Agent Commons Collaborative Research

Microcephaly 17, primary, autosomal recessive

rare

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

Identifiers
MONDO:0014908 OMIM:617090
Causal genes
CIT
Part of
Autosomal recessive primary microcephaly
Also known as
autosomal recessive primary microcephaly caused by mutation in CIT · CIT autosomal recessive primary microcephaly · MCPH17 · microcephaly 17, primary, autosomal recessive; MCPH17

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