Search results for myh9

126 hits were found for myh9

# Family MCID Name MIFTS Score
1
MCR359 Macrothrombocytopenia and Granulocyte Inclusions with or Without Nephritis or Sensorineural Hearing Loss 47 19.536
2
c DFN200 Deafness, Autosomal Dominant 17 43 6.100
3
P SNS001 Sensorineural Hearing Loss 60 4.032
4
P THR014 Thrombocytopenia 67 3.997
5
P BRS047 Breast Cancer 97 3.449
6
P KDN018 Kidney Disease 72 3.414
7
P ALP004 Alport Syndrome 68 3.179
8
END086 End Stage Renal Disease 51 3.096
9
P FCL005 Focal Segmental Glomerulosclerosis 57 3.019
10
c CHR684 Chronic Kidney Disease 70 2.914
11
P GLM007 Glomerulonephritis 57 2.834
12
P BRN019 Bernard-Soulier Syndrome 60 2.796
13
P HMN010 Hemangioma 61 2.702
14
P CTR002 Cataract 60 2.632
15
CLF027 Cleft Palate, Isolated 64 2.299
16
ATS252 Autosomal Recessive Non-Syndromic Sensorineural Deafness Type Dfnb 32 2.274
17
RRG078 Rare Genetic Deafness 29 2.274
18
c HYP595 Hypertension, Essential 84 2.248
19
BLD053 Blood Platelet Disease 49 2.248
20
P ORF002 Orofacial Cleft 44 2.248
21
P USH001 Usher Syndrome 60 2.217
22
NTR046 Neutrophil Migration 50 2.217
23
PSD016 Pseudosarcomatous Fibromatosis 37 2.217
24
c NNS007 Nonsyndromic Deafness 35 2.217
25
FSC004 Fasciitis 50 2.181
26
P INN002 Inner Ear Disease 47 2.181
27
c ATS005 Autosomal Dominant Nonsyndromic Deafness 26 2.181
29
P ATS208 Autosomal Dominant Macrothrombocytopenia 27 1.707
30
ATS251 Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna 31 1.683
31
c HMN027 Hemangioma, Capillary Infantile 37 1.625
32
c XLN231 X-Linked Alport Syndrome 33 1.589
33
PTN001 Patent Foramen Ovale 60 1.542
34
GRY002 Gray Platelet Syndrome 59 1.542
35
P SYP003 Syphilis 58 1.542
36
c CRD085 Cardiomyopathy, Familial Hypertrophic, 4 52 1.542
37
P RNL015 Renal Hypertension 47 1.542
38
P BLD051 Blood Coagulation Disease 46 1.542
39
MLC004 Mulchandani-Bhoj-Conlin Syndrome 44 1.542
40
P VTL001 Vitelliform Macular Dystrophy 42 1.542
41
ASY002 Asymptomatic Neurosyphilis 41 1.542
42
c SCN006 Secondary Syphilis 40 1.542
43
c ATS018 Autosomal Recessive Alport Syndrome 40 1.542
44
c CNG033 Congenital Syphilis 40 1.542
45
P MYP105 Myopathy, Myosin Storage, Autosomal Dominant 39 1.542
46
c ACQ005 Acquired Thrombocytopenia 39 1.542
47
LTN001 Latent Syphilis 38 1.542
48
P YWS001 Yaws 36 1.542
49
TBS001 Tabes Dorsalis 34 1.542
50
P LNS003 Lens Disease 34 1.542
51
TRT003 Tertiary Syphilis 33 1.542
52
c ATS015 Autosomal Dominant Alport Syndrome 31 1.542
53
c PRM022 Primary Syphilis 31 1.542
54
PRT034 Peritoneal Serous Adenocarcinoma 27 1.542
55
MNN005 Meningovascular Neurosyphilis 26 1.542
57
INT055 Intravascular Fasciitis 22 1.542
58
TRT002 Tertiary Neurosyphilis 22 1.542
59
PRL005 Proliferative Fasciitis 20 1.542
60
c BRN108 Branchiootic Syndrome 1 62 0.340
61
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.247
62
PRP030 Purpura 54 0.150
63
