Search results for val

171 hits were found for val

# Family MCID Name MIFTS Score
1
ANG066 Angel-Shaped Phalangoepiphyseal Dysplasia 33 0.235
2
P SCH015 Schizophrenia 71 0.185
3
c BLD140 Blood Group, I System 37 0.131
4
P BRS047 Breast Cancer 100 0.123
5
P THL005 Thalassemia 65 0.115
6
P ALZ034 Alzheimer Disease 95 0.107
7
THR024 Thrombosis 61 0.098
8
VNW001 Von Willebrand's Disease 61 0.098
9
P BPL003 Bipolar Disorder 61 0.098
10
ECH005 Echo Virus 11 Sensitivity 15 0.098
11
P LKM002 Leukemia 75 0.087
12
c THR092 Thrombophilia Due to Thrombin Defect 61 0.087
13
P PLY019 Polyneuropathy 58 0.087
14
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.087
15
P LVR013 Liver Disease 76 0.076
16
P HPT021 Hepatitis 75 0.076
17
ANX010 Anxiety 72 0.076
18
VSC007 Vascular Disease 71 0.076
19
c BTT014 Beta-Thalassemia 70 0.076
20
SYS004 Systemic Mastocytosis 65 0.076
21
AGN016 Aging 65 0.076
22
P HML002 Hemolytic Anemia 62 0.076
23
c ALP101 Alpha-Thalassemia 60 0.076
24
P CRN300 Coronary Heart Disease 1 57 0.076
25
P HYP750 Hypertriglyceridemia, Familial 55 0.076
26
c HYP555 Hypertriglyceridemia, Transient Infantile 34 0.076
27
P LNG032 Lung Cancer 99 0.062
28
P CLR023 Colorectal Cancer 98 0.062
29
P PRS040 Prostate Cancer 88 0.062
30
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.062
31
P MLT020 Multiple Sclerosis 85 0.062
32
P MYC007 Myocardial Infarction 81 0.062
33
P HRT032 Heart Disease 80 0.062
34
CNG034 Congestive Heart Failure 74 0.062
35
c HPT073 Hepatitis C Virus 73 0.062
36
ISC006 Ischemic Heart Disease 73 0.062
37
c HPT001 Hepatitis C 73 0.062
38
P DBT009 Diabetes Mellitus 72 0.062
39
P CRN018 Coronary Artery Anomaly 69 0.062
40
ISC004 Ischemia 66 0.062
41
P HYP061 Hypertrophic Cardiomyopathy 65 0.062
42
P PRS038 Personality Disorder 65 0.062
43
GLL008 Gilles De La Tourette Syndrome 64 0.062
44
c HPT003 Hepatitis a 63 0.062
45
P ART021 Arteriosclerosis 62 0.062
46
KRT019 Keratitis, Hereditary 62 0.062
47
ANR040 Aneurysm 61 0.062
48
ALP103 Alpha-1-Antitrypsin Deficiency 60 0.062
49
P PLY018 Polycythemia 60 0.062
50
PRS047 Prostatitis 59 0.062
51
P MNC007 Monocytic Leukemia 59 0.062
52
P LTR001 Lateral Sclerosis 58 0.062
53
FCT003 Factor X Deficiency 58 0.062
54
BRN071 Brain Injury 54 0.062
55
TRM010 Traumatic Brain Injury 54 0.062
56
P DBT005 Diabetes Insipidus 54 0.062
57
ART140 Arteries, Anomalies of 51 0.062
58
STR072 Stromal Keratitis 50 0.062
59
BRD004 Borderline Personality Disorder 50 0.062
60
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.062
61
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.062
62
TKN001 Takenouchi-Kosaki Syndrome 30 0.062
63
GST053 Gastric Cancer 84 0.044
64
STR067 Stroke, Ischemic 84 0.044
65
c LKM061 Leukemia, Acute Myeloid 81 0.044
66
P PLM037 Pulmonary Hypertension 79 0.044
67
c HYP595 Hypertension, Essential 78 0.044
68
P INF038 Influenza 77 0.044
69
SQM006 Squamous Cell Carcinoma 74 0.044
70
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.044
71
P NRB001 Neuroblastoma 73 0.044
72
MLN008 Melanoma 72 0.044
73
c CHR089 Chronic Kidney Failure 72 0.044
74
WLS001 Wilson Disease 72 0.044
75
P KDN018 Kidney Disease 69 0.044
76
P MYL006 Myeloid Leukemia 69 0.044
77
P ATR011 Atrial Fibrillation 68 0.044
78
OBS002 Obsessive-Compulsive Disorder 68 0.044
79
LNG099 Lung Disease 67 0.044
80
P ATT013 Attention Deficit-Hyperactivity Disorder 67 0.044
81
c PLM164 Pulmonary Hypertension, Primary, 1 67 0.044
82
c SML038 Small Cell Cancer of the Lung 67 0.044
83
BRT054 Brittle Bone Disorder 67 0.044
84
VSC011 Vasculitis 66 0.044
85
GLN010 Glanzmann Thrombasthenia 66 0.044
86
ACQ007 Acquired Immunodeficiency Syndrome 65 0.044
87
SND001 Sandhoff Disease 65 0.044
88
MLT157 Multiple System Atrophy 1 65 0.044
89
c ACT075 Acute Myocardial Infarction 64 0.044
90
c MCP049 Mucopolysaccharidosis, Type Vii 64 0.044
