Search results for tjp1

165 hits were found for tjp1

# Family MCID Name MIFTS Score
1
P CLR023 Colorectal Cancer 100 18.311
2
MLR004 Malaria 78 13.728
3
CLT003 Colitis 63 12.191
4
P INF037 Inflammatory Bowel Disease 53 12.151
5
P ENC004 Encephalitis 61 12.103
6
P CLC063 Celiac Disease 1 66 10.046
8
BRN004 Brain Edema 54 9.858
9
P PRK057 Parkinson Disease, Late-Onset 79 9.707
10
P CRN276 Corneal Endothelial Dystrophy 52 9.707
11
HMN044 Human Immunodeficiency Virus Type 1 76 9.707
12
c WLM013 Wilms Tumor 1 65 9.707
13
P DMY001 Demyelinating Polyneuropathy 41 9.707
14
P CRN025 Corneal Dystrophy 49 9.707
15
NVS001 Neovascular Glaucoma 52 9.707
16
P INT143 Interstitial Cystitis 59 9.707
17
P CYS018 Cystitis 59 9.707
18
P OBS001 Obstructive Jaundice 49 9.707
19
P BRS044 Breast Adenocarcinoma 58 9.707
20
P CTR002 Cataract 59 9.707
21
P RTN008 Retinitis Pigmentosa 79 6.864
22
DRR013 Diarrhea 8, Secretory Sodium, Congenital 35 6.864
23
LBR036 Leber Plus Disease 67 6.864
24
P CRN024 Corneal Disease 43 6.864
25
ATM015 Autoimmune Disease of Gastrointestinal Tract 27 6.864
26
c SPS215 Spastic Paraplegia 3, Autosomal Dominant 62 6.864
27
P CRN026 Corneal Edema 42 6.864
28
DSS008 Disease of Mental Health 74 6.864
29
c HRD010 Hereditary Spastic Paraplegia 65 6.864
30
SNL004 Senile Ectropion 28 6.864
31
FCH001 Fuchs' Endothelial Dystrophy 48 6.864
32
MCL006 Macular Retinal Edema 56 6.864
33
INT010 Intracranial Embolism 48 6.864
34
ACN004 Acantholytic Acanthoma 28 6.864
35
FND002 Fundus Dystrophy 55 6.864
36
ACT060 Acute Vascular Insufficiency of Intestine 27 6.864
37
PRN019 Perinatal Necrotizing Enterocolitis 60 6.864
38
VTR005 Vitreous Disease 40 6.864
39
c ATR087 Atrial Standstill 1 74 1.858
40
MYL069 Myeloma, Multiple 77 1.468
41
P LMY004 Leiomyosarcoma 62 1.328
42
SFT003 Soft Tissue Sarcoma 57 1.328
43
PRT251 Proteinuria, Chronic Benign 58 1.254
44
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 1.254
45
c DLT002 Dilated Cardiomyopathy 79 1.254
46
P HPT023 Hepatocellular Carcinoma 95 1.217
47
P GST053 Gastric Cancer 82 1.128
48
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 1.107
49
P ANG001 Angelman Syndrome 65 1.088
50
MLG077 Malignant Peripheral Nerve Sheath Tumor 54 1.040
51
P NRF002 Neurofibromatosis 60 1.040
52
P RRT020 Rare Tumor 39 1.040
53
IRN008 Iron Overload in Africa 51 0.955
54
RJS001 Ruijs-Aalfs Syndrome 47 0.955
55
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.955
56
HPT079 Hepatoid Adenocarcinoma 39 0.955
57
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 57 0.955
58
c HPT073 Hepatitis C Virus 71 0.955
59
ADL096 Adult Hepatocellular Carcinoma 60 0.955
60
PDT042 Pediatric Hepatocellular Carcinoma 50 0.955
61
PTY007 Pityriasis Rotunda 26 0.955
62
FBR086 Fibrolamellar Carcinoma 59 0.955
63
HPT011 Hepatocellular Clear Cell Carcinoma 45 0.955
64
P BRS047 Breast Cancer 97 0.896
65
P OVR042 Ovarian Cancer 88 0.888
66
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.872
67
P MDL005 Medulloblastoma 75 0.872
68
RHB011 Rhabdoid Tumor Predisposition Syndrome 2 28 0.872
69
LNG019 Lung Combined Type Small Cell Carcinoma 32 0.872
70
P LNG021 Lung Occult Small Cell Carcinoma 20 0.872
71
P SCH015 Schizophrenia 74 0.517
72
CHR662 Chromosome 15q13.3 Deletion Syndrome 37 0.517
73
P ATS364 Autism 72 0.517
74
P PNC035 Pancreatic Cancer 86 0.517
75
P BLD134 Bladder Cancer 79 0.428
76
ATR057 Atrioventricular Block 54 0.428
77
c MCR133 Microvascular Complications of Diabetes 4 41 0.371
78
c MCR113 Microvascular Complications of Diabetes 3 52 0.371
79
c MCR130 Microvascular Complications of Diabetes 6 41 0.371
80
c MCR120 Microvascular Complications of Diabetes 7 47 0.371
81
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.339
82
P MLN007 Male Infertility 56 0.339
83
CCC002 Coccidiosis 50 0.339
84
ULC004 Ulcerative Colitis 74 0.339
