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GENATLAS PHENOTYPE
last update : 12-01-2017
Symbol MRMC
Location 9p13.3
Name mental retardation and secondary microcephaly
Corresponding gene RUSC2
Other symbol(s) MRT61
Main clinical features
  • central hypotonia, microcephaly, and moderate to severe intellectual disability
  • Genetic determination autosomal recessive
    Function/system disorder mental retardation
    Type disease
    Remark(s)