Disease #07067 (NEDEPH (neurodevelopmental disorder with epilepsy and hemochromatosis), OMIM:301072)
| Official abbreviation |
NEDEPH |
| Name |
neurodevelopmental disorder with epilepsy and hemochromatosis |
| OMIM ID |
301072 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
PIGA |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2024-02-02 17:32:25 +01:00 (CET) |
| Date last edited |
N/A |
Individuals
|