Search results for cdh5

143 hits were found for cdh5

# Family MCID Name MIFTS Score
1
P PRS040 Prostate Cancer 95 15.056
2
P MLN008 Melanoma 75 12.897
3
P MYC007 Myocardial Infarction 69 12.807
4
c ACT075 Acute Myocardial Infarction 55 12.807
5
LPP008 Lipoprotein Quantitative Trait Locus 65 12.744
6
P EPT012 Epithelioid Sarcoma 41 12.591
7
c MCR115 Microvascular Complications of Diabetes 5 65 10.685
8
P CRB048 Cerebral Cavernous Malformations 63 10.623
10
P MLN069 Melanoma, Uveal 59 10.545
11
c ART115 Aortic Valve Disease 1 72 10.280
12
c HYP595 Hypertension, Essential 84 10.280
13
c HRD002 Hereditary Angioedema 61 10.280
14
c DLT002 Dilated Cardiomyopathy 79 10.280
15
PRP002 Periapical Granuloma 38 10.280
16
P CRB154 Cerebrocostomandibular Syndrome 55 7.269
17
DYS160 Dyssegmental Dysplasia, Silverman-Handmaker Type 48 7.269
18
VNH007 Von Hippel-Lindau Syndrome 73 7.269
19
INT051 Intussusception 53 7.269
20
c EXD008 Exudative Vitreoretinopathy 1 71 7.269
21
c SPS215 Spastic Paraplegia 3, Autosomal Dominant 62 7.269
22
c NPH076 Nephrotic Syndrome, Type 10 37 7.269
23
HNT019 Hantavirus Hemorrhagic Fever with Renal Syndrome 44 7.269
24
c HRD010 Hereditary Spastic Paraplegia 65 7.269
25
HNT002 Hantavirus Pulmonary Syndrome 55 7.269
26
HYP266 Hypoxia 56 1.574
27
GLB002 Glioblastoma 67 1.556
28
P BRS047 Breast Cancer 97 1.300
29
P GST053 Gastric Cancer 82 1.289
30
RTN003 Retinal Ischemia 48 1.286
31
GST040 Gastric Adenocarcinoma 66 1.091
32
SKN019 Skin Melanoma 70 0.931
33
P BLD134 Bladder Cancer 79 0.811
34
P LNG032 Lung Cancer 98 0.782
35
P OVR042 Ovarian Cancer 88 0.731
36
P PNC035 Pancreatic Cancer 86 0.731
37
P ADN016 Adenocarcinoma 63 0.667
38
ESP021 Esophageal Cancer 84 0.658
39
c MSM022 Mismatch Repair Cancer Syndrome 1 69 0.658
40
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.658
41
BLD173 Bladder Small Cell Carcinoma 44 0.658
42
c GLM043 Glioma Susceptibility 9 30 0.658
43
c GLM047 Glioma Susceptibility 3 32 0.658
44
c GLM025 Glioma Susceptibility 2 29 0.658
45
GST103 Gastric Cancer, Hereditary Diffuse 68 0.658
46
MLN065 Melanocytic Nevus Syndrome, Congenital 61 0.658
47
P GLM040 Glioma Susceptibility 1 70 0.658
48
SML009 Small Intestine Adenocarcinoma 57 0.658
49
LNG019 Lung Combined Type Small Cell Carcinoma 32 0.658
50
P OLG002 Oligodendroglioma 66 0.658
51
MNN043 Meningioma, Familial 79 0.658
52
GLM045 Glioma 62 0.658
53
P LNG021 Lung Occult Small Cell Carcinoma 20 0.658
54
MYL005 Myelofibrosis 70 0.517
55
P LNG064 Lung Cancer Susceptibility 3 70 0.459
56
RTN020 Retinal Vascular Disease 45 0.433
57
HYP066 Hyperglycemia 60 0.405
58
ATH013 Atherosclerosis Susceptibility 63 0.375
59
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.375
60
OVR029 Ovarian Hyperstimulation Syndrome 63 0.375
61
c PLM164 Pulmonary Hypertension, Primary, 1 80 0.375
62
MRF001 Marfan Syndrome 76 0.342
63
P CLR023 Colorectal Cancer 100 0.342
64
LPD008 Lipid Metabolism Disorder 61 0.342
65
CVR010 Cavernous Malformation 29 0.342
66
P PRD008 Periodontitis 64 0.342
67
LMB062 Limb Ischemia 55 0.306
68
MYL031 Myeloproliferative Neoplasm 66 0.306
69
P ADL010 Adult Respiratory Distress Syndrome 71 0.306
70
ART016 Aortic Aneurysm 69 0.306
71
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.265
