Summary Literature (0)

MIM:614852 - MICROCEPHALY 9, PRIMARY, AUTOSOMAL RECESSIVE; MCPH9

Xenbase Genes: cep152

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013923 - microcephaly 9, primary, autosomal recessive

MONDO:0016660 - autosomal recessive primary microcephaly