Disease #01197 (KEL (blood group system, Kell (KEL)), OMIM:110900)

Official abbreviation KEL
Name blood group system, Kell (KEL)
OMIM ID 110900
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene KEL
Associated tissues -
Disease features -
Remarks -