Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:608716 - MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE; MCPH5

Xenbase Genes: aspm

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012106 - microcephaly 5, primary, autosomal recessive
MONDO:0016660 - autosomal recessive primary microcephaly

Disease Ontology (DO):
DOID:10907 - microcephaly