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| | '''Gastroenterologic''' | | | '''Gastroenterologic''' |
| |bgcolor="Beige"| | | |bgcolor="Beige"| |
| [[Acute pancreatitis]], [[Ascites]], [[Autoimmune pancreatitis]], [[Bezoar]], [[Biliary atresia]], [[Blind loop syndrome]], [[Bowel obstruction]], [[Cholangiocarcinoma]], [[Cholecystitis]], [[Choledochal cyst]], [[Cholelithiasis]], [[Cirrhosis]], [[Colonic diverticulitis]], [[Congenital hypertrophic pyloric stenosis]], [[Congenital megacolon]], [[Constipation]], [[Crohn's disease]], [[Distal intestinal obstruction syndrome]], [[Gastroschisis]], [[Hepatomegaly]], [[Hirschsprung's disease]], Liver [[granuloma]], Palpable gallbladder [[Courvoisier's sign]], [[Pancreatic pseudocyst]], [[Pyloric stenosis]], [[Riedel lobe of liver]], [[Splenosis]], [[Toxic megacolon]],
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| [[Urachal cyst]], [[Vermiform appendix]], [[Volvulus]], [[Wandering spleen]], [[Yersinia enterocolitica]].
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| |-bgcolor="LightSteelBlue" | | |-bgcolor="LightSteelBlue" |
| | '''Genetic''' | | | '''Genetic''' |
| |bgcolor="Beige"|[[Acanthocheilonemiasis ]], [[Alpha-L-iduronidase deficiency (Hurler syndrome)]], [[Alpha-L-iduronidase deficiency (Hurler-Scheie syndrome)]], [[Alpha-mannosidase deficiency]], Apolipoprotein C-II deficiency, Beta [[thalassaemia]] (heterozygous), [[Chanarin-Dorfman disease]], [[Chediak-Higashi disease ]], [[Cholesterol ester storage disease ]], [[Common variable hypogammaglobulinaemia]], [[Congenital dyserythropoietic anaemia type 1]], [[Congenital erythropoeitic porphyria]], [[Coproporphyria, hereditary ]], [[Cruveilhier-Baumgarten syndrome]], [[Familial alphalipoprotein deficiency]], [[Familial histiocytic reticulosis]], [[Familial hypertriglyceridaemia]], [[Farber lipogranulomatosis]], [[Fucosidosis ]], [[Fumarase deficiency ]], [[Galactose epimerase deficiency]], [[Galactose-1-phosphate uridyltransferase deficiency]], [[Gangliosidosis GM1 type 1]], [[Gangliosidosis GM1 type 3]], [[Gangliosidosis GM3]], [[Gaucher disease ]], [[Geleophysic dysplasia]], [[Glucose phosphate isomerase deficiency]], [[Glycogenosis type 4]], [[Granulocyte colony stimulating factor]], [[Haemochromatosis ]], [[Haemoglobin C disease]], [[Haemoglobin E disease]], [[Haemoglobin SC disease]], [[Haemolytic disease of the newborn]], [[Hereditary spherocytosis ]], [[Iduronate-2-sulfatase deficiency]], [[Iminodipeptiduria ]][[Kartagener syndrome ]], [[Long chain hydroxyacyl-CoA dehydrogenase deficiency]], [[Macrophage activation syndrome]], [[McLeod phenotype]], [[Mevalonate kinase deficiency]], [[Mucopolysaccharidosis VI ]], [[Neutrophilia, hereditary,]] [[Niemann-Pick disease type B]], [[Niemann-Pick Disease, Type C]], [[ Norrbottnian Gaucher disease]], [[Salla disease ]], [[Sandhoff disease ]], [[Sanfilippo disease]], [[Sarcoidosis ]], [[Sickle cell disease]], [[Zimmermann-Laband syndrome]]. | | |bgcolor="Beige"| |
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| |-bgcolor="LightSteelBlue" | | |-bgcolor="LightSteelBlue" |
| | '''Hematologic''' | | | '''Hematologic''' |
| |bgcolor="Beige"|[[Chediak-Higashi disease ]], [[Extramedullary haemopoiesis]], [[Familial histiocytic reticulosis]], [[Fanconi-Bickel syndrome]], [[Haemochromatosis ]], [[Sickle cell crisis ]], [[Haemoglobin C disease]], [[Haemoglobin E disease]], [[Haemoglobin SC disease]], [[Haemolytic disease of the newborn]], [[Hereditary spherocytosis ]], [[Mastocytosis ]], [[Myelofibrosis ]], [[Hereditary neutrophilia]], [[Vitamin B12 deficiency]]. | | |bgcolor="Beige"| |
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| |-bgcolor="LightSteelBlue" | | |-bgcolor="LightSteelBlue" |