COX15
Deellabo: | PGD DNA |
Gen (Gen Code): | COX15 |
Aliases Gen: | COX15 |
Gen ID (NCBI): | 1355 |
OMIM Gen ID: | 603646 |
Chromosomale locatie: | 10q24.2 |
Genetische aandoening / Analyse: | Leigh syndroom (LS) - COX15 |
OMIM aandoening ID: | 256000 |
Overerving: | AR |
Aliases aandoening: | LEIGH SYNDROME; LS LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY, INCLUDED LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX II DEFICIENCY, INCLUDED LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX III DEFICIENCY, INCLUDED LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX IV DEFICIENCY, INCLUDED LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX V DEFICIENCY, INCLUDED |