Microcephaly 13, primary, autosomal recessive

MONDO:0014473

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

Also known as: CENPE autosomal recessive primary microcephaly, autosomal recessive primary microcephaly caused by mutation in CENPE, microcephaly 13, primary, autosomal recessive, MCPH13

0 clinical trials for this condition and its sub-types, 0 tagged with Microcephaly 13, primary, autosomal recessive itself.

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↑ Primordial dwarfism and slender bone disorder (9) ↑ Autosomal recessive primary microcephaly (8) ↑ Seckel syndrome (1)

Including sub-types (0) Tagged with Microcephaly 13, primary, autosomal recessive (0)

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