Disease #00092

Official abbreviation COXPD1
Name Combined oxidative phosphorylation deficiency 1, 609060 (3)
OMIM ID 609060
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene GFM1
Associated tissues -
Disease features -
Remarks -

  Powered by LOVD v.3.0 Build 21
LOVD software ©2004-2018 Leiden University Medical Center