic Paraplegia
0.110 GeneticVariation disease BEFREE Loss of DDHD2, whose mutation causes spastic paraplegia, promotes reactive oxygen species generation and apoptosis. 30038238 2018
CUI: C0037772
Disease: Spastic Paraplegia
Spastic Paraplegia
0.110 Biomarker disease HPO