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

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	KEL
Name	blood group system, Kell (KEL)
OMIM ID	110900
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	KEL
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2016-03-20 12:15:43 +01:00 (CET)

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