# |
|
Family |
MCID |
Name |
MIFTS |
Score |
1 |
|
|
HYP781 |
Hypoascorbemia |
51 |
4.731 |
|
2 |
|
|
MTH054 |
Methylmalonic Aciduria and Homocystinuria, Cblc Type |
54 |
3.602 |
|
3 |
|
|
RCK004 |
Rickets |
68 |
0.962 |
|
4 |
|
c
|
HPT001 |
Hepatitis C |
62 |
0.802 |
|
5 |
|
c
|
HPT073 |
Hepatitis C Virus |
72 |
0.742 |
|
6 |
|
P
|
HPT021 |
Hepatitis |
67 |
0.470 |
|
7 |
|
|
KRT002 |
Keratomalacia |
47 |
0.446 |
|
8 |
|
|
HYP276 |
Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant |
54 |
0.431 |
|
9 |
|
P
|
LVR013 |
Liver Disease |
68 |
0.406 |
|
10 |
|
|
VTM002 |
Vitamin B12 Deficiency |
48 |
0.368 |
|
11 |
|
P
|
KDN018 |
Kidney Disease |
72 |
0.362 |
|
12 |
|
|
LVR012 |
Liver Cirrhosis |
62 |
0.356 |
|
13 |
|
P
|
HYP069 |
Hyperparathyroidism |
63 |
0.349 |
|
14 |
|
c
|
CHR684 |
Chronic Kidney Disease |
70 |
0.328 |
|
15 |
|
P
|
BRS047 |
Breast Cancer |
97 |
0.323 |
|
16 |
|
P
|
OST002 |
Osteoporosis |
74 |
0.320 |
|
17 |
|
P
|
CLR023 |
Colorectal Cancer |
99 |
0.308 |
|
18 |
|
P
|
BNM029 |
Bone Mineral Density Quantitative Trait Locus 15 |
48 |
0.303 |
|
19 |
|
c
|
BNM022 |
Bone Mineral Density Quantitative Trait Locus 8 |
42 |
0.302 |
|
20 |
|
|
ATM095 |
Autoimmune Disease |
62 |
0.301 |
|
21 |
|
|
VTM033 |
Vitamin K Deficiency Bleeding |
48 |
0.281 |
|
22 |
|
|
DFC004 |
Deficiency Anemia |
70 |
0.277 |
|
23 |
|
P
|
HPT023 |
Hepatocellular Carcinoma |
100 |
0.272 |
|
24 |
|
c
|
SCN007 |
Secondary Hyperparathyroidism |
51 |
0.270 |
|
25 |
|
|
BNR002 |
Bone Resorption Disease |
48 |
0.264 |
|
26 |
|
|
ANM044 |
Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities |
67 |
0.262 |
|
27 |
|
P
|
RTN008 |
Retinitis Pigmentosa |
79 |
0.253 |
|
28 |
|
c
|
HPT016 |
Hepatitis B |
59 |
0.242 |
|
29 |
|
c
|
PRC016 |
Pre-Eclampsia |
63 |
0.240 |
|
30 |
|
P
|
PRT133 |
Proteasome-Associated Autoinflammatory Syndrome 1 |
81 |
0.240 |
|
31 |
|
|
OST011 |
Osteomalacia |
52 |
0.239 |
|
32 |
|
P
|
BND020 |
Bone Disease |
59 |
0.237 |
|
33 |
|
|
48X005 |
48,xyyy |
39 |
0.235 |
|
34 |
|
c
|
VRL010 |
Viral Hepatitis |
52 |
0.234 |
|
35 |
|
|
FTT001 |
Fatty Liver Disease |
61 |
0.232 |
|
36 |
|
|
END086 |
End Stage Renal Disease |
51 |
0.232 |
|
37 |
|
P
|
PRS040 |
Prostate Cancer |
97 |
0.231 |
|
38 |
|
P
|
CRN300 |
Coronary Heart Disease 1 |
63 |
0.231 |
|
39 |
|
|
ATH013 |
Atherosclerosis Susceptibility |
65 |
0.230 |
|
40 |
|
c
|
HYP836 |
Hypercholesterolemia, Familial, 1 |
73 |
0.229 |
|
41 |
|
c
|
HPT003 |
Hepatitis a |
62 |
0.227 |
|
42 |
|
P
|
VSC007 |
Vascular Disease |
63 |
0.225 |
|
43 |
|
P
|
DBT009 |
Diabetes Mellitus |
64 |
0.224 |
|
44 |
|
|
RPD005 |
Rapidly Involuting Congenital Hemangioma |
38 |
0.223 |
|
45 |
|
|
IRN002 |
Iron Metabolism Disease |
57 |
0.219 |
|
46 |
|
P
|
DRR001 |
Diarrhea |
55 |
0.219 |
|
47 |
|
|
CYS001 |
Cystic Fibrosis |
81 |
0.217 |
|
48 |
|
P
|
NRP001 |
Neuropathy |
56 |
0.217 |
|
49 |
|
P
|
PSR002 |
Psoriasis |
62 |
0.217 |
|
50 |
|
|
HMC014 |
Homocysteinemia |
53 |
0.217 |
|
|
52 |
|
|
PST011 |
Pustulosis of Palm and Sole |
52 |
0.213 |
|
53 |
|
|
LPP008 |
Lipoprotein Quantitative Trait Locus |
62 |
0.210 |
|
54 |
|
P
|
INF037 |
Inflammatory Bowel Disease |
54 |
0.209 |
|
55 |
|
P
|
LKM002 |
Leukemia |
68 |
0.206 |
|
56 |
|
P
|
DBT026 |
Diabetes Mellitus, Noninsulin-Dependent |
90 |
0.204 |
|
57 |
|
P
|
HRT032 |
Heart Disease |
75 |
0.204 |
|
58 |
|
P
|
HYP724 |
Hyperlipoproteinemia, Type Iii |
73 |
0.203 |
|
59 |
|
|
NNL005 |
Non-Alcoholic Fatty Liver Disease |
61 |
0.203 |
|
60 |
|
|
LPD008 |
Lipid Metabolism Disorder |
62 |
0.203 |
|
61 |
|
|
ALP042 |
Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity |
66 |
0.202 |
|
62 |
|
c
|
BDY007 |
Body Mass Index Quantitative Trait Locus 1 |
42 |
0.201 |
|
63 |
|
|
YMN001 |
Yemenite Deaf-Blind Hypopigmentation Syndrome |
65 |
0.200 |
|
64 |
|
P
|
CRD246 |
Cardiovascular System Disease |
57 |
0.199 |
|
65 |
|
|
ART140 |
Arteries, Anomalies of |
52 |
0.198 |
|
66 |
|
P
|
ALZ034 |
Alzheimer Disease |
88 |
0.197 |
|
67 |
|
|
HLX001 |
Helix Syndrome |
47 |
0.197 |
|
68 |
|
|
CYT002 |
Cytokine Deficiency |
42 |
0.197 |
|
69 |
|
|
HMN044 |
Human Immunodeficiency Virus Type 1 |
71 |
0.197 |
|
70 |
|
c
|
THR092 |
Thrombophilia Due to Thrombin Defect |
73 |
0.197 |
|
71 |
|
|
ISC004 |
Ischemia |
58 |
0.194 |
|
72 |
|
P
|
ATR011 |
Atrial Fibrillation |
66 |
0.193 |
|
73 |
|
P
|
SKN015 |
Skin Carcinoma |
66 |
0.193 |
|
74 |
|
P
|
MYL006 |
Myeloid Leukemia |
60 |
0.193 |
|
75 |
|
|
NRL016 |
Neural Tube Defects |
82 |
0.191 |
|
76 |
|
P
|
MLT020 |
Multiple Sclerosis |
72 |
0.190 |
|
77 |
|
P
|
LNG032 |
Lung Cancer |
98 |
0.190 |
|
78 |
|
|
PRN011 |
Pernicious Anemia |
53 |
0.188 |
|
79 |
|
P
|
ADN016 |
Adenocarcinoma |
64 |
0.187 |
|
80 |
|
P
|
BDY004 |
Body Mass Index Quantitative Trait Locus 11 |
76 |
0.186 |
|
81 |
|
|
CRH001 |
Crohn's Disease |
74 |
0.186 |
|
82 |
|
|
PRT037 |
Pertussis |
65 |
0.185 |
|
83 |
|
|
DRM006 |
Dermatitis |
61 |
0.185 |
|
84 |
|
c
|
SYS001 |
Systemic Lupus Erythematosus |
86 |
0.185 |
|
85 |
|
|
ADN018 |
Adenoma |
59 |
0.184 |
|
86 |
|
c
|
ATR087 |
Atrial Standstill 1 |
75 |
0.183 |
|
87 |
|
c
|
LKM061 |
Leukemia, Acute Myeloid |
84 |
0.182 |
|
88 |
|
|
ATX038 |
Ataxia and Polyneuropathy, Adult-Onset |
45 |
0.182 |
|
89 |
|
|
STR067 |
Stroke, Ischemic |
81 |
0.181 |
|
90 |
|
P
|
BLD134 |
Bladder Cancer |
79 |
0.181 |
|
91 |
|
P
|
LYN001 |
Lynch Syndrome |
77 |
0.181 |
|
92 |
|
P
|
FTT008 |
Fatty Liver Disease, Nonalcoholic 1 |
60 |
0.180 |
|
93 |
|
P
|
MYP004 |
Myopathy |
70 |
0.179 |
|
94 |
|
c
|
NRF023 |
Neurofibromatosis, Type Ii |
80 |
0.179 |
|
95 |
|
P
|
LYM118 |
Lymphoma |
68 |
0.178 |
|
96 |
|
P
|
GST053 |
Gastric Cancer |
83 |
