Search results for "MYH9"

74 hits were found for 'MYH9'

# Family MCID Name MIFTS Score
1
P MYH004 Myh9 Related Thrombocytopenia 46 31.917
2
P ALP004 Alport Syndrome 63 5.500
3
MYH002 Myh9-Related Disorders 17 5.500
4
MCR139 Macrothrombocytopenia and Progressive Sensorineural Deafness 23 5.477
5
P BRN019 Bernard-Soulier Syndrome 64 4.482
6
c DFN200 Deafness, Autosomal Dominant 17 13 3.855
7
c ATS015 Autosomal Dominant Alport Syndrome 54 3.222
8
P DFN023 Deafness, Autosomal Dominant Nonsyndromic Sensorineural 17 14 2.278
9
P DFN102 Deafness, Autosomal Dominant 3b 43 2.226
10
DFN052 Dfna17 Nonsyndromic Hearing Loss and Deafness 5 2.226
11
c KDN018 Kidney Disease 62 0.154
12
GLM011 Glomerulosclerosis 47 0.141
13
P FCL005 Focal Segmental Glomerulosclerosis 72 0.126
14
c THR014 Thrombocytopenia 69 0.126
15
CLF001 Cleft Lip 59 0.109
16
NPH051 Nephritis 53 0.109
17
P HYP075 Hypertension 85 0.089
18
PRP030 Purpura 65 0.089
19
PRT039 Proteinuria 57 0.089
20
c CTR002 Cataract 57 0.089
21
LPS007 Lupus Nephritis 52 0.089
22
P CLF002 Cleft Palate 51 0.089
23
DBT061 Diabetic Nephropathy 47 0.089
24
c NNS007 Nonsyndromic Deafness 38 0.089
25
c TYP009 Type 2 Diabetes Mellitus 100 0.063
26
P SCH015 Schizophrenia 84 0.063
27
AND002 Androgen Insensitivity Syndrome 80 0.063
28
c DBT009 Diabetes Mellitus 73 0.063
29
c PRM002 Primary Hyperoxaluria 73 0.063
30
c AXN002 Axenfeld-Rieger Syndrome 69 0.063
31
P SHR002 Short Stature 68 0.063
32
c NPH012 Nephrotic Syndrome 67 0.063
33
c AMY001 Amyotrophic Lateral Sclerosis 66 0.063
34
ACN002 Acanthosis Nigricans 64 0.063
35
c AMY077 Amyotrophic Lateral Sclerosis Type 18 63 0.063
36
HV1006 Hiv-1 63 0.063
37
LRN003 Learning Disability 62 0.063
38
P ANP001 Anaplastic Large Cell Lymphoma 62 0.063
39
SCK005 Sickle Cell Disease 61 0.063
40
c BRC006 Brachydactyly 60 0.063
41
P AMY074 Amyotrophic Lateral Sclerosis Type 14 59 0.063
42
MYC002 Mycobacterium Avium Complex Disease 58 0.063
43
END030 End Stage Renal Failure 57 0.063
44
SNS001 Sensorineural Hearing Loss 57 0.063
45
c MCR010 Microcephaly 56 0.063
46
P DWR001 Dwarfism 54 0.063
47
THR013 Thoracic Outlet Syndrome 52 0.063
48
END072 Endotheliitis 50 0.063
49
c ORF002 Orofacial Cleft 48 0.063
50
P ATX010 Ataxia Neuropathy Spectrum 47 0.063
51
EVN001 Evans' Syndrome 45 0.063
52
SYN036 Syncope 44 0.063
53
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 43 0.063
54
TTH002 Tooth Agenesis 42 0.063
55
TTH016 Tooth Agenesis, Selective, 1, with or Without Orofacial Cleft 40 0.063
56
AND001 Anodontia 39 0.063
57
GST053 Gastric Cancer 38 0.063
58
CLF027 Cleft Palate, Isolated 37 0.063
59
OLV002 Oliver Syndrome 36 0.063
60
ADS002 Adie Syndrome 35 0.063
61
SYN053 Syndromic Diarrhea 34 0.063
62
FCT013 Factor V Leiden Thrombophilia 34 0.063
63
BRN065 Bernard-Soulier Syndrome Type C 32 0.063
64
c ADM004 Adams Oliver Syndrome 30 0.063
65
HNM002 Hinman Syndrome 28 0.063
66
BFD003 Bifid Uvula 22 0.063
67
c BNG076 Benign Exophthalmos Syndrome 22 0.063
68
AND005 Androgen Insensitivity Syndrome, Mild 21 0.063
69
ISL075 Isolated Pierre Robin Sequence 20 0.063
70
CMP053 Camptodactyly of Fingers 18 0.063
71
c BRC069 Brachydactyly of Toes 17 0.063
72
SBM006 Submucosal Cleft Palate 16 0.063
73
LKC003 Leukocyte Disease 10 0.063
74
VNT005 Ventricular Extrasystoles with Syncopal Episodes - Perodactyly - Robin Sequence 9 0.063