# |
|
Family |
MCID |
Name |
MIFTS |
Score |
1 |
|
P
|
RHM011 |
Rheumatoid Arthritis |
82 |
38.610 |
|
2 |
|
P
|
ART022 |
Arthritis |
71 |
30.841 |
|
3 |
|
|
CTR172 |
Citrullinemia, Classic |
65 |
20.640 |
|
4 |
|
|
CTR030 |
Citrulline Transport Defect |
9 |
18.733 |
|
5 |
|
|
ALP042 |
Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity |
65 |
16.340 |
|
6 |
|
|
ORN008 |
Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to |
62 |
13.011 |
|
7 |
|
|
URC002 |
Urea Cycle Disorder |
51 |
12.785 |
|
8 |
|
|
ATM095 |
Autoimmune Disease |
61 |
12.301 |
|
9 |
|
P
|
PRD008 |
Periodontitis |
64 |
10.855 |
|
10 |
|
P
|
SHR001 |
Short Bowel Syndrome |
53 |
9.677 |
|
11 |
|
|
PLC002 |
Plica Syndrome |
35 |
9.550 |
|
12 |
|
|
SYN007 |
Synovitis |
55 |
9.550 |
|
13 |
|
|
TRD008 |
Triiodothyronine Receptor Auxiliary Protein |
33 |
8.808 |
|
14 |
|
P
|
PLM037 |
Pulmonary Hypertension |
72 |
8.759 |
|
15 |
|
|
LNG099 |
Lung Disease |
62 |
8.286 |
|
16 |
|
|
CRB197 |
Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to |
57 |
7.883 |
|
17 |
|
|
PSR001 |
Psoriatic Arthritis |
62 |
7.750 |
|
18 |
|
c
|
JVN010 |
Juvenile Rheumatoid Arthritis |
66 |
7.736 |
|
19 |
|
|
ENT004 |
Enthesopathy |
51 |
7.701 |
|
20 |
|
|
INT066 |
Interstitial Lung Disease |
60 |
6.623 |
|
21 |
|
|
CNN005 |
Connective Tissue Disease |
67 |
6.204 |
|
22 |
|
|
CRH001 |
Crohn's Disease |
80 |
6.083 |
|
23 |
|
|
SPN051 |
Spondylitis |
51 |
6.053 |
|
24 |
|
|
INF009 |
Inflammatory Spondylopathy |
30 |
6.053 |
|
25 |
|
c
|
SPN225 |
Spondyloarthropathy 1 |
70 |
5.982 |
|
26 |
|
|
PPL052 |
Papillomatosis, Confluent and Reticulated |
34 |
5.973 |
|
27 |
|
P
|
LPS004 |
Lupus Erythematosus |
61 |
5.680 |
|
28 |
|
P
|
VSC007 |
Vascular Disease |
63 |
5.649 |
|
29 |
|
c
|
SYS001 |
Systemic Lupus Erythematosus |
87 |
5.589 |
|
30 |
|
P
|
SCK005 |
Sickle Cell Disease |
56 |
5.469 |
|
31 |
|
|
PLM129 |
Pulmonary Disease, Chronic Obstructive |
74 |
5.469 |
|
32 |
|
|
MTC023 |
Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes |
44 |
5.466 |
|
33 |
|
|
ENT011 |
Enterocolitis |
55 |
5.379 |
|
34 |
|
|
48X005 |
48,xyyy |
39 |
5.363 |
|
35 |
|
P
|
CTR177 |
Citrullinemia, Type Ii, Adult-Onset |
55 |
5.332 |
|
36 |
|
|
MTC114 |
Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes |
62 |
5.281 |
|
37 |
|
|
LYS003 |
Lysinuric Protein Intolerance |
57 |
5.238 |
|
38 |
|
P
|
ART023 |
Arthropathy |
61 |
5.237 |
|
39 |
|
|
MCS002 |
Mucositis |
56 |
5.196 |
|
40 |
|
|
PRN019 |
Perinatal Necrotizing Enterocolitis |
60 |
5.152 |
|
41 |
|
|
TXC005 |
Toxic Shock Syndrome |
62 |
5.081 |
|
42 |
|
c
|
SCL052 |
Scleroderma, Familial Progressive |
61 |
5.034 |
|
43 |
|
|
ISC004 |
Ischemia |
61 |
4.962 |
|
44 |
|
P
|
CTR077 |
Citrullinemia, Type Ii, Neonatal-Onset |
41 |
4.933 |
|
45 |
|
|
HYP266 |
Hypoxia |
57 |
4.932 |
|
46 |
|
P
|
INT068 |
Intestinal Disease |
53 |
4.922 |
|
47 |
|
P
|
MLT020 |
Multiple Sclerosis |
79 |
4.835 |
|
48 |
|
c
|
PRC016 |
Pre-Eclampsia |
65 |
4.771 |
|
49 |
|
P
|
MSC005 |
Muscular Dystrophy |
67 |
4.745 |
|
50 |
|
P
|
CLC063 |
Celiac Disease 1 |
66 |
4.662 |
|
51 |
|
P
|
HRT032 |
Heart Disease |
81 |
4.647 |
|
52 |
|
|
SYS071 |
Systemic Autoimmune Disease |
35 |
4.502 |
|
53 |
|
|
IMP005 |
Impotence |
52 |
4.471 |
|
54 |
|
P
|
LCT001 |
Lactic Acidosis |
51 |
4.436 |
|
55 |
|
P
|
VSC011 |
Vasculitis |
61 |
4.429 |
|
56 |
|
|
47X002 |
47,xyy |
48 |
4.405 |
|
57 |
|
|
CYT002 |
Cytokine Deficiency |
43 |
4.377 |
|
58 |
|
|
HYP774 |
Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome |
54 |
4.352 |
|
59 |
|
P
|
ADL010 |
Adult Respiratory Distress Syndrome |
71 |
4.340 |
|
60 |
|
P
|
LVR013 |
Liver Disease |
69 |
4.304 |
|
61 |
|
P
|
PRN023 |
Prion Disease |
60 |
4.257 |
|
62 |
|
P
|
MTC069 |
Mitochondrial Disorders |
57 |
4.237 |
|
63 |
|
|
FTT001 |
Fatty Liver Disease |
62 |
4.204 |
|
64 |
|
|
ULC004 |
Ulcerative Colitis |
74 |
4.199 |
|
65 |
|
|
BRN056 |
Bronchopulmonary Dysplasia |
56 |
4.175 |
|
66 |
|
c
|
PRD040 |
Periodontitis, Chronic |
52 |
4.165 |
|
67 |
|
|
ARG002 |
Argininosuccinic Aciduria |
61 |
4.118 |
|
68 |
|
|
NNL005 |
Non-Alcoholic Fatty Liver Disease |
63 |
4.075 |
|
69 |
|
P
|
INF037 |
Inflammatory Bowel Disease |
53 |
4.070 |
|
70 |
|
|
ATH013 |
Atherosclerosis Susceptibility |
63 |
4.043 |
|
71 |
|
P
|
SPN052 |
Spondyloarthropathy |
55 |
4.002 |
|
72 |
|
|
ALL014 |
Allergic Encephalomyelitis |
34 |
3.908 |
|
73 |
|
P
|
PLY041 |
Polymyositis |
59 |
3.858 |
|
74 |
|
|
MTC004 |
Mitochondrial Encephalomyopathy |
42 |
3.842 |
|
75 |
|
|
CHL068 |
Cholestasis |
61 |
3.836 |
|
76 |
|
|
ART140 |
Arteries, Anomalies of |
53 |
3.829 |
|
77 |
|
P
|
PLM036 |
Pulmonary Fibrosis |
66 |
3.827 |
|
78 |
|
|
SCK003 |
Sickle Cell Anemia |
74 |
3.822 |
|
79 |
|
P
|
PRT133 |
Proteasome-Associated Autoinflammatory Syndrome 1 |
80 |
3.807 |
|
80 |
|
|
DFC004 |
Deficiency Anemia |
74 |
3.745 |
|
81 |
|
|
AGN016 |
Aging |
54 |
3.728 |
|
82 |
|
c
|
TYP009 |
Type 2 Diabetes Mellitus |
92 |
3.657 |
|
83 |
|
P
|
SJG008 |
Sjogren Syndrome |
61 |
3.655 |
|
84 |
|
|
MSC157 |
Muscular Dystrophy, Duchenne Type |
79 |
3.650 |
|
85 |
|
c
|
CHR684 |
Chronic Kidney Disease |
69 |
3.634 |
|
86 |
|
c
|
HYP595 |
Hypertension, Essential |
85 |
3.598 |
|
87 |
|
P
|
DRR001 |
Diarrhea |
55 |
3.570 |
|
|
89 |
|
|
ANT039 |
Antisynthetase Syndrome |
55 |
3.530 |
|
90 |
|
P
|
CRN300 |
Coronary Heart Disease 1 |
73 |
3.523 |
|
91 |
|
|
SCR011 |
Scrapie |
39 |
3.505 |
|
92 |
|
|
OCL069 |
Ocular Motor Apraxia |
57 |
3.503 |
|
93 |
|
c
|
BDY010 |
Body Mass Index Quantitative Trait Locus 4 |
46 |
3.451 |
|
94 |
|
c
|
BDY011 |
Body Mass Index Quantitative Trait Locus 10 |
45 |
3.451 |
|
95 |
|
c
|
BDY005 |
Body Mass Index Quantitative Trait Locus 9 |
47 |
3.451 |
|
96 |
|
c
|
BDY012 |
Body Mass Index Quantitative Trait Locus 7 |
44 |
3.451 |
|
97 |
|
P
|
BDY004 |
Body Mass Index Quantitative Trait Locus 11 |
83 |
3.451 |
|
98 |
|
c
|
BDY006 |
Body Mass Index Quantitative Trait Locus 8 |
44 |
3.451 |
|
99 |
|
c
|
BDY017 |
Body Mass Index Quantitative Trait Locus 14 |
45 |
3.451 |
|
100 |
|
c
|
BDY020 |
Body Mass Index Quantitative Trait Locus 19 |
52 |
3.451 |
|
101 |
|
c
|
BDY015 |
Body Mass Index Quantitative Trait Locus 12 |
46 |
3.451 |
|
102 |
|
c
|
BDY019 |
Body Mass Index Quantitative Trait Locus 18 |
47 |
3.451 |
|
103 |
|
P
|
ALZ034 |
Alzheimer Disease |
87 |
3.450 |
|
104 |
|
P
|
ENC018 |
Encephalopathy |
62 |
3.450 |
|
105 |
|
|
ACT228 |
Acute Radiation Syndrome |
30 |
3.439 |
|
106 |
|
|
MTC005 |
Mitochondrial Metabolism Disease |
45 |
3.394 |
|
107 |
|
P
|
SYS005 |
Systemic Scleroderma |
74 |
3.376 |
|
108 |
|
|
PLN005 |
Palindromic Rheumatism |
43 |
3.372 |
|
109 |
|
|
PRP027 |
Peripheral Vascular Disease |
71 |
3.361 |
|
110 |
|
P
|
MYP004 |
Myopathy |
67 |
3.343 |
|
111 |
|
P
|
DBT009 |
Diabetes Mellitus |
67 |
3.339 |
|
112 |
|
c
|
HPT001 |
Hepatitis C |
62 |
3.252 |
|
113 |
|
|
CRT072 |
Creutzfeldt-Jakob Disease |
68 |
3.200 |
|
114 |
|
|
RCT015 |
Reactive Arthritis |
61 |
3.183 |
|
115 |
|
|
CRH005 |
Crohn's Colitis |
53 |
3.173 |
|
116 |
|
c
|
ACT027 |
Acute Pancreatitis |
60 |
3.166 |
|
117 |
|
|
DMY004 |
Demyelinating Disease |
50 |
3.166 |
|
118 |
|
P
|
GRF003 |
