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<p>storage diseases are generally classified by the nature of the primary stored material involved, and can be broadly broken into the following: (<a href="page.php?w=ICD">ICD-10</a> codes are provided where available)<br/>
* (E75) <a href="page.php?w=Lipid_storage_disorder">Lipid storage disorder</a>s<br/>
** <a href="page.php?w=Gangliosidosis">Gangliosidoses</a> (including <a href="page.php?w=Tay-Sachs_disease">Tay-Sachs disease</a> (E75.0-E75.1) - they are a subtype of sphingolipidoses<br/>
** <a href="page.php?w=Sphingolipidoses">Sphingolipidoses</a></p><p>
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