91
RSP006 Respiratory System Disease 63 0.044
92
P NRP001 Neuropathy 63 0.044
93
P CHR285 Chronic Myelomonocytic Leukemia 63 0.044
94
P SPN046 Spinal Muscular Atrophy 63 0.044
95
FTT001 Fatty Liver Disease 62 0.044
96
PRP030 Purpura 61 0.044
97
HYP266 Hypoxia 61 0.044
98
P DYS154 Dystonia 61 0.044
99
ETN001 Eating Disorder 61 0.044
100
LMY014 Leiomyoma, Uterine 61 0.044
101
P MCP040 Mucopolysaccharidosis-Plus Syndrome 61 0.044
102
PRT058 Pure Autonomic Failure 60 0.044
103
PST028 Post-Traumatic Stress Disorder 59 0.044
104
TRD006 Tardive Dyskinesia 59 0.044
105
ORL015 Oral Squamous Cell Carcinoma 59 0.044
106
P ENC018 Encephalopathy 58 0.044
107
LMY002 Leiomyoma 58 0.044
108
URN009 Urinary System Disease 58 0.044
109
EPD016 Epidermolysis Bullosa 57 0.044
110
P PNC025 Panic Disorder 57 0.044
111
P ANG015 Angioedema 57 0.044
112
CYT008 Cytomegalovirus Infection 57 0.044
113
HYP052 Hyperkalemic Periodic Paralysis 57 0.044
114
AND002 Androgen Insensitivity Syndrome 57 0.044
115
NNL002 Nonalcoholic Steatohepatitis 56 0.044
116
HYP060 Hyperinsulinism 56 0.044
117
IGR001 Ige Responsiveness, Atopic 56 0.044
118
P THY032 Thyroiditis 56 0.044
119
P MSC003 Muscular Atrophy 55 0.044
120
SPS003 Spastic Diplegia 55 0.044
121
MGR028 Migraine with or Without Aura 1 55 0.044
122
TBC004 Tobacco Addiction 55 0.044
123
INT007 Intermediate Coronary Syndrome 55 0.044
124
CND002 Conduct Disorder 54 0.044
125
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 54 0.044
126
OPT003 Opiate Dependence 54 0.044
127
ANG054 Angina Pectoris 53 0.044
128
HMG005 Hemoglobinopathy 53 0.044
129
P EPD003 Epidermolysis Bullosa Simplex 53 0.044
130
c GRV008 Graves Disease 1 52 0.044
131
DBT004 Diabetic Polyneuropathy 51 0.044
132
ATN002 Autonomic Nervous System Disease 51 0.044
133
ATN005 Autonomic Dysfunction 51 0.044
134
P DYS026 Dysfibrinogenemia 51 0.044
135
P LCT001 Lactic Acidosis 51 0.044
136
c BPL002 Bipolar I Disorder 50 0.044
137
P CRV039 Cervicitis 49 0.044
138
ANX004 Anoxia 49 0.044
139
AND020 Androgen Insensitivity, Partial 49 0.044
140
HRT015 Heritable Pulmonary Arterial Hypertension 48 0.044
141
P DYS021 Dysautonomia 47 0.044
142
CMP034 Complete Androgen Insensitivity Syndrome 47 0.044
143
END072 Endotheliitis 46 0.044
144
THR035 Thrombasthenia 46 0.044
145
CRV043 Cervical Dystonia 45 0.044
146
P PRP034 Purpura Fulminans 44 0.044
147
BSL008 Basal Ganglia Disease 44 0.044
148
c CHR095 Chronic Progressive External Ophthalmoplegia 44 0.044
149
SYS003 Systolic Heart Failure 44 0.044
150
c HYP768 Hyperlipoproteinemia, Type I 44 0.044
151
HRN003 Heroin Dependence 43 0.044
152
CRB009 Cerebritis 41 0.044
153
PRG039 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 40 0.044
154
MVM001 Movement Disease 40 0.044
155
PRM057 Paramyotonia Congenita of Von Eulenburg 39 0.044
156
GLC008 Glucose Metabolism Disease 38 0.044
157
P VSC018 Visceral Steatosis 38 0.044
158
P MYG005 Myoglobinuria 37 0.044
159
PPL059 Popliteal Pterygium Syndrome, Lethal Type 37 0.044
160
FML330 Familial Lcat Deficiency 37 0.044
161
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 36 0.044
162
c MLT151 Multiple Mitochondrial Dysfunctions Syndrome 5 36 0.044
163
PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 36 0.044
164
PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 35 0.044
165
PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 35 0.044
166
P SMK004 Smoking As a Quantitative Trait Locus 3 34 0.044
167
c MYG004 Myoglobinuria, Acute Recurrent, Autosomal Recessive 33 0.044
168
DFC001 Defective Apolipoprotein B-100 31 0.044
169
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 29 0.044
170
PPL052 Papillomatosis, Confluent and Reticulated 26 0.044
171
BLD138 Blood Group--Diego System 18 0.044
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