0.178 |
|
97 |
|
P
|
HRD086 |
Hereditary Hypophosphatemic Rickets |
40 |
0.178 |
|
98 |
|
|
IMM167 |
Immune Deficiency Disease |
78 |
0.177 |
|
99 |
|
P
|
OVR042 |
Ovarian Cancer |
88 |
0.176 |
|
100 |
|
P
|
PNC035 |
Pancreatic Cancer |
84 |
0.175 |
|
101 |
|
|
NTR005 |
Nutritional Deficiency Disease |
62 |
0.174 |
|
102 |
|
c
|
MCL042 |
Macular Degeneration, Age-Related, 1 |
85 |
0.174 |
|
103 |
|
P
|
PRD008 |
Periodontitis |
64 |
0.174 |
|
104 |
|
|
OST159 |
Osteogenic Sarcoma |
66 |
0.174 |
|
105 |
|
P
|
NRB001 |
Neuroblastoma |
72 |
0.174 |
|
106 |
|
P
|
PLY011 |
Polycystic Ovary Syndrome |
56 |
0.173 |
|
107 |
|
|
CNG034 |
Congestive Heart Failure |
69 |
0.173 |
|
108 |
|
|
TXC005 |
Toxic Shock Syndrome |
62 |
0.173 |
|
109 |
|
P
|
LPS004 |
Lupus Erythematosus |
61 |
0.173 |
|
110 |
|
P
|
THL005 |
Thalassemia |
60 |
0.173 |
|
111 |
|
P
|
PRP019 |
Peripheral Nervous System Disease |
58 |
0.172 |
|
112 |
|
|
HYP066 |
Hyperglycemia |
61 |
0.171 |
|
113 |
|
|
SKN016 |
Skin Disease |
63 |
0.171 |
|
114 |
|
|
CRB039 |
Cerebrovascular Disease |
67 |
0.171 |
|
115 |
|
|
MSL001 |
Measles |
62 |
0.170 |
|
116 |
|
|
INS024 |
Insulin-Like Growth Factor I |
79 |
0.170 |
|
117 |
|
P
|
MYC007 |
Myocardial Infarction |
70 |
0.170 |
|
118 |
|
|
GST033 |
Gestational Diabetes |
61 |
0.169 |
|
119 |
|
c
|
MCR120 |
Microvascular Complications of Diabetes 7 |
47 |
0.169 |
|
120 |
|
P
|
HYP086 |
Hypothyroidism |
69 |
0.169 |
|
121 |
|
|
PLM129 |
Pulmonary Disease, Chronic Obstructive |
73 |
0.167 |
|
122 |
|
P
|
ALP008 |
Alopecia |
54 |
0.167 |
|
123 |
|
P
|
THR014 |
Thrombocytopenia |
67 |
0.167 |
|
124 |
|
c
|
MCR113 |
Microvascular Complications of Diabetes 3 |
52 |
0.167 |
|
125 |
|
P
|
NTR004 |
Neutropenia |
63 |
0.166 |
|
126 |
|
|
PYR009 |
Pyridoxine Deficiency Anemia |
34 |
0.166 |
|
127 |
|
c
|
MCR130 |
Microvascular Complications of Diabetes 6 |
41 |
0.166 |
|
128 |
|
c
|
HYP595 |
Hypertension, Essential |
84 |
0.165 |
|
129 |
|
c
|
MCR133 |
Microvascular Complications of Diabetes 4 |
41 |
0.165 |
|
130 |
|
|
CHL068 |
Cholestasis |
61 |
0.165 |
|
131 |
|
P
|
ATX030 |
Ataxia-Telangiectasia |
82 |
0.165 |
|
132 |
|
|
LNG099 |
Lung Disease |
60 |
0.164 |
|
133 |
|
P
|
CTR002 |
Cataract |
60 |
0.164 |
|
134 |
|
|
OST012 |
Osteoarthritis |
78 |
0.163 |
|
135 |
|
P
|
GST044 |
Gastritis |
56 |
0.162 |
|
136 |
|
|
DPR016 |
Depression |
63 |
0.161 |
|
137 |
|
P
|
HYP061 |
Hypertrophic Cardiomyopathy |
70 |
0.161 |
|
138 |
|
P
|
RHM011 |
Rheumatoid Arthritis |
80 |
0.160 |
|
139 |
|
|
TTN003 |
Tetanus |
65 |
0.159 |
|
140 |
|
|
AST005 |
Asthma |
76 |
0.159 |
|
141 |
|
c
|
BDY020 |
Body Mass Index Quantitative Trait Locus 19 |
52 |
0.158 |
|
142 |
|
|
VSL002 |
Visual Epilepsy |
59 |
0.158 |
|
143 |
|
c
|
BDY010 |
Body Mass Index Quantitative Trait Locus 4 |
46 |
0.158 |
|
144 |
|
P
|
MLN008 |
Melanoma |
69 |
0.158 |
|
145 |
|
c
|
BDY021 |
Body Mass Index Quantitative Trait Locus 20 |
52 |
0.158 |
|
146 |
|
c
|
BDY005 |
Body Mass Index Quantitative Trait Locus 9 |
48 |
0.158 |
|
147 |
|
c
|
BDY019 |
Body Mass Index Quantitative Trait Locus 18 |
47 |
0.158 |
|
148 |
|
c
|
BDY015 |
Body Mass Index Quantitative Trait Locus 12 |
46 |
0.158 |
|
149 |
|
c
|
BDY017 |
Body Mass Index Quantitative Trait Locus 14 |
45 |
0.158 |
|
150 |
|
c
|
BDY011 |
Body Mass Index Quantitative Trait Locus 10 |
45 |
0.158 |
|
151 |
|
c
|
BDY006 |
Body Mass Index Quantitative Trait Locus 8 |
44 |
0.158 |
|
152 |
|
c
|
BDY012 |
Body Mass Index Quantitative Trait Locus 7 |
44 |
0.158 |
|
153 |
|
|
NNL006 |
Non-Alcoholic Steatohepatitis |
54 |
0.157 |
|
154 |
|
|
PLM001 |
Pulmonary Tuberculosis |
69 |
0.156 |
|
155 |
|
|
ALL026 |
Allergic Hypersensitivity Disease |
62 |
0.156 |
|
156 |
|
P
|
DRM053 |
Dermatitis, Atopic |
66 |
0.156 |
|
157 |
|
P
|
ECL001 |
Eclampsia |
50 |
0.155 |
|
158 |
|
|
THR024 |
Thrombosis |
57 |
0.155 |
|
159 |
|
|
ULC004 |
Ulcerative Colitis |
73 |
0.155 |
|
160 |
|
c
|
PRM005 |
Primary Hyperparathyroidism |
58 |
0.153 |
|
161 |
|
|
AGN016 |
Aging |
56 |
0.152 |
|
162 |
|
|
PRP030 |
Purpura |
54 |
0.152 |
|
163 |
|
|
47X002 |
47,xyy |
49 |
0.151 |
|
164 |
|
|
MLT161 |
Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly |
57 |
0.151 |
|
165 |
|
|
LGH007 |
Leigh Syndrome |
70 |
0.151 |
|
166 |
|
|
RNL114 |
Renal Cell Carcinoma, Nonpapillary |
78 |
0.149 |
|
167 |
|
P
|
BCL017 |
B-Cell Lymphoma |
58 |
0.149 |
|
168 |
|
|
THY029 |
Thyroid Carcinoma |
59 |
0.149 |
|
169 |
|
|
ATX019 |
Ataxia with Vitamin E Deficiency |
42 |
0.148 |
|
170 |
|
|
ALC007 |
Alcohol Dependence |
66 |
0.148 |
|
171 |
|
|
VTM027 |
Vitamin D-Dependent Rickets, Type 2a |
56 |
0.147 |
|
172 |
|
P
|
GLM007 |
Glomerulonephritis |
57 |
0.147 |
|
173 |
|
P
|
PNM007 |
Pneumonia |
68 |
0.146 |
|
174 |
|
P
|
HML002 |
Hemolytic Anemia |
63 |
0.146 |
|
175 |
|
|
MNT002 |
Mental Depression |
58 |
0.145 |
|
176 |
|
P
|
NGH001 |
Night Blindness |
48 |
0.143 |
|
177 |
|
P
|
GLM045 |
Glioma |
63 |
0.143 |
|
178 |
|
|
SQM006 |
Squamous Cell Carcinoma |
60 |
0.143 |
|
179 |
|
P
|
VSC011 |
Vasculitis |
62 |
0.143 |
|
180 |
|
|
PRT011 |
Protein C Deficiency |
44 |
0.142 |
|
181 |
|
|
MGL001 |
Megaloblastic Anemia |
51 |
0.141 |
|
182 |
|
|
CHL079 |
Children's Interstitial Lung Disease |
26 |
0.141 |
|
183 |
|
|
GLL048 |
Glial Tumor |
45 |
0.141 |
|
184 |
|
|
HMS001 |
Hemosiderosis |
54 |
0.140 |
|
185 |
|
|
TRD008 |
Triiodothyronine Receptor Auxiliary Protein |
34 |
0.140 |
|
186 |
|
|
GLC003 |
Glucose Intolerance |
54 |
0.139 |
|
187 |
|
|
CLT003 |
Colitis |
62 |
0.139 |
|
188 |
|
|
VRL011 |
Viral Infectious Disease |
61 |
0.139 |
|
189 |
|
P
|
MSC005 |
Muscular Dystrophy |
66 |
0.139 |
|
190 |
|
|
CMM005 |
Common Cold |
57 |
0.139 |
|
191 |
|
|
ACQ007 |
Acquired Immunodeficiency Syndrome |
60 |
0.139 |
|
192 |
|
P
|
ART062 |
Arthrogryposis, Renal Dysfunction, and Cholestasis 1 |
65 |
0.138 |
|
193 |
|
|
ESP021 |
Esophageal Cancer |
90 |
0.138 |
|
194 |
|
P
|
CNR004 |
Cone-Rod Dystrophy 2 |
73 |
0.138 |
|
195 |
|
P
|
SZR006 |
Seizure Disorder |
56 |
0.136 |
|
196 |
|
|
HMN014 |
Human Immunodeficiency Virus Infectious Disease |
55 |
0.136 |
|
197 |
|
c
|
ACT075 |
Acute Myocardial Infarction |
57 |
0.136 |
|
198 |
|
|
BCT022 |
Bacterial Infectious Disease |
56 |
0.136 |
|
199 |
|
|
HYP017 |
Hypophosphatemia |
50 |
0.136 |
|
200 |
|
|
CRY004 |
Cryoglobulinemia |
48 |
0.135 |
|
201 |
|
P
|
ART022 |
Arthritis |
69 |
0.135 |
|
202 |
|
P
|
THY032 |
Thyroiditis |
52 |
0.135 |
|
203 |
|
P
|
ENC018 |
Encephalopathy |
61 |
0.135 |
|
204 |
|
P
|
INF032 |
Infertility |
57 |
0.135 |
|
205 |
|
c
|
RHB024 |
Rhabdomyosarcoma 2 |
67 |
0.134 |
|
206 |
|
P
|
RRH023 |
Rare Hereditary Hemochromatosis |
41 |
0.134 |
|
207 |
|
P
|
ATS364 |
Autism |
70 |
0.133 |
|
208 |
|
P
|
MCR115 |
Microvascular Complications of Diabetes 5 |
66 |
0.133 |
|
209 |
|
P
|
TRN020 |
Turner Syndrome |
67 |
0.132 |
|
210 |
|
P
|
HYP076 |
Hyperthyroidism |
55 |
0.132 |
|
211 |
|
|
KRT001 |
Keratoconjunctivitis Sicca |
49 |
0.132 |
|
212 |
|
|
PRP027 |
Peripheral Vascular Disease |
71 |
0.132 |
|
213 |
|
|
XRP001 |
Xerophthalmia |
41 |
0.132 |
|
214 |
|
c
|
ATS007 |
Autism Spectrum Disorder |
67 |
0.132 |
|
215 |
|
|
INT323 |
Intraocular Pressure Quantitative Trait Locus |
62 |
0.131 |
|
216 |
|
P
|
SRC025 |
Sarcoidosis 1 |
70 |
0.131 |
|
217 |
|
c
|
MTR018 |
Maturity-Onset Diabetes of the Young, Type 1 |
62 |
0.130 |
|
218 |
|
P
|
RTN024 |
Retinoblastoma |
73 |
0.130 |
|
219 |
|
|
DWN001 |
Down Syndrome |
70 |
0.130 |
|
220 |
|
|
MYL009 |
Myelodysplastic Syndrome |
70 |
0.130 |
|
221 |
|
P
|
ART021 |
Arteriosclerosis |
54 |
0.130 |
|
222 |
|
P
|
ALC033 |
Alcohol Use Disorder |
58 |
0.130 |
|
223 |
|
c
|
SML038 |
Small Cell Cancer of the Lung |
65 |
0.129 |
|
224 |
|
c
|
DLT002 |
Dilated Cardiomyopathy |
79 |
0.129 |
|
225 |
|
P
|
EXN002 |
Exanthem |
57 |
0.128 |
|
226 |
|
c
|
PRM038 |
Primary Agammaglobulinemia |
44 |
0.128 |
|
227 |
|
|
NPH009 |
Nephrolithiasis |
55 |
0.128 |
|
228 |
|
c
|
AMY091 |
Amyotrophic Lateral Sclerosis 1 |
89 |
0.128 |
|
229 |
|
c
|
NRD033 |
Neurodegeneration with Brain Iron Accumulation 2a |
69 |
0.127 |
|
230 |
|
c
|
NRF024 |
Neurofibromatosis, Type I |
77 |
0.127 |
|
231 |
|
P
|
MYC084 |
Mycobacterium Tuberculosis 1 |
68 |
0.127 |
|
232 |
|
c
|
MLN055 |
Melanoma, Cutaneous Malignant 10 |
52 |
0.127 |
|
233 |
|
P
|
LKM062 |
Leukemia, Acute Lymphoblastic |
69 |
0.127 |
|
234 |
|
|
ATS010 |
Autosomal Recessive Disease |
48 |
0.127 |
|
235 |
|
c
|
FML346 |
Familial Adenomatous Polyposis 1 |
66 |
0.127 |
|
236 |
|
|
GST019 |
Gastrointestinal Stromal Tumor |
78 |
0.126 |
|
237 |
|
P
|
PHC003 |
Pheochromocytoma |
71 |
0.126 |
|
238 |
|
|
HYP266 |
Hypoxia |
57 |
0.126 |
|
239 |
|
|
GLB015 |
Glioblastoma Multiforme |
75 |
0.126 |
|
240 |
|
c
|
DBT099 |
Diabetes Mellitus, Type I |
65 |
0.126 |
|
241 |
|
c
|
FNC027 |
Fanconi Anemia, Complementation Group a |
81 |
0.126 |
|
242 |
|
|
STM007 |
Stomatitis |
50 |
0.125 |
|
243 |
|
c
|
BTT014 |
Beta-Thalassemia |
74 |
0.125 |
|
244 |
|
c
|
HYP260 |
Hypophosphatemic Rickets, Autosomal Dominant |
60 |
0.125 |
|
245 |
|
P
|
NPH012 |
Nephrotic Syndrome |
60 |
0.124 |
|
246 |
|
P
|
LCH002 |
Lichen Planus |
53 |
0.123 |
|
247 |
|
|
URM002 |
Uremia |
49 |
0.123 |
|
248 |
|
P
|
SCK005 |
Sickle Cell Disease |
50 |
0.122 |
|
249 |
|
P
|
HYP750 |
Hypertriglyceridemia, Familial |
62 |
0.122 |
|
250 |
|
P
|
CHR071 |
Charcot-Marie-Tooth Disease |
65 |
0.122 |
|
251 |
|
P
|
INF038 |
Influenza |
68 |
0.122 |
|
252 |
|
|
ANG054 |
Angina Pectoris |
66 |
0.122 |
|
253 |
|
P
|
RHN004 |
Rhinitis |
57 |
0.122 |
|
254 |
|
|
PLM033 |
Pulmonary Embolism |
59 |
0.121 |
|
255 |
|
P
|
CHR345 |
Chronic Pain |
44 |
0.121 |
|
256 |
|
|
LPT014 |
Leptin Deficiency or Dysfunction |
74 |
0.120 |
|
257 |
|
|
IRN001 |
Iron Deficiency Anemia |
59 |
0.120 |
|
258 |
|
|
LYM133 |
Lymphoma, Hodgkin, Classic |
69 |
0.120 |
|
259 |
|
|
MYL069 |
Myeloma, Multiple |
85 |
0.120 |
|
260 |
|
P
|
HYP024 |
Hypoparathyroidism |
56 |
0.120 |
|
261 |
|
|
DPH001 |
Diphtheria |
60 |
0.120 |
|
262 |
|
P
|
DMN002 |
Dementia |
66 |
0.119 |
|
263 |
|
P
|
PLY019 |
Polyneuropathy |
56 |
0.119 |
|
264 |
|
P
|
PRM011 |
Primary Ciliary Dyskinesia |
69 |
0.119 |
|
265 |
|
|
PPL061 |
Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome |
25 |
0.119 |
|
266 |
|
P
|
PRM006 |
Primary Biliary Cirrhosis |
62 |
0.119 |
|
267 |
|
|
DSR002 |
Disorders of Intracellular Cobalamin Metabolism |
31 |
0.118 |
|
268 |
|
|
CLR108 |
Colorectal Adenoma |
64 |
0.118 |
|
269 |
|
|
TQP001 |
Taqi Polymorphism |
32 |
0.118 |
|
270 |
|
c
|
ACT071 |
Acute Kidney Failure |
60 |
0.117 |
|
271 |
|
c
|
THR082 |
Thrombophilia Due to Activated Protein C Resistance |
61 |
0.117 |
|
272 |
|
P
|
LTR001 |
Lateral Sclerosis |
54 |
0.116 |
|
273 |
|
P
|
HYP726 |
Hypercalcemia, Infantile, 1 |
58 |
0.116 |
|
274 |
|
P
|
PRK057 |
Parkinson Disease, Late-Onset |
78 |
0.116 |
|
275 |
|
P
|
HMC002 |
Homocystinuria |
53 |
0.116 |
|
276 |
|
|
HLC007 |
Helicobacter Pylori Infection |
59 |
0.115 |
|
277 |
|
|
SVR004 |
Severe Combined Immunodeficiency |
73 |
0.115 |
|
278 |
|
P
|
MNN013 |
Meningitis |
66 |
0.115 |
|
279 |
|
c
|
TBR025 |
Tuberous Sclerosis 1 |
77 |
0.115 |
|
280 |
|
|
LYM143 |
Lymphoma, Non-Hodgkin, Familial |
72 |
0.115 |
|
281 |
|
|
PRT013 |
Portal Hypertension |
59 |
0.114 |
|
282 |
|
P
|
CLC063 |
Celiac Disease 1 |
66 |
0.114 |
|
283 |
|
|
MNN028 |
Mononeuropathy of the Median Nerve, Mild |
46 |
0.114 |
|
284 |
|
|
HYP025 |
Hyperphosphatemia |
48 |
0.114 |
|
285 |
|
P
|
THR015 |
Thrombophilia |
51 |
0.113 |
|
286 |
|
c
|
FML001 |
Familial Atrial Fibrillation |
65 |
0.113 |
|
287 |
|
|
FND002 |
Fundus Dystrophy |
55 |
0.113 |
|
288 |
|
|
INT007 |
Intermediate Coronary Syndrome |
55 |
0.113 |
|
289 |
|
|
SPN186 |
Spinal Cord Injury |
60 |
0.113 |
|
290 |
|
c
|
FML008 |
Familial Retinoblastoma |
53 |
0.113 |
|
291 |
|
|
HYP056 |
Hypoglycemia |
66 |
0.113 |
|
292 |
|
P
|
MJR001 |
Major Depressive Disorder |
68 |
0.113 |
|
293 |
|
|
LSH001 |
Leishmaniasis |
63 |
0.113 |
|
294 |
|
P
|
KLZ004 |
Kala-Azar 1 |
41 |
0.113 |
|
295 |
|
c
|
MGR028 |
Migraine with or Without Aura 1 |
67 |
0.112 |
|
296 |
|
P
|
RSP003 |
Respiratory Failure |
74 |
0.112 |
|
297 |
|
c
|
EXD008 |
Exudative Vitreoretinopathy 1 |
71 |
0.112 |
|
298 |
|
P
|
MTH008 |
Methylmalonic Acidemia |
50 |
0.111 |
|
299 |
|
|
HYP060 |
Hyperinsulinism |
54 |
0.111 |
|
300 |
|
P
|
END044 |
Endometriosis |
63 |
0.111 |
|
301 |
|
c
|
BNM018 |
Bone Mineral Density Quantitative Trait Locus 3 |
33 |
0.111 |
|
302 |
|
|
VTM028 |
Vitamin E, Familial Isolated Deficiency of |
52 |
0.111 |
|
303 |
|
|
XRD010 |
Xeroderma Pigmentosum, Variant Type |
73 |
0.111 |
|
304 |
|
c
|
PCH010 |
Pachyonychia Congenita 3 |
44 |
0.111 |
|
305 |
|
|
NPH091 |
Nephrolithiasis, Calcium Oxalate |
60 |
0.110 |
|
306 |
|
P
|
CRY007 |
Cryoglobulinemia, Familial Mixed |
50 |
0.109 |
|
307 |
|
P
|
GRV001 |
Graves' Disease |
55 |
0.109 |
|
308 |
|
c
|
ATM011 |
Autoimmune Hepatitis |
63 |
0.109 |
|
309 |
|
P
|
ART106 |
Arterial Calcification, Generalized, of Infancy, 1 |
46 |
0.109 |
|
310 |
|
|
ALL014 |
Allergic Encephalomyelitis |
38 |
0.109 |
|
311 |
|
P
|
HMP007 |
Hemophilia |
51 |
0.109 |
|
312 |
|
P
|
ABD014 |
Abdominal Obesity-Metabolic Syndrome 1 |
64 |
0.108 |
|
313 |
|
c
|
GLC092 |
Glaucoma, Primary Open Angle |
62 |
0.108 |
|
314 |
|
|
CHL014 |
Cholera |
59 |
0.108 |
|
315 |
|
P
|
HRP006 |
Herpes Simplex |
65 |
0.108 |
|
316 |
|
c
|
PLM164 |
Pulmonary Hypertension, Primary, 1 |
75 |
0.108 |
|
317 |
|
|
KRT009 |
Keratosis |
51 |
0.108 |
|
318 |
|
P
|
EPL164 |
Epilepsy |
71 |
0.108 |
|
319 |
|
P
|
HYP802 |
Hypocalcemia, Autosomal Dominant 1 |
69 |
0.107 |
|
320 |
|
c
|
PRD040 |
Periodontitis, Chronic |
53 |
0.107 |
|
321 |
|
P
|
RCT021 |
Rectum Cancer |
52 |
0.107 |
|
322 |
|
|
CRV035 |
Cervical Cancer |
76 |
0.107 |
|
323 |
|
c
|
INH030 |
Inherited Retinal Disorder |
51 |
0.107 |
|
324 |
|
|
ALL003 |
Allergic Rhinitis |
67 |
0.107 |
|
325 |
|
|
ADL002 |
Adult Syndrome |
70 |
0.107 |
|
326 |
|
|
EYD002 |
Eye Disease |
58 |
0.106 |
|
327 |
|
|
MLR004 |
Malaria |
81 |
0.106 |
|
328 |
|
c
|
NMN015 |
Niemann-Pick Disease, Type C1 |
68 |
0.106 |
|
329 |
|
P
|
GRF003 |
Graft-Versus-Host Disease |
72 |
0.106 |
|
330 |
|
c
|
ACT073 |
Acute Leukemia |
58 |
0.106 |
|
331 |
|
P
|
LNG064 |
Lung Cancer Susceptibility 3 |
78 |
0.105 |
|
332 |
|
|
CVD001 |
Covid-19 |
44 |
0.105 |
|
333 |
|
c
|
DWL002 |
Dowling-Degos Disease 1 |
58 |
0.105 |
|
334 |
|
|
RTN023 |
Retinitis |
46 |
0.105 |
|
335 |
|
|
NRR001 |
Neuroretinitis |
42 |
0.105 |
|
336 |
|
P
|
ATR005 |
Atrophic Gastritis |
50 |
0.105 |
|
337 |
|
c
|
ACT027 |
Acute Pancreatitis |
60 |
0.104 |
|
338 |
|
|
GST106 |
Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets |
64 |
0.104 |
|
339 |
|
P
|
HYP058 |
Hypervitaminosis a |
48 |
0.104 |
|
340 |
|
P
|
NRP063 |
Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive |
57 |
0.104 |
|
341 |
|
|
SPL018 |
Splenomegaly |
48 |
0.104 |
|
342 |
|
|
RNL011 |
Renal Osteodystrophy |
50 |
0.104 |
|
343 |
|
|
ABT001 |
Abetalipoproteinemia |
69 |
0.104 |
|
344 |
|
|
ANX010 |
Anxiety |
73 |
0.104 |
|
345 |
|
|
DBT010 |
Diabetic Neuropathy |
54 |
0.103 |
|
346 |
|
|
PLM031 |
Poliomyelitis |
64 |
0.103 |
|
347 |
|
|
NSS002 |
Neisseria Meningitidis Infection |
47 |
0.103 |
|
348 |
|
c
|
BRN108 |
Branchiootic Syndrome 1 |
62 |
0.103 |
|
349 |
|
P
|
OPN001 |
Open-Angle Glaucoma |
49 |
0.103 |
|
350 |
|
c
|
SPN225 |
Spondyloarthropathy 1 |
73 |
0.102 |
|
351 |
|
|
LYM019 |
Lymphosarcoma |
46 |
0.102 |
|
352 |
|
P
|
3MT016 |
3-Methylglutaconic Aciduria, Type Iii |
67 |
0.101 |
|
353 |
|
|
CNS004 |
Constipation |
58 |
0.101 |
|
354 |
|
|
KRT019 |
Keratitis, Hereditary |
65 |
0.101 |
|
355 |
|
|
MTC097 |
Mitochondrial Complex Iv Deficiency |
59 |
0.101 |
|
356 |
|
|
MRF001 |
Marfan Syndrome |
77 |
0.101 |
|
357 |
|
|
ATX031 |
Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus |
58 |
0.101 |
|
358 |
|
P
|
SLP006 |
Sleep Apnea |
69 |
0.101 |
|
359 |
|
c
|
INF071 |
Inflammatory Bowel Disease 1 |
67 |
0.101 |
|
360 |
|
P
|
NMN002 |
Niemann-Pick Disease |
59 |
0.100 |
|
361 |
|
|
PLC008 |
Placenta Disease |
50 |
0.100 |
|
362 |
|
|
SCK003 |
Sickle Cell Anemia |
74 |
0.100 |
|
363 |
|
P
|
SYP003 |
Syphilis |
58 |
0.100 |
|
364 |
|
P
|
PRP029 |
Porphyria |
62 |
0.100 |
|
365 |
|
P
|
SCH015 |
Schizophrenia |
74 |
0.100 |
|
366 |
|
P
|
BRB001 |
Beriberi |
46 |
0.100 |
|
367 |
|
P
|
MLN007 |
Male Infertility |
55 |
0.100 |
|
368 |
|
|
PPT005 |
Peptic Ulcer Disease |
59 |
0.099 |
|
369 |
|
|
PNC001 |
Pancytopenia |
54 |
0.099 |
|
370 |
|
P
|
PLM036 |
Pulmonary Fibrosis |
65 |
0.099 |
|
371 |
|
P
|
HDC001 |
Headache |
57 |
0.099 |
|
372 |
|
|
RLP002 |
Relapsing-Remitting Multiple Sclerosis |
56 |
0.099 |
|
373 |
|
|
RTN135 |
Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome |
40 |
0.098 |
|
374 |
|
|
PNC129 |
Pancreatic Adenocarcinoma |
68 |
0.098 |
|
375 |
|
|
MCS002 |
Mucositis |
56 |
0.098 |
|
376 |
|
|
DSS009 |
Disseminated Intravascular Coagulation |
57 |
0.098 |
|
377 |
|
P
|
OVR082 |
Overgrowth Syndrome |
50 |
0.098 |
|
378 |
|
|
BRN056 |
Bronchopulmonary Dysplasia |
57 |
0.098 |
|
379 |
|
|
VTM009 |
Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 1 |
31 |
0.098 |
|
380 |
|
|
PHN003 |
Phenylketonuria |
75 |
0.097 |
|
381 |
|
|
DFF005 |
Diffuse Large B-Cell Lymphoma |
55 |
0.097 |
|
382 |
|
P
|
HMR003 |
Hemorrhagic Disease |
53 |
0.097 |
|
383 |
|
c
|
FML021 |
Familial Hypercholesterolemia |
66 |
0.097 |
|
384 |
|
c
|
SVR001 |
Severe Acute Respiratory Syndrome |
62 |
0.097 |
|
385 |
|
|
HRW001 |
Hair Whorl |
36 |
0.097 |
|
386 |
|
c
|
CNG411 |
Congenital Disorder of Glycosylation, Type in |
68 |
0.097 |
|
387 |
|
P
|
PNC044 |
Pancreatitis |
61 |
0.097 |
|
388 |
|
P
|
CRD119 |
Cardiac Arrest |
67 |
0.096 |
|
389 |
|
|
BRK010 |
Burkitt Lymphoma |
67 |
0.096 |
|
390 |
|
|
TRN015 |
Transient Cerebral Ischemia |
63 |
0.096 |
|
391 |
|
|
HYP081 |
Hypolipoproteinemia |
51 |
0.096 |
|
392 |
|
|
SKN019 |
Skin Melanoma |
68 |
0.096 |
|
393 |
|
|
MDD011 |
Mood Disorder |
62 |
0.096 |
|
394 |
|
|
FDL002 |
Food Allergy |
51 |
0.096 |
|
395 |
|
P
|
VTL004 |
Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 |
60 |
0.096 |
|
396 |
|
P
|
IMR002 |
Imerslund-Grasbeck Syndrome 1 |
43 |
0.096 |
|
397 |
|
|
PRT036 |
Peritonitis |
64 |
0.096 |
|
398 |
|
|
DNT012 |
Dental Caries |
53 |
0.096 |
|
399 |
|
c
|
VTL009 |
Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 |
42 |
0.096 |
|
400 |
|
P
|
TRM003 |
Tremor |
54 |
0.096 |
|
401 |
|
|
BSL036 |
Basal Cell Nevus Syndrome |
73 |
0.095 |
|
402 |
|
P
|
TBR001 |
Tuberous Sclerosis |
70 |
0.095 |
|
403 |
|
|
ENT011 |
Enterocolitis |
51 |
0.095 |
|
404 |
|
|
BRN071 |
Brain Injury |
49 |
0.095 |
|
405 |
|
|
GST050 |
Gastrointestinal System Disease |
56 |
0.094 |
|
406 |
|
|
ORL011 |
Oral Cancer |
60 |
0.094 |
|
407 |
|
P
|
HYP098 |
Hypereosinophilic Syndrome |
67 |
0.094 |
|
408 |
|
P
|
URT039 |
Urticaria |
58 |
0.094 |
|
409 |
|
|
CHL123 |
Chlamydia |
59 |
0.094 |
|
410 |
|
|
URL001 |
Urolithiasis |
45 |
0.094 |
|
411 |
|
|
FBR047 |
Fibromyalgia |
58 |
0.094 |
|
412 |
|
c
|
LKM063 |
Leukemia, Chronic Myeloid |
72 |
0.094 |
|
413 |
|
c
|
HMC039 |
Hemochromatosis, Type 1 |
74 |
0.094 |
|
414 |
|
P
|
HYP609 |
Hypophosphatemic Rickets, X-Linked Dominant |
64 |
0.094 |
|
415 |
|
|
PPL052 |
Papillomatosis, Confluent and Reticulated |
33 |
0.094 |
|
416 |
|
|
GTR002 |
Goiter |
53 |
0.094 |
|
417 |
|
P
|
INS002 |
in Situ Carcinoma |
53 |
0.094 |
|
418 |
|
|
ACT119 |
Acute Promyelocytic Leukemia |
63 |
0.093 |
|
419 |
|
|
OCL069 |
Ocular Motor Apraxia |
51 |
0.093 |
|
420 |
|
|
MSC157 |
Muscular Dystrophy, Duchenne Type |
72 |
0.093 |
|
421 |
|
|
IGR001 |
Ige Responsiveness, Atopic |
59 |
0.093 |
|
422 |
|
|
GST045 |
Gastroenteritis |
59 |
0.093 |
|
423 |
|
|
IRR002 |
Irritable Bowel Syndrome |
65 |
0.093 |
|
424 |
|
|
NPH003 |
Nephrocalcinosis |
51 |
0.092 |
|
425 |
|
|
PRP080 |
Peripheral Artery Disease |
53 |
0.092 |
|
426 |
|
|
SPN051 |
Spondylitis |
51 |
0.092 |
|
427 |
|
|
BRN024 |
Bronchitis |
68 |
0.092 |
|
428 |
|
|
BLR008 |
Bilirubin Metabolic Disorder |
57 |
0.092 |
|
429 |
|
|
INF009 |
Inflammatory Spondylopathy |
31 |
0.092 |
|
430 |
|
P
|
HYP265 |
Hypotonia |
43 |
0.092 |
|
431 |
|
P
|
RTN016 |
Retinal Degeneration |
53 |
0.091 |
|
432 |
|
P
|
SBS003 |
Substance Abuse |
55 |
0.091 |
|
433 |
|
c
|
HYP798 |
Hypophosphatemic Rickets, X-Linked Recessive |
60 |
0.091 |
|
434 |
|
c
|
PNS012 |
Paine Syndrome |
61 |
0.091 |
|
435 |
|
|
END057 |
Endometrial Cancer |
74 |
0.091 |
|
436 |
|
P
|
LKM071 |
Leukemia, Chronic Lymphocytic |
79 |
0.091 |
|
437 |
|
P
|
PLR004 |
Pleuropulmonary Blastoma |
65 |
0.091 |
|
438 |
|
|
ALL006 |
Allergic Asthma |
56 |
0.091 |
|
439 |
|
|
HSH003 |
Hashimoto Thyroiditis |
62 |
0.090 |
|
440 |
|
c
|
SCL052 |
Scleroderma, Familial Progressive |
61 |
0.090 |
|
441 |
|
|
PRS045 |
Prostatic Hypertrophy |
53 |
0.090 |
|
442 |
|
P
|
FBR017 |
Fibrosarcoma |
56 |
0.090 |
|
443 |
|
|
SQM013 |
Squamous Cell Carcinoma, Head and Neck |
80 |
0.090 |
|
444 |
|
|
VRC005 |
Varicose Veins |
60 |
0.090 |
|
445 |
|
|
HNS001 |
Hansen's Disease |
34 |
0.090 |
|
446 |
|
|
ERY051 |
Erythroleukemia, Familial |
56 |
0.090 |
|
447 |
|
|
CRH005 |
Crohn's Colitis |
53 |
0.089 |
|
448 |
|
P
|
LPR021 |
Leprosy 3 |
69 |
0.089 |
|
449 |
|
P
|
BPL003 |
Bipolar Disorder |
56 |
0.089 |
|
450 |
|
c
|
FNC043 |
Fanconi Anemia, Complementation Group E |
62 |
0.089 |
|
451 |
|
P
|
MSC003 |
Muscular Atrophy |
52 |
0.089 |
|
452 |
|
P
|
ANT006 |
Antiphospholipid Syndrome |
55 |
0.089 |
|
453 |
|
|
PPL022 |
Papilloma |
54 |
0.089 |
|
454 |
|
|
VCC001 |
Vaccinia |
49 |
0.089 |
|
455 |
|
c
|
ACT068 |
Acute Cystitis |
63 |
0.089 |
|
456 |
|
c
|
MJR024 |
Major Affective Disorder 9 |
41 |
0.088 |
|
457 |
|
c
|
MJR022 |
Major Affective Disorder 8 |
38 |
0.088 |
|
458 |
|
c
|
DRR009 |
Diarrhea 6 |
46 |
0.088 |
|
459 |
|
|
CMP080 |
Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy |
38 |
0.088 |
|
460 |
|
|
3HY005 |
3-Hydroxyacyl-Coa Dehydrogenase Deficiency |
62 |
0.088 |
|
461 |
|
|
TRN018 |
Transitional Cell Carcinoma |
56 |
0.088 |
|
462 |
|
|
THY030 |
Thyroid Gland Disease |
52 |
0.088 |
|
463 |
|
|
BRT054 |
Brittle Bone Disorder |
72 |
0.088 |
|
464 |
|
c
|
NRP053 |
Neuropathy, Hereditary Sensory and Autonomic, Type Iia |
65 |
0.088 |
|
465 |
|
|
PND002 |
Pendred Syndrome |
65 |
0.088 |
|
466 |
|
c
|
HYP057 |
Hypervitaminosis D |
42 |
0.088 |
|
467 |
|
P
|
ANR048 |
Aniridia 1 |
63 |
0.088 |
|
468 |
|
|
ORL015 |
Oral Squamous Cell Carcinoma |
43 |
0.088 |
|
469 |
|
|
MST005 |
Mastitis |
53 |
0.088 |
|
470 |
|
|
GST040 |
Gastric Adenocarcinoma |
70 |
0.087 |
|
471 |
|
|
HMP009 |
Haemophilus Influenzae |
43 |
0.087 |
|
472 |
|
P
|
NSP012 |
Nasopharyngeal Carcinoma |
66 |
0.087 |
|
473 |
|
|
DRR016 |
Diarrhea 2, with Microvillus Atrophy |
60 |
0.087 |
|
474 |
|
P
|
AMY004 |
Amyloidosis |
70 |
0.087 |
|
475 |
|
P
|
ATT013 |
Attention Deficit-Hyperactivity Disorder |
65 |
0.086 |
|
476 |
|
|
CNT047 |
Contact Dermatitis |
58 |
0.086 |
|
477 |
|
|
BRN002 |
Bronchiolitis |
59 |
0.086 |
|
478 |
|
|
PRS129 |
Prostatic Hyperplasia, Benign |
49 |
0.086 |
|
479 |
|
P
|
SYS005 |
Systemic Scleroderma |
68 |
0.086 |
|
480 |
|
|
PSY004 |
Psychotic Disorder |
67 |
0.085 |
|
481 |
|
P
|
MYC008 |
Myocarditis |
59 |
0.085 |
|
482 |
|
P
|
PLM037 |
Pulmonary Hypertension |
67 |
0.085 |
|
483 |
|
|
RNL065 |
Renal Cell Carcinoma, Papillary, 1 |
73 |
0.085 |
|
484 |
|
|
SRC014 |
Sarcoma |
65 |
0.085 |
|
485 |
|
|
SCH014 |
Schistosomiasis |
57 |
0.085 |
|
486 |
|
|
SCH060 |
Schistosoma Mansoni Infection, Susceptibility/ |
39 |
0.085 |
|
487 |
|
|
MSC007 |
Muscle Hypertrophy |
64 |
0.085 |
|
488 |
|
|
EPL118 |
Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation |
65 |
0.085 |
|
489 |
|
|
KHL003 |
Kohlschutter-Tonz Syndrome |
65 |
0.085 |
|
490 |
|
|
PRS021 |
Prostatic Adenoma |
51 |
0.085 |
|
491 |
|
c
|
EPS039 |
Episodic Pain Syndrome, Familial, 1 |
42 |
0.085 |
|
492 |
|
P
|
HYD006 |
Hydrocephalus |
66 |
0.085 |
|
493 |
|
P
|
MYP006 |
Myopia |
55 |
0.084 |
|
494 |
|
|
ANR007 |
Anorexia Nervosa |
63 |
0.084 |
|
495 |
|
|
EPL131 |
Epilepsy, Pyridoxine-Dependent |
49 |
0.084 |
|
496 |
|
|
MTH078 |
Methylmalonic Aciduria, Cblb Type |
51 |
0.084 |
|
497 |
|
|
MCR017 |
Macrocytic Anemia |
44 |
0.084 |
|
498 |
|
|
TRM010 |
Traumatic Brain Injury |
51 |
0.084 |
|
499 |
|
P
|
OST001 |
Osteopetrosis |
70 |
0.084 |
|
500 |
|
P
|
VTM026 |
Vitamin D Hydroxylation-Deficient Rickets, Type 1a |
38 |
0.084 |
|
501 |
|
|
BCK006 |
Back Pain |
42 |
0.084 |
|
502 |
|
P
|
KDN017 |
Kidney Cancer |
60 |
0.084 |
|
503 |
|
c
|
BSL007 |
Basal Cell Carcinoma |
68 |
0.084 |
|
504 |
|
|
CNN005 |
Connective Tissue Disease |
68 |
0.084 |
|
505 |
|
P
|
SLP005 |
Sleep Disorder |
59 |
0.084 |
|
506 |
|
c
|
NGH026 |
Night Blindness, Congenital Stationary, Type 1a |
52 |
0.084 |
|
507 |
|
c
|
MCR129 |
Microvascular Complications of Diabetes 1 |
66 |
0.083 |
|
508 |
|
|
SHR059 |
Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis |
47 |
0.083 |
|
509 |
|
P
|
DYS154 |
Dystonia |
65 |
0.083 |
|
510 |
|
P
|
LCT001 |
Lactic Acidosis |
51 |
0.083 |
|
511 |
|
c
|
PRS136 |
Prostate Cancer, Hereditary, 6 |
33 |
0.083 |
|
512 |
|
|
DSS008 |
Disease of Mental Health |
58 |
0.083 |
|
513 |
|
c
|
TBR026 |
Tuberous Sclerosis 2 |
72 |
0.083 |
|
514 |
|
|
SQM002 |
Squamous Cell Papilloma |
46 |
0.083 |
|
515 |
|
|
LMY002 |
Leiomyoma |
52 |
0.083 |
|
516 |
|
c
|
PRS130 |
Prostate Cancer, Hereditary, 8 |
32 |
0.083 |
|
517 |
|
|
JNT004 |
Joint Laxity, Short Stature, and Myopia |
45 |
0.083 |
|
518 |
|
P
|
PRP003 |
Porphyria Cutanea Tarda |
67 |
0.083 |
|
519 |
|
P
|
ART153 |
Arthrochalasia Ehlers-Danlos Syndrome |
55 |
0.082 |
|
520 |
|
P
|
OPT006 |
Optic Nerve Disease |
60 |
0.082 |
|
521 |
|
|
MTH077 |
Methylmalonic Aciduria, Cbla Type |
42 |
0.082 |
|
522 |
|
|
ENT004 |
Enthesopathy |
49 |
0.082 |
|
523 |
|
|
PRT038 |
Protein-Energy Malnutrition |
54 |
0.082 |
|
524 |
|
|
CLN015 |
Colon Adenocarcinoma |
65 |
0.082 |
|
525 |
|
c
|
VNT034 |
Ventricular Fibrillation, Paroxysmal Familial, 1 |
67 |
0.082 |
|
526 |
|
|
SPN035 |
Spindle Cell Sarcoma |
53 |
0.081 |
|
527 |
|
P
|
SCL018 |
Scoliosis |
60 |
0.081 |
|
528 |
|
P
|
SPP010 |
Suppressor of Tumorigenicity 3 |
51 |
0.081 |
|
529 |
|
|
HPT004 |
Hepatic Coma |
45 |
0.081 |
|
530 |
|
|
PST092 |
Posttransplant Acute Limbic Encephalitis |
29 |
0.081 |
|
531 |
|
|
ORL013 |
Oral Lichen Planus |
45 |
0.080 |
|
532 |
|
P
|
ATS308 |
Autosomal Dominant Cerebellar Ataxia |
60 |
0.080 |
|
533 |
|
P
|
ADL010 |
Adult Respiratory Distress Syndrome |
65 |
0.080 |
|
534 |
|
|
HRD160 |
Hereditary Combined Deficiency of Vitamin K-Dependent Clotting Factors |
22 |
0.080 |
|
535 |
|
|
SBC016 |
Subacute Delirium |
44 |
0.080 |
|
536 |
|
|
PNG002 |
Pain Agnosia |
51 |
0.080 |
|
537 |
|
|
OTT002 |
Otitis Media |
72 |
0.080 |
|
538 |
|
|
CLC006 |
Calcinosis |
48 |
0.080 |
|
539 |
|
c
|
CWD006 |
Cowden Syndrome 1 |
78 |
0.080 |
|
540 |
|
|
DMY004 |
Demyelinating Disease |
52 |
0.080 |
|
541 |
|
|
GNG013 |
Gingivitis |
59 |
0.080 |
|
542 |
|
c
|
HMP029 |
Hemophilia a |
67 |
0.080 |
|
543 |
|
|
CMR002 |
Coumarin Resistance |
56 |
0.080 |
|
544 |
|
|
HPT019 |
Hepatic Encephalopathy |
60 |
0.080 |
|
545 |
|
|
OVR094 |
Ovarian Epithelial Cancer |
38 |
0.079 |
|
546 |
|
c
|
PK3005 |
Pik3ca-Related Overgrowth Syndrome |
34 |
0.079 |
|
547 |
|
|
WRN001 |
Werner Syndrome |
69 |
0.079 |
|
548 |
|
P
|
ART023 |
Arthropathy |
62 |
0.079 |
|
549 |
|
|
CLF027 |
Cleft Palate, Isolated |
64 |
0.079 |
|
550 |
|
|
PLM134 |
Pulmonary Fibrosis, Idiopathic |
77 |
0.079 |
|
551 |
|
P
|
ALP009 |
Alopecia Areata |
60 |
0.079 |
|
552 |
|
|
CHL065 |
Cholangiocarcinoma |
68 |
0.078 |
|
553 |
|
P
|
OCL013 |
Oculodentodigital Dysplasia |
69 |
0.078 |
|
554 |
|
c
|
ACT134 |
Acute Liver Failure |
56 |
0.078 |
|
555 |
|
|
ALC028 |
Alacrima, Achalasia, and Mental Retardation Syndrome |
64 |
0.078 |
|
556 |
|
|
BRC012 |
Brucellosis |
64 |
0.078 |
|
557 |
|
c
|
LKM060 |
Leukemia, Acute Lymphoblastic 3 |
56 |
0.078 |
|
558 |
|
|
MTB004 |
Metabolic Acidosis |
50 |
0.078 |
|
559 |
|
|
CRB037 |
Cerebral Palsy |
69 |
0.078 |
|
560 |
|
P
|
FML018 |
Familial Mediterranean Fever |
73 |
0.078 |
|
561 |
|
|
INT079 |
Intrahepatic Cholangiocarcinoma |
51 |
0.078 |
|
562 |
|
|
