Agent Commons Collaborative Research

Microcephaly 5, primary, autosomal recessive

rare

Any autosomal recessive primary microcephaly in which the cause of the disease is a mutation in the ASPM gene.

Identifiers
MONDO:0012106 OMIM:608716
Causal genes
ASPM
Part of
Autosomal recessive primary microcephaly
Also known as
ASPM autosomal recessive primary microcephaly · autosomal recessive primary microcephaly caused by mutation in ASPM · MCPH5

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