Graft-Versus-Host Disease |
71 |
3.149 |
|
119 |
|
|
ATS010 |
Autosomal Recessive Disease |
42 |
3.132 |
|
120 |
|
P
|
PSR002 |
Psoriasis |
63 |
3.091 |
|
121 |
|
|
PST011 |
Pustulosis of Palm and Sole |
52 |
3.091 |
|
122 |
|
|
LPP008 |
Lipoprotein Quantitative Trait Locus |
65 |
3.088 |
|
123 |
|
c
|
ATM011 |
Autoimmune Hepatitis |
63 |
3.080 |
|
124 |
|
|
PLM134 |
Pulmonary Fibrosis, Idiopathic |
76 |
3.071 |
|
125 |
|
|
BNR002 |
Bone Resorption Disease |
47 |
3.071 |
|
126 |
|
P
|
BRN022 |
Bronchiectasis |
60 |
3.071 |
|
127 |
|
|
HTT002 |
Hutterite Cerebroosteonephrodysplasia Syndrome |
25 |
3.036 |
|
128 |
|
P
|
MSC003 |
Muscular Atrophy |
52 |
3.010 |
|
129 |
|
c
|
PLM164 |
Pulmonary Hypertension, Primary, 1 |
76 |
2.989 |
|
130 |
|
P
|
NTR004 |
Neutropenia |
63 |
2.986 |
|
131 |
|
P
|
PNC044 |
Pancreatitis |
61 |
2.986 |
|
132 |
|
|
TTN003 |
Tetanus |
65 |
2.973 |
|
133 |
|
P
|
TMP003 |
Temporal Arteritis |
69 |
2.934 |
|
134 |
|
|
MSC152 |
Muscular Dystrophy, Becker Type |
69 |
2.927 |
|
135 |
|
P
|
AST005 |
Asthma |
76 |
2.924 |
|
136 |
|
|
PRP080 |
Peripheral Artery Disease |
54 |
2.900 |
|
137 |
|
P
|
MYS005 |
Myositis |
56 |
2.898 |
|
138 |
|
P
|
ECL001 |
Eclampsia |
52 |
2.892 |
|
139 |
|
|
CLT003 |
Colitis |
63 |
2.861 |
|
140 |
|
|
TNS014 |
Tenosynovitis |
46 |
2.860 |
|
141 |
|
c
|
HYP836 |
Hypercholesterolemia, Familial, 1 |
73 |
2.851 |
|
142 |
|
|
FLT011 |
Felty Syndrome |
52 |
2.843 |
|
143 |
|
|
BRC012 |
Brucellosis |
66 |
2.823 |
|
144 |
|
P
|
DRM010 |
Dermatomyositis |
61 |
2.819 |
|
145 |
|
|
HPT004 |
Hepatic Coma |
43 |
2.761 |
|
146 |
|
|
RYS001 |
Reye Syndrome |
49 |
2.753 |
|
147 |
|
|
LVR012 |
Liver Cirrhosis |
63 |
2.735 |
|
148 |
|
c
|
ACT135 |
Acute Graft Versus Host Disease |
51 |
2.708 |
|
149 |
|
|
CRB186 |
Carbamoyl Phosphate Synthetase I Deficiency, Hyperammonemia Due to |
50 |
2.698 |
|
150 |
|
|
NCT003 |
N-Acetylglutamate Synthase Deficiency |
43 |
2.661 |
|
151 |
|
|
ARG007 |
Argininemia |
58 |
2.660 |
|
152 |
|
|
URM002 |
Uremia |
47 |
2.658 |
|
153 |
|
|
RPD005 |
Rapidly Involuting Congenital Hemangioma |
46 |
2.651 |
|
154 |
|
|
BCT022 |
Bacterial Infectious Disease |
56 |
2.621 |
|
155 |
|
|
PRT038 |
Protein-Energy Malnutrition |
53 |
2.616 |
|
156 |
|
|
HYP066 |
Hyperglycemia |
61 |
2.585 |
|
157 |
|
|
HPT019 |
Hepatic Encephalopathy |
59 |
2.566 |
|
158 |
|
c
|
HPT073 |
Hepatitis C Virus |
71 |
2.563 |
|
159 |
|
P
|
KLZ004 |
Kala-Azar 1 |
41 |
2.559 |
|
160 |
|
|
LSH001 |
Leishmaniasis |
64 |
2.559 |
|
161 |
|
|
END086 |
End Stage Renal Disease |
52 |
2.541 |
|
162 |
|
P
|
RSP003 |
Respiratory Failure |
74 |
2.522 |
|
163 |
|
c
|
TYP008 |
Type 1 Diabetes Mellitus |
70 |
2.512 |
|
164 |
|
|
OST012 |
Osteoarthritis |
77 |
2.512 |
|
165 |
|
|
ORN004 |
Ornithinemia |
13 |
2.497 |
|
166 |
|
|
SPN119 |
Spondylarthropathy |
38 |
2.494 |
|
167 |
|
|
ESN011 |
Eisenmenger Syndrome |
47 |
2.480 |
|
168 |
|
P
|
PLY187 |
Polyarticular Juvenile Idiopathic Arthritis |
39 |
2.471 |
|
169 |
|
P
|
GLM007 |
Glomerulonephritis |
60 |
2.471 |
|
170 |
|
|
ORT008 |
Orotic Aciduria |
57 |
2.462 |
|
171 |
|
|
LPD008 |
Lipid Metabolism Disorder |
62 |
2.462 |
|
172 |
|
P
|
FML018 |
Familial Mediterranean Fever |
73 |
2.437 |
|
173 |
|
c
|
AMY091 |
Amyotrophic Lateral Sclerosis 1 |
88 |
2.431 |
|
174 |
|
c
|
MGR028 |
Migraine with or Without Aura 1 |
64 |
2.431 |
|
175 |
|
P
|
LTR001 |
Lateral Sclerosis |
58 |
2.431 |
|
176 |
|
|
YMN001 |
Yemenite Deaf-Blind Hypopigmentation Syndrome |
66 |
2.425 |
|
177 |
|
|
CRB039 |
Cerebrovascular Disease |
66 |
2.391 |
|
178 |
|
c
|
CHR464 |
Chronic Intestinal Failure |
24 |
2.368 |
|
179 |
|
|
PRT251 |
Proteinuria, Chronic Benign |
57 |
2.353 |
|
180 |
|
c
|
BDY007 |
Body Mass Index Quantitative Trait Locus 1 |
40 |
2.351 |
|
181 |
|
|
PPL022 |
Papilloma |
53 |
2.349 |
|
182 |
|
|
SQM002 |
Squamous Cell Papilloma |
46 |
2.349 |
|
183 |
|
P
|
MYC008 |
Myocarditis |
59 |
2.349 |
|
184 |
|
|
PLM031 |
Poliomyelitis |
63 |
2.326 |
|
185 |
|
|
PRT013 |
Portal Hypertension |
59 |
2.315 |
|
186 |
|
|
GT001 |
Gout |
64 |
2.307 |
|
187 |
|
|
MTB004 |
Metabolic Acidosis |
48 |
2.276 |
|
188 |
|
|
MLR004 |
Malaria |
80 |
2.276 |
|
189 |
|
|
SKN016 |
Skin Disease |
63 |
2.274 |
|
190 |
|
|
MXD005 |
Mixed Connective Tissue Disease |
57 |
2.274 |
|
191 |
|
P
|
TRN020 |
Turner Syndrome |
67 |
2.269 |
|
192 |
|
|
TBL029 |
Tubulin, Beta |
28 |
2.263 |
|
193 |
|
P
|
KDN018 |
Kidney Disease |
72 |
2.263 |
|
194 |
|
P
|
ADN016 |
Adenocarcinoma |
63 |
2.263 |
|
195 |
|
|
VSC003 |
Visceral Leishmaniasis |
55 |
2.246 |
|
196 |
|
P
|
PRP019 |
Peripheral Nervous System Disease |
58 |
2.246 |
|
197 |
|
|
PRM236 |
Primary Biliary Cholangitis |
60 |
2.224 |
|
198 |
|
c
|
HPT016 |
Hepatitis B |
62 |
2.219 |
|
199 |
|
|
BRN002 |
Bronchiolitis |
57 |
2.173 |
|
200 |
|
|
ANX004 |
Anoxia |
40 |
2.172 |
|
201 |
|
|
TRM010 |
Traumatic Brain Injury |
51 |
2.172 |
|
202 |
|
|
HYP060 |
Hyperinsulinism |
54 |
2.172 |
|
203 |
|
|
SPL018 |
Splenomegaly |
49 |
2.172 |
|
204 |
|
|
ANC002 |
Anca-Associated Vasculitis |
44 |
2.172 |
|
205 |
|
|
PYR037 |
Pyruvate Carboxylase Deficiency |
45 |
2.171 |
|
206 |
|
P
|
CLR023 |
Colorectal Cancer |
100 |
2.154 |
|
207 |
|
P
|
TRM003 |
Tremor |
48 |
2.154 |
|
208 |
|
|
CNG034 |
Congestive Heart Failure |
69 |
2.154 |
|
209 |
|
|
ADL002 |
Adult Syndrome |
70 |
2.143 |
|
210 |
|
|
THR024 |
Thrombosis |
56 |
2.128 |
|
211 |
|
|
SCH060 |
Schistosoma Mansoni Infection, Susceptibility/ |
38 |
2.124 |
|
212 |
|
c
|
MCR130 |
Microvascular Complications of Diabetes 6 |
41 |
2.124 |
|
213 |
|
c
|
MCR120 |
Microvascular Complications of Diabetes 7 |
47 |
2.124 |
|
214 |
|
|
CLR109 |
Colorectal Adenocarcinoma |
50 |
2.124 |
|
215 |
|
c
|
MCR113 |
Microvascular Complications of Diabetes 3 |
52 |
2.124 |
|
216 |
|
c
|
MCR133 |
Microvascular Complications of Diabetes 4 |
41 |
2.124 |
|
217 |
|
|
SCH014 |
Schistosomiasis |
56 |
2.124 |
|
218 |
|
|
BRN004 |
Brain Edema |
54 |
2.111 |
|
219 |
|
c
|
DLT002 |
Dilated Cardiomyopathy |
78 |
2.111 |
|
220 |
|
c
|
INH020 |
Inherited Metabolic Disorder |
48 |
2.094 |
|
221 |
|
|
RCK004 |
Rickets |
68 |
2.075 |
|
222 |
|
P
|
MNN013 |
Meningitis |
65 |
2.075 |
|
223 |
|
P
|
HPT021 |
Hepatitis |
69 |
2.072 |
|
224 |
|
|
OST159 |
Osteogenic Sarcoma |
66 |
2.068 |
|
225 |
|
|
RNL114 |
Renal Cell Carcinoma, Nonpapillary |
80 |
2.068 |
|
226 |
|
P
|
ANT006 |
Antiphospholipid Syndrome |
55 |
2.068 |
|
227 |
|
|
DPR016 |
Depression |
65 |
2.068 |
|
228 |
|
|
CVD001 |
Covid-19 |
57 |
2.066 |
|
229 |
|
|
LGH007 |
Leigh Syndrome |
70 |
2.046 |
|
230 |
|
|
SPR126 |
Superior Semicircular Canal Dehiscence |
41 |
2.026 |
|
231 |
|
c
|
HMG029 |
Hemoglobin Se Disease |
40 |
2.026 |
|
232 |
|
c
|
ACT071 |
Acute Kidney Failure |
60 |
2.023 |
|
233 |
|
c
|
RNG008 |
Ring Chromosome 13 |
30 |
2.023 |
|
234 |
|
c
|
LKM061 |
Leukemia, Acute Myeloid |
83 |
2.023 |
|
235 |
|
|
PRT037 |
Pertussis |
65 |
2.023 |
|
236 |
|
|
SVR004 |
Severe Combined Immunodeficiency |
72 |
2.023 |
|
237 |
|
|
BRN071 |
Brain Injury |
50 |
2.023 |
|
238 |
|
P
|
ATR001 |
Atrioventricular Septal Defect |
55 |
1.979 |
|
239 |
|
P
|
VNT002 |
Ventricular Septal Defect |
58 |
1.979 |
|
