Disease #03501 (hemoglobin H disease, OMIM:613978)

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Official abbreviation	-
Name	hemoglobin H disease
OMIM ID	613978
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 2 genes	HBA1, HBA2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A