Example image of eyePlorer eyePlorer map for 'Fragile X syndrome': Genetic disorder Syndrome FMR1 Trinucleotide repeat disorder X chromosome Microcephaly Gene Mutation Female Male Genetic code Allele DNA DNA methylation Protein Chromosome Axon Chemical synapse Messenger RNA X-inactivation Sherman paradox Hypotonia Macroorchidism Cluttered speech Social anxiety Social cognition Hyperactivity Dementia Obsessive–compulsive disorder Psychoticism Somatization Executive functions Intelligence quotient Etiology Olfaction Fight-or-flight response Perseveration Strabismus Amblyopia Cytogenetics Restriction enzyme Southern blot In vitro RNA-binding protein Metabotropic glutamate receptor Metabotropic glutamate receptor 5 Behaviour therapy Special education Genetic counseling Conditions comorbid to autism spectrum disorders