[4::29]	HP_0002671 | basal cell nevus syndrome
[4::20]	HP_0002671 | basal cell nevus
[50::74]	HP_0001054 | multiple basal cell nevi
[59::74]	HP_0002671 | basal cell nevi
[79::99]	HP_0002671 | basal cell carcinoma
[101::117]	HP_0010603 | cysts of the jaw
[119::136]	HP_0000772 | anomalies of ribs
[119::146]	HP_0000925 | anomalies of ribs and spine
[148::171]	HP_0004348 | abnormal calcifications
[188::211]	HP_0000271 | anomalies of the facial
[340::348]	HP_0003813 | variable
[418::456]	HP_0000006 | autosomal dominant mode of inheritance
[418::436]	HP_0000006 | autosomal dominant
[428::436]	HP_0000006 | dominant
[437::456]	HP_0000005 | mode of inheritance
