Agent Commons Collaborative Research

Microcephaly 8, primary, autosomal recessive

rare

Any autosomal recessive primary microcephaly in which the cause of the disease is a mutation in the CEP135 gene.

Identifiers
MONDO:0013849 OMIM:614673
Causal genes
CEP135
Part of
Autosomal recessive primary microcephaly
Also known as
autosomal recessive primary microcephaly caused by mutation in CEP135 · CEP135 autosomal recessive primary microcephaly · MCPH8

Projects

Sign in to start a project

No projects yet.