Search results for ephb4

222 hits were found for ephb4

# Family MCID Name MIFTS Score
1
CPL015 Capillary Malformation-Arteriovenous Malformation 2 29 47.075
2
c LYM150 Lymphatic Malformation 7 43 37.689
4
P BRS047 Breast Cancer 97 22.252
5
P CLR023 Colorectal Cancer 100 22.201
6
END057 Endometrial Cancer 71 19.815
7
P OVR042 Ovarian Cancer 88 19.482
8
P ART005 Arteriovenous Malformation 65 18.470
9
P TTR001 Tetralogy of Fallot 69 16.881
10
SQM013 Squamous Cell Carcinoma, Head and Neck 75 13.569
11
P CPL014 Capillary Malformation-Arteriovenous Malformation 1 53 12.846
12
P HRD008 Hereditary Hemorrhagic Telangiectasia 65 12.179
13
P MCR129 Microvascular Complications of Diabetes 1 68 10.967
14
HNN001 Hennekam Syndrome 52 8.420
15
WBR001 Weber Syndrome 38 7.781
16
PRK003 Parkes Weber Syndrome 41 7.781
17
CRD007 Cardiovascular Organ Benign Neoplasm 25 7.583
18
BRN011 Brain Stem Astrocytic Neoplasm 20 7.583
19
SKN001 Skin Angiosarcoma 30 7.583
20
LVR003 Liver Carcinoma in Situ 19 7.583
21
P GST053 Gastric Cancer 82 4.281
22
P PRS040 Prostate Cancer 95 3.227
23
P HPT023 Hepatocellular Carcinoma 95 3.024
24
P MLN008 Melanoma 75 2.596
25
GLM045 Glioma 62 2.550
26
GLL048 Glial Tumor 52 2.550
27
P LNG064 Lung Cancer Susceptibility 3 70 2.512
28
P LNG032 Lung Cancer 98 2.441
29
BNR002 Bone Resorption Disease 47 2.437
30
c LKM063 Leukemia, Chronic Myeloid 71 2.427
31
c PRC016 Pre-Eclampsia 64 2.359
32
P MYL006 Myeloid Leukemia 60 2.271
33
P BNG032 Benign Mesothelioma 53 2.240
34
HYD038 Hydrops Fetalis, Nonimmune 57 2.239
35
P ADN016 Adenocarcinoma 63 2.229
36
P PNC035 Pancreatic Cancer 86 2.151
37
SQM006 Squamous Cell Carcinoma 59 2.150
38
HYP266 Hypoxia 56 2.009
39
ESP021 Esophageal Cancer 84 1.973
40
IMM039 Immune Hydrops Fetalis 33 1.878
41
GLB002 Glioblastoma 67 1.830
42
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.803
43
c THY109 Thyroid Cancer, Nonmedullary, 1 55 1.564
44
THY029 Thyroid Carcinoma 54 1.564
45
INS024 Insulin-Like Growth Factor I 77 1.535
46
c SML038 Small Cell Cancer of the Lung 69 1.520
47
P FBR017 Fibrosarcoma 55 1.520
48
P LKM062 Leukemia, Acute Lymphoblastic 69 1.489
49
SFT003 Soft Tissue Sarcoma 57 1.489
50
P BND020 Bone Disease 60 1.472
51
P RHB003 Rhabdomyosarcoma 66 1.472
52
TLN003 Telangiectasis 51 1.438
53
RTR008 Root Resorption 44 1.343
54
c MST023 Mesothelioma, Malignant 56 1.321
55
P PRD008 Periodontitis 64 1.274
56
P LKM002 Leukemia 66 1.247
57
SRC014 Sarcoma 64 1.232
58
SPN035 Spindle Cell Sarcoma 51 1.232
59
PLM173 Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and 46,xx Sex Reversal 34 1.203
60
SKN022 Skin Squamous Cell Carcinoma 54 1.203
61
GST040 Gastric Adenocarcinoma 66 1.203
62
PSD011 Pseudovascular Skin Squamous Cell Carcinoma 16 1.203
63
BRR014 Barrett Esophagus 66 1.199
64
ISC004 Ischemia 61 1.199
65
P END044 Endometriosis 62 1.181
66
MLG079 Malignant Pleural Mesothelioma 42 1.163
67
END062 Endometrial Hyperplasia 48 1.145
68
SVR004 Severe Combined Immunodeficiency 71 1.126
69
c LKM061 Leukemia, Acute Myeloid 83 1.106
70
P BLD134 Bladder Cancer 79 1.085
71
P CRB048 Cerebral Cavernous Malformations 63 1.085
72
SRC027 Sarcoma, Synovial 58 1.085
73
P LPS002 Liposarcoma 64 1.085
74
48X005 48,xyyy 39 1.085
75
OST012 Osteoarthritis 77 1.085
76
P NRB001 Neuroblastoma 66 1.064
77
ART141 Arteriovenous Malformations of the Brain 58 1.041
78
