# |
|
Family |
MCID |
Name |
MIFTS |
Score |
1 |
|
|
MTH026 |
Methemoglobinemia Due to Deficiency of Methemoglobin Reductase |
35 |
44.624 |
|
2 |
|
|
MTC146 |
Mitochondrial Complex I Deficiency, Nuclear Type 1 |
61 |
41.306 |
|
3 |
|
P
|
MTH007 |
Methemoglobinemia |
46 |
10.669 |
|
4 |
|
P
|
MPL001 |
Maple Syrup Urine Disease |
70 |
10.018 |
|
5 |
|
|
PYR031 |
Pyruvate Dehydrogenase E3-Binding Protein Deficiency |
43 |
9.193 |
|
6 |
|
|
DHY010 |
Dihydrolipoamide Dehydrogenase Deficiency |
47 |
9.193 |
|
7 |
|
|
ANX004 |
Anoxia |
40 |
9.107 |
|
8 |
|
c
|
CNG223 |
Congenital Methemoglobinemia |
39 |
9.019 |
|
9 |
|
P
|
MYP004 |
Myopathy |
67 |
7.725 |
|
10 |
|
P
|
LCT001 |
Lactic Acidosis |
51 |
6.566 |
|
11 |
|
|
HYP266 |
Hypoxia |
57 |
6.490 |
|
12 |
|
|
MTC005 |
Mitochondrial Metabolism Disease |
45 |
6.409 |
|
13 |
|
P
|
OPT006 |
Optic Nerve Disease |
58 |
6.115 |
|
14 |
|
P
|
MTC133 |
Mitochondrial Myopathy |
50 |
6.080 |
|
15 |
|
P
|
HRD217 |
Hereditary Optic Neuropathy |
36 |
6.041 |
|
16 |
|
P
|
NRP001 |
Neuropathy |
60 |
5.193 |
|
17 |
|
P
|
MTC069 |
Mitochondrial Disorders |
57 |
5.133 |
|
18 |
|
|
CYN002 |
Cyanosis, Transient Neonatal |
43 |
5.128 |
|
19 |
|
|
FTT001 |
Fatty Liver Disease |
62 |
5.036 |
|
20 |
|
|
LBR038 |
Leber Hereditary Optic Neuropathy, Modifier of |
62 |
4.935 |
|
21 |
|
P
|
MYC084 |
Mycobacterium Tuberculosis 1 |
68 |
4.843 |
|
22 |
|
|
HLX001 |
Helix Syndrome |
48 |
4.715 |
|
23 |
|
P
|
PRK039 |
Parkinsonism |
55 |
4.638 |
|
24 |
|
|
HYP066 |
Hyperglycemia |
61 |
4.603 |
|
25 |
|
P
|
NRB001 |
Neuroblastoma |
66 |
4.383 |
|
26 |
|
c
|
ATS307 |
Autosomal Recessive Cerebellar Ataxia |
39 |
4.211 |
|
27 |
|
|
LGH007 |
Leigh Syndrome |
70 |
4.202 |
|
28 |
|
P
|
ENC018 |
Encephalopathy |
62 |
3.978 |
|
29 |
|
|
MTC004 |
Mitochondrial Encephalomyopathy |
42 |
3.966 |
|
30 |
|
|
CHR066 |
Chronic Fatigue Syndrome |
60 |
3.873 |
|
31 |
|
|
GLL048 |
Glial Tumor |
52 |
3.855 |
|
32 |
|
|
GLM045 |
Glioma |
63 |
3.855 |
|
33 |
|
|
NNL005 |
Non-Alcoholic Fatty Liver Disease |
63 |
3.843 |
|
34 |
|
|
CHG001 |
Chagas Disease |
66 |
3.801 |
|
35 |
|
P
|
ALZ034 |
Alzheimer Disease |
87 |
3.781 |
|
36 |
|
c
|
ATR087 |
Atrial Standstill 1 |
74 |
3.559 |
|
37 |
|
|
AGN016 |
Aging |
54 |
3.540 |
|
38 |
|
|
HYP056 |
Hypoglycemia |
65 |
3.461 |
|
39 |
|
|
ECH003 |
Echinococcosis |
53 |
3.428 |
|
40 |
|
|
TRD008 |
Triiodothyronine Receptor Auxiliary Protein |
33 |
3.374 |
|
41 |
|
|
CHL014 |
Cholera |
62 |
3.319 |
|
42 |
|
|
MTC114 |
Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes |
62 |
3.287 |
|
43 |
|
|
LPD008 |
Lipid Metabolism Disorder |
62 |
3.287 |
|
44 |
|
P
|
3MT016 |
3-Methylglutaconic Aciduria, Type Iii |
68 |
3.227 |
|
45 |
|
|
MTC023 |
Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes |
44 |
3.189 |
|
46 |
|
|
BRN071 |
Brain Injury |
50 |
3.088 |
|
47 |
|
|
CRB197 |
Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to |
57 |
3.079 |
|
48 |
|
|
PRT037 |
Pertussis |
65 |
3.066 |
|
49 |
|
|
ATX038 |
Ataxia and Polyneuropathy, Adult-Onset |
46 |
3.043 |
|
50 |
|
P
|
HYP265 |
Hypotonia |
42 |
3.043 |
|
51 |
|
P
|
FTT008 |
Fatty Liver Disease, Nonalcoholic 1 |
48 |
2.998 |
|
52 |
|
P
|
BRS047 |
Breast Cancer |
98 |
2.959 |
|
53 |
|
c
|
MCR115 |
Microvascular Complications of Diabetes 5 |
65 |
2.922 |
|
54 |
|
|
CYS001 |
Cystic Fibrosis |
78 |
2.899 |
|
55 |
|
P
|
CHR012 |
Chronic Granulomatous Disease |
69 |
2.890 |
|
56 |
|
|
MTB004 |
Metabolic Acidosis |
48 |
2.885 |
|
57 |
|
P
|
KLZ004 |
Kala-Azar 1 |
41 |
2.857 |
|
58 |
|
|
LSH001 |
Leishmaniasis |
64 |
2.857 |
|
59 |
|
|
IRN002 |
Iron Metabolism Disease |
57 |
2.857 |
|
60 |
|
|
48X005 |
48,xyyy |
39 |
2.827 |
|
61 |
|
P
|
MSC005 |
Muscular Dystrophy |
67 |
2.797 |
|
62 |
|
|
47X002 |
47,xyy |
48 |
2.793 |
|
63 |
|
P
|
DYS154 |
Dystonia |
64 |
2.786 |
|
64 |
|
|
HMP009 |
Haemophilus Influenzae |
41 |
2.786 |
|
65 |
|
|
CTR172 |
Citrullinemia, Classic |
65 |
2.736 |
|
66 |
|
|
CRT015 |
Carotid Artery Occlusion |
45 |
2.705 |
|
67 |
|
P
|
PRK057 |
Parkinson Disease, Late-Onset |
80 |
2.691 |
|
68 |
|
|
OST159 |
Osteogenic Sarcoma |
66 |
2.691 |
|
69 |
|
P
|
HNT016 |
Huntington Disease |
73 |
2.656 |
|
70 |
|
|
CRB004 |
Cerebral Artery Occlusion |
45 |
2.642 |
|
71 |
|
|
ISC004 |
Ischemia |
61 |
2.635 |
|
72 |
|
|
MTH072 |
Methemoglobin Reductase Deficiency |
15 |
2.597 |
|
73 |
|
c
|
MJR022 |
Major Affective Disorder 8 |
38 |
2.595 |
|
74 |
|
c
|
MJR024 |
Major Affective Disorder 9 |
41 |
2.595 |
|
75 |
|
P
|
BPL003 |
Bipolar Disorder |
56 |
2.595 |
|
76 |
|
|
TRM010 |
Traumatic Brain Injury |
51 |
2.584 |
|
77 |
|
P
|
HYP061 |
Hypertrophic Cardiomyopathy |
69 |
2.566 |
|
78 |
|
|
LBR036 |
Leber Plus Disease |
66 |
2.546 |
|
79 |
|
|
GLB002 |
Glioblastoma |
67 |
2.546 |
|
80 |
|
|
ALC007 |
Alcohol Dependence |
66 |
2.509 |
|
81 |
|
c
|
DLT002 |
Dilated Cardiomyopathy |
78 |
2.440 |
|
82 |
|
P
|
GST053 |
Gastric Cancer |
83 |
2.425 |
|
83 |
|
|
CYS008 |
Cystic Echinococcosis |
57 |
2.420 |
|
84 |
|
P
|
MSC003 |
Muscular Atrophy |
52 |
2.404 |
|
85 |
|
P
|
SZR006 |
Seizure Disorder |
70 |
2.389 |
|
86 |
|
|
MLR004 |
Malaria |
80 |
2.389 |
|
87 |
|
|
RNL114 |
Renal Cell Carcinoma, Nonpapillary |
80 |
2.389 |
|
88 |
|
|
HRW001 |
Hair Whorl |
35 |
2.389 |
|
89 |
|
|
DYS015 |
Dysentery |
50 |
2.381 |
|
90 |
|
|
NRM005 |
Neuromuscular Disease |
63 |
2.367 |
|
91 |
|
|
PST092 |
Posttransplant Acute Limbic Encephalitis |
28 |
2.347 |
|
92 |
|
P
|
CTR177 |
Citrullinemia, Type Ii, Adult-Onset |
55 |
2.334 |
|
93 |
|
|
ART140 |
Arteries, Anomalies of |
53 |
2.334 |
|
94 |
|
|
LPP008 |
Lipoprotein Quantitative Trait Locus |
65 |
2.334 |
|
95 |
|
|
SCC003 |
Succinic Acidemia |
10 |
2.308 |
|
96 |
|
|
ATH013 |
Atherosclerosis Susceptibility |
63 |
2.304 |
|
97 |
|
|
KRN002 |
Kearns-Sayre Syndrome |
63 |
2.292 |
|
98 |
|
|
CRN030 |
Coronary Stenosis |
50 |
2.285 |
|
99 |
|
c
|
BRN108 |
Branchiootic Syndrome 1 |
62 |
2.260 |
|
100 |
|
|
DNT012 |
Dental Caries |
53 |
2.260 |
|
101 |
|
c
|
AMY091 |
Amyotrophic Lateral Sclerosis 1 |
88 |
2.253 |
|
102 |
|
P
|
LTR001 |
Lateral Sclerosis |
58 |
2.253 |
|
103 |
|
|
HYP060 |
Hyperinsulinism |
54 |
2.253 |
|
104 |
|
|
CHL068 |
Cholestasis |
61 |
2.244 |
|
105 |
|
|
ATS010 |
Autosomal Recessive Disease |
42 |
2.235 |
|
106 |
|
P
|
SPP010 |
Suppressor of Tumorigenicity 3 |
51 |
2.215 |
|
107 |
|
P
|
CTR002 |
Cataract |
60 |
2.215 |
|
108 |
|
|
STN013 |
Stenotrophomonas Maltophilia Infection |
26 |
2.213 |
|
109 |
|
c
|
HPT001 |
Hepatitis C |
62 |
2.213 |
|
110 |
|
P
|
MLN008 |
Melanoma |
76 |
2.183 |
|
111 |
|
P
|
PHC003 |
Pheochromocytoma |
69 |
2.172 |
|
112 |
|
|
CNG393 |
Congenital Muscular Dystrophy with Hyperlaxity |
12 |
2.172 |
|
113 |
|
c
|
HPT073 |
Hepatitis C Virus |
71 |
2.131 |
|
114 |
|
|
SLP001 |
Sleeping Sickness |
56 |
2.119 |
|
115 |
|
P
|
VSC007 |
Vascular Disease |
63 |
2.119 |
|
116 |
|
|
ALL014 |
Allergic Encephalomyelitis |
34 |
2.119 |
|
117 |
|
c
|
HYP836 |
Hypercholesterolemia, Familial, 1 |
73 |
2.088 |
|
118 |
|
|
ORL011 |
Oral Cancer |
60 |
2.088 |
|
119 |
|
P
|
RSP003 |
Respiratory Failure |
74 |
2.069 |
|
120 |
|
P
|
LVR013 |
Liver Disease |
69 |
2.054 |
|
121 |
|
|
SQM006 |
Squamous Cell Carcinoma |
60 |
2.044 |
|
122 |
|
P
|
BRS044 |
Breast Adenocarcinoma |
58 |
2.017 |
|
123 |
|
|
GLC003 |
Glucose Intolerance |
54 |
1.998 |
|
124 |
|
|
CRB090 |
Cerebral Hypoxia |
42 |
1.998 |
|
125 |
|
c
|
DNT047 |
Dentinogenesis Imperfecta Type 2 |
35 |
1.998 |
|
126 |
|
P
|
ATS364 |
Autism |
69 |
1.951 |
|
127 |
|
c
|
HYP595 |
Hypertension, Essential |
85 |
1.951 |
|
128 |
|
|
MTC015 |
Mitochondrial Dna-Associated Leigh Syndrome and Narp |
17 |
1.951 |
|
129 |
|
|
PRM329 |
Premature Aging |
36 |
1.905 |
|
130 |
|
P
|
INF032 |
Infertility |
57 |
1.905 |
|
131 |
|
P
|
LPR021 |
Leprosy 3 |
71 |
1.903 |
|
132 |
|
|
URT049 |
Urate Oxidase, Pseudogene |
24 |
1.903 |
|
133 |
|
P
|
MCR010 |
Microcephaly |
60 |
1.903 |
|
134 |
|
|
HNS001 |
Hansen's Disease |
32 |
1.903 |
|
135 |
|
|
CND006 |
Candida Glabrata |
30 |
1.903 |
|
136 |
|
P
|
PRT133 |
Proteasome-Associated Autoinflammatory Syndrome 1 |
80 |
1.853 |
|
137 |
|
|
RPD005 |
Rapidly Involuting Congenital Hemangioma |
46 |
1.853 |
|
138 |
|
|
HYP014 |
Hyperuricemia |
51 |
1.853 |
|
139 |
|
|
CNT047 |
Contact Dermatitis |
57 |
1.846 |
|
140 |
|
c
|
MCR130 |
Microvascular Complications of Diabetes 6 |
41 |
1.845 |
|
141 |
|
c
|
MCR120 |
Microvascular Complications of Diabetes 7 |
47 |
1.845 |
|
142 |
|
c
|
MCR113 |
Microvascular Complications of Diabetes 3 |
52 |
1.845 |
|
143 |
|
c
|
MCR133 |
Microvascular Complications of Diabetes 4 |
41 |
1.845 |
|
144 |
|
P
|
SCK005 |
Sickle Cell Disease |
56 |
1.845 |
|
145 |
|
|
YMN001 |
Yemenite Deaf-Blind Hypopigmentation Syndrome |
66 |
1.800 |
|
146 |
|
|
HMC014 |
Homocysteinemia |
52 |
1.800 |
|
147 |
|
P
|
SCH015 |
Schizophrenia |
74 |
1.800 |
|
148 |
|
P
|
PRS040 |
Prostate Cancer |
95 |
1.800 |
|
149 |
|
c
|
CHR095 |
Chronic Progressive External Ophthalmoplegia |
49 |
1.800 |
|
150 |
|
P
|
LPS004 |
Lupus Erythematosus |
61 |
1.800 |
|
151 |
|
P
|
MYC033 |
Myoclonus |
47 |
1.800 |
|
152 |
|
c
|
THY056 |
Thyroid Dyshormonogenesis 3 |
31 |
1.782 |
|
153 |
|
|
CHL065 |
Cholangiocarcinoma |
58 |
1.782 |
|
154 |
|
|
TRN015 |
Transient Cerebral Ischemia |
63 |
1.782 |
|
155 |
|
|
INT079 |
Intrahepatic Cholangiocarcinoma |
51 |
1.782 |
|
156 |
|
P
|
PLM037 |
Pulmonary Hypertension |
72 |
1.770 |
|
157 |
|
|
DBT010 |
Diabetic Neuropathy |
54 |
1.770 |
|
158 |
|
P
|
THL005 |
Thalassemia |
56 |
1.746 |
|
159 |
|
|
CRV035 |
Cervical Cancer |
73 |
1.746 |
|
160 |
|
c
|
SYS001 |
Systemic Lupus Erythematosus |
87 |
1.746 |
|
161 |
|
P
|
MLT020 |
Multiple Sclerosis |
79 |
1.746 |
|
162 |
|
P
|
FBR017 |
Fibrosarcoma |
56 |
1.746 |
|
163 |
|
|
HDN002 |
Head Injury |
44 |
1.746 |
|
164 |
|
|
CRV040 |
Cervix Carcinoma |
50 |
1.715 |
|
165 |
|
|
PPL052 |
Papillomatosis, Confluent and Reticulated |
34 |
1.691 |
|
166 |
|
|
ART002 |
Arts Syndrome |
66 |
1.689 |
|
167 |
|
P
|
PRG130 |
Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 |
54 |
1.689 |
|
168 |
|
P
|
ANP001 |
Anaplastic Large Cell Lymphoma |
61 |
1.689 |
|
169 |
|
c
|
LKM061 |
Leukemia, Acute Myeloid |
83 |
1.689 |
|
170 |
|
c
|
ACT068 |
Acute Cystitis |
61 |
1.689 |
|
171 |
|
|
TTN003 |
Tetanus |
65 |
1.689 |
|
172 |
|
P
|
PTS002 |
Ptosis |
52 |
1.689 |
|
173 |
|
c
|
BDY010 |
Body Mass Index Quantitative Trait Locus 4 |
46 |
1.650 |
|
174 |
|
c
|
BDY011 |
Body Mass Index Quantitative Trait Locus 10 |
45 |
1.650 |
|
175 |
|
c
|
BDY005 |
Body Mass Index Quantitative Trait Locus 9 |
47 |
1.650 |
|
176 |
|
c
|
BDY012 |
Body Mass Index Quantitative Trait Locus 7 |
44 |
1.650 |
|
177 |
|
c
|
BDY006 |
Body Mass Index Quantitative Trait Locus 8 |
44 |
1.650 |
|
178 |
|
c
|
BDY017 |
Body Mass Index Quantitative Trait Locus 14 |
45 |
1.650 |
|
179 |
|
c
|
BDY020 |
Body Mass Index Quantitative Trait Locus 19 |
52 |
1.650 |
|
180 |
|
c
|
BDY015 |
Body Mass Index Quantitative Trait Locus 12 |
46 |
1.650 |
|
181 |
|
c
|
TYP009 |
Type 2 Diabetes Mellitus |
92 |
1.650 |
|
182 |
|
P
|
PRD008 |
Periodontitis |
64 |
1.650 |
|
183 |
|
c
|
BDY019 |
Body Mass Index Quantitative Trait Locus 18 |
47 |
1.650 |
|
184 |
|
|
TXC005 |
Toxic Shock Syndrome |
62 |
1.650 |
|
185 |
|
|
STT001 |
Status Epilepticus |
59 |
1.650 |
|
186 |
|
|
SPS057 |
Spasticity |
42 |
1.629 |
|
187 |
|
|
VLV047 |
Volvulus of Midgut |
52 |
1.629 |
|
188 |
|
P
|
EXN002 |
Exanthem |
58 |
1.629 |
|
189 |
|
|
SCK003 |
Sickle Cell Anemia |
74 |
1.629 |
|
190 |
|
c
|
PRG038 |
Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 |
49 |
1.629 |
|
191 |
|
|
OCL069 |
Ocular Motor Apraxia |
57 |
1.629 |
|
192 |
|
c
|
PRG040 |
Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 |
53 |
1.629 |
|
193 |
|
c
|
HYP807 |
Hyperinsulinemic Hypoglycemia, Familial, 6 |
52 |
1.629 |
|
194 |
|
|
ORL015 |
Oral Squamous Cell Carcinoma |
43 |
1.629 |
|
195 |
|
P
|
CRD119 |
Cardiac Arrest |
67 |
1.629 |
|
196 |
|
P
|
MYC008 |
Myocarditis |
59 |
1.629 |
|
197 |
|
P
|
CTR077 |
Citrullinemia, Type Ii, Neonatal-Onset |
41 |
1.608 |
|
198 |
|
P
|
LNG032 |
Lung Cancer |
98 |
1.566 |
|
199 |
|
P
|
BLD134 |
Bladder Cancer |
79 |
1.566 |
|
200 |
|
|
ACT098 |
Acute Erythroid Leukemia |
55 |
1.566 |
|
201 |
|
P
|
FRD001 |
Friedreich Ataxia |
61 |
1.566 |
|
202 |
|
|
DBT084 |
Diabetes Mellitus, Ketosis-Prone |
60 |
1.566 |
|
203 |
|
P
|
MLG056 |
Malignant Hyperthermia |
66 |
1.566 |
|
204 |
|
P
|
CRV031 |
Cervical Adenocarcinoma |
48 |
1.566 |
|
205 |
|
|
INS001 |
Insulinoma |
59 |
1.566 |
|
206 |
|
P
|
GST044 |
Gastritis |
55 |
1.566 |
|
207 |
|
|
INT071 |
Intestinal Perforation |
49 |
1.566 |
|
208 |
|
|
ALV002 |
Alveolar Echinococcosis |
57 |
1.566 |
|
209 |
|
P
|
HPT021 |
Hepatitis |
69 |
1.566 |
|
210 |
|
|
FLR002 |
Filariasis |
55 |
1.566 |
|
211 |
|
P
|
BDY004 |
Body Mass Index Quantitative Trait Locus 11 |
83 |
1.566 |
|
212 |
|
|
PHN003 |
Phenylketonuria |
76 |
1.566 |
|
213 |
|
|
PLM129 |
Pulmonary Disease, Chronic Obstructive |
74 |
1.564 |
|
214 |
|
P
|
PSR002 |
Psoriasis |
63 |
1.564 |
|
215 |
|
|
PST011 |
Pustulosis of Palm and Sole |
52 |
1.564 |
|
216 |
|
|
GRD001 |
Giardiasis |
46 |
1.564 |
|
217 |
|
|
CRB037 |
Cerebral Palsy |
67 |
1.564 |
|
218 |
|
|
ADR040 |
Adrenal Gland Pheochromocytoma |
46 |
1.521 |
|
219 |
|
c
|
PK3005 |
Pik3ca-Related Overgrowth Syndrome |
33 |
1.521 |
|
220 |
|
P
|
BCL017 |
B-Cell Lymphoma |
59 |
1.521 |
|
221 |
|
P
|
SKN015 |
Skin Carcinoma |
71 |
1.521 |
|
222 |
|
c
|
ACT071 |
Acute Kidney Failure |
60 |
1.521 |
|
223 |
|
c
|
MGR028 |
Migraine with or Without Aura 1 |
64 |
1.499 |
|
224 |
|
|
OTT002 |
Otitis Media |
71 |
1.499 |
|
225 |
|
P
|
MYL006 |
Myeloid Leukemia |
61 |
1.499 |
|
226 |
|
c
|
PRC016 |
Pre-Eclampsia |
65 |
1.499 |
|
227 |
|
|
HGH043 |
High Grade Glioma |
45 |
1.499 |
|
228 |
|
|
LTH004 |
Lathyrism |
15 |
1.499 |
|
229 |
|
|
SVR001 |
Severe Acute Respiratory Syndrome |
67 |
1.477 |
|
230 |
|
P
|
GLC113 |
Galactosemia I |
66 |
1.476 |
|
231 |
|
|
HPT022 |
Hepatoblastoma |
54 |
1.476 |
|
232 |
|
|
CNG034 |
Congestive Heart Failure |
69 |
1.476 |
|
233 |
|
P
|
TRM003 |
Tremor |
48 |
1.429 |
|
234 |
|
P
|
LNG064 |
Lung Cancer Susceptibility 3 |
70 |
1.429 |
|
235 |
|
|
INS024 |
Insulin-Like Growth Factor I |
78 |
1.426 |
|
236 |
|
|
VSC003 |
Visceral Leishmaniasis |
55 |
1.426 |
|
237 |
|
|
RSC001 |
Rosacea |
55 |
1.426 |
|
238 |
|
|
PRM236 |
Primary Biliary Cholangitis |
60 |
1.426 |
|
239 |
|
|
ONC002 |
Onchocerciasis |
51 |
1.426 |
|
240 |
|
|
PTH003 |
Pathologic Nystagmus |
52 |
1.426 |
|
241 |
|
|
DYS073 |
Dysphagia |
53 |
1.426 |
|
242 |
|
c
|
RNG015 |
