- OMIM ID
-
100300
- OMIM term:
- ADAMS-OLIVER SYNDROME 1; AOS1
- Alternative terms:
-
AOS
ABSENCE DEFECT OF LIMBS, SCALP, AND SKULL
CONGENITAL SCALP DEFECTS WITH DISTAL LIMB REDUCTION ANOMALIES
APLASIA CUTIS CONGENITA WITH TERMINAL TRANSVERSE LIMB DEFECTS APLASIA CUTIS CONGENITA, CONGENITAL HEART DEFECT, AND FRONTONASAL CYSTS, INCLUDED
- (∗) Location:
- 3q13.33
- (†) Associated OMIM genes:
- ARHGAP31
- (‡) Associated MGI genes:
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