240 |
|
|
HRT011 |
Heart Septal Defect |
49 |
1.979 |
|
241 |
|
|
END057 |
Endometrial Cancer |
72 |
1.976 |
|
242 |
|
|
RHM033 |
Rheumatoid Factor-Positive Polyarticular Juvenile Idiopathic Arthritis |
19 |
1.976 |
|
243 |
|
|
GLM045 |
Glioma |
63 |
1.976 |
|
244 |
|
|
HLX001 |
Helix Syndrome |
48 |
1.970 |
|
245 |
|
|
GNG013 |
Gingivitis |
59 |
1.970 |
|
246 |
|
P
|
NRP001 |
Neuropathy |
60 |
1.945 |
|
247 |
|
P
|
LPR021 |
Leprosy 3 |
71 |
1.939 |
|
248 |
|
|
HNS001 |
Hansen's Disease |
32 |
1.939 |
|
249 |
|
|
ALL006 |
Allergic Asthma |
56 |
1.929 |
|
250 |
|
|
GLL048 |
Glial Tumor |
52 |
1.929 |
|
251 |
|
P
|
CRD119 |
Cardiac Arrest |
67 |
1.929 |
|
252 |
|
|
HSH003 |
Hashimoto Thyroiditis |
60 |
1.915 |
|
253 |
|
P
|
PNC035 |
Pancreatic Cancer |
86 |
1.879 |
|
254 |
|
P
|
MLN008 |
Melanoma |
76 |
1.879 |
|
255 |
|
|
CLN019 |
Colonic Disease |
47 |
1.879 |
|
256 |
|
|
SPN035 |
Spindle Cell Sarcoma |
54 |
1.857 |
|
257 |
|
|
TNS005 |
Tonsillitis |
57 |
1.857 |
|
258 |
|
|
SRC014 |
Sarcoma |
65 |
1.857 |
|
259 |
|
P
|
CRD246 |
Cardiovascular System Disease |
56 |
1.854 |
|
260 |
|
c
|
ACT134 |
Acute Liver Failure |
59 |
1.828 |
|
261 |
|
P
|
OST002 |
Osteoporosis |
76 |
1.828 |
|
262 |
|
P
|
EXN002 |
Exanthem |
58 |
1.828 |
|
263 |
|
c
|
BNM022 |
Bone Mineral Density Quantitative Trait Locus 8 |
45 |
1.828 |
|
264 |
|
P
|
BNM029 |
Bone Mineral Density Quantitative Trait Locus 15 |
48 |
1.828 |
|
265 |
|
|
MND021 |
Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome |
66 |
1.828 |
|
266 |
|
P
|
OPN001 |
Open-Angle Glaucoma |
55 |
1.828 |
|
267 |
|
P
|
HDC001 |
Headache |
57 |
1.828 |
|
268 |
|
|
DWN001 |
Down Syndrome |
70 |
1.815 |
|
269 |
|
c
|
CHL116 |
Cholestasis, Intrahepatic, of Pregnancy, 1 |
52 |
1.804 |
|
270 |
|
P
|
FTT008 |
Fatty Liver Disease, Nonalcoholic 1 |
48 |
1.796 |
|
271 |
|
|
DHY010 |
Dihydrolipoamide Dehydrogenase Deficiency |
47 |
1.796 |
|
272 |
|
|
PLM001 |
Pulmonary Tuberculosis |
69 |
1.796 |
|
273 |
|
|
BNN003 |
Bone Inflammation Disease |
48 |
1.796 |
|
274 |
|
|
ANK001 |
Ankylosis |
51 |
1.796 |
|
275 |
|
|
MCR088 |
Microscopic Polyangiitis |
51 |
1.796 |
|
276 |
|
P
|
LNG032 |
Lung Cancer |
98 |
1.775 |
|
277 |
|
|
CLF027 |
Cleft Palate, Isolated |
64 |
1.775 |
|
278 |
|
c
|
SML038 |
Small Cell Cancer of the Lung |
69 |
1.775 |
|
279 |
|
c
|
GLC092 |
Glaucoma, Primary Open Angle |
62 |
1.775 |
|
280 |
|
|
CLF001 |
Cleft Lip |
53 |
1.775 |
|
281 |
|
|
FBR047 |
Fibromyalgia |
58 |
1.775 |
|
282 |
|
|
CMB007 |
Combined Immunodeficiency |
57 |
1.775 |
|
283 |
|
|
PRP030 |
Purpura |
54 |
1.775 |
|
284 |
|
|
ACT017 |
Acute Chest Syndrome |
50 |
1.765 |
|
285 |
|
|
INT002 |
Intermittent Claudication |
61 |
1.759 |
|
286 |
|
|
ACR041 |
Acromelic Frontonasal Dysostosis |
53 |
1.755 |
|
287 |
|
|
NWB001 |
Newborn Respiratory Distress Syndrome |
56 |
1.755 |
|
288 |
|
|
CYS013 |
Cystinuria |
66 |
1.750 |
|
289 |
|
P
|
AGG001 |
Aggressive Periodontitis |
55 |
1.738 |
|
290 |
|
P
|
CTR002 |
Cataract |
60 |
1.731 |
|
291 |
|
c
|
THR092 |
Thrombophilia Due to Thrombin Defect |
74 |
1.719 |
|
292 |
|
P
|
ORF002 |
Orofacial Cleft |
43 |
1.719 |
|
293 |
|
P
|
PRS040 |
Prostate Cancer |
95 |
1.719 |
|
294 |
|
P
|
HPT023 |
Hepatocellular Carcinoma |
96 |
1.719 |
|
295 |
|
P
|
MYC007 |
Myocardial Infarction |
70 |
1.719 |
|
296 |
|
|
CLF056 |
Cleft Lip with or Without Cleft Palate |
42 |
1.719 |
|
297 |
|
P
|
INT070 |
Intestinal Obstruction |
57 |
1.719 |
|
298 |
|
P
|
DMN002 |
Dementia |
66 |
1.719 |
|
299 |
|
P
|
UVT001 |
Uveitis |
57 |
1.719 |
|
300 |
|
|
RYN005 |
Raynaud Phenomenon |
45 |
1.719 |
|
301 |
|
P
|
PNM007 |
Pneumonia |
67 |
1.686 |
|
302 |
|
|
SVR001 |
Severe Acute Respiratory Syndrome |
67 |
1.665 |
|
303 |
|
|
IMM166 |
Immunodeficiency 27a |
60 |
1.662 |
|
304 |
|
|
ISL109 |
Isolated Cleft Lip |
33 |
1.661 |
|
305 |
|
P
|
LYM118 |
Lymphoma |
67 |
1.661 |
|
306 |
|
P
|
SRC025 |
Sarcoidosis 1 |
71 |
1.661 |
|
307 |
|
|
ESP021 |
Esophageal Cancer |
83 |
1.661 |
|
308 |
|
|
URT010 |
Ureteral Obstruction |
45 |
1.661 |
|
309 |
|
|
ORF053 |
Orofacial Clefting Syndrome |
31 |
1.661 |
|
310 |
|
|
INS001 |
Insulinoma |
59 |
1.661 |
|
311 |
|
|
ADN018 |
Adenoma |
59 |
1.661 |
|
312 |
|
|
ALL029 |
Allergic Disease |
59 |
1.661 |
|
313 |
|
|
HGH043 |
High Grade Glioma |
45 |
1.661 |
|
314 |
|
|
NNS002 |
Nonspecific Interstitial Pneumonia |
42 |
1.661 |
|
315 |
|
|
GST045 |
Gastroenteritis |
58 |
1.661 |
|
316 |
|
P
|
HYP265 |
Hypotonia |
42 |
1.661 |
|
317 |
|
c
|
RNG015 |
Ring Chromosome 2 |
22 |
1.661 |
|
318 |
|
c
|
JVN061 |
Juvenile Arthritis |
56 |
1.658 |
|
319 |
|
|
LYM133 |
Lymphoma, Hodgkin, Classic |
74 |
1.600 |
|
320 |
|
|
SPN186 |
Spinal Cord Injury |
61 |
1.600 |
|
321 |
|
c
|
SCN036 |
Secondary Progressive Multiple Sclerosis |
55 |
1.600 |
|
322 |
|
|
INT323 |
Intraocular Pressure Quantitative Trait Locus |
64 |
1.600 |
|
323 |
|
|
MYL069 |
Myeloma, Multiple |
77 |
1.600 |
|
324 |
|
P
|
THY032 |
Thyroiditis |
57 |
1.600 |
|
325 |
|
P
|
MTR014 |
Motor Neuron Disease |
65 |
1.600 |
|
326 |
|
P
|
BNG032 |
Benign Mesothelioma |
53 |
1.600 |
|
327 |
|
|
VSC002 |
Vascular Dementia |
60 |
1.600 |
|
328 |
|
|
END072 |
Endotheliitis |
36 |
1.590 |
|
329 |
|
|
PPL061 |
Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome |
26 |
1.590 |
|
330 |
|
|
NNL006 |
Non-Alcoholic Steatohepatitis |
54 |
1.588 |
|
331 |
|
|
IMM167 |
Immune Deficiency Disease |
78 |
1.588 |
|
332 |
|
|
CHC001 |
Chickenpox |
57 |
1.588 |
|
333 |
|
c
|
VRL010 |
Viral Hepatitis |
53 |
1.588 |
|
334 |
|
|
CRT015 |
Carotid Artery Occlusion |
45 |
1.588 |
|
335 |
|
c
|
BNM018 |
Bone Mineral Density Quantitative Trait Locus 3 |
33 |
1.569 |
|
336 |
|
|
LYM017 |
Lyme Disease |
62 |
1.569 |
|
337 |
|
|
STR067 |
Stroke, Ischemic |
80 |
1.551 |
|
338 |
|
|
PRT036 |
Peritonitis |
65 |
1.551 |
|
339 |
|
|
STT001 |
Status Epilepticus |
59 |
1.551 |
|
340 |
|
|
MLT161 |
Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly |
55 |
1.536 |
|
341 |
|
|
ANR007 |
Anorexia Nervosa |
60 |
1.536 |
|
342 |
|
P
|
MYC084 |
Mycobacterium Tuberculosis 1 |
68 |
1.536 |
|
343 |
|
|
PLY150 |
Polykaryocytosis Inducer |
29 |
1.536 |
|
344 |
|
|
DSS032 |
Disease by Infectious Agent |
55 |
1.536 |
|
345 |
|
|
LNG091 |
Lung Mucoepidermoid Carcinoma |
32 |
1.536 |
|
346 |
|
|
OBS082 |
Obstructive Nephropathy |
41 |
1.536 |
|
347 |
|
|
MCP006 |
Mucoepidermoid Carcinoma |
48 |
1.536 |
|
348 |
|
|
GST106 |
Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets |
65 |
1.536 |
|
349 |
|
|
CHG001 |
Chagas Disease |
66 |
1.536 |
|
350 |
|
P
|
HYD006 |
Hydrocephalus |
61 |
1.536 |
|
351 |
|
|
HML018 |
Homologous Wasting Disease |
21 |
1.536 |
|
352 |
|
P
|
HNT016 |
Huntington Disease |
73 |
1.505 |
|
353 |
|
P
|
HYP086 |
Hypothyroidism |
69 |
1.505 |
|
354 |
|
|
GST033 |
Gestational Diabetes |
61 |
1.505 |
|
355 |
|
c
|
PRM038 |
Primary Agammaglobulinemia |
47 |
1.488 |
|
356 |
|
c
|
SPS158 |
Spastic Paraplegia 9a, Autosomal Dominant |
44 |
1.485 |
|
357 |
|
P
|
BLD134 |
Bladder Cancer |
79 |
1.467 |
|
358 |
|
|
SMT004 |
Smith-Lemli-Opitz Syndrome |
70 |
1.467 |
|
359 |
|
c
|
ATR087 |
Atrial Standstill 1 |
74 |
1.467 |
|
360 |
|
c
|
CLC042 |
Celiac Disease 9 |
