Disease #01203 (blood group P (blood group system, P1PK), OMIM:111400)

Official abbreviation blood group P
Name blood group system, P1PK
OMIM ID 111400
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 2 genes A4GALT, B3GALNT1
Associated tissues -
Disease features -
Remarks -