Disease #06158 ({?Erythroleukemia, familial, susceptibility to}, OMIM:133180)

Official abbreviation -
Name {?Erythroleukemia, familial, susceptibility to}
OMIM ID 133180
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene ERBB3
Associated tissues -
Disease features -
Remarks -

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