Disease #00408 (AHDS;MCT-8 (Allan-Herndon-Dudley syndrome (AHDS, monocarboxylate transporter-8 deficiency (MCT-8))), OMIM:300523)
| Official abbreviation |
AHDS;MCT-8 |
| Name |
Allan-Herndon-Dudley syndrome (AHDS, monocarboxylate transporter-8 deficiency (MCT-8)) |
| OMIM ID |
300523 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
SLC16A2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-06-08 10:18:16 +02:00 (CEST) |
| Date last edited |
N/A |
|
