Term Name: combined oxidative phosphorylation deficiency 54
Synonyms: COXPD54
Definition: A combined oxidative phosphorylation deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the PRORP gene on chromosome 14q13.
Ontology: Human Disease [DOID:0070427]   ( DOID:0070427 )

Relationships
is a type of: autosomal recessive disease combined oxidative phosphorylation deficiency