Disease #03048 (COXPD5 (combined oxidative phosphorylation deficiency, type 5 (COXPD-5)), OMIM:611719)
Official abbreviation |
COXPD5 |
Name |
combined oxidative phosphorylation deficiency, type 5 (COXPD-5) |
OMIM ID |
611719 |
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 |
MRPS22 |
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
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