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Microcephaly 9, primary, autosomal recessive

rare

Any autosomal recessive primary microcephaly in which the cause of the disease is a mutation in the CEP152 gene.

Identifiers
MONDO:0013923 OMIM:614852
Causal genes
CEP152
Part of
Autosomal recessive primary microcephaly
Also known as
autosomal recessive primary microcephaly caused by mutation in CEP152 · CEP152 autosomal recessive primary microcephaly · MCPH9

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