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Differential Diagnosis For Splenomegaly: Metabolic, Storage Disorders

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List of current finding(s):

Metabolic, Storage Disorders: next: Congenital Causes
Hypertriglyceridemia
Congenital erythropoetic porphyria
Mucopolysaccharidoses
Amyloidosis, hepatosplenic
Amyloidosis, secondary
Chylomicronemia syndrome
Hemochromatosis
Histiocytosis, pulmonary
Hurler's mucopolysaccharidosis syndrome
Phosphoglycerate Kinase Deficiency/Systemic homozygous PGKD
Cerebral Gaucher's of infants (acute)
Cerebral lipidosis disorder
Wilsons Disease
Wolman Disease
Amylopectinosis (Andersen's) disease (GSD IV)
Beta-glucuronidase deficiency syndrome (MPS VII)
Cholesteryl ester storage disease
DiFerrente syndrome (Mucopolysaccharidosis VIII)
Farber disease/ceramide lipidosis
Fucosidosis (Anderson-Fabry)
Gangliosidosis, generalized (GM1)
Gaucher's disease
Histiocytosis X
Hunter's mucopolysaccharidosis syndrome
Morquio's mucopolysaccharidosis synd.
Niemann-Pick disease
Sandhoff disease
Sanfilippo's mucopolysaccharidosis synd
Storage (storage-cell) disorders
Tangier's disease
Familial hypertriglyceridemia/VLDL/Type IV
Goldberg Syndrome
Lysosome Storage Disease
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