Search results for "MYH9"

50 hits were found for 'MYH9'

# Family MCID Name MIFTS Score
1
MYH002 Myh9-Related Disorders 20 14.014
2
c MYH004 Myh9 Related Thrombocytopenia 27 13.759
3
FCH003 Fechtner Syndrome 42 9.421
4
SBS006 Sebastian Syndrome 28 9.338
5
EPS006 Epstein Syndrome 30 9.312
6
MYH001 May-Hegglin Anomaly 43 7.833
7
P ALP004 Alport Syndrome 69 5.329
8
MCR139 Macrothrombocytopenia and Progressive Sensorineural Deafness 21 5.264
9
P ATS208 Autosomal Dominant Macrothrombocytopenia 30 4.371
10
c DFN200 Deafness, Autosomal Dominant 17 14 3.802
11
P DFN023 Deafness, Autosomal Dominant Nonsyndromic Sensorineural 17 15 2.258
12
ATS251 Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna 32 2.153
13
DFN052 Dfna17 Nonsyndromic Hearing Loss and Deafness 5 2.153
14
P KDN018 Kidney Disease 64 0.175
15
GLM011 Glomerulosclerosis 46 0.160
16
P THR014 Thrombocytopenia 69 0.143
17
P FCL005 Focal Segmental Glomerulosclerosis 68 0.143
18
P SCH015 Schizophrenia 88 0.101
19
CLF001 Cleft Lip 59 0.101
20
P CTR002 Cataract 58 0.101
21
NPH051 Nephritis 53 0.101
22
LPS007 Lupus Nephritis 51 0.101
23
PRT039 Proteinuria 50 0.101
24
HV1006 Hiv-1 79 0.071
25
AND015 Androgen Insensitivity 78 0.071
26
P PRM002 Primary Hyperoxaluria 78 0.071
27
P NPH012 Nephrotic Syndrome 68 0.071
28
ACN002 Acanthosis Nigricans 63 0.071
29
PRP030 Purpura 63 0.071
30
P ANP001 Anaplastic Large Cell Lymphoma 62 0.071
31
SCK005 Sickle Cell Disease 61 0.071
32
MYC002 Mycobacterium Avium Complex Disease 59 0.071
33
P AXN010 Axenfeld-Rieger Syndrome, Type 3 57 0.071
34
END030 End Stage Renal Failure 57 0.071
35
SNS001 Sensorineural Hearing Loss 55 0.071
36
P ADM011 Adams-Oliver Syndrome 52 0.071
37
THR013 Thoracic Outlet Syndrome 52 0.071
38
END072 Endotheliitis 51 0.071
39
BRN082 Bernard-Soulier Syndrome, Type C 47 0.071
40
c ALP073 Alport Syndrome, Autosomal Recessive 45 0.071
41
P TRC086 Trichohepatoenteric Syndrome 1 45 0.071
42
P ORF002 Orofacial Cleft 44 0.071
43
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 42 0.071
44
c NNS007 Nonsyndromic Deafness 39 0.071
45
c ALP074 Alport Syndrome, Autosomal Dominant 38 0.071
46
OLV002 Oliver Syndrome 38 0.071
47
FCT013 Factor V Leiden Thrombophilia 35 0.071
48
P ATX010 Ataxia Neuropathy Spectrum 29 0.071
49
c BNG076 Benign Exophthalmos Syndrome 21 0.071
50
AND005 Androgen Insensitivity Syndrome, Mild 19 0.071