Search results for "MYH9"

67 hits were found for 'MYH9'

# Family MCID Name MIFTS Score
1
P MYH004 Myh9 Related Thrombocytopenia 41 31.066
2
ALP004 Alport Syndrome 60 5.605
3
MCR139 Macrothrombocytopenia and Progressive Sensorineural Deafness 17 5.100
4
MYH002 Myh9-Related Disorders 17 4.595
5
P BRN019 Bernard-Soulier Syndrome 64 4.567
6
P ATS015 Autosomal Dominant Alport Syndrome 52 3.284
7
c DFN200 Deafness, Autosomal Dominant 17 11 3.208
8
P DFN266 Deafness, Autosomal Dominant 4b 46 2.268
9
DFN052 Dfna17 Nonsyndromic Hearing Loss and Deafness 5 2.268
10
c KDN018 Kidney Disease 62 0.144
11
GLM011 Glomerulosclerosis 46 0.144
12
P FCL005 Focal Segmental Glomerulosclerosis 72 0.129
13
c THR014 Thrombocytopenia 70 0.129
14
CLF001 Cleft Lip 59 0.112
15
NPH051 Nephritis 54 0.112
16
P HYP075 Hypertension 85 0.091
17
P SCH015 Schizophrenia 82 0.091
18
PRT039 Proteinuria 57 0.091
19
c CTR002 Cataract 57 0.091
20
LPS007 Lupus Nephritis 52 0.091
21
P CLF002 Cleft Palate 52 0.091
22
DBT061 Diabetic Nephropathy 40 0.091
23
P NNS007 Nonsyndromic Deafness 36 0.091
24
P AMY001 Amyotrophic Lateral Sclerosis 98 0.065
25
c TYP009 Type 2 Diabetes Mellitus 95 0.065
26
AND002 Androgen Insensitivity Syndrome 80 0.065
27
c DBT009 Diabetes Mellitus 78 0.065
28
c PRM002 Primary Hyperoxaluria 72 0.065
29
ACN002 Acanthosis Nigricans 69 0.065
30
c NPH012 Nephrotic Syndrome 66 0.065
31
c AXN002 Axenfeld-Rieger Syndrome 66 0.065
32
PRP030 Purpura 64 0.065
33
P SHR002 Short Stature 64 0.065
34
LRN003 Learning Disability 62 0.065
35
P ANP001 Anaplastic Large Cell Lymphoma 62 0.065
36
HV1006 Hiv-1 61 0.065
37
SCK005 Sickle Cell Disease 58 0.065
38
MYC002 Mycobacterium Avium Complex Disease 58 0.065
39
END030 End Stage Renal Failure 58 0.065
40
SNS001 Sensorineural Hearing Loss 57 0.065
41
c BRC006 Brachydactyly 55 0.065
42
P DWR001 Dwarfism 55 0.065
43
MCR010 Microcephaly 54 0.065
44
THR013 Thoracic Outlet Syndrome 52 0.065
45
END072 Endotheliitis 50 0.065
46
c ORF002 Orofacial Cleft 47 0.065
47
SYN036 Syncope 44 0.065
48
P ATX010 Ataxia Neuropathy Spectrum 41 0.065
49
TTH016 Tooth Agenesis, Selective, 1, with or Without Orofacial Cleft 40 0.065
50
AND001 Anodontia 39 0.065
51
CLF027 Cleft Palate, Isolated 36 0.065
52
OLV002 Oliver Syndrome 35 0.065
53
ADS002 Adie Syndrome 35 0.065
54
FCT013 Factor V Leiden Thrombophilia 33 0.065
55
SYN053 Syndromic Diarrhea 32 0.065
56
c ADM004 Adams Oliver Syndrome 30 0.065
57
BRN065 Bernard-Soulier Syndrome Type C 30 0.065
58
HNM002 Hinman Syndrome 27 0.065
59
c BNG076 Benign Exophthalmos Syndrome 22 0.065
60
BFD003 Bifid Uvula 21 0.065
61
AND005 Androgen Insensitivity Syndrome, Mild 21 0.065
62
c BRC069 Brachydactyly of Toes 18 0.065
63
ISL075 Isolated Pierre Robin Sequence 17 0.065
64
CMP053 Camptodactyly of Fingers 16 0.065
65
SBM006 Submucosal Cleft Palate 16 0.065
66
P DFN023 Deafness, Autosomal Dominant Nonsyndromic Sensorineural 17 12 0.065
67
VNT005 Ventricular Extrasystoles with Syncopal Episodes - Perodactyly - Robin Sequence 5 0.065