- OMIM ID
-
305400
- OMIM term:
- AARSKOG-SCOTT SYNDROME; AAS
- Alternative terms:
-
FACIOGENITAL DYSPLASIA; FGDY
FACIODIGITOGENITAL SYNDROME
AARSKOG SYNDROME, X-LINKED FACIOGENITAL DYSPLASIA WITH ATTENTION DEFICIT-HYPERACTIVITY DISORDER, INCLUDED
MENTAL RETARDATION, X-LINKED, SYNDROMIC 16, INCLUDED; MRXS16, INCLUDED
- (∗) Location:
- Xp11.22
- (†) Associated OMIM genes:
- FGD1
- (‡) Associated MGI genes:
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