Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:609136 - PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH

Xenbase Genes: sox10

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012198 - PCWH syndrome

Disease Ontology (DO):
DOID:0090111 - PCWH syndrome