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Differential Diagnosis For Palpable Liver/Hepatomegaly: Metabolic, Storage Disorders

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List of current finding(s):

Metabolic, Storage Disorders: next: Deficiency Causes
Diabetes mellitus
Hypertriglyceridemia
Amyloidosis, heart
Mucopolysaccharidoses
Amyloidosis, hepatosplenic
Amyloidosis, secondary
Amyloidosis, systemic
Chylomicronemia syndrome
Hemochromatosis
Hurler's mucopolysaccharidosis syndrome
Cerebral Gaucher's of infants (acute)
MCAD/Medium chain OH-CoA Dehydrogenase def
Wilsons Disease
Wolman Disease
Beta-glucuronidase deficiency syndrome (MPS VII)
Cholesteryl ester storage disease
DiFerrente syndrome (Mucopolysaccharidosis VIII)
Dubin-Johnson syndrome
Fructose intolerance, hereditary
Fucosidosis (Anderson-Fabry)
Galactosemia
Gangliosidosis, generalized (GM1)
Gaucher's disease
Glycogen storage diseases
Glycogen storage muscle disease/Pompe
Hepatophosphorylase def. glycogenosis
Histiocytosis X
Homocystinuria/homocystinemia
Hunter's mucopolysaccharidosis syndrome
Morquio's mucopolysaccharidosis synd.
Niemann-Pick disease
Phosphoenolpyruvate carboxykinase defic (PEPCK)
Sandhoff disease
Sanfilippo's mucopolysaccharidosis synd
Tangier's disease
Von Gierke's disease/glycogenosis I
Fatty acid oxidation/metabolic syndromes
Unclassified fatty oxidation syndromes (U-FAOD)
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