| Disease Aliases (20) | Bxl4-related early-onset mitochondrial encephalopathy Encephalomyopathic mitochondrial dna depletion syndrome-13 F-box and leucine rich repeat protein 4 related mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form Fbxl4 (f-box and leucine rich repeat protein 4) related early onset mitochondrial encephalopathy Fbxl4 deficiency Fbxl4 mitochondrial dna depletion syndrome Fbxl4-related early onset mitochondrial encephalopathy Fbxl4-related encephalomyopathic mitochondrial dna depletion syndrome Mtdps13 Mitochondrial dna depletion syndrome 13 (encephalomyopathic type) Mitochondrial dna depletion syndrome 13 encephalomyopathic type Mitochondrial dna depletion syndrome, encephalomyopathic form with variable craniofacial anomalies Encephalomyopathic form with variable craniofacial anomalies Mitochondrial dna depletion syndrome 13 Mitochondrial dna depletion syndrome 13 (encephalomyopathic type); mtdps13 Mitochondrial dna depletion syndrome 13, encephalomyopathic type Mitochondrial dna depletion syndrome caused by mutation in fbxl4 Mitochondrial dna depletion syndrome type 13 Mtdna depletion syndrome Mtdna depletion syndrome, encephalomyopathic form with variable craniofacial anomalies |
Associated Genes (1) NCBI-RefSeq: FBXL4 (F-box and leucine rich repeat protein 4) External Links: gnomAD browser Ensembl GeneCards
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| Cross-references of Mitochondrial DNA depletion syndrome 13 | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |