Disease-gene associations mined from literature

Human genes for neutral lipid storage disease

Neutral lipid storage disease [DOID:0050729]

A lipid storage disease that is characterized by accumulation of triglycerides in the cytoplasm of leukocytes, muscle, liver, fibroblasts, and other tissues.

Synonyms:  neutral lipid storage disease,  DOID:0050729,  neutral lipid storage disorder,  neutral lipid storage syndrome,  Chanarin-Dorfman syndrome ...

Linkouts:  OMIM