# |
|
Family |
MCID |
Name |
MIFTS |
Score |
1 |
|
P
|
PRS040 |
Prostate Cancer |
95 |
49.298 |
|
2 |
|
|
EWN003 |
Ewing Sarcoma |
70 |
41.052 |
|
3 |
|
P
|
LKM002 |
Leukemia |
67 |
29.932 |
|
4 |
|
P
|
MYL006 |
Myeloid Leukemia |
61 |
29.638 |
|
5 |
|
|
SRC014 |
Sarcoma |
65 |
26.962 |
|
6 |
|
|
NRR001 |
Neuroretinitis |
42 |
18.591 |
|
7 |
|
|
RTN023 |
Retinitis |
46 |
18.591 |
|
8 |
|
P
|
RTN008 |
Retinitis Pigmentosa |
80 |
17.912 |
|
9 |
|
P
|
RTN016 |
Retinal Degeneration |
52 |
16.377 |
|
10 |
|
|
YMN001 |
Yemenite Deaf-Blind Hypopigmentation Syndrome |
66 |
16.138 |
|
11 |
|
|
MYX005 |
Myxoid Liposarcoma |
65 |
14.504 |
|
12 |
|
P
|
NGH001 |
Night Blindness |
52 |
14.412 |
|
13 |
|
P
|
RTN018 |
Retinal Disease |
53 |
13.325 |
|
14 |
|
c
|
MCR115 |
Microvascular Complications of Diabetes 5 |
65 |
12.714 |
|
15 |
|
c
|
RTN035 |
Retinal Cone Dystrophy 3b |
32 |
12.472 |
|
16 |
|
|
PRS006 |
Prostatic Acinar Adenocarcinoma |
25 |
11.782 |
|
17 |
|
P
|
CNG010 |
Congenital Stationary Night Blindness |
56 |
11.773 |
|
18 |
|
c
|
LKM061 |
Leukemia, Acute Myeloid |
83 |
11.615 |
|
19 |
|
c
|
MCL042 |
Macular Degeneration, Age-Related, 1 |
85 |
11.150 |
|
20 |
|
P
|
CND005 |
Cone Dystrophy |
47 |
9.986 |
|
21 |
|
|
INT323 |
Intraocular Pressure Quantitative Trait Locus |
64 |
9.883 |
|
22 |
|
|
RTN017 |
Retinal Detachment |
60 |
9.616 |
|
23 |
|
c
|
NRF024 |
Neurofibromatosis, Type I |
72 |
9.599 |
|
24 |
|
P
|
RTN209 |
Retinoschisis 1, X-Linked, Juvenile |
60 |
9.513 |
|
|
26 |
|
|
PTH003 |
Pathologic Nystagmus |
52 |
8.952 |
|
27 |
|
P
|
JVN042 |
Juvenile Retinoschisis |
39 |
8.702 |
|
28 |
|
P
|
MYP006 |
Myopia |
56 |
8.157 |
|
29 |
|
|
SPN035 |
Spindle Cell Sarcoma |
54 |
8.086 |
|
30 |
|
P
|
CNR004 |
Cone-Rod Dystrophy 2 |
74 |
7.868 |
|
31 |
|
P
|
LKM062 |
Leukemia, Acute Lymphoblastic |
69 |
7.778 |
|
32 |
|
|
SCT002 |
Scotoma |
42 |
7.763 |
|
33 |
|
|
RTN003 |
Retinal Ischemia |
49 |
7.728 |
|
34 |
|
c
|
INH030 |
Inherited Retinal Disorder |
28 |
7.359 |
|
35 |
|
|
FND002 |
Fundus Dystrophy |
55 |
7.338 |
|
36 |
|
P
|
RTN022 |
Retinal Vein Occlusion |
54 |
7.027 |
|
37 |
|
|
CNT016 |
Central Retinal Vein Occlusion |
54 |
6.982 |
|
38 |
|
|
XLN247 |
X-Linked Congenital Retinoschisis |
20 |
6.790 |
|
39 |
|
|
MCL006 |
Macular Retinal Edema |
57 |
6.779 |
|
40 |
|
P
|
OPT006 |
Optic Nerve Disease |
58 |
6.774 |
|
41 |
|
P
|
3MT016 |
3-Methylglutaconic Aciduria, Type Iii |
68 |
6.754 |
|
42 |
|
P
|
ACH003 |
Achromatopsia |
62 |
6.691 |
|
43 |
|
P
|
ADN016 |
Adenocarcinoma |
63 |
6.664 |
|
44 |
|
P
|
UVT001 |
Uveitis |
57 |
6.475 |
|
45 |
|
c
|
ACT073 |
Acute Leukemia |
58 |
6.469 |
|
46 |
|
|
RFR003 |
Refractive Error |
41 |
6.246 |
|
47 |
|
|
OCL006 |
Ocular Hypertension |
53 |
6.244 |
|
48 |
|
P
|
LNG032 |
Lung Cancer |
98 |
6.241 |
|
49 |
|
P
|
CTR002 |
Cataract |
60 |
6.041 |
|
50 |
|
P
|
MSC005 |
Muscular Dystrophy |
67 |
5.945 |
|
51 |
|
P
|
OPN001 |
Open-Angle Glaucoma |
55 |
5.934 |
|
52 |
|
|
DWN001 |
Down Syndrome |
70 |
5.910 |
|
53 |
|
|
SPP007 |
Suppression Amblyopia |
38 |
5.756 |
|
54 |
|
|
AMB002 |
Amblyopia |
50 |
5.756 |
|
55 |
|
|
NRT004 |
Neuritis |
53 |
5.750 |
|
56 |
|
P
|
OGC005 |
Oguchi Disease |
45 |
5.748 |
|
57 |
|
|
PRC049 |
Precursor T-Cell Acute Lymphoblastic Leukemia |
45 |
5.737 |
|
58 |
|
|
SPP011 |
Suppression of Tumorigenicity 12 |
61 |
5.554 |
|
59 |
|
c
|
NGH029 |
Night Blindness, Congenital Stationary, Type 1e |
37 |
5.530 |
|
60 |
|
P
|
STR022 |
Stargardt Disease |
61 |
5.528 |
|
61 |
|
|
SML031 |
Small Cell Carcinoma of the Bladder |
46 |
5.493 |
|
62 |
|
|
RTN020 |
Retinal Vascular Disease |
46 |
5.485 |
|
63 |
|
|
OCC002 |
Occult Macular Dystrophy |
46 |
5.430 |
|
64 |
|
|
LBR036 |
Leber Plus Disease |
66 |
5.345 |
|
65 |
|
P
|
OPT009 |
Optic Neuritis |
57 |
5.327 |
|
66 |
|
|
MSC157 |
Muscular Dystrophy, Duchenne Type |
79 |
5.325 |
|
67 |
|
|
KRT002 |
Keratomalacia |
55 |
5.319 |
|
68 |
|
P
|
RTN024 |
Retinoblastoma |
73 |
5.318 |
|
69 |
|
P
|
GST053 |
Gastric Cancer |
83 |
5.263 |
|
70 |
|
|
ENH001 |
Enhanced S-Cone Syndrome |
58 |
5.245 |
|
71 |
|
|
FND001 |
Fundus Albipunctatus |
55 |
5.182 |
|
72 |
|
|
PRS045 |
Prostatic Hypertrophy |
53 |
5.150 |
|
73 |
|
P
|
BLD134 |
Bladder Cancer |
79 |
5.117 |
|
74 |
|
c
|
EXD008 |
Exudative Vitreoretinopathy 1 |
71 |
5.016 |
|
75 |
|
P
|
USH001 |
Usher Syndrome |
64 |
4.999 |
|
76 |
|
|
MCL003 |
Macular Holes |
44 |
4.993 |
|
77 |
|
P
|
EYD002 |
Eye Disease |
57 |
4.984 |
|
78 |
|
P
|
SML001 |
Small Cell Carcinoma |
52 |
4.976 |
|
79 |
|
|
PRS021 |
Prostatic Adenoma |
43 |
4.913 |
|
80 |
|
P
|
RTN014 |
Retinal Artery Occlusion |
47 |
4.889 |
|
81 |
|
|
BRN026 |
Branch Retinal Artery Occlusion |
41 |
4.889 |
|
82 |
|
|
MLN046 |
Melanoma-Associated Retinopathy |
24 |
4.757 |
|
83 |
|
|
RTN187 |
Retinitis Pigmentosa-Deafness Syndrome |
48 |
4.754 |
|
84 |
|
|
ANG020 |
Angiosarcoma |
64 |
4.742 |
|
85 |
|
|
END057 |
Endometrial Cancer |
72 |
4.737 |
|
86 |
|
|
47X002 |
47,xyy |
48 |
4.672 |
|
87 |
|
|
CHR178 |
Chromosomal Triplication |
34 |
4.625 |
|
88 |
|
P
|
LNG028 |
Long Qt Syndrome |
64 |
4.620 |
|
89 |
|
P
|
NRP001 |
Neuropathy |
60 |
4.504 |
|
90 |
|
|
CNC014 |
Cancer-Associated Retinopathy |
42 |
4.469 |
|
91 |
|
|
CYT019 |
Cytogenetically Normal Acute Myeloid Leukemia |
30 |
4.424 |
|
92 |
|
P
|
MCR129 |
Microvascular Complications of Diabetes 1 |
68 |
4.422 |
|
93 |
|
c
|
MCR112 |
Microvascular Complications of Diabetes 2 |
42 |
4.422 |
|
94 |
|
P
|
END047 |
Endophthalmitis |
53 |
4.408 |
|
95 |
|
|
BST008 |
Bestrophinopathy, Autosomal Recessive |
46 |
4.377 |
|
96 |
|
|
CNT028 |
Central Retinal Artery Occlusion |
43 |
4.356 |
|
97 |
|
|
PRS129 |
Prostatic Hyperplasia, Benign |
49 |
4.255 |
|
98 |
|
|
MNN043 |
Meningioma, Familial |
79 |
4.108 |
|
99 |
|
|
ALB002 |
Albinism |
47 |
4.008 |
|
100 |
|
|
OPT070 |
Optic Nerve Hypoplasia, Bilateral |
56 |
3.976 |
|
101 |
|
|
GST040 |
Gastric Adenocarcinoma |
67 |
3.875 |
|
102 |
|
P
|
LNG064 |
Lung Cancer Susceptibility 3 |
70 |
3.875 |
|
103 |
|
|
ADN011 |
Adenoid Cystic Carcinoma |
68 |
3.863 |
|
104 |
|
P
|
LPS002 |
Liposarcoma |
64 |
3.834 |
|
105 |
|
c
|
GLC092 |
Glaucoma, Primary Open Angle |
62 |
3.830 |
|
106 |
|
|
BRD025 |
Birdshot Chorioretinopathy |
48 |
3.810 |
|
107 |
|
|
SVR004 |
Severe Combined Immunodeficiency |
72 |
3.807 |
|
108 |
|
c
|
OGC001 |
Oguchi Disease 1 |
39 |
3.740 |
|
109 |
|
P
|
CNG024 |
Congenital Nystagmus |
36 |
3.696 |
|
110 |
|
|
GST103 |
Gastric Cancer, Hereditary Diffuse |
68 |
3.689 |
|
111 |
|
P
|
OVR042 |
Ovarian Cancer |
88 |
3.629 |
|
112 |
|
|
CHR081 |
Choroideremia |
58 |
3.568 |
|
113 |
|
|
ATM076 |
Autoimmune Retinopathy |
27 |
3.564 |
|
114 |
|
|
ISC004 |
Ischemia |
61 |
3.561 |
|
115 |
|
c
|
CRD186 |
Ceroid Lipofuscinosis, Neuronal, 3 |
63 |
3.559 |
|
116 |
|
P
|
EPT012 |
Epithelioid Sarcoma |
41 |
3.557 |
|
117 |
|
P
|
SCH015 |
Schizophrenia |
74 |
3.550 |
|
118 |
|
|
ATX038 |
Ataxia and Polyneuropathy, Adult-Onset |
46 |
3.548 |
|
119 |
|
P
|
LYM118 |
Lymphoma |
67 |
3.521 |
|
120 |
|
|
HYP066 |
Hyperglycemia |
61 |
3.499 |
|
121 |
|
|
GLM045 |
Glioma |
63 |
3.495 |
|
122 |
|
P
|
NRN021 |
Neuronal Ceroid Lipofuscinosis |
65 |
3.474 |
|
123 |
|
|
KHN001 |
Kuhnt-Junius Degeneration |
48 |
3.473 |
|
124 |
|
|
ACT250 |
Acute Megakaryocytic Leukemia |
60 |
3.457 |
|
125 |
|
|
DBT006 |
Diabetic Macular Edema |
48 |
3.401 |
|
126 |
|
|
HYP266 |
Hypoxia |
57 |
3.398 |
|
127 |
|
P
|
VTL001 |
Vitelliform Macular Dystrophy |
46 |
3.364 |
|
128 |
|
P
|
STR020 |
Strabismus |
56 |
3.361 |
|
129 |
|
|
MCH006 |
Mechanical Strabismus |
40 |
3.361 |
|
130 |
|
|
SKN019 |
Skin Melanoma |
71 |
3.358 |
|
131 |
|
P
|
GLM040 |
Glioma Susceptibility 1 |
71 |
3.351 |
|
132 |
|
P
|
MLT020 |
Multiple Sclerosis |
79 |
3.317 |
|
133 |
|
P
|
CLR019 |
Color Blindness |
48 |
3.317 |
|
134 |
|
|
OST159 |
Osteogenic Sarcoma |
66 |
3.313 |
|
135 |
|
|
MSN004 |
Mesenchymal Cell Neoplasm |
42 |
3.306 |
|
136 |
|
P
|
VTR007 |
Vitreoretinopathy |
46 |
3.292 |
|
137 |
|
c
|
PCH010 |
Pachyonychia Congenita 3 |
43 |
3.279 |
|
138 |
|
P
|
SDR002 |
Siderosis |
43 |
3.279 |
|
139 |
|
|
RPD005 |
Rapidly Involuting Congenital Hemangioma |
46 |
3.197 |
|
140 |
|
|
HMN016 |
Hemangioendothelioma |
34 |
3.184 |
|
141 |
|
|
PPL052 |
Papillomatosis, Confluent and Reticulated |
34 |
3.183 |
|
142 |
|
|
BCK003 |
Background Diabetic Retinopathy |
47 |
3.173 |
|
143 |
|
|
ACT098 |
Acute Erythroid Leukemia |
55 |
3.148 |
|
144 |
|
|
MSC152 |
Muscular Dystrophy, Becker Type |
69 |
3.148 |
|
145 |
|
|
SML009 |
Small Intestine Adenocarcinoma |
57 |
3.144 |
|
146 |
|
P
|
BRS047 |
Breast Cancer |
98 |
3.097 |
|
147 |
|
c
|
STR084 |
Stargardt Disease 1 |
53 |
3.067 |
|
148 |
|
|
XLN012 |
X-Linked Congenital Stationary Night Blindness |
28 |
3.067 |
|
149 |
|
|
FST001 |
Foster-Kennedy Syndrome |
39 |
3.066 |
|
150 |
|
|
ACT120 |
Acute Zonal Occult Outer Retinopathy |
24 |
3.059 |
|
151 |
|
|
AGN016 |
Aging |
54 |
3.054 |
|
152 |
|
|
AST006 |
Astigmatism |
47 |
3.044 |
|
153 |
|
|
CHL152 |
Childhood Acute Lymphocytic Leukemia |
50 |
3.024 |
|
154 |
|
P
|
BRD002 |
Bardet-Biedl Syndrome |
66 |
3.019 |
|
155 |
|
|
CLR033 |
Color Vision Deficiency |
40 |
3.019 |
|
156 |
|
|
LNG039 |
Lung Squamous Cell Carcinoma |
57 |
3.004 |
|
157 |
|
|
CLN015 |
Colon Adenocarcinoma |
65 |
2.973 |
|
158 |
|
|
PTT037 |
Pituitary Tumors |
44 |
2.952 |
|
159 |
|
|
ATS010 |
Autosomal Recessive Disease |
42 |
2.920 |
|
160 |
|
|
RNL114 |
Renal Cell Carcinoma, Nonpapillary |
80 |
2.906 |
|
161 |
|
|
CNT060 |
Central Serous Chorioretinopathy |
38 |
2.895 |
|
162 |
|
P
|
TMR010 |
Tumor Predisposition Syndrome |
67 |
2.882 |
|
163 |
|
|
ADN089 |
Adenosquamous Lung Carcinoma |
49 |
2.882 |
|
164 |
|
|
BRN015 |
Bronchiolo-Alveolar Adenocarcinoma |
55 |
2.882 |
|
165 |
|
c
|
BRN108 |
Branchiootic Syndrome 1 |
62 |
2.872 |
|
166 |
|
P
|
EPT020 |
Epithelioid Hemangioendothelioma |
44 |
2.843 |
|
167 |
|
|
TCL027 |
T-Cell Acute Lymphoblastic Leukemia |
51 |
2.832 |
|
168 |
|
c
|
NNS043 |
Nonsyndromic Retinitis Pigmentosa |
27 |
2.817 |
|
169 |
|
c
|
NGH007 |
Night Blindness, Congenital Stationary, Type 1b |
42 |
2.813 |
|
170 |
|
|
TRT020 |
Tritanopia |
50 |
2.801 |
|
171 |
|
c
|
SML038 |
Small Cell Cancer of the Lung |
69 |
2.797 |
|
172 |
|
|
KRN002 |
Kearns-Sayre Syndrome |
63 |
2.769 |
|
173 |
|
c
|
PLY162 |
Polyposis Syndrome, Hereditary Mixed, 1 |
60 |
2.768 |
|
174 |
|
c
|
CLR087 |
Colorectal Cancer 12 |
34 |
2.768 |
|
175 |
|
P
|
HMN010 |
Hemangioma |
62 |
2.767 |
|
176 |
|
c
|
LBR004 |
Leber Congenital Amaurosis 1 |
52 |
2.764 |
|
177 |
|
|
PRL047 |
Prolonged Electroretinal Response Suppression |
43 |
2.738 |
|
178 |
|
c
|
USH035 |
Usher Syndrome Type 2 |
52 |
2.708 |
|
179 |
|
c
|
PST005 |
Posterior Uveitis |
54 |
2.708 |
|
180 |
|
P
|
SNS001 |
Sensorineural Hearing Loss |
59 |
2.708 |
|
181 |
|
|
MYL031 |
Myeloproliferative Neoplasm |
66 |
2.704 |
|
182 |
|
|
CHL149 |
Childhood Acute Myeloid Leukemia |
43 |
2.697 |
|
183 |
|
c
|
RTN150 |
Retinitis Pigmentosa 10 |
44 |
2.693 |
|
184 |
|
|
48X005 |
48,xyyy |
39 |
2.680 |
|
185 |
|
c
|
LNG047 |
Long Qt Syndrome 2 |
59 |
2.661 |
|
186 |
|
|
WST001 |
West Syndrome |
59 |
2.652 |
|
187 |
|
|
PST092 |
Posttransplant Acute Limbic Encephalitis |
28 |
2.652 |
|
188 |
|
|
BLC001 |
Blue Cone Monochromacy |
45 |
2.649 |
|
189 |
|
P
|
BLY001 |
B-Lymphoblastic Leukemia/lymphoma |
52 |
2.645 |
|
190 |
|
P
|
RHB003 |
Rhabdomyosarcoma |
66 |
2.645 |
|
191 |
|
P
|
VSC007 |
Vascular Disease |
63 |
2.645 |
|
192 |
|
c
|
LBR012 |
Leber Congenital Amaurosis 2 |
52 |
2.615 |
|
193 |
|
c
|
MJR022 |
Major Affective Disorder 8 |
38 |
2.615 |
|
194 |
|
c
|
MJR024 |
Major Affective Disorder 9 |
41 |
2.615 |
|
195 |
|
P
|
BPL003 |
Bipolar Disorder |
56 |
2.615 |
|
196 |
|
c
|
GLM047 |
Glioma Susceptibility 3 |
33 |
2.567 |
|
197 |
|
c
|
MSM022 |
Mismatch Repair Cancer Syndrome 1 |
70 |
2.567 |
|
198 |
|
c
|
GLM025 |
Glioma Susceptibility 2 |
30 |
2.567 |
|
199 |
|
c
|
GLM043 |
Glioma Susceptibility 9 |
30 |
2.567 |
|
200 |
|
P
|
OLG002 |
Oligodendroglioma |
66 |
2.567 |
|
201 |
|
|
CYT005 |
Cytomegalovirus Retinitis |
50 |
2.565 |
|
202 |
|
|
NRN005 |
Neuronal Ceroid-Lipofuscinoses |
61 |
2.554 |
|
203 |
|
P
|
HRD217 |
Hereditary Optic Neuropathy |
36 |
2.548 |
|
204 |
|
P
|
MLN008 |
Melanoma |
76 |
2.530 |
|
205 |
|
|
STR046 |
Stargardt Macular Degeneration |
27 |
2.530 |
|
206 |
|
c
|
BDY010 |
Body Mass Index Quantitative Trait Locus 4 |
46 |
2.515 |
|
207 |
|
c
|
BDY011 |
Body Mass Index Quantitative Trait Locus 10 |
45 |
2.515 |
|
208 |
|
c
|
BDY005 |
Body Mass Index Quantitative Trait Locus 9 |
47 |
2.515 |
|
209 |
|
|
PLY150 |
Polykaryocytosis Inducer |
29 |
2.515 |
|
210 |
|
c
|
BDY012 |
Body Mass Index Quantitative Trait Locus 7 |
44 |
2.515 |
|
211 |
|
|
MYL009 |
Myelodysplastic Syndrome |
67 |
2.515 |
|
212 |
|
P
|
BDY004 |
Body Mass Index Quantitative Trait Locus 11 |
83 |
2.515 |
|
213 |
|
c
|
BDY006 |
Body Mass Index Quantitative Trait Locus 8 |
44 |
2.515 |
|
214 |
|
c
|
BDY017 |
Body Mass Index Quantitative Trait Locus 14 |
45 |
2.515 |
|
215 |
|
c
|
BDY020 |
Body Mass Index Quantitative Trait Locus 19 |
52 |
2.515 |
|
216 |
|
c
|
BDY015 |
Body Mass Index Quantitative Trait Locus 12 |
46 |
2.515 |
|
217 |
|
c
|
BDY019 |
Body Mass Index Quantitative Trait Locus 18 |
47 |
2.515 |
|
218 |
|
P
|
VSC011 |
Vasculitis |
61 |
2.505 |
|
219 |
|
P
|
HYP265 |
Hypotonia |
42 |
2.505 |
|
220 |
|
|
VTR013 |
Vitreoretinopathy, Neovascular Inflammatory |
62 |
2.456 |
|
221 |
|
c
|
NGH010 |
Night Blindness, Congenital Stationary, Autosomal Dominant 2 |
46 |
2.446 |
|
222 |
|
P
|
NRB001 |
Neuroblastoma |
66 |
2.446 |
|
223 |
|
|
IMP005 |
Impotence |
52 |
2.446 |
|
224 |
|
|
CHR078 |
Chorioretinitis |
51 |
2.443 |
|
225 |
|
c
|
RTN172 |
Retinitis Pigmentosa 1 |
44 |
2.441 |
|
226 |
|
|
ALN001 |
Aland Island Eye Disease |
55 |
2.411 |
|
227 |
|
P
|
MJR001 |
Major Depressive Disorder |
68 |
2.406 |
|
228 |
|
|
CRB159 |
Cerebral Visual Impairment |
34 |
2.379 |
|
229 |
|
P
|
CHN012 |
Chondrosarcoma |
57 |
2.374 |
|
230 |
|
|
GYR004 |
Gyrate Atrophy of Choroid and Retina |
58 |
2.374 |
|
231 |
|
|
RHB024 |
Rhabdomyosarcoma 2 |
67 |
2.373 |
|
232 |
|
c
|
NGH026 |
Night Blindness, Congenital Stationary, Type 1a |
47 |
2.307 |
|
233 |
|
|
SRC027 |
Sarcoma, Synovial |
58 |
2.300 |
|
234 |
|
|
OCL069 |
Ocular Motor Apraxia |
57 |
2.294 |
|
235 |
|
c
|
MCL066 |
Macular Dystrophy, Vitelliform, 2 |
48 |
2.293 |
|
236 |
|
|
BRS099 |
Breast Ductal Carcinoma |
61 |
2.286 |
|
237 |
|
|
MNC001 |
