[hereditary persistence of alpha-fetoprotein] Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://www.omim.org/entry/615970
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1 genes associated with the [hereditary persistence of alpha-fetoprotein] phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
AFP alpha-fetoprotein