PRDX5, peroxiredoxin 5, 25824

N. diseases: 153; N. variants: 4
Disease: Leukodystrophy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy 		0.020 GeneticVariation disease BEFREE Pelizaeus-Merzbacher disease (PMD) can now be defined as an X-linked recessive leukodystrophy that is caused by a mutation in the proteolipid protein (PLP) gene on chromosome Xq22. 12230321 2002
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy 		0.020 GeneticVariation disease BEFREE Pelizaeus-Merzbacher disease (PMD) is a leukodystrophy associated with mutations in the proteolipid protein (PLP) gene. 10401787 1999