Familial myeloproliferative disease. A new syndrome closely simulating myelogenous leukemia in childhood.
D000469:Alkaline Phosphatase; D000740:Anemia / Q000235:genetics*; D001855:Bone Marrow Diseases / Q000235:genetics*; D002675:Child, Preschool; D002875:Chromosomes; D003937:Diagnosis, Differential; D005260:Female; D006529:Hepatomegaly / Q000235:genetics*; D006801:Humans; D007223:Infant; D007621:Karyotyping; D007951:Leukemia, Myeloid / Q000175:diagnosis*; D007964:Leukocytosis / Q000235:genetics*; D008297:Male; D013156:Splenectomy; D013163:Splenomegaly / Q000235:genetics*; D013921:Thrombocytopenia / Q000235:genetics*