- OMIM ID
-
309500
- OMIM term:
- RENPENNING SYNDROME 1; RENS1
- Alternative terms:
-
MENTAL RETARDATION, X-LINKED, RENPENNING TYPE
SUTHERLAND-HAAN X-LINKED MENTAL RETARDATION SYNDROME; SHS
GOLABI-ITO-HALL SYNDROME
MENTAL RETARDATION, X-LINKED, WITH SPASTIC DIPLEGIA
MENTAL RETARDATION, X-LINKED, SYNDROMIC 3; MRXS3
MENTAL RETARDATION, X-LINKED, SYNDROMIC 8; MRXS8
MENTAL RETARDATION, X-LINKED 55; MRX55
- (∗) Location:
- Xp11.23
- (†) Associated OMIM genes:
- PQBP1
- (‡) Associated MGI genes:
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