Disease #00016
Official abbreviation |
252011 |
Name |
Mitochondrial complex II deficiency, 252011 (3) |
OMIM ID |
252011 |
Human Phenotype Ontology Project (HPO) |
HPO |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 3 genes |
SDHA, SDHAF1, SDHD |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|