Disease #03108 (Myd88 deficiency, OMIM:612260)

Official abbreviation -
Name Myd88 deficiency
OMIM ID 612260
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene MYD88
Associated tissues -
Disease features -
Remarks -