- OMIM ID
-
300055
- OMIM term:
- MENTAL RETARDATION, X-LINKED, SYNDROMIC 13; MRXS13 MENTAL RETARDATION, X-LINKED 79; MRX79
- Alternative terms:
-
MENTAL RETARDATION, X-LINKED 16; MRX16
MENTAL RETARDATION, X-LINKED, WITH SPASTICITY
MENTAL RETARDATION WITH PSYCHOSIS, PYRAMIDAL SIGNS, AND MACROORCHIDISM; PPMX
- (∗) Location:
- Xq28
- (†) Associated OMIM genes:
- MECP2
- (‡) Associated MGI genes:
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