Ring Chromosome 2 |
22 |
1.426 |
|
243 |
|
P
|
MYP087 |
Myopathy, Tubular Aggregate, 1 |
49 |
1.416 |
|
244 |
|
c
|
TYP008 |
Type 1 Diabetes Mellitus |
70 |
1.381 |
|
245 |
|
|
BRN004 |
Brain Edema |
54 |
1.381 |
|
246 |
|
|
RBF001 |
Riboflavin Deficiency |
49 |
1.378 |
|
247 |
|
|
LCT008 |
Lactate Dehydrogenase Deficiency |
14 |
1.377 |
|
248 |
|
|
CYN003 |
Cyanide Poisoning |
22 |
1.347 |
|
249 |
|
|
MSC007 |
Muscle Hypertrophy |
64 |
1.347 |
|
250 |
|
|
INF034 |
Infective Endocarditis |
54 |
1.347 |
|
251 |
|
c
|
THY071 |
Thyroid Dyshormonogenesis 1 |
31 |
1.347 |
|
252 |
|
|
RTN212 |
Retinal Dystrophy with or Without Macular Staphyloma |
31 |
1.347 |
|
253 |
|
P
|
MTH008 |
Methylmalonic Acidemia |
52 |
1.347 |
|
254 |
|
|
PRT036 |
Peritonitis |
65 |
1.347 |
|
255 |
|
|
CLR030 |
Clear Cell Renal Cell Carcinoma |
54 |
1.347 |
|
256 |
|
P
|
CCK001 |
Cockayne Syndrome |
68 |
1.347 |
|
257 |
|
P
|
ECL001 |
Eclampsia |
52 |
1.347 |
|
258 |
|
|
GLC009 |
Glucosephosphate Dehydrogenase Deficiency |
53 |
1.347 |
|
259 |
|
|
CHL123 |
Chlamydia |
58 |
1.347 |
|
260 |
|
P
|
END033 |
Endocarditis |
58 |
1.347 |
|
261 |
|
P
|
BNG032 |
Benign Mesothelioma |
53 |
1.347 |
|
262 |
|
P
|
PRP029 |
Porphyria |
60 |
1.347 |
|
263 |
|
|
ISL099 |
Isolated Methylmalonic Acidemia |
36 |
1.347 |
|
|
265 |
|
|
DFC004 |
Deficiency Anemia |
74 |
1.330 |
|
266 |
|
|
BCT022 |
Bacterial Infectious Disease |
56 |
1.330 |
|
267 |
|
|
MTH071 |
Methane Production |
25 |
1.278 |
|
268 |
|
P
|
BRG001 |
Brugada Syndrome |
69 |
1.278 |
|
269 |
|
|
ARG004 |
Argyria |
26 |
1.278 |
|
270 |
|
|
CYS005 |
Cysticercosis |
60 |
1.278 |
|
271 |
|
|
PRP027 |
Peripheral Vascular Disease |
71 |
1.260 |
|
272 |
|
|
ANG054 |
Angina Pectoris |
66 |
1.260 |
|
|
274 |
|
|
MST004 |
Mast Cell Neoplasm |
42 |
1.260 |
|
275 |
|
P
|
HRD018 |
Hair Disease |
44 |
1.260 |
|
276 |
|
|
HLL004 |
Hellp Syndrome |
53 |
1.260 |
|
277 |
|
|
KRT002 |
Keratomalacia |
55 |
1.240 |
|
278 |
|
c
|
SPR086 |
Spermatogenic Failure 3 |
46 |
1.224 |
|
279 |
|
|
SCH060 |
Schistosoma Mansoni Infection, Susceptibility/ |
38 |
1.224 |
|
280 |
|
P
|
PNC035 |
Pancreatic Cancer |
86 |
1.224 |
|
281 |
|
P
|
HML002 |
Hemolytic Anemia |
62 |
1.224 |
|
282 |
|
P
|
RRH023 |
Rare Hereditary Hemochromatosis |
54 |
1.224 |
|
283 |
|
|
ENC067 |
Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis |
50 |
1.224 |
|
284 |
|
|
HMS001 |
Hemosiderosis |
48 |
1.224 |
|
285 |
|
|
SCH014 |
Schistosomiasis |
56 |
1.224 |
|
286 |
|
P
|
HYP076 |
Hyperthyroidism |
53 |
1.224 |
|
287 |
|
|
HRT015 |
Heritable Pulmonary Arterial Hypertension |
46 |
1.224 |
|
288 |
|
|
BRN056 |
Bronchopulmonary Dysplasia |
56 |
1.224 |
|
289 |
|
|
CRT020 |
Cortisone Reductase Deficiency |
34 |
1.209 |
|
290 |
|
c
|
PLM164 |
Pulmonary Hypertension, Primary, 1 |
76 |
1.167 |
|
291 |
|
P
|
ALC033 |
Alcohol Use Disorder |
61 |
1.167 |
|
292 |
|
|
ATX031 |
Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus |
58 |
1.167 |
|
293 |
|
P
|
LKM002 |
Leukemia |
67 |
1.167 |
|
294 |
|
c
|
ACT027 |
Acute Pancreatitis |
60 |
1.167 |
|
295 |
|
|
MNK001 |
Menkes Disease |
64 |
1.161 |
|
296 |
|
|
BRK010 |
Burkitt Lymphoma |
66 |
1.161 |
|
297 |
|
|
LBR031 |
Leber Optic Atrophy and Dystonia |
39 |
1.161 |
|
298 |
|
|
DWN001 |
Down Syndrome |
70 |
1.161 |
|
299 |
|
|
ESP021 |
Esophageal Cancer |
83 |
1.161 |
|
300 |
|
|
ORG002 |
Organic Acidemia |
44 |
1.161 |
|
301 |
|
|
PRX097 |
Paroxysmal Dystonia |
32 |
1.161 |
|
302 |
|
|
LYD001 |
Leydig Cell Tumor |
45 |
1.161 |
|
303 |
|
P
|
HYD006 |
Hydrocephalus |
61 |
1.161 |
|
304 |
|
|
CRB039 |
Cerebrovascular Disease |
66 |
1.161 |
|
305 |
|
P
|
LRY044 |
Larynx Cancer |
54 |
1.161 |
|
306 |
|
c
|
SPR009 |
Sporadic Breast Cancer |
42 |
1.108 |
|
307 |
|
c
|
THY107 |
Thymoma, Familial |
42 |
1.107 |
|
308 |
|
|
ONC007 |
Oncocytoma |
50 |
1.107 |
|
309 |
|
P
|
OVR042 |
Ovarian Cancer |
88 |
1.107 |
|
310 |
|
P
|
CLR023 |
Colorectal Cancer |
100 |
1.107 |
|
311 |
|
c
|
DVL036 |
Developmental and Epileptic Encephalopathy 39 |
39 |
1.107 |
|
312 |
|
P
|
HPT023 |
Hepatocellular Carcinoma |
96 |
1.107 |
|
313 |
|
|
DSS032 |
Disease by Infectious Agent |
55 |
1.107 |
|
314 |
|
|
HPT004 |
Hepatic Coma |
43 |
1.107 |
|
315 |
|
c
|
CHR684 |
Chronic Kidney Disease |
69 |
1.107 |
|
316 |
|
P
|
MLN007 |
Male Infertility |
56 |
1.107 |
|
317 |
|
|
HPT019 |
Hepatic Encephalopathy |
59 |
1.107 |
|
318 |
|
|
DPH001 |
Diphtheria |
59 |
1.107 |
|
319 |
|
P
|
HRT032 |
Heart Disease |
81 |
1.107 |
|
320 |
|
P
|
MYG005 |
Myoglobinuria |
40 |
1.107 |
|
321 |
|
P
|
PRP019 |
Peripheral Nervous System Disease |
58 |
1.107 |
|
322 |
|
P
|
THY023 |
Thymoma |
64 |
1.107 |
|
323 |
|
|
LKS001 |
Leukostasis |
41 |
1.107 |
|
324 |
|
P
|
RRT020 |
Rare Tumor |
39 |
1.044 |
|
325 |
|
P
|
DFN349 |
Deafness, Nonsyndromic Sensorineural, Mitochondrial |
34 |
1.044 |
|
326 |
|
|
KRT058 |
Keratoderma, Palmoplantar, with Deafness |
43 |
1.044 |
|
327 |
|
|
HMM004 |
Hamamy Syndrome |
39 |
1.044 |
|
328 |
|
|
SNG007 |
Sengers Syndrome |
45 |
1.044 |
|
329 |
|
|
MYL069 |
Myeloma, Multiple |
77 |
1.044 |
|
330 |
|
|
PLT031 |
Platelet Membrane Fluidity |
28 |
1.044 |
|
331 |
|
|
SCR011 |
Scrapie |
39 |
1.044 |
|
332 |
|
|
PRS034 |
Parasitic Helminthiasis Infectious Disease |
51 |
1.044 |
|
333 |
|
|
ALL010 |
Allergic Contact Dermatitis |
56 |
1.044 |
|
334 |
|
P
|
BRN006 |
Branchiootorenal Syndrome |
50 |
1.044 |
|
335 |
|
|
CNR001 |
Coenurosis |
26 |
1.044 |
|
336 |
|
|
TNS005 |
Tonsillitis |
57 |
1.044 |
|
337 |
|
P
|
GRV001 |
Graves' Disease |
55 |
1.044 |
|
338 |
|
|
ANS011 |
Anus Cancer |
57 |
1.044 |
|
339 |
|
|
NNS010 |
Nonsyndromic Hearing Loss and Deafness, Mitochondrial |
13 |
1.044 |
|
340 |
|
|
PRS119 |
Persistent Genital Arousal Disorder |
18 |
1.044 |
|
341 |
|
P
|
LKM062 |
Leukemia, Acute Lymphoblastic |
69 |
1.044 |
|
342 |
|
|
BRT005 |
Barth Syndrome |
56 |
1.044 |
|
343 |
|
|
RCH002 |
Richards-Rundle Syndrome |
31 |
1.044 |
|
344 |
|
P
|
SCL018 |
Scoliosis |
57 |
1.044 |
|
345 |
|
|
THY029 |
Thyroid Carcinoma |
51 |
1.044 |
|
346 |
|
P
|
DBT009 |
Diabetes Mellitus |
67 |
1.044 |
|
347 |
|
|
YLL002 |
Yellow Fever |
61 |
1.044 |
|
348 |
|
|
PLC005 |
Placental Insufficiency |
56 |
1.044 |
|
349 |
|
|
MLT006 |
Multidrug-Resistant Tuberculosis |
47 |
1.044 |
|
350 |
|
|
ADN018 |
Adenoma |
59 |
1.044 |
|
351 |
|
|
END086 |
End Stage Renal Disease |
52 |
1.044 |
|
352 |
|
P
|
BRB001 |
Beriberi |
44 |
1.044 |
|
353 |
|
P
|
ADN016 |
Adenocarcinoma |
63 |
1.044 |
|
354 |
|
P
|
INS002 |
in Situ Carcinoma |
53 |
1.044 |
|
355 |
|
|
SPN186 |
Spinal Cord Injury |
61 |
0.976 |
|
356 |
|
c
|
ACT134 |
Acute Liver Failure |
59 |
0.976 |
|
357 |
|
|
ACR009 |
Acromesomelic Dysplasia, Hunter-Thompson Type |
41 |
0.976 |
|
358 |
|
P
|
RTN008 |
Retinitis Pigmentosa |
80 |
0.976 |
|
359 |
|
c
|
OPT053 |
Optic Atrophy 1 |
62 |
0.976 |
|
360 |
|
c
|
L2H001 |
L-2-Hydroxyglutaric Aciduria |
49 |
0.976 |
|
361 |
|
P
|
APL001 |
Aplastic Anemia |
73 |
0.976 |
|
362 |
|
c
|
2HY001 |
2-Hydroxyglutaric Aciduria |
38 |
0.976 |
|
363 |
|
c
|
MCL042 |
Macular Degeneration, Age-Related, 1 |
85 |
0.976 |
|
364 |
|
|
BTT016 |
Batten-Turner Congenital Myopathy |
53 |
0.976 |
|
365 |
|
c
|
CHL116 |
Cholestasis, Intrahepatic, of Pregnancy, 1 |
52 |
0.976 |
|
366 |
|
|
NRR001 |
Neuroretinitis |
42 |
0.976 |
|
367 |
|
|
