| Human Disease |
Term: Mitochondrial DNA Depletion Syndrome 5 (encephalomyopathic with Methylmalonic Aciduria); MTDPS5
OMIM ID: 612073
|
| Synonyms |
Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form, with Methylmalonic Aciduria, Autosomal Recessive, Sucla2-Related |
| Associated Genes |
Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.
Mouse Gene |
Human Gene |
|
Characteristics of this human disease are associated with mutations in... |
| |
|
|
|
|
 ...the human gene.
MGI data currently do not associate this disease with mutations in the orthologous mouse gene. |
| |
|
|
|
Analysis Tools