101 hits were found for 'MYH9'

# ++ Fam MCID Name MIFTS Score
1
MYH004 Myh9 Related Thrombocytopenia 31 18.939
2
SBS006 Sebastian Syndrome 25 6.710
3
MCR139 Macrothrombocytopenia and Progressive Sensorineural Deafness 6 5.188
4
c DFN200 Deafness, Autosomal Dominant 17 5 4.196
5
ALP004 Alport Syndrome 55 3.700
6
MYH002 Myh9-Related Disorders 15 3.044
7
P ATS015 Autosomal Dominant Alport Syndrome 43 3.021
8
P BRN019 Bernard-Soulier Syndrome 56 2.995
9
MCR041 Macrothrombocytopenia Progressive Deafness 5 2.995
10
c KDN018 Kidney Disease 52 2.701
11
c THR014 Thrombocytopenia 66 2.679
12
NPH051 Nephritis 55 2.655
13
P PRT039 Proteinuria 51 2.655
14
c CTR002 Cataract 48 2.655
15
P CLF002 Cleft Palate 60 2.630
16
SNS001 Sensorineural Hearing Loss 55 2.602
17
LKM002 Leukemia 70 2.570
18
MYL006 Myeloid Leukemia 64 2.570
19
P GRF002 Graft Versus Host Disease 64 2.570
20
P GLM007 Glomerulonephritis 60 2.570
21
c ACT135 Acute Graft Versus Host Disease 55 2.570
22
END072 Endotheliitis 51 2.570
23
WSR001 Was-Related Disorders 22 2.570
24
DFN052 Dfna17 Nonsyndromic Hearing Loss and Deafness 2 2.570
25
c NNS007 Nonsyndromic Deafness 37 2.267
26
P FCL005 Focal Segmental Glomerulosclerosis 64 2.222
27
P SCH015 Schizophrenia 69 2.168
28
LPS007 Lupus Nephritis 55 2.168
29
P HYP075 Hypertension 76 2.136
30
c DBT009 Diabetes Mellitus 68 2.136
31
c NPH012 Nephrotic Syndrome 57 2.136
32
P ANP001 Anaplastic Large Cell Lymphoma 56 2.136
33
P ORF002 Orofacial Cleft 41 2.136
34
ACT019 Acute Myeloid Leukemia 87 2.098
35
P BRS047 Breast Cancer 85 2.098
36
P PRS040 Prostate Cancer 76 2.098
37
KPS001 Kaposi's Sarcoma 73 2.098
38
P CLR023 Colorectal Cancer 66 2.098
39
c ESS002 Essential Hypertension 64 2.098
40
ACT073 Acute Leukemia 62 2.098
41
P ADN016 Adenocarcinoma 60 2.098
42
P HRP006 Herpes Simplex 57 2.098
43
CHR090 Chronic Lymphocytic Leukemia 56 2.098
44
SRC014 Sarcoma 54 2.098
45
RTN023 Retinitis 53 2.098
46
KLD001 Keloids 52 2.098
47
P ESP024 Esophagitis 51 2.098
48
P MYC008 Myocarditis 51 2.098
49
PRS047 Prostatitis 50 2.098
50
CLF001 Cleft Lip 47 2.098
51
P INF037 Inflammatory Bowel Disease 44 2.098
52
FSC004 Fasciitis 44 2.098
53
CLN015 Colon Adenocarcinoma 41 2.098
54
DBT061 Diabetic Nephropathy 50 1.571
55
SCK005 Sickle Cell Disease 58 1.533
56
P TYP009 Type 2 Diabetes Mellitus 80 1.484
57
P MLT019 Multiple Myeloma 76 1.484
58
HML002 Hemolytic Anemia 60 1.484
59
c SYP003 Syphilis 55 1.484
60
c MYL007 Myeloma 53 1.484
61
HV1006 Hiv-1 42 1.484
62
c DFN266 Deafness, Autosomal Dominant 4b 33 1.484
63
P NNS014 Nonsyndromic Hearing Loss and Deafness 28 1.484
64
DFN003 Deafness and Hereditary Hearing Loss 26 1.484
65
c NNS015 Nonsyndromic Hearing Loss and Deafness, Autosomal Dominant 21 1.484
66
BRS089 Breast and Colorectal Cancer 20 1.484
67
P DFN023 Deafness, Autosomal Dominant Nonsyndromic Sensorineural 17 10 0.180
68
HNM001 Hinman's Syndrome 28 0.134
69
FCL008 Focal Glomerulosclerosis 57 0.120
70
NSY001 N Syndrome 57 0.120
71
RTC002 Reticular Dysgenesis 51 0.120
72
FCT013 Factor V Leiden Thrombophilia 31 0.120
73
P EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 23 0.120
74
THR013 Thoracic Outlet Syndrome 53 0.104
75
CHL079 Children's Interstitial Lung Disease 39 0.104
76
c HVY001 Heavy Chain Disease 27 0.104
77
ACN002 Acanthosis Nigricans 70 0.085
78
MYC002 Mycobacterium Avium Complex Disease 56 0.085
79
KDS001 Kid Syndrome 55 0.085
80
P THR090 Thrombocythemia 1 48 0.085
81
P SPR013 Spiradenoma 38 0.085
82
BRN065 Bernard-Soulier Syndrome Type C 13 0.085
83
P AMY001 Amyotrophic Lateral Sclerosis 87 0.060
84
AND002 Androgen Insensitivity Syndrome 75 0.060
85
WST001 West Syndrome 64 0.060
86
c PRM002 Primary Hyperoxaluria 63 0.060
87
PRP030 Purpura 60 0.060
88
c AXN002 Axenfeld-Rieger Syndrome 57 0.060
89
RNL015 Renal Hypertension 52 0.060
90
HYP030 Hypoactive Sexual Desire Disorder 39 0.060
91
c ATX010 Ataxia Neuropathy Spectrum 33 0.060
92
ADS002 Adie Syndrome 32 0.060
93
OLV002 Oliver Syndrome 31 0.060
94
c ADM004 Adams Oliver Syndrome 27 0.060
95
c MCH003 Mu Chain Disease 20 0.060
96
AND005 Androgen Insensitivity Syndrome, Mild 19 0.060
97
c BNG076 Benign Exophthalmos Syndrome 17 0.060
98
c BRN064 Bernard-Soulier Syndrome Type B 14 0.060
99
c RRD005 Rare Deafness 10 0.060
100
c BRN063 Bernard-Soulier Syndrome Type a 10 0.060
101
c BRN110 Bernard-Soulier Syndrome, Type A1 4 0.060