[33::46]	HP_0001425 | heterogeneous
[72::90]	HP_0000006 | autosomal dominant
[117::126]	HP_0009794 | branchial
[117::145]	HP_0009794 | branchial arch abnormalities
[147::159]	HP_0000365 | hearing loss
[164::183]	HP_0000077 | renal abnormalities
