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GENATLAS PHENOTYPE
last update : 08-01-2015
Symbol NSMR9
Location 1q43
Name non syndromic mental retardation 9
Corresponding gene FMN2
Main clinical features
  • nonsyndromic autosomal-recessive intellectual disability
    • Genetic determination autosomal recessive
    Function/system disorder mental retardation
    Type disease
    Mechanism(s)
    Gene mutationChromosome rearrangementEffectComments
    various types   truncated protein  
    Remark(s)