Search results for val

229 hits were found for val

# Family MCID Name MIFTS Score
1
P SCH015 Schizophrenia 77 0.162
2
P BRS047 Breast Cancer 100 0.111
3
P THL005 Thalassemia 64 0.104
4
THR024 Thrombosis 57 0.088
5
P LKM002 Leukemia 71 0.079
6
P BPL003 Bipolar Disorder 62 0.079
7
P PLY019 Polyneuropathy 56 0.079
8
P CRD011 Cardiomyopathy 68 0.068
9
P HML002 Hemolytic Anemia 62 0.068
10
P HYP117 Hypertriglyceridemia 61 0.068
11
c SYS004 Systemic Mastocytosis 60 0.068
12
P MST009 Mastocytosis 56 0.068
13
BRN071 Brain Injury 52 0.068
14
P CLR023 Colorectal Cancer 97 0.056
15
P LNG032 Lung Cancer 95 0.056
16
P PRS040 Prostate Cancer 90 0.056
17
P HRT032 Heart Disease 75 0.056
18
CNG034 Congestive Heart Failure 72 0.056
19
KRT004 Keratitis 71 0.056
20
P HPT021 Hepatitis 69 0.056
21
VSC007 Vascular Disease 67 0.056
22
ATH003 Atherosclerosis 65 0.056
23
P PRS038 Personality Disorder 62 0.056
24
GLL008 Gilles De La Tourette Syndrome 62 0.056
25
FCT003 Factor X Deficiency 61 0.056
26
P PLY018 Polycythemia 58 0.056
27
ART021 Arteriosclerosis 58 0.056
28
PRS047 Prostatitis 56 0.056
29
ART111 Artery Disease 55 0.056
30
P MNC007 Monocytic Leukemia 55 0.056
31
P LTR001 Lateral Sclerosis 53 0.056
32
P DBT005 Diabetes Insipidus 53 0.056
33
TRM010 Traumatic Brain Injury 52 0.056
34
BRD004 Borderline Personality Disorder 47 0.056
35
STR072 Stromal Keratitis 46 0.056
36
SYS003 Systolic Heart Failure 43 0.056
37
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.039
38
P PLM037 Pulmonary Hypertension 79 0.039
39
P MYC007 Myocardial Infarction 79 0.039
40
GST053 Gastric Cancer 78 0.039
41
P LVR013 Liver Disease 75 0.039
42
STR067 Stroke, Ischemic 75 0.039
43
P CRN211 Coronary Artery Disease 74 0.039
44
c HPT073 Hepatitis C Virus 73 0.039
45
WLS001 Wilson Disease 72 0.039
46
P RSP003 Respiratory Failure 71 0.039
47
MLT021 Multiple System Atrophy 70 0.039
48
P NRB001 Neuroblastoma 70 0.039
49
SQM006 Squamous Cell Carcinoma 70 0.039
50
c HYP595 Hypertension, Essential 69 0.039
51
ATT013 Attention Deficit-Hyperactivity Disorder 69 0.039
52
P OST005 Osteogenesis Imperfecta 69 0.039
53
PRP027 Peripheral Vascular Disease 68 0.039
54
c HPT001 Hepatitis C 68 0.039
55
ISC006 Ischemic Heart Disease 68 0.039
56
PCK002 Pick Disease 68 0.039
57
ANX002 Anxiety Disorder 67 0.039
58
P MYP004 Myopathy 67 0.039
59
P ATR011 Atrial Fibrillation 66 0.039
60
P KDN018 Kidney Disease 66 0.039
61
c CHR089 Chronic Kidney Failure 66 0.039
62
P MYL006 Myeloid Leukemia 66 0.039
63
OBS002 Obsessive-Compulsive Disorder 66 0.039
64
ATP002 Atopy 66 0.039
65
P DYS154 Dystonia 65 0.039
66
P SPN046 Spinal Muscular Atrophy 65 0.039
67
AND015 Androgen Insensitivity 64 0.039
68
DFC004 Deficiency Anemia 64 0.039
69
LNG099 Lung Disease 64 0.039
70
CHR066 Chronic Fatigue Syndrome 64 0.039
71
CRB039 Cerebrovascular Disease 63 0.039
72
GLN010 Glanzmann Thrombasthenia 63 0.039
73
LPP001 Lipoprotein Lipase Deficiency 63 0.039
74
PLM129 Pulmonary Disease, Chronic Obstructive 63 0.039
75
MLN008 Melanoma 62 0.039
76
VSC011 Vasculitis 62 0.039
77
APH001 Aphthous Stomatitis 62 0.039
78
ISC004 Ischemia 61 0.039
79
HPY002 H. Pylori Infection 61 0.039
80
c ACT075 Acute Myocardial Infarction 60 0.039
81
P MCP010 Mucopolysaccharidosis 60 0.039
82
c VRL010 Viral Hepatitis 60 0.039
83
WLL001 Williams-Beuren Syndrome 60 0.039
84
P PNC025 Panic Disorder 60 0.039
85
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.039
86
c HPT003 Hepatitis a 59 0.039
87
P ENC018 Encephalopathy 59 0.039
88
FTT001 Fatty Liver Disease 59 0.039
89
P NRP001 Neuropathy 59 0.039
90
WLL006 Wells Syndrome 59 0.039
91
PRP030 Purpura 58 0.039
92
P HYP060 Hyperinsulinism 58 0.039
93
ETN001 Eating Disorder 58 0.039
94
RSP006 Respiratory System Disease 58 0.039
95
PST028 Post-Traumatic Stress Disorder 57 0.039
96
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 57 0.039
97
ART017 Aortic Disease 57 0.039
98
c FML108 Familial Breast Cancer 57 0.039
99
ORL015 Oral Squamous Cell Carcinoma 57 0.039
100
EPD016 Epidermolysis Bullosa 57 0.039
101
HYP266 Hypoxia 56 0.039
102
CHR285 Chronic Myelomonocytic Leukemia 56 0.039
103
PRP019 Peripheral Nervous System Disease 55 0.039
104
c THR092 Thrombophilia Due to Thrombin Defect 54 0.039
105
P MMB011 Membranous Nephropathy 54 0.039
106
P THY032 Thyroiditis 54 0.039
107
LMY002 Leiomyoma 54 0.039
108
CND002 Conduct Disorder 54 0.039
109
P MTC069 Mitochondrial Disorders 53 0.039
110
P EPD003 Epidermolysis Bullosa Simplex 53 0.039
111
ADL002 Adult Syndrome 52 0.039
112
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.039
113
P FRC002 Fructose Intolerance 52 0.039
114
PRT058 Pure Autonomic Failure 52 0.039
115
P ANG015 Angioedema 52 0.039
116
CYT008 Cytomegalovirus Infection 52 0.039
117
HMG005 Hemoglobinopathy 52 0.039
118
ALL026 Allergic Hypersensitivity Disease 52 0.039
119
P MSC033 Muscle Disorders 52 0.039
120
P SPS003 Spastic Diplegia 52 0.039
121
DBT004 Diabetic Polyneuropathy 52 0.039
122
P LCT001 Lactic Acidosis 51 0.039
123
ATR060 Atrial Standstill, Digenic 51 0.039
124
CRN030 Coronary Stenosis 51 0.039
125
INT007 Intermediate Coronary Syndrome 50 0.039
126
P MSC003 Muscular Atrophy 50 0.039
127
OPT003 Opiate Dependence 50 0.039
128
NNL002 Nonalcoholic Steatohepatitis 50 0.039
129
URN009 Urinary System Disease 50 0.039
130
c ACT134 Acute Liver Failure 50 0.039
131
CSY001 C Syndrome 50 0.039
132
ANG054 Angina Pectoris 50 0.039
133
HYP006 Hypertensive Heart Disease 50 0.039
134
P URF003 Urofacial Syndrome 1 50 0.039
135
TRD006 Tardive Dyskinesia 49 0.039
136
MVM001 Movement Disease 49 0.039
137
LPD009 Lipid Storage Disease 49 0.039
138
c INH020 Inherited Metabolic Disorder 49 0.039
139
ATN005 Autonomic Dysfunction 49 0.039
140
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.039
141
LPD004 Lipoid Nephrosis 48 0.039
142
P CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 48 0.039
143
PRM028 Paramyotonia Congenita 48 0.039
144
OCL006 Ocular Hypertension 48 0.039
145
CRN017 Coronary Thrombosis 48 0.039
146
ATN002 Autonomic Nervous System Disease 48 0.039
147
VND001 Vein Disease 47 0.039
148
c BPL002 Bipolar I Disorder 47 0.039
149
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.039
150
BLD053 Blood Platelet Disease 46 0.039
151
GLT021 Glutaricaciduria, Type I 46 0.039
152
P CRV039 Cervicitis 45 0.039
153
P DYS026 Dysfibrinogenemia 45 0.039
154
HRT015 Heritable Pulmonary Arterial Hypertension 45 0.039
155
ALN001 Aland Island Eye Disease 45 0.039
156
GDS001 Good Syndrome 44 0.039
157
CRV043 Cervical Dystonia 44 0.039
158
c CHR095 Chronic Progressive External Ophthalmoplegia 44 0.039
159
