Search results for "MYH9"

74 hits were found for 'MYH9'

# Family MCID Name MIFTS Score
1
P MYH004 Myh9 Related Thrombocytopenia 45 31.917
2
ALP004 Alport Syndrome 61 5.500
3
MYH002 Myh9-Related Disorders 17 5.500
4
MCR139 Macrothrombocytopenia and Progressive Sensorineural Deafness 20 5.477
5
P BRN019 Bernard-Soulier Syndrome 65 4.482
6
c DFN200 Deafness, Autosomal Dominant 17 11 3.855
7
P ATS015 Autosomal Dominant Alport Syndrome 54 3.222
8
P DFN023 Deafness, Autosomal Dominant Nonsyndromic Sensorineural 17 13 2.278
9
P DFN102 Deafness, Autosomal Dominant 3b 41 2.226
10
DFN052 Dfna17 Nonsyndromic Hearing Loss and Deafness 5 2.226
11
c KDN018 Kidney Disease 63 0.154
12
GLM011 Glomerulosclerosis 48 0.141
13
c THR014 Thrombocytopenia 71 0.126
14
P FCL005 Focal Segmental Glomerulosclerosis 70 0.126
15
CLF001 Cleft Lip 60 0.109
16
NPH051 Nephritis 54 0.109
17
P HYP075 Hypertension 87 0.089
18
PRP030 Purpura 66 0.089
19
PRT039 Proteinuria 58 0.089
20
c CTR002 Cataract 57 0.089
21
LPS007 Lupus Nephritis 53 0.089
22
P CLF002 Cleft Palate 52 0.089
23
DBT061 Diabetic Nephropathy 47 0.089
24
P NNS007 Nonsyndromic Deafness 35 0.089
25
c TYP009 Type 2 Diabetes Mellitus 100 0.063
26
P SCH015 Schizophrenia 82 0.063
27
AND002 Androgen Insensitivity Syndrome 80 0.063
28
c DBT009 Diabetes Mellitus 74 0.063
29
c PRM002 Primary Hyperoxaluria 74 0.063
30
P SHR002 Short Stature 68 0.063
31
c NPH012 Nephrotic Syndrome 67 0.063
32
c AXN002 Axenfeld-Rieger Syndrome 67 0.063
33
c AMY001 Amyotrophic Lateral Sclerosis 67 0.063
34
HV1006 Hiv-1 64 0.063
35
ACN002 Acanthosis Nigricans 63 0.063
36
LRN003 Learning Disability 63 0.063
37
P ANP001 Anaplastic Large Cell Lymphoma 63 0.063
38
SCK005 Sickle Cell Disease 62 0.063
39
c AMY077 Amyotrophic Lateral Sclerosis Type 18 60 0.063
40
MYC002 Mycobacterium Avium Complex Disease 59 0.063
41
END030 End Stage Renal Failure 58 0.063
42
SNS001 Sensorineural Hearing Loss 57 0.063
43
c BRC006 Brachydactyly 57 0.063
44
P AMY074 Amyotrophic Lateral Sclerosis Type 14 56 0.063
45
P DWR001 Dwarfism 55 0.063
46
MCR010 Microcephaly 53 0.063
47
THR013 Thoracic Outlet Syndrome 52 0.063
48
END072 Endotheliitis 51 0.063
49
c ORF002 Orofacial Cleft 49 0.063
50
EVN001 Evans' Syndrome 46 0.063
51
SYN036 Syncope 44 0.063
52
TTH002 Tooth Agenesis 43 0.063
53
P ATX010 Ataxia Neuropathy Spectrum 43 0.063
54
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 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 36 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
c ADM004 Adams Oliver Syndrome 30 0.063
64
BRN065 Bernard-Soulier Syndrome Type C 30 0.063
65
HNM002 Hinman Syndrome 28 0.063
66
c BNG076 Benign Exophthalmos Syndrome 22 0.063
67
AND005 Androgen Insensitivity Syndrome, Mild 21 0.063
68
BFD003 Bifid Uvula 21 0.063
69
ISL075 Isolated Pierre Robin Sequence 20 0.063
70
c BRC069 Brachydactyly of Toes 18 0.063
71
CMP053 Camptodactyly of Fingers 16 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 5 0.063