has material basis in germline mutation in SPTA1 familial hemolytic anemia elliptocytosis 2 https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/elliptocytosis_2 MEDGEN:343643 OMIM:130600 Any hereditary elliptocytosis in which the cause of the disease is a mutation in the SPTA1 gene. MONDO:0007533 elliptocytosis type 2 hereditary elliptocytosis caused by mutation in SPTA1 elliptocytosis 2 EL2 SPTA1 hereditary elliptocytosis MESH:C565058 UMLS:C1851741 elliptocytosis-2 GARD:0015064 hereditary elliptocytosis