Monocular Esotropia |
30 |
2.278 |
|
238 |
|
|
EST005 |
Esotropia |
43 |
2.278 |
|
239 |
|
|
ALL029 |
Allergic Disease |
59 |
2.278 |
|
240 |
|
P
|
ATS308 |
Autosomal Dominant Cerebellar Ataxia |
64 |
2.278 |
|
241 |
|
c
|
MCR122 |
Microphthalmia, Isolated 5 |
39 |
2.264 |
|
242 |
|
|
NNR004 |
Nonarteritic Anterior Ischemic Optic Neuropathy |
57 |
2.261 |
|
243 |
|
P
|
ANR048 |
Aniridia 1 |
64 |
2.251 |
|
244 |
|
c
|
CHR095 |
Chronic Progressive External Ophthalmoplegia |
49 |
2.251 |
|
245 |
|
|
NVS001 |
Neovascular Glaucoma |
52 |
2.243 |
|
246 |
|
|
PHC015 |
Phacoanaphylactic Uveitis |
18 |
2.221 |
|
247 |
|
|
VTR003 |
Vitreous Detachment |
41 |
2.219 |
|
248 |
|
P
|
THL005 |
Thalassemia |
56 |
2.208 |
|
249 |
|
P
|
BCL017 |
B-Cell Lymphoma |
59 |
2.208 |
|
250 |
|
|
HYP056 |
Hypoglycemia |
65 |
2.208 |
|
251 |
|
|
LTN004 |
Late-Onset Retinal Degeneration |
60 |
2.201 |
|
252 |
|
c
|
PLM164 |
Pulmonary Hypertension, Primary, 1 |
76 |
2.180 |
|
253 |
|
|
ACT119 |
Acute Promyelocytic Leukemia |
62 |
2.180 |
|
254 |
|
P
|
EPL164 |
Epilepsy |
68 |
2.172 |
|
255 |
|
P
|
FLL037 |
Follicular Lymphoma |
74 |
2.153 |
|
256 |
|
P
|
OCL002 |
Oculocutaneous Albinism |
59 |
2.135 |
|
257 |
|
|
MCP033 |
Mucopolysaccharidoses |
44 |
2.135 |
|
258 |
|
P
|
DBT009 |
Diabetes Mellitus |
67 |
2.134 |
|
259 |
|
|
PRP099 |
Peripheral Cone Dystrophy |
14 |
2.122 |
|
260 |
|
|
ACT235 |
Acute Macular Neuroretinopathy |
16 |
2.097 |
|
261 |
|
P
|
MYP004 |
Myopathy |
67 |
2.097 |
|
262 |
|
|
CMB007 |
Combined Immunodeficiency |
57 |
2.097 |
|
263 |
|
|
SPN050 |
Spinocerebellar Degeneration |
39 |
2.095 |
|
264 |
|
c
|
PRS134 |
Prostate Cancer, Hereditary, 3 |
20 |
2.095 |
|
265 |
|
c
|
USH036 |
Usher Syndrome, Type I |
61 |
2.076 |
|
266 |
|
|
ATX031 |
Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus |
58 |
2.076 |
|
267 |
|
|
ANX004 |
Anoxia |
40 |
2.063 |
|
268 |
|
P
|
MCP040 |
Mucopolysaccharidosis-Plus Syndrome |
70 |
2.058 |
|
269 |
|
|
SPL018 |
Splenomegaly |
49 |
2.058 |
|
270 |
|
|
ART016 |
Aortic Aneurysm |
68 |
2.051 |
|
271 |
|
|
RHB001 |
Rhabdoid Cancer |
68 |
2.051 |
|
272 |
|
|
OST012 |
Osteoarthritis |
77 |
2.051 |
|
273 |
|
P
|
ART022 |
Arthritis |
71 |
2.046 |
|
274 |
|
c
|
CNR007 |
Cone-Rod Dystrophy 6 |
52 |
2.029 |
|
275 |
|
|
BRN041 |
Bornholm Eye Disease |
34 |
2.019 |
|
276 |
|
c
|
RTN032 |
Retinal Cone Dystrophy 1 |
24 |
2.018 |
|
277 |
|
|
DSM007 |
Desmoplastic Small Round Cell Tumor |
54 |
2.018 |
|
278 |
|
c
|
RNG015 |
Ring Chromosome 2 |
22 |
2.016 |
|
279 |
|
|
SMT004 |
Smith-Lemli-Opitz Syndrome |
70 |
2.011 |
|
280 |
|
|
ANR040 |
Aneurysm |
61 |
2.004 |
|
281 |
|
|
ALS001 |
Alstrom Syndrome |
65 |
2.002 |
|
282 |
|
c
|
BRD010 |
Bardet-Biedl Syndrome 1 |
64 |
1.985 |
|
283 |
|
|
INT082 |
Intraocular Retinoblastoma |
29 |
1.985 |
|
|
285 |
|
|
VTL009 |
Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 |
42 |
1.978 |
|
286 |
|
|
DFF005 |
Diffuse Large B-Cell Lymphoma |
54 |
1.978 |
|
287 |
|
P
|
VTL004 |
Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 |
60 |
1.978 |
|
288 |
|
c
|
ART138 |
Aortic Aneurysm, Familial Abdominal, 1 |
61 |
1.957 |
|
289 |
|
|
MYL069 |
Myeloma, Multiple |
77 |
1.957 |
|
290 |
|
|
ATN005 |
Autonomic Dysfunction |
46 |
1.957 |
|
291 |
|
P
|
CLR023 |
Colorectal Cancer |
100 |
1.954 |
|
292 |
|
|
KRT019 |
Keratitis, Hereditary |
66 |
1.936 |
|
293 |
|
|
KPS004 |
Kaposi Sarcoma |
77 |
1.936 |
|
294 |
|
c
|
NGH025 |
Night Blindness, Congenital Stationary, Type 2a |
44 |
1.922 |
|
295 |
|
P
|
PNC035 |
Pancreatic Cancer |
86 |
1.920 |
|
296 |
|
|
HRD016 |
Hereditary Retinal Dystrophy |
34 |
1.907 |
|
297 |
|
|
PRS047 |
Prostatitis |
58 |
1.906 |
|
298 |
|
|
HPT046 |
Hepatic Veno-Occlusive Disease |
62 |
1.900 |
|
299 |
|
|
ADN018 |
Adenoma |
59 |
1.893 |
|
300 |
|
|
INT054 |
Intraocular Lymphoma |
48 |
1.893 |
|
301 |
|
|
RTN001 |
Retinal Vasculitis |
46 |
1.893 |
|
302 |
|
P
|
MYT002 |
Myotonic Dystrophy |
51 |
1.893 |
|
303 |
|
c
|
CND011 |
Cone Dystrophy 3 |
40 |
1.891 |
|
304 |
|
c
|
TYP008 |
Type 1 Diabetes Mellitus |
70 |
1.890 |
|
305 |
|
|
HLX001 |
Helix Syndrome |
48 |
1.890 |
|
306 |
|
P
|
RHM011 |
Rheumatoid Arthritis |
82 |
1.857 |
|
307 |
|
c
|
OPT053 |
Optic Atrophy 1 |
62 |
1.857 |
|
308 |
|
|
CLB010 |
Coloboma of Macula |
53 |
1.857 |
|
309 |
|
|
CYS001 |
Cystic Fibrosis |
78 |
1.855 |
|
310 |
|
|
MYP002 |
Myoepithelial Carcinoma |
46 |
1.855 |
|
311 |
|
P
|
CHR637 |
Choroidal Dystrophy, Central Areolar, 1 |
49 |
1.848 |
|
312 |
|
|
CHL014 |
Cholera |
62 |
1.848 |
|
313 |
|
c
|
LBR016 |
Leber Congenital Amaurosis 6 |
42 |
1.834 |
|
314 |
|
|
BTT001 |
Bietti Crystalline Corneoretinal Dystrophy |
48 |
1.823 |
|
315 |
|
|
ACT038 |
Acute Retrobulbar Neuritis |
24 |
1.823 |
|
316 |
|
c
|
CRD183 |
Ceroid Lipofuscinosis, Neuronal, 2 |
56 |
1.808 |
|
317 |
|
c
|
RTN054 |
Retinitis Pigmentosa 25 |
42 |
1.806 |
|
318 |
|
|
CLR132 |
Colorblindness, Partial, Deutan Series |
30 |
1.802 |
|
319 |
|
|
LNG073 |
Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency |
58 |
1.802 |
|
320 |
|
P
|
PRG130 |
Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 |
54 |
1.801 |
|
321 |
|
|
MLR004 |
Malaria |
80 |
1.801 |
|
322 |
|
c
|
PRG038 |
Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 |
49 |
1.801 |
|
323 |
|
c
|
PRG040 |
Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 |
53 |
1.801 |
|
324 |
|
|
CHL061 |
Childhood Leukemia |
47 |
1.801 |
|
325 |
|
c
|
MGR028 |
Migraine with or Without Aura 1 |
64 |
1.789 |
|
326 |
|
|
SFT003 |
Soft Tissue Sarcoma |
57 |
1.789 |
|
327 |
|
c
|
RTN162 |
Retinitis Pigmentosa 2 |
45 |
1.754 |
|
328 |
|
|
MCR013 |
Microphthalmia |
60 |
1.754 |
|
329 |
|
|
MTR001 |
Mature Cataract |
29 |
1.754 |
|
330 |
|
|
MSC012 |
Muscular Dystrophy, Duchenne and Becker Type |
33 |
1.754 |
|
331 |
|
|
SYN149 |
Syndromic Rod-Cone Dystrophy |
21 |
1.754 |
|
332 |
|
|
RLP002 |
Relapsing-Remitting Multiple Sclerosis |
56 |
1.754 |
|
333 |
|
|
OPT001 |
Optic Disk Drusen |
34 |
1.754 |
|
334 |
|
|
CHN010 |
Chondroma |
43 |
1.754 |
|
335 |
|
P
|
BNC003 |
Bone Cancer |
58 |
1.754 |
|
336 |
|
|
CND006 |
Candida Glabrata |
30 |
1.754 |
|
337 |
|
|
ACT186 |
Acute Megakaryoblastic Leukemia in Down Syndrome |
15 |
1.744 |
|
338 |
|
|
MCL057 |
Macular Dystrophy with Central Cone Involvement |
28 |
1.729 |
|
339 |
|
P
|
PLM025 |
Pulmonary Venoocclusive Disease |
44 |
1.707 |
|
340 |
|
|
3HY005 |
3-Hydroxyacyl-Coa Dehydrogenase Deficiency |
62 |
1.705 |
|
341 |
|
|
CHN053 |
Chondromyxoid Fibroma |
39 |
1.705 |
|
342 |
|
|
HRL003 |
Hurler Syndrome |
66 |
1.705 |
|
343 |
|
|
CRD223 |
Cardiac Arrhythmia |
63 |
1.705 |
|
344 |
|
|
CHR072 |
Chordoma |
57 |
1.705 |
|
345 |
|
|
FBR054 |
Fibroma |
44 |
1.705 |
|
346 |
|
P
|
MSN005 |
Mesenchymal Chondrosarcoma |
47 |
1.705 |
|
347 |
|
P
|
ENC018 |
Encephalopathy |
62 |
1.705 |
|
348 |
|
|
CNR033 |
Cone-Rod Synaptic Disorder, Congenital Nonprogressive |
35 |
1.698 |
|
349 |
|
|
LNG111 |
Lung Non-Squamous Non-Small Cell Carcinoma |
56 |
1.693 |
|
350 |
|
c
|
ATM099 |
Autoimmune Uveitis |
45 |
1.683 |
|
351 |
|
P
|
PLY006 |
Polydactyly |
59 |
1.683 |
|
352 |
|
|
CRH001 |
Crohn's Disease |
80 |
1.683 |
|
353 |
|
|
CRN030 |
Coronary Stenosis |
50 |
1.683 |
|
354 |
|
|
IRD001 |
Iridocyclitis |
53 |
1.683 |
|
355 |
|
|
VNH007 |
