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Summary Literature (0)
MIM:141749 - FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 1; HBFQTL1

Xenbase Genes: hbg2, hbg1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0016489 - delta-beta-thalassemia
MONDO:0016672 - hereditary persistence of fetal hemoglobin-sickle cell disease syndrome
MONDO:0018749 - hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome