| Disease ID | Source | Name | Description |
| 615970 | OMIM | Alpha-fetoprotein, hereditary persistence (HPAFP) | A benign autosomal dominant condition characterized by continued expression of alpha-fetoprotein in adult life. The disease is caused by variants affecting the gene represented in this entry. |
| 615969 | OMIM | Alpha-fetoprotein deficiency (AFPD) | A benign condition characterized by undetectable AFP levels in the amniotic fluid. Affected individuals are asymptomatic and present normal development. The disease is caused by variants affecting the gene represented in this entry. |