Search results for "[genes] MYH9"

35 hits were found for '[genes] MYH9'

# Family MCID Name MIFTS Score
1
FCH003 Fechtner Syndrome 36 23.134
2
EPS006 Epstein Syndrome 36 23.134
3
SBS006 Sebastian Syndrome 34 23.134
4
MYH001 May-Hegglin Anomaly 43 21.947
5
P ALP004 Alport Syndrome 66 19.356
6
SNS001 Sensorineural Hearing Loss 49 17.920
7
c DFN200 Deafness, Autosomal Dominant 17 21 17.920
8
MCR139 Macrothrombocytopenia and Progressive Sensorineural Deafness 20 17.920
9
P THR014 Thrombocytopenia 50 16.358
10
MYH002 Myh9-Related Disorders 19 14.631
11
END030 End Stage Renal Failure 51 12.671
12
BRN082 Bernard-Soulier Syndrome, Type C 51 12.671
13
P ACT135 Acute Graft Versus Host Disease 44 12.671
14
FSC004 Fasciitis 40 12.671
15
BLD053 Blood Platelet Disease 32 12.671
16
LNS003 Lens Disease 26 12.671
17
P ATS208 Autosomal Dominant Macrothrombocytopenia 24 12.671
18
c MYH004 Myh9 Related Thrombocytopenia 22 12.671
19
P FCL005 Focal Segmental Glomerulosclerosis 65 10.346
20
c CHR089 Chronic Kidney Failure 61 10.346
21
P SYP003 Syphilis 44 10.346
22
YWS001 Yaws 38 10.346
23
INN002 Inner Ear Disease 38 10.346
24
c CNG033 Congenital Syphilis 35 10.346
25
c PRM022 Primary Syphilis 35 10.346
26
LTN001 Latent Syphilis 33 10.346
27
ASY002 Asymptomatic Neurosyphilis 33 10.346
28
TRT003 Tertiary Syphilis 31 10.346
29
TRT002 Tertiary Neurosyphilis 30 10.346
30
SLF001 Sulfhemoglobinemia 25 10.346
31
PTN001 Patent Foramen Ovale 48 7.316
32
ATS251 Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna 24 7.316
33
P DFN023 Deafness, Autosomal Dominant Nonsyndromic Sensorineural 17 13 7.316
34
DFN052 Dfna17 Nonsyndromic Hearing Loss and Deafness 5 7.316
35
MCR041 Macrothrombocytopenia Progressive Deafness 5 7.316