Hereditary Persistence of Fetal Hemoglobin Genotype
Either homozygosity or heterozygosity for the HPFH1 mutation, a 106-KB deletion in the beta globin gene cluster.
Sickle Cell Disease Ontology Project
Term info
created by
clair ingram
creation date
2018-09-23T14:42:19.655Z
curator note
Request inclusion into relevant ontology
dc:creator
SCDO (Jade Hotchkiss)
definition source
https://www.ncbi.nlm.nih.gov/pubmed/603615