Human genes for fragile X syndrome
Fragile X syndrome [DOID:14261]
A syndrome that is characterized by moderate to severe mental retardation, macroorchidism, and distinct facial features, including long face, large ears, and prominent jaw, and has_material_basis_in X-linked inheritance and a loss of FMR1 function.
Synonyms: fragile X syndrome, DOID:14261, fragile X disease, fragile X disorder, fragile X syndromes ...
Linkouts: OMIM