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Human Disease

mitochondrial DNA depletion syndrome 18

Term ID
DOID:0070449
Synonyms
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 )
Relationships
is a type of
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Genes Involved
Zebrafish Models