14 |
1.467 |
|
361 |
|
P
|
MPL001 |
Maple Syrup Urine Disease |
70 |
1.467 |
|
362 |
|
|
PHN003 |
Phenylketonuria |
76 |
1.467 |
|
363 |
|
P
|
BCL017 |
B-Cell Lymphoma |
59 |
1.467 |
|
364 |
|
P
|
ACN011 |
Acne |
57 |
1.467 |
|
365 |
|
|
TLN003 |
Telangiectasis |
51 |
1.467 |
|
366 |
|
|
SYS003 |
Systolic Heart Failure |
49 |
1.467 |
|
367 |
|
P
|
MYC033 |
Myoclonus |
47 |
1.467 |
|
368 |
|
|
HMP009 |
Haemophilus Influenzae |
41 |
1.467 |
|
369 |
|
c
|
MCR115 |
Microvascular Complications of Diabetes 5 |
65 |
1.457 |
|
370 |
|
|
AND005 |
Androgen Insensitivity Syndrome, Mild |
21 |
1.433 |
|
371 |
|
P
|
DYS154 |
Dystonia |
64 |
1.419 |
|
372 |
|
c
|
MTC200 |
Mitochondrial Dna Depletion Syndrome 17 |
20 |
1.413 |
|
373 |
|
|
CRB004 |
Cerebral Artery Occlusion |
45 |
1.407 |
|
374 |
|
|
RFR013 |
Refractory Celiac Disease |
33 |
1.393 |
|
375 |
|
P
|
HYP111 |
Hyperprolinemia |
45 |
1.393 |
|
376 |
|
|
SXL003 |
Sexual Disorder |
49 |
1.393 |
|
377 |
|
|
HLC007 |
Helicobacter Pylori Infection |
67 |
1.393 |
|
378 |
|
|
LYM143 |
Lymphoma, Non-Hodgkin, Familial |
75 |
1.393 |
|
379 |
|
P
|
ASP006 |
Aspergillosis |
72 |
1.393 |
|
380 |
|
|
GYR004 |
Gyrate Atrophy of Choroid and Retina |
58 |
1.393 |
|
381 |
|
c
|
FML116 |
Familial Cold Autoinflammatory Syndrome 1 |
55 |
1.393 |
|
382 |
|
|
GLC003 |
Glucose Intolerance |
54 |
1.393 |
|
383 |
|
|
ENC067 |
Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis |
50 |
1.393 |
|
384 |
|
P
|
MYG005 |
Myoglobinuria |
40 |
1.393 |
|
385 |
|
P
|
TRT010 |
Teratoma |
51 |
1.393 |
|
386 |
|
|
MRP001 |
Morphine Dependence |
42 |
1.393 |
|
387 |
|
|
CRY004 |
Cryoglobulinemia |
48 |
1.393 |
|
388 |
|
|
GST023 |
Gastric Ulcer |
52 |
1.393 |
|
389 |
|
|
TLR001 |
Tularemia |
56 |
1.393 |
|
390 |
|
|
RHM014 |
Rheumatoid Vasculitis |
37 |
1.393 |
|
391 |
|
P
|
CLS010 |
Cluster Headache |
42 |
1.393 |
|
392 |
|
c
|
MYT029 |
Myotonia Congenita, Autosomal Recessive |
40 |
1.391 |
|
393 |
|
|
END021 |
Endomyocardial Fibrosis |
56 |
1.391 |
|
394 |
|
c
|
BDY021 |
Body Mass Index Quantitative Trait Locus 20 |
49 |
1.376 |
|
395 |
|
P
|
SZR006 |
Seizure Disorder |
70 |
1.356 |
|
396 |
|
|
INS024 |
Insulin-Like Growth Factor I |
78 |
1.356 |
|
397 |
|
|
CYS001 |
Cystic Fibrosis |
78 |
1.356 |
|
398 |
|
|
ART016 |
Aortic Aneurysm |
68 |
1.356 |
|
399 |
|
|
PMP006 |
Pemphigus Vulgaris, Familial |
58 |
1.319 |
|
400 |
|
P
|
PMP001 |
Pemphigus |
55 |
1.319 |
|
401 |
|
P
|
RBL001 |
Rubella |
58 |
1.319 |
|
402 |
|
P
|
EYD002 |
Eye Disease |
57 |
1.319 |
|
403 |
|
|
GST009 |
Gastroschisis |
53 |
1.313 |
|
404 |
|
|
SMT017 |
Somatomammotropinoma |
17 |
1.313 |
|
405 |
|
|
PTT048 |
Pituitary Adenoma, Prolactin-Secreting |
64 |
1.313 |
|
406 |
|
P
|
LKM071 |
Leukemia, Chronic Lymphocytic |
75 |
1.313 |
|
407 |
|
P
|
PRK057 |
Parkinson Disease, Late-Onset |
80 |
1.313 |
|
408 |
|
|
HYP780 |
Hypoadrenocorticism, Familial |
61 |
1.313 |
|
409 |
|
|
PLG003 |
Polg-Related Disorders |
20 |
1.313 |
|
410 |
|
|
DST006 |
Diastolic Heart Failure |
45 |
1.313 |
|
411 |
|
P
|
ENC004 |
Encephalitis |
61 |
1.313 |
|
412 |
|
|
ABD010 |
Abdominal Wall Defect |
39 |
1.313 |
|
413 |
|
|
BNS003 |
Binswanger's Disease |
41 |
1.313 |
|
414 |
|
|
ATX038 |
Ataxia and Polyneuropathy, Adult-Onset |
46 |
1.303 |
|
415 |
|
c
|
ART138 |
Aortic Aneurysm, Familial Abdominal, 1 |
61 |
1.303 |
|
416 |
|
P
|
HYP750 |
Hypertriglyceridemia, Familial |
62 |
1.303 |
|
417 |
|
|
CHR100 |
Chronic Ulcer of Skin |
57 |
1.248 |
|
418 |
|
|
HYP056 |
Hypoglycemia |
65 |
1.248 |
|
419 |
|
|
NTR005 |
Nutritional Deficiency Disease |
61 |
1.235 |
|
420 |
|
|
INT276 |
Interatrial Communication |
51 |
1.227 |
|
421 |
|
|
TRG019 |
Trigonocephaly with Short Stature and Developmental Delay |
38 |
1.227 |
|
422 |
|
P
|
ATR010 |
Atrial Heart Septal Defect |
58 |
1.227 |
|
423 |
|
|
KPS004 |
Kaposi Sarcoma |
77 |
1.224 |
|
424 |
|
|
ARG004 |
Argyria |
26 |
1.224 |
|
425 |
|
c
|
PK3005 |
Pik3ca-Related Overgrowth Syndrome |
33 |
1.224 |
|
426 |
|
|
XLN228 |
X-Linked Recessive Disease |
24 |
1.224 |
|
427 |
|
P
|
CHL066 |
Cholangitis |
52 |
1.224 |
|
428 |
|
c
|
HMG001 |
Hemoglobin C Disease |
41 |
1.224 |
|
429 |
|
|
UND007 |
Undifferentiated Connective Tissue Disease |
28 |
1.224 |
|
430 |
|
P
|
CHR345 |
Chronic Pain |
50 |
1.224 |
|
431 |
|
|
RMT001 |
Remitting Seronegative Symmetrical Synovitis with Pitting Edema |
17 |
1.224 |
|
432 |
|
|
MTC112 |
Mitochondrial Dna-Associated Leigh Syndrome |
32 |
1.205 |
|
433 |
|
|
SPS057 |
Spasticity |
42 |
1.190 |
|
434 |
|
|
HMC014 |
Homocysteinemia |
52 |
1.190 |
|
435 |
|
P
|
END033 |
Endocarditis |
58 |
1.190 |
|
436 |
|
|
PLM033 |
Pulmonary Embolism |
58 |
1.190 |
|
437 |
|
P
|
DRM053 |
Dermatitis, Atopic |
65 |
1.128 |
|
438 |
|
P
|
MJR001 |
Major Depressive Disorder |
68 |
1.128 |
|
439 |
|
|
CHL067 |
Cholecystitis |
60 |
1.128 |
|
440 |
|
|
MNT002 |
Mental Depression |
57 |
1.128 |
|
441 |
|
|
ILS001 |
Ileus |
50 |
1.128 |
|
442 |
|
|
DYS064 |
Dystonia 3, Torsion, X-Linked |
45 |
1.123 |
|
443 |
|
c
|
MST023 |
Mesothelioma, Malignant |
56 |
1.123 |
|
444 |
|
c
|
SYS045 |
Systemic Lupus Erythematosus 14 |
13 |
1.123 |
|
445 |
|
|
KRT019 |
Keratitis, Hereditary |
66 |
1.123 |
|
446 |
|
c
|
CTS029 |
Cutis Laxa, Autosomal Recessive, Type Iiia |
53 |
1.123 |
|
447 |
|
|
MLT157 |
Multiple System Atrophy 1 |
69 |
1.123 |
|
448 |
|
P
|
CRY007 |
Cryoglobulinemia, Familial Mixed |
49 |
1.123 |
|
449 |
|
P
|
PRK039 |
Parkinsonism |
55 |
1.123 |
|
450 |
|
|
SCN068 |
Secondary Interstitial Lung Disease in Childhood and Adulthood Associated with a Connective Tissue Disease |
19 |
1.123 |
|
451 |
|
P
|
HYP098 |
Hypereosinophilic Syndrome |
66 |
1.123 |
|
452 |
|
P
|
CYS018 |
Cystitis |
59 |
1.123 |
|
453 |
|
P
|
RTN016 |
Retinal Degeneration |
52 |
1.123 |
|
454 |
|
|
BRN012 |
Bronchiolitis Obliterans |
56 |
1.123 |
|
455 |
|
|
HYP068 |
Hyperostosis |
47 |
1.123 |
|
456 |
|
|
MNN009 |
Meningoencephalitis |
48 |
1.123 |
|
457 |
|
|
SPT004 |
Septic Arthritis |
58 |
1.123 |
|
458 |
|
|
MLT016 |
Multicentric Reticulohistiocytosis |
39 |
1.123 |
|
459 |
|
c
|
SVR005 |
Severe Pre-Eclampsia |
50 |
1.123 |
|
460 |
|
|
HRP004 |
Herpes Zoster |
61 |
1.123 |
|
461 |
|
|
KDN013 |
Kidney Hypertrophy |
34 |
1.123 |
|
462 |
|
P
|
OVR042 |
Ovarian Cancer |
88 |
1.064 |
|
463 |
|
P
|
BRS047 |
Breast Cancer |
98 |
1.064 |
|
464 |
|
P
|
ANP001 |
Anaplastic Large Cell Lymphoma |
61 |
1.064 |
|
465 |
|
P
|
URN019 |
Urinary Tract Infection |
49 |
1.064 |
|
466 |
|
P
|
LKM062 |
Leukemia, Acute Lymphoblastic |
69 |
1.064 |
|
467 |
|
|
ALC028 |
Alacrima, Achalasia, and Mental Retardation Syndrome |
68 |
1.064 |
|
468 |
|
c
|
ATS307 |
Autosomal Recessive Cerebellar Ataxia |
39 |
1.064 |
|
469 |
|
P
|
AMY004 |
Amyloidosis |
70 |
1.064 |
|
470 |
|
|
LRN003 |
Learning Disability |
49 |
1.064 |
|
471 |
|
|
RHM036 |
Rheumatoid Arthritis Interstitial Lung Disease |
31 |
1.064 |
|
472 |
|
P
|
PLM006 |
Pulmonary Alveolar Proteinosis |
53 |
1.064 |
|
473 |
|
|
BLR001 |
Biliary Atresia |
55 |
1.064 |
|
474 |
|
|
PST106 |
Post-Cardiac Arrest Syndrome |
31 |
1.064 |
|
475 |
|
P
|
KDN017 |
Kidney Cancer |
61 |
1.064 |
|
476 |
|
|
SBC016 |
Subacute Delirium |
43 |
