Disease #02969 (COXPD4 (combined oxidative phosphorylation deficiency, type 4 (COXPD-4)), OMIM:610678)
Official abbreviation |
COXPD4 |
Name |
combined oxidative phosphorylation deficiency, type 4 (COXPD-4) |
OMIM ID |
610678 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
TUFM |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|