| Disease ID | Source | Name | Description |
| 612300 | OMIM | Hemolytic anemia, CD59-mediated, with or without polyneuropathy (HACD59) | An autosomal recessive disorder characterized by infantile onset of chronic hemolysis and a relapsing-remitting polyneuropathy, often exacerbated by infection, and manifested as hypotonia, limb muscle weakness, and hyporeflexia. The disease is caused by variants affecting the gene represented in this entry. |