OBO ID: DOID:0060333 |
Term Name: | mitochondrial complex V (ATP synthase) deficiency nuclear type 4 | Search Ontology: | |
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Synonyms: |
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Definition: | A mitochondrial complex V (ATP synthase) deficiency that has_material_basis_in mutation in the ATP5F1A gene on chromosome 18q21.1. (2) | ||
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Ontology: | Human Disease ( DOID:0060333 ) |
OTHER mitochondrial complex V (ATP synthase) deficiency nuclear type 4 PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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