Von Hippel-Lindau Syndrome |
73 |
1.672 |
|
356 |
|
|
MCL029 |
Macular Degeneration, X-Linked Atrophic |
17 |
1.668 |
|
357 |
|
|
SHR107 |
Short Stature-Obesity Syndrome |
25 |
1.653 |
|
358 |
|
c
|
SPN294 |
Spinocerebellar Ataxia 1 |
53 |
1.653 |
|
359 |
|
|
HYP020 |
Hyperprolactinemia |
63 |
1.653 |
|
360 |
|
P
|
THR014 |
Thrombocytopenia |
66 |
1.653 |
|
|
362 |
|
|
CLR005 |
Clear Cell Chondrosarcoma |
37 |
1.653 |
|
363 |
|
|
OST011 |
Osteomalacia |
52 |
1.653 |
|
364 |
|
|
BLT001 |
Bilateral Retinoblastoma |
35 |
1.653 |
|
365 |
|
|
CHN003 |
Chondroblastic Osteosarcoma |
30 |
1.653 |
|
366 |
|
|
PSR001 |
Psoriatic Arthritis |
62 |
1.646 |
|
367 |
|
c
|
ATS169 |
Autosomal Recessive Congenital Stationary Night Blindness |
30 |
1.646 |
|
368 |
|
c
|
MCL013 |
Mucolipidosis Iv |
65 |
1.646 |
|
369 |
|
c
|
CNR038 |
Cone-Rod Dystrophy, X-Linked, 3 |
36 |
1.623 |
|
370 |
|
c
|
NGH008 |
Night Blindness, Congenital Stationary, Autosomal Dominant 3 |
36 |
1.623 |
|
371 |
|
c
|
DWL002 |
Dowling-Degos Disease 1 |
58 |
1.608 |
|
372 |
|
P
|
MYC084 |
Mycobacterium Tuberculosis 1 |
68 |
1.608 |
|
373 |
|
|
CLT003 |
Colitis |
63 |
1.608 |
|
374 |
|
P
|
HNT016 |
Huntington Disease |
73 |
1.608 |
|
375 |
|
P
|
KRT007 |
Keratoconus |
50 |
1.608 |
|
376 |
|
|
VGT001 |
Vogt-Koyanagi-Harada Disease |
56 |
1.608 |
|
377 |
|
P
|
PLM037 |
Pulmonary Hypertension |
72 |
1.599 |
|
378 |
|
|
SVR002 |
Severe Nonproliferative Diabetic Retinopathy |
36 |
1.599 |
|
379 |
|
|
RRV005 |
Rare Vascular Tumor |
17 |
1.599 |
|
380 |
|
|
ILS001 |
Ileus |
50 |
1.599 |
|
381 |
|
P
|
CRN026 |
Corneal Edema |
42 |
1.599 |
|
382 |
|
|
ONC003 |
Oncogenic Osteomalacia |
42 |
1.599 |
|
383 |
|
|
SKN022 |
Skin Squamous Cell Carcinoma |
54 |
1.577 |
|
384 |
|
|
LBL001 |
Lobular Neoplasia |
55 |
1.577 |
|
385 |
|
|
MYL005 |
Myelofibrosis |
71 |
1.573 |
|
386 |
|
P
|
RRT020 |
Rare Tumor |
39 |
1.569 |
|
387 |
|
P
|
JBR020 |
Joubert Syndrome 1 |
74 |
1.569 |
|
388 |
|
c
|
TYP009 |
Type 2 Diabetes Mellitus |
92 |
1.569 |
|
389 |
|
|
DGN002 |
Degenerative Myopia |
31 |
1.569 |
|
390 |
|
c
|
INT064 |
Intermediate Uveitis |
54 |
1.569 |
|
391 |
|
|
PTT063 |
Pattern Dystrophy |
36 |
1.569 |
|
392 |
|
c
|
CND012 |
Cone Dystrophy 4 |
30 |
1.563 |
|
393 |
|
|
TTR011 |
Tetraploidy |
43 |
1.542 |
|
394 |
|
c
|
LKM070 |
Leukemia, Acute Monocytic |
56 |
1.542 |
|
395 |
|
|
MLT157 |
Multiple System Atrophy 1 |
69 |
1.542 |
|
396 |
|
|
SCH036 |
Scheie Syndrome |
73 |
1.542 |
|
397 |
|
P
|
ISL078 |
Isolated Ectopia Lentis |
58 |
1.542 |
|
398 |
|
|
PRS042 |
Prostate Disease |
42 |
1.542 |
|
399 |
|
|
INT075 |
Intracranial Hypertension |
53 |
1.542 |
|
400 |
|
P
|
MTC133 |
Mitochondrial Myopathy |
50 |
1.542 |
|
401 |
|
|
SRC030 |
Sarcomatoid Carcinoma |
42 |
1.542 |
|
402 |
|
|
SCR001 |
Secretory Meningioma |
40 |
1.542 |
|
403 |
|
|
LYM002 |
Lymphoplasmacyte-Rich Meningioma |
35 |
1.542 |
|
404 |
|
P
|
MNC007 |
Monocytic Leukemia |
47 |
1.542 |
|
405 |
|
|
PNC001 |
Pancytopenia |
53 |
1.542 |
|
406 |
|
|
ATY005 |
Atypical Teratoid Rhabdoid Tumor |
69 |
1.542 |
|
407 |
|
|
SPN021 |
Spinal Meningioma |
50 |
1.542 |
|
408 |
|
|
ACT200 |
Acute Monoblastic Leukemia |
41 |
1.542 |
|
409 |
|
c
|
ATS007 |
Autism Spectrum Disorder |
72 |
1.529 |
|
410 |
|
P
|
MGR001 |
Migraine Without Aura |
49 |
1.529 |
|
411 |
|
P
|
PNV001 |
Panuveitis |
49 |
1.529 |
|
412 |
|
|
LKS001 |
Leukostasis |
41 |
1.529 |
|
413 |
|
|
RTN021 |
Retinal Vascular Occlusion |
45 |
1.529 |
|
414 |
|
|
ESP021 |
Esophageal Cancer |
83 |
1.514 |
|
415 |
|
|
END041 |
Endometrial Adenocarcinoma |
64 |
1.514 |
|
416 |
|
c
|
PRS097 |
Prostate Cancer, Hereditary, 1 |
39 |
1.490 |
|
417 |
|
c
|
PRS070 |
Prostate Cancer, Hereditary, 12 |
22 |
1.490 |
|
418 |
|
c
|
PRS071 |
Prostate Cancer, Hereditary, 13 |
25 |
1.490 |
|
419 |
|
c
|
PRS117 |
Prostate Cancer, Hereditary, 11 |
24 |
1.490 |
|
420 |
|
c
|
PRS114 |
Prostate Cancer, Hereditary, 2 |
33 |
1.490 |
|
421 |
|
|
PRS015 |
Prostate Signet Ring Cell Adenocarcinoma |
25 |
1.490 |
|
422 |
|
|
PRP030 |
Purpura |
54 |
1.489 |
|
423 |
|
|
LYS002 |
Lysosomal Storage Disease |
51 |
1.489 |
|
424 |
|
P
|
PTS002 |
Ptosis |
52 |
1.489 |
|
425 |
|
c
|
ATS168 |
Autosomal Dominant Congenital Stationary Night Blindness |
24 |
1.489 |
|
426 |
|
|
ONC007 |
Oncocytoma |
50 |
1.481 |
|
427 |
|
|
APR001 |
Apraxia |
52 |
1.481 |
|
428 |
|
|
ALP042 |
Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity |
65 |
1.481 |
|
429 |
|
P
|
CHR071 |
Charcot-Marie-Tooth Disease |
64 |
1.481 |
|
430 |
|
P
|
HYP086 |
Hypothyroidism |
69 |
1.481 |
|
431 |
|
P
|
ART005 |
Arteriovenous Malformation |
65 |
1.481 |
|
432 |
|
c
|
DNT047 |
Dentinogenesis Imperfecta Type 2 |
35 |
1.481 |
|
433 |
|
|
BTH002 |
Bothnia Retinal Dystrophy |
35 |
1.452 |
|
434 |
|
|
FML292 |
Familial Drusen |
34 |
1.447 |
|
435 |
|
|
RTN078 |
Retinoschisis of Fovea |
19 |
1.447 |
|
436 |
|
P
|
AST005 |
Asthma |
76 |
1.447 |
|
437 |
|
c
|
CNG411 |
Congenital Disorder of Glycosylation, Type in |
67 |
1.447 |
|
438 |
|
|
PPL021 |
Papilledema |
49 |
1.447 |
|
439 |
|
|
MNT002 |
Mental Depression |
57 |
1.447 |
|
440 |
|
|
ALT003 |
Alternating Exotropia |
33 |
1.447 |
|
441 |
|
P
|
MCR010 |
Microcephaly |
60 |
1.447 |
|
442 |
|
|
EXT022 |
Exotropia |
42 |
1.447 |
|
443 |
|
|
DPR016 |
Depression |
65 |
1.447 |
|
444 |
|
|
CRV035 |
Cervical Cancer |
73 |
1.417 |
|
445 |
|
|
ASK001 |
Askin's Tumor |
32 |
1.417 |
|
446 |
|
c
|
VNT034 |
Ventricular Fibrillation, Paroxysmal Familial, 1 |
67 |
1.417 |
|
447 |
|
|
GST019 |
Gastrointestinal Stromal Tumor |
78 |
1.417 |
|
448 |
|
|
PST048 |
Postural Orthostatic Tachycardia Syndrome |
46 |
1.417 |
|
449 |
|
|
CRT012 |
Cortical Blindness |
42 |
1.417 |
|
450 |
|
P
|
CRB059 |
Cerebellar Degeneration |
36 |
1.417 |
|
451 |
|
c
|
PRS136 |
Prostate Cancer, Hereditary, 6 |
33 |
1.409 |
|
452 |
|
c
|
PRS130 |
Prostate Cancer, Hereditary, 8 |
32 |
1.409 |
|
453 |
|
c
|
STR040 |
Stargardt Disease 3 |
34 |
1.404 |
|
454 |
|
c
|
THY107 |
Thymoma, Familial |
42 |
1.404 |
|
455 |
|
c
|
RTN058 |
Retinitis Pigmentosa 3 |
43 |
1.404 |
|
456 |
|
|
ANG054 |
Angina Pectoris |
66 |
1.404 |
|
457 |
|
P
|
OCL001 |
Ocular Albinism |
48 |
1.404 |
|
458 |
|
c
|
RTN066 |
Retinitis Pigmentosa 4 |
42 |
1.404 |
|
459 |
|
P
|
EXD001 |
Exudative Vitreoretinopathy |
56 |
1.404 |
|
460 |
|
P
|
ATR011 |
Atrial Fibrillation |
66 |
1.404 |
|
461 |
|
c
|
SPN291 |
Spinocerebellar Ataxia 7 |
53 |
1.404 |
|
462 |
|
P
|
MYC007 |
Myocardial Infarction |
70 |
1.404 |
|
463 |
|
|
CRN019 |
Coronary Artery Vasospasm |
47 |
1.404 |
|
464 |
|
P
|
THY023 |
Thymoma |
64 |
1.404 |
|
465 |
|
P
|
MCL035 |
Macular Dystrophy, Retinal, 2 |
27 |
1.378 |
|
466 |
|
c
|
USH046 |
Usher Syndrome, Type 1m |
17 |
1.378 |
|
467 |
|
|
ATM095 |
Autoimmune Disease |
61 |
1.359 |
|
468 |
|
|
PRS012 |
Pars Planitis |
47 |
1.359 |
|
469 |
|
|
THR100 |
Thrombocytopenic Purpura, Autoimmune |
61 |
1.359 |
|
470 |
|
P
|
PSR002 |
Psoriasis |
63 |
1.359 |
|
471 |
|
|
PST011 |
Pustulosis of Palm and Sole |
52 |
1.359 |
|
472 |
|
|
TLN003 |
Telangiectasis |
51 |
1.359 |
|
473 |
|
P
|
NPH005 |
Nephronophthisis |
56 |
1.359 |
|
474 |
|
P
|
LBR033 |
Leber Congenital Amaurosis / Early-Onset Severe Retinal Dystrophy |
22 |
1.359 |
|
475 |
|
|
MSC007 |
Muscle Hypertrophy |
