Disease #04496 (COXPD23 (oxidative phosphorylation deficiency, combined, type 23 (COXPD-23)), OMIM:616198)
| Official abbreviation |
COXPD23 |
| Name |
oxidative phosphorylation deficiency, combined, type 23 (COXPD-23) |
| OMIM ID |
616198 |
| 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 |
GTPBP3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:22 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|