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. Author manuscript; available in PMC: 2017 Mar 8.
Published in final edited form as: Clin Genet. 2015 Oct 6;89(4):466–472. doi: 10.1111/cge.12677

Table 2.

Diagnosis by Mode of Inheritance

Inheritance n of patients Genes n of patients % of all solved patients
AD 18 KCNQ4 4 7.5 %
WFS1 4 7.5 %
MYO6 3 5.7 %
TECTA 2 3.8 %
TMC1 2 3.8 %
MYH14, MYO7A, P2RX2 1 each 1.9 %
AR 34 MYO15A 6 11.3 %
CDH23 5 9.4 %
SLC26A4 4 7.5 %
OTOF 3 5.7 %
STRC 3 5.7 %
LOXHD1, PCDH15 PTPRQ MT-RNR1 (961T>C) 2 each 3.8 %
GPR98, MYO7A, TECTA, TMPRSS3 1 each 1.9 %
X linked POU3F4 1 each 1.9 %