72
P FML011 Familial Adenomatous Polyposis 71 0.265
73
P BNG032 Benign Mesothelioma 53 0.265
74
c ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.265
75
CNT060 Central Serous Chorioretinopathy 39 0.265
76
NRR002 Norrie Disease 60 0.216
77
CRV035 Cervical Cancer 72 0.216
78
P PLM037 Pulmonary Hypertension 69 0.216
79
P LYM118 Lymphoma 69 0.216
80
ANG020 Angiosarcoma 63 0.216
81
BRT054 Brittle Bone Disorder 74 0.216
82
c SML038 Small Cell Cancer of the Lung 69 0.216
83
c SCL052 Scleroderma, Familial Progressive 60 0.216
84
SMT018 Smith-Mccort Dysplasia 2 33 0.216
85
P HPT023 Hepatocellular Carcinoma 95 0.216
86
P EXD001 Exudative Vitreoretinopathy 55 0.216
87
ISC004 Ischemia 61 0.216
88
CNG034 Congestive Heart Failure 69 0.216
89
P MTR012 Mitral Valve Disease 57 0.216
90
P VSC007 Vascular Disease 62 0.216
91
GST033 Gestational Diabetes 61 0.216
92
P ART021 Arteriosclerosis 53 0.216
93
c CRB191 Cerebral Cavernous Malformations 2 45 0.216
94
SFT003 Soft Tissue Sarcoma 57 0.216
95
P VTR007 Vitreoretinopathy 45 0.216
96
THY029 Thyroid Carcinoma 54 0.216
97
ART140 Arteries, Anomalies of 52 0.153
98
P SRC025 Sarcoidosis 1 70 0.153
99
CRN048 Craniofacial-Deafness-Hand Syndrome 52 0.153
100
DWN001 Down Syndrome 70 0.153
101
c MCR133 Microvascular Complications of Diabetes 4 41 0.153
102
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.153
103
TBL029 Tubulin, Beta 28 0.153
104
c BRT029 Brittle Cornea Syndrome 2 33 0.153
105
MCR013 Microphthalmia 60 0.153
106
c PRC016 Pre-Eclampsia 64 0.153
107
P MDL005 Medulloblastoma 75 0.153
108
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.153
109
END020 Endocardial Fibroelastosis 54 0.153
110
c ATS007 Autism Spectrum Disorder 72 0.153
111
RNL077 Renal Fibrosis 46 0.153
112
P SCL048 Sclerosteosis 58 0.153
113
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 59 0.153
114
c MST023 Mesothelioma, Malignant 56 0.153
115
c MCR113 Microvascular Complications of Diabetes 3 52 0.153
116
c MCR130 Microvascular Complications of Diabetes 6 41 0.153
117
c MCR120 Microvascular Complications of Diabetes 7 47 0.153
118
P ART005 Arteriovenous Malformation 65 0.153
119
P ATS364 Autism 72 0.153
120
c HRD202 Hereditary Lymphedema I 55 0.153
121
PRP027 Peripheral Vascular Disease 71 0.153
122
MST005 Mastitis 52 0.153
123
CRT013 Carotid Stenosis 51 0.153
124
P SBS003 Substance Abuse 54 0.153
125
P INF032 Infertility 60 0.153
126
c BNG019 Benign Intermediate Mesothelioma 13 0.153
127
CNN005 Connective Tissue Disease 66 0.153
128
P KDN017 Kidney Cancer 60 0.153
129
SQM006 Squamous Cell Carcinoma 59 0.153
130
TLN003 Telangiectasis 51 0.153
131
P LKM002 Leukemia 66 0.153
132
P PLM036 Pulmonary Fibrosis 65 0.153
133
c LKM061 Leukemia, Acute Myeloid 83 0.153
134
c CRB094 Cerebral Cavernous Malformations 3 41 0.153
135
P HRD008 Hereditary Hemorrhagic Telangiectasia 65 0.153
136
P MYL006 Myeloid Leukemia 60 0.153
137
P NRB001 Neuroblastoma 66 0.153
138
P BRT047 Brittle Cornea Syndrome 42 0.153
139
CHR178 Chromosomal Triplication 34 0.153
140
MLG079 Malignant Pleural Mesothelioma 42 0.153
141
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.153
142
c MNS008 Monosomy 21 24 0.153
143
P OVR082 Overgrowth Syndrome 42 0.153
Content
Loading form....