Search results for "[genes] MYH9"

48 hits were found for '[genes] MYH9'

# Family MCID Name MIFTS Score
1
EPS006 Epstein Syndrome 39 22.101
2
FCH003 Fechtner Syndrome 37 22.101
3
SBS006 Sebastian Syndrome 35 22.101
4
MYH001 May-Hegglin Anomaly 43 20.967
5
c DFN200 Deafness, Autosomal Dominant 17 37 18.491
6
P ALP004 Alport Syndrome 69 17.119
7
SNS001 Sensorineural Hearing Loss 57 17.119
8
MCR139 Macrothrombocytopenia and Progressive Sensorineural Deafness 19 17.119
9
P KDN018 Kidney Disease 66 15.628
10
P THR014 Thrombocytopenia 64 15.628
11
P FCL005 Focal Segmental Glomerulosclerosis 60 15.628
12
MYH015 Myh-9 Related Disease 19 15.628
13
END030 End Stage Renal Failure 55 13.978
14
P ACT135 Acute Graft Versus Host Disease 53 13.978
15
BRN082 Bernard-Soulier Syndrome, Type C 50 13.978
16
FSC004 Fasciitis 48 13.978
17
BLD053 Blood Platelet Disease 46 13.978
18
c MYH004 Myh9 Related Thrombocytopenia 22 13.978
19
P SYP003 Syphilis 53 12.105
20
INN002 Inner Ear Disease 49 12.105
21
YWS001 Yaws 42 12.105
22
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 12.105
23
c CNG033 Congenital Syphilis 39 12.105
24
ASY002 Asymptomatic Neurosyphilis 36 12.105
25
c PRM022 Primary Syphilis 33 12.105
26
LNS003 Lens Disease 33 12.105
27
PSD016 Pseudosarcomatous Fibromatosis 32 12.105
28
TRT003 Tertiary Syphilis 31 12.105
29
LTN001 Latent Syphilis 27 12.105
30
P ATS208 Autosomal Dominant Macrothrombocytopenia 27 12.105
31
SLF001 Sulfhemoglobinemia 19 12.105
32
P DFN023 Deafness, Autosomal Dominant Nonsyndromic Sensorineural 17 13 12.105
33
DFN052 Dfna17 Nonsyndromic Hearing Loss and Deafness 4 12.105
34
PTN001 Patent Foramen Ovale 55 9.884
35
c ALP073 Alport Syndrome, Autosomal Recessive 43 9.884
36
c ALP074 Alport Syndrome, Autosomal Dominant 43 9.884
37
c NNS007 Nonsyndromic Deafness 42 9.884
38
BLD130 Bladder Exstrophy 42 9.884
39
c DFN196 Deafness, Autosomal Dominant 22 41 9.884
40
ADT003 Auditory System Disease 40 9.884
41
c DFN203 Deafness, Autosomal Recessive 30 40 9.884
42
c DFN197 Deafness, Autosomal Recessive 37 39 9.884
43
c DFN202 Deafness, Autosomal Dominant 48 38 9.884
44
c ATS336 Autosomal Recessive Nonsyndromic Deafness 3 31 9.884
45
TRT002 Tertiary Neurosyphilis 27 9.884
46
ATS251 Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna 26 9.884
47
MCR041 Macrothrombocytopenia Progressive Deafness 5 9.884
48
ATS252 Autosomal Recessive Non-Syndromic Sensorineural Deafness Type Dfnb 24 6.989