Search Ontology:
Human Disease
mitochondrial DNA depletion syndrome 18
- Term ID
- DOID:0070449
- Synonyms
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- Definition
- A mitochondrial DNA depletion syndrome characterized by early onset progressive weakness, atrophy of the distal limb muscles, and multiple mitochondrial oxidative phosphorylation deficiencies that has_material_basis_in homozygous mutation in the SLC25A21 gene on chromosome 14q11.3. https://pubmed.ncbi.nlm.nih.gov/29517768/
- References
- Ontology
- Human Disease ( DOID:0070449 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models