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Summary Literature (0)
MIM:617913 - NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CATARACTS, AND RENAL ABNORMALITIES; NEDMCR

Xenbase Genes: gemin4

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0060664 - neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities

Disease Ontology (DO):
DOID:0081263 - neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities