All diseases

OMIM ID
300624
OMIM term:
FRAGILE X MENTAL RETARDATION SYNDROME
Alternative terms:
FRAGILE X SYNDROME
MENTAL RETARDATION, X-LINKED, ASSOCIATED WITH marXq28
X-LINKED MENTAL RETARDATION AND MACROORCHIDISM
MARKER X SYNDROME
MARTIN-BELL SYNDROME PRIMARY OVARIAN INSUFFICIENCY, FRAGILE X-ASSOCIATED, INCLUDED
FRAGILE X PREMATURE OVARIAN FAILURE, INCLUDED
(∗) Location:
Xq27.3  
(†) Associated OMIM genes:
FMR1  
(‡) Associated MGI genes:
Fmr1  

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