[48::66]	HP_0000006 | autosomal-dominant
[58::66]	HP_0000006 | dominant
[67::79]	HP_0000175 | cleft palate
[80::101]	HP_0002260 | craniofacial disorder
[107::115]	HP_0003813 | variable
[107::128]	HP_0003828 | variable expressivity
[157::176]	HP_0000951 | cutaneous anomalies
[188::225]	HP_0000377 | infra- and/or supra-auricular defects
[254::270]	HP_0000284 | ocular anomalies
[287::304]	HP_0001999 | facial appearance
[306::322]	HP_0000356 | malformed pinnae
[324::335]	HP_0000202 | oral clefts
[329::335]	HP_0009794 | clefts
[358::406]	HP_0000077 | renal and ectodermal (dental and hair) anomalies
[368::406]	HP_0000164 | ectodermal (dental and hair) anomalies
[824::831]	HP_0003745 | de novo
[1095::1116]	HP_0001425 | genetic heterogeneity
[1103::1116]	HP_0001425 | heterogeneity
