Microcephaly 9, primary, autosomal recessive

MONDO:0013923

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

Also known as: CEP152 autosomal recessive primary microcephaly, autosomal recessive primary microcephaly caused by mutation in CEP152, microcephaly 9, primary, autosomal recessive, MCPH9

0 clinical trials for this condition and its sub-types, 0 tagged with Microcephaly 9, primary, autosomal recessive itself.

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↑ Autosomal recessive primary microcephaly (8)

Including sub-types (0) Tagged with Microcephaly 9, primary, autosomal recessive (0)

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