Search results for val

160 hits were found for val

# Family MCID Name MIFTS Score
1
P SCH015 Schizophrenia 69 0.194
2
P THL005 Thalassemia 64 0.141
3
P BRS047 Breast Cancer 100 0.109
4
P ALZ034 Alzheimer Disease 87 0.109
5
DPR016 Depression 72 0.100
6
ANX010 Anxiety 72 0.100
7
THR024 Thrombosis 61 0.100
8
VNW001 Von Willebrand's Disease 60 0.100
9
P BPL003 Bipolar Disorder 59 0.100
10
P LKM002 Leukemia 72 0.089
11
c BTT014 Beta-Thalassemia 69 0.089
12
c THR092 Thrombophilia Due to Thrombin Defect 67 0.089
13
P PLY019 Polyneuropathy 57 0.089
14
P HPT021 Hepatitis 76 0.077
15
P LVR013 Liver Disease 75 0.077
16
VSC007 Vascular Disease 68 0.077
17
SYS004 Systemic Mastocytosis 65 0.077
18
c CRN300 Coronary Heart Disease 1 64 0.077
19
AGN016 Aging 64 0.077
20
P HML002 Hemolytic Anemia 62 0.077
21
c ALP101 Alpha-Thalassemia 59 0.077
22
OCL033 Oculocerebral Syndrome with Hypopigmentation 45 0.077
23
P LNG032 Lung Cancer 98 0.063
24
P CLR023 Colorectal Cancer 97 0.063
25
P PRS040 Prostate Cancer 90 0.063
26
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.063
27
P MYC007 Myocardial Infarction 79 0.063
28
P MLT020 Multiple Sclerosis 78 0.063
29
P HRT032 Heart Disease 74 0.063
30
ISC006 Ischemic Heart Disease 72 0.063
31
CNG034 Congestive Heart Failure 72 0.063
32
c HPT073 Hepatitis C Virus 72 0.063
33
c HPT001 Hepatitis C 71 0.063
34
P CRN018 Coronary Artery Anomaly 68 0.063
35
ART140 Arteries, Anomalies of 65 0.063
36
ISC004 Ischemia 65 0.063
37
P HYP061 Hypertrophic Cardiomyopathy 64 0.063
38
P DBT009 Diabetes Mellitus 64 0.063
39
P PRS038 Personality Disorder 64 0.063
40
GLL008 Gilles De La Tourette Syndrome 63 0.063
41
ALP103 Alpha-1-Antitrypsin Deficiency 61 0.063
42
c HPT003 Hepatitis a 61 0.063
43
ANR040 Aneurysm 60 0.063
44
DBT087 Diabetes Insipidus, Neurohypophyseal 60 0.063
45
P ART021 Arteriosclerosis 60 0.063
46
PRS047 Prostatitis 60 0.063
47
P LTR001 Lateral Sclerosis 58 0.063
48
P PLY018 Polycythemia 58 0.063
49
P MNC007 Monocytic Leukemia 57 0.063
50
FCT003 Factor X Deficiency 57 0.063
51
TYP041 Type I 56 0.063
52
TRM010 Traumatic Brain Injury 55 0.063
53
P DBT005 Diabetes Insipidus 54 0.063
54
BRN071 Brain Injury 53 0.063
55
STR072 Stromal Keratitis 50 0.063
56
BRD004 Borderline Personality Disorder 49 0.063
57
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.045
58
STR067 Stroke, Ischemic 82 0.045
59
c LKM061 Leukemia, Acute Myeloid 80 0.045
60
GST053 Gastric Cancer 77 0.045
61
c HYP595 Hypertension, Essential 76 0.045
62
P INF038 Influenza 76 0.045
63
P PLM037 Pulmonary Hypertension 75 0.045
64
MLT157 Multiple System Atrophy 1 73 0.045
65
P NRB001 Neuroblastoma 72 0.045
66
c CHR089 Chronic Kidney Failure 72 0.045
67
PLM129 Pulmonary Disease, Chronic Obstructive 72 0.045
68
WLS001 Wilson Disease 71 0.045
69
BRT054 Brittle Bone Disorder 69 0.045
70
P ATR011 Atrial Fibrillation 68 0.045
71
c SML038 Small Cell Cancer of the Lung 68 0.045
72
P KDN018 Kidney Disease 68 0.045
73
P MYL006 Myeloid Leukemia 68 0.045
74
LNG099 Lung Disease 67 0.045
75
ANG054 Angina Pectoris 66 0.045
76
c PLM164 Pulmonary Hypertension, Primary, 1 66 0.045
77
OBS002 Obsessive-Compulsive Disorder 66 0.045
78
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.045
79
CRT072 Creutzfeldt-Jakob Disease 65 0.045
80
VSC011 Vasculitis 65 0.045
81
GLN010 Glanzmann Thrombasthenia 65 0.045
82
P DYS154 Dystonia 64 0.045
83
SND001 Sandhoff Disease 64 0.045
84
P SPN046 Spinal Muscular Atrophy 63 0.045
