Disease #01363 (HBFQTL1 (hemoglobin, fetal, quantitative trait locus 1 (HBFQTL-1)), OMIM:141749)

Official abbreviation HBFQTL1
Name hemoglobin, fetal, quantitative trait locus 1 (HBFQTL-1)
OMIM ID 141749
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 2
Associated with 3 genes HBB, HBG1, HBG2
Associated tissues -
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Individuals

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00305905 20 - - M - China - - - - - HBFQTL1 - HBG2 HBG2 1 1 Sha Hong
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