1.064 |
|
477 |
|
c
|
SCN046 |
Secondary Short Bowel Syndrome |
14 |
1.036 |
|
478 |
|
|
PHS029 |
Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic |
26 |
1.036 |
|
479 |
|
|
GST050 |
Gastrointestinal System Disease |
55 |
1.028 |
|
480 |
|
|
DSR072 |
Disorder of Energy Metabolism |
10 |
1.013 |
|
481 |
|
P
|
PRC031 |
Preeclampsia/eclampsia 1 |
43 |
1.013 |
|
482 |
|
c
|
HYP724 |
Hyperlipoproteinemia, Type Iii |
67 |
1.013 |
|
483 |
|
|
AGG012 |
Aggressive Nk-Cell Leukemia |
46 |
1.013 |
|
484 |
|
|
PST020 |
Postpoliomyelitis Syndrome |
43 |
1.013 |
|
485 |
|
|
HRT015 |
Heritable Pulmonary Arterial Hypertension |
46 |
1.013 |
|
486 |
|
P
|
MYS003 |
Myasthenia Gravis |
68 |
1.004 |
|
487 |
|
|
OTT002 |
Otitis Media |
71 |
1.004 |
|
488 |
|
|
CHR005 |
Chorioamnionitis |
50 |
1.004 |
|
489 |
|
P
|
FML011 |
Familial Adenomatous Polyposis |
71 |
1.004 |
|
490 |
|
|
CHK001 |
Chikungunya |
60 |
1.004 |
|
491 |
|
|
PMP004 |
Pemphigus Foliaceus |
43 |
1.004 |
|
492 |
|
|
TQP001 |
Taqi Polymorphism |
29 |
1.004 |
|
493 |
|
|
CVT001 |
Cavitary Optic Disc Anomalies |
37 |
1.004 |
|
494 |
|
|
HYD003 |
Hydrarthrosis |
30 |
1.004 |
|
495 |
|
P
|
RHB003 |
Rhabdomyosarcoma |
66 |
1.004 |
|
496 |
|
|
INT182 |
Intermittent Hydrarthrosis |
17 |
1.004 |
|
497 |
|
|
IGG001 |
Iga Glomerulonephritis |
50 |
1.004 |
|
498 |
|
|
BRD005 |
Borderline Leprosy |
28 |
1.004 |
|
499 |
|
|
RFL002 |
Reflex Epilepsy |
41 |
1.004 |
|
500 |
|
|
SPP004 |
Suppurative Cholangitis |
23 |
1.004 |
|
501 |
|
|
IDP011 |
Idiopathic Interstitial Pneumonia |
59 |
1.004 |
|
502 |
|
|
LPR001 |
Lepromatous Leprosy |
49 |
1.004 |
|
503 |
|
|
TBR006 |
Tuberculoid Leprosy |
43 |
1.004 |
|
504 |
|
P
|
OBS001 |
Obstructive Jaundice |
48 |
1.004 |
|
505 |
|
P
|
SCL015 |
Scleritis |
48 |
1.004 |
|
506 |
|
|
PST046 |
Post-Transplant Lymphoproliferative Disease |
53 |
1.004 |
|
507 |
|
P
|
PHC003 |
Pheochromocytoma |
69 |
0.995 |
|
508 |
|
|
ADR040 |
Adrenal Gland Pheochromocytoma |
46 |
0.995 |
|
509 |
|
|
GLB002 |
Glioblastoma |
67 |
0.995 |
|
510 |
|
|
PRP016 |
Paraplegia |
52 |
0.995 |
|
511 |
|
P
|
LKM002 |
Leukemia |
67 |
0.995 |
|
512 |
|
c
|
ACT068 |
Acute Cystitis |
61 |
0.995 |
|
513 |
|
P
|
MCR010 |
Microcephaly |
60 |
0.995 |
|
514 |
|
P
|
CTS001 |
Cutis Laxa |
65 |
0.995 |
|
515 |
|
P
|
ACT105 |
Acute Mountain Sickness |
52 |
0.995 |
|
516 |
|
P
|
OVR082 |
Overgrowth Syndrome |
49 |
0.921 |
|
517 |
|
|
INF034 |
Infective Endocarditis |
54 |
0.921 |
|
518 |
|
|
MLD018 |
Mild Cognitive Impairment |
48 |
0.921 |
|
519 |
|
|
VRC005 |
Varicose Veins |
60 |
0.921 |
|
520 |
|
P
|
NRB001 |
Neuroblastoma |
66 |
0.921 |
|
521 |
|
P
|
HRP006 |
Herpes Simplex |
65 |
0.921 |
|
522 |
|
P
|
HML002 |
Hemolytic Anemia |
62 |
0.921 |
|
523 |
|
P
|
ALP008 |
Alopecia |
54 |
0.921 |
|
524 |
|
P
|
THR014 |
Thrombocytopenia |
66 |
0.921 |
|
525 |
|
|
BLR008 |
Bilirubin Metabolic Disorder |
57 |
0.921 |
|
526 |
|
|
CHL014 |
Cholera |
62 |
0.921 |
|
527 |
|
|
ESP002 |
Esophageal Varix |
51 |
0.921 |
|
528 |
|
|
DSS009 |
Disseminated Intravascular Coagulation |
57 |
0.921 |
|
529 |
|
c
|
FML021 |
Familial Hypercholesterolemia |
72 |
0.921 |
|
530 |
|
P
|
PLY019 |
Polyneuropathy |
52 |
0.921 |
|
531 |
|
|
ADL030 |
Adult-Onset Still's Disease |
59 |
0.921 |
|
532 |
|
|
IRN002 |
Iron Metabolism Disease |
57 |
0.921 |
|
533 |
|
|
CRB037 |
Cerebral Palsy |
67 |
0.921 |
|
534 |
|
|
AMN006 |
Aminoaciduria |
37 |
0.921 |
|
535 |
|
c
|
HMC039 |
Hemochromatosis, Type 1 |
73 |
0.848 |
|
536 |
|
|
RST023 |
Resting Heart Rate, Variation in |
40 |
0.848 |
|
537 |
|
|
CRT084 |
Creatinine Clearance Quantitative Trait Locus |
25 |
0.848 |
|
538 |
|
c
|
RTN047 |
Retinitis Pigmentosa 18 |
46 |
0.848 |
|
539 |
|
|
DFF005 |
Diffuse Large B-Cell Lymphoma |
54 |
0.848 |
|
540 |
|
|
CRS005 |
Crest Syndrome |
36 |
0.848 |
|
541 |
|
c
|
SPN226 |
Spondyloarthropathy 2 |
15 |
0.848 |
|
542 |
|
c
|
SYS046 |
Systemic Lupus Erythematosus 3 |
18 |
0.848 |
|
543 |
|
|
ALV005 |
Alveolar Soft Part Sarcoma |
61 |
0.848 |
|
544 |
|
c
|
PSR033 |
Psoriasis 12 |
26 |
0.848 |
|
545 |
|
|
ORB013 |
Orbital Disease |
42 |
0.848 |
|
546 |
|
P
|
BCL004 |
B-Cell Non-Hodgkin Lymphoma |
42 |
0.848 |
|
547 |
|
P
|
EPL164 |
Epilepsy |
68 |
0.848 |
|
548 |
|
|
MNC006 |
Monoclonal Gammopathy of Uncertain Significance |
47 |
0.848 |
|
549 |
|
|
EXT034 |
Extrinsic Allergic Alveolitis |
57 |
0.848 |
|
550 |
|
c
|
ACT004 |
Acute Diarrhea |
40 |
0.848 |
|
551 |
|
|
CRY001 |
Cryptogenic Organizing Pneumonia |
54 |
0.848 |
|
552 |
|
|
FRZ001 |
Frozen Shoulder |
55 |
0.848 |
|
553 |
|
|
EXS001 |
Exostosis |
49 |
0.848 |
|
554 |
|
|
BRS064 |
Bursitis |
51 |
0.848 |
|
555 |
|
|
SCL011 |
Sclerosing Keratitis |
24 |
0.848 |
|
556 |
|
|
CLC006 |
Calcinosis |
47 |
0.848 |
|
557 |
|
P
|
MRC003 |
Mercury Poisoning |
49 |
0.848 |
|
558 |
|
|
RTB001 |
Rat Bite Fever |
26 |
0.848 |
|
559 |
|
|
CHR178 |
Chromosomal Triplication |
34 |
0.848 |
|
560 |
|
P
|
RTN008 |
Retinitis Pigmentosa |
80 |
0.841 |
|
561 |
|
|
NRP045 |
Neuropathy, Ataxia, and Retinitis Pigmentosa |
47 |
0.841 |
|
562 |
|
|
RTN017 |
Retinal Detachment |
60 |
0.841 |
|
563 |
|
|
MRF001 |
Marfan Syndrome |
76 |
0.841 |
|
564 |
|
P
|
MCR129 |
Microvascular Complications of Diabetes 1 |
68 |
0.841 |
|
565 |
|
P
|
GST053 |
Gastric Cancer |
83 |
0.841 |
|
566 |
|
P
|
GLC113 |
Galactosemia I |
66 |
0.841 |
|
567 |
|
P
|
GLM040 |
Glioma Susceptibility 1 |
71 |
0.841 |
|
568 |
|
|
HRW001 |
Hair Whorl |
35 |
0.841 |
|
569 |
|
|
HYD058 |
Hydrops, Lactic Acidosis, and Sideroblastic Anemia |
60 |
0.841 |
|
570 |
|
|
ORG002 |
Organic Acidemia |
44 |
0.841 |
|
571 |
|
|
NRR001 |
Neuroretinitis |
42 |
0.841 |
|
572 |
|
c
|
ACT075 |
Acute Myocardial Infarction |
56 |
0.841 |
|
573 |
|
|
RTN023 |
Retinitis |
46 |
0.841 |
|
574 |
|
P
|
HMC002 |
Homocystinuria |
53 |
0.841 |
|
575 |
|
P
|
MYL006 |
Myeloid Leukemia |
61 |
0.841 |
|
576 |
|
P
|
MTH008 |
Methylmalonic Acidemia |
52 |
0.841 |
|
577 |
|
P
|
BRS044 |
Breast Adenocarcinoma |
58 |
0.841 |
|
578 |
|
|
APP008 |
Appendicitis |
62 |
0.841 |
|
579 |
|
|
MLG079 |
Malignant Pleural Mesothelioma |
42 |
0.841 |
|
580 |
|
c
|
MCR112 |
Microvascular Complications of Diabetes 2 |
42 |
0.841 |
|
581 |
|
P
|
HMP002 |
Hemophagocytic Lymphohistiocytosis |
61 |
0.841 |
|
582 |
|
P
|
GRV001 |
Graves' Disease |
55 |
0.841 |
|
583 |
|
|
DNT012 |
Dental Caries |
53 |
0.841 |
|
584 |
|
|
PYL006 |
Pyloric Stenosis |
48 |
0.841 |
|
585 |
|
|
MLG169 |
Malignant Astrocytoma |
57 |
0.841 |
|
586 |
|
|
HNC001 |
Henoch-Schoenlein Purpura |
54 |
0.841 |
|
587 |
|
P
|
RHN004 |
Rhinitis |
57 |
0.841 |
|
588 |
|
|
THY030 |
Thyroid Gland Disease |
50 |
0.841 |
|
589 |
|
P
|
INF032 |
Infertility |
57 |
0.841 |
|
590 |
|
P
|
HYP076 |
Hyperthyroidism |
53 |
0.841 |
|
591 |
|
P
|
ART021 |
Arteriosclerosis |
54 |
0.841 |
|
592 |
|
|
PLG002 |
Plague |
58 |
0.841 |
|
593 |
|
|
PLM010 |
Pulmonary Edema |
55 |
0.841 |
|
594 |
|
|
KRT001 |
Keratoconjunctivitis Sicca |
50 |
0.841 |
|
595 |
|
c
|
MTC014 |
Mitochondrial Dna Deletion Syndromes |
16 |
0.841 |
|
596 |
|
|
THR123 |
Thrombotic Microangiopathy |
40 |
0.752 |
|
597 |
|
c
|
SPR086 |
Spermatogenic Failure 3 |
46 |
0.752 |
|
598 |
|
|
HYP003 |
Hypermethioninemia |
51 |
0.752 |
|
599 |
|
|
MSC007 |
Muscle Hypertrophy |
64 |
0.752 |
|
600 |
|
|
CHL152 |
Childhood Acute Lymphocytic Leukemia |
50 |
0.752 |
|
601 |
|
P
|
CRP001 |
Carpal Tunnel Syndrome |
66 |
0.752 |
|
602 |
|
c
|
CTR129 |
Cataract 31, Multiple Types |
36 |
0.752 |
|
603 |
|
c
|
SPS159 |
Spastic Paraplegia 9b, Autosomal Recessive |
40 |
0.752 |
|
604 |
|
P
|
TYR004 |
Tyrosinemia |
50 |
0.752 |
|
605 |
|
|
PRP007 |
Priapism |
47 |
0.752 |
|
606 |
|
|
PRC013 |
Pericarditis |
53 |
0.752 |
|
607 |
|
P
|
GST044 |
Gastritis |
55 |
0.752 |
|
608 |
|
|
ACT049 |
Acute Disseminated Encephalomyelitis |
48 |
0.752 |
|
609 |
|
|
PRP009 |
Peripartum Cardiomyopathy |
55 |
0.752 |
|
610 |
|
|
CRN017 |
Coronary Thrombosis |
46 |
0.752 |
|
611 |
|
|
ASP003 |
Aseptic Meningitis |
50 |
0.752 |
|
612 |
|
|
DYS015 |
Dysentery |
50 |
0.752 |
|
613 |
|
|
PNC001 |
Pancytopenia |
53 |
0.752 |
|
614 |
|
|
ALC006 |
Alcoholic Hepatitis |
61 |
0.752 |
|
615 |
|
|
CNS004 |
Constipation |
56 |
0.752 |
|
616 |
|
P
|
HMN010 |
Hemangioma |
62 |
0.752 |
|
617 |
|
P
|
NPH012 |
Nephrotic Syndrome |
60 |
0.752 |
|
618 |
|
c
|
HRD010 |
Hereditary Spastic Paraplegia |
66 |
0.752 |
|
619 |
|
|
CLN015 |
Colon Adenocarcinoma |
65 |
0.752 |
|
620 |
|
|
HMP001 |
Hemopericardium |
47 |
0.752 |
|
621 |
|
|
CRD001 |
Cardiac Tamponade |
43 |
0.752 |
|
622 |
|
P
|
PRC012 |
Pericardial Effusion |
50 |
0.752 |
|
623 |
|
|
ALC005 |
Alcoholic Pancreatitis |
38 |
0.752 |
|
624 |
|
|
PNC041 |
Pancreatic Ductal Adenocarcinoma |
51 |
0.752 |
|
625 |
|
|
SFT003 |
Soft Tissue Sarcoma |
57 |
0.752 |
|
626 |
|
|
BCK006 |
Back Pain |
47 |
0.752 |
|
627 |
|
|
ANR040 |
Aneurysm |
61 |
0.752 |
|
628 |
|
c
|
DVL105 |
Developmental and Epileptic Encephalopathy 82 |
23 |
0.733 |
|
629 |
|
c
|
BLD140 |
Blood Group, I System |
46 |
0.702 |
|
630 |
|
|
CHY002 |
Chylomicron Retention Disease |
64 |
0.702 |
|
631 |
|
c
|
INF071 |
Inflammatory Bowel Disease 1 |
65 |
0.702 |
|
632 |
|
c
|
MTR018 |
Maturity-Onset Diabetes of the Young, Type 1 |
63 |
0.702 |
|
633 |
|
P
|
ATS364 |
Autism |
69 |
0.652 |
|
634 |
|
|
DFF031 |
Diffuse Alveolar Hemorrhage |
31 |
0.652 |
|
635 |
|
c
|
SPS042 |
Spastic Paraplegia 9 |
21 |
0.652 |
|
636 |
|
|
STN013 |
Stenotrophomonas Maltophilia Infection |
26 |
0.652 |
|
637 |
|
|
SQM013 |
Squamous Cell Carcinoma, Head and Neck |
73 |
0.652 |
|
638 |
|
|
PRS127 |
Pearson Marrow-Pancreas Syndrome |
52 |
0.652 |
|
639 |
|
P
|
SCH015 |
Schizophrenia |
74 |
0.652 |
|
640 |
|
c
|
EXD008 |
Exudative Vitreoretinopathy 1 |
71 |
0.652 |
|
641 |
|
|
ALC007 |
Alcohol Dependence |
66 |
0.652 |
|
642 |
|
|
3HY001 |
3-Hydroxyisobutyric Aciduria |
26 |
0.652 |
|
643 |
|
P
|
HYP769 |
Hyperlysinemia, Type I |
42 |
0.652 |
|
644 |
|
|
HMN044 |
Human Immunodeficiency Virus Type 1 |
78 |
0.652 |
|
645 |
|
|
AGN018 |
Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome |
57 |
0.652 |
|
646 |
|
|
ANG054 |
Angina Pectoris |
66 |
0.652 |
|
647 |
|
P
|
ADL017 |
Adult T-Cell Leukemia |
56 |
0.652 |
|
648 |
|
|
WST001 |
West Syndrome |
59 |
0.652 |
|
649 |
|
c
|
CHR711 |
Chronic Asthma |
41 |
0.652 |
|
650 |
|
P
|
FTL001 |
Fetal Alcohol Syndrome |
55 |
0.652 |
|
651 |
|
|
KRN002 |
Kearns-Sayre Syndrome |
63 |
0.652 |
|
652 |
|
c
|
BRN108 |
Branchiootic Syndrome 1 |
62 |
0.652 |
|
653 |
|
c
|
MCL042 |
Macular Degeneration, Age-Related, 1 |
85 |
0.652 |
|
654 |
|
P
|
ABD014 |
Abdominal Obesity-Metabolic Syndrome 1 |
63 |
0.652 |
|
655 |
|
c
|
CTS041 |
Cutis Laxa, Autosomal Dominant 3 |
45 |
0.652 |
|
656 |
|
|
PRT082 |
Preterm Premature Rupture of the Membranes |
57 |
0.652 |
|
657 |
|
|
THY029 |
Thyroid Carcinoma |
51 |
0.652 |
|
658 |
|
|
CWP001 |
Cowpox |
45 |
0.652 |
|
659 |
|
|
CMP010 |
Complex Regional Pain Syndrome |
60 |
0.652 |
|
660 |
|
P
|
PLY017 |
Polyarteritis Nodosa |
60 |
0.652 |
|
661 |
|
P
|
RNV001 |
Renovascular Hypertension |
49 |
0.652 |
|
662 |
|
P
|
CHR012 |
Chronic Granulomatous Disease |
69 |
0.652 |
|
663 |
|
|
VCC001 |
Vaccinia |
47 |
0.652 |
|
664 |
|
P
|
CND004 |
Candidiasis |
58 |
0.652 |
|
665 |
|
P
|
AGN002 |
Agnosia |
54 |
0.652 |
|
666 |
|
|
PPT005 |
Peptic Ulcer Disease |
58 |
0.652 |
|
667 |
|
|
LYM027 |
Lymphopenia |
56 |
0.652 |
|
668 |
|
|
ATX031 |
Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus |
58 |
0.652 |
|
669 |
|
|
XRP001 |
Xerophthalmia |
41 |
0.652 |
|
670 |
|
|
PLR008 |
Pleurisy |
50 |
0.652 |
|
671 |
|
|
HMS001 |
Hemosiderosis |
48 |
0.652 |
|
672 |
|
P
|
MLN007 |
Male Infertility |
56 |
0.652 |
|
673 |
|
|
ACR007 |
Acromegaly |
70 |
0.652 |
|
674 |
|
|
RTN020 |
Retinal Vascular Disease |
46 |
0.652 |
|
675 |
|
|
NNT012 |
Neonatal Jaundice |
53 |
0.652 |
|
676 |
|
|
URT001 |
Urethritis |
53 |
0.652 |
|
677 |
|
|
IRN001 |
Iron Deficiency Anemia |
58 |
0.652 |
|
678 |
|
|
MST005 |
Mastitis |
53 |
0.652 |
|
679 |
|
P
|
FNC004 |
Fanconi Syndrome |
60 |
0.652 |
|
680 |
|
|
BRN024 |
Bronchitis |
67 |
0.652 |
|
681 |
|
|
TCL028 |
T-Cell Lymphoblastic Leukemia/lymphoma |
46 |
0.652 |
|
682 |
|
P
|
CRV039 |
Cervicitis |
52 |
0.652 |
|
683 |
|
|
PLS007 |
Plasmodium Falciparum Malaria |
52 |
0.652 |
|
684 |
|
|
PNN001 |
Panniculitis |
52 |
0.652 |
|
685 |
|
c
|
THR001 |
Thrombocytopenia Due to Platelet Alloimmunization |
60 |
0.652 |
|
686 |
|
P
|
HYP009 |
Hypertrophic Pyloric Stenosis |
41 |
0.652 |
|
687 |
|
|
HDR002 |
Hidradenitis Suppurativa |
54 |
0.652 |
|
688 |
|
|
HDR003 |
Hidradenitis |
50 |
0.652 |
|
689 |
|
|
SQM006 |
Squamous Cell Carcinoma |
60 |
0.652 |
|
690 |
|
|
ISL099 |
Isolated Methylmalonic Acidemia |
36 |
0.652 |
|
691 |
|
|
NRF007 |
Neurofibroma |
64 |
0.652 |
|
692 |
|
|
IRR002 |
Irritable Bowel Syndrome |
65 |
0.652 |
|
693 |
|
c
|
LKM005 |
Leukemia, T-Cell, Chronic |
34 |
0.652 |
|
694 |
|
P
|
FML187 |
Familial Hypertension |
34 |
0.652 |
|
695 |
|
|
SNG003 |
Single Ventricular Heart |
30 |
0.532 |
|
696 |
|
|
GRW007 |
Growth Hormone Deficiency |
46 |
0.532 |
|
697 |
|
|
ADR022 |
Adrenomyeloneuropathy |
39 |
0.532 |
|
698 |
|
P
|
AVS003 |
Avascular Necrosis |
41 |
0.532 |
|
699 |
|
|
SPS019 |
Spastic Paraparesis |
38 |
0.532 |
|
700 |
|
|
PRC049 |
Precursor T-Cell Acute Lymphoblastic Leukemia |
45 |
0.532 |
|
701 |
|
|
FRN006 |
Frontotemporal Dementia |
68 |
0.532 |
|
702 |
|
|
ADR007 |
Adrenoleukodystrophy |
73 |
0.532 |
|
703 |
|
c
|
THY107 |
Thymoma, Familial |
42 |
0.532 |
|
704 |
|
|
CRD132 |
Cardiac Conduction Defect |
60 |
0.532 |
|
705 |
|
|
ACR056 |
Acrodermatitis Enteropathica, Zinc-Deficiency Type |
56 |
0.532 |
|
706 |
|
|
ALL003 |
Allergic Rhinitis |
67 |
0.532 |
|
707 |
|
|
MTC029 |
Mitochondrial Complex V Deficiency, Nuclear Type 1 |
40 |
0.532 |
|
708 |
|
c
|
PSR029 |
Psoriasis 9 |
24 |
0.532 |
|
709 |
|
|
ANX010 |
Anxiety |
70 |
0.532 |
|
710 |
|
c
|
PNC108 |
Pancreatitis, Hereditary |
69 |
0.532 |
|
711 |
|
|
BRK010 |
Burkitt Lymphoma |
66 |
0.532 |
|
712 |
|
P
|
ATX030 |
Ataxia-Telangiectasia |
80 |
0.532 |
|
713 |
|
|
NRD100 |
Neurodevelopmental, Jaw, Eye, and Digital Syndrome |
49 |
0.532 |
|
714 |
|
|
FDB001 |
Foodborne Botulism |
55 |
0.532 |
|
715 |
|
P
|
MLT008 |
Multinodular Goiter |
42 |
0.532 |
|
716 |
|
|
ALC001 |
Alcohol-Related Birth Defect |
36 |
0.532 |
|