64 |
1.349 |
|
476 |
|
c
|
MCL030 |
Macular Degeneration, Age-Related, 10 |
24 |
1.349 |
|
477 |
|
P
|
NJM001 |
Nijmegen Breakage Syndrome |
76 |
1.349 |
|
478 |
|
c
|
WLM013 |
Wilms Tumor 1 |
66 |
1.349 |
|
479 |
|
P
|
SPP010 |
Suppressor of Tumorigenicity 3 |
51 |
1.349 |
|
480 |
|
|
CRB006 |
Cribriform Carcinoma |
34 |
1.349 |
|
481 |
|
|
GLB002 |
Glioblastoma |
67 |
1.349 |
|
482 |
|
|
ENC067 |
Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis |
50 |
1.349 |
|
483 |
|
|
ACT113 |
Acute Myeloblastic Leukemia with Maturation |
46 |
1.349 |
|
484 |
|
|
LYM116 |
Lymph Node Disease |
42 |
1.349 |
|
485 |
|
|
CHR167 |
Chorioretinal Atrophy, Progressive Bifocal |
27 |
1.335 |
|
486 |
|
c
|
RTN036 |
Retinal Cone Dystrophy 4 |
35 |
1.335 |
|
|
488 |
|
P
|
SZR006 |
Seizure Disorder |
70 |
1.313 |
|
489 |
|
|
CRT072 |
Creutzfeldt-Jakob Disease |
68 |
1.313 |
|
490 |
|
c
|
MCR130 |
Microvascular Complications of Diabetes 6 |
41 |
1.313 |
|
491 |
|
P
|
FTL001 |
Fetal Alcohol Syndrome |
55 |
1.313 |
|
492 |
|
|
IMM167 |
Immune Deficiency Disease |
78 |
1.313 |
|
493 |
|
c
|
MCR120 |
Microvascular Complications of Diabetes 7 |
47 |
1.313 |
|
494 |
|
P
|
HMC002 |
Homocystinuria |
53 |
1.313 |
|
495 |
|
c
|
MCR113 |
Microvascular Complications of Diabetes 3 |
52 |
1.313 |
|
496 |
|
c
|
MCR133 |
Microvascular Complications of Diabetes 4 |
41 |
1.313 |
|
497 |
|
c
|
PRC016 |
Pre-Eclampsia |
65 |
1.313 |
|
498 |
|
P
|
PLY019 |
Polyneuropathy |
52 |
1.313 |
|
499 |
|
|
SQM006 |
Squamous Cell Carcinoma |
60 |
1.313 |
|
500 |
|
|
RP6003 |
Rpe65-Related Leber Congenital Amaurosis / Early-Onset Severe Retinal Dystrophy |
9 |
1.313 |
|
501 |
|
P
|
GRF003 |
Graft-Versus-Host Disease |
71 |
1.299 |
|
502 |
|
c
|
CNR013 |
Cone-Rod Dystrophy 12 |
36 |
1.295 |
|
503 |
|
P
|
SNR003 |
Senior-Loken Syndrome 1 |
58 |
1.295 |
|
504 |
|
|
CRD132 |
Cardiac Conduction Defect |
60 |
1.274 |
|
505 |
|
|
HRL004 |
Hurler-Scheie Syndrome |
57 |
1.274 |
|
506 |
|
|
CNG410 |
Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly |
61 |
1.274 |
|
507 |
|
|
SVR001 |
Severe Acute Respiratory Syndrome |
67 |
1.274 |
|
508 |
|
P
|
HRM001 |
Hermansky-Pudlak Syndrome |
65 |
1.274 |
|
509 |
|
P
|
NPH012 |
Nephrotic Syndrome |
60 |
1.274 |
|
510 |
|
P
|
OST001 |
Osteopetrosis |
71 |
1.274 |
|
511 |
|
|
LTT006 |
Littoral Cell Angioma of the Spleen |
18 |
1.274 |
|
512 |
|
|
PRT058 |
Pure Autonomic Failure |
58 |
1.274 |
|
513 |
|
P
|
ATS364 |
Autism |
69 |
1.265 |
|
514 |
|
|
RTN208 |
Retinopathy, Pericentral Pigmentary, Autosomal Recessive |
16 |
1.265 |
|
515 |
|
|
ALC007 |
Alcohol Dependence |
66 |
1.265 |
|
516 |
|
|
ALC028 |
Alacrima, Achalasia, and Mental Retardation Syndrome |
68 |
1.265 |
|
517 |
|
P
|
RTN034 |
Retinal Cone Dystrophy 3a |
28 |
1.265 |
|
518 |
|
|
TRM010 |
Traumatic Brain Injury |
51 |
1.265 |
|
519 |
|
P
|
HYP087 |
Hypotrichosis |
42 |
1.265 |
|
520 |
|
c
|
HPT001 |
Hepatitis C |
62 |
1.265 |
|
521 |
|
|
CRT015 |
Carotid Artery Occlusion |
45 |
1.265 |
|
522 |
|
P
|
TRT010 |
Teratoma |
51 |
1.265 |
|
523 |
|
|
KRT001 |
Keratoconjunctivitis Sicca |
50 |
1.265 |
|
524 |
|
|
CLR030 |
Clear Cell Renal Cell Carcinoma |
54 |
1.238 |
|
525 |
|
|
PLM173 |
Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and 46,xx Sex Reversal |
34 |
1.226 |
|
526 |
|
|
PSD011 |
Pseudovascular Skin Squamous Cell Carcinoma |
16 |
1.226 |
|
527 |
|
|
SQM013 |
Squamous Cell Carcinoma, Head and Neck |
73 |
1.215 |
|
528 |
|
c
|
CNR003 |
Cone-Rod Dystrophy 1 |
31 |
1.215 |
|
529 |
|
|
ALC001 |
Alcohol-Related Birth Defect |
36 |
1.215 |
|
530 |
|
c
|
BTT014 |
Beta-Thalassemia |
72 |
1.215 |
|
531 |
|
P
|
NNP021 |
Nanophthalmos |
39 |
1.215 |
|
532 |
|
P
|
MTH008 |
Methylmalonic Acidemia |
52 |
1.215 |
|
533 |
|
P
|
ANT006 |
Antiphospholipid Syndrome |
55 |
1.215 |
|
534 |
|
|
XRP001 |
Xerophthalmia |
41 |
1.215 |
|
535 |
|
|
GT001 |
Gout |
64 |
1.215 |
|
536 |
|
|
HYP008 |
Hypertensive Retinopathy |
39 |
1.215 |
|
537 |
|
|
STT001 |
Status Epilepticus |
59 |
1.215 |
|
538 |
|
|
SNL007 |
Senile Cataract |
40 |
1.215 |
|
539 |
|
P
|
VTR008 |
Vitreoretinal Degeneration |
29 |
1.215 |
|
540 |
|
P
|
HDC001 |
Headache |
57 |
1.215 |
|
541 |
|
P
|
GNG009 |
Gangliosidosis |
44 |
1.215 |
|
542 |
|
P
|
CNR031 |
Cone-Rod Dystrophy, X-Linked, 1 |
37 |
1.201 |
|
543 |
|
|
ATM096 |
Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia |
65 |
1.201 |
|
544 |
|
P
|
LBR014 |
Leber Congenital Amaurosis 4 |
56 |
1.201 |
|
545 |
|
c
|
NGH030 |
Night Blindness, Congenital Stationary, Type 1f |
25 |
1.201 |
|
546 |
|
P
|
BLD062 |
Bile Duct Cancer |
67 |
1.197 |
|
547 |
|
P
|
LNG021 |
Lung Occult Small Cell Carcinoma |
20 |
1.197 |
|
548 |
|
|
LNG019 |
Lung Combined Type Small Cell Carcinoma |
32 |
1.197 |
|
549 |
|
|
CVD001 |
Covid-19 |
57 |
1.191 |
|
550 |
|
P
|
GLL032 |
Galloway-Mowat Syndrome |
46 |
1.191 |
|
551 |
|
|
EST007 |
Estrogen Resistance |
41 |
1.191 |
|
552 |
|
P
|
HMN036 |
Hemangiopericytoma, Malignant |
58 |
1.191 |
|
553 |
|
|
MYL003 |
Myeloid Sarcoma |
48 |
1.191 |
|
554 |
|
c
|
RTN048 |
Retinitis Pigmentosa 19 |
39 |
1.189 |
|
555 |
|
c
|
RTN230 |
Retinitis Pigmentosa 88 |
23 |
1.189 |
|
556 |
|
c
|
RTN233 |
Retinitis Pigmentosa 89 |
20 |
1.189 |
|
557 |
|
|
NRR002 |
Norrie Disease |
61 |
1.164 |
|
558 |
|
c
|
USH037 |
Usher Syndrome, Type Iia |
48 |
1.164 |
|
559 |
|
P
|
LKM071 |
Leukemia, Chronic Lymphocytic |
75 |
1.164 |
|
560 |
|
|
MCL069 |
Macular Dystrophy, Retinal, 1, North Carolina Type |
38 |
1.164 |
|
561 |
|
P
|
LSS002 |
Lissencephaly |
50 |
1.164 |
|
562 |
|
|
DFC004 |
Deficiency Anemia |
74 |
1.164 |
|
563 |
|
P
|
MCL001 |
Mucolipidosis |
49 |
1.164 |
|
564 |
|
P
|
RBL001 |
Rubella |
58 |
1.164 |
|
565 |
|
P
|
CHL066 |
Cholangitis |
52 |
1.164 |
|
566 |
|
|
SKN016 |
Skin Disease |
63 |
1.164 |
|
567 |
|
|
CRT013 |
Carotid Stenosis |
51 |
1.164 |
|
568 |
|
P
|
SCL009 |
Sclerosing Cholangitis |
48 |
1.164 |
|
569 |
|
|
THR004 |
Thrombocytosis |
53 |
1.164 |
|
570 |
|
P
|
BLP003 |
Blepharospasm |
46 |
1.164 |
|
571 |
|
|
HYP080 |
Hypogonadism |
50 |
1.164 |
|
572 |
|
P
|
LMY004 |
Leiomyosarcoma |
62 |
1.164 |
|
573 |
|
c
|
RNG021 |
Ring Chromosome 5 |
20 |
1.164 |
|
574 |
|
|
MTH021 |
Methylmalonic Acidemia with Homocystinuria |
44 |
1.164 |
|
575 |
|
|
PRR004 |
Preretinal Fibrosis |
34 |
1.127 |
|
576 |
|
|
HYP781 |
Hypoascorbemia |
52 |
1.119 |
|
577 |
|
|
MTH047 |
Methanol Poisoning |
37 |
1.110 |
|
578 |
|
P
|
ALZ034 |
Alzheimer Disease |
87 |
1.110 |
|
579 |
|
P
|
PHC003 |
Pheochromocytoma |
69 |
1.110 |
|
580 |
|
|
ATR057 |
Atrioventricular Block |
54 |
1.110 |
|
581 |
|
|
DBT090 |
Diabetes and Deafness, Maternally Inherited |
45 |
1.110 |
|
582 |
|
|
NRN008 |
Neuronal Intranuclear Inclusion Disease |
47 |
1.110 |
|
583 |
|
|
MYP106 |
Myopathy, Myosin Storage, Autosomal Recessive |
33 |
1.110 |
|
584 |
|
|
ADR040 |
Adrenal Gland Pheochromocytoma |
46 |
1.110 |
|
585 |
|
|
SCR011 |
Scrapie |
39 |
1.110 |
|
586 |
|
P
|
ALP008 |
Alopecia |
54 |
1.110 |
|
587 |
|
P
|
CRN024 |
Corneal Disease |
44 |
1.110 |
|
588 |
|
P
|
NTR004 |
Neutropenia |
63 |
1.110 |
|
589 |
|
P
|
SBS003 |
Substance Abuse |
54 |
1.110 |
|
590 |
|
|
ABS022 |
Absolute Glaucoma |
33 |
1.110 |
|
591 |
|
|
VCN001 |
Vcan-Related Vitreoretinopathy |
20 |
1.110 |
|
592 |
