[81::93]	HP_0000365 | hearing loss
[172::233]	HP_0000478 | ophthalmic, orofacial, articular, and auditory manifestations
[184::233]	HP_0000153 | orofacial, articular, and auditory manifestations
[195::233]	HP_0001367 | articular, and auditory manifestations
[210::233]	HP_0000364 | auditory manifestations
[289::307]	HP_0000006 | autosomal dominant
[289::313]	HP_0000006 | autosomal dominant trait
[299::307]	HP_0000006 | dominant
[299::313]	HP_0000006 | dominant trait
[327::362]	HP_0009794 | branchial, otic and renal anomalies
[327::336]	HP_0009794 | branchial
[338::362]	HP_0000598 | otic and renal anomalies
[347::362]	HP_0000077 | renal anomalies
[564::576]	HP_0000365 | hearing loss
[581::593]	HP_0000175 | cleft palate
[638::644]	HP_0000545 | myopia
[673::689]	HP_0007773 | vitreous anomaly
[696::705]	HP_0000272 | flat face
[966::984]	HP_0004467 | pre-auricular pits
[970::984]	HP_0004467 | auricular pits
[980::984]	HP_0004467 | pits
[986::995]	HP_0009794 | branchial
[986::1004]	HP_0009795 | branchial fistulae
[1009::1023]	HP_0000104 | renal agenesis
[1222::1229]	HP_0003745 | de novo
