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:300475 - DEAFNESS, DYSTONIA, AND CEREBRAL HYPOMYELINATION; DDCH


Xenbase Genes: bcap31

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010334 - severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome
MONDO:0018247 - CADDS

Disease Ontology (DO):
DOID:0112123 - deafness, dystonia, and cerebral hypomyelination