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<div class="main-content lit-style"><div class="body-content whole_rhythm"><div id="cask-dis.Tc" class="table"><p class="large-table-link" style="display:none"><span class="right"><a href="/books/NBK169825/table/cask-dis.Tc/?report=objectonly" target="object">View in own window</a></span></p><div class="large_tbl" id="__cask-dis.Tc_lrgtbl__"><table class="no_bottom_margin"><thead><tr><th id="hd_h_cask-dis.Tc_1_1_1_1" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:top;"><i>CASK</i> Disorders: Included Phenotypes&#x000a0;<sup>1</sup></th></tr></thead><tbody><tr><td headers="hd_h_cask-dis.Tc_1_1_1_1" rowspan="1" colspan="1" style="text-align:left;vertical-align:top;"><ul><li class="half_rhythm"><div>Intellectual disability and microcephaly with pontine and cerebellar hypoplasia (MICPCH)</div></li><li class="half_rhythm"><div><a class="def" href="/books/n/gene/glossary/def-item/x-linked/">X-linked</a> intellectual disability (XLID) with or without nystagmus</div></li></ul>
</td></tr></tbody></table></div><div><div><dl class="temp-labeled-list small"><dt></dt><dd><div><p class="no_margin">For synonyms and outdated names see <a href="/books/NBK169825/#cask-dis.Nomenclature" target="mainwindow">Nomenclature</a>.</p></div></dd><dt>1. </dt><dd><div id="cask-dis.TF.c.1"><p class="no_margin">For other genetic causes of these phenotypes see <a href="/books/NBK169825/#cask-dis.Differential_Diagnosis" target="mainwindow">Differential Diagnosis</a>.</p></div></dd></dl></div></div></div><div id="bk_toc_contnr"></div></div></div>
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