Term Name: | combined oxidative phosphorylation deficiency 24 |
---|---|
Synonyms: | COXPD24 |
Definition: | A combined oxidative phosphorylation deficiency typically characterized by delayed neurodevelopment, refractory seizures, hypotonia, and hearing impairment that has_material_basis_in homozygous or compound heterozygous mutation in the NARS2 gene on chromosome 11q14.1. |
Ontology: | Human Disease [DOID:0111485] ( DOID:0111485 ) |