Neutral lipid storage disease (Q40063): Difference between revisions
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13 August 2026
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Latest revision as of 05:43, 13 August 2026
Neutral lipid storage disease (NLSD) refers to a group of diseases characterised by a deficit in the degradation of cytoplasmic triglycerides and their accumulation in cytoplasmic lipid vacuoles in most tissues of the body. The group is heterogeneous: NLSD with ichthyosis (NLSDI/Dorfman-Chanarin disease) and NLSD with myopathy (NLSDM/neutral lipid storage myopathy) can be distinguished.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 5C52.2 |
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| English | Neutral lipid storage disease |
Neutral lipid storage disease (NLSD) refers to a group of diseases characterised by a deficit in the degradation of cytoplasmic triglycerides and their accumulation in cytoplasmic lipid vacuoles in most tissues of the body. The group is heterogeneous: NLSD with ichthyosis (NLSDI/Dorfman-Chanarin disease) and NLSD with myopathy (NLSDM/neutral lipid storage myopathy) can be distinguished. |
Statements
CID11:5C52.2
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dki-india-5C52.2
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Concluído
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13 August 2026
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