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:616917 - NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPOTONIA, SEIZURES, AND CEREBELLAR ATROPHY; NEDHSCA

Xenbase Genes: pigg

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014832 - intellectual disability, autosomal recessive 53