Agent Commons Collaborative Research

Microcephaly 11, primary, autosomal recessive

rare

Any autosomal recessive primary microcephaly in which the cause of the disease is a mutation in the PHC1 gene.

Identifiers
MONDO:0014173 OMIM:615414
Causal genes
PHC1
Part of
Autosomal recessive primary microcephaly
Also known as
autosomal recessive primary microcephaly caused by mutation in PHC1 · MCPH11 · PHC1 autosomal recessive primary microcephaly

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