| Label | Id | |
|---|---|---|
| aplasia cutis congenita, congenital heart defect, and frontonasal cysts | C4551482 | |
| Adams-Oliver syndrome caused by mutation in ARHGAP31 | C4551482 | |
| Familial aplasia cutis congenita of the scalp | C4551482 | |
| absence defect of limbs, scalp, and skull | C4551482 | |
| ARHGAP31 Adams-Oliver syndrome | C4551482 | |
| Adams Oliver syndrome | C4551482 | |
| Congenital defect of skull and scalp | C4551482 | |
| Scalp defects with ectrodactyly | C4551482 |