Search results for "MYH9"

51 hits were found for 'MYH9'

# Family MCID Name MIFTS Score
1
MYH002 Myh9-Related Disorders 18 13.893
2
c MYH004 Myh9 Related Thrombocytopenia 22 12.723
3
FCH003 Fechtner Syndrome 38 9.315
4
EPS006 Epstein Syndrome 28 9.257
5
SBS006 Sebastian Syndrome 25 9.209
6
MYH001 May-Hegglin Anomaly 39 7.750
7
P ALP004 Alport Syndrome 60 5.254
8
MCR139 Macrothrombocytopenia and Progressive Sensorineural Deafness 16 4.856
9
P ATS208 Autosomal Dominant Macrothrombocytopenia 27 4.310
10
c DFN200 Deafness, Autosomal Dominant 17 11 3.749
11
P DFN023 Deafness, Autosomal Dominant Nonsyndromic Sensorineural 17 13 2.227
12
MCR041 Macrothrombocytopenia Progressive Deafness 5 2.227
13
ATS251 Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna 28 2.123
14
DFN052 Dfna17 Nonsyndromic Hearing Loss and Deafness 4 2.123
15
P KDN018 Kidney Disease 57 0.174
16
GLM011 Glomerulosclerosis 40 0.159
17
P FCL005 Focal Segmental Glomerulosclerosis 58 0.142
18
P THR014 Thrombocytopenia 56 0.142
19
P SCH015 Schizophrenia 79 0.101
20
CLF001 Cleft Lip 51 0.101
21
P CTR002 Cataract 50 0.101
22
NPH051 Nephritis 46 0.101
23
LPS007 Lupus Nephritis 44 0.101
24
PRT039 Proteinuria 43 0.101
25
HV1006 Hiv-1 83 0.071
26
P PRM002 Primary Hyperoxaluria 68 0.071
27
AND015 Androgen Insensitivity 69 0.071
28
P NPH012 Nephrotic Syndrome 60 0.071
29
END030 End Stage Renal Failure 56 0.071
30
ACN002 Acanthosis Nigricans 55 0.071
31
PRP030 Purpura 54 0.071
32
SCK005 Sickle Cell Disease 54 0.071
33
P ANP001 Anaplastic Large Cell Lymphoma 53 0.071
34
MYC002 Mycobacterium Avium Complex Disease 51 0.071
35
P AXN010 Axenfeld-Rieger Syndrome, Type 3 50 0.071
36
SNS001 Sensorineural Hearing Loss 48 0.071
37
P ADM011 Adams-Oliver Syndrome 46 0.071
38
THR013 Thoracic Outlet Syndrome 45 0.071
39
END072 Endotheliitis 44 0.071
40
BRN082 Bernard-Soulier Syndrome, Type C 42 0.071
41
c ALP073 Alport Syndrome, Autosomal Recessive 40 0.071
42
P TRC086 Trichohepatoenteric Syndrome 1 39 0.071
43
P ORF002 Orofacial Cleft 38 0.071
44
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 38 0.071
45
c NNS007 Nonsyndromic Deafness 34 0.071
46
OLV002 Oliver Syndrome 33 0.071
47
c ALP074 Alport Syndrome, Autosomal Dominant 34 0.071
48
FCT013 Factor V Leiden Thrombophilia 31 0.071
49
P ATX010 Ataxia Neuropathy Spectrum 29 0.071
50
c BNG076 Benign Exophthalmos Syndrome 19 0.071
51
AND005 Androgen Insensitivity Syndrome, Mild 17 0.071