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#618952 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 46; COXPD46
Cytogenetic locations: mutation
Gene summaries Genetic tests Medical literature
#618835 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 40; COXPD40
Cytogenetic locations: 616823
#618239 - MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 17; MC1DN17
Cytogenetic locations: Phosphatidylinositol
*617209 - GLUTAMINYL-tRNA AMIDOTRANSFERASE SUBUNIT QRSL1; QRSL1
#615457 - BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 18; BMIQ18
Cytogenetic locations: 19390624
*615410 - MELANOCORTIN 2 RECEPTOR ACCESSORY PROTEIN 2; MRAP2
Cytogenetic locations: 23869017
#610678 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 4; COXPD4
Cytogenetic locations: 17160893
*601421 - LYSYL-tRNA SYNTHETASE 1; KARS1
Cytogenetic locations: 28887846
#300952 - LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 3; LSDMCA3
Cytogenetic locations: 610877
*300403 - NADH-UBIQUINONE OXIDOREDUCTASE 1 BETA SUBCOMPLEX, 11; NDUFB11
*300102 - PATATIN-LIKE PHOSPHOLIPASE DOMAIN-CONTAINING PROTEIN 4; PNPLA4
Cytogenetic locations: 27806223
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