| Disease ID | Source | Name | Description |
| 301310 | OMIM | Anemia, sideroblastic, spinocerebellar ataxia (ASAT) | An X-linked recessive disorder characterized by an infantile to early childhood onset of non-progressive cerebellar ataxia and mild anemia, with hypochromia and microcytosis. The disease is caused by variants affecting the gene represented in this entry. |