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Neutral lipid storage disease
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Congenital autosomal recessive disorder
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Neutral lipid storage disease (also known as Chanarin–Dorfman syndrome) is a congenital autosomal recessive disorder characterized by accumulation of triglycerides in the cytoplasm of leukocytes (Jordans' anomaly), muscle, liver, fibroblasts, and other tissues. It commonly occurs as one of two subtypes, cardiomyopathic neutral lipid storage...

Instance of
Rare disease
class of disease
Subclass of
Lipid storage disorder
rare dyslipidemia
disorder of phospholipids, sphingolipids and fatty acids biosynthesis with skeletal muscle predominant involvement
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