Search results for "[genes] MYH9"

37 hits were found for '[genes] MYH9'

# Family MCID Name MIFTS Score
1
EPS006 Epstein Syndrome 40 22.855
2
FCH003 Fechtner Syndrome 37 22.855
3
SBS006 Sebastian Syndrome 37 22.855
4
MYH001 May-Hegglin Anomaly 43 21.682
5
P ALP004 Alport Syndrome 68 17.704
6
SNS001 Sensorineural Hearing Loss 57 17.704
7
MCR139 Macrothrombocytopenia and Progressive Sensorineural Deafness 19 17.704
8
P THR014 Thrombocytopenia 64 16.161
9
c DFN200 Deafness, Autosomal Dominant 17 21 16.161
10
P FCL005 Focal Segmental Glomerulosclerosis 59 14.455
11
P ACT135 Acute Graft Versus Host Disease 53 12.518
12
END030 End Stage Renal Failure 52 12.518
13
BRN082 Bernard-Soulier Syndrome, Type C 50 12.518
14
BLD053 Blood Platelet Disease 46 12.518
15
FSC004 Fasciitis 46 12.518
16
P ATS208 Autosomal Dominant Macrothrombocytopenia 26 12.518
17
c MYH004 Myh9 Related Thrombocytopenia 21 12.518
18
THR009 Thrombocytopenia-Absent Radius Syndrome 54 10.221
19
P SYP003 Syphilis 53 10.221
20
INN002 Inner Ear Disease 50 10.221
21
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 44 10.221
22
c PRM022 Primary Syphilis 42 10.221
23
YWS001 Yaws 41 10.221
24
c CNG033 Congenital Syphilis 39 10.221
25
LNS003 Lens Disease 38 10.221
26
ASY002 Asymptomatic Neurosyphilis 33 10.221
27
TRT003 Tertiary Syphilis 31 10.221
28
PSD016 Pseudosarcomatous Fibromatosis 29 10.221
29
LTN001 Latent Syphilis 27 10.221
30
SLF001 Sulfhemoglobinemia 20 10.221
31
MYH015 Myh-9 Related Disease 11 10.221
32
PTN001 Patent Foramen Ovale 54 7.227
33
ADT003 Auditory System Disease 51 7.227
34
ATS251 Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna 25 7.227
35
P DFN023 Deafness, Autosomal Dominant Nonsyndromic Sensorineural 17 13 7.227
36
MCR041 Macrothrombocytopenia Progressive Deafness 5 7.227
37
DFN052 Dfna17 Nonsyndromic Hearing Loss and Deafness 4 7.227