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

Official abbreviation -
Name hemoglobin H disease
OMIM ID 613978
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 2 genes HBA1, HBA2
Associated tissues -
Disease features -
Remarks -