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 1.041
79
c PCH010 Pachyonychia Congenita 3 43 1.041
80
CRB039 Cerebrovascular Disease 65 1.041
81
P VTR007 Vitreoretinopathy 45 1.041
82
RPD005 Rapidly Involuting Congenital Hemangioma 48 1.017
83
CHL152 Childhood Acute Lymphocytic Leukemia 50 1.017
84
LMB062 Limb Ischemia 55 1.017
85
THR100 Thrombocytopenic Purpura, Autoimmune 60 1.017
86
TRN018 Transitional Cell Carcinoma 56 1.017
87
BLD131 Bladder Urothelial Carcinoma 59 1.017
88
c CRB094 Cerebral Cavernous Malformations 3 41 1.017
89
PRP030 Purpura 54 1.017
90
P INS002 in Situ Carcinoma 53 1.017
91
CVR010 Cavernous Malformation 29 1.017
92
P PLM037 Pulmonary Hypertension 69 0.991
93
CRB004 Cerebral Artery Occlusion 46 0.991
94
P OST002 Osteoporosis 77 0.991
95
P FML011 Familial Adenomatous Polyposis 71 0.991
96
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.991
97
INT051 Intussusception 53 0.991
98
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.991
99
P GLM040 Glioma Susceptibility 1 70 0.991
100
MLG169 Malignant Astrocytoma 57 0.991
101
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 0.991
102
HRT011 Heart Septal Defect 49 0.977
103
RHB024 Rhabdomyosarcoma 2 65 0.964
104
PPL002 Papillary Carcinoma 46 0.964
105
LYM116 Lymph Node Disease 42 0.964
106
CRT069 Cortical Malformations, Occipital 31 0.934
107
c DPH024 Diaphragmatic Hernia, Congenital 64 0.934
108
c DLT002 Dilated Cardiomyopathy 79 0.934
109
P TMR010 Tumor Predisposition Syndrome 69 0.932
110
ADN011 Adenoid Cystic Carcinoma 68 0.932
111
BLD173 Bladder Small Cell Carcinoma 44 0.932
112
MLN065 Melanocytic Nevus Syndrome, Congenital 61 0.932
113
ADN089 Adenosquamous Lung Carcinoma 49 0.932
114
LNG039 Lung Squamous Cell Carcinoma 57 0.932
115
BRN015 Bronchiolo-Alveolar Adenocarcinoma 55 0.932
116
c ATS007 Autism Spectrum Disorder 72 0.901
117
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.901
118
PRV004 Periventricular Leukomalacia 52 0.901
119
c SPR009 Sporadic Breast Cancer 42 0.901
120
GLM044 Glomerular Disease 34 0.901
121
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.863
122
P HNN005 Hennekam Lymphangiectasia-Lymphedema Syndrome 1 40 0.837
123
P KRB001 Krabbe Disease 69 0.837
124
P ATR010 Atrial Heart Septal Defect 58 0.837
125
INT276 Interatrial Communication 50 0.837
126
LMN016 Luminal Breast Carcinoma B 28 0.761
127
P LMN015 Luminal Breast Carcinoma a 34 0.761
128
GST103 Gastric Cancer, Hereditary Diffuse 68 0.761
129
SML009 Small Intestine Adenocarcinoma 57 0.761
130
THY124 Thyroid Gland Papillary Carcinoma 38 0.761
131
SKN019 Skin Melanoma 70 0.761
132
PYG006 Pyogenic Granuloma 36 0.621
133
IRN008 Iron Overload in Africa 51 0.538
134
RJS001 Ruijs-Aalfs Syndrome 47 0.538
135
P LRG012 Large Congenital Melanocytic Nevus 47 0.538
136
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.538
137
HPT079 Hepatoid Adenocarcinoma 39 0.538
138
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 57 0.538
139
c HPT073 Hepatitis C Virus 71 0.538
140
ADL096 Adult Hepatocellular Carcinoma 60 0.538
141
END002 Endometrioid Ovary Carcinoma 52 0.538
142
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 0.538
143
PDT042 Pediatric Hepatocellular Carcinoma 50 0.538
144
PTY007 Pityriasis Rotunda 26 0.538
145
FBR086 Fibrolamellar Carcinoma 59 0.538
146
HPT011 Hepatocellular Clear Cell Carcinoma 45 0.538
147
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.492
