[61::75]	HP_0001627 | cardiac defect
[77::96]	HP_0001759 | ossicular anomalies
[101::122]	HP_0000006 | dominant transmission
[101::109]	HP_0000006 | dominant
[128::153]	HP_0003822 | intrafamilial variability
[128::170]	HP_0003822 | intrafamilial variability of the phenotype
[142::153]	HP_0003812 | variability
[206::220]	HP_0001420 | isolated cases
