Search results for "[genes] MYH9"

35 hits were found for '[genes] MYH9'

# Family MCID Name MIFTS Score
1
EPS006 Epstein Syndrome 40 23.033
2
FCH003 Fechtner Syndrome 36 23.033
3
SBS006 Sebastian Syndrome 36 23.033
4
MYH001 May-Hegglin Anomaly 41 21.851
5
P ALP004 Alport Syndrome 68 17.842
6
MCR139 Macrothrombocytopenia and Progressive Sensorineural Deafness 20 17.842
7
c DFN200 Deafness, Autosomal Dominant 17 19 16.287
8
SNS001 Sensorineural Hearing Loss 52 14.568
9
P THR014 Thrombocytopenia 63 14.568
10
MYH002 Myh9-Related Disorders 18 14.568
11
BRN082 Bernard-Soulier Syndrome, Type C 51 12.616
12
c MYH004 Myh9 Related Thrombocytopenia 21 12.616
13
END030 End Stage Renal Failure 53 12.616
14
FSC004 Fasciitis 47 12.616
15
P ATS208 Autosomal Dominant Macrothrombocytopenia 26 12.616
16
YWS001 Yaws 41 10.301
17
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 10.301
18
INN002 Inner Ear Disease 48 10.301
19
P SYP003 Syphilis 51 10.301
20
LNS003 Lens Disease 37 10.301
21
c CNG033 Congenital Syphilis 39 10.301
22
TRT003 Tertiary Syphilis 33 10.301
23
ASY002 Asymptomatic Neurosyphilis 35 10.301
24
PSD016 Pseudosarcomatous Fibromatosis 25 10.301
25
TRT002 Tertiary Neurosyphilis 28 10.301
26
c PRM022 Primary Syphilis 39 10.301
27
LTN001 Latent Syphilis 39 10.301
28
SLF001 Sulfhemoglobinemia 20 10.301
29
ADT003 Auditory System Disease 49 7.284
30
PTN001 Patent Foramen Ovale 55 7.284
31
P DFN023 Deafness, Autosomal Dominant Nonsyndromic Sensorineural 17 14 7.284
32
BLD053 Blood Platelet Disease 44 7.284
33
ATS251 Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna 26 7.284
34
MCR041 Macrothrombocytopenia Progressive Deafness 5 7.284
35
DFN052 Dfna17 Nonsyndromic Hearing Loss and Deafness 4 7.284