|
c
|
MNS014 |
Monosomy 22 |
35 |
1.097 |
|
593 |
|
P
|
TMP003 |
Temporal Arteritis |
69 |
1.097 |
|
594 |
|
|
LNG099 |
Lung Disease |
62 |
1.097 |
|
595 |
|
|
DNG001 |
Dengue Shock Syndrome |
40 |
1.097 |
|
596 |
|
P
|
DNG005 |
Dengue Virus |
56 |
1.097 |
|
597 |
|
|
DNG002 |
Dengue Hemorrhagic Fever |
60 |
1.097 |
|
598 |
|
|
HMP001 |
Hemopericardium |
47 |
1.097 |
|
599 |
|
P
|
PRC012 |
Pericardial Effusion |
50 |
1.097 |
|
600 |
|
P
|
HYP076 |
Hyperthyroidism |
53 |
1.097 |
|
601 |
|
|
DBF001 |
D-Bifunctional Protein Deficiency |
55 |
1.089 |
|
602 |
|
|
SRS007 |
Sorsby Fundus Dystrophy |
51 |
1.089 |
|
603 |
|
c
|
CRB175 |
Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 |
70 |
1.089 |
|
604 |
|
c
|
LBR005 |
Leber Congenital Amaurosis 10 |
45 |
1.075 |
|
605 |
|
c
|
LBR018 |
Leber Congenital Amaurosis 8 |
47 |
1.075 |
|
606 |
|
c
|
LBR006 |
Leber Congenital Amaurosis 11 |
35 |
1.075 |
|
607 |
|
c
|
LBR017 |
Leber Congenital Amaurosis 7 |
37 |
1.075 |
|
608 |
|
|
LYM133 |
Lymphoma, Hodgkin, Classic |
74 |
1.053 |
|
609 |
|
|
MLT161 |
Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly |
55 |
1.053 |
|
610 |
|
c
|
FML294 |
Familial Short Qt Syndrome |
43 |
1.053 |
|
611 |
|
|
INS024 |
Insulin-Like Growth Factor I |
78 |
1.053 |
|
612 |
|
c
|
USH038 |
Usher Syndrome, Type Iiia |
51 |
1.053 |
|
613 |
|
c
|
SPN225 |
Spondyloarthropathy 1 |
70 |
1.053 |
|
614 |
|
|
FTL006 |
Fetal Alcohol Spectrum Disorder |
43 |
1.053 |
|
615 |
|
c
|
SHR030 |
Short Qt Syndrome |
44 |
1.053 |
|
616 |
|
c
|
BRD017 |
Bardet-Biedl Syndrome 5 |
38 |
1.053 |
|
617 |
|
c
|
CHL119 |
Cholangitis, Primary Sclerosing |
58 |
1.053 |
|
618 |
|
|
ALL006 |
Allergic Asthma |
56 |
1.053 |
|
619 |
|
|
ULC004 |
Ulcerative Colitis |
74 |
1.053 |
|
620 |
|
|
SPN051 |
Spondylitis |
51 |
1.053 |
|
621 |
|
|
ADN009 |
Adenosquamous Carcinoma |
48 |
1.053 |
|
622 |
|
c
|
DLT002 |
Dilated Cardiomyopathy |
78 |
1.053 |
|
623 |
|
|
DNG003 |
Dengue Disease |
65 |
1.053 |
|
624 |
|
|
INF009 |
Inflammatory Spondylopathy |
30 |
1.053 |
|
625 |
|
|
DBT008 |
Diabetic Angiopathy |
45 |
1.053 |
|
626 |
|
|
DMY004 |
Demyelinating Disease |
50 |
1.053 |
|
627 |
|
|
KRT008 |
Keratopathy |
46 |
1.053 |
|
628 |
|
|
HYP060 |
Hyperinsulinism |
54 |
1.053 |
|
629 |
|
P
|
NRF002 |
Neurofibromatosis |
57 |
1.053 |
|
630 |
|
c
|
NNS007 |
Nonsyndromic Deafness |
33 |
1.053 |
|
631 |
|
P
|
MTC069 |
Mitochondrial Disorders |
57 |
1.053 |
|
632 |
|
c
|
ACT135 |
Acute Graft Versus Host Disease |
51 |
1.042 |
|
633 |
|
P
|
CNR040 |
Cone-Rod Dystrophy and Hearing Loss 1 |
26 |
1.027 |
|
634 |
|
|
CLP005 |
Ciliopathy |
41 |
0.992 |
|
635 |
|
c
|
MCP050 |
Mucopolysaccharidosis, Type Ii |
74 |
0.992 |
|
636 |
|
|
CRT084 |
Creatinine Clearance Quantitative Trait Locus |
25 |
0.992 |
|
637 |
|
c
|
ATR087 |
Atrial Standstill 1 |
74 |
0.992 |
|
638 |
|
|
TRD008 |
Triiodothyronine Receptor Auxiliary Protein |
33 |
0.992 |
|
639 |
|
|
MNT001 |
Mantle Cell Lymphoma |
67 |
0.992 |
|
640 |
|
c
|
NGH027 |
Night Blindness, Congenital Stationary, Type 1c |
36 |
0.992 |
|
641 |
|
P
|
CTN015 |
Cutaneous T Cell Lymphoma |
48 |
0.992 |
|
642 |
|
|
CRH005 |
Crohn's Colitis |
53 |
0.992 |
|
643 |
|
c
|
LBR015 |
Leber Congenital Amaurosis 5 |
42 |
0.992 |
|
644 |
|
c
|
BRD011 |
Bardet-Biedl Syndrome 10 |
49 |
0.992 |
|
645 |
|
|
CHR607 |
Chorea, Childhood-Onset, with Psychomotor Retardation |
39 |
0.992 |
|
646 |
|
|
LBR038 |
Leber Hereditary Optic Neuropathy, Modifier of |
62 |
0.992 |
|
647 |
|
c
|
ACH020 |
Achromatopsia 2 |
48 |
0.992 |
|
648 |
|
P
|
ATT013 |
Attention Deficit-Hyperactivity Disorder |
64 |
0.992 |
|
649 |
|
P
|
EST001 |
Estrogen-Receptor Positive Breast Cancer |
49 |
0.992 |
|
650 |
|
|
OPT010 |
Optic Papillitis |
38 |
0.992 |
|
651 |
|
c
|
CHR684 |
Chronic Kidney Disease |
69 |
0.992 |
|
652 |
|
|
SCH012 |
Schizoaffective Disorder |
50 |
0.992 |
|
653 |
|
|
NRM001 |
Neuromyelitis Optica |
61 |
0.992 |
|
654 |
|
|
GLL048 |
Glial Tumor |
52 |
0.992 |
|
655 |
|
|
DBT010 |
Diabetic Neuropathy |
54 |
0.992 |
|
656 |
|
|
MYP060 |
Myopic Macular Degeneration |
19 |
0.992 |
|
657 |
|
P
|
FBR017 |
Fibrosarcoma |
56 |
0.992 |
|
658 |
|
P
|
CND004 |
Candidiasis |
58 |
0.992 |
|
659 |
|
P
|
LCT001 |
Lactic Acidosis |
51 |
0.992 |
|
660 |
|
P
|
SYP003 |
Syphilis |
59 |
0.992 |
|
661 |
|
P
|
ACN011 |
Acne |
57 |
0.992 |
|
662 |
|
|
RDG001 |
Red-Green Color Blindness |
28 |
0.992 |
|
663 |
|
|
PRS025 |
Presbyopia |
38 |
0.992 |
|
664 |
|
|
UNL002 |
Unilateral Retinoblastoma |
37 |
0.992 |
|
665 |
|
|
DRM006 |
Dermatitis |
62 |
0.992 |
|
666 |
|
|
TXC008 |
Toxic Optic Neuropathy |
27 |
0.992 |
|
667 |
|
|
CHR073 |
Choreatic Disease |
54 |
0.992 |
|
668 |
|
|
ENT004 |
Enthesopathy |
51 |
0.992 |
|
669 |
|
c
|
HPT016 |
Hepatitis B |
62 |
0.992 |
|
670 |
|
P
|
ACT105 |
Acute Mountain Sickness |
52 |
0.992 |
|
671 |
|
|
BRN071 |
Brain Injury |
50 |
0.992 |
|
672 |
|
P
|
MYC033 |
Myoclonus |
47 |
0.992 |
|
673 |
|
|
ACT177 |
Acute Basophilic Leukemia |
34 |
0.985 |
|
674 |
|
|
DRM014 |
Dermatofibrosarcoma Protuberans |
65 |
0.985 |
|
675 |
|
P
|
SYS005 |
Systemic Scleroderma |
74 |
0.985 |
|
676 |
|
|
AMT001 |
Ametropic Amblyopia |
26 |
0.985 |
|
677 |
|
|
VSC002 |
Vascular Dementia |
60 |
0.985 |
|
678 |
|
|
ACT193 |
Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) |
54 |
0.985 |
|
679 |
|
|
AMR003 |
Amaurosis Fugax |
33 |
0.985 |
|
680 |
|
c
|
SNR004 |
Senior-Loken Syndrome 4 |
26 |
0.944 |
|
681 |
|
c
|
MSC045 |
Muscular Dystrophy-Dystroglycanopathy , Type a, 3 |
36 |
0.944 |
|
682 |
|
c
|
LBR011 |
Leber Congenital Amaurosis 16 |
38 |
0.944 |
|
683 |
|
c
|
LBR009 |
Leber Congenital Amaurosis 14 |
41 |
0.944 |
|
684 |
|
|
HPT070 |
Hepatosplenic T-Cell Lymphoma |
36 |
0.940 |
|
685 |
|
P
|
DBT005 |
Diabetes Insipidus |
54 |
0.928 |
|
686 |
|
|
PRM155 |
Primary Cutaneous Anaplastic Large Cell Lymphoma |
34 |
0.928 |
|
687 |
|
|
SHK001 |
Shaken Baby Syndrome |
21 |
0.928 |
|
688 |
|
c
|
MCP049 |
Mucopolysaccharidosis, Type Vii |
63 |
0.928 |
|
689 |
|
|
DNN001 |
Danon Disease |
59 |
0.928 |
|
690 |
|
|
MYC006 |
Mycosis Fungoides |
65 |
0.928 |
|
691 |
|
c
|
USH041 |
Usher Syndrome, Type if |
47 |
0.928 |
|
692 |
|
|
HMC014 |
Homocysteinemia |
52 |
0.928 |
|
693 |
|
|
BRK010 |
Burkitt Lymphoma |
66 |
0.928 |
|
694 |
|
c
|
THR092 |
Thrombophilia Due to Thrombin Defect |
74 |
0.928 |
|
695 |
|
|
HMN044 |
Human Immunodeficiency Virus Type 1 |
78 |
0.928 |
|
696 |
|
P
|
ANP001 |
Anaplastic Large Cell Lymphoma |
61 |
0.928 |
|
697 |
|
P
|
SLP006 |
Sleep Apnea |
69 |
0.928 |
|
698 |
|
P
|
INF037 |
Inflammatory Bowel Disease |
53 |
0.928 |
|
699 |
|
c
|
RTN044 |
Retinitis Pigmentosa 14 |
37 |
0.928 |
|
700 |
|
P
|
TYS001 |
Tay-Sachs Disease |
69 |
0.928 |
|
701 |
|
|
LGH007 |
Leigh Syndrome |
70 |
0.928 |
|
702 |
|
c
|
USH020 |
Usher Syndrome, Type Iic |
45 |
0.928 |
|
703 |
|
P
|
PRN026 |
Porencephaly |
55 |
0.928 |
|
704 |
|
|
PRT037 |
Pertussis |
65 |
0.928 |
|
705 |
|
P
|
PRK039 |
Parkinsonism |
55 |
0.928 |
|
706 |
|
|
MTC004 |
Mitochondrial Encephalomyopathy |
42 |
0.928 |
|
707 |
|
P
|
HYP098 |
Hypereosinophilic Syndrome |
66 |
0.928 |
|
708 |
|
P
|
RRH023 |
Rare Hereditary Hemochromatosis |
54 |
0.928 |
|
709 |
|
|
NRN001 |
Neuroendocrine Carcinoma |
47 |
0.928 |
|
710 |
|
P
|
