Search results for "[genes] COCH"

16 hits were found for '[genes] COCH'

# Family MCID Name MIFTS Score
1
SNS001 Sensorineural Hearing Loss 44 18.046
2
c DFN136 Deafness, Autosomal Dominant 9 22 18.046
3
MNR002 Meniere's Disease 42 16.140
4
c GLC062 Glaucoma 1, Open Angle, E 45 13.978
5
c NNS007 Nonsyndromic Deafness 41 13.978
6
INN002 Inner Ear Disease 38 11.413
7
c USH010 Usher Syndrome, Type 1f 38 11.413
8
ADT003 Auditory System Disease 37 11.413
9
LBY003 Labyrinthine Disease 32 11.413
10
PRP028 Peripheral Vertigo 31 11.413
11
SPN012 Spindle Cell Hemangioma 30 11.413
12
c ATS005 Autosomal Dominant Nonsyndromic Deafness 24 11.413
13
c CHR097 Chronic Purulent Otitis Media 22 11.413
14
PRL021 Perilymphatic Fistula 22 11.413
15
ATS251 Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna 26 8.070
16
DFN047 Dfna 9 Nonsyndromic Hearing Loss and Deafness 10 8.070