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238710 - HYPERLYSINEMIA DUE TO DEFECT IN LYSINE TRANSPORT INTO MITOCHONDRIA
Gene summaries Genetic tests Medical literature
258470 - OPHTHALMOPLEGIC NEUROMUSCULAR DISORDER WITH ABNORMAL MITOCHONDRIA
255140 - MYOPATHY WITH GIANT ABNORMAL MITOCHONDRIA
600706 - PROXIMAL MYOPATHY WITH FOCAL DEPLETION OF MITOCHONDRIA
*617298 - APOPTOSIS-INDUCING FACTOR, MITOCHONDRIA-ASSOCIATED, 3; AIFM3
Cytogenetic locations: 617843
238800 - HYPERMETABOLISM DUE TO UNCOUPLED MITOCHONDRIAL OXIDATIVE PHOSPHORYLATION 1; HUMOP1
*605159 - APOPTOSIS-INDUCING FACTOR, MITOCHONDRIA-ASSOCIATED, 2; AIFM2
Cytogenetic locations: 611309
*616184 - CLUSTERED MITOCHONDRIA, D. DISCOIDEUM, HOMOLOG OF; CLUH
Cytogenetic locations: 29734811
*601148 - SPERM MITOCHONDRIA-ASSOCIATED CYSTEINE-RICH PROTEIN; SMCP
Cytogenetic locations: 11940662
*619684 - MITOCHONDRIA-LOCALIZED GLUTAMIC ACID-RICH PROTEIN; MGARP
Cytogenetic locations: 23900018
*614336 - PRESEQUENCE TRANSLOCASE-ASSOCIATED MOTOR 16; PAM16
Cytogenetic locations: 20053669
#302060 - BARTH SYNDROME; BTHS
Cytogenetic locations: CT47A9
*605219 - DIRECT IAP-BINDING PROTEIN WITH LOW pI; DIABLO
Cytogenetic locations: 11140638
*300169 - APOPTOSIS-INDUCING FACTOR, MITOCHONDRIA-ASSOCIATED, 1; AIFM1
Cytogenetic locations: -
262900 - PLEOCONIAL MYOPATHY WITH SALT CRAVING
#550500 - MYOGLOBINURIA, RECURRENT
251945 - MITOCHONDRIAL MYOPATHY WITH A DEFECT IN MITOCHONDRIAL-PROTEIN TRANSPORT
253320 - CHUDLEY SYNDROME
#251950 - MITOCHONDRIAL MYOPATHY WITH LACTIC ACIDOSIS; MMLA
Cytogenetic locations: 25512002
#617644 - SPERMATOGENIC FAILURE 21; SPGF21
Cytogenetic locations: 28199965
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