OLV001 |
Olivopontocerebellar Atrophy |
51 |
0.928 |
|
711 |
|
P
|
PNC025 |
Panic Disorder |
52 |
0.928 |
|
712 |
|
P
|
MGR003 |
Migraine with Aura |
52 |
0.928 |
|
713 |
|
|
HMS001 |
Hemosiderosis |
48 |
0.928 |
|
714 |
|
|
CHR008 |
Choroiditis |
48 |
0.928 |
|
715 |
|
|
CYS010 |
Cystinosis |
62 |
0.928 |
|
716 |
|
|
LVR012 |
Liver Cirrhosis |
63 |
0.928 |
|
717 |
|
|
OPT007 |
Optic Nerve Glioma |
40 |
0.928 |
|
718 |
|
|
MDD011 |
Mood Disorder |
62 |
0.928 |
|
719 |
|
|
DSR002 |
Disorders of Intracellular Cobalamin Metabolism |
29 |
0.928 |
|
720 |
|
|
PRS063 |
Paresthesia |
39 |
0.928 |
|
721 |
|
|
ALL014 |
Allergic Encephalomyelitis |
34 |
0.928 |
|
722 |
|
|
MLN065 |
Melanocytic Nevus Syndrome, Congenital |
62 |
0.888 |
|
723 |
|
|
PLS025 |
Plasmablastic Lymphoma |
56 |
0.888 |
|
724 |
|
|
MLT165 |
Multilocular Cystic Renal Neoplasm of Low Malignant Potential |
28 |
0.888 |
|
725 |
|
|
MLT003 |
Multilocular Clear Cell Renal Cell Carcinoma |
32 |
0.888 |
|
726 |
|
|
OVR062 |
Ovary Serous Adenocarcinoma |
25 |
0.888 |
|
727 |
|
|
PRM126 |
Primary Peritoneal Carcinoma |
62 |
0.888 |
|
728 |
|
|
NGH031 |
Night Blindness, Congenital Stationary, Type1i |
19 |
0.862 |
|
729 |
|
|
CHR603 |
Chronic Enteropathy Associated with Slco2a1 Gene |
25 |
0.859 |
|
730 |
|
|
CTS003 |
Coats Disease |
53 |
0.859 |
|
731 |
|
|
ACR008 |
Acrocallosal Syndrome |
70 |
0.859 |
|
732 |
|
|
ANG004 |
Angioid Streaks |
40 |
0.859 |
|
733 |
|
|
MNK001 |
Menkes Disease |
64 |
0.859 |
|
734 |
|
|
HYP332 |
Hypotrichosis, Congenital, with Juvenile Macular Dystrophy |
41 |
0.859 |
|
735 |
|
|
KSH004 |
Kashin-Beck Disease |
38 |
0.859 |
|
736 |
|
|
VTR010 |
Vitreoretinochoroidopathy |
49 |
0.859 |
|
737 |
|
c
|
HYP836 |
Hypercholesterolemia, Familial, 1 |
73 |
0.859 |
|
738 |
|
c
|
BRD013 |
Bardet-Biedl Syndrome 12 |
44 |
0.859 |
|
739 |
|
|
NRT011 |
Neurotrophic Keratopathy |
36 |
0.859 |
|
740 |
|
c
|
LRG001 |
Large Cell Carcinoma |
48 |
0.859 |
|
741 |
|
|
INT007 |
Intermediate Coronary Syndrome |
54 |
0.859 |
|
742 |
|
|
LRN003 |
Learning Disability |
49 |
0.859 |
|
743 |
|
P
|
SKN015 |
Skin Carcinoma |
71 |
0.859 |
|
744 |
|
P
|
DMN002 |
Dementia |
66 |
0.859 |
|
745 |
|
|
BLR001 |
Biliary Atresia |
55 |
0.859 |
|
746 |
|
|
HYD002 |
Hydronephrosis |
58 |
0.859 |
|
747 |
|
P
|
STC001 |
Stickler Syndrome |
60 |
0.859 |
|
748 |
|
|
TRC008 |
Trachoma |
53 |
0.859 |
|
749 |
|
P
|
SHR001 |
Short Bowel Syndrome |
53 |
0.859 |
|
750 |
|
|
HYD001 |
Hydranencephaly |
43 |
0.859 |
|
751 |
|
|
TCL028 |
T-Cell Lymphoblastic Leukemia/lymphoma |
46 |
0.859 |
|
752 |
|
P
|
KDN017 |
Kidney Cancer |
61 |
0.859 |
|
753 |
|
c
|
GM2006 |
Gm2 Gangliosidosis |
46 |
0.859 |
|
754 |
|
P
|
TMP001 |
Temporal Lobe Epilepsy |
49 |
0.859 |
|
755 |
|
|
LST001 |
Listeriosis |
59 |
0.859 |
|
756 |
|
c
|
MCP001 |
Mucopolysaccharidosis Iii |
69 |
0.859 |
|
757 |
|
c
|
LKM005 |
Leukemia, T-Cell, Chronic |
34 |
0.859 |
|
758 |
|
|
MCL079 |
Macular Telangiectasia Type 2 |
27 |
0.859 |
|
759 |
|
|
MLT035 |
Multifocal Choroiditis |
31 |
0.859 |
|
760 |
|
|
ORN004 |
Ornithinemia |
13 |
0.859 |
|
761 |
|
P
|
KNB001 |
Knobloch Syndrome |
38 |
0.859 |
|
762 |
|
P
|
HYP058 |
Hypervitaminosis a |
47 |
0.847 |
|
763 |
|
|
CLL002 |
Collecting Duct Carcinoma |
54 |
0.846 |
|
764 |
|
|
ACR014 |
Acral Lentiginous Melanoma |
52 |
0.846 |
|
765 |
|
|
LNG012 |
Lung Occult Squamous Cell Carcinoma |
20 |
0.846 |
|
766 |
|
|
PPL004 |
Papillary Squamous Carcinoma |
39 |
0.846 |
|
767 |
|
|
PNS010 |
Penis Squamous Cell Carcinoma |
45 |
0.846 |
|
768 |
|
|
LNG007 |
Lung Mixed Small Cell and Squamous Cell Carcinoma |
21 |
0.846 |
|
769 |
|
|
PNS005 |
Penis Mixed Squamous Cell Carcinoma |
12 |
0.846 |
|
770 |
|
|
SSC001 |
Susac Syndrome |
32 |
0.840 |
|
771 |
|
c
|
OPT051 |
Opitz Gbbb Syndrome, Type I |
46 |
0.840 |
|
772 |
|
P
|
PRK057 |
Parkinson Disease, Late-Onset |
80 |
0.840 |
|
773 |
|
P
|
FML011 |
Familial Adenomatous Polyposis |
71 |
0.840 |
|
774 |
|
|
MYP067 |
Myopathy, Distal, Tateyama Type |
28 |
0.840 |
|
775 |
|
|
CD4003 |
Cd40 Ligand Deficiency |
54 |
0.840 |
|
776 |
|
P
|
ASP006 |
Aspergillosis |
72 |
0.840 |
|
777 |
|
|
IMM174 |
Immunodeficiency with Hyper-Igm, Type 1 |
64 |
0.840 |
|
778 |
|
|
ISC001 |
Ischemic Neuropathy |
27 |
0.840 |
|
779 |
|
c
|
CV3001 |
Cav3-Related Distal Myopathy |
17 |
0.840 |
|
780 |
|
c
|
ACH038 |
Achromatopsia 7 |
37 |
0.839 |
|
781 |
|
c
|
NGH022 |
Night Blindness, Congenital Stationary, Type 1g |
20 |
0.839 |
|
782 |
|
c
|
CNR012 |
Cone-Rod Dystrophy 11 |
27 |
0.839 |
|
783 |
|
|
KNB006 |
Knobloch Syndrome 1 |
43 |
0.839 |
|
784 |
|
|
RTN193 |
Retinitis Pigmentosa and Erythrocytic Microcytosis |
52 |
0.839 |
|
785 |
|
c
|
RTN192 |
Retinitis Pigmentosa 77 |
22 |
0.839 |
|
786 |
|
c
|
RTN196 |
Retinitis Pigmentosa 78 |
20 |
0.839 |
|
787 |
|
c
|
RTN219 |
Retinitis Pigmentosa 85 |
18 |
0.839 |
|
788 |
|
|
CNR041 |
Cone-Rod Dystrophy and Hearing Loss 2 |
19 |
0.839 |
|
789 |
|
c
|
RTN157 |
Retinitis Pigmentosa 37 |
34 |
0.839 |
|
790 |
|
c
|
RTN227 |
Retinitis Pigmentosa 86 |
21 |
0.839 |
|
791 |
|
|
RTN232 |
Retinal Dystrophy, Optic Nerve Edema, Splenomegaly, Anhidrosis, and Migraine Headache Syndrome |
25 |
0.839 |
|
792 |
|
c
|
RTN213 |
Retinitis Pigmentosa 80 |
27 |
0.839 |
|
793 |
|
c
|
RTN217 |
Retinitis Pigmentosa 83 |
20 |
0.839 |
|
794 |
|
c
|
RTN234 |
Retinitis Pigmentosa 90 |
23 |
0.839 |
|
795 |
|
|
TCL023 |
T-Cell Lymphoma, Subcutaneous Panniculitis-Like |
50 |
0.814 |
|
796 |
|
|
ACT201 |
Acute Posterior Multifocal Placoid Pigment Epitheliopathy |
21 |
0.785 |
|
797 |
|
|
OPT077 |
Optic Disc Pit |
17 |
0.785 |
|
798 |
|
c
|
TRN053 |
Transient Pseudohypoaldosteronism |
24 |
0.785 |
|
799 |
|
|
OCL015 |
Oculomotor Apraxia |
39 |
0.785 |
|
800 |
|
|
SPS057 |
Spasticity |
42 |
0.785 |
|
801 |
|
P
|
OVR082 |
Overgrowth Syndrome |
49 |
0.785 |
|
802 |
|
|
LRY022 |
Laryngoonychocutaneous Syndrome |
43 |
0.785 |
|
803 |
|
|
SCH018 |
Schizencephaly |
52 |
0.785 |
|
804 |
|
|
EPD052 |
Epidermolysis Bullosa Simplex Superficialis |
17 |
0.785 |
|
805 |
|
c
|
BRD015 |
Bardet-Biedl Syndrome 3 |
48 |
0.785 |
|
806 |
|
c
|
RTN069 |
Retinitis Pigmentosa 7 |
44 |
0.785 |
|
807 |
|
|
OCL008 |
Oculopharyngeal Muscular Dystrophy |
53 |
0.785 |
|
808 |
|
c
|
MCL059 |
Macular Dystrophy, Patterned, 1 |
29 |
0.785 |
|
809 |
|
P
|
ATX030 |
Ataxia-Telangiectasia |
80 |
0.785 |
|
810 |
|
|
LNN001 |
Lennox-Gastaut Syndrome |
61 |
0.785 |
|
811 |
|
c
|
OGC002 |
Oguchi Disease 2 |
35 |
0.785 |
|
812 |
|
|
BRN032 |
Brain Glioma |
45 |
0.785 |
|
813 |
|
|
GNY003 |
Guanylate Cyclase 2e, Pseudogene |
12 |
0.785 |
|
814 |
|
c
|
BRD019 |
Bardet-Biedl Syndrome 7 |
43 |
0.785 |
|
815 |
|
c
|
DFN093 |
Deafness, Autosomal Recessive 23 |
38 |
0.785 |
|
816 |
|
c
|
MSC165 |
Muscular Dystrophy, Congenital, Lmna-Related |
65 |
0.785 |
|
817 |
|
c
|
ALB009 |
Albinism, Oculocutaneous, Type Ia |
53 |
0.785 |
|
818 |
|
|
MTC027 |
Mitochondrial Trifunctional Protein Deficiency |
57 |
0.785 |
|
819 |
|
|
NRM019 |
Neuraminidase Deficiency |
48 |
0.785 |
|
820 |
|
P
|
PSD087 |
Pseudoxanthoma Elasticum |
67 |
0.785 |
|
821 |
|
|
PTR032 |
Peters-Plus Syndrome |
63 |
0.785 |
|
822 |
|
c
|
BRD014 |
Bardet-Biedl Syndrome 2 |
53 |
0.785 |
|
823 |
|
|
ADN001 |
Adenosine Deaminase Deficiency |
