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TPP2

tripeptidyl peptidase 2

gene with protein productOMIM: 1904701 заболевание
GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Disease-causing germline mutation(s) (loss of function) in1
Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome due to TPP2 deficiencyORPHA:444463
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Данные: Orphadata (CC-BY-4.0)