Disease #05954 (MC4DN3 (mitochondrial complex IV deficiency, nuclear, type 3 (MC4DN3)), OMIM:619046)
| Official abbreviation |
MC4DN3 |
| Name |
mitochondrial complex IV deficiency, nuclear, type 3 (MC4DN3) |
| OMIM ID |
619046 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
COX10 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-07-23 10:40:01 +02:00 (CEST) |
| Date last edited |
N/A |
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