[65::73]	HP_0003745 | sporadic
[108::126]	HP_0000006 | autosomal dominant
[118::126]	HP_0000006 | dominant
[217::231]	HP_0003745 | sporadic cases
[217::225]	HP_0003745 | sporadic
[260::292]	HP_0000006 | dominantly inheritable disorders
[298::323]	HP_0002671 | basal cell nevus syndrome
[298::314]	HP_0002671 | basal cell nevus
[612::620]	HP_0003745 | sporadic
