Search results for "[genes] COCH"

16 hits were found for '[genes] COCH'

# Family MCID Name MIFTS Score
1
SNS001 Sensorineural Hearing Loss 56 18.046
2
c DFN136 Deafness, Autosomal Dominant 9 19 18.046
3
MNR002 Meniere's Disease 53 16.140
4
c GLC062 Glaucoma 1, Open Angle, E 49 13.978
5
c NNS007 Nonsyndromic Deafness 42 13.978
6
INN002 Inner Ear Disease 51 11.413
7
ADT003 Auditory System Disease 48 11.413
8
LBY003 Labyrinthine Disease 45 11.413
9
PRP028 Peripheral Vertigo 43 11.413
10
c USH010 Usher Syndrome, Type 1f 37 11.413
11
SPN012 Spindle Cell Hemangioma 32 11.413
12
c CHR097 Chronic Purulent Otitis Media 26 11.413
13
c ATS005 Autosomal Dominant Nonsyndromic Deafness 25 11.413
14
PRL021 Perilymphatic Fistula 24 11.413
15
ATS251 Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna 27 8.070
16
DFN047 Dfna 9 Nonsyndromic Hearing Loss and Deafness 11 8.070