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

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Official abbreviation	HBFQTL-1
Name	hemoglobin, fetal, quantitative trait locus 1 (HBFQTL-1)
OMIM ID	141749
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 3 genes	HBB, HBG1, HBG2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A