Disease #03847 (D2L2AD (aciduria, combined d-2- and l-2-hydroxyglutaric (D2L2AD), OMIM:615182)
| Official abbreviation |
D2L2AD |
| Name |
aciduria, combined d-2- and l-2-hydroxyglutaric (D2L2AD |
| OMIM ID |
615182 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
SLC25A1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2020-08-05 11:53:54 +02:00 (CEST) |
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