Microcephaly 1, primary, autosomal recessive

Any autosomal recessive primary microcephaly in which the cause of the disease is a mutation in the MCPH1 gene.

Also known as: MCPH1 autosomal recessive primary microcephaly, autosomal recessive primary microcephaly caused by mutation in MCPH1, microcephaly 1, primary, autosomal recessive, MCPH1, PCC syndrome, premature chromosome condensation syndrome, premature chromosome condensation with microcephaly and intellectual disability, premature chromosome condensation with microcephaly and mental retardation

23 clinical trials for this condition and its sub-types.