717 |
|
c
|
MJR022 |
Major Affective Disorder 8 |
38 |
0.532 |
|
718 |
|
|
PYR012 |
Pyruvate Dehydrogenase E1-Beta Deficiency |
41 |
0.532 |
|
719 |
|
|
LMB062 |
Limb Ischemia |
55 |
0.532 |
|
720 |
|
|
TND005 |
Tendinitis |
54 |
0.532 |
|
721 |
|
|
PYR010 |
Peyronie's Disease |
50 |
0.532 |
|
722 |
|
P
|
ERY036 |
Erythema Nodosum |
49 |
0.532 |
|
723 |
|
c
|
ATS007 |
Autism Spectrum Disorder |
72 |
0.532 |
|
724 |
|
P
|
PLY014 |
Polycystic Kidney Disease |
69 |
0.532 |
|
725 |
|
P
|
BLY001 |
B-Lymphoblastic Leukemia/lymphoma |
52 |
0.532 |
|
726 |
|
|
APH002 |
Aphasia |
56 |
0.532 |
|
727 |
|
|
ILT001 |
Ileitis |
48 |
0.532 |
|
728 |
|
|
HPT046 |
Hepatic Veno-Occlusive Disease |
62 |
0.532 |
|
729 |
|
c
|
ATM022 |
Autoimmune Myocarditis |
36 |
0.532 |
|
730 |
|
P
|
3MT016 |
3-Methylglutaconic Aciduria, Type Iii |
68 |
0.532 |
|
731 |
|
|
NRL016 |
Neural Tube Defects |
81 |
0.532 |
|
732 |
|
c
|
DPH024 |
Diaphragmatic Hernia, Congenital |
64 |
0.532 |
|
733 |
|
|
PRP001 |
Propionic Acidemia |
65 |
0.532 |
|
734 |
|
|
DBT084 |
Diabetes Mellitus, Ketosis-Prone |
60 |
0.532 |
|
735 |
|
c
|
MJR024 |
Major Affective Disorder 9 |
41 |
0.532 |
|
736 |
|
c
|
CHL119 |
Cholangitis, Primary Sclerosing |
58 |
0.532 |
|
737 |
|
|
PRL045 |
Proline-Negative Auxotroph of Hamster, Complementation of |
16 |
0.532 |
|
738 |
|
c
|
THY109 |
Thyroid Cancer, Nonmedullary, 1 |
55 |
0.532 |
|
739 |
|
P
|
SPP010 |
Suppressor of Tumorigenicity 3 |
51 |
0.532 |
|
740 |
|
c
|
PYL018 |
Pyloric Stenosis, Infantile Hypertrophic, 1 |
35 |
0.532 |
|
741 |
|
P
|
STR020 |
Strabismus |
56 |
0.532 |
|
742 |
|
P
|
UNC017 |
Uncombable Hair Syndrome 1 |
32 |
0.532 |
|
743 |
|
P
|
ATT013 |
Attention Deficit-Hyperactivity Disorder |
64 |
0.532 |
|
744 |
|
P
|
CRC039 |
Coarctation of Aorta |
46 |
0.532 |
|
745 |
|
|
DNB001 |
Danubian Endemic Familial Nephropathy |
41 |
0.532 |
|
746 |
|
|
MYL057 |
Myelopathy, Htlv-1-Associated |
38 |
0.532 |
|
747 |
|
|
HND015 |
Hand Skill, Relative |
30 |
0.532 |
|
748 |
|
P
|
HRS035 |
Hirschsprung Disease 1 |
66 |
0.532 |
|
749 |
|
|
AMY087 |
Amyloidosis, Hereditary, Transthyretin-Related |
65 |
0.532 |
|
750 |
|
|
PLM124 |
Pulmonary Hypertension, Neonatal |
20 |
0.532 |
|
751 |
|
|
OST017 |
Osteomyelitis |
63 |
0.532 |
|
752 |
|
P
|
PLY188 |
Polyendocrinopathy |
31 |
0.532 |
|
753 |
|
|
PMP014 |
Pemphigoid |
51 |
0.532 |
|
754 |
|
P
|
MYP006 |
Myopia |
56 |
0.532 |
|
755 |
|
P
|
LCH002 |
Lichen Planus |
54 |
0.532 |
|
756 |
|
|
INT075 |
Intracranial Hypertension |
53 |
0.532 |
|
757 |
|
|
ACH005 |
Achalasia |
55 |
0.532 |
|
758 |
|
|
MCH006 |
Mechanical Strabismus |
40 |
0.532 |
|
759 |
|
|
KRT006 |
Keratoconjunctivitis |
53 |
0.532 |
|
760 |
|
P
|
MTC133 |
Mitochondrial Myopathy |
50 |
0.532 |
|
761 |
|
|
DBT010 |
Diabetic Neuropathy |
54 |
0.532 |
|
762 |
|
P
|
RRH023 |
Rare Hereditary Hemochromatosis |
54 |
0.532 |
|
763 |
|
P
|
ALC033 |
Alcohol Use Disorder |
61 |
0.532 |
|
764 |
|
P
|
PTT006 |
Pituitary Adenoma |
55 |
0.532 |
|
765 |
|
P
|
BPL003 |
Bipolar Disorder |
56 |
0.532 |
|
766 |
|
P
|
FBR017 |
Fibrosarcoma |
56 |
0.532 |
|
767 |
|
P
|
MST009 |
Mastocytosis |
64 |
0.532 |
|
768 |
|
|
PNM008 |
Pneumothorax |
54 |
0.532 |
|
769 |
|
|
CRV038 |
Cervical Squamous Cell Carcinoma |
58 |
0.532 |
|
770 |
|
P
|
SYP003 |
Syphilis |
59 |
0.532 |
|
771 |
|
|
HRT012 |
Heart Valve Disease |
53 |
0.532 |
|
772 |
|
P
|
NLD001 |
Nail Disease |
51 |
0.532 |
|
773 |
|
c
|
VRL007 |
Viral Encephalitis |
50 |
0.532 |
|
774 |
|
P
|
INF038 |
Influenza |
68 |
0.532 |
|
775 |
|
|
BLL006 |
Bullous Pemphigoid |
61 |
0.532 |
|
776 |
|
P
|
MMB011 |
Membranous Nephropathy |
50 |
0.532 |
|
777 |
|
P
|
CRN024 |
Corneal Disease |
44 |
0.532 |
|
778 |
|
|
NSP002 |
Nasopharyngitis |
45 |
0.532 |
|
779 |
|
c
|
ATM104 |
Autoimmune Vasculitis |
37 |
0.532 |
|
780 |
|
|
INT060 |
Intestinal Atresia |
41 |
0.532 |
|
781 |
|
P
|
HYP061 |
Hypertrophic Cardiomyopathy |
69 |
0.532 |
|
782 |
|
|
GTR002 |
Goiter |
53 |
0.532 |
|
783 |
|
|
TRN015 |
Transient Cerebral Ischemia |
63 |
0.532 |
|
784 |
|
P
|
PST095 |
Post-Thrombotic Syndrome |
51 |
0.532 |
|
785 |
|
|
RLP002 |
Relapsing-Remitting Multiple Sclerosis |
56 |
0.532 |
|
786 |
|
P
|
SCL009 |
Sclerosing Cholangitis |
48 |
0.532 |
|
787 |
|
|
NRT004 |
Neuritis |
53 |
0.532 |
|
788 |
|
|
HYP072 |
Hypersensitivity Reaction Type Iii Disease |
39 |
0.532 |
|
789 |
|
|
KRT009 |
Keratosis |
53 |
0.532 |
|
790 |
|
|
GLS001 |
Gliosarcoma |
64 |
0.532 |
|
791 |
|
|
PPL018 |
Papillary Adenocarcinoma |
44 |
0.532 |
|
792 |
|
P
|
INT143 |
Interstitial Cystitis |
60 |
0.532 |
|
793 |
|
|
PRS036 |
Parasitic Protozoa Infectious Disease |
44 |
0.532 |
|
794 |
|
|
HPT014 |
Hepatorenal Syndrome |
49 |
0.532 |
|
795 |
|
P
|
THR005 |
Thrombotic Thrombocytopenic Purpura |
64 |
0.532 |
|
796 |
|
P
|
BND020 |
Bone Disease |
59 |
0.532 |
|
797 |
|
|
PLP001 |
Pulpitis |
48 |
0.532 |
|
798 |
|
|
CHL123 |
Chlamydia |
58 |
0.532 |
|
799 |
|
P
|
CHN059 |
Chondrocalcinosis |
52 |
0.532 |
|
800 |
|
c
|
VRL005 |
Viral Pneumonia |
53 |
0.532 |
|
801 |
|
|
HMN014 |
Human Immunodeficiency Virus Infectious Disease |
54 |
0.532 |
|
802 |
|
|
OST016 |
Osteochondrosis |
52 |
0.532 |
|
803 |
|
|
BRS099 |
Breast Ductal Carcinoma |
61 |
0.532 |
|
804 |
|
|
CYS009 |
Cystadenoma |
43 |
0.532 |
|
805 |
|
|
ACR005 |
Acrodermatitis |
38 |
0.532 |
|
806 |
|
P
|
THY023 |
Thymoma |
64 |
0.532 |
|
807 |
|
c
|
CNT035 |
Central Nervous System Disease |
54 |
0.532 |
|
808 |
|
|
MDD011 |
Mood Disorder |
62 |
0.532 |
|
809 |
|
|
DRM006 |
Dermatitis |
62 |
0.532 |
|
810 |
|
|
TRP002 |
Tropical Spastic Paraparesis |
49 |
0.532 |
|
811 |
|
|
TYP007 |
Typhoid Fever |
64 |
0.532 |
|
812 |
|
P
|
GND004 |
Gonadal Dysgenesis |
47 |
0.532 |
|
813 |
|
|
EXC002 |
Exocrine Pancreatic Insufficiency |
42 |
0.532 |
|
814 |
|
|
FML035 |
Familial Hyperlipidemia |
55 |
0.532 |
|
815 |
|
|
MGC001 |
Megacolon |
48 |
0.532 |
|
816 |
|
|
AMN003 |
Amnestic Disorder |
54 |
0.532 |
|
817 |
|
|
QDR001 |
Quadriplegia |
50 |
0.532 |
|
818 |
|
|
HYP014 |
Hyperuricemia |
51 |
0.532 |
|
819 |
|
|
HYP080 |
Hypogonadism |
50 |
0.532 |
|
820 |
|
|
HST011 |
Histoplasmosis |
55 |
0.532 |
|
821 |
|
|
PST028 |
Post-Traumatic Stress Disorder |
59 |
0.532 |
|
822 |
|
|
NCR007 |
Necrotizing Fasciitis |
49 |
0.532 |
|
823 |
|
|
HYP141 |
Hyperphenylalaninemia |
42 |
0.532 |
|
824 |
|
P
|
INS002 |
in Situ Carcinoma |
53 |
0.532 |
|
825 |
|
|
FSC004 |
Fasciitis |
49 |
0.532 |
|
826 |
|
P
|
TXP001 |
Toxoplasmosis |
60 |
0.532 |
|
827 |
|
|
STM007 |
Stomatitis |
54 |
0.532 |
|
828 |
|
|
HTL001 |
Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis |
38 |
0.532 |
|
829 |
|
|
MST020 |
Mast Cell Activation Syndrome |
28 |
0.532 |
|
830 |
|
|
TRC096 |
Trichothiodystrophy |
55 |
0.532 |
|
831 |
|
|
HDN002 |
Head Injury |
44 |
0.532 |
|
832 |
|
|
MCR225 |
Macrophage Activation Syndrome |
45 |
0.532 |
|
833 |
|
c
|
ATM075 |
Autoimmune Encephalitis |
40 |
0.532 |
|
834 |
|
|
ENT007 |
Enteropathica |
25 |
0.532 |
|
835 |
|
P
|
NRV007 |
Nervous System Disease |
67 |
0.532 |
|
836 |
|
c
|
HMN021 |
Human T-Cell Leukemia Virus Type 1 |
47 |
0.532 |
|
837 |
|
|
MTT004 |
Metatarsus Adductus |
17 |
0.532 |
|
838 |
|
|
