Congenital splenomegaly

Common: Anemia; Congenital transplacental infection; Dysgammaglobulinemia; Gaucher disease; Glycogen storage disease type 1; Glycogen storage disease type 3; GM1 gangliosidosis; Hemochromatosis; Langerhans cell histiocytosis; Mucolipidosis; Mucopolysaccharidosis; Niemann-Pick disease; Pyruvate kinase deficiency; Sickle cell disease; Spherocytosis; Thalassemia
Uncommon: Aase syndrome; Alpha1-antitrypsin deficiency; Aspartylglucosaminuria; Beckwith-Wiedemann syndrome; Chédiak-Higashi syndrome; Cholesterol ester storage disease; Cogan syndrome; Cruveilhier-Baumgarten syndrome; Cystinosis; Ethanolaminosis; Farber disease; Felty syndrome; Fucosidosis; Galactosialidosis; Hepatic fibrosis-renal cystic disease; Hyperlipoproteinemia; Infantile multisystem inflammatory disease; Lipodystrophy; Mannosidosis; Osteopetrosis; POEMS syndrome; Sea-blue histiocyte syndrome; Tyrosinemia type 1; Vaquez-Osler syndrome; Wilson disease; Wolman disease; Zellweger syndrome