85
ACQ007 Acquired Immunodeficiency Syndrome 63 0.045
86
c MCP049 Mucopolysaccharidosis, Type Vii 63 0.045
87
P NRP001 Neuropathy 63 0.045
88
RSP006 Respiratory System Disease 63 0.045
89
P ENC018 Encephalopathy 62 0.045
90
MLN008 Melanoma 62 0.045
91
P CHR285 Chronic Myelomonocytic Leukemia 62 0.045
92
ETN001 Eating Disorder 61 0.045
93
PRP030 Purpura 61 0.045
94
HYP266 Hypoxia 61 0.045
95
TBC004 Tobacco Addiction 60 0.045
96
FTT001 Fatty Liver Disease 60 0.045
97
MVM001 Movement Disease 60 0.045
98
PRP019 Peripheral Nervous System Disease 60 0.045
99
PRT058 Pure Autonomic Failure 59 0.045
100
TRD006 Tardive Dyskinesia 59 0.045
101
SQM006 Squamous Cell Carcinoma 59 0.045
102
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 59 0.045
103
PST028 Post-Traumatic Stress Disorder 58 0.045
104
c ACT075 Acute Myocardial Infarction 58 0.045
105
FBR047 Fibromyalgia 57 0.045
106
LMY002 Leiomyoma 57 0.045
107
P ANG015 Angioedema 57 0.045
108
EPD016 Epidermolysis Bullosa 56 0.045
109
HYP060 Hyperinsulinism 56 0.045
110
CYT008 Cytomegalovirus Infection 56 0.045
111
AND002 Androgen Insensitivity Syndrome 56 0.045
112
HYP052 Hyperkalemic Periodic Paralysis 55 0.045
113
URN009 Urinary System Disease 55 0.045
114
P PNC025 Panic Disorder 55 0.045
115
P THY032 Thyroiditis 55 0.045
116
P MSC003 Muscular Atrophy 54 0.045
117
SPS003 Spastic Diplegia 54 0.045
118
OPT003 Opiate Dependence 54 0.045
119
CND002 Conduct Disorder 54 0.045
120
LMY014 Leiomyoma, Uterine 53 0.045
121
HMG005 Hemoglobinopathy 53 0.045
122
GLC008 Glucose Metabolism Disease 52 0.045
123
INT007 Intermediate Coronary Syndrome 52 0.045
124
P EPD003 Epidermolysis Bullosa Simplex 51 0.045
125
ATN002 Autonomic Nervous System Disease 51 0.045
126
P NNL004 Nonalcoholic Fatty Liver Disease 51 0.045
127
DBT004 Diabetic Polyneuropathy 51 0.045
128
P LCT001 Lactic Acidosis 50 0.045
129
P DYS026 Dysfibrinogenemia 50 0.045
130
ATN005 Autonomic Dysfunction 50 0.045
131
P CRV039 Cervicitis 49 0.045
132
ANX004 Anoxia 49 0.045
133
c BPL002 Bipolar I Disorder 49 0.045
134
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 48 0.045
135
HRT015 Heritable Pulmonary Arterial Hypertension 48 0.045
136
CMP034 Complete Androgen Insensitivity Syndrome 47 0.045
137
c MTR002 Mitral Valve Insufficiency 46 0.045
138
SYS003 Systolic Heart Failure 46 0.045
139
BSL008 Basal Ganglia Disease 46 0.045
140
THR035 Thrombasthenia 45 0.045
141
P PRP034 Purpura Fulminans 45 0.045
142
END072 Endotheliitis 45 0.045
143
ORL015 Oral Squamous Cell Carcinoma 45 0.045
144
P DYS021 Dysautonomia 43 0.045
145
c CHR095 Chronic Progressive External Ophthalmoplegia 43 0.045
146
CRV043 Cervical Dystonia 41 0.045
147
FML330 Familial Lcat Deficiency 41 0.045
148
CRB009 Cerebritis 41 0.045
149
PRG039 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 40 0.045
150
HRN003 Heroin Dependence 40 0.045
151
c FTT008 Fatty Liver Disease, Nonalcoholic 1 39 0.045
152
KR002 Kuru 38 0.045
153
P MYG005 Myoglobinuria 37 0.045
154
P VSC018 Visceral Steatosis 37 0.045
155
PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 36 0.045
156
PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 36 0.045
157
P SMK004 Smoking As a Quantitative Trait Locus 3 36 0.045
158
PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 36 0.045
159
DFC001 Defective Apolipoprotein B-100 31 0.045
160
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 29 0.045
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