59 |
0.785 |
|
824 |
|
P
|
HRD018 |
Hair Disease |
44 |
0.785 |
|
825 |
|
|
CLR017 |
Clear Cell Sarcoma |
44 |
0.785 |
|
826 |
|
P
|
PRD008 |
Periodontitis |
64 |
0.785 |
|
827 |
|
P
|
HYP061 |
Hypertrophic Cardiomyopathy |
69 |
0.785 |
|
828 |
|
|
CNS004 |
Constipation |
56 |
0.785 |
|
829 |
|
P
|
DMN001 |
Diamond-Blackfan Anemia |
71 |
0.785 |
|
830 |
|
c
|
BSL007 |
Basal Cell Carcinoma |
68 |
0.785 |
|
831 |
|
|
MLG169 |
Malignant Astrocytoma |
57 |
0.785 |
|
832 |
|
|
PRT018 |
Portal Vein Thrombosis |
50 |
0.785 |
|
833 |
|
|
ASP004 |
Asphyxia Neonatorum |
50 |
0.785 |
|
834 |
|
|
ACQ002 |
Acquired Night Blindness |
20 |
0.785 |
|
835 |
|
P
|
PRP019 |
Peripheral Nervous System Disease |
58 |
0.785 |
|
836 |
|
c
|
GM1007 |
Gm1 Gangliosidosis |
65 |
0.785 |
|
837 |
|
|
GLY031 |
Glycoproteinosis |
49 |
0.785 |
|
838 |
|
P
|
BNG032 |
Benign Mesothelioma |
53 |
0.785 |
|
839 |
|
|
VSC006 |
Vascular Cancer |
46 |
0.785 |
|
840 |
|
|
HST011 |
Histoplasmosis |
55 |
0.785 |
|
841 |
|
P
|
INS002 |
in Situ Carcinoma |
53 |
0.785 |
|
842 |
|
|
MSC077 |
Muscle Eye Brain Disease |
52 |
0.785 |
|
843 |
|
|
MSL001 |
Measles |
61 |
0.785 |
|
844 |
|
|
MCR055 |
Microcephaly Nonsyndromal |
9 |
0.785 |
|
845 |
|
|
PCH002 |
Pachygyria |
32 |
0.785 |
|
846 |
|
|
RTC011 |
Reticular Dystrophy of Retinal Pigment Epithelium |
18 |
0.724 |
|
847 |
|
c
|
CNR005 |
Cone-Rod Dystrophy 3 |
40 |
0.724 |
|
848 |
|
c
|
CNR014 |
Cone-Rod Dystrophy 16 |
42 |
0.724 |
|
849 |
|
|
ADR022 |
Adrenomyeloneuropathy |
39 |
0.702 |
|
850 |
|
c
|
RRR006 |
Rare Retinal Disorder |
8 |
0.702 |
|
851 |
|
|
MTR087 |
Maternal Uniparental Disomy |
28 |
0.702 |
|
852 |
|
c
|
JVN041 |
Juvenile Nephronophthisis |
43 |
0.702 |
|
853 |
|
|
CNG506 |
Congenital Amyoplasia |
27 |
0.702 |
|
854 |
|
|
BTT011 |
Butterfly-Shaped Pigment Dystrophy |
31 |
0.702 |
|
855 |
|
|
ATX010 |
Ataxia Neuropathy Spectrum |
34 |
0.702 |
|
856 |
|
|
OLG014 |
Oligocone Trichromacy |
25 |
0.702 |
|
857 |
|
c
|
NRF023 |
Neurofibromatosis, Type Ii |
71 |
0.702 |
|
858 |
|
|
ATH013 |
Atherosclerosis Susceptibility |
63 |
0.702 |
|
859 |
|
|
DRV001 |
Dravet Syndrome |
69 |
0.702 |
|
860 |
|
|
MST006 |
Mast Syndrome |
40 |
0.702 |
|
861 |
|
|
ADR007 |
Adrenoleukodystrophy |
73 |
0.702 |
|
862 |
|
c
|
RTN053 |
Retinitis Pigmentosa 24 |
27 |
0.702 |
|
863 |
|
c
|
DFN146 |
Deafness, X-Linked 3 |
27 |
0.702 |
|
864 |
|
c
|
MCL046 |
Mucolipidosis Iii Alpha/beta |
60 |
0.702 |
|
865 |
|
c
|
MCL016 |
Mucolipidosis Iii Gamma |
50 |
0.702 |
|
866 |
|
|
SNS008 |
Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis |
60 |
0.702 |
|
867 |
|
c
|
RTN068 |
Retinitis Pigmentosa 6 |
27 |
0.702 |
|
868 |
|
P
|
SPR120 |
Supranuclear Palsy, Progressive, 1 |
69 |
0.702 |
|
869 |
|
c
|
CRD185 |
Ceroid Lipofuscinosis, Neuronal, 6 |
53 |
0.702 |
|
870 |
|
|
MTC114 |
Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes |
62 |
0.702 |
|
871 |
|
P
|
KLZ004 |
Kala-Azar 1 |
41 |
0.702 |
|
872 |
|
|
MCL027 |
Macular Dystrophy, Dominant Cystoid |
51 |
0.702 |
|
873 |
|
c
|
NRD017 |
Neurodegeneration with Brain Iron Accumulation 1 |
63 |
0.702 |
|
874 |
|
P
|
DST002 |
Distal Arthrogryposis |
65 |
0.702 |
|
875 |
|
|
MRG003 |
Marginal Zone B-Cell Lymphoma |
52 |
0.702 |
|
876 |
|
c
|
LNG050 |
Long Qt Syndrome 5 |
46 |
0.702 |
|
877 |
|
c
|
RTN143 |
Retinitis Pigmentosa 47 |
41 |
0.702 |
|
878 |
|
c
|
NGH028 |
Night Blindness, Congenital Stationary, Type 1d |
26 |
0.702 |
|
879 |
|
|
BTT017 |
Beta-Thalassemia Major |
51 |
0.702 |
|
880 |
|
c
|
USH040 |
Usher Syndrome, Type Id |
47 |
0.702 |
|
881 |
|
P
|
FRD001 |
Friedreich Ataxia |
61 |
0.702 |
|
882 |
|
|
LYM143 |
Lymphoma, Non-Hodgkin, Familial |
75 |
0.702 |
|
883 |
|
|
RTN135 |
Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome |
34 |
0.702 |
|
884 |
|
c
|
NNP011 |
Nanophthalmos 2 |
26 |
0.702 |
|
885 |
|
c
|
RTN133 |
Retinitis Pigmentosa 43 |
29 |
0.702 |
|
886 |
|
|
MGL003 |
Megalocornea |
47 |
0.702 |
|
887 |
|
|
CHN016 |
Cohen Syndrome |
60 |
0.702 |
|
888 |
|
|
GLC012 |
Galactosialidosis |
56 |
0.702 |
|
889 |
|
|
PGM007 |
Pigmented Paravenous Chorioretinal Atrophy |
42 |
0.702 |
|
890 |
|
c
|
BNM018 |
Bone Mineral Density Quantitative Trait Locus 3 |
33 |
0.702 |
|
891 |
|
|
GLC003 |
Glucose Intolerance |
54 |
0.702 |
|
892 |
|
|
PRM329 |
Premature Aging |
36 |
0.702 |
|
893 |
|
|
THY029 |
Thyroid Carcinoma |
51 |
0.702 |
|
894 |
|
|
XLN228 |
X-Linked Recessive Disease |
24 |
0.702 |
|
895 |
|
P
|
NRD007 |
Neurodegeneration with Brain Iron Accumulation |
52 |
0.702 |
|
896 |
|
c
|
CRD179 |
Ceroid Lipofuscinosis, Neuronal, 7 |
49 |
0.702 |
|
897 |
|
P
|
RNG032 |
Ring Chromosome |
39 |
0.702 |
|
898 |
|
P
|
ZLL001 |
Zellweger Syndrome |
65 |
0.702 |
|
899 |
|
P
|
FBR003 |
Fibrous Histiocytoma |
43 |
0.702 |
|
900 |
|
|
GLC001 |
Glaucomatocyclitic Crisis |
27 |
0.702 |
|
901 |
|
|
KRT006 |
Keratoconjunctivitis |
53 |
0.702 |
|
902 |
|
P
|
HRP006 |
Herpes Simplex |
65 |
0.702 |
|
903 |
|
|
LSH001 |
Leishmaniasis |
64 |
0.702 |
|
904 |
|
P
|
TRM003 |
Tremor |
48 |
0.702 |
|
905 |
|
c
|
ATS025 |
Autosomal Dominant Progressive External Ophthalmoplegia |
45 |
0.702 |
|
906 |
|
P
|
TXC009 |
Toxic Maculopathy |
21 |
0.702 |
|
907 |
|
|
SPS087 |
Spasmus Nutans |
21 |
0.702 |
|
908 |
|
|
PNM008 |
Pneumothorax |
54 |
0.702 |
|
909 |
|
|
MLG077 |
Malignant Peripheral Nerve Sheath Tumor |
54 |
0.702 |
|
910 |
|
|
SMN007 |
Seminoma |
42 |
0.702 |
|
911 |
|
P
|
GRV001 |
Graves' Disease |
55 |
0.702 |
|
912 |
|
c
|
SCN007 |
Secondary Hyperparathyroidism |
51 |
0.702 |
|
913 |
|
|
PRP026 |
Peripheral Retinal Degeneration |
29 |
0.702 |
|
914 |
|
P
|
HYP069 |
Hyperparathyroidism |
62 |
0.702 |
|
915 |
|
|
RBS002 |
Rubeosis Iridis |
32 |
0.702 |
|
916 |
|
P
|
ECL001 |
Eclampsia |
52 |
0.702 |
|
917 |
|
|
ACC002 |
Accommodative Spasm |
25 |
0.702 |
|
918 |
|
P
|
PRN023 |
Prion Disease |
60 |
0.702 |
|
919 |
|
P
|
INT068 |
Intestinal Disease |
53 |
0.702 |
|
920 |
|
|
ERL001 |
Early Myoclonic Encephalopathy |
62 |
0.702 |
|
921 |
|
P
|
CPL006 |
Capillary Hemangioma |
53 |
0.702 |
|
922 |
|
|
LNS001 |
Lens Subluxation |
39 |
0.702 |
|
923 |
|
|
DBT007 |
Diabetic Cataract |
36 |
0.702 |
|
924 |
|
P
|
ACT028 |
Acute Closed-Angle Glaucoma |
32 |
0.702 |
|
925 |
|
|
LKC002 |
Leukocoria |
33 |
0.702 |
|
926 |
|
|
SLR002 |
Solar Retinopathy |
28 |
0.702 |
|
927 |
|
|
RTN004 |
Retinal Microaneurysm |
33 |
0.702 |
|
928 |
|
|
DBT004 |
Diabetic Polyneuropathy |
50 |
0.702 |
|
929 |
|
|
CRB033 |
Cerebral Degeneration |
39 |
0.702 |
|
930 |
|
|
HDR002 |
Hidradenitis Suppurativa |
54 |
0.702 |
|
931 |
|
|
HDR003 |
Hidradenitis |
50 |
0.702 |
|
932 |
|
|
IRN002 |
Iron Metabolism Disease |
57 |
0.702 |
|
933 |
|
|
NRN004 |
Neuroendocrine Tumor |
59 |
0.702 |
|
934 |
|
P
|
MRQ003 |
Morquio Syndrome |
35 |
0.702 |
|
935 |
|
|
PLM033 |
Pulmonary Embolism |
58 |
0.702 |
|
936 |
|
|
DYS032 |
Dystrophinopathies |
47 |
0.702 |
|
937 |
|
|
PLG003 |
Polg-Related Disorders |
20 |
0.702 |
|
938 |
|
|
STM007 |
Stomatitis |
54 |
0.702 |
|
939 |
|
P
|
SCK005 |
Sickle Cell Disease |
56 |
0.702 |
|
940 |
|
|
MYT011 |
Myotonia |
39 |
0.702 |
|
941 |
|
|
PRN039 |
Paraneoplastic Syndromes |
37 |
0.702 |
|
942 |
|
|
FRS019 |
Farsightedness |
36 |
0.702 |
|
943 |
|
P
|
NNS072 |
Nonsyndromic Hearing Loss |