|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Hereditary persistence of alpha-fetoprotein is a benign genetic condition characterized by persistence of high alpha-fetoprotein (AFP) levels throughout life, with no associated clinical disability and thus no need for specific therapy (Orphanet Rare Disease Ontology, Orphanet_168615)|
|Downloads & Tools|
1 genes associated with the [hereditary persistence of alpha-fetoprotein] phenotype from the curated OMIM Gene-Disease Associations dataset.