Disease #00623 (MEGDEL (3-methylglutaconic aciduria with deafness, encephalopathy, Leigh-like syndrome (MEGDEL)), OMIM:614739)
| Official abbreviation |
MEGDEL |
| Name |
3-methylglutaconic aciduria with deafness, encephalopathy, Leigh-like syndrome (MEGDEL) |
| OMIM ID |
614739 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
SERAC1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
|
