Search results for "[genes] MYH9"

36 hits were found for '[genes] MYH9'

# Family MCID Name MIFTS Score
1
EPS006 Epstein Syndrome 40 23.061
2
SBS006 Sebastian Syndrome 36 23.061
3
FCH003 Fechtner Syndrome 36 23.061
4
MYH001 May-Hegglin Anomaly 40 21.878
5
P ALP004 Alport Syndrome 68 17.863
6
SNS001 Sensorineural Hearing Loss 56 17.863
7
MCR139 Macrothrombocytopenia and Progressive Sensorineural Deafness 17 17.863
8
P THR014 Thrombocytopenia 62 16.307
9
c DFN200 Deafness, Autosomal Dominant 17 21 16.307
10
MYH002 Myh9-Related Disorders 20 14.585
11
P GLM007 Glomerulonephritis 61 12.631
12
END030 End Stage Renal Failure 58 12.631
13
P ACT135 Acute Graft Versus Host Disease 56 12.631
14
BRN082 Bernard-Soulier Syndrome, Type C 52 12.631
15
FSC004 Fasciitis 51 12.631
16
BLD053 Blood Platelet Disease 47 12.631
17
P ATS208 Autosomal Dominant Macrothrombocytopenia 29 12.631
18
c MYH004 Myh9 Related Thrombocytopenia 21 12.631
19
c CHR089 Chronic Kidney Failure 67 10.313
20
P SYP003 Syphilis 56 10.313
21
PTN001 Patent Foramen Ovale 55 10.313
22
INN002 Inner Ear Disease 51 10.313
23
c PRM022 Primary Syphilis 44 10.313
24
YWS001 Yaws 43 10.313
25
LTN001 Latent Syphilis 43 10.313
26
ASY002 Asymptomatic Neurosyphilis 39 10.313
27
c CNG033 Congenital Syphilis 39 10.313
28
LNS003 Lens Disease 39 10.313
29
TRT003 Tertiary Syphilis 34 10.313
30
SLF001 Sulfhemoglobinemia 33 10.313
31
TRT002 Tertiary Neurosyphilis 30 10.313
32
ADT003 Auditory System Disease 48 7.293
33
ATS251 Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna 27 7.293
34
P DFN023 Deafness, Autosomal Dominant Nonsyndromic Sensorineural 17 10 7.293
35
MCR041 Macrothrombocytopenia Progressive Deafness 6 7.293
36
DFN052 Dfna17 Nonsyndromic Hearing Loss and Deafness 5 7.293