Sporadic congenital spherocytosis associated with congenital hypoplastic thrombocytopenia and malformations.
D017487:Ankyrins / Q000172:deficiency; D002648:Child; D006402:Hematologic Diseases; D006801:Humans; D007223:Infant; D011696:Purpura, Thrombocytopenic; D013103:Spherocytosis, Hereditary
D017487:Ankyrins
BLOOD DISEASES/in infant and child