Congenital Amegakaryocytic Thrombocytopenia

specific

A rare, autosomal recessive inherited disorder caused by mutation in the c-Mpl gene. It is characterized by thrombocytopenia and absence of megakaryocytes. It presents with bleeding in the first month of life.

9

Centers

0

Active Trials

Cancer Funding

Top Centers for Congenital Amegakaryocytic Thrombocytopenia(9)

Ranked by research excellence score (trials · grants · publications). Methodology →

#CenterScore
1
NCI Comprehensive
55.6
255.6
3
NCI Comprehensive
55.6
455.6
5
NCI Comprehensive
55.6
6
NCI Comprehensive
55.6
755.6
855.6
955.6

Research tier badges reflect trial volume, NIH grant funding, and publication impact — not clinical outcomes or patient satisfaction. Learn about our methodology →