Gen-Panel
Nicht-syndromale Schwerhörigkeit, autosomal-dominant (DFNA): ID091.04, 60 Gene
ABCC1,
ACTG1,
ATOH1,
ATP2B2,
ATP11A,
CCDC50,
CD164,
CEACAM16,
COCH,
COL11A1,
COL11A2,
CRYM,
DIABLO,
DIAPH1,
DMXL2,
DSPP,
ELMOD3,
EPHA10,
EYA4,
GJB2,
GJB3,
GJB6,
GREB1L,
GRHL2,
GSDME,
HOMER2,
KCNQ4,
KITLG,
LMX1A,
MAP1B,
MCM2,
MT-RNR1,
MYH9,
MYH14,
MYO3A,
MYO6,
MYO7A,
NLRP3,
OSBPL2,
P2RX2,
PDE1C,
PI4KB,
PLS1,
POU4F3,
PTPRQ,
REST,
RIPOR2,
SCD5,
SIX1,
SLC12A2,
SLC17A8,
SLC44A4,
TBC1D24,
TECTA,
THOC1,
TMC1,
TNC,
TRRAP,
USP48,
WFS1
HPO Terms
Autosomal dominant inheritance, Sensorineural hearing impairment, Progressive sensorineural hearing impairment, High-frequency hearing impairment, Tinnitus, Adult onset, Hearing impairment, Hearing loss, Hearing abnormality, Abnormal inner ear morphology, Abnormal cochlear morphology, Abnormal vestibular function, Abnormal vestibulocochlear nerve morphology, Abnormal semicircular canal morphology, Postlingual sensorineural hearing impairment, Auditory neuropathy, Auditory processing disorder, Abnormal ear morphology, Abnormal auditory nerve morphology, Low-frequency sensorineural hearing impairment