MDD018 |
Middle East Respiratory Syndrome |
44 |
0.976 |
|
368 |
|
|
RTN023 |
Retinitis |
46 |
0.976 |
|
369 |
|
P
|
MVM001 |
Movement Disease |
61 |
0.976 |
|
370 |
|
P
|
RNV001 |
Renovascular Hypertension |
49 |
0.976 |
|
371 |
|
|
SKN016 |
Skin Disease |
63 |
0.976 |
|
372 |
|
P
|
CNT004 |
Centronuclear Myopathy |
57 |
0.976 |
|
373 |
|
|
SPN035 |
Spindle Cell Sarcoma |
54 |
0.976 |
|
374 |
|
P
|
RTN016 |
Retinal Degeneration |
52 |
0.976 |
|
375 |
|
P
|
PLM175 |
Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 |
51 |
0.976 |
|
376 |
|
P
|
SNS001 |
Sensorineural Hearing Loss |
59 |
0.976 |
|
377 |
|
|
RLP002 |
Relapsing-Remitting Multiple Sclerosis |
56 |
0.976 |
|
378 |
|
P
|
BRS053 |
Breast Fibroadenoma |
49 |
0.976 |
|
379 |
|
P
|
GLY013 |
Glycogen Storage Disease |
60 |
0.976 |
|
380 |
|
|
SRC014 |
Sarcoma |
65 |
0.976 |
|
381 |
|
|
LVR012 |
Liver Cirrhosis |
63 |
0.976 |
|
382 |
|
P
|
ADL010 |
Adult Respiratory Distress Syndrome |
71 |
0.976 |
|
383 |
|
|
CYT002 |
Cytokine Deficiency |
43 |
0.976 |
|
384 |
|
|
MSC157 |
Muscular Dystrophy, Duchenne Type |
79 |
0.904 |
|
385 |
|
|
STR067 |
Stroke, Ischemic |
80 |
0.904 |
|
386 |
|
P
|
MYS005 |
Myositis |
56 |
0.904 |
|
387 |
|
c
|
PRM108 |
Primary Progressive Multiple Sclerosis |
51 |
0.904 |
|
388 |
|
c
|
SCN036 |
Secondary Progressive Multiple Sclerosis |
55 |
0.904 |
|
389 |
|
|
ALC028 |
Alacrima, Achalasia, and Mental Retardation Syndrome |
68 |
0.904 |
|
390 |
|
c
|
PCH010 |
Pachyonychia Congenita 3 |
43 |
0.904 |
|
391 |
|
P
|
ASP006 |
Aspergillosis |
72 |
0.904 |
|
392 |
|
P
|
GLM040 |
Glioma Susceptibility 1 |
71 |
0.904 |
|
393 |
|
|
RNL077 |
Renal Fibrosis |
46 |
0.904 |
|
394 |
|
P
|
PLY041 |
Polymyositis |
59 |
0.904 |
|
395 |
|
|
INT075 |
Intracranial Hypertension |
53 |
0.904 |
|
396 |
|
P
|
RBL001 |
Rubella |
58 |
0.904 |
|
397 |
|
|
VCC001 |
Vaccinia |
47 |
0.904 |
|
398 |
|
|
TRY001 |
Trypanosomiasis |
50 |
0.904 |
|
399 |
|
P
|
DRM010 |
Dermatomyositis |
61 |
0.904 |
|
400 |
|
|
RCK004 |
Rickets |
68 |
0.904 |
|
401 |
|
|
TLN003 |
Telangiectasis |
51 |
0.904 |
|
402 |
|
|
ALC006 |
Alcoholic Hepatitis |
61 |
0.904 |
|
403 |
|
|
PSY004 |
Psychotic Disorder |
66 |
0.904 |
|
404 |
|
|
CCC002 |
Coccidiosis |
50 |
0.904 |
|
405 |
|
|
MLG169 |
Malignant Astrocytoma |
57 |
0.904 |
|
406 |
|
|
ERL001 |
Early Myoclonic Encephalopathy |
62 |
0.904 |
|
407 |
|
P
|
KDN017 |
Kidney Cancer |
61 |
0.904 |
|
408 |
|
|
GST045 |
Gastroenteritis |
58 |
0.904 |
|
409 |
|
|
DBT007 |
Diabetic Cataract |
36 |
0.904 |
|
410 |
|
|
IDP022 |
Idiopathic Spinal Cord Herniation |
17 |
0.904 |
|
411 |
|
P
|
DBT005 |
Diabetes Insipidus |
54 |
0.891 |
|
412 |
|
P
|
MCH002 |
Machado-Joseph Disease |
62 |
0.891 |
|
413 |
|
|
ALZ029 |
Alzheimer Disease Mitochondrial |
24 |
0.891 |
|
414 |
|
|
ARG002 |
Argininosuccinic Aciduria |
61 |
0.891 |
|
415 |
|
|
ASP002 |
Aspartylglucosaminuria |
58 |
0.891 |
|
416 |
|
|
SPS007 |
Spastic Cerebral Palsy |
46 |
0.891 |
|
417 |
|
|
APR001 |
Apraxia |
52 |
0.891 |
|
418 |
|
|
PNB004 |
Panbronchiolitis, Diffuse |
34 |
0.891 |
|
419 |
|
|
HYP690 |
Hyper-Beta-Alaninemia |
24 |
0.891 |
|
420 |
|
|
EST002 |
Estrogen-Receptor Negative Breast Cancer |
45 |
0.891 |
|
421 |
|
P
|
BLD062 |
Bile Duct Cancer |
67 |
0.891 |
|
422 |
|
|
PTN001 |
Patent Foramen Ovale |
62 |
0.891 |
|
423 |
|
P
|
DRR001 |
Diarrhea |
55 |
0.891 |
|
424 |
|
|
MYP161 |
Myopathy, Congenital Proximal, with Minicore Lesions |
17 |
0.855 |
|
425 |
|
|
PRS129 |
Prostatic Hyperplasia, Benign |
49 |
0.825 |
|
426 |
|
|
FRN006 |
Frontotemporal Dementia |
68 |
0.825 |
|
427 |
|
|
PLY150 |
Polykaryocytosis Inducer |
29 |
0.825 |
|
428 |
|
P
|
ATX030 |
Ataxia-Telangiectasia |
80 |
0.825 |
|
429 |
|
|
HMN044 |
Human Immunodeficiency Virus Type 1 |
78 |
0.825 |
|
430 |
|
c
|
ATS007 |
Autism Spectrum Disorder |
72 |
0.825 |
|
431 |
|
|
CLT003 |
Colitis |
63 |
0.825 |
|
432 |
|
c
|
VNT034 |
Ventricular Fibrillation, Paroxysmal Familial, 1 |
67 |
0.825 |
|
433 |
|
P
|
MYC007 |
Myocardial Infarction |
70 |
0.825 |
|
434 |
|
P
|
HYP098 |
Hypereosinophilic Syndrome |
66 |
0.825 |
|
435 |
|
P
|
CND004 |
Candidiasis |
58 |
0.825 |
|
436 |
|
P
|
RNL017 |
Renal Oncocytoma |
54 |
0.825 |
|
437 |
|
|
PRP016 |
Paraplegia |
52 |
0.825 |
|
438 |
|
|
CHL045 |
Choline Deficiency Disease |
39 |
0.825 |
|
439 |
|
|
STR103 |
Streptococcus Pneumonia |
47 |
0.825 |
|
440 |
|
|
CRN019 |
Coronary Artery Vasospasm |
47 |
0.825 |
|
441 |
|
|
CNS004 |
Constipation |
56 |
0.825 |
|
442 |
|
|
PRS021 |
Prostatic Adenoma |
43 |
0.825 |
|
443 |
|
c
|
BSL007 |
Basal Cell Carcinoma |
68 |
0.825 |
|
444 |
|
|
FCL014 |
Focal Epilepsy |
53 |
0.825 |
|
445 |
|
P
|
RNL015 |
Renal Hypertension |
45 |
0.825 |
|
446 |
|
|
LYM017 |
Lyme Disease |
62 |
0.825 |
|
447 |
|
|
PRS045 |
Prostatic Hypertrophy |
53 |
0.825 |
|
448 |
|
|
SVR004 |
Severe Combined Immunodeficiency |
72 |
0.825 |
|
449 |
|
P
|
ART021 |
Arteriosclerosis |
54 |
0.825 |
|
450 |
|
P
|
OVR049 |
Ovarian Disease |
52 |
0.825 |
|
451 |
|
P
|
LMB006 |
Limb-Girdle Muscular Dystrophy |
52 |
0.825 |
|
452 |
|
|
STM007 |
Stomatitis |
54 |
0.825 |
|
453 |
|
|
MYC005 |
Myocardial Stunning |
46 |
0.825 |
|
454 |
|
|
WLL004 |
Wallerian Degeneration |
38 |
0.825 |
|
455 |
|
P
|
MRC003 |
Mercury Poisoning |
49 |
0.825 |
|
456 |
|
P
|
MYC026 |
Myoclonus Epilepsy |
35 |
0.825 |
|
457 |
|
|
MYC015 |
Mycobacterium Fortuitum |
28 |
0.825 |
|
458 |
|
|
ADR022 |
Adrenomyeloneuropathy |
39 |
0.738 |
|
459 |
|
|
PRC049 |
Precursor T-Cell Acute Lymphoblastic Leukemia |
45 |
0.738 |
|
460 |
|
P
|
CRN300 |
Coronary Heart Disease 1 |
73 |
0.738 |
|
461 |
|
|
ADR007 |
Adrenoleukodystrophy |
73 |
0.738 |
|
462 |
|
|
ANM045 |
Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency |
50 |
0.738 |
|
463 |
|
P
|
ART067 |
Aortic Aneurysm, Familial Thoracic 1 |
61 |
0.738 |
|
464 |
|
c
|
ATM006 |
Autoimmune Lymphoproliferative Syndrome |
75 |
0.738 |
|
465 |
|
|
ATM095 |
Autoimmune Disease |
61 |
0.738 |
|
466 |
|
|
AGN018 |
Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome |
57 |
0.738 |
|
467 |
|
P
|
SLP006 |
Sleep Apnea |
69 |
0.738 |
|
468 |
|
|
FML037 |
Female Breast Cancer |
51 |
0.738 |
|
469 |
|
|
CHK001 |
Chikungunya |
60 |
0.738 |
|
470 |
|
P
|
URN019 |
Urinary Tract Infection |
49 |
0.738 |
|
471 |
|
|
NNL006 |
Non-Alcoholic Steatohepatitis |
54 |
0.738 |
|
472 |
|
|
HLC007 |
Helicobacter Pylori Infection |
67 |
0.738 |
|
473 |
|
|
VRC005 |
Varicose Veins |
60 |
0.738 |
|
474 |
|
c
|
HYP368 |
Hyperphenylalaninemia, Bh4-Deficient, C |
37 |
0.738 |
|
475 |
|
|
MNN043 |
Meningioma, Familial |
79 |
0.738 |
|
476 |
|
|
FSC002 |
Fascioliasis |
44 |
0.738 |
|
477 |
|
c
|
ACT075 |
Acute Myocardial Infarction |
56 |
0.738 |
|
478 |
|
P
|
KDN018 |
Kidney Disease |
72 |
0.738 |
|
479 |
|
P
|
RHB003 |
Rhabdomyosarcoma |
66 |
0.738 |
|
480 |
|
|
GSG001 |
Gas Gangrene |
52 |
0.738 |
|
481 |
|
|
ULC004 |
Ulcerative Colitis |
74 |
0.738 |
|
482 |
|
|
CHR074 |
Choriocarcinoma |
46 |
0.738 |
|
483 |
|
c
|
CHR688 |
Chronic Acquired Demyelinating Polyneuropathy |
16 |
0.738 |
|
484 |
|
P
|
PTT006 |
Pituitary Adenoma |
55 |
0.738 |
|
485 |
|
|
TRC003 |
Trichomoniasis |
53 |
0.738 |
|
486 |
|
|
ART016 |
Aortic Aneurysm |
68 |
0.738 |
|
487 |
|
|
GLC008 |
Glucose Metabolism Disease |
40 |
0.738 |
|
488 |
|
|
SCR001 |
Secretory Meningioma |
40 |
0.738 |
|
489 |
|
|
LYM002 |
Lymphoplasmacyte-Rich Meningioma |
35 |
0.738 |
|
490 |
|
|
LNG099 |
Lung Disease |
62 |
0.738 |
|
491 |
|
P
|
KRT007 |
Keratoconus |
50 |
0.738 |
|
492 |
|
P
|
CHR071 |
Charcot-Marie-Tooth Disease |
64 |
0.738 |
|
493 |
|
P
|
SPN046 |
Spinal Muscular Atrophy |
63 |
0.738 |
|
494 |
|
|
KRT009 |
Keratosis |
53 |
0.738 |
|
495 |
|
|
CLN015 |
Colon Adenocarcinoma |
65 |
0.738 |
|
496 |
|
|
HMG005 |
Hemoglobinopathy |
56 |
0.738 |
|
497 |
|
P
|
MYS079 |
Miyoshi Muscular Dystrophy |
54 |
0.738 |
|
498 |
|
P
|
BND020 |
Bone Disease |
59 |
0.738 |
|
499 |
|
|
TTH006 |
Tooth Disease |
51 |
0.738 |
|
500 |
|
P
|
PLY011 |
Polycystic Ovary Syndrome |
57 |
0.738 |
|
501 |
|
P
|
PRN023 |
Prion Disease |
60 |
0.738 |
|
502 |
|
P
|
PNC044 |
Pancreatitis |
61 |
0.738 |
|
503 |
|
P
|
EYD002 |
Eye Disease |
57 |
0.738 |
|
504 |
|
P
|
PRM002 |
Primary Hyperoxaluria |
65 |
0.738 |
|
505 |
|
P
|
OBS001 |
Obstructive Jaundice |
48 |
0.738 |
|
506 |
|
|
IDP070 |
Idiopathic Scoliosis |
42 |
0.738 |
|
507 |
|
|
FML035 |
Familial Hyperlipidemia |
55 |
0.738 |
|
508 |
|
|
SPN021 |
Spinal Meningioma |
50 |
0.738 |
|
509 |
|
P
|
CRD246 |
Cardiovascular System Disease |
56 |
0.738 |
|
510 |
|
|
HYP141 |
Hyperphenylalaninemia |
42 |
0.738 |
|
511 |
|
P
|
MYT002 |
Myotonic Dystrophy |
51 |
0.738 |
|
512 |
|
|
NCL011 |
Nuclear Gene-Encoded Leigh Syndrome Spectrum |
21 |
0.738 |
|
513 |
|
P
|
TXP001 |
Toxoplasmosis |
60 |
0.738 |
|
514 |
|
|
AGR019 |
Age-Related Hearing Loss |
41 |
0.738 |
|
515 |
|
|
ANR040 |
Aneurysm |
61 |
0.738 |
|
516 |
|
|
FST010 |
Fasting Hypoglycemia |
33 |
0.738 |
|
517 |
|
|
HYP781 |
Hypoascorbemia |
52 |
0.719 |
|
518 |
|
|
RHB024 |
Rhabdomyosarcoma 2 |
67 |
0.719 |
|
519 |
|
|
ANT039 |
Antisynthetase Syndrome |
55 |
0.719 |
|
520 |
|
|
FST001 |
Foster-Kennedy Syndrome |
39 |
0.719 |
|
521 |
|
|
FRC013 |
Fructose Utilization |
15 |
0.639 |
|
522 |
|
|
PLY100 |
Polyploidy |
36 |
0.639 |
|
523 |
|
|
ETH012 |
Ethylene Glycol Poisoning |
29 |
0.639 |
|
524 |
|
c
|
ACQ047 |
Acquired Methemoglobinemia |
30 |
0.639 |
|
525 |
|
P
|
RTT002 |
Rett Syndrome |
79 |
0.639 |
|
526 |
|
c
|
GLL024 |
Gallbladder Disease 1 |
52 |
0.639 |
|
527 |
|
|
MHR001 |
Mohr-Tranebjaerg Syndrome |
49 |
0.639 |
|
528 |
|
P
|
MTR004 |
Maturity-Onset Diabetes of the Young |
68 |
0.639 |
|
529 |
|
|
DGL002 |
D-Glyceric Aciduria |
41 |
0.639 |
|
530 |
|
|
MTC205 |
Mitochondrial Complex Iv Deficiency, Nuclear Type 1 |
57 |
0.639 |
|
531 |
|
|
HYP814 |
Hypermethioninemia with S-Adenosylhomocysteine Hydrolase Deficiency |
34 |
0.639 |
|
532 |
|
c
|
MSC106 |
Mosaic Variegated Aneuploidy Syndrome 2 |
41 |
0.639 |
|
533 |
|
P
|
INF037 |
Inflammatory Bowel Disease |
53 |
0.639 |
|
534 |
|
|
DFF005 |
Diffuse Large B-Cell Lymphoma |
54 |
0.639 |
|
535 |
|
|
LMB062 |
Limb Ischemia |
55 |
0.639 |
|
536 |
|
|
INV001 |
Invasive Aspergillosis |
49 |
0.639 |
|
537 |
|
P
|
BLY001 |
B-Lymphoblastic Leukemia/lymphoma |
52 |
0.639 |
|
538 |
|
|
MLD018 |
Mild Cognitive Impairment |
48 |
0.639 |
|
539 |
|
|
DBT090 |
Diabetes and Deafness, Maternally Inherited |
45 |
0.639 |
|
540 |
|
|
CRY035 |
Cryptorchidism, Unilateral or Bilateral |
58 |
0.639 |
|
541 |
|
|
TRD006 |
Tardive Dyskinesia |
53 |
0.639 |
|
542 |
|
|
WRN002 |
Wernicke-Korsakoff Syndrome |
50 |
0.639 |
|
543 |
|
c
|
HYP602 |
Hyperoxaluria, Primary, Type Ii |
49 |
0.639 |
|
544 |
|
P
|
ART106 |
Arterial Calcification, Generalized, of Infancy, 1 |
48 |
0.639 |
|
545 |
|
c
|
THY109 |
Thyroid Cancer, Nonmedullary, 1 |
55 |
0.639 |
|
546 |
|
P
|
SCL057 |
Scoliosis, Isolated 1 |
40 |
0.639 |
|
547 |
|
c
|
MTR019 |
Maturity-Onset Diabetes of the Young, Type 2 |
53 |
0.639 |
|
548 |
|
|
INC002 |
Inclusion Body Myositis |
57 |
0.639 |
|
549 |
|
|
CMR002 |
Coumarin Resistance |
59 |
0.639 |
|
550 |
|
|
OPT066 |
Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy |
55 |
0.639 |
|
551 |
|
|
ACH004 |
Achondroplasia |
66 |
0.639 |
|
552 |
|
|
RHM034 |
Rahman Syndrome |
37 |
0.639 |
|
553 |
|
c
|
ACT073 |
Acute Leukemia |
58 |
0.639 |
|
554 |
|
P
|
ZLL001 |
Zellweger Syndrome |
65 |
0.639 |
|
555 |
|
|
BRR002 |
Barrett's Adenocarcinoma |
37 |
0.639 |
|
556 |
|
|
URM002 |
Uremia |
47 |
0.639 |
|
557 |
|
|
CRC021 |
Carcinosarcoma |
64 |
0.639 |
|
558 |
|
|
SKN019 |
Skin Melanoma |
71 |
0.639 |
|
559 |
|
|
MSC193 |
Muscular Lipidosis |
22 |
0.639 |
|
560 |
|
c
|
PRG106 |
Progressive Muscular Dystrophy |
32 |
0.639 |
|
561 |
|
|
PNC129 |
Pancreatic Adenocarcinoma |
65 |
0.639 |
|
562 |
|
P
|
EPL164 |
Epilepsy |
68 |
0.639 |
|
563 |
|
P
|
PLM036 |
Pulmonary Fibrosis |
66 |
0.639 |
|
564 |
|
|
GST040 |
Gastric Adenocarcinoma |
67 |
0.639 |
|
565 |
|
|
ANV001 |
Anovulation |
47 |
0.639 |
|
566 |
|
|
OVR063 |
Overnutrition |
42 |
0.639 |
|
567 |
|
P
|
BNG002 |
Benign Meningioma |
36 |
0.639 |
|
568 |
|
|
PPT005 |
Peptic Ulcer Disease |
58 |
0.639 |
|
569 |
|
P
|
PLL002 |
Pellagra |
46 |
0.639 |
|
570 |
|
P
|
ART022 |
Arthritis |
71 |
0.639 |
|
571 |
|
|
OST012 |
Osteoarthritis |
77 |
0.639 |
|
572 |
|
P
|
INT070 |
Intestinal Obstruction |
57 |
0.639 |
|
573 |
|
P
|
DNG005 |
Dengue Virus |
56 |
0.639 |
|
574 |
|
|
SPR006 |
Sparganosis |
35 |
0.639 |
|
575 |
|
P
|
DMN002 |
Dementia |
66 |
0.639 |
|
576 |
|
|
ALL029 |
Allergic Disease |
59 |
0.639 |
|
577 |
|
|
VRC001 |
Varicocele |
48 |
0.639 |
|
578 |
|
|
PCD001 |
Pica Disease |
38 |
0.639 |
|
579 |
|
|
SKN005 |
Skin Atrophy |
41 |
0.639 |
|
580 |
|
|
NRT004 |
Neuritis |
53 |
0.639 |
|
581 |
|
P
|
HYP086 |
Hypothyroidism |
69 |
0.639 |
|
582 |
|
|
GLN002 |
Glanders |
38 |
0.639 |
|
583 |
|
|
GST033 |
Gestational Diabetes |
61 |
0.639 |
|
584 |
|
|
MST005 |
Mastitis |
53 |
0.639 |
|
585 |
|
P
|
FNC004 |
Fanconi Syndrome |
60 |
0.639 |
|
586 |
|
|
BRN024 |
Bronchitis |
67 |
0.639 |
|
587 |
|
P
|
CWD010 |
Cowden Syndrome |
70 |
0.639 |
|
588 |
|
|
NRT001 |
Neurotic Disorder |
56 |
0.639 |
|
589 |
|
P
|
RTN018 |
Retinal Disease |
53 |
0.639 |
|
590 |
|
|
ACT058 |
Active Peptic Ulcer Disease |
56 |
0.639 |
|
591 |
|
|
MDD011 |
Mood Disorder |
62 |
0.639 |
|
592 |
|
P
|
GLM007 |
Glomerulonephritis |
60 |
0.639 |
|
593 |
|
|
DMY004 |
Demyelinating Disease |
50 |
0.639 |
|
594 |
|
P
|
PLY019 |
Polyneuropathy |
52 |
0.639 |
|
595 |
|
|
GST023 |
Gastric Ulcer |
52 |
0.639 |
|
596 |
|
|
QDR001 |
Quadriplegia |
50 |
0.639 |
|
597 |
|
P
|
ATS308 |
Autosomal Dominant Cerebellar Ataxia |
64 |
0.639 |
|
598 |
|
c
|
HPT016 |
Hepatitis B |
62 |
0.639 |
|
599 |
|
|
GRN017 |
Granulocytopenia |
42 |
0.639 |
|
600 |
|
|
SYS003 |
Systolic Heart Failure |
49 |
0.639 |
|
601 |
|
P
|
DRM053 |
Dermatitis, Atopic |
65 |
0.522 |
|
602 |
|
c
|
ALP101 |
Alpha-Thalassemia |
62 |
0.522 |
|
603 |
|
c
|
LCT020 |
Lactic Acidosis, Chronic Adult Form |
8 |
0.522 |
|
604 |
|
|
PLG003 |
Polg-Related Disorders |
20 |
0.522 |
|
605 |
|
|
MTH047 |
Methanol Poisoning |
37 |
0.522 |
|
606 |
|
|
CNG506 |
Congenital Amyoplasia |
27 |
0.522 |
|
607 |
|
|
GRN033 |
Granulomatous Mastitis |
32 |
0.522 |
|
608 |
|
|
GLM044 |
Glomerular Disease |
35 |
0.522 |
|
609 |
|
c
|
BDY007 |
Body Mass Index Quantitative Trait Locus 1 |
40 |
0.522 |
|
610 |
|
P
|
NSP012 |
Nasopharyngeal Carcinoma |
61 |
0.522 |
|
611 |
|
|
CHR696 |
Charcot-Marie-Tooth Disease, X-Linked Recessive, 4, with or Without Cerebellar Ataxia |
32 |
0.522 |
|
612 |
|
|
PLM134 |
Pulmonary Fibrosis, Idiopathic |
76 |
0.522 |
|
613 |
|
|
3HY007 |
3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency |
51 |
0.522 |
|
614 |
|
P
|
MYS003 |
Myasthenia Gravis |
68 |
0.522 |
|
615 |
|
|
SCC001 |
Succinic Semialdehyde Dehydrogenase Deficiency |
59 |
0.522 |
|
616 |
|
c
|
SPS222 |
Spastic Paraplegia 20, Autosomal Recessive |
56 |
0.522 |
|
617 |
|
|
SQM013 |
Squamous Cell Carcinoma, Head and Neck |
73 |
0.522 |
|
618 |
|
P
|
ALB003 |
Albinism-Deafness Syndrome |
34 |
0.522 |
|
619 |
|
|
CMB017 |
Combined Oxidative Phosphorylation Deficiency 6 |
41 |
0.522 |
|
620 |
|
|
CRD223 |
Cardiac Arrhythmia |
63 |
0.522 |
|
621 |
|
|
ANR007 |
Anorexia Nervosa |
60 |
0.522 |
|
622 |
|
|
ALL003 |
Allergic Rhinitis |
67 |
0.522 |
|
623 |
|
c
|
CTR132 |
Cataract 3, Multiple Types |
42 |
0.522 |
|
624 |
|
|
PRK088 |
Parkinson Disease, Mitochondrial |
19 |
0.522 |
|
625 |
|
|
MTC029 |
Mitochondrial Complex V Deficiency, Nuclear Type 1 |
40 |
0.522 |
|
626 |
|
|
END057 |
Endometrial Cancer |
72 |
0.522 |
|
627 |
|
P
|
TRC072 |
Treacher Collins Syndrome 1 |
62 |
0.522 |
|
628 |
|
|
HMF006 |
Hemifacial Microsomia |
55 |
0.522 |
|
629 |
|
|
PHS025 |
Phosphatase, Acid, of Tissues |
28 |
0.522 |
|
630 |
|
|
CRT072 |
Creutzfeldt-Jakob Disease |
68 |
0.522 |
|
631 |
|
|
CRZ001 |
Crouzon Syndrome |
65 |
0.522 |
|
632 |
|
|
VTL009 |
Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 |
42 |
0.522 |
|
633 |
|
c
|
LKM063 |
Leukemia, Chronic Myeloid |
71 |
0.522 |
|
634 |
|
|
CHR100 |
Chronic Ulcer of Skin |
57 |
0.522 |
|
635 |
|
|
EPD015 |
Epidemic Typhus |
44 |
0.522 |
|
636 |
|
|
ALC001 |
Alcohol-Related Birth Defect |
36 |
0.522 |
|
637 |
|
P
|
FML011 |
Familial Adenomatous Polyposis |
71 |
0.522 |
|
638 |
|
|
VTM002 |
Vitamin B12 Deficiency |
48 |
0.522 |
|
639 |
|
P
|
PRG013 |
Paraganglioma |
57 |
0.522 |
|
640 |
|
|
CRB150 |
Cerebral Creatine Deficiency Syndrome 2 |
54 |
0.522 |
|
641 |
|
|
PYR012 |
Pyruvate Dehydrogenase E1-Beta Deficiency |
41 |
0.522 |
|
642 |
|
|
PRT251 |
Proteinuria, Chronic Benign |
57 |
0.522 |
|
643 |
|
|
NRN005 |
Neuronal Ceroid-Lipofuscinoses |
61 |
0.522 |
|
644 |
|
|
BCT021 |
Bacterial Sepsis |
43 |
0.522 |
|
645 |
|
P
|
HYP111 |
Hyperprolinemia |
45 |
0.522 |
|
646 |
|
P
|
PLY014 |
Polycystic Kidney Disease |
69 |
0.522 |
|
647 |
|
P
|
ATR011 |
Atrial Fibrillation |
66 |
0.522 |
|
648 |
|
P
|
FTL001 |
Fetal Alcohol Syndrome |
55 |
0.522 |
|
649 |
|
|
CRD231 |
Cardiomyopathy, Infantile Histiocytoid |
45 |
0.522 |
|
650 |
|
|
SLF014 |
Sulfite Oxidase Deficiency, Isolated |
53 |
0.522 |
|
651 |
|
|
CNT105 |
Central Core Disease of Muscle |
59 |
0.522 |
|
652 |
|
P
|
ABD014 |
Abdominal Obesity-Metabolic Syndrome 1 |
63 |
0.522 |
|
653 |
|
P
|
MCR129 |
Microvascular Complications of Diabetes 1 |
68 |
0.522 |
|
654 |
|
c
|
MTH083 |
Methemoglobinemia, Beta Type |
22 |
0.522 |
|
655 |
|
c
|
MTH084 |
Methemoglobinemia, Alpha Type |
11 |
0.522 |
|
656 |
|
|
INT323 |
Intraocular Pressure Quantitative Trait Locus |
64 |
0.522 |
|
657 |
|
|
EWN003 |
Ewing Sarcoma |
70 |
0.522 |
|
658 |
|
P
|
MJR001 |
Major Depressive Disorder |
68 |
0.522 |
|
659 |
|
|
ACT119 |
Acute Promyelocytic Leukemia |
62 |
0.522 |
|
660 |
|
c
|
BRS111 |
Breast-Ovarian Cancer, Familial 2 |
53 |
0.522 |
|
661 |
|
c
|
SCH079 |
Schizophrenia 1 |
44 |
0.522 |
|
662 |
|
|
TBL029 |
Tubulin, Beta |
28 |
0.522 |
|
663 |
|
P
|
VTL004 |
Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 |
60 |
0.522 |
|
664 |
|
c
|
HYP597 |
Hyperprolinemia, Type Ii |
43 |
0.522 |
|
665 |
|
P
|
TRT019 |
Torticollis |
47 |
0.522 |
|
666 |
|
c
|
NRD033 |
Neurodegeneration with Brain Iron Accumulation 2a |
70 |
0.522 |
|
667 |
|
|
KRT071 |
Keratosis, Seborrheic |
56 |
0.522 |
|
668 |
|
|
PTR032 |
Peters-Plus Syndrome |
63 |
0.522 |
|
669 |
|
|
RFS006 |
Refsum Disease, Classic |
63 |
0.522 |
|
670 |
|
c
|
TBR025 |
Tuberous Sclerosis 1 |
84 |
0.522 |
|
671 |
|
c
|
CRD086 |
Cardiomyopathy, Familial Hypertrophic, 1 |
69 |
0.522 |
|
672 |
|
c
|
SML038 |
Small Cell Cancer of the Lung |
69 |
0.522 |
|
673 |
|
P
|
HYP726 |
Hypercalcemia, Infantile, 1 |
58 |
0.522 |
|
674 |
|
P
|
HYP750 |
Hypertriglyceridemia, Familial |
62 |
0.522 |
|
675 |
|
|
MLT157 |
Multiple System Atrophy 1 |
69 |
0.522 |
|
676 |
|
P
|
MDL005 |
Medulloblastoma |
75 |
0.522 |
|
677 |
|
|
NPH091 |
Nephrolithiasis, Calcium Oxalate |
61 |
0.522 |
|
678 |
|
P
|
MYP105 |
Myopathy, Myosin Storage, Autosomal Dominant |
40 |
0.522 |
|
679 |
|
c
|
CHR489 |
Charcot-Marie-Tooth Disease, Axonal, Type 2q |
32 |
0.522 |
|
680 |
|
|
MLD001 |
Melioidosis |
67 |
0.522 |
|
681 |
|
|
MTC155 |
Mitochondrial Complex I Deficiency, Nuclear Type 7 |
22 |
0.522 |
|
682 |
|
|
CHR431 |
Chronic Venous Insufficiency |
48 |
0.522 |
|
683 |
|
|
CRD137 |
Cardiogenic Shock |
56 |
0.522 |
|
684 |
|
P
|
NRD007 |
Neurodegeneration with Brain Iron Accumulation |
52 |
0.522 |
|
685 |
|
c
|
CHR697 |
Charcot-Marie-Tooth Disease X-Linked Recessive 4 |
31 |
0.522 |
|
686 |
|
P
|
HRD144 |
Hereditary Mixed Polyposis Syndrome |
54 |
0.522 |
|
687 |
|
|
RGD003 |
Rigid Spine Muscular Dystrophy 1 |
56 |
0.522 |
|
688 |
|
|
LMY002 |
Leiomyoma |
51 |
0.522 |
|
689 |
|
P
|
FML068 |
Familial Hypocalciuric Hypercalcemia |
55 |
0.522 |
|
690 |
|
|
FBR009 |
Fibrous Dysplasia |
48 |
0.522 |
|
691 |
|
P
|
CRB210 |
Cerebrofacial Arteriovenous Metameric Syndrome |
27 |
0.522 |
|
692 |
|
P
|
SDR003 |
Sideroblastic Anemia |
51 |
0.522 |
|
693 |
|
|
SCT002 |
Scotoma |
42 |
0.522 |
|
694 |
|
P
|
HLP001 |
Holoprosencephaly |
69 |
0.522 |
|
695 |
|
|
NTR005 |
Nutritional Deficiency Disease |
61 |
0.522 |
|
696 |
|
|
URT010 |
Ureteral Obstruction |
45 |
0.522 |
|
697 |
|
P
|
EMB005 |
Embryonal Rhabdomyosarcoma |
53 |
0.522 |
|
698 |
|
|
INT007 |
Intermediate Coronary Syndrome |
54 |
0.522 |
|
699 |
|
|
DRM011 |
Dermatophytosis |
52 |
0.522 |
|
700 |
|
|
BLT006 |
Bilateral Breast Cancer |
48 |
0.522 |
|
701 |
|
|
GLY085 |
Glycogen Storage Disease Due to Lactate Dehydrogenase Deficiency |
16 |
0.522 |
|
702 |
|
|
EMR021 |
Emery-Dreifuss Syndrome |
11 |
0.522 |
|
703 |
|
c
|
VRL010 |
Viral Hepatitis |
53 |
0.522 |
|
704 |
|
|
MNT002 |
Mental Depression |
57 |
0.522 |
|
705 |
|
|
PSD009 |
Pseudohermaphroditism |
46 |
0.522 |
|
706 |
|
|
PYD002 |
Pyoderma |
50 |
0.522 |
|
707 |
|
|
MLG077 |
Malignant Peripheral Nerve Sheath Tumor |
54 |
0.522 |
|
708 |
|
|
ACQ007 |
Acquired Immunodeficiency Syndrome |
59 |
0.522 |
|
709 |
|
|
ILS001 |
Ileus |
50 |
0.522 |
|
710 |
|
|
NPH009 |
Nephrolithiasis |
54 |
0.522 |
|
711 |
|
|
TNC002 |
Tinea Capitis |
42 |
0.522 |
|
712 |
|
|
CMB007 |
Combined Immunodeficiency |
57 |
0.522 |
|
713 |
|
P
|
VNS003 |
Venous Insufficiency |
55 |
0.522 |
|
714 |
|
c
|
MCR112 |
Microvascular Complications of Diabetes 2 |
42 |
0.522 |
|
715 |
|
c
|
DVL110 |
Developmental and Epileptic Encephalopathy 88 |
20 |
0.522 |
|
716 |
|
P
|
MGR003 |
Migraine with Aura |
52 |
0.522 |
|
717 |
|
|
OST003 |
Osteonecrosis |
61 |
0.522 |
|
718 |
|
|
ANT018 |
Anthracosis |
51 |
0.522 |
|
719 |
|
|
OST011 |
Osteomalacia |
52 |
0.522 |
|
720 |
|
P
|
MGR001 |
Migraine Without Aura |
49 |
0.522 |
|
721 |
|
|
ALC010 |
Alcoholic Cardiomyopathy |
42 |
0.522 |
|
722 |
|
|
GT001 |
Gout |
64 |
0.522 |
|
723 |
|
|
DNG003 |
Dengue Disease |
65 |
0.522 |
|
724 |
|
|
CRY005 |
Cryptococcosis |