P DYS021 Dysautonomia 44 0.039
160
PHY002 Physical Disorder 43 0.039
161
CMP034 Complete Androgen Insensitivity Syndrome 43 0.039
162
RNL097 Renal Artery Disease 43 0.039
163
LKC003 Leukocyte Disease 43 0.039
164
MLT001 Multiple Chemical Sensitivity 43 0.039
165
CRB008 Cerebral Atherosclerosis 43 0.039
166
P CRB088 Cerebral Atrophy 42 0.039
167
END072 Endotheliitis 42 0.039
168
GLC008 Glucose Metabolism Disease 42 0.039
169
P BLD051 Blood Coagulation Disease 42 0.039
170
BRN080 Brain Ischemia 41 0.039
171
P ABD016 Abdominal Obesity-Metabolic Syndrome 41 0.039
172
DCB001 Decubitus Ulcer 41 0.039
173
CHR413 Chronic Myocardial Ischemia 41 0.039
174
P PRP034 Purpura Fulminans 41 0.039
175
THL017 Thalassemia Intermedia 40 0.039
176
ACT084 Acute Stress Disorder 40 0.039
177
GST078 Gastrointestinal Allergy 40 0.039
178
CRN019 Coronary Artery Vasospasm 40 0.039
179
BSL008 Basal Ganglia Disease 40 0.039
180
HRN003 Heroin Dependence 40 0.039
181
c CHR096 Chronic Pulmonary Heart Disease 40 0.039
182
CRB009 Cerebritis 39 0.039
183
HYP540 Hypertension, Diastolic 39 0.039
184
ACT088 Acute Insulin Response 39 0.039
185
THR035 Thrombasthenia 39 0.039
186
c HYP072 Hypersensitivity Reaction Type Iii Disease 38 0.039
187
BLD054 Blood Protein Disease 37 0.039
188
CHR415 Chronic Venous Leg Ulcers 37 0.039
189
PRP080 Peripheral Artery Disease 37 0.039
190
VSC018 Visceral Steatosis 37 0.039
191
NSY001 N Syndrome 36 0.039
192
c INH004 Inherited Blood Coagulation Disease 36 0.039
193
MTC005 Mitochondrial Metabolism Disease 36 0.039
194
P MYG005 Myoglobinuria 35 0.039
195
MSC004 Muscle Tissue Disease 34 0.039
196
FML330 Familial Lcat Deficiency 34 0.039
197
IMP003 Impaired Renal Function Disease 34 0.039
198
c ABD013 Abdominal Obesity-Metabolic Syndrome 3 32 0.039
199
MTC028 Mitochondrial Cardiomyopathy 32 0.039
200
NTM001 Nutmeg Liver 31 0.039
201
RNL001 Renal Artery Obstruction 31 0.039
202
TYP015 Type 2b Von Willebrand Disease 30 0.039
203
P FTT008 Fatty Liver Disease, Nonalcoholic 1 30 0.039
204
VTM003 Vitamin Metabolic Disorder 30 0.039
205
DFC001 Defective Apolipoprotein B-100 29 0.039
206
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.039
207
c PLM128 Pulmonary Hypertension, Primary, 2 28 0.039
208
c MYC058 Myocardial Infarction 2 28 0.039
209
CKS001 Ck Syndrome 27 0.039
210
TYP027 Type 1 Diabetes Mellitus 10 27 0.039
211
CRB031 Cerebral Arterial Disease 27 0.039
212
YNG002 Young Syndrome 26 0.039
213
SPN031 Supine Hypotensive Syndrome 25 0.039
214
c CRN214 Coronary Heart Disease 5 22 0.039
215
P CRN178 Coronary Heart Disease 6 21 0.039
216
ULC005 Ulcer of Lower Limbs 20 0.039
217
c CRN174 Coronary Heart Disease 2 20 0.039
218
c CRN175 Coronary Heart Disease 4 19 0.039
219
c CRN172 Coronary Heart Disease 3 19 0.039
220
c CRN173 Coronary Heart Disease 8 18 0.039
221
c DYS033 Dysautonomia Like Disorder 16 0.039
222
c FTT007 Fatty Liver Disease, Nonalcoholic 2 16 0.039
223
c DLT012 Delta-Thalassemia 15 0.039
224
WSC001 Wisconsin Syndrome 14 0.039
225
BLN008 Blind Hypotensive Eye 14 0.039
226
SGM003 Segmentation Syndrome 1 12 0.039
227
HRD059 Hereditary Peripheral Nervous Disorder 11 0.039
228
IDP075 Idiopathic and/or Familial Pulmonary Arterial Hypertension 11 0.039
229
HYP159 Hyperinsulinism, Focal 9 0.039
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