Any autosomal recessive primary microcephaly in which the cause of the disease is a mutation in the CIT gene.
Comprehensive, easy-to-understand information about this condition
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microcephaly 1, primary, autosomal recessive
MONDO:0009617
microcephaly with simplified gyral pattern
MONDO:0011372
microcephaly 2, primary, autosomal recessive, with or without cortical malformations
MONDO:0011435
microcephaly 4, primary, autosomal recessive
MONDO:0011437
microcephaly 3, primary, autosomal recessive
MONDO:0011488
microcephaly 5, primary, autosomal recessive
MONDO:0012106