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LMSSIO

Fragile X Syndrome

Fragile X Syndrome is a genetic disorder caused by a mutation on the FMR1 gene located on the X chromosome. This mutation leads to a lack of the fragile X mental retardation protein (FMRP), which is crucial for normal brain development.

IRI: http://lmss.sali.org/RBm4FfOtNNc2YXqnz3Pkqce
Branch: Legal Entity
Source: https://www.ssa.gov/disability/professionals/bluebook/10.00-

Also known as

FXS, Fragile X Mental Retardation Syndrome

Ancestry path

Legal Entity Individual Person Characteristics Disability Physical Disability Congenital Disorders that Affect Multiple Body Systems

Generated from sali-legal/LMSS at 3f9ac0c9357b (2026-03-10). JSON