| Disease ID | Source | Name | Description |
| 301015 | OMIM | Hemolytic anemia, congenital, X-linked (HAXL) | An X-linked hematologic disease characterized by shortened survival of erythrocytes due to congenital hemolysis that cannot be compensated by bone marrow activity. Clinical features are mild jaundice and anemia. Red cells morphology is normal. The disease is caused by variants affecting the gene represented in this entry. |