60 |
0.522 |
|
725 |
|
|
GTR002 |
Goiter |
53 |
0.522 |
|
726 |
|
|
FLR001 |
Filarial Elephantiasis |
59 |
0.522 |
|
727 |
|
|
PNC001 |
Pancytopenia |
53 |
0.522 |
|
728 |
|
|
CRT012 |
Cortical Blindness |
42 |
0.522 |
|
729 |
|
|
NRX001 |
Neuroaxonal Dystrophy |
38 |
0.522 |
|
730 |
|
P
|
NRN021 |
Neuronal Ceroid Lipofuscinosis |
65 |
0.522 |
|
731 |
|
|
RYS001 |
Reye Syndrome |
49 |
0.522 |
|
732 |
|
c
|
ATM011 |
Autoimmune Hepatitis |
63 |
0.522 |
|
733 |
|
P
|
CRN037 |
Craniosynostosis |
68 |
0.522 |
|
734 |
|
P
|
TBR001 |
Tuberous Sclerosis |
69 |
0.522 |
|
735 |
|
P
|
LNG028 |
Long Qt Syndrome |
64 |
0.522 |
|
736 |
|
P
|
END044 |
Endometriosis |
62 |
0.522 |
|
737 |
|
|
ING001 |
Inguinal Hernia |
59 |
0.522 |
|
738 |
|
P
|
MTC010 |
Mitochondrial Dna Depletion Syndrome |
47 |
0.522 |
|
739 |
|
|
LPR001 |
Lepromatous Leprosy |
49 |
0.522 |
|
740 |
|
|
HMP005 |
Hemiplegia |
54 |
0.522 |
|
741 |
|
|
VTM033 |
Vitamin K Deficiency Bleeding |
48 |
0.522 |
|
742 |
|
|
MCR013 |
Microphthalmia |
60 |
0.522 |
|
743 |
|
c
|
INH020 |
Inherited Metabolic Disorder |
48 |
0.522 |
|
744 |
|
P
|
PSD003 |
Pseudohypoaldosteronism |
44 |
0.522 |
|
745 |
|
P
|
SLP005 |
Sleep Disorder |
61 |
0.522 |
|
746 |
|
P
|
AXN001 |
Axonal Neuropathy |
35 |
0.522 |
|
747 |
|
|
CCN002 |
Cocaine Abuse |
49 |
0.522 |
|
748 |
|
P
|
TRT010 |
Teratoma |
51 |
0.522 |
|
749 |
|
|
INT066 |
Interstitial Lung Disease |
60 |
0.522 |
|
750 |
|
|
MLG067 |
Malignant Giant Cell Tumor |
28 |
0.522 |
|
751 |
|
P
|
MTR014 |
Motor Neuron Disease |
65 |
0.522 |
|
752 |
|
P
|
TMP001 |
Temporal Lobe Epilepsy |
49 |
0.522 |
|
753 |
|
|
BRS051 |
Breast Disease |
58 |
0.522 |
|
754 |
|
|
PNC041 |
Pancreatic Ductal Adenocarcinoma |
51 |
0.522 |
|
755 |
|
|
LYS002 |
Lysosomal Storage Disease |
51 |
0.522 |
|
756 |
|
|
AMN001 |
Amenorrhea |
54 |
0.522 |
|
757 |
|
|
KLB003 |
Klebsiella Pneumonia |
50 |
0.522 |
|
758 |
|
|
OPS001 |
Opisthorchiasis |
41 |
0.522 |
|
759 |
|
|
DBT002 |
Diabetic Autonomic Neuropathy |
41 |
0.522 |
|
760 |
|
|
LCH001 |
Leech Infestation |
38 |
0.522 |
|
761 |
|
|
MYS004 |
Myiasis |
39 |
0.522 |
|
762 |
|
|
HYP080 |
Hypogonadism |
50 |
0.522 |
|
763 |
|
|
PST028 |
Post-Traumatic Stress Disorder |
59 |
0.522 |
|
764 |
|
|
BBS001 |
Babesiosis |
49 |
0.522 |
|
765 |
|
|
INV005 |
Inverted Follicular Keratosis |
32 |
0.522 |
|
766 |
|
P
|
NRF002 |
Neurofibromatosis |
57 |
0.522 |
|
767 |
|
|
DST006 |
Diastolic Heart Failure |
45 |
0.522 |
|
768 |
|
|
HYD005 |
Hydrocele |
46 |
0.522 |
|
769 |
|
|
TTR005 |
Tetrahydrobiopterin Deficiency |
48 |
0.522 |
|
770 |
|
P
|
RDC010 |
Reducing Body Myopathy |
33 |
0.522 |
|
771 |
|
|
DPR016 |
Depression |
65 |
0.522 |
|
772 |
|
P
|
CRB088 |
Cerebral Atrophy |
33 |
0.522 |
|
773 |
|
|
MYT011 |
Myotonia |
39 |
0.522 |
|
774 |
|
|
OVR094 |
Ovarian Epithelial Cancer |
39 |
0.522 |
|
775 |
|
|
GST039 |
Gastroduodenitis |
37 |
0.522 |
|
776 |
|
|
LYM133 |
Lymphoma, Hodgkin, Classic |
74 |
0.369 |
|
777 |
|
|
SPN050 |
Spinocerebellar Degeneration |
39 |
0.369 |
|
778 |
|
|
CLF004 |
Cleft Lip/palate |
57 |
0.369 |
|
779 |
|
P
|
OTT001 |
Otitis Externa |
42 |
0.369 |
|
780 |
|
c
|
BCT007 |
Bacterial Meningitis |
55 |
0.369 |
|
781 |
|
|
SCL025 |
Scleromyxedema |
32 |
0.369 |
|
782 |
|
|
VNZ002 |
Venezuelan Equine Encephalitis |
46 |
0.369 |
|
783 |
|
|
SLN002 |
Selenium Poisoning |
10 |
0.369 |
|
784 |
|
|
CNN002 |
Cannabis Abuse |
45 |
0.369 |
|
785 |
|
c
|
INF185 |
Infantile Epilepsy Syndrome |
29 |
0.369 |
|
786 |
|
|
RFR010 |
Refractory Anemia |
49 |
0.369 |
|
787 |
|
|
ACT181 |
Acute Motor Axonal Neuropathy |
22 |
0.369 |
|
788 |
|
|
MTB016 |
Metabolic Myopathy |
30 |
0.369 |
|
789 |
|
|
IDP079 |
Idiopathic Dropped Head Syndrome |
10 |
0.369 |
|
790 |
|
|
BNG077 |
Benign Idiopathic Neonatal Seizures |
23 |
0.369 |
|
791 |
|
|
NRM022 |
Neurometabolic Disease |
24 |
0.369 |
|
792 |
|
|
CCN009 |
Cocaine Intoxication |
30 |
0.369 |
|
793 |
|
|
PRC051 |
Paracetamol Poisoning |
29 |
0.369 |
|
794 |
|
c
|
ADL084 |
Adult-Onset Myasthenia Gravis |
21 |
0.369 |
|
795 |
|
|
SPS019 |
Spastic Paraparesis |
38 |
0.369 |
|
796 |
|
|
SDD008 |
Sudden Sensorineural Hearing Loss |
41 |
0.369 |
|
797 |
|
|
GNT167 |
Genetic Obesity |
30 |
0.369 |
|
798 |
|
|
THY128 |
Thyroid Tumor |
35 |
0.369 |
|
799 |
|
c
|
AMY088 |
Amyotrophic Lateral Sclerosis 3 |
31 |
0.369 |
|
800 |
|
c
|
ART068 |
Aortic Aneurysm, Familial Thoracic 2 |
33 |
0.369 |
|
801 |
|
|
EPL050 |
Epilepsy, Partial, with Pericentral Spikes |
26 |
0.369 |
|
802 |
|
c
|
SPS128 |
Spastic Paraplegia 7, Autosomal Recessive |
58 |
0.369 |
|
803 |
|
|
SPP011 |
Suppression of Tumorigenicity 12 |
61 |
0.369 |
|
804 |
|
|
PLM061 |
Pulmonary Edema of Mountaineers |
26 |
0.369 |
|
805 |
|
c
|
SCL052 |
Scleroderma, Familial Progressive |
61 |
0.369 |
|
806 |
|
P
|
DNT020 |
Dent Disease 1 |
63 |
0.369 |
|
807 |
|
|
DNN001 |
Danon Disease |
59 |
0.369 |
|
808 |
|
|
MSC152 |
Muscular Dystrophy, Becker Type |
69 |
0.369 |
|
809 |
|
|
MTC147 |
Mitochondrial Complex I Deficiency, Nuclear Type 12 |
21 |
0.369 |
|
810 |
|
|
CRD132 |
Cardiac Conduction Defect |
60 |
0.369 |
|
811 |
|
c
|
MCL013 |
Mucolipidosis Iv |
65 |
0.369 |
|
812 |
|
|
ACY010 |
Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of |
64 |
0.369 |
|
813 |
|
|
LPD012 |
Lipoid Congenital Adrenal Hyperplasia |
70 |
0.369 |
|
814 |
|
|
ALK013 |
Alkaptonuria |
59 |
0.369 |
|
815 |
|
|
FBR012 |
Fabry Disease |
70 |
0.369 |
|
816 |
|
|
KFR001 |
Kufor-Rakeb Syndrome |
59 |
0.369 |
|
817 |
|
|
SNS008 |
Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis |
60 |
0.369 |
|
818 |
|
|
MTC149 |
Mitochondrial Complex I Deficiency, Mitochondrial Type 1 |
14 |
0.369 |
|
819 |
|
c
|
NPH049 |
Nephrotic Syndrome, Type 2 |
51 |
0.369 |
|
820 |
|
P
|
SPR120 |
Supranuclear Palsy, Progressive, 1 |
69 |
0.369 |
|
821 |
|
|
ENC055 |
Encephalopathy, Ethylmalonic |
51 |
0.369 |
|
822 |
|
|
PRS127 |
Pearson Marrow-Pancreas Syndrome |
52 |
0.369 |
|
823 |
|
c
|
MTR020 |
Maturity-Onset Diabetes of the Young, Type 3 |
54 |
0.369 |
|
824 |
|
P
|
D2H002 |
D-2-Hydroxyglutaric Aciduria 1 |
52 |
0.369 |
|
825 |
|
|
ASC010 |
Ascaris Lumbricoides Infection |
49 |
0.369 |
|
826 |
|
P
|
RHM011 |
Rheumatoid Arthritis |
82 |
0.369 |
|
827 |
|
|
HRD029 |
Hereditary Leiomyomatosis and Renal Cell Cancer |
56 |
0.369 |
|
828 |
|
P
|
FCS012 |
Facioscapulohumeral Muscular Dystrophy 1 |
68 |
0.369 |
|
829 |
|
P
|
OST002 |
Osteoporosis |
76 |
0.369 |
|
830 |
|
P
|
LKM071 |
Leukemia, Chronic Lymphocytic |
75 |
0.369 |
|
831 |
|
|
CLF027 |
Cleft Palate, Isolated |
64 |
0.369 |
|
832 |
|
c
|
SPN225 |
Spondyloarthropathy 1 |
70 |
0.369 |
|
833 |
|
c
|
SYN084 |
Synpolydactyly 1 |
36 |
0.369 |
|
834 |
|
|
SYR010 |
Syringomyelia, Noncommunicating Isolated |
36 |
0.369 |
|
835 |
|
c
|
THR092 |
Thrombophilia Due to Thrombin Defect |
74 |
0.369 |
|
836 |
|
|
ARG007 |
Argininemia |
58 |
0.369 |
|
837 |
|
|
CYS019 |
Cystathioninuria |
46 |
0.369 |
|
838 |
|
c
|
NRD017 |
Neurodegeneration with Brain Iron Accumulation 1 |
63 |
0.369 |
|
839 |
|
|
ATM096 |
Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia |
65 |
0.369 |
|
840 |
|
|
SRB001 |
Sorbitol Dehydrogenase Deficiency with Peripheral Neuropathy |
21 |
0.369 |
|
841 |
|
c
|
FNC066 |
Fanconi Renotubular Syndrome 5 |
27 |
0.369 |
|
842 |
|
|
ADR016 |
Adrenal Cortical Carcinoma |
