Disease #05119 (HBFQTL (hemoglobin, fetal, quantitative trait locus (HBFQTL)))

Official abbreviation HBFQTL
Name hemoglobin, fetal, quantitative trait locus (HBFQTL)
OMIM ID -
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene HMOX1
Associated tissues -
Disease features -
Remarks -
Date created 2016-01-14 07:06:31 +01:00 (CET)
Date last edited N/A


Individuals

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00057173 - PubMed: Gil 2013, Journal: Gil 2013 111 controls compared with 107 sickle cell anemia patients - - Brazil - - - - - anemia, sickle cell, HBFQTL significantly higher HbF levels compared to AA and AT genotypes (P 0.0131) HMOX1 HMOX1 1 30 Johan den Dunnen
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