ATN011 |
Autoinflammation with Infantile Enterocolitis |
45 |
0.496 |
|
839 |
|
|
RSP019 |
Respiratory Distress Syndrome in Premature Infants |
52 |
0.496 |
|
840 |
|
P
|
ANR048 |
Aniridia 1 |
64 |
0.496 |
|
841 |
|
|
CHR661 |
Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction |
49 |
0.496 |
|
842 |
|
c
|
DRR009 |
Diarrhea 6 |
45 |
0.496 |
|
843 |
|
|
TRP004 |
Tropical Sprue |
39 |
0.496 |
|
844 |
|
|
ENT001 |
Enterocele |
42 |
0.496 |
|
845 |
|
P
|
CMP008 |
Compartment Syndrome |
50 |
0.496 |
|
846 |
|
P
|
CLL015 |
Collagen Disease |
48 |
0.496 |
|
847 |
|
|
RSP007 |
Respiratory Distress Syndrome, Infant |
40 |
0.496 |
|
848 |
|
|
DDN006 |
Duodenitis |
50 |
0.496 |
|
849 |
|
c
|
ATS392 |
Autosomal Recessive Cutis Laxa Type Iii |
48 |
0.472 |
|
850 |
|
|
GRN020 |
Granulomatous Hypophysitis |
14 |
0.472 |
|
851 |
|
|
DMN042 |
Diaminopentanuria |
14 |
0.376 |
|
852 |
|
|
RNL024 |
Renal Glucosuria |
60 |
0.376 |
|
853 |
|
|
CLF004 |
Cleft Lip/palate |
57 |
0.376 |
|
854 |
|
|
NNT033 |
Neonatal Hypoxic and Ischemic Brain Injury |
42 |
0.376 |
|
855 |
|
|
PCH007 |
Pouchitis |
42 |
0.376 |
|
856 |
|
P
|
NNT042 |
Neonatal Lupus Erythematosus |
37 |
0.376 |
|
857 |
|
|
ERY014 |
Erythrokeratoderma |
26 |
0.376 |
|
858 |
|
|
MTR087 |
Maternal Uniparental Disomy |
28 |
0.376 |
|
859 |
|
P
|
HRD217 |
Hereditary Optic Neuropathy |
36 |
0.376 |
|
860 |
|
|
GRN033 |
Granulomatous Mastitis |
32 |
0.376 |
|
861 |
|
c
|
INH030 |
Inherited Retinal Disorder |
28 |
0.376 |
|
862 |
|
|
SMT007 |
Smith-Fineman-Myers Syndrome |
32 |
0.376 |
|
863 |
|
|
THP001 |
Thiopurine S Methyltranferase Deficiency |
20 |
0.376 |
|
864 |
|
P
|
THL005 |
Thalassemia |
56 |
0.376 |
|
865 |
|
|
SDD008 |
Sudden Sensorineural Hearing Loss |
41 |
0.376 |
|
866 |
|
|
CNG491 |
Congenital Portosystemic Shunt |
17 |
0.376 |
|
867 |
|
|
PFF001 |
Pfeiffer Syndrome |
77 |
0.376 |
|
868 |
|
c
|
LKM056 |
Leukemia, Chronic Lymphocytic 2 |
48 |
0.376 |
|
869 |
|
P
|
NSP012 |
Nasopharyngeal Carcinoma |
61 |
0.376 |
|
870 |
|
c
|
CRD186 |
Ceroid Lipofuscinosis, Neuronal, 3 |
63 |
0.376 |
|
871 |
|
|
FMR004 |
Fumarase Deficiency |
50 |
0.376 |
|
872 |
|
c
|
DRM040 |
Dermatitis Herpetiformis, Familial |
35 |
0.376 |
|
873 |
|
|
BRT054 |
Brittle Bone Disorder |
74 |
0.376 |
|
874 |
|
|
LPM012 |
Lipomatosis, Multiple |
60 |
0.376 |
|
875 |
|
P
|
MCR364 |
Macrodactyly |
40 |
0.376 |
|
876 |
|
|
PRL019 |
Prolidase Deficiency |
50 |
0.376 |
|
877 |
|
|
CRD002 |
Cri-Du-Chat Syndrome |
49 |
0.376 |
|
878 |
|
|
EPD002 |
Epidermolytic Hyperkeratosis |
56 |
0.376 |
|
879 |
|
|
GST092 |
Gastroesophageal Reflux |
61 |
0.376 |
|
880 |
|
|
VLV047 |
Volvulus of Midgut |
52 |
0.376 |
|
881 |
|
P
|
PTY003 |
Pityriasis Rubra Pilaris |
57 |
0.376 |
|
882 |
|
|
PRG071 |
Progressive Pseudorheumatoid Dysplasia |
45 |
0.376 |
|
883 |
|
c
|
FNC027 |
Fanconi Anemia, Complementation Group a |
81 |
0.376 |
|
884 |
|
|
ISV001 |
Isovaleric Acidemia |
54 |
0.376 |
|
885 |
|
|
HYP001 |
Hypochromic Microcytic Anemia |
37 |
0.376 |
|
886 |
|
|
FTL006 |
Fetal Alcohol Spectrum Disorder |
43 |
0.376 |
|
887 |
|
|
MNT001 |
Mantle Cell Lymphoma |
67 |
0.376 |
|
888 |
|
|
MYL009 |
Myelodysplastic Syndrome |
67 |
0.376 |
|
889 |
|
|
BTN004 |
Biotin Deficiency |
45 |
0.376 |
|
890 |
|
|
HYP346 |
Hypotrichosis and Recurrent Skin Vesicles |
29 |
0.376 |
|
891 |
|
|
NRN005 |
Neuronal Ceroid-Lipofuscinoses |
61 |
0.376 |
|
892 |
|
|
KSH004 |
Kashin-Beck Disease |
38 |
0.376 |
|
893 |
|
|
IGG007 |
Igg4-Related Disease |
48 |
0.376 |
|
894 |
|
|
ART074 |
Aortic Dissection |
53 |
0.376 |
|
895 |
|
|
C1N001 |
C1 Inhibitor Deficiency |
43 |
0.376 |
|
896 |
|
|
APR001 |
Apraxia |
52 |
0.376 |
|
897 |
|
P
|
ATR011 |
Atrial Fibrillation |
66 |
0.376 |
|
898 |
|
|
RSP021 |
Respiratory Allergy |
41 |
0.376 |
|
899 |
|
P
|
LYM033 |
Lymphoproliferative Syndrome |
59 |
0.376 |
|
900 |
|
|
INT072 |
Intestinal Pseudo-Obstruction |
62 |
0.376 |
|
901 |
|
|
HYP025 |
Hyperphosphatemia |
48 |
0.376 |
|
902 |
|
P
|
BRC006 |
Brachydactyly |
51 |
0.376 |
|
903 |
|
|
LMB024 |
Limbic Encephalitis |
43 |
0.376 |
|
904 |
|
c
|
RTN041 |
Retinitis Pigmentosa 11 |
42 |
0.376 |
|
905 |
|
P
|
FNC044 |
Fanconi Anemia, Complementation Group C |
56 |
0.376 |
|
906 |
|
c
|
FNC042 |
Fanconi Anemia, Complementation Group D2 |
54 |
0.376 |
|
907 |
|
|
GLT014 |
Glutathionuria |
37 |
0.376 |
|
908 |
|
|
GDP001 |
Goodpasture Syndrome |
55 |
0.376 |
|
909 |
|
|
TRD006 |
Tardive Dyskinesia |
53 |
0.376 |
|
910 |
|
c
|
GRV008 |
Graves Disease 1 |
54 |
0.376 |
|
911 |
|
|
CHR288 |
Chronic Recurrent Multifocal Osteomyelitis |
60 |
0.376 |
|
912 |
|
c
|
CHR627 |
Charcot-Marie-Tooth Disease, Demyelinating, Type 1a |
56 |
0.376 |
|
913 |
|
c
|
CHR320 |
Chiari Malformation Type I |
46 |
0.376 |
|
914 |
|
|
ICH001 |
Ichthyosis Vulgaris |
53 |
0.376 |
|
915 |
|
|
SPN019 |
Spondylolisthesis |
52 |
0.376 |
|
916 |
|
P
|
PRD006 |
Prader-Willi Syndrome |
61 |
0.376 |
|
917 |
|
c
|
VNT034 |
Ventricular Fibrillation, Paroxysmal Familial, 1 |
67 |
0.376 |
|
918 |
|
|
LGH019 |
Light Fixation Seizure Syndrome |
27 |
0.376 |
|
919 |
|
|
LNG108 |
Langerhans Cell Histiocytosis |
58 |
0.376 |
|
920 |
|
|
BLD063 |
Bile Duct Cysts |
42 |
0.376 |
|
921 |
|
|
CNG510 |
Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi |
63 |
0.376 |
|
922 |
|
|
AKL001 |
Au-Kline Syndrome |
39 |
0.376 |
|
923 |
|
|
SPS204 |
Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity |
44 |
0.376 |
|
924 |
|
|
EWN003 |
Ewing Sarcoma |
70 |
0.376 |
|
925 |
|
|
TMP012 |
Temple Syndrome |
38 |
0.376 |
|
926 |
|
|
ACT119 |
Acute Promyelocytic Leukemia |
62 |
0.376 |
|
927 |
|
|
MTC068 |
Mitochondrial Complex V Deficiency, Nuclear Type 2 |
31 |
0.376 |
|
928 |
|
c
|
SYS040 |
Systemic Lupus Erythematosus 10 |
22 |
0.376 |
|
929 |
|
|
SCC002 |
Saccharopinuria |
26 |
0.376 |
|
930 |
|
c
|
ANM035 |
Anemia, Hypochromic Microcytic, with Iron Overload 1 |
36 |
0.376 |
|
931 |
|
|
LBR038 |
Leber Hereditary Optic Neuropathy, Modifier of |
62 |
0.376 |
|
932 |
|
P
|
ART106 |
Arterial Calcification, Generalized, of Infancy, 1 |
48 |
0.376 |
|
933 |
|
P
|
HRT035 |
Heart Block, Congenital |
43 |
0.376 |
|
934 |
|
c
|
PLM167 |
Pulmonary Venoocclusive Disease 2, Autosomal Recessive |
38 |
0.376 |
|
935 |
|
P
|
HYP058 |
Hypervitaminosis a |
47 |
0.376 |
|
936 |
|
|
INT303 |
Intracranial Hypertension, Idiopathic |
56 |
0.376 |
|
937 |
|
|
LRN002 |
Laron Syndrome |
63 |
0.376 |
|
938 |
|
|
THR100 |
Thrombocytopenic Purpura, Autoimmune |
61 |
0.376 |
|
939 |
|
P
|
PLM085 |
Pulmonary Hemosiderosis |
44 |
0.376 |
|
940 |
|
P
|
MJR007 |
Major Affective Disorder 1 |
42 |
0.376 |
|
941 |
|
|
INC002 |
Inclusion Body Myositis |
57 |
0.376 |
|
942 |
|
|
CMP040 |
Complement Component 4, Partial Deficiency of |
34 |
0.376 |
|
943 |
|
|
OPT066 |
Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy |
55 |
0.376 |
|
944 |
|
|
DMN031 |
Dementia, Lewy Body |
65 |
0.376 |
|
945 |
|
|
DYS053 |
Dystelephalangy |
14 |
0.376 |
|
946 |
|
P
|
PYR039 |
Peyronie Disease |
39 |
0.376 |
|
947 |
|
P
|
MYP105 |
Myopathy, Myosin Storage, Autosomal Dominant |
40 |
0.376 |
|
948 |
|
c
|
SYS069 |
Systemic Lupus Erythematosus 6 |
21 |
0.376 |
|
949 |
|