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Summary Literature (0)
MIM:617090 - MICROCEPHALY 17, PRIMARY, AUTOSOMAL RECESSIVE; MCPH17

Xenbase Genes: cit

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014908 - microcephaly 17, primary, autosomal recessive
MONDO:0016660 - autosomal recessive primary microcephaly