Search results for kcnq4

Showing 25 of 156 hits for kcnq4
# Family MCID Name MIFTS Score
1
c DFN190 Deafness, Autosomal Dominant 2a 38 44.217
2
DFN001 Dfna2 Nonsyndromic Hearing Loss 13 31.246
3
P NNS072 Nonsyndromic Hearing Loss 43 23.370
4
RRG078 Rare Genetic Deafness 37 22.105
5
NNS044 Non-Syndromic Genetic Deafness 44 20.683
6
P SNS001 Sensorineural Hearing Loss 59 19.157
7
DFN245 Deafness, Autosomal Recessive 4, with Enlarged Vestibular Aqueduct 53 9.626
8
P LNG028 Long Qt Syndrome 63 8.511
9
c DFN136 Deafness, Autosomal Dominant 9 46 8.426
10
c LNG044 Long Qt Syndrome 1 67 8.381
11
ATS251 Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna 27 8.222
12
c ATS005 Autosomal Dominant Nonsyndromic Deafness 27 7.835
13
BNG006 Benign Familial Neonatal Epilepsy 53 7.155
14
P BNG026 Benign Neonatal Seizures 51 7.155
15
MNR012 Meniere Disease 56 6.962
16
c DFN097 Deafness, Autosomal Recessive 1a 51 6.914
17
c BRN131 Branchiootorenal Syndrome 1 46 6.914
18
c USH036 Usher Syndrome, Type I 63 6.851
19
c DFN196 Deafness, Autosomal Dominant 22 45 6.851
20
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 6.732
21
c WRD030 Waardenburg Syndrome, Type 1 55 6.699
22
c DFN118 Deafness, Autosomal Dominant 44 29 6.699
23
c DFN165 Deafness, Autosomal Recessive 14 19 6.699
24
c DFN107 Deafness, Autosomal Dominant 10 40 6.699
25
c DFN155 Deafness, Autosomal Dominant 41 34 6.699
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