Search results for "[genes] MYH9"

36 hits were found for '[genes] MYH9'

# Family MCID Name MIFTS Score
1
FCH003 Fechtner Syndrome 39 23.061
2
EPS006 Epstein Syndrome 35 23.061
3
SBS006 Sebastian Syndrome 31 23.061
4
MYH001 May-Hegglin Anomaly 43 21.878
5
P ALP004 Alport Syndrome 66 17.863
6
SNS001 Sensorineural Hearing Loss 44 17.863
7
MCR139 Macrothrombocytopenia and Progressive Sensorineural Deafness 20 17.863
8
P THR014 Thrombocytopenia 54 16.307
9
c DFN200 Deafness, Autosomal Dominant 17 19 16.307
10
MYH002 Myh9-Related Disorders 18 14.585
11
BRN082 Bernard-Soulier Syndrome, Type C 51 12.631
12
P GLM007 Glomerulonephritis 50 12.631
13
END030 End Stage Renal Failure 50 12.631
14
P ACT135 Acute Graft Versus Host Disease 45 12.631
15
FSC004 Fasciitis 41 12.631
16
BLD053 Blood Platelet Disease 35 12.631
17
P ATS208 Autosomal Dominant Macrothrombocytopenia 28 12.631
18
c MYH004 Myh9 Related Thrombocytopenia 23 12.631
19
c CHR089 Chronic Kidney Failure 58 10.313
20
PTN001 Patent Foramen Ovale 48 10.313
21
P SYP003 Syphilis 46 10.313
22
INN002 Inner Ear Disease 38 10.313
23
YWS001 Yaws 38 10.313
24
LTN001 Latent Syphilis 37 10.313
25
ASY002 Asymptomatic Neurosyphilis 36 10.313
26
c PRM022 Primary Syphilis 35 10.313
27
c CNG033 Congenital Syphilis 34 10.313
28
TRT003 Tertiary Syphilis 32 10.313
29
SLF001 Sulfhemoglobinemia 32 10.313
30
TRT002 Tertiary Neurosyphilis 28 10.313
31
LNS003 Lens Disease 25 10.313
32
ADT003 Auditory System Disease 37 7.293
33
ATS251 Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna 26 7.293
34
P DFN023 Deafness, Autosomal Dominant Nonsyndromic Sensorineural 17 13 7.293
35
MCR041 Macrothrombocytopenia Progressive Deafness 5 7.293
36
DFN052 Dfna17 Nonsyndromic Hearing Loss and Deafness 4 7.293