85
IRR002 Irritable Bowel Syndrome 65 0.339
86
c TYP008 Type 1 Diabetes Mellitus 77 0.303
87
ISC004 Ischemia 61 0.303
88
P DBT009 Diabetes Mellitus 67 0.303
89
c EPL200 Epilepsy, Childhood Absence 1 30 0.262
90
P SHR001 Short Bowel Syndrome 53 0.262
91
P LNG064 Lung Cancer Susceptibility 3 70 0.262
92
P DRR001 Diarrhea 55 0.262
93
c NPH055 Nephrotic Syndrome, Type 1 52 0.262
94
c ALB021 Albinism, Oculocutaneous, Type Ii 58 0.214
95
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.214
96
c EXS019 Exostoses, Multiple, Type I 54 0.214
97
c EXS020 Exostoses, Multiple, Type Ii 38 0.214
98
c SML038 Small Cell Cancer of the Lung 69 0.214
99
P CRB048 Cerebral Cavernous Malformations 63 0.214
100
c NGH027 Night Blindness, Congenital Stationary, Type 1c 36 0.214
101
P CNG010 Congenital Stationary Night Blindness 56 0.214
102
URT010 Ureteral Obstruction 45 0.214
103
ORC001 Orchitis 44 0.214
104
LNG039 Lung Squamous Cell Carcinoma 57 0.214
105
ART002 Arts Syndrome 66 0.214
106
P PTN014 Patent Ductus Arteriosus 1 59 0.214
107
CYT002 Cytokine Deficiency 43 0.214
108
CRH001 Crohn's Disease 80 0.214
109
P NGH001 Night Blindness 52 0.214
110
P PRS040 Prostate Cancer 95 0.151
111
HLC007 Helicobacter Pylori Infection 67 0.151
112
c NPH049 Nephrotic Syndrome, Type 2 52 0.151
113
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.151
114
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 0.151
115
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.151
116
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.151
117
TBL029 Tubulin, Beta 28 0.151
118
WST005 West Nile Virus 55 0.151
119
P END046 Endometritis 46 0.151
120
c PRC016 Pre-Eclampsia 64 0.151
121
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.151
122
CRB004 Cerebral Artery Occlusion 46 0.151
123
PLY150 Polykaryocytosis Inducer 29 0.151
124
P MLN069 Melanoma, Uveal 59 0.151
125
MCR191 Microscopic Colitis 46 0.151
126
CLL021 Collagenous Colitis 41 0.151
127
LYM042 Lymphocytic Colitis 40 0.151
128
PLL012 Pollen Allergy 44 0.151
129
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.151
130
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.151
131
P ESP035 Esophagitis, Eosinophilic, 1 57 0.151
132
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.151
133
ALL003 Allergic Rhinitis 66 0.151
134
P MJR001 Major Depressive Disorder 68 0.151
135
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.151
136
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.151
137
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.151
138
c CHL143 Cholestasis, Progressive Familial Intrahepatic, 4 40 0.151
139
SNT005 Sinoatrial Node Disease 47 0.151
140
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.151
141
P SCK002 Sick Sinus Syndrome 55 0.151
142
CHL068 Cholestasis 61 0.151
143
CRB039 Cerebrovascular Disease 65 0.151
144
THY020 Thyroid Hyalinizing Trabecular Adenoma 19 0.151
145
P INF032 Infertility 60 0.151
146
c INF023 Inflammatory Breast Carcinoma 48 0.151
147
P MLN008 Melanoma 75 0.151
148
MNT002 Mental Depression 56 0.151
149
AZS001 Azoospermia 45 0.151
150
P ESP024 Esophagitis 60 0.151
151
KHN001 Kuhnt-Junius Degeneration 48 0.151
152
P NPH012 Nephrotic Syndrome 62 0.151
153
P RHN004 Rhinitis 57 0.151
154
c FML015 Familial Nephrotic Syndrome 47 0.151
155
c CRB191 Cerebral Cavernous Malformations 2 45 0.151
156
OST159 Osteogenic Sarcoma 66 0.151
157
DPR016 Depression 65 0.151
158
P INS002 in Situ Carcinoma 53 0.151
159
P SLW003 Slow-Channel Congenital Myasthenic Syndrome 35 0.151
160
HYP266 Hypoxia 56 0.151
161
P INF038 Influenza 68 0.151
162
P BCL017 B-Cell Lymphoma 57 0.151
163
P MYT002 Myotonic Dystrophy 51 0.151
164
P FML355 Familial Intrahepatic Cholestasis 42 0.151
165
P VTR007 Vitreoretinopathy 45 0.151
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