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Summary Literature (0)
MIM:617051 - NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY AND GRAY SCLERAE; NEDMIGS

Xenbase Genes: pus3

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014886 - severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome