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:616577 - NEURODEVELOPMENTAL DISORDER WITH HEARING LOSS, SEIZURES, AND BRAIN ABNORMALITIES; NEDHSB

Xenbase Genes: afg2a

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014698 - microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome