# |
|
Family |
MCID |
Name |
MIFTS |
Score |
1 |
|
P
|
CHR654 |
Charcot-Marie-Tooth Disease, Axonal, Type 2e |
58 |
42.633 |
|
2 |
|
c
|
WRD033 |
Waardenburg Syndrome, Type 2e |
53 |
32.084 |
|
3 |
|
c
|
MSC176 |
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4 |
48 |
28.406 |
|
4 |
|
c
|
PNT034 |
Pontocerebellar Hypoplasia, Type 2e |
52 |
24.797 |
|
5 |
|
c
|
MSC170 |
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 2 |
66 |
22.497 |
|
6 |
|
c
|
PSD092 |
Pseudohypoaldosteronism, Type Iie |
48 |
20.020 |
|
7 |
|
c
|
MSC169 |
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 1 |
61 |
18.415 |
|
8 |
|
|
IMM140 |
Immunodeficiency 47 |
56 |
15.692 |
|
9 |
|
|
GNY003 |
Guanylate Cyclase 2e, Pseudogene |
12 |
10.141 |
|
10 |
|
c
|
ART054 |
Arthrogryposis, Distal, Type 2e |
14 |
9.506 |
|
11 |
|
P
|
LMB006 |
Limb-Girdle Muscular Dystrophy |
52 |
6.612 |
|
12 |
|
P
|
MSC005 |
Muscular Dystrophy |
67 |
6.458 |
|
13 |
|
P
|
ICH004 |
Ichthyosis |
56 |
4.366 |
|
14 |
|
|
ICH002 |
Ichthyosis Bullosa of Siemens |
41 |
4.313 |
|
15 |
|
P
|
CHR071 |
Charcot-Marie-Tooth Disease |
64 |
4.155 |
|
16 |
|
|
TTH006 |
Tooth Disease |
51 |
4.155 |
|
17 |
|
|
KRT009 |
Keratosis |
53 |
4.050 |
|
18 |
|
P
|
NRP001 |
Neuropathy |
60 |
3.944 |
|
19 |
|
|
EPD002 |
Epidermolytic Hyperkeratosis |
56 |
3.731 |
|
20 |
|
|
TRD008 |
Triiodothyronine Receptor Auxiliary Protein |
33 |
3.729 |
|
21 |
|
P
|
ATS411 |
Autosomal Dominant Epidermolytic Ichthyosis |
36 |
3.673 |
|
22 |
|
P
|
QLT011 |
Qualitative or Quantitative Defects of Sarcoglycan |
26 |
3.474 |
|
23 |
|
c
|
PLM127 |
Pulmonary Hypertension, Primary, 3 |
34 |
3.093 |
|
24 |
|
P
|
VNW001 |
Von Willebrand's Disease |
65 |
3.039 |
|
25 |
|
P
|
HML001 |
Hemolytic-Uremic Syndrome |
52 |
2.808 |
|
26 |
|
c
|
HYP836 |
Hypercholesterolemia, Familial, 1 |
73 |
2.780 |
|
27 |
|
c
|
FML021 |
Familial Hypercholesterolemia |
72 |
2.780 |
|
28 |
|
P
|
PRP019 |
Peripheral Nervous System Disease |
58 |
2.679 |
|
29 |
|
|
HLX001 |
Helix Syndrome |
48 |
2.342 |
|
30 |
|
|
NRL005 |
Neurilemmoma |
60 |
2.342 |
|
31 |
|
|
EXF002 |
Exfoliative Ichthyosis |
25 |
2.291 |
|
32 |
|
|
ATM095 |
Autoimmune Disease |
61 |
2.281 |
|
33 |
|
|
HRW001 |
Hair Whorl |
35 |
2.281 |
|
34 |
|
|
SNS003 |
Sensory Peripheral Neuropathy |
52 |
2.241 |
|
35 |
|
|
GLM045 |
Glioma |
63 |
2.217 |
|
36 |
|
|
MSC157 |
Muscular Dystrophy, Duchenne Type |
79 |
2.189 |
|
37 |
|
c
|
CHR656 |
Charcot-Marie-Tooth Disease, Demyelinating, Type 1f |
46 |
2.184 |
|
38 |
|
c
|
DWL002 |
Dowling-Degos Disease 1 |
58 |
2.044 |
|
|
40 |
|
c
|
HPT073 |
Hepatitis C Virus |
71 |
2.005 |
|
41 |
|
|
ALP042 |
Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity |
65 |
2.005 |
|
42 |
|
P
|
NRB001 |
Neuroblastoma |
66 |
2.005 |
|
43 |
|
|
ACT098 |
Acute Erythroid Leukemia |
55 |
1.926 |
|
44 |
|
c
|
VNW005 |
Von Willebrand Disease, Type 1 |
45 |
1.926 |
|
45 |
|
|
LPD008 |
Lipid Metabolism Disorder |
62 |
1.926 |
|
46 |
|
|
NRR001 |
Neuroretinitis |
42 |
1.921 |
|
47 |
|
|
RTN023 |
Retinitis |
46 |
1.921 |
|
48 |
|
|
RPD005 |
Rapidly Involuting Congenital Hemangioma |
46 |
1.882 |
|
49 |
|
|
HYP066 |
Hyperglycemia |
61 |
1.882 |
|
50 |
|
P
|
SCH015 |
Schizophrenia |
74 |
1.843 |
|
51 |
|
P
|
HYP750 |
Hypertriglyceridemia, Familial |
62 |
1.843 |
|
52 |
|
|
ALL014 |
Allergic Encephalomyelitis |
34 |
1.843 |
|
53 |
|
P
|
SZR006 |
Seizure Disorder |
70 |
1.792 |
|
54 |
|
|
ATX038 |
Ataxia and Polyneuropathy, Adult-Onset |
46 |
1.776 |
|
55 |
|
P
|
RTN008 |
Retinitis Pigmentosa |
80 |
1.776 |
|
56 |
|
P
|
CLR023 |
Colorectal Cancer |
100 |
1.768 |
|
57 |
|
P
|
PNC035 |
Pancreatic Cancer |
86 |
1.753 |
|
58 |
|
c
|
PCH010 |
Pachyonychia Congenita 3 |
43 |
1.753 |
|
59 |
|
P
|
BCL017 |
B-Cell Lymphoma |
59 |
1.753 |
|
60 |
|
P
|
TRM003 |
Tremor |
48 |
1.753 |
|
61 |
|
P
|
HPT023 |
Hepatocellular Carcinoma |
96 |
1.656 |
|
62 |
|
P
|
LNG064 |
Lung Cancer Susceptibility 3 |
70 |
1.646 |
|
63 |
|
c
|
MSC171 |
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 5 |
42 |
1.624 |
|
64 |
|
P
|
AXN001 |
Axonal Neuropathy |
35 |
1.587 |
|
65 |
|
|
MNN043 |
Meningioma, Familial |
79 |
1.548 |
|
66 |
|
|
SCR001 |
Secretory Meningioma |
40 |
1.548 |
|
67 |
|
|
LYM002 |
Lymphoplasmacyte-Rich Meningioma |
35 |
1.548 |
|
68 |
|
|
SPN021 |
Spinal Meningioma |
50 |
1.548 |
|
69 |
|
|
CHR178 |
Chromosomal Triplication |
34 |
1.548 |
|
70 |
|
P
|
LKM062 |
Leukemia, Acute Lymphoblastic |
69 |
1.544 |
|
71 |
|
P
|
OPT006 |
Optic Nerve Disease |
58 |
1.514 |
|
72 |
|
P
|
BRS047 |
Breast Cancer |
98 |
1.444 |
|
73 |
|
P
|
DRR001 |
Diarrhea |
55 |
1.444 |
|
74 |
|
|
ESP021 |
Esophageal Cancer |
83 |
1.426 |
|
75 |
|
|
YMN001 |
Yemenite Deaf-Blind Hypopigmentation Syndrome |
66 |
1.408 |
|
76 |
|
c
|
MCL042 |
Macular Degeneration, Age-Related, 1 |
85 |
1.370 |
|
77 |
|
c
|
MSC177 |
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 3 |
42 |
1.356 |
|
78 |
|
c
|
CHR676 |
Charcot-Marie-Tooth Disease, Dominant Intermediate G |
24 |
1.355 |
|
79 |
|
c
|
WRD029 |
Waardenburg Syndrome, Type 2b |
29 |
1.315 |
|
80 |
|
c
|
WRD031 |
Waardenburg Syndrome, Type 3 |
45 |
1.315 |
|
81 |
|
c
|
WRD032 |
Waardenburg Syndrome, Type 2a |
47 |
1.315 |
|
82 |
|
P
|
WRD001 |
Waardenburg's Syndrome |
60 |
1.315 |
|
83 |
|
|
ANS002 |
Aniseikonia |
32 |
1.291 |
|
84 |
|
|
NNR004 |
Nonarteritic Anterior Ischemic Optic Neuropathy |
57 |
1.291 |
|
85 |
|
|
SCT002 |
Scotoma |
42 |
1.291 |
|
86 |
|
c
|
HPT001 |
Hepatitis C |
62 |
1.291 |
|
87 |
|
|
ANX004 |
Anoxia |
40 |
1.281 |
|
88 |
|
|
HGH043 |
High Grade Glioma |
45 |
1.281 |
|
89 |
|
|
PRG009 |
Progressive Multifocal Leukoencephalopathy |
58 |
1.281 |
|
90 |
|
|
GST045 |
Gastroenteritis |
58 |
1.281 |
|
91 |
|
|
EPD050 |
Epidermolysis Bullosa Simplex with Muscular Dystrophy |
56 |
1.231 |
|
92 |
|
|
BNG077 |
Benign Idiopathic Neonatal Seizures |
23 |
1.208 |
|
93 |
|
P
|
KLZ004 |
Kala-Azar 1 |
41 |
1.208 |
|
94 |
|
|
LSH001 |
Leishmaniasis |
64 |
1.208 |
|
95 |
|
|
SVR001 |
Severe Acute Respiratory Syndrome |
67 |
1.208 |
|
96 |
|
|
CLN015 |
Colon Adenocarcinoma |
65 |
1.208 |
|
97 |
|
|
HMN044 |
Human Immunodeficiency Virus Type 1 |
78 |
1.141 |
|
98 |
|
|
LBR036 |
Leber Plus Disease |
66 |
1.141 |
|
99 |
|
P
|
MSC003 |
Muscular Atrophy |
52 |
1.141 |
|
100 |
|
|
ACQ007 |
Acquired Immunodeficiency Syndrome |
59 |
1.141 |
|
101 |
|
|
ATX031 |
Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus |
58 |
1.141 |
|
102 |
|
P
|
SPN046 |
Spinal Muscular Atrophy |
63 |
1.141 |
|
103 |
|
|
NRT004 |
Neuritis |
53 |
1.141 |
|
104 |
|
|
NRF007 |
Neurofibroma |
64 |
1.141 |
|
105 |
|
c
|
BRN108 |
Branchiootic Syndrome 1 |
62 |
1.131 |
|
106 |
|
P
|
EPL164 |
Epilepsy |
68 |
1.131 |
|
107 |
|
|
MCR013 |
Microphthalmia |
60 |
1.131 |
|
108 |
|
P
|
LNG032 |
Lung Cancer |
98 |
1.118 |
|
109 |
|
P
|
RTN209 |
Retinoschisis 1, X-Linked, Juvenile |
60 |
1.118 |
|
110 |
|
|
CLR109 |
Colorectal Adenocarcinoma |
50 |
1.118 |
|
111 |
|
|
CMB039 |
Combined Pulmonary Fibrosis-Emphysema Syndrome |
18 |
1.118 |
|
112 |
|
|
GLL048 |
Glial Tumor |
52 |
1.118 |
|
113 |
|
P
|
FBR017 |
Fibrosarcoma |
56 |
1.118 |
|
114 |
|
P
|
RTN018 |
Retinal Disease |
53 |
1.118 |
|
115 |
|
|
XLN247 |
X-Linked Congenital Retinoschisis |
20 |
1.118 |
|
116 |
|
P
|
JVN042 |
Juvenile Retinoschisis |
39 |
1.118 |
|
117 |
|
|
MTR087 |
Maternal Uniparental Disomy |
28 |
1.092 |
|
118 |
|
c
|
MTR062 |
Maternal Uniparental Disomy of Chromosome 4 |
18 |
1.092 |
|
119 |
|
c
|
ATR087 |
Atrial Standstill 1 |
74 |
1.092 |
|
120 |
|
c
|
LKM063 |
Leukemia, Chronic Myeloid |
71 |
1.092 |
|
121 |
|
c
|
PLM121 |
Pulmonary Hypertension, Primary, 4 |
28 |
1.092 |
|
122 |
|
c
|
TYP009 |
Type 2 Diabetes Mellitus |
92 |
1.092 |
|
123 |
|
P
|
HYP077 |
Hypertrichosis |
46 |
1.092 |
|
124 |
|
|
DBT010 |
Diabetic Neuropathy |
54 |
1.092 |
|
125 |
|
|
GLB002 |
Glioblastoma |
67 |
1.092 |
|
126 |
|
P
|
THY032 |
Thyroiditis |
57 |
1.092 |
|
127 |
|
|
BRN028 |
Brain Cancer |
74 |
1.092 |
|
128 |
|
P
|
MLN008 |
Melanoma |
76 |
1.092 |
|
129 |
|
|
STT001 |
Status Epilepticus |
59 |
1.092 |
|
130 |
|
|
BRN071 |
Brain Injury |
50 |
1.092 |
|
131 |
|
P
|
ALZ034 |
Alzheimer Disease |
87 |
1.021 |
|
132 |
|
|
SCH060 |
Schistosoma Mansoni Infection, Susceptibility/ |
38 |
1.021 |
|
133 |
|
P
|
SRC025 |
Sarcoidosis 1 |
71 |
1.021 |
|
134 |
|
|
BCT022 |
Bacterial Infectious Disease |
56 |
1.021 |
|
135 |
|
P
|
MYP006 |
Myopia |
56 |
1.021 |
|
136 |
|
|
DRM011 |
Dermatophytosis |
52 |
1.021 |
|
137 |
|
|
VSC003 |
Visceral Leishmaniasis |
55 |
1.021 |
|
138 |
|
P
|
BRS044 |
Breast Adenocarcinoma |
58 |
1.021 |
|
139 |
|
|
CMM005 |
Common Cold |
56 |
1.021 |
|
140 |
|
|
GLS001 |
Gliosarcoma |
64 |
1.021 |
|
141 |
|
|
SCH014 |
Schistosomiasis |
56 |
1.021 |
|
142 |
|
P
|
HRT032 |
Heart Disease |
81 |
1.021 |
|
143 |
|
c
|
HPT016 |
Hepatitis B |
62 |
1.021 |
|
144 |
|
c
|
RNG007 |
Ring Chromosome 12 |
27 |
1.021 |
|
145 |
|
|
DSS012 |
Disseminated Infection with Mycobacterium Avium Complex |
19 |
1.021 |
|
146 |
|
P
|
3MT016 |
3-Methylglutaconic Aciduria, Type Iii |
68 |
0.952 |
|
147 |
|
P
|
VTL004 |
Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 |
60 |
0.952 |
|
148 |
|
c
|
CHR352 |
Charcot-Marie-Tooth Disease, Axonal, Type 2f |
45 |
0.952 |
|
149 |
|
c
|
NRN041 |
Neuronopathy, Distal Hereditary Motor, Type Iib |
33 |
0.952 |
|
150 |
|
c
|
DST106 |
Distal Hereditary Motor Neuronopathy Type 2 |
41 |
0.952 |
|
151 |
|
c
|
CHR699 |
Charcot-Marie-Tooth Disease Type 2a2a |
28 |
0.952 |
|
152 |
|
P
|
MVM001 |
Movement Disease |
61 |
0.952 |
|
153 |
|
|
MFN001 |
Mfn2 Hereditary Motor and Sensory Neuropathy |
13 |
0.952 |
|
154 |
|
|
DYS073 |
Dysphagia |
53 |
0.952 |
|
155 |
|
P
|
PSR002 |
Psoriasis |
63 |
0.927 |
|
156 |
|
P
|
CRN300 |
Coronary Heart Disease 1 |
73 |
0.913 |
|
157 |
|
|
END057 |
Endometrial Cancer |
72 |
0.913 |
|
158 |
|
P
|
MLT020 |
Multiple Sclerosis |
79 |
0.913 |
|
159 |
|
P
|
PRK057 |
Parkinson Disease, Late-Onset |
80 |
0.913 |
|
160 |
|
P
|
ANP001 |
Anaplastic Large Cell Lymphoma |
61 |
0.913 |
|
161 |
|
|
LWG006 |
Low Grade Glioma |
41 |
0.913 |
|
162 |
|
P
|
LYM118 |
Lymphoma |
67 |
0.913 |
|
163 |
|
|
NNL005 |
Non-Alcoholic Fatty Liver Disease |
63 |
0.913 |
|
164 |
|
|
IMM167 |
Immune Deficiency Disease |
78 |
0.913 |
|
165 |
|
P
|
GST053 |
Gastric Cancer |
83 |
0.913 |
|
166 |
|
|
SZR028 |
Seizures, Scoliosis, and Macrocephaly/microcephaly Syndrome |
36 |
0.913 |
|
167 |
|
P
|
PRK039 |
Parkinsonism |
55 |
0.913 |
|
168 |
|
|
TRM010 |
Traumatic Brain Injury |
51 |
0.913 |
|
169 |
|
P
|
DBT009 |
Diabetes Mellitus |
67 |
0.913 |
|
170 |
|
|
CRB004 |
Cerebral Artery Occlusion |
45 |
0.913 |
|
171 |
|
|
CNT016 |
Central Retinal Vein Occlusion |
54 |
0.913 |
|
172 |
|
P
|
HPT021 |
Hepatitis |
69 |
0.913 |
|
173 |
|
|
SVR004 |
Severe Combined Immunodeficiency |
72 |
0.913 |
|
174 |
|
|
LVR012 |
Liver Cirrhosis |
63 |
0.913 |
|
175 |
|
P
|
GLM007 |
Glomerulonephritis |
60 |
0.913 |
|
176 |
|
P
|
HMP007 |
Hemophilia |
52 |
0.913 |
|
177 |
|
|
HNM002 |
Hinman Syndrome |
27 |
0.858 |
|
178 |
|
c
|
BLD140 |
Blood Group, I System |
46 |
0.858 |
|
179 |
|
|
ADP007 |
Adie Pupil |
40 |
0.858 |
|
180 |
|
P
|
NSP012 |
Nasopharyngeal Carcinoma |
61 |
0.791 |
|
181 |
|
|
CRV035 |
Cervical Cancer |
73 |
0.791 |
|
182 |
|
|
ANX010 |
Anxiety |
70 |
0.791 |
|
183 |
|
|
PLY150 |
Polykaryocytosis Inducer |
29 |
0.791 |
|
|
185 |
|
P
|
URN019 |
Urinary Tract Infection |
49 |
0.791 |
|
186 |
|
P
|
BLY001 |
B-Lymphoblastic Leukemia/lymphoma |
52 |
0.791 |
|
187 |
|
P
|
PRT133 |
Proteasome-Associated Autoinflammatory Syndrome 1 |
80 |
0.791 |
|
188 |
|
|
NRL016 |
Neural Tube Defects |
81 |
0.791 |
|
189 |
|
|
DWN001 |
Down Syndrome |
70 |
0.791 |
|
190 |
|
c
|
SML038 |
Small Cell Cancer of the Lung |
69 |
0.791 |
|
191 |
|
|
HND015 |
Hand Skill, Relative |
30 |
0.791 |
|
192 |
|
P
|
MYP004 |
Myopathy |
67 |
0.791 |
|
193 |
|
|
PRM133 |
Primary Pulmonary Lymphoma |
16 |
0.791 |
|
194 |
|
P
|
LVR013 |
Liver Disease |
69 |
0.791 |
|
195 |
|
|
PRT036 |
Peritonitis |
65 |
0.791 |
|
196 |
|
|
ANT024 |
Anthrax Disease |
58 |
0.791 |
|
197 |
|
c
|
PLM128 |
Pulmonary Hypertension, Primary, 2 |
28 |
0.791 |
|
198 |
|
|
TRY001 |
Trypanosomiasis |
50 |
0.791 |
|
199 |
|
|
GST027 |
Gastric Lymphoma |
46 |
0.791 |
|
200 |
|
|
CHG001 |
Chagas Disease |
66 |
0.791 |
|
201 |
|
|
PTS001 |
Patau Syndrome |
56 |
0.791 |
|
202 |
|
|
STM006 |
Stomach Disease |
47 |
0.791 |
|
203 |
|
c
|
ACT071 |
Acute Kidney Failure |
60 |
0.791 |
|
204 |
|
|
LNG013 |
Lung Lymphoma |
31 |
0.791 |
|
205 |
|
c
|
ATS246 |
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2c |
33 |
0.711 |
|
206 |
|
c
|
ATS277 |
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2d |
41 |
0.711 |
|
207 |
|
P
|
CLP009 |
Calpain-3-Related Limb-Girdle Muscular Dystrophy R1 |
30 |
0.711 |
|
208 |
|
P
|
CNT116 |
Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a |
54 |
0.701 |
|
209 |
|
|
CRZ002 |
Crouzon Syndrome with Acanthosis Nigricans |
58 |
0.701 |
|
210 |
|
|
VSL002 |
Visual Epilepsy |
39 |
0.701 |
|
211 |
|
|
CLF004 |
Cleft Lip/palate |
57 |
0.646 |
|
212 |
|
P
|
HRD217 |
Hereditary Optic Neuropathy |
36 |
0.646 |
|
213 |
|
|
OBN001 |
Ouabain Resistance |
16 |
0.646 |
|
214 |
|
|
AMN014 |
Aminopterin Syndrome Sine Aminopterin |
32 |
0.646 |
|
215 |
|
c
|
SCL052 |
Scleroderma, Familial Progressive |
61 |
0.646 |
|
216 |
|
c
|
MSC172 |
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 8 |
44 |
0.646 |
|
217 |
|
c
|
MYS033 |
Miyoshi Muscular Dystrophy 1 |
52 |
0.646 |
|
218 |
|
|
INS024 |
Insulin-Like Growth Factor I |
78 |
0.646 |
|
219 |
|
|
ART002 |
Arts Syndrome |
66 |
0.646 |
|
220 |
|
|
AGN016 |
Aging |
54 |
0.646 |
|
221 |
|
|
NRP045 |
Neuropathy, Ataxia, and Retinitis Pigmentosa |
47 |
0.646 |
|
222 |
|
c
|
MSC174 |
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 7 |
42 |
0.646 |
|
223 |
|
c
|
THR092 |
Thrombophilia Due to Thrombin Defect |
74 |
0.646 |
|
224 |
|
|
CHR005 |
Chorioamnionitis |
50 |
0.646 |
|
225 |
|
c
|
VNW010 |
Von Willebrand Disease, Type 2 |
48 |
0.646 |
|
226 |
|
|
TTH002 |
Tooth Agenesis |
61 |
0.646 |
|
227 |
|
|
DFF005 |
Diffuse Large B-Cell Lymphoma |
54 |
0.646 |
|
228 |
|
P
|
FTT008 |
Fatty Liver Disease, Nonalcoholic 1 |
48 |
0.646 |
|
229 |
|
P
|
STR022 |
Stargardt Disease |
61 |
0.646 |
|
230 |
|
|
CLT003 |
Colitis |
63 |
0.646 |
|
231 |
|
|
BNR002 |
Bone Resorption Disease |
47 |
0.646 |
|
232 |
|
|
THR024 |
Thrombosis |
56 |
0.646 |
|
233 |
|
P
|
CNG010 |
Congenital Stationary Night Blindness |
56 |
0.646 |
|
234 |
|
|
INT017 |
Intestinal Schistosomiasis |
51 |
0.646 |
|
235 |
|
c
|
LKM061 |
Leukemia, Acute Myeloid |
83 |
0.646 |
|
236 |
|
|
MLC004 |
Mulchandani-Bhoj-Conlin Syndrome |
51 |
0.646 |
|
237 |
|
|
INT323 |
Intraocular Pressure Quantitative Trait Locus |
64 |
0.646 |
|
238 |
|
c
|
MSC165 |
Muscular Dystrophy, Congenital, Lmna-Related |
65 |
0.646 |
|
239 |
|
|
LBR038 |
Leber Hereditary Optic Neuropathy, Modifier of |
62 |
0.646 |
|
240 |
|
|
TTH030 |
Teeth, Supernumerary |
33 |
0.646 |
|
241 |
|
P
|
PRS040 |
Prostate Cancer |
95 |
0.646 |
|
242 |
|
c
|
GLC092 |
Glaucoma, Primary Open Angle |
62 |
0.646 |
|
243 |
|
|
PRT112 |
Portal Hypertension, Noncirrhotic |
30 |
0.646 |
|
244 |
|
|
ORL015 |
Oral Squamous Cell Carcinoma |
43 |
0.646 |
|
245 |
|
P
|
OPN001 |
Open-Angle Glaucoma |
55 |
0.646 |
|
246 |
|
|
BRN004 |
Brain Edema |
54 |
0.646 |
|
247 |
|
P
|
EPD003 |
Epidermolysis Bullosa Simplex |
57 |
0.646 |
|
248 |
|
|
BNM001 |
Bone Marrow Cancer |
46 |
0.646 |
|
249 |
|
|
NRM001 |
Neuromyelitis Optica |
61 |
0.646 |
|
250 |
|
P
|
NRC002 |
Narcolepsy |
56 |
0.646 |
|
251 |
|
|
CLF001 |
Cleft Lip |
53 |
0.646 |
|
252 |
|
|
CHC001 |
Chickenpox |
57 |
0.646 |
|
253 |
|
|
YLL002 |
Yellow Fever |
61 |
0.646 |
|
254 |
|
|
47X002 |
47,xyy |
48 |
0.646 |
|
255 |
|
|
SKN016 |
Skin Disease |
63 |
0.646 |
|
256 |
|
P
|
SKN015 |
Skin Carcinoma |
71 |
0.646 |
|
257 |
|
P
|
RTN016 |
Retinal Degeneration |
52 |
0.646 |
|
258 |
|
|
PPT005 |
Peptic Ulcer Disease |
58 |
0.646 |
|
259 |
|
P
|
ART022 |
Arthritis |
71 |
0.646 |
|
260 |
|
|
OST012 |
Osteoarthritis |
77 |
0.646 |
|
261 |
|
P
|
NGH001 |
Night Blindness |
52 |
0.646 |
|
262 |
|
|
SLP001 |
Sleeping Sickness |
56 |
0.646 |
|
263 |
|
P
|
DNG005 |
Dengue Virus |
56 |
0.646 |
|
264 |
|
P
|
DMN002 |
Dementia |
66 |
0.646 |
|
265 |
|
P
|
UVT001 |
Uveitis |
57 |
0.646 |
|
266 |
|
|
GT001 |
Gout |
64 |
0.646 |
|
267 |
|
|
ALL029 |
Allergic Disease |
59 |
0.646 |
|
268 |
|
|
CRY005 |
Cryptococcosis |
60 |
0.646 |
|
269 |
|
P
|
OPT009 |
Optic Neuritis |
57 |
0.646 |
|
270 |
|
P
|
LKM002 |
Leukemia |
67 |
0.646 |
|
271 |
|
|
DNT012 |
Dental Caries |
53 |
0.646 |
|
272 |
|
P
|
ACH003 |
Achromatopsia |
62 |
0.646 |
|
273 |
|
|
GST033 |
Gestational Diabetes |
61 |
0.646 |
|
274 |
|
|
CNG034 |
Congestive Heart Failure |
69 |
0.646 |
|
275 |
|
|
ISC004 |
Ischemia |
61 |
0.646 |
|
276 |
|
|
EMB004 |
Embryonal Carcinoma |
56 |
0.646 |
|
277 |
|
P
|
EPD016 |
Epidermolysis Bullosa |
53 |
0.646 |
|
278 |
|
|
DRM006 |
Dermatitis |
62 |
0.646 |
|
279 |
|
P
|
PTS002 |
Ptosis |
52 |
0.646 |
|
280 |
|
|
GST023 |
Gastric Ulcer |
52 |
0.646 |
|
281 |
|
|
IRN002 |
Iron Metabolism Disease |
57 |
0.646 |
|
282 |
|
P
|
BNC003 |
Bone Cancer |
58 |
0.646 |
|
283 |
|
|
DYS032 |
Dystrophinopathies |
47 |
0.646 |
|
284 |
|
|
RFR003 |
Refractive Error |
41 |
0.646 |
|
285 |
|
|
DPR016 |
Depression |
65 |
0.646 |
|
286 |
|
P
|
CHR345 |
Chronic Pain |
50 |
0.646 |
|
287 |
|
|
CRD132 |
Cardiac Conduction Defect |
60 |
0.635 |
|
288 |
|
|
ADG002 |
Audiogenic Seizures |
25 |
0.635 |
|
289 |
|
|
INS001 |
Insulinoma |
59 |
0.635 |
|
290 |
|
|
3HY005 |
3-Hydroxyacyl-Coa Dehydrogenase Deficiency |
62 |
0.495 |
|
291 |
|
|
GNT176 |
Genetic Motor Neuron Disease |
20 |
0.495 |
|
292 |
|
c
|
ATS452 |
Autosomal Recessive Axonal Hereditary Motor and Sensory Neuropathy |
18 |
0.495 |
|
293 |
|
|
SPS019 |
Spastic Paraparesis |
38 |
0.495 |
|
294 |
|
c
|
WRD010 |
Waardenburg Syndrome Type 4 |
30 |
0.495 |
|
295 |
|
c
|
AXN013 |
Axonal Hereditary Motor and Sensory Neuropathy |
13 |
0.495 |
|
296 |
|
c
|
SPS128 |
Spastic Paraplegia 7, Autosomal Recessive |
58 |
0.495 |
|
297 |
|
P
|
SPS133 |
Spastic Paraplegia 2, X-Linked |
50 |
0.495 |
|
298 |
|
c
|
CHR646 |
Charcot-Marie-Tooth Disease, Axonal, Type 2b |
50 |
0.495 |
|
299 |
|
|
MST006 |
Mast Syndrome |
40 |
0.495 |
|
300 |
|
c
|
SPS108 |
Spastic Paraplegia 5a, Autosomal Recessive |
42 |
0.495 |
|
301 |
|
c
|
PNT044 |
Pontocerebellar Hypoplasia, Type 2a |
41 |
0.495 |
|
302 |
|
|
ALB025 |
Albinism, Ocular, with Late-Onset Sensorineural Deafness |
49 |
0.495 |
|
303 |
|
c
|
SPS222 |
Spastic Paraplegia 20, Autosomal Recessive |
56 |
0.495 |
|
304 |
|
|
ATX047 |
Ataxia, Spastic, Childhood-Onset, Autosomal Recessive, with Optic Atrophy and Mental Retardation |
23 |
0.495 |
|
305 |
|
c
|
SPS219 |
Spastic Paraplegia 17, Autosomal Dominant |
42 |
0.495 |
|
306 |
|
c
|
SPS125 |
Spastic Paraplegia 15, Autosomal Recessive |
49 |
0.495 |
|
307 |
|
c
|
NRP053 |
Neuropathy, Hereditary Sensory and Autonomic, Type Iia |
67 |
0.495 |
|
308 |
|
c
|
AMY058 |
Amyotrophic Lateral Sclerosis 2, Juvenile |
41 |
0.495 |
|
309 |
|
c
|
WRD026 |
Waardenburg Syndrome, Type 2c |
26 |
0.495 |
|
310 |
|
c
|
SPS110 |
Spastic Paraplegia 19, Autosomal Dominant |
29 |
0.495 |
|
311 |
|
|
MYP136 |
Myopathy, Centronuclear, X-Linked |
59 |
0.495 |
|
312 |
|
c
|
AMY045 |
Amyotrophic Lateral Sclerosis 4, Juvenile |
49 |
0.495 |
|
313 |
|
c
|
SPS127 |
Spastic Paraplegia 6, Autosomal Dominant |
48 |
0.495 |
|
314 |
|
c
|
NRN037 |
Neuronopathy, Distal Hereditary Motor, Type Va |
49 |
0.495 |
|
315 |
|
c
|
CHR649 |
Charcot-Marie-Tooth Disease, Axonal, Type 2d |
46 |
0.495 |
|
316 |
|
c
|
SPS151 |
Spastic Paraplegia 11, Autosomal Recessive |
49 |
0.495 |
|
317 |
|
|
NRP049 |
Neuropathy, Hereditary Sensory and Autonomic, Type I, with Cough and Gastroesophageal Reflux |
32 |
0.495 |
|
318 |
|
c
|
CHR350 |
Charcot-Marie-Tooth Disease, Axonal, Type 2k |
47 |
0.495 |
|
319 |
|
P
|
DYS193 |
Dystonia 11, Myoclonic |
55 |
0.495 |
|
320 |
|
|
NRP051 |
Neuropathy, Hereditary, with Liability to Pressure Palsies |
54 |
0.495 |
|
321 |
|
c
|
AMY091 |
Amyotrophic Lateral Sclerosis 1 |
88 |
0.495 |
|
322 |
|
|
MLN065 |
Melanocytic Nevus Syndrome, Congenital |
62 |
0.495 |
|
323 |
|
|
TTZ003 |
Tietz Albinism-Deafness Syndrome |
59 |
0.495 |
|
324 |
|
|
PPL049 |
Papillon-Lefevre Syndrome |
66 |
0.495 |
|
325 |
|
|
SLW005 |
Slowed Nerve Conduction Velocity, Autosomal Dominant |
35 |
0.495 |
|
326 |
|
c
|
CHR353 |
Charcot-Marie-Tooth Disease, Axonal, Type 2l |
41 |
0.495 |
|
327 |
|
|
PRP066 |
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease |
50 |
0.495 |
|
328 |
|
|
GLD006 |
Goldberg-Shprintzen Syndrome |
49 |
0.495 |
|
329 |
|
P
|
OCL001 |
Ocular Albinism |
48 |
0.495 |
|
330 |
|
P
|
DST002 |
Distal Arthrogryposis |
65 |
0.495 |
|
331 |
|
|
DYS001 |
Dyskinetic Cerebral Palsy |
31 |
0.495 |
|
332 |
|
P
|
PRR025 |
Perrault Syndrome |
42 |
0.495 |
|
333 |
|
c
|
SPS123 |
Spastic Paraplegia 32, Autosomal Recessive |
33 |
0.495 |
|
334 |
|
c
|
NRP039 |
Neuropathy, Hereditary Sensory, Type Id |
39 |
0.495 |
|
335 |
|
c
|
NRP029 |
Neuropathy, Hereditary Sensory, Type Iic |
36 |
0.495 |
|
336 |
|
c
|
CHR026 |
Charcot-Marie-Tooth Disease Type X |
25 |
0.495 |
|
337 |
|
c
|
CHR025 |
Charcot-Marie-Tooth Disease Intermediate Type |
29 |
0.495 |
|
338 |
|
P
|
HRD021 |
Hereditary Sensory Neuropathy |
48 |
0.495 |
|
339 |
|
c
|
SPN444 |
Spinal Muscular Atrophy Type 0 |
22 |
0.495 |
|
340 |
|
c
|
AMY081 |
Amyotrophic Lateral Sclerosis Type 12 |
28 |
0.495 |
|
341 |
|
c
|
AMY074 |
Amyotrophic Lateral Sclerosis Type 14 |
21 |
0.495 |
|
342 |
|
c
|
AMY079 |
Amyotrophic Lateral Sclerosis Type 15 |
26 |
0.495 |
|
343 |
|
|
INT072 |
Intestinal Pseudo-Obstruction |
62 |
0.495 |
|
344 |
|
c
|
AMY022 |
Amyotrophic Lateral Sclerosis Type 5 |
33 |
0.495 |
|
345 |
|
c
|
AMY023 |
Amyotrophic Lateral Sclerosis Type 6 |
34 |
0.495 |
|
346 |
|
c
|
OPT023 |
Optic Atrophy 2 |
32 |
0.495 |
|
347 |
|
c
|
CHR647 |
Charcot-Marie-Tooth Disease, Demyelinating, Type 1c |
46 |
0.495 |
|
348 |
|
c
|
CHR521 |
Charcot-Marie-Tooth Disease, Type 4b1 |
47 |
0.495 |
|
349 |
|
c
|
CHR376 |
Charcot-Marie-Tooth Disease, Type 4d |
47 |
0.495 |
|
350 |
|
c
|
CHR516 |
Charcot-Marie-Tooth Disease, Type 4c |
48 |
0.495 |
|
351 |
|
c
|
AMY094 |
Amyotrophic Lateral Sclerosis 5, Juvenile |
31 |
0.495 |
|
352 |
|
c
|
PNT043 |
Pontocerebellar Hypoplasia, Type 4 |
41 |
0.495 |
|
353 |
|
c
|
WRD020 |
Waardenburg Syndrome, Type 4a |
49 |
0.495 |
|
354 |
|
c
|
SPS198 |
Spastic Paraplegia 16, X-Linked |
30 |
0.495 |
|
355 |
|
P
|
PHS005 |
Peho Syndrome |
44 |
0.495 |
|
356 |
|
P
|
CHR625 |
Charcot-Marie-Tooth Disease, Demyelinating, Type 1b |
57 |
0.495 |
|
357 |
|
c
|
CHR626 |
Charcot-Marie-Tooth Disease, Axonal, Type 2a1 |
36 |
0.495 |
|
358 |
|
c
|
CHR627 |
Charcot-Marie-Tooth Disease, Demyelinating, Type 1a |
56 |
0.495 |
|
359 |
|
|
CHR629 |
Charcot-Marie-Tooth Disease and Deafness |
50 |
0.495 |
|
360 |
|
c
|
SPS117 |
Spastic Paraplegia 10, Autosomal Dominant |
48 |
0.495 |
|
361 |
|
c
|
CHR650 |
Charcot-Marie-Tooth Disease, Axonal, Type 2b1 |
45 |
0.495 |
|
362 |
|
c
|
CHR651 |
Charcot-Marie-Tooth Disease, Axonal, Type 2b2 |
39 |
0.495 |
|
363 |
|
P
|
HRD094 |
Hereditary Motor and Sensory Neuropathy, Type Iic |
48 |
0.495 |
|
364 |
|
c
|
SPS149 |
Spastic Paraplegia 8, Autosomal Dominant |
48 |
0.495 |
|
365 |
|
P
|
SPN408 |
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 1 |
51 |
0.495 |
|
366 |
|
|
NRP009 |
Neuropathy, Hereditary Motor and Sensory, Okinawa Type |
32 |
0.495 |
|
367 |
|
c
|
SPS068 |
Spastic Paraplegia 14, Autosomal Recessive |
29 |
0.495 |
|
368 |
|
P
|
NRP063 |
Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive |
58 |
0.495 |
|
369 |
|
c
|
SPS097 |
Spastic Paraplegia 13, Autosomal Dominant |
41 |
0.495 |
|
370 |
|
|
NRP010 |
Neuropathy, Hereditary Motor and Sensory, Russe Type |
36 |
0.495 |
|
371 |
|
c
|
SPN326 |
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 2 |
38 |
0.495 |
|
372 |
|
c
|
ALZ053 |
Alzheimer Disease 7 |
32 |
0.495 |
|
373 |
|
c
|
CHR519 |
Charcot-Marie-Tooth Disease, Type 4b2 |
48 |
0.495 |
|
374 |
|
c
|
SPS131 |
Spastic Paraplegia 12, Autosomal Dominant |
41 |
0.495 |
|
375 |
|
c
|
SPS103 |
Spastic Paraplegia 50, Autosomal Recessive |
41 |
0.495 |
|
376 |
|
c
|
MYP081 |
Myopathy, Myofibrillar, 6 |
41 |
0.495 |
|
377 |
|
c
|
SPS071 |
Spastic Paraplegia 48, Autosomal Recessive |
44 |
0.495 |
|
378 |
|
c
|
CHR671 |
Charcot-Marie-Tooth Disease, Axonal, Type 2r |
37 |
0.495 |
|
379 |
|
|
ALC028 |
Alacrima, Achalasia, and Mental Retardation Syndrome |
68 |
0.495 |
|
380 |
|
c
|
CRT074 |
Cortical Dysplasia, Complex, with Other Brain Malformations 6 |
32 |
0.495 |
|
381 |
|
|
PLY118 |
Polyglucosan Body Myopathy 1 with or Without Immunodeficiency |
55 |
0.495 |
|
382 |
|
c
|
CHR514 |
Charcot-Marie-Tooth Disease, Recessive Intermediate D |
27 |
0.495 |
|
383 |
|
c
|
CHR544 |
Charcot-Marie-Tooth Disease, Axonal, Type 2w |
34 |
0.495 |
|
384 |
|
c
|
CHR618 |
Charcot-Marie-Tooth Disease, Axonal, Type 2cc |
28 |
0.495 |
|
385 |
|
|
CHR607 |
Chorea, Childhood-Onset, with Psychomotor Retardation |
39 |
0.495 |
|
386 |
|
c
|
PNT036 |
Pontocerebellar Hypoplasia, Type 6 |
46 |
0.495 |
|
387 |
|
|
GLC105 |
Glucocorticoid Deficiency 4 with or Without Mineralocorticoid Deficiency |
33 |
0.495 |
|
388 |
|
c
|
CHR670 |
Charcot-Marie-Tooth Disease, Demyelinating, Type 4f |
43 |
0.495 |
|
389 |
|
c
|
SPS106 |
Spastic Paraplegia 54, Autosomal Recessive |
42 |
0.495 |
|
390 |
|
c
|
SPS119 |
Spastic Paraplegia 55, Autosomal Recessive |
39 |
0.495 |
|
391 |
|
|
CLD014 |
Cole Disease |
38 |
0.495 |
|
392 |
|
c
|
SPS137 |
Spastic Paraplegia 57, Autosomal Recessive |
39 |
0.495 |
|
393 |
|
c
|
SPS157 |
Spastic Paraplegia 64, Autosomal Recessive |
40 |
0.495 |
|
394 |
|
c
|
SPS141 |
Spastic Paraplegia 61, Autosomal Recessive |
37 |
0.495 |
|
395 |
|
c
|
SPS228 |
Spastic Paraplegia 63, Autosomal Recessive |
35 |
0.495 |
|
396 |
|
c
|
SPS107 |
Spastic Paraplegia 18, Autosomal Recessive |
41 |
0.495 |
|
397 |
|
P
|
AMY106 |
Amyotrophic Lateral Sclerosis 10 with or Without Frontotemporal Dementia |
44 |
0.495 |
|
398 |
|
c
|
SPS096 |
Spastic Paraplegia 44, Autosomal Recessive |
38 |
0.495 |
|
399 |
|
c
|
WRD024 |
Waardenburg Syndrome, Type 4c |
43 |
0.495 |
|
400 |
|
c
|
WRD019 |
Waardenburg Syndrome, Type 4b |
45 |
0.495 |
|
401 |
|
c
|
CHR351 |
Charcot-Marie-Tooth Disease, Axonal, Type 2n |
41 |
0.495 |
|
402 |
|
c
|
SPS115 |
Spastic Paraplegia 41, Autosomal Dominant |
29 |
0.495 |
|
403 |
|
c
|
NRN018 |
Neuronopathy, Distal Hereditary Motor, Type Iic |
34 |
0.495 |
|
404 |
|
c
|
NRP040 |
Neuropathy, Hereditary Sensory and Autonomic, Type Ic |
42 |
0.495 |
|
405 |
|
c
|
CHR666 |
Charcot-Marie-Tooth Disease, Recessive Intermediate B |
36 |
0.495 |
|
406 |
|
c
|
PNT049 |
Pontocerebellar Hypoplasia, Type 2d |
43 |
0.495 |
|
407 |
|
c
|
SPS095 |
Spastic Paraplegia 47, Autosomal Recessive |
43 |
0.495 |
|
408 |
|
c
|
SPS122 |
Spastic Paraplegia 52, Autosomal Recessive |
39 |
0.495 |
|
409 |
|
c
|
CHR420 |
Charcot-Marie-Tooth Disease, Type 4j |
48 |
0.495 |
|
410 |
|
c
|
AMY085 |
Amyotrophic Lateral Sclerosis 9 |
36 |
0.495 |
|
411 |
|
c
|
SPS129 |
Spastic Paraplegia 39, Autosomal Recessive |
44 |
0.495 |
|
412 |
|
c
|
SPS153 |
Spastic Paraplegia 35, Autosomal Recessive |
50 |
0.495 |
|
413 |
|
c
|
SPS099 |
Spastic Paraplegia 42, Autosomal Dominant |
40 |
0.495 |
|
414 |
|
c
|
SPS113 |
Spastic Paraplegia 33, Autosomal Dominant |
37 |
0.495 |
|
415 |
|
|
PHS023 |
Phosphoserine Aminotransferase Deficiency |
41 |
0.495 |
|
416 |
|
P
|
CHR640 |
Charcot-Marie-Tooth Disease, X-Linked Dominant, 1 |
51 |
0.495 |
|
417 |
|
c
|
CHR641 |
Charcot-Marie-Tooth Disease, X-Linked Recessive, 2 |
33 |
0.495 |
|
418 |
|
|
MSS001 |
Masa Syndrome |
60 |
0.495 |
|
419 |
|
|
SPN402 |
Spinal Muscular Atrophy, X-Linked 2 |
48 |
0.495 |
|
420 |
|
c
|
PNT046 |
Pontocerebellar Hypoplasia, Type 5 |
30 |
0.495 |
|
421 |
|
c
|
SPS148 |
Spastic Paraplegia 31, Autosomal Dominant |
47 |
0.495 |
|
422 |
|
c
|
SPN191 |
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 |
46 |
0.495 |
|
423 |
|
|
ALX003 |
Alexander Disease |
61 |
0.495 |
|
424 |
|
c
|
LBR004 |
Leber Congenital Amaurosis 1 |
52 |
0.495 |
|
425 |
|
c
|
AMY090 |
Amyotrophic Lateral Sclerosis 8 |
43 |
0.495 |
|
426 |
|
c
|
NRP037 |
Neuropathy, Hereditary Sensory and Autonomic, Type V |
55 |
0.495 |
|
427 |
|
c
|
WRD022 |
Waardenburg Syndrome, Type 2d |
33 |
0.495 |
|
428 |
|
c
|
SPS116 |
Spastic Paraplegia 26, Autosomal Recessive |
40 |
0.495 |
|
429 |
|
c
|
CHR421 |
Charcot-Marie-Tooth Disease, Type 4h |
46 |
0.495 |
|
430 |
|
c
|
SPS124 |
Spastic Paraplegia 28, Autosomal Recessive |
41 |
0.495 |
|
431 |
|
|
BHR001 |
Behr Syndrome |
51 |
0.495 |
|
432 |
|
c
|
CHR517 |
Charcot-Marie-Tooth Disease, Type 4a |
45 |
0.495 |
|
433 |
|
|
YNS002 |
Yunis-Varon Syndrome |
50 |
0.495 |
|
434 |
|
|
HLN001 |
Halo Nevi |
27 |
0.495 |
|
435 |
|
c
|
WRD030 |
Waardenburg Syndrome, Type 1 |
53 |
0.495 |
|
436 |
|
c
|
GNT049 |
Giant Axonal Neuropathy 1, Autosomal Recessive |
48 |
0.495 |
|
437 |
|
|
PYC001 |
Pycnodysostosis |
55 |
0.495 |
|
438 |
|
|
TLC001 |
Telecanthus |
35 |
0.495 |
|
439 |
|
|
SCP002 |
Scapuloperoneal Spinal Muscular Atrophy |
55 |
0.495 |
|
440 |
|
c
|
SPS147 |
Spastic Paraplegia 4, Autosomal Dominant |
55 |
0.495 |
|
|
442 |
|
|
DLT018 |
Dilution, Pigmentary |
25 |
0.495 |
|
443 |
|
|
HYP186 |
Hypertrophic Neuropathy of Dejerine-Sottas |
51 |
0.495 |
|
444 |
|
P
|
HYP535 |
Hypogonadotropic Hypogonadism 7 with or Without Anosmia |
57 |
0.495 |
|
445 |
|
|
PBL005 |
Piebald Trait |
59 |
0.495 |
|
446 |
|
|
HTR005 |
Heterochromia Iridis |
21 |
0.495 |
|
447 |
|
P
|
HRS035 |
Hirschsprung Disease 1 |
66 |
0.495 |
|
448 |
|
P
|
CMP005 |
Campomelic Dysplasia |
65 |
0.495 |
|
449 |
|
c
|
NRN040 |
Neuronopathy, Distal Hereditary Motor, Type Viib |
45 |
0.495 |
|
450 |
|
c
|
CHR371 |
Charcot-Marie-Tooth Disease, Dominant Intermediate C |
41 |
0.495 |
|
451 |
|
c
|
CHR658 |
Charcot-Marie-Tooth Disease, Recessive Intermediate a |
38 |
0.495 |
|
452 |
|
c
|
AMY063 |
Amyotrophic Lateral Sclerosis 20 |
31 |
0.495 |
|
453 |
|
c
|
CHR547 |
Charcot-Marie-Tooth Disease, Axonal, Type 2u |
38 |
0.495 |
|
454 |
|
c
|
DVL055 |
Developmental and Epileptic Encephalopathy 29 |
37 |
0.495 |
|
455 |
|
c
|
LKD023 |
Leukodystrophy, Hypomyelinating, 12 |
38 |
0.495 |
|
456 |
|
c
|
CHR542 |
Charcot-Marie-Tooth Disease, Axonal, Type 2t |
36 |
0.495 |
|
457 |
|
|
HYD058 |
Hydrops, Lactic Acidosis, and Sideroblastic Anemia |
60 |
0.495 |
|
458 |
|
c
|
CHR652 |
Charcot-Marie-Tooth Disease, Axonal, Type 2i |
38 |
0.495 |
|
459 |
|
c
|
CHR653 |
Charcot-Marie-Tooth Disease, Demyelinating, Type 1d |
39 |
0.495 |
|
460 |
|
|
CHR655 |
Charcot-Marie-Tooth Disease, Axonal, with Vocal Cord Paresis, Autosomal Recessive |
32 |
0.495 |
|
461 |
|
c
|
CHR545 |
Charcot-Marie-Tooth Disease, Axonal, Type 2h |
27 |
0.495 |
|
462 |
|
c
|
CHR657 |
Charcot-Marie-Tooth Disease, Axonal, Type 2j |
39 |
0.495 |
|
463 |
|
c
|
CHR481 |
Charcot-Marie-Tooth Disease, Dominant Intermediate D |
32 |
0.495 |
|
464 |
|
c
|
DNJ004 |
Dnajb2-Related Charcot-Marie-Tooth Disease Type 2 |
15 |
0.495 |
|
465 |
|
|
NNS061 |
Non-Syndromic Pontocerebellar Hypoplasia |
20 |
0.495 |
|
466 |
|
P
|
PNT019 |
Pontocerebellar Hypoplasia |
46 |
0.495 |
|
467 |
|
P
|
HYP730 |
Hypogonadotropic Hypogonadism |
53 |
0.495 |
|
468 |
|
c
|
GNT045 |
Giant Axonal Neuropathy 2 |
24 |
0.495 |
|
469 |
|
c
|
HRD210 |
Hereditary Spastic Paraplegia 23 |
22 |
0.495 |
|
470 |
|
c
|
ATS425 |
Autosomal Recessive Distal Hereditary Motor Neuronopathy |
20 |
0.495 |
|
471 |
|
P
|
ATS426 |
Autosomal Dominant Distal Hereditary Motor Neuronopathy |
33 |
0.495 |
|
472 |
|
c
|
HRD220 |
Hereditary Spastic Paraplegia 30 |
32 |
0.495 |
|
473 |
|
c
|
HRD186 |
Hereditary Spastic Paraplegia 51 |
29 |
0.495 |
|
474 |
|
c
|
HRD188 |
Hereditary Spastic Paraplegia 72 |
28 |
0.495 |
|
475 |
|
c
|
CHR422 |
Charcot-Marie-Tooth Disease, Dominant Intermediate B |
46 |
0.495 |
|
476 |
|
c
|
CHR491 |
Charcot-Marie-Tooth Disease, Dominant Intermediate a |
30 |
0.495 |
|
477 |
|
c
|
CHR608 |
Charcot-Marie-Tooth Disease, Axonal, Type 2p |
45 |
0.495 |
|
478 |
|
|
LSN001 |
Lesion of Sciatic Nerve |
22 |
0.495 |
|
479 |
|
P
|
SPN423 |
Spinal Muscular Atrophy with Lower Extremity Predominance |
26 |
0.495 |
|
480 |
|
P
|
OCL062 |
Ocular Albinism with Congenital Sensorineural Deafness |
23 |
0.495 |
|
481 |
|
P
|
DYS154 |
Dystonia |
64 |
0.495 |
|
482 |
|
P
|
KLL001 |
Kallmann Syndrome |
65 |
0.495 |
|
483 |
|
P
|
ACT008 |
Actinic Keratosis |
54 |
0.495 |
|
484 |
|
|
CCH001 |
Cochlear Disease |
28 |
0.495 |
|
485 |
|
P
|
DST101 |
Distal Hereditary Motor Neuropathies |
23 |
0.495 |
|
486 |
|
|
BRC011 |
Brachial Plexus Neuropathy |
38 |
0.495 |
|
487 |
|
|
PRG001 |
Progressive Muscular Atrophy |
41 |
0.495 |
|
488 |
|
|
ANG018 |
Angiomyolipoma |
46 |
0.495 |
|
489 |
|
P
|
CNT004 |
Centronuclear Myopathy |
57 |
0.495 |
|
490 |
|
|
NRM005 |
Neuromuscular Disease |
63 |
0.495 |
|
491 |
|
|
PRP016 |
Paraplegia |
52 |
0.495 |
|
492 |
|
|
DFF013 |
Diffuse Meningeal Melanocytosis |
20 |
0.495 |
|
493 |
|
c
|
CHR522 |
Charcot-Marie-Tooth Disease, Dominant Intermediate E |
40 |
0.495 |
|
494 |
|
c
|
MLN043 |
Melanoma, Cutaneous Malignant 8 |
37 |
0.495 |
|
495 |
|
|
EPT001 |
Epithelioid Cell Melanoma |
21 |
0.495 |
|
496 |
|
c
|
SPS101 |
Spastic Paraplegia 56, Autosomal Recessive |
39 |
0.495 |
|
497 |
|
c
|
SPS126 |
Spastic Paraplegia 49, Autosomal Recessive |
44 |
0.495 |
|
498 |
|
c
|
CHR504 |
Charcot-Marie-Tooth Disease, Type 4b3 |
45 |
0.495 |
|
499 |
|
|
ALK024 |
Alkuraya-Kucinskas Syndrome |
45 |
0.495 |
|
500 |
|
|
ENC067 |
Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis |
50 |
0.495 |
|
501 |
|
P
|
SNS001 |
Sensorineural Hearing Loss |
59 |
0.495 |
|
502 |
|
c
|
AMY083 |
Amyotrophic Lateral Sclerosis 11 |
39 |
0.495 |
|
503 |
|
c
|
SPS109 |
Spastic Paraplegia 46, Autosomal Recessive |
42 |
0.495 |
|
504 |
|
c
|
AMY057 |
Amyotrophic Lateral Sclerosis 16, Juvenile |
38 |
0.495 |
|
505 |
|
P
|
LTR001 |
Lateral Sclerosis |
58 |
0.495 |
|
506 |
|
|
MTR007 |
Motor Peripheral Neuropathy |
40 |
0.495 |
|
507 |
|
|
ARG003 |
Argyll Robertson Pupil |
23 |
0.495 |
|
508 |
|
c
|
HRD010 |
Hereditary Spastic Paraplegia |
66 |
0.495 |
|
509 |
|
P
|
PPL023 |
Pupil Disease |
26 |
0.495 |
|
510 |
|
|
MLG005 |
Malignant Spindle Cell Melanoma |
39 |
0.495 |
|
511 |
|
|
MLN079 |
Melanoma in Congenital Melanocytic Nevus |
37 |
0.495 |
|
512 |
|
c
|
CHR571 |
Charcot-Marie-Tooth Disease Type 5 |
23 |
0.495 |
|
513 |
|
P
|
MCR010 |
Microcephaly |
60 |
0.495 |
|
514 |
|
|
SPS004 |
Spastic Quadriplegia |
40 |
0.495 |
|
515 |
|
|
ABN004 |
Abnormal Pupillary Function |
15 |
0.495 |
|
516 |
|
|
MLG061 |
Malignant Choroid Melanoma |
33 |
0.495 |
|
517 |
|
|
CHL010 |
Childhood Kidney Cell Carcinoma |
38 |
0.495 |
|
518 |
|
|
GLL012 |
Gallbladder Melanoma |
25 |
0.495 |
|
519 |
|
P
|
MTR014 |
Motor Neuron Disease |
65 |
0.495 |
|
520 |
|
P
|
PLY019 |
Polyneuropathy |
52 |
0.495 |
|
521 |
|
|
MNN017 |
Mononeuropathy |
41 |
0.495 |
|
522 |
|
|
MLN005 |
Melanoacanthoma |
22 |
0.495 |
|
523 |
|
|
MGC001 |
Megacolon |
48 |
0.495 |
|
524 |
|
|
SPS003 |
Spastic Diplegia |
53 |
0.495 |
|
525 |
|
|
QDR001 |
Quadriplegia |
50 |
0.495 |
|
526 |
|
|
CHR073 |
Choreatic Disease |
54 |
0.495 |
|
527 |
|
|
OCH001 |
Ochronosis |
40 |
0.495 |
|
528 |
|
|
HYP080 |
Hypogonadism |
50 |
0.495 |
|
529 |
|
|
CRB037 |
Cerebral Palsy |
67 |
0.495 |
|
530 |
|
|
BSC002 |
Bscl2-Related Neurologic Disorders/seipinopathy |
10 |
0.495 |
|
531 |
|
|
ALB002 |
Albinism |
47 |
0.495 |
|
532 |
|
c
|
SPS092 |
Spastic Paraplegia 11 |
33 |
0.495 |
|
533 |
|
|
TSN004 |
Tsen54 Pontocerebellar Hypoplasia |
15 |
0.495 |
|
534 |
|
P
|
PRX014 |
Proximal Spinal Muscular Atrophy |
42 |
0.495 |
|
535 |
|
c
|
ERL012 |
Early-Onset Glaucoma |
24 |
0.495 |
|
536 |
|
P
|
ENC018 |
Encephalopathy |
62 |
0.495 |
|
537 |
|
P
|
CHR453 |
Charcot-Marie-Tooth Hereditary Neuropathy |
39 |
0.495 |
|
538 |
|
P
|
GNT009 |
Giant Axonal Neuropathy |
46 |
0.495 |
|
539 |
|
P
|
CRB088 |
Cerebral Atrophy |
33 |
0.495 |
|
540 |
|
|
ATN005 |
Autonomic Dysfunction |
46 |
0.495 |
|
541 |
|
c
|
HRD088 |
Hereditary Neuropathies |
33 |
0.495 |
|
542 |
|
P
|
MYC033 |
Myoclonus |
47 |
0.495 |
|
543 |
|
|
HYP213 |
Hypomelanotic Disorder |
22 |
0.495 |
|
544 |
|
|
ANC002 |
Anca-Associated Vasculitis |
44 |
0.495 |
|
545 |
|
c
|
ATS272 |
Autosomal Dominant Intermediate Charcot-Marie-Tooth |
19 |
0.495 |
|
546 |
|
c
|
CHR135 |
Charcot-Marie-Tooth Disease Type 2a |
23 |
0.495 |
|
547 |
|
|
PRX008 |
Paroxysmal Cold Hemoglobinuria |
26 |
0.495 |
|
548 |
|
|
ARC025 |
Arachnoid Cysts, Intracranial |
37 |
0.457 |
|
549 |
|
c
|
TYP008 |
Type 1 Diabetes Mellitus |
70 |
0.457 |
|
550 |
|
|
LYM133 |
Lymphoma, Hodgkin, Classic |
74 |
0.457 |
|
551 |
|
|
QLT002 |
Qualitative or Quantitative Defects of Dystrophin |
19 |
0.457 |
|
552 |
|
|
ERY002 |
Erythema Infectiosum |
35 |
0.457 |
|
553 |
|
|
APN006 |
Apnea of Prematurity |
24 |
0.457 |
|
554 |
|
|
CYN003 |
Cyanide Poisoning |
22 |
0.457 |
|
555 |
|
P
|
OVR082 |
Overgrowth Syndrome |
49 |
0.457 |
|
556 |
|
|
ATH013 |
Atherosclerosis Susceptibility |
63 |
0.457 |
|
557 |
|
P
|
BLD134 |
Bladder Cancer |
79 |
0.457 |
|
558 |
|
c
|
BDY010 |
Body Mass Index Quantitative Trait Locus 4 |
46 |
0.457 |
|
559 |
|
|
PLM134 |
Pulmonary Fibrosis, Idiopathic |
76 |
0.457 |
|
560 |
|
P
|
ULL002 |
Ullrich Congenital Muscular Dystrophy 1 |
57 |
0.457 |
|
561 |
|
P
|
MYS003 |
Myasthenia Gravis |
68 |
0.457 |
|
562 |
|
|
MSC152 |
Muscular Dystrophy, Becker Type |
69 |
0.457 |
|
563 |
|
c
|
MSC036 |
Muscular Dystrophy-Dystroglycanopathy , Type C, 5 |
64 |
0.457 |
|
564 |
|
|
PSR001 |
Psoriatic Arthritis |
62 |
0.457 |
|
565 |
|
c
|
BDY011 |
Body Mass Index Quantitative Trait Locus 10 |
45 |
0.457 |
|
566 |
|
|
SHR097 |
Short Tarsus with Absence of Lower Eyelashes |
25 |
0.457 |
|
567 |
|
c
|
HRD138 |
Hereditary Motor and Sensory Neuropathy V |
32 |
0.457 |
|
568 |
|
|
STR067 |
Stroke, Ischemic |
80 |
0.457 |
|
569 |
|
c
|
BDY005 |
Body Mass Index Quantitative Trait Locus 9 |
47 |
0.457 |
|
570 |
|
P
|
DRM053 |
Dermatitis, Atopic |
65 |
0.457 |
|
571 |
|
c
|
PLM164 |
Pulmonary Hypertension, Primary, 1 |
76 |
0.457 |
|
572 |
|
|
RTN017 |
Retinal Detachment |
60 |
0.457 |
|
573 |
|
P
|
RHM011 |
Rheumatoid Arthritis |
82 |
0.457 |
|
574 |
|
|
LTH043 |
Lithium Transport |
17 |
0.457 |
|
575 |
|
|
MRF001 |
Marfan Syndrome |
76 |
0.457 |
|
576 |
|
P
|
BTH005 |
Bethlem Myopathy 1 |
62 |
0.457 |
|
577 |
|
P
|
OST002 |
Osteoporosis |
76 |
0.457 |
|
578 |
|
|
TRT017 |
Teratoma, Ovarian |
28 |
0.457 |
|
579 |
|
c
|
PCH015 |
Pachyonychia Congenita 1 |
60 |
0.457 |
|
580 |
|
P
|
LKM071 |
Leukemia, Chronic Lymphocytic |
75 |
0.457 |
|
581 |
|
c
|
SYS001 |
Systemic Lupus Erythematosus |
87 |
0.457 |
|
582 |
|
P
|
OVR042 |
Ovarian Cancer |
88 |
0.457 |
|
583 |
|
|
MNT107 |
Mental Retardation, Fra12a Type |
20 |
0.457 |
|
584 |
|
|
GLL008 |
Gilles De La Tourette Syndrome |
65 |
0.457 |
|
585 |
|
|
ALC007 |
Alcohol Dependence |
66 |
0.457 |
|
586 |
|
c
|
SPN225 |
Spondyloarthropathy 1 |
70 |
0.457 |
|
587 |
|
|
GST092 |
Gastroesophageal Reflux |
61 |
0.457 |
|
588 |
|
c
|
SYN084 |
Synpolydactyly 1 |
36 |
0.457 |
|
589 |
|
|
VTL009 |
Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 |
42 |
0.457 |
|
590 |
|
P
|
CLC063 |
Celiac Disease 1 |
66 |
0.457 |
|
591 |
|
|
HYD038 |
Hydrops Fetalis, Nonimmune |
59 |
0.457 |
|
592 |
|
c
|
BDY012 |
Body Mass Index Quantitative Trait Locus 7 |
44 |
0.457 |
|
593 |
|
P
|
PLM037 |
Pulmonary Hypertension |
72 |
0.457 |
|
594 |
|
|
MTR088 |
Mature T-Cell and Nk-Cell Lymphoma |
42 |
0.457 |
|
595 |
|
P
|
SLP006 |
Sleep Apnea |
69 |
0.457 |
|
596 |
|
|
FTL006 |
Fetal Alcohol Spectrum Disorder |
43 |
0.457 |
|
597 |
|
|
PRP036 |
Peripheral T-Cell Lymphoma |
53 |
0.457 |
|
598 |
|
|
MLR004 |
Malaria |
80 |
0.457 |
|
599 |
|
c
|
BNM022 |
Bone Mineral Density Quantitative Trait Locus 8 |
45 |
0.457 |
|
600 |
|
c
|
MJR022 |
Major Affective Disorder 8 |
38 |
0.457 |
|
601 |
|
c
|
MCR130 |
Microvascular Complications of Diabetes 6 |
41 |
0.457 |
|
602 |
|
|
HYP561 |
Hypertelorism, Preauricular Sinus, Punctal Pits, and Deafness |
27 |
0.457 |
|
603 |
|
P
|
BNM029 |
Bone Mineral Density Quantitative Trait Locus 15 |
48 |
0.457 |
|
604 |
|
|
CYN002 |
Cyanosis, Transient Neonatal |
43 |
0.457 |
|
605 |
|
|
NDL024 |
Nodal Marginal Zone Lymphoma |
37 |
0.457 |
|
606 |
|
c
|
ATS007 |
Autism Spectrum Disorder |
72 |
0.457 |
|
607 |
|
|
ART074 |
Aortic Dissection |
53 |
0.457 |
|
608 |
|
|
HMN047 |
Human Cytomegalovirus Infection |
57 |
0.457 |
|
609 |
|
P
|
CTN015 |
Cutaneous T Cell Lymphoma |
48 |
0.457 |
|
610 |
|
P
|
SYN012 |
Synpolydactyly |
38 |
0.457 |
|
611 |
|
P
|
ATR011 |
Atrial Fibrillation |
66 |
0.457 |
|
612 |
|
P
|
FTL001 |
Fetal Alcohol Syndrome |
55 |
0.457 |
|
613 |
|
P
|
SML001 |
Small Cell Carcinoma |
52 |
0.457 |
|
614 |
|
P
|
BSL038 |
Basal Ganglia Calcification, Idiopathic, 1 |
53 |
0.457 |
|
615 |
|
|
CRY035 |
Cryptorchidism, Unilateral or Bilateral |
58 |
0.457 |
|
616 |
|
P
|
BDY004 |
Body Mass Index Quantitative Trait Locus 11 |
83 |
0.457 |
|
617 |
|
|
CNT105 |
Central Core Disease of Muscle |
59 |
0.457 |
|
618 |
|
|
HSH003 |
Hashimoto Thyroiditis |
60 |
0.457 |
|
619 |
|
c
|
BDY006 |
Body Mass Index Quantitative Trait Locus 8 |
44 |
0.457 |
|
620 |
|
|
RNL065 |
Renal Cell Carcinoma, Papillary, 1 |
79 |
0.457 |
|
621 |
|
|
ALV005 |
Alveolar Soft Part Sarcoma |
61 |
0.457 |
|
622 |
|
|
LYM143 |
Lymphoma, Non-Hodgkin, Familial |
75 |
0.457 |
|
623 |
|
|
AST006 |
Astigmatism |
47 |
0.457 |
|
624 |
|
|
EWN003 |
Ewing Sarcoma |
70 |
0.457 |
|
625 |
|
c
|
BDY017 |
Body Mass Index Quantitative Trait Locus 14 |
45 |
0.457 |
|
626 |
|
c
|
LSS030 |
Lissencephaly 7 with Cerebellar Hypoplasia |
21 |
0.457 |
|
627 |
|
c
|
CHR617 |
Charcot-Marie-Tooth Disease, Axonal, Type 2z |
35 |
0.457 |
|
628 |
|
c
|
BDY020 |
Body Mass Index Quantitative Trait Locus 19 |
52 |
0.457 |
|
629 |
|
P
|
MJR001 |
Major Depressive Disorder |
68 |
0.457 |
|
630 |
|
c
|
MJR024 |
Major Affective Disorder 9 |
41 |
0.457 |
|
631 |
|
|
ACT119 |
Acute Promyelocytic Leukemia |
62 |
0.457 |
|
632 |
|
c
|
MCR120 |
Microvascular Complications of Diabetes 7 |
47 |
0.457 |
|
633 |
|
c
|
BDY015 |
Body Mass Index Quantitative Trait Locus 12 |
46 |
0.457 |
|
634 |
|
P
|
DVL012 |
Developmental Dysplasia of the Hip 1 |
46 |
0.457 |
|
635 |
|
|
TBL029 |
Tubulin, Beta |
28 |
0.457 |
|
636 |
|
c
|
CHR660 |
Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2a2a |
35 |
0.457 |
|
637 |
|
P
|
HMN036 |
Hemangiopericytoma, Malignant |
58 |
0.457 |
|
638 |
|
|
MYL005 |
Myelofibrosis |
71 |
0.457 |
|
639 |
|
|
OCL069 |
Ocular Motor Apraxia |
57 |
0.457 |
|
640 |
|
P
|
RTN024 |
Retinoblastoma |
73 |
0.457 |
|
641 |
|
|
OST159 |
Osteogenic Sarcoma |
66 |
0.457 |
|
642 |
|
P
|
STR020 |
Strabismus |
56 |
0.457 |
|
643 |
|
P
|
ATT013 |
Attention Deficit-Hyperactivity Disorder |
64 |
0.457 |
|
644 |
|
c
|
HYP595 |
Hypertension, Essential |
85 |
0.457 |
|
645 |
|
|
CRN238 |
Corneal Dystrophy, Epithelial Basement Membrane |
32 |
0.457 |
|
646 |
|
|
RNL114 |
Renal Cell Carcinoma, Nonpapillary |
80 |
0.457 |
|
647 |
|
|
OPT066 |
Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy |
55 |
0.457 |
|
648 |
|
|
LYM129 |
Lymphoma, Mucosa-Associated Lymphoid Type |
72 |
0.457 |
|
649 |
|
P
|
MDL005 |
Medulloblastoma |
75 |
0.457 |
|
650 |
|
P
|
GLM040 |
Glioma Susceptibility 1 |
71 |
0.457 |
|
651 |
|
|
MMM006 |
Mammographic Density |
39 |
0.457 |
|
652 |
|
|
CHL065 |
Cholangiocarcinoma |
58 |
0.457 |
|
653 |
|
|
DCT002 |
Ductal Carcinoma in Situ |
58 |
0.457 |
|
654 |
|
|
PNG002 |
Pain Agnosia |
51 |
0.457 |
|
655 |
|
P
|
PTN014 |
Patent Ductus Arteriosus 1 |
59 |
0.457 |
|
656 |
|
|
DSS032 |
Disease by Infectious Agent |
55 |
0.457 |
|
657 |
|
|
TNG009 |
Tongue Squamous Cell Carcinoma |
43 |
0.457 |
|
658 |
|
|
ARG004 |
Argyria |
26 |
0.457 |
|
659 |
|
c
|
ATS331 |
Autosomal Recessive Limb-Girdle Muscular Dystrophy |
40 |
0.457 |
|
660 |
|
|
TNG007 |
Tongue Carcinoma |
52 |
0.457 |
|
661 |
|
|
MDD018 |
Middle East Respiratory Syndrome |
44 |
0.457 |
|
662 |
|
|
PRT037 |
Pertussis |
65 |
0.457 |
|
663 |
|
P
|
LPS004 |
Lupus Erythematosus |
61 |
0.457 |
|
664 |
|
P
|
AMY004 |
Amyloidosis |
70 |
0.457 |
|
665 |
|
c
|
ACT075 |
Acute Myocardial Infarction |
56 |
0.457 |
|
666 |
|
P
|
FBR003 |
Fibrous Histiocytoma |
43 |
0.457 |
|
667 |
|
|
CLR011 |
Clear Cell Ependymoma |
31 |
0.457 |
|
668 |
|
P
|
EPD009 |
Epidermolysis Bullosa Dystrophica |
66 |
0.457 |
|
669 |
|
|
NTR005 |
Nutritional Deficiency Disease |
61 |
0.457 |
|
670 |
|
|
NRL001 |
Neurilemmoma of the Fifth Cranial Nerve |
26 |
0.457 |
|
671 |
|
P
|
RHB003 |
Rhabdomyosarcoma |
66 |
0.457 |
|
672 |
|
|
CRV002 |
Cervix Uteri Carcinoma in Situ |
47 |
0.457 |
|
673 |
|
|
IRD001 |
Iridocyclitis |
53 |
0.457 |
|
674 |
|
|
MCH006 |
Mechanical Strabismus |
40 |
0.457 |
|
675 |
|
P
|
HRP006 |
Herpes Simplex |
65 |
0.457 |
|
676 |
|
|
LRN003 |
Learning Disability |
49 |
0.457 |
|
677 |
|
|
ULC004 |
Ulcerative Colitis |
74 |
0.457 |
|
678 |
|
|
FTT001 |
Fatty Liver Disease |
62 |
0.457 |
|
679 |
|
P
|
HML002 |
Hemolytic Anemia |
62 |
0.457 |
|
680 |
|
|
CLL010 |
Cellular Ependymoma |
57 |
0.457 |
|
681 |
|
|
PST092 |
Posttransplant Acute Limbic Encephalitis |
28 |
0.457 |
|
682 |
|
|
LMN005 |
Lmna-Related Cardiocutaneous Progeria Syndrome |
28 |
0.457 |
|
683 |
|
P
|
ALP008 |
Alopecia |
54 |
0.457 |
|
684 |
|
c
|
PRG106 |
Progressive Muscular Dystrophy |
32 |
0.457 |
|
685 |
|
P
|
ALC033 |
Alcohol Use Disorder |
61 |
0.457 |
|
686 |
|
P
|
THR014 |
Thrombocytopenia |
66 |
0.457 |
|
687 |
|
P
|
CYS018 |
Cystitis |
59 |
0.457 |
|
688 |
|
|
SKN022 |
Skin Squamous Cell Carcinoma |
54 |
0.457 |
|
689 |
|
P
|
OLG002 |
Oligodendroglioma |
66 |
0.457 |
|
690 |
|
|
TRC003 |
Trichomoniasis |
53 |
0.457 |
|
691 |
|
|
VCC001 |
Vaccinia |
47 |
0.457 |
|
692 |
|
P
|
BPL003 |
Bipolar Disorder |
56 |
0.457 |
|
693 |
|
|
MNT002 |
Mental Depression |
57 |
0.457 |
|
694 |
|
P
|
PLM036 |
Pulmonary Fibrosis |
66 |
0.457 |
|
695 |
|
P
|
ART023 |
Arthropathy |
61 |
0.457 |
|
696 |
|
P
|
INF038 |
Influenza |
68 |
0.457 |
|
697 |
|
|
PST011 |
Pustulosis of Palm and Sole |
52 |
0.457 |
|
698 |
|
|
PPT002 |
Peptic Ulcer Perforation |
34 |
0.457 |
|
699 |
|
|
SPN051 |
Spondylitis |
51 |
0.457 |
|
700 |
|
|
EXT034 |
Extrinsic Allergic Alveolitis |
57 |
0.457 |
|
701 |
|
|
LNG099 |
Lung Disease |
62 |
0.457 |
|
702 |
|
P
|
BNG030 |
Benign Ependymoma |
51 |
0.457 |
|
703 |
|
|
MYL001 |
Myelitis |
50 |
0.457 |
|
704 |
|
P
|
PLY020 |
Polyradiculoneuropathy |
46 |
0.457 |
|
705 |
|
|
DFF016 |
Diffuse Astrocytoma |
45 |
0.457 |
|
706 |
|
P
|
PRD008 |
Periodontitis |
64 |
0.457 |
|
707 |
|
P
|
INT070 |
Intestinal Obstruction |
57 |
0.457 |
|
708 |
|
c
|
BDY019 |
Body Mass Index Quantitative Trait Locus 18 |
47 |
0.457 |
|
709 |
|
|
PGM003 |
Pigmentation Disease |
45 |
0.457 |
|
710 |
|
P
|
KRT007 |
Keratoconus |
50 |
0.457 |
|
711 |
|
|
NSP002 |
Nasopharyngitis |
45 |
0.457 |
|
712 |
|
P
|
GRF003 |
Graft-Versus-Host Disease |
71 |
0.457 |
|
713 |
|
c
|
MCR113 |
Microvascular Complications of Diabetes 3 |
52 |
0.457 |
|
714 |
|
c
|
MCR133 |
Microvascular Complications of Diabetes 4 |
41 |
0.457 |
|
715 |
|
|
GST106 |
Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets |
65 |
0.457 |
|
716 |
|
|
THY006 |
Thymus Lymphoma |
27 |
0.457 |
|
717 |
|
c
|
DLT002 |
Dilated Cardiomyopathy |
78 |
0.457 |
|
718 |
|
|
DNG003 |
Dengue Disease |
65 |
0.457 |
|
719 |
|
P
|
MLN007 |
Male Infertility |
56 |
0.457 |
|
720 |
|
P
|
ESP024 |
Esophagitis |
60 |
0.457 |
|
721 |
|
|
INF009 |
Inflammatory Spondylopathy |
30 |
0.457 |
|
722 |
|
|
DYS015 |
Dysentery |
50 |
0.457 |
|
723 |
|
|
TST004 |
Testicular Lymphoma |
39 |
0.457 |
|
724 |
|
|
RLP002 |
Relapsing-Remitting Multiple Sclerosis |
56 |
0.457 |
|
725 |
|
P
|
HMN010 |
Hemangioma |
62 |
0.457 |
|
726 |
|
|
BLR008 |
Bilirubin Metabolic Disorder |
57 |
0.457 |
|
727 |
|
|
RTN020 |
Retinal Vascular Disease |
46 |
0.457 |
|
728 |
|
P
|
HYP086 |
Hypothyroidism |
69 |
0.457 |
|
729 |
|
P
|
ADN016 |
Adenocarcinoma |
63 |
0.457 |
|
730 |
|
|
MLG169 |
Malignant Astrocytoma |
57 |
0.457 |
|
731 |
|
|
URT001 |
Urethritis |
53 |
0.457 |
|
732 |
|
|
BCT004 |
Bacteriuria |
47 |
0.457 |
|
733 |
|
|
BRC012 |
Brucellosis |
66 |
0.457 |
|
734 |
|
P
|
MYG005 |
Myoglobinuria |
40 |
0.457 |
|
735 |
|
|
CYT005 |
Cytomegalovirus Retinitis |
50 |
0.457 |
|
736 |
|
|
MST005 |
Mastitis |
53 |
0.457 |
|
737 |
|
|
HMP005 |
Hemiplegia |
54 |
0.457 |
|
738 |
|
P
|
RSP003 |
Respiratory Failure |
74 |
0.457 |
|
739 |
|
|
RBS001 |
Rabies |
58 |
0.457 |
|
740 |
|
P
|
PYL005 |
Pyelonephritis |
57 |
0.457 |
|
741 |
|
|
PRT038 |
Protein-Energy Malnutrition |
53 |
0.457 |
|
742 |
|
|
RCT015 |
Reactive Arthritis |
61 |
0.457 |
|
743 |
|
c
|
INF023 |
Inflammatory Breast Carcinoma |
49 |
0.457 |
|
744 |
|
|
INT079 |
Intrahepatic Cholangiocarcinoma |
51 |
0.457 |
|
745 |
|
c
|
ESS001 |
Essential Tremor |
57 |
0.457 |
|
746 |
|
|
CHR070 |
Chronic Inflammatory Demyelinating Polyradiculoneuropathy |
57 |
0.457 |
|
747 |
|
|
HMN014 |
Human Immunodeficiency Virus Infectious Disease |
54 |
0.457 |
|
748 |
|
P
|
INT068 |
Intestinal Disease |
53 |
0.457 |
|
749 |
|
|
OVR109 |
Ovarian Germ Cell Teratoma |
32 |
0.457 |
|
750 |
|
P
|
PNM007 |
Pneumonia |
67 |
0.457 |
|
751 |
|
|
CCN002 |
Cocaine Abuse |
49 |
0.457 |
|
752 |
|
P
|
TRT010 |
Teratoma |
51 |
0.457 |
|
753 |
|
|
PLM029 |
Palmoplantar Keratosis |
48 |
0.457 |
|
754 |
|
|
INT066 |
Interstitial Lung Disease |
60 |
0.457 |
|
755 |
|
P
|
LRY044 |
Larynx Cancer |
54 |
0.457 |
|
756 |
|
P
|
KDN017 |
Kidney Cancer |
61 |
0.457 |
|
757 |
|
P
|
TCD001 |
Tic Disorder |
49 |
0.457 |
|
758 |
|
|
BRS051 |
Breast Disease |
58 |
0.457 |
|
759 |
|
P
|
JNC001 |
Junctional Epidermolysis Bullosa |
53 |
0.457 |
|
760 |
|
|
DMY004 |
Demyelinating Disease |
50 |
0.457 |
|
761 |
|
|
PLR005 |
Pleuropneumonia |
33 |
0.457 |
|
762 |
|
P
|
EHL001 |
Ehlers-Danlos Syndrome |
58 |
0.457 |
|
763 |
|
|
PLS007 |
Plasmodium Falciparum Malaria |
52 |
0.457 |
|
764 |
|
|
AZS001 |
Azoospermia |
45 |
0.457 |
|
765 |
|
|
ENT004 |
Enthesopathy |
51 |
0.457 |
|
766 |
|
|
HYP014 |
Hyperuricemia |
51 |
0.457 |
|
767 |
|
|
RTN021 |
Retinal Vascular Occlusion |
45 |
0.457 |
|
768 |
|
|
SQM006 |
Squamous Cell Carcinoma |
60 |
0.457 |
|
769 |
|
|
NRN004 |
Neuroendocrine Tumor |
59 |
0.457 |
|
770 |
|
P
|
RTN022 |
Retinal Vein Occlusion |
54 |
0.457 |
|
771 |
|
|
PLM033 |
Pulmonary Embolism |
58 |
0.457 |
|
772 |
|
P
|
INS002 |
in Situ Carcinoma |
53 |
0.457 |
|
773 |
|
|
HYP706 |
Hypermobile Ehlers-Danlos Syndrome |
55 |
0.457 |
|
774 |
|
P
|
MYC008 |
Myocarditis |
59 |
0.457 |
|
775 |
|
|
HRP004 |
Herpes Zoster |
61 |
0.457 |
|
776 |
|
|
PTH003 |
Pathologic Nystagmus |
52 |
0.457 |
|
777 |
|
|
SFT003 |
Soft Tissue Sarcoma |
57 |
0.457 |
|
778 |
|
|
SPL018 |
Splenomegaly |
49 |
0.457 |
|
779 |
|
|
48X005 |
48,xyyy |
39 |
0.457 |
|
780 |
|
|
PRN039 |
Paraneoplastic Syndromes |
37 |
0.457 |
|
781 |
|
|
CND006 |
Candida Glabrata |
30 |
0.457 |
|
782 |
|
|
CYT002 |
Cytokine Deficiency |
43 |
0.457 |
|
783 |
|
|
CRV045 |
Cervical Intraepithelial Neoplasia |
39 |
0.457 |
|
784 |
|
|
HMP009 |
Haemophilus Influenzae |
41 |
0.457 |
|
785 |
|
|
MYC019 |
Mycobacterium Marinum |
29 |
0.457 |
|
786 |
|
|
CHR176 |
Chromophil Renal Cell Carcinoma |
23 |
0.457 |
|
787 |
|
c
|
LMB030 |
Limb-Girdle Muscular Dystrophy Type 1c |
27 |
0.457 |
|
788 |
|
|
LYM051 |
Lymphomatoid Granulomatosis |
45 |
0.457 |
|
789 |
|
|
MYC015 |
Mycobacterium Fortuitum |
28 |
0.457 |
|