Disease #00308 (HAG (anemia, hemolytic, due to G6PD deficiency (HAG, incl favism)), OMIM:300908)
| Official abbreviation |
HAG |
| Name |
anemia, hemolytic, due to G6PD deficiency (HAG, incl favism) |
| OMIM ID |
300908 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
X-linked dominant |
| Individuals reported having this disease |
10573 |
| Phenotype entries for this disease |
10573 |
| Associated with 1 gene |
G6PD |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
X-linked dominant |
| Date created |
2014-01-24 11:32:05 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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