Term Name: | combined oxidative phosphorylation deficiency 44 |
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Synonyms: | COXPD44 |
Definition: | A combined oxidative phosphorylation deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the FASTKD2 gene on chromosome 2q33. |
Ontology: | Human Disease [DOID:0070424] ( DOID:0070424 ) |