148
GST092 Gastroesophageal Reflux 60 0.397
149
P FLL037 Follicular Lymphoma 73 0.397
150
KPS004 Kaposi Sarcoma 76 0.371
151
ADN027 Adenomyosis 59 0.343
153
END041 Endometrial Adenocarcinoma 63 0.343
154
RTN020 Retinal Vascular Disease 45 0.343
155
OST159 Osteogenic Sarcoma 66 0.343
156
CYT002 Cytokine Deficiency 43 0.343
157
ORL015 Oral Squamous Cell Carcinoma 43 0.313
158
HMN009 Hemangioblastoma 53 0.313
159
MMM001 Mammary Paget's Disease 53 0.313
160
MSL001 Measles 61 0.313
161
P ALZ034 Alzheimer Disease 87 0.280
162
c MCR115 Microvascular Complications of Diabetes 5 65 0.280
163
ATH013 Atherosclerosis Susceptibility 63 0.280
164
CNG034 Congestive Heart Failure 69 0.280
165
CRN027 Corneal Neovascularization 47 0.280
166
ARG004 Argyria 26 0.280
167
HMC014 Homocysteinemia 52 0.243
168
c MCR112 Microvascular Complications of Diabetes 2 42 0.243
169
P MDL005 Medulloblastoma 75 0.243
170
c EXD008 Exudative Vitreoretinopathy 1 71 0.243
171
c SCL052 Scleroderma, Familial Progressive 60 0.243
172
HGH043 High Grade Glioma 46 0.243
173
P GST044 Gastritis 55 0.243
174
P SML001 Small Cell Carcinoma 52 0.198
175
PRT013 Portal Hypertension 59 0.198
176
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.198
177
P HMN036 Hemangiopericytoma, Malignant 57 0.198
178
P MYC007 Myocardial Infarction 69 0.198
179
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.198
180
CHL065 Cholangiocarcinoma 58 0.198
181
c HRD202 Hereditary Lymphedema I 55 0.198
182
INT079 Intrahepatic Cholangiocarcinoma 51 0.198
183
P VNT002 Ventricular Septal Defect 58 0.198
184
P HRT032 Heart Disease 84 0.198
185
P PLM036 Pulmonary Fibrosis 65 0.198
186
HYP066 Hyperglycemia 60 0.198
187
c TLN011 Telangiectasia, Hereditary Hemorrhagic, Type 2 45 0.198
188
OVR094 Ovarian Epithelial Cancer 39 0.198
189
NDL013 Nodular Regenerative Hyperplasia 46 0.198
190
P SCH015 Schizophrenia 74 0.140
191
CRN005 Craniofrontonasal Syndrome 57 0.140
192
NRR002 Norrie Disease 60 0.140
193
MYL069 Myeloma, Multiple 77 0.140
194
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.140
195
c HMP013 Hemophagocytic Lymphohistiocytosis, Familial, 3 47 0.140
196
MYL009 Myelodysplastic Syndrome 67 0.140
197
ACT119 Acute Promyelocytic Leukemia 62 0.140
198
P INF037 Inflammatory Bowel Disease 53 0.140
199
DDN010 Duodenum Cancer 52 0.140
200
ANG020 Angiosarcoma 63 0.140
201
KLP010 Klippel-Trenaunay-Weber Syndrome 59 0.140
202
CLF027 Cleft Palate, Isolated 64 0.140
203
c HMP023 Hemophagocytic Lymphohistiocytosis, Familial, 5 42 0.140
204
c TLN006 Telangiectasia, Hereditary Hemorrhagic, Type 1 56 0.140
205
P CPL006 Capillary Hemangioma 53 0.140
206
PLC001 Placenta Accreta 44 0.140
207
HDR003 Hidradenitis 50 0.140
208
P VSC007 Vascular Disease 62 0.140
209
P HMN010 Hemangioma 61 0.140
210
P RTN022 Retinal Vein Occlusion 54 0.140
211
PRM236 Primary Biliary Cholangitis 62 0.140
212
CLN015 Colon Adenocarcinoma 64 0.140
213
HDR002 Hidradenitis Suppurativa 54 0.140
214
OST032 Osteofibrous Dysplasia 52 0.140
215
STR067 Stroke, Ischemic 79 0.140
216
HYP082 Hypopharynx Cancer 47 0.140
217
HND011 Hendra Virus Infection 11 0.140
218
LNG099 Lung Disease 62 0.140
219
CRH001 Crohn's Disease 80 0.140
220
P LPS004 Lupus Erythematosus 61 0.140
221
ULC004 Ulcerative Colitis 74 0.140
222
CCN002 Cocaine Abuse 49 0.140
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