Disease #01881 (SCOTD (succinyl-CoA acetoacetate transferase deficiency (SCOTD)), OMIM:245050)
| Official abbreviation |
SCOTD |
| Name |
succinyl-CoA acetoacetate transferase deficiency (SCOTD) |
| OMIM ID |
245050 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
3 |
| Phenotype entries for this disease |
3 |
| Associated with 1 gene |
OXCT1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2019-03-09 15:41:33 +01:00 (CET) |
Individuals
|