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:614800 - SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY; SOPH

Xenbase Genes: nbas

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013889 - short stature-optic atrophy-Pelger-Huët anomaly syndrome