Search results for val

182 hits were found for val

# Family MCID Name MIFTS Score
1
P SCH015 Schizophrenia 71 0.176
2
P BRS047 Breast Cancer 100 0.121
3
P THL005 Thalassemia 61 0.113
4
THR024 Thrombosis 43 0.096
5
P LKM002 Leukemia 72 0.086
6
P BPL003 Bipolar Disorder 60 0.086
7
P PLY019 Polyneuropathy 54 0.086
8
P LVR013 Liver Disease 72 0.074
9
P HPT021 Hepatitis 68 0.074
10
P CRD011 Cardiomyopathy 67 0.074
11
VSC007 Vascular Disease 65 0.074
12
P HYP117 Hypertriglyceridemia 61 0.074
13
P HML002 Hemolytic Anemia 61 0.074
14
SYS004 Systemic Mastocytosis 60 0.074
15
BRN071 Brain Injury 50 0.074
16
P CLR023 Colorectal Cancer 95 0.060
17
P LNG032 Lung Cancer 94 0.060
18
P PRS040 Prostate Cancer 88 0.060
19
P MYC007 Myocardial Infarction 77 0.060
20
P HRT032 Heart Disease 75 0.060
21
P CRN211 Coronary Artery Disease 73 0.060
22
c HPT073 Hepatitis C Virus 70 0.060
23
CNG034 Congestive Heart Failure 70 0.060
24
KRT004 Keratitis 70 0.060
25
ATH003 Atherosclerosis 65 0.060
26
GLL008 Gilles De La Tourette Syndrome 63 0.060
27
c HPT001 Hepatitis C 62 0.060
28
P PRS038 Personality Disorder 61 0.060
29
ISC004 Ischemia 59 0.060
30
FCT003 Factor X Deficiency 59 0.060
31
ART021 Arteriosclerosis 57 0.060
32
P PLY018 Polycythemia 56 0.060
33
c HPT003 Hepatitis a 56 0.060
34
ART111 Artery Disease 55 0.060
35
PRS047 Prostatitis 55 0.060
36
P MNC007 Monocytic Leukemia 54 0.060
37
P LTR001 Lateral Sclerosis 53 0.060
38
ISC006 Ischemic Heart Disease 53 0.060
39
P DBT005 Diabetes Insipidus 52 0.060
40
TRM010 Traumatic Brain Injury 51 0.060
41
STR072 Stromal Keratitis 47 0.060
42
BRD004 Borderline Personality Disorder 45 0.060
43
P OBS005 Obesity 91 0.043
44
P PLM037 Pulmonary Hypertension 77 0.043
45
WLS001 Wilson Disease 73 0.043
46
P INF038 Influenza 71 0.043
47
P NRB001 Neuroblastoma 71 0.043
48
MLT021 Multiple System Atrophy 70 0.043
49
MLN008 Melanoma 70 0.043
50
SQM006 Squamous Cell Carcinoma 69 0.043
51
P OST005 Osteogenesis Imperfecta 68 0.043
52
PCK002 Pick Disease 68 0.043
53
ANX002 Anxiety Disorder 66 0.043
54
ATT013 Attention Deficit-Hyperactivity Disorder 66 0.043
55
c HYP595 Hypertension, Essential 66 0.043
56
P ATR011 Atrial Fibrillation 65 0.043
57
P KDN018 Kidney Disease 65 0.043
58
PRP027 Peripheral Vascular Disease 65 0.043
59
c CHR089 Chronic Kidney Failure 65 0.043
60
OBS002 Obsessive-Compulsive Disorder 64 0.043
61
GLN010 Glanzmann Thrombasthenia 64 0.043
62
P MYL006 Myeloid Leukemia 64 0.043
63
AND015 Androgen Insensitivity 63 0.043
64
P SPN046 Spinal Muscular Atrophy 63 0.043
65
VSC011 Vasculitis 62 0.043
66
PLM129 Pulmonary Disease, Chronic Obstructive 62 0.043
67
LNG099 Lung Disease 61 0.043
68
ATP002 Atopy 61 0.043
69
P DYS154 Dystonia 61 0.043
70
RSP006 Respiratory System Disease 60 0.043
71
HPY002 H. Pylori Infection 60 0.043
72
ACQ007 Acquired Immunodeficiency Syndrome 60 0.043
73
c ACT075 Acute Myocardial Infarction 59 0.043
74
LPP001 Lipoprotein Lipase Deficiency 59 0.043
75
FTT001 Fatty Liver Disease 59 0.043
76
P PNC025 Panic Disorder 58 0.043
77
P CHR285 Chronic Myelomonocytic Leukemia 58 0.043
78
WLL006 Wells Syndrome 58 0.043
79
PRP030 Purpura 57 0.043
80
P HYP060 Hyperinsulinism 57 0.043
81
P NRP001 Neuropathy 57 0.043
82
ADL002 Adult Syndrome 57 0.043
83
ART017 Aortic Disease 57 0.043
84
ETN001 Eating Disorder 56 0.043
85
ORL015 Oral Squamous Cell Carcinoma 55 0.043
86
EPD016 Epidermolysis Bullosa 55 0.043
87
P MTC069 Mitochondrial Disorders 55 0.043
88
HYP266 Hypoxia 55 0.043
89
PST028 Post-Traumatic Stress Disorder 55 0.043
90
P THY032 Thyroiditis 53 0.043
91
CND002 Conduct Disorder 53 0.043
92
PRP019 Peripheral Nervous System Disease 53 0.043
93
LMY002 Leiomyoma 53 0.043
94
P EPD003 Epidermolysis Bullosa Simplex 53 0.043
95
P ANG015 Angioedema 52 0.043
96
P SPS003 Spastic Diplegia 52 0.043
97
P ENC018 Encephalopathy 52 0.043
98
