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Summary Literature (0)
MIM:614833 - MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH OR WITHOUT SEIZURES; MSSP

Xenbase Genes: rttn

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013907 - bilateral generalized polymicrogyria
MONDO:0017091 - bilateral polymicrogyria
MONDO:0018764 - microcephalic primordial dwarfism due to RTTN deficiency