- OMIM ID
-
309580
- OMIM term:
- MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1
- Alternative terms:
-
SMITH-FINEMAN-MYERS SYNDROME 1; SFM1
SFMS
XLMR-HYPOTONIC FACIES SYNDROME
CARPENTER-WAZIRI SYNDROME
CHUDLEY-LOWRY SYNDROME
JUBERG-MARSIDI SYNDROME; JMS
HOLMES-GANG SYNDROME
MENTAL RETARDATION, X-LINKED, WITH GROWTH RETARDATION, DEAFNESS, AND MICROGENITALISM
- (∗) Location:
- Xq21.1
- (†) Associated OMIM genes:
- ATRX
- (‡) Associated MGI genes:
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