c MCR113 Microvascular Complications of Diabetes 3 52 0.150
64
c MCR120 Microvascular Complications of Diabetes 7 47 0.150
65
c MCR130 Microvascular Complications of Diabetes 6 41 0.150
66
c MCR133 Microvascular Complications of Diabetes 4 41 0.150
67
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.127
68
P HPT023 Hepatocellular Carcinoma 100 0.113
69
CLF001 Cleft Lip 53 0.113
70
NPH010 Nephrosclerosis 50 0.113
71
c SYS001 Systemic Lupus Erythematosus 86 0.098
72
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.098
73
CLF056 Cleft Lip with or Without Cleft Palate 47 0.098
74
GLM044 Glomerular Disease 37 0.098
75
IMM167 Immune Deficiency Disease 78 0.080
76
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.080
77
ESP020 Esophageal Atresia 62 0.080
78
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 55 0.080
79
P SCK005 Sickle Cell Disease 50 0.080
80
PYL006 Pyloric Stenosis 48 0.080
81
SNL007 Senile Cataract 42 0.080
82
P NNS072 Nonsyndromic Hearing Loss 41 0.080
83
c FCL082 Focal Segmental Glomerulosclerosis 4 22 0.080
84
c MCL073 Macular Dystrophy, Vitelliform, 1 21 0.080
85
P CLR023 Colorectal Cancer 99 0.057
86
P LNG032 Lung Cancer 98 0.057
87
P OVR042 Ovarian Cancer 88 0.057
88
c LKM061 Leukemia, Acute Myeloid 84 0.057
89
P GST053 Gastric Cancer 83 0.057
90
DWN001 Down Syndrome 70 0.057
91
RCK004 Rickets 68 0.057
92
OST159 Osteogenic Sarcoma 66 0.057
93
P NSP012 Nasopharyngeal Carcinoma 66 0.057
94
P MCR115 Microvascular Complications of Diabetes 5 66 0.057
95
c SML038 Small Cell Cancer of the Lung 65 0.057
96
P ART005 Arteriovenous Malformation 65 0.057
97
PRT036 Peritonitis 64 0.057
98
P PRD008 Periodontitis 64 0.057
99
CLT003 Colitis 62 0.057
100
ATM095 Autoimmune Disease 62 0.057
101
P LPS004 Lupus Erythematosus 61 0.057
102
P MYL006 Myeloid Leukemia 60 0.057
103
P NPH012 Nephrotic Syndrome 60 0.057
104
SQM006 Squamous Cell Carcinoma 60 0.057
105
THY029 Thyroid Carcinoma 59 0.057
106
PLM033 Pulmonary Embolism 59 0.057
107
VSL002 Visual Epilepsy 59 0.057
108
P ADM011 Adams-Oliver Syndrome 59 0.057
109
P ANP001 Anaplastic Large Cell Lymphoma 58 0.057
110
P SZR006 Seizure Disorder 56 0.057
111
GST050 Gastrointestinal System Disease 56 0.057
112
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.057
113
CLF004 Cleft Lip/palate 54 0.057
114
P HMR003 Hemorrhagic Disease 53 0.057
115
URM002 Uremia 49 0.057
116
IGG001 Iga Glomerulonephritis 48 0.057
117
P OST028 Osteochondroma 45 0.057
119
RTN187 Retinitis Pigmentosa-Deafness Syndrome 42 0.057
120
OLV002 Oliver Syndrome 42 0.057
121
48X005 48,xyyy 39 0.057
122
OVR094 Ovarian Epithelial Cancer 38 0.057
123
c ORF048 Orofacial Cleft 1 29 0.057
124
P C1Q005 C1q Nephropathy 22 0.057
125
c CNG578 Congenital Hemangioma 21 0.057
126
c DFN023 Deafness, Autosomal Dominant Nonsyndromic Sensorineural 17 9 0.057
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