Disease #00525
Official abbreviation |
617086 |
Name |
Encephalopathy due to defective mitochondrial and peroxisomal fission 2, 617086 (3) |
OMIM ID |
617086 |
Human Phenotype Ontology Project (HPO) |
HPO |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
MFF |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|