HYP080 |
Hypogonadism |
50 |
0.078 |
|
563 |
|
P
|
BLD124 |
Bleeding Disorder, Platelet-Type, 11 |
63 |
0.078 |
|
564 |
|
|
PRN019 |
Perinatal Necrotizing Enterocolitis |
59 |
0.077 |
|
565 |
|
|
CRD132 |
Cardiac Conduction Defect |
58 |
0.077 |
|
566 |
|
|
LYM027 |
Lymphopenia |
58 |
0.077 |
|
567 |
|
|
NWC001 |
Newcastle Disease |
45 |
0.077 |
|
568 |
|
P
|
APL001 |
Aplastic Anemia |
74 |
0.077 |
|
569 |
|
P
|
UVT001 |
Uveitis |
57 |
0.077 |
|
570 |
|
|
DYS073 |
Dysphagia |
50 |
0.077 |
|
571 |
|
|
CRB004 |
Cerebral Artery Occlusion |
45 |
0.077 |
|
572 |
|
|
LKP003 |
Leukoplakia |
39 |
0.077 |
|
573 |
|
P
|
MPL001 |
Maple Syrup Urine Disease |
69 |
0.077 |
|
574 |
|
P
|
MVM001 |
Movement Disease |
63 |
0.077 |
|
575 |
|
P
|
ALP004 |
Alport Syndrome |
68 |
0.077 |
|
576 |
|
|
CRP001 |
Carpal Tunnel Syndrome |
67 |
0.076 |
|
577 |
|
P
|
CRN037 |
Craniosynostosis |
68 |
0.076 |
|
578 |
|
|
HYP014 |
Hyperuricemia |
52 |
0.076 |
|
579 |
|
|
PRM020 |
Premenstrual Tension |
40 |
0.076 |
|
580 |
|
c
|
FML035 |
Familial Hyperlipidemia |
55 |
0.076 |
|
581 |
|
P
|
ENC004 |
Encephalitis |
61 |
0.076 |
|
582 |
|
c
|
PSR023 |
Psoriasis 1 |
52 |
0.076 |
|
583 |
|
P
|
GLM040 |
Glioma Susceptibility 1 |
81 |
0.076 |
|
584 |
|
P
|
AST007 |
Astrocytoma |
51 |
0.076 |
|
585 |
|
|
BRN028 |
Brain Cancer |
74 |
0.075 |
|
586 |
|
|
IMP005 |
Impotence |
52 |
0.075 |
|
587 |
|
|
ERY029 |
Erythermalgia, Primary |
58 |
0.075 |
|
588 |
|
|
ATM052 |
Autoimmune Disease 1 |
37 |
0.075 |
|
589 |
|
c
|
SVR005 |
Severe Pre-Eclampsia |
50 |
0.075 |
|
590 |
|
|
CHR066 |
Chronic Fatigue Syndrome |
61 |
0.075 |
|
591 |
|
|
MMM001 |
Mammary Paget's Disease |
53 |
0.075 |
|
592 |
|
|
BLD131 |
Bladder Urothelial Carcinoma |
62 |
0.074 |
|
593 |
|
|
ADR040 |
Adrenal Gland Pheochromocytoma |
46 |
0.074 |
|
594 |
|
|
PLY118 |
Polyglucosan Body Myopathy 1 with or Without Immunodeficiency |
53 |
0.074 |
|
595 |
|
P
|
PLL002 |
Pellagra |
46 |
0.074 |
|
596 |
|
|
ANR040 |
Aneurysm |
59 |
0.074 |
|
597 |
|
|
PPL049 |
Papillon-Lefevre Syndrome |
65 |
0.074 |
|
598 |
|
c
|
GRV008 |
Graves Disease 1 |
56 |
0.074 |
|
599 |
|
|
HMG005 |
Hemoglobinopathy |
56 |
0.074 |
|
600 |
|
c
|
HYP272 |
Hypercholesterolemia, Familial, 3 |
44 |
0.074 |
|
601 |
|
|
NRL018 |
Neural Tube Defects, Folate-Sensitive |
48 |
0.074 |
|
602 |
|
c
|
MCR112 |
Microvascular Complications of Diabetes 2 |
41 |
0.074 |
|
603 |
|
c
|
PSR017 |
Psoriasis 2 |
53 |
0.073 |
|
604 |
|
|
INT324 |
Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies |
58 |
0.073 |
|
605 |
|
P
|
CHL066 |
Cholangitis |
51 |
0.073 |
|
606 |
|
P
|
HYP818 |
Hypobetalipoproteinemia, Familial, 1 |
56 |
0.073 |
|
607 |
|
|
TLN003 |
Telangiectasis |
52 |
0.073 |
|
608 |
|
|
HYP005 |
Hypokalemia |
55 |
0.072 |
|
609 |
|
P
|
END033 |
Endocarditis |
57 |
0.072 |
|
610 |
|
P
|
PLY170 |
Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease |
64 |
0.072 |
|
611 |
|
|
CRN030 |
Coronary Stenosis |
50 |
0.072 |
|
612 |
|
|
GT001 |
Gout |
64 |
0.072 |
|
613 |
|
c
|
ALP101 |
Alpha-Thalassemia |
62 |
0.072 |
|
614 |
|
|
MTC114 |
Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes |
61 |
0.072 |
|
615 |
|
|
THY111 |
Thyroid Carcinoma, Familial Medullary |
67 |
0.072 |
|
616 |
|
|
MYL005 |
Myelofibrosis |
70 |
0.072 |
|
617 |
|
|
CMP010 |
Complex Regional Pain Syndrome |
58 |
0.072 |
|
618 |
|
P
|
BNG032 |
Benign Mesothelioma |
46 |
0.072 |
|
619 |
|
|
VSC003 |
Visceral Leishmaniasis |
55 |
0.072 |
|
620 |
|
P
|
DNG005 |
Dengue Virus |
59 |
0.072 |
|
621 |
|
|
NRT004 |
Neuritis |
52 |
0.072 |
|
622 |
|
|
GST023 |
Gastric Ulcer |
53 |
0.072 |
|
623 |
|
|
49X006 |
49, Xxxxy Syndrome |
41 |
0.072 |
|
624 |
|
|
TRD006 |
Tardive Dyskinesia |
54 |
0.072 |
|
625 |
|
P
|
INT068 |
Intestinal Disease |
53 |
0.072 |
|
626 |
|
|
PNC041 |
Pancreatic Ductal Adenocarcinoma |
51 |
0.071 |
|
627 |
|
|
FCT007 |
Factor Vii Deficiency |
67 |
0.071 |
|
628 |
|
|
END040 |
Endogenous Depression |
55 |
0.071 |
|
629 |
|
|
APH001 |
Aphthous Stomatitis |
57 |
0.071 |
|
630 |
|
|
ANX004 |
Anoxia |
40 |
0.071 |
|
631 |
|
|
ART016 |
Aortic Aneurysm |
69 |
0.071 |
|
632 |
|
P
|
SHR001 |
Short Bowel Syndrome |
53 |
0.071 |
|
633 |
|
|
CHR178 |
Chromosomal Triplication |
35 |
0.071 |
|
634 |
|
|
HYP043 |
Hyperandrogenism |
48 |
0.071 |
|
635 |
|
|
DGN001 |
Degenerative Disc Disease |
48 |
0.071 |
|
636 |
|
|
ACR007 |
Acromegaly |
71 |
0.071 |
|
637 |
|
P
|
FRN006 |
Frontotemporal Dementia |
68 |
0.071 |
|
638 |
|
|
PRM329 |
Premature Aging |
35 |
0.070 |
|
639 |
|
|
ACT113 |
Acute Myeloblastic Leukemia with Maturation |
46 |
0.070 |
|
640 |
|
c
|
GLL024 |
Gallbladder Disease 1 |
53 |
0.070 |
|
641 |
|
|
LNG031 |
Lung Benign Neoplasm |
51 |
0.070 |
|
642 |
|
P
|
LFR001 |
Li-Fraumeni Syndrome |
72 |
0.070 |
|
643 |
|
P
|
PRC031 |
Preeclampsia/eclampsia 1 |
38 |
0.070 |
|
644 |
|
|
PSR001 |
Psoriatic Arthritis |
61 |
0.070 |
|
645 |
|
P
|
BRS044 |
Breast Adenocarcinoma |
59 |
0.070 |
|
646 |
|
|
MMB001 |
Membranoproliferative Glomerulonephritis |
55 |
0.070 |
|
647 |
|
|
WLS001 |
Wilson Disease |
71 |
0.070 |
|
648 |
|
|
BLR001 |
Biliary Atresia |
50 |
0.070 |
|
649 |
|
P
|
MLT074 |
Multiple Endocrine Neoplasia |
56 |
0.070 |
|
650 |
|
|
NRT001 |
Neurotic Disorder |
53 |
0.070 |
|
651 |
|
c
|
PNC108 |
Pancreatitis, Hereditary |
70 |
0.070 |
|
652 |
|
P
|
LKD017 |
Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism |
57 |
0.070 |
|
653 |
|
|
NWB001 |
Newborn Respiratory Distress Syndrome |
58 |
0.069 |
|
654 |
|
c
|
EPL184 |
Epileptic Encephalopathy, Early Infantile, 6 |
70 |
0.069 |
|
655 |
|
P
|
RTN018 |
Retinal Disease |
53 |
0.069 |
|
656 |
|
|
VSC002 |
Vascular Dementia |
57 |
