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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-HuC+t anomaly syndrome