- OMIM ID
-
301900
- OMIM term:
- BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS
- Alternative terms:
-
MENTAL RETARDATION, X-LINKED, SYNDROMIC, BORJESON-FORSSMAN-LEHMANN TYPE; MRXSBFL
BORJESON SYNDROME; BORJ
MENTAL RETARDATION, EPILEPSY, AND ENDOCRINE DISORDERS
- (∗) Location:
- Xq26.2
- (†) Associated OMIM genes:
- PHF6
- (‡) Associated MGI genes:
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