62 |
0.369 |
|
843 |
|
P
|
LSS002 |
Lissencephaly |
50 |
0.369 |
|
844 |
|
|
END014 |
Endemic Typhus |
32 |
0.369 |
|
845 |
|
|
HYP017 |
Hypophosphatemia |
49 |
0.369 |
|
846 |
|
|
CRR001 |
Carrion's Disease |
31 |
0.369 |
|
847 |
|
c
|
BNM022 |
Bone Mineral Density Quantitative Trait Locus 8 |
45 |
0.369 |
|
848 |
|
|
DSR012 |
Disordered Steroidogenesis Due to Cytochrome P450 Oxidoreductase Deficiency |
39 |
0.369 |
|
849 |
|
c
|
LBR006 |
Leber Congenital Amaurosis 11 |
35 |
0.369 |
|
850 |
|
P
|
MGL010 |
Megalencephalic Leukoencephalopathy with Subcortical Cysts 2a |
40 |
0.369 |
|
851 |
|
c
|
BTT014 |
Beta-Thalassemia |
72 |
0.369 |
|
852 |
|
|
MYL009 |
Myelodysplastic Syndrome |
67 |
0.369 |
|
853 |
|
P
|
HRD021 |
Hereditary Sensory Neuropathy |
48 |
0.369 |
|
854 |
|
P
|
BNM029 |
Bone Mineral Density Quantitative Trait Locus 15 |
48 |
0.369 |
|
855 |
|
c
|
RTN143 |
Retinitis Pigmentosa 47 |
41 |
0.369 |
|
856 |
|
|
HRS016 |
Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction |
26 |
0.369 |
|
857 |
|
P
|
HMG032 |
Hemoglobin H Disease |
51 |
0.369 |
|
858 |
|
|
MLT150 |
Multiple Mitochondrial Dysfunctions Syndrome 2 with Hyperglycinemia |
36 |
0.369 |
|
859 |
|
|
HMN002 |
Human Granulocytic Anaplasmosis |
31 |
0.369 |
|
860 |
|
|
RCK002 |
Rocky Mountain Spotted Fever |
34 |
0.369 |
|
861 |
|
P
|
MCL001 |
Mucolipidosis |
49 |
0.369 |
|
862 |
|
|
THY121 |
Thyroid Gland Anaplastic Carcinoma |
67 |
0.369 |
|
863 |
|
|
ADT001 |
Auditory Agnosia |
26 |
0.369 |
|
864 |
|
|
CRT007 |
Cortical Deafness |
26 |
0.369 |
|
865 |
|
|
HMN047 |
Human Cytomegalovirus Infection |
57 |
0.369 |
|
866 |
|
c
|
HRD201 |
Hereditary Sensory and Autonomic Neuropathy Type 1 |
43 |
0.369 |
|
867 |
|
|
OLG022 |
Oligoasthenoteratozoospermia |
36 |
0.369 |
|
868 |
|
c
|
3MT007 |
3-Methylglutaconic Aciduria |
37 |
0.369 |
|
869 |
|
|
PLL012 |
Pollen Allergy |
45 |
0.369 |
|
870 |
|
|
PHY002 |
Physical Disorder |
41 |
0.369 |
|
871 |
|
|
CHL152 |
Childhood Acute Lymphocytic Leukemia |
50 |
0.369 |
|
872 |
|
P
|
LYM118 |
Lymphoma |
67 |
0.369 |
|
873 |
|
|
HYP025 |
Hyperphosphatemia |
48 |
0.369 |
|
874 |
|
c
|
PRM032 |
Primary Congenital Glaucoma |
41 |
0.369 |
|
875 |
|
|
TNS007 |
Taeniasis |
46 |
0.369 |
|
876 |
|
|
INT017 |
Intestinal Schistosomiasis |
51 |
0.369 |
|
877 |
|
P
|
MYF003 |
Myofibrillar Myopathy |
49 |
0.369 |
|
878 |
|
|
PYR022 |
Pyruvate Dehydrogenase E1-Alpha Deficiency |
64 |
0.369 |
|
879 |
|
c
|
DFN251 |
Deafness, Autosomal Dominant 11 |
44 |
0.369 |
|
880 |
|
c
|
HYP839 |
Hyperlipidemia, Familial Combined, 1 |
30 |
0.369 |
|
881 |
|
c
|
PRX059 |
Peroxisome Biogenesis Disorder 1a |
56 |
0.369 |
|
882 |
|
|
CYS044 |
Cystic Disease of Lung |
20 |
0.369 |
|
883 |
|
c
|
GLC112 |
Galactosemia Iii |
51 |
0.369 |
|
884 |
|
P
|
HYP768 |
Hyperlipoproteinemia, Type I |
67 |
0.369 |
|
885 |
|
c
|
GRV008 |
Graves Disease 1 |
54 |
0.369 |
|
886 |
|
|
MYC079 |
Myoclonic Epilepsy of Lafora |
64 |
0.369 |
|
887 |
|
|
NNR004 |
Nonarteritic Anterior Ischemic Optic Neuropathy |
57 |
0.369 |
|
888 |
|
|
SPN354 |
Spinal Arachnoiditis |
36 |
0.369 |
|
889 |
|
|
CTY001 |
Cat Eye Syndrome |
44 |
0.369 |
|
890 |
|
|
HTC003 |
Hutchinson-Gilford Progeria Syndrome |
65 |
0.369 |
|
891 |
|
c
|
PRT132 |
Protoporphyria, Erythropoietic, 1 |
61 |
0.369 |
|
892 |
|
P
|
PLV020 |
Pelvic Organ Prolapse |
58 |
0.369 |
|
893 |
|
|
KRT019 |
Keratitis, Hereditary |
66 |
0.369 |
|
894 |
|
|
KPS004 |
Kaposi Sarcoma |
77 |
0.369 |
|
895 |
|
|
GRG001 |
Greig Cephalopolysyndactyly Syndrome |
64 |
0.369 |
|
896 |
|
|
EXF001 |
Exfoliation Syndrome |
56 |
0.369 |
|
897 |
|
|
CHD004 |
Chudley-Mccullough Syndrome |
48 |
0.369 |
|
898 |
|
c
|
TTH012 |
Tooth Agenesis, Selective, 3 |
25 |
0.369 |
|
899 |
|
P
|
ORT004 |
Orthostatic Intolerance |
63 |
0.369 |
|
900 |
|
|
LTN004 |
Late-Onset Retinal Degeneration |
60 |
0.369 |
|
901 |
|
c
|
TTH011 |
Tooth Agenesis, Selective, 2 |
13 |
0.369 |
|
902 |
|
c
|
LNG048 |
Long Qt Syndrome 3 |
53 |
0.369 |
|
903 |
|
c
|
MLT068 |
Multiple Mitochondrial Dysfunctions Syndrome 1 |
45 |
0.369 |
|
904 |
|
|
LYM143 |
Lymphoma, Non-Hodgkin, Familial |
75 |
0.369 |
|
905 |
|
|
PHL006 |
Phelan-Mcdermid Syndrome |
60 |
0.369 |
|
906 |
|
c
|
LNG047 |
Long Qt Syndrome 2 |
59 |
0.369 |
|
907 |
|
c
|
ART101 |
Aortic Valve Disease 2 |
66 |
0.369 |
|
908 |
|
|
MND021 |
Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome |
66 |
0.369 |
|
909 |
|
|
MYP099 |
Myopathy, Isolated Mitochondrial, Autosomal Dominant |
27 |
0.369 |
|
910 |
|
|
AKL001 |
Au-Kline Syndrome |
39 |
0.369 |
|
911 |
|
|
HRT037 |
Heart and Brain Malformation Syndrome |
31 |
0.369 |
|
912 |
|
|
CHR607 |
Chorea, Childhood-Onset, with Psychomotor Retardation |
39 |
0.369 |
|
913 |
|
|
MLC004 |
Mulchandani-Bhoj-Conlin Syndrome |
51 |
0.369 |
|
914 |
|
|
INT258 |
Interstitial Nephritis, Karyomegalic |
45 |
0.369 |
|
915 |
|
c
|
RTN140 |
Retinitis Pigmentosa 67 |
32 |
0.369 |
|
916 |
|
c
|
DFN360 |
Deafness, Autosomal Dominant 69 |
34 |
0.369 |
|
917 |
|
c
|
MCR312 |
Microphthalmia, Syndromic 10 |
40 |
0.369 |
|
918 |
|
|
HRN029 |
Hearing Loss, Noise-Induced |
37 |
0.369 |
|
919 |
|
c
|
MSC165 |
Muscular Dystrophy, Congenital, Lmna-Related |
65 |
0.369 |
|
920 |
|
|
WST005 |
West Nile Virus |
57 |
0.369 |
|
921 |
|
|
ADR042 |
Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency |
50 |
0.369 |
|
922 |
|
|
2MN001 |
2-Aminoadipic 2-Oxoadipic Aciduria |
34 |
0.369 |
|
923 |
|
|
PRP083 |
Porphyria, Acute Intermittent |
65 |
0.369 |
|
924 |
|
c
|
NTR047 |
Neutropenia, Severe Congenital, 1, Autosomal Dominant |
37 |
0.369 |
|
925 |
|
|
MLL018 |
Miller-Dieker Lissencephaly Syndrome |
52 |
0.369 |
|
926 |
|
|
MTC207 |
Mitochondrial Complex Ii Deficiency, Nuclear Type 1 |
55 |
0.369 |
|
927 |
|
|
ADR054 |
Adrenocortical Carcinoma, Hereditary |
47 |
0.369 |
|
928 |
|
c
|
MTC056 |
Mitochondrial Dna Depletion Syndrome 4a |
62 |
0.369 |
|
929 |
|
|
LWC002 |
Lowe Oculocerebrorenal Syndrome |
68 |
0.369 |
|
930 |
|
|
LGN006 |
Legionnaire Disease |
52 |
0.369 |
|
931 |
|
c
|
MYC058 |
Myocardial Infarction 2 |
24 |
0.369 |
|
932 |
|
|
PSD063 |
Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak |
56 |
0.369 |
|
933 |
|
|
ALP042 |
Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity |
65 |
0.369 |
|
934 |
|
|
ENT011 |
Enterocolitis |
55 |
0.369 |
|
935 |
|
c
|
GLY008 |
Glycogen Storage Disease Ii |
72 |
0.369 |
|
936 |
|
|
HLT002 |
Halothane Hepatitis |
31 |
0.369 |
|
937 |
|
P
|
HYP058 |
Hypervitaminosis a |
47 |
0.369 |
|
938 |
|
|
HYP784 |
Hypogonadism, Male |
43 |
0.369 |
|
939 |
|
|
TRG002 |
Trigeminal Neuralgia |
61 |
0.369 |
|
940 |
|
|
CRN295 |
Carnitine Palmitoyltransferase I Deficiency |
55 |
0.369 |
|
941 |
|
|
MYP091 |
Myopathy, Congenital, with Fiber-Type Disproportion |
43 |
0.369 |
|
942 |
|
|
MYL013 |
Myeloperoxidase Deficiency |
44 |
0.369 |
|
943 |
|
c
|
PRD040 |
Periodontitis, Chronic |
52 |
0.369 |
|
944 |
|
|
PLY001 |
Polycythemia Vera |
69 |
0.369 |
|
945 |
|
|
MYC080 |
Myoclonic Epilepsy of Unverricht and Lundborg |
53 |
0.369 |
|
946 |
|
|
MYP097 |
Myopathy with Lactic Acidosis, Hereditary |
31 |
0.369 |
|
947 |
|
c
|
NPH055 |
Nephrotic Syndrome, Type 1 |
52 |
0.369 |
|
948 |
|
P
|
TTR001 |
Tetralogy of Fallot |
69 |
0.369 |
|
949 |
|
|
WLF001 |
Wolff-Parkinson-White Syndrome |
65 |
|