ALL026 Allergic Hypersensitivity Disease 52 0.043
99
P MSC033 Muscle Disorders 52 0.043
100
MVM001 Movement Disease 52 0.043
101
CYT008 Cytomegalovirus Infection 51 0.043
102
HMG005 Hemoglobinopathy 51 0.043
103
INT007 Intermediate Coronary Syndrome 50 0.043
104
P LCT001 Lactic Acidosis 50 0.043
105
PRT058 Pure Autonomic Failure 50 0.043
106
TRD006 Tardive Dyskinesia 50 0.043
107
ANG054 Angina Pectoris 49 0.043
108
P MSC003 Muscular Atrophy 49 0.043
109
URN009 Urinary System Disease 49 0.043
110
PRM028 Paramyotonia Congenita 49 0.043
111
OPT003 Opiate Dependence 49 0.043
112
VND001 Vein Disease 49 0.043
113
CRN030 Coronary Stenosis 49 0.043
114
ALP007 Alpha 1-Antitrypsin Deficiency 48 0.043
115
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 48 0.043
116
ATN002 Autonomic Nervous System Disease 48 0.043
117
DBT004 Diabetic Polyneuropathy 47 0.043
118
CRN017 Coronary Thrombosis 47 0.043
119
P DYS026 Dysfibrinogenemia 47 0.043
120
LKC003 Leukocyte Disease 46 0.043
121
BLD053 Blood Platelet Disease 46 0.043
122
GDS001 Good Syndrome 46 0.043
123
c BPL002 Bipolar I Disorder 46 0.043
124
P DYS021 Dysautonomia 45 0.043
125
P CRV039 Cervicitis 45 0.043
126
ATN005 Autonomic Dysfunction 45 0.043
127
CMP034 Complete Androgen Insensitivity Syndrome 44 0.043
128
GLC008 Glucose Metabolism Disease 44 0.043
129
BSL008 Basal Ganglia Disease 44 0.043
130
HRT015 Heritable Pulmonary Arterial Hypertension 44 0.043
131
ANX004 Anoxia 44 0.043
132
SYS003 Systolic Heart Failure 43 0.043
133
P BLD051 Blood Coagulation Disease 43 0.043
134
c CHR095 Chronic Progressive External Ophthalmoplegia 43 0.043
135
P HYP729 Hypersensitivity Reaction Disease 43 0.043
136
PHY002 Physical Disorder 43 0.043
137
CRV043 Cervical Dystonia 43 0.043
138
CRB008 Cerebral Atherosclerosis 43 0.043
139
RNL097 Renal Artery Disease 42 0.043
140
END072 Endotheliitis 41 0.043
141
THR035 Thrombasthenia 41 0.043
142
VSC018 Visceral Steatosis 41 0.043
143
CHR413 Chronic Myocardial Ischemia 41 0.043
144
P ABD016 Abdominal Obesity-Metabolic Syndrome 41 0.043
145
P PRP034 Purpura Fulminans 40 0.043
146
THL017 Thalassemia Intermedia 40 0.043
147
c CHR096 Chronic Pulmonary Heart Disease 40 0.043
148
HRN003 Heroin Dependence 39 0.043
149
BLD054 Blood Protein Disease 39 0.043
150
c INH004 Inherited Blood Coagulation Disease 39 0.043
151
CRB009 Cerebritis 39 0.043
152
ACT088 Acute Insulin Response 38 0.043
153
MTC005 Mitochondrial Metabolism Disease 38 0.043
154
MSC004 Muscle Tissue Disease 37 0.043
155
IMP003 Impaired Renal Function Disease 36 0.043
156
c ABD013 Abdominal Obesity-Metabolic Syndrome 3 36 0.043
157
P MYG005 Myoglobinuria 34 0.043
158
FML330 Familial Lcat Deficiency 34 0.043
159
CKS001 Ck Syndrome 32 0.043
160
P FTT008 Fatty Liver Disease, Nonalcoholic 1 31 0.043
161
VTM003 Vitamin Metabolic Disorder 31 0.043
162
NTM001 Nutmeg Liver 31 0.043
163
TYP015 Type 2b Von Willebrand Disease 30 0.043
164
c PLM128 Pulmonary Hypertension, Primary, 2 30 0.043
165
c PLM121 Pulmonary Hypertension, Primary, 4 29 0.043
166
YNG002 Young Syndrome 29 0.043
167
DFC001 Defective Apolipoprotein B-100 29 0.043
168
c MYC058 Myocardial Infarction 2 28 0.043
169
NLL002 Null Syndrome 26 0.043
170
SPN031 Supine Hypotensive Syndrome 24 0.043
171
P CRN178 Coronary Heart Disease 6 22 0.043
172
c CRN214 Coronary Heart Disease 5 22 0.043
173
c CRN174 Coronary Heart Disease 2 21 0.043
174
c CRN172 Coronary Heart Disease 3 20 0.043
175
c CRN175 Coronary Heart Disease 4 20 0.043
176
c FTT007 Fatty Liver Disease, Nonalcoholic 2 19 0.043
177
c CRN173 Coronary Heart Disease 8 19 0.043
178
WSC001 Wisconsin Syndrome 18 0.043
179
c DLT012 Delta-Thalassemia 16 0.043
180
SGM003 Segmentation Syndrome 1 14 0.043
181
HRD059 Hereditary Peripheral Nervous Disorder 13 0.043
182
HYP159 Hyperinsulinism, Focal 11 0.043
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