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:617330 - HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS

Xenbase Genes: ebf3

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0015021 - forelimb endochondral element

Disease Ontology (DO):
DOID:0081176 - hypotonia, ataxia, and delayed development syndrome