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
|