0.069 |
|
657 |
|
P
|
CND004 |
Candidiasis |
58 |
0.069 |
|
658 |
|
P
|
PLM175 |
Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 |
51 |
0.069 |
|
659 |
|
|
OST003 |
Osteonecrosis |
61 |
0.069 |
|
660 |
|
|
DYS015 |
Dysentery |
52 |
0.069 |
|
661 |
|
|
SNS003 |
Sensory Peripheral Neuropathy |
54 |
0.069 |
|
662 |
|
c
|
WLM013 |
Wilms Tumor 1 |
65 |
0.069 |
|
663 |
|
P
|
SJG008 |
Sjogren Syndrome |
61 |
0.069 |
|
664 |
|
|
CHG001 |
Chagas Disease |
66 |
0.069 |
|
665 |
|
c
|
ACT135 |
Acute Graft Versus Host Disease |
52 |
0.069 |
|
666 |
|
|
BRR014 |
Barrett Esophagus |
65 |
0.069 |
|
667 |
|
P
|
MDL005 |
Medulloblastoma |
77 |
0.069 |
|
668 |
|
c
|
CNG006 |
Congenital Hypothyroidism |
64 |
0.069 |
|
669 |
|
|
MNN020 |
Meningococcal Infection |
46 |
0.069 |
|
670 |
|
|
ATX029 |
Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia |
65 |
0.069 |
|
671 |
|
P
|
PSD087 |
Pseudoxanthoma Elasticum |
65 |
0.069 |
|
672 |
|
|
CHC001 |
Chickenpox |
60 |
0.068 |
|
673 |
|
|
MTH009 |
Mouth Disease |
56 |
0.068 |
|
674 |
|
P
|
MTC069 |
Mitochondrial Disorders |
56 |
0.068 |
|
675 |
|
c
|
HYP604 |
Hyperinsulinemic Hypoglycemia, Familial, 2 |
65 |
0.068 |
|
676 |
|
|
THY125 |
Thyroid Gland Medullary Carcinoma |
50 |
0.068 |
|
677 |
|
P
|
DYS007 |
Dyskeratosis Congenita |
67 |
0.068 |
|
678 |
|
|
RBF001 |
Riboflavin Deficiency |
49 |
0.068 |
|
679 |
|
P
|
TRC086 |
Trichohepatoenteric Syndrome 1 |
62 |
0.068 |
|
680 |
|
|
PLY150 |
Polykaryocytosis Inducer |
31 |
0.068 |
|
681 |
|
|
ALP103 |
Alpha-1-Antitrypsin Deficiency |
64 |
0.068 |
|
682 |
|
P
|
PLY014 |
Polycystic Kidney Disease |
62 |
0.068 |
|
683 |
|
|
ADR007 |
Adrenoleukodystrophy |
75 |
0.068 |
|
684 |
|
|
INT066 |
Interstitial Lung Disease |
60 |
0.068 |
|
685 |
|
c
|
LKM005 |
Leukemia, T-Cell, Chronic |
34 |
0.068 |
|
686 |
|
c
|
HYP843 |
Hypoalphalipoproteinemia, Primary, 2 |
52 |
0.068 |
|
687 |
|
c
|
PRT132 |
Protoporphyria, Erythropoietic, 1 |
61 |
0.068 |
|
688 |
|
|
HYD058 |
Hydrops, Lactic Acidosis, and Sideroblastic Anemia |
59 |
0.067 |
|
689 |
|
c
|
HYP841 |
Hypoalphalipoproteinemia, Primary, 1 |
41 |
0.067 |
|
690 |
|
|
PLM010 |
Pulmonary Edema |
54 |
0.067 |
|
691 |
|
|
HMC040 |
Homocystinuria Due to Cystathionine Beta-Synthase Deficiency |
52 |
0.067 |
|
692 |
|
P
|
BRL012 |
Bare Lymphocyte Syndrome, Type Ii |
66 |
0.067 |
|
693 |
|
|
OST017 |
Osteomyelitis |
64 |
0.067 |
|
694 |
|
P
|
NRV007 |
Nervous System Disease |
66 |
0.067 |
|
695 |
|
|
KPS004 |
Kaposi Sarcoma |
75 |
0.067 |
|
696 |
|
P
|
MST009 |
Mastocytosis |
64 |
0.067 |
|
697 |
|
|
PYR016 |
Pyridoxine Deficiency |
30 |
0.067 |
|
698 |
|
|
CHR074 |
Choriocarcinoma |
47 |
0.067 |
|
699 |
|
c
|
NMN014 |
Niemann-Pick Disease, Type C2 |
51 |
0.067 |
|
700 |
|
c
|
LTN004 |
Late-Onset Retinal Degeneration |
59 |
0.067 |
|
701 |
|
|
ALC006 |
Alcoholic Hepatitis |
61 |
0.067 |
|
702 |
|
|
HRP004 |
Herpes Zoster |
60 |
0.067 |
|
703 |
|
|
FML307 |
Familial Calcium Pyrophosphate Deposition |
40 |
0.067 |
|
704 |
|
|
TNG002 |
Tangier Disease |
65 |
0.067 |
|
705 |
|
P
|
ANG001 |
Angelman Syndrome |
69 |
0.067 |
|
706 |
|
c
|
SPN207 |
Spinocerebellar Ataxia, Autosomal Recessive 8 |
49 |
0.067 |
|
707 |
|
P
|
DDN001 |
Duodenal Ulcer |
52 |
0.066 |
|
708 |
|
|
CTN007 |
Cutaneous Leishmaniasis |
62 |
0.066 |
|
709 |
|
|
ISL099 |
Isolated Methylmalonic Acidemia |
29 |
0.066 |
|
710 |
|
c
|
CRV002 |
Cervix Uteri Carcinoma in Situ |
46 |
0.066 |
|
711 |
|
|
CRV045 |
Cervical Intraepithelial Neoplasia |
39 |
0.066 |
|
712 |
|
|
STT001 |
Status Epilepticus |
60 |
0.066 |
|
713 |
|
|
MTH076 |
Methylmalonic Aciduria Due to Methylmalonyl-Coa Mutase Deficiency |
50 |
0.066 |
|
714 |
|
|
APN008 |
Apnea, Obstructive Sleep |
64 |
0.066 |
|
715 |
|
|
CHN016 |
Cohen Syndrome |
63 |
0.066 |
|
716 |
|
P
|
PRS038 |
Personality Disorder |
65 |
0.066 |
|
717 |
|
c
|
MYT021 |
Myotonic Dystrophy 1 |
69 |
0.066 |
|
718 |
|
P
|
VTR007 |
Vitreoretinopathy |
46 |
0.066 |
|
719 |
|
|
BDD001 |
Budd-Chiari Syndrome |
63 |
0.066 |
|
720 |
|
P
|
LBR014 |
Leber Congenital Amaurosis 4 |
56 |
0.066 |
|
721 |
|
|
OST062 |
Osteoarthritis with Mild Chondrodysplasia |
47 |
0.066 |
|
722 |
|
P
|
CYS018 |
Cystitis |
59 |
0.066 |
|
723 |
|
c
|
MLT156 |
Multiple Endocrine Neoplasia, Type I |
72 |
0.066 |
|
724 |
|
P
|
VSC018 |
Visceral Steatosis |
33 |
0.066 |
|
725 |
|
|
CLR109 |
Colorectal Adenocarcinoma |
51 |
0.066 |
|
726 |
|
|
HYL004 |
Hyaline Fibromatosis Syndrome |
67 |
0.066 |
|
727 |
|
P
|
PLY018 |
Polycythemia |
56 |
0.066 |
|
728 |
|
|
BRS051 |
Breast Disease |
58 |
0.066 |
|
729 |
|
|
AND019 |
Andersen Cardiodysrhythmic Periodic Paralysis |
65 |
0.066 |
|
730 |
|
P
|
HML001 |
Hemolytic-Uremic Syndrome |
53 |
0.066 |
|
731 |
|
P
|
HYP733 |
Hypercalciuria, Absorptive, 2 |
45 |
0.066 |
|
732 |
|
P
|
HNT016 |
Huntington Disease |
72 |
0.065 |
|
733 |
|
|
INT002 |
Intermittent Claudication |
61 |
0.065 |
|
734 |
|
|
ESP002 |
Esophageal Varix |
51 |
0.065 |
|
735 |
|
|
CYS036 |
Cystinosis, Nephropathic |
51 |
0.065 |
|
736 |
|
c
|
XNT010 |
Xanthinuria, Type I |
53 |
0.065 |
|
737 |
|
|
THR004 |
Thrombocytosis |
51 |
0.065 |
|
738 |
|
P
|
PRP034 |
Purpura Fulminans |
43 |
0.065 |
|
739 |
|
|
MND021 |
Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome |
65 |
0.065 |
|
740 |
|
c
|
INH020 |
Inherited Metabolic Disorder |
47 |
0.065 |
|
741 |
|
P
|
ICH004 |
Ichthyosis |
54 |
0.065 |
|
742 |
|
P
|
FLL037 |
Follicular Lymphoma |
67 |
0.065 |
|
743 |
|
c
|
HYP243 |
Hyperparathyroidism 1 |
51 |
0.065 |
|
744 |
|
|
SCN001 |
Secondary Hyperparathyroidism of Renal Origin |
27 |
0.065 |
|
745 |
|
P
|
ESP024 |
Esophagitis |
62 |
0.065 |
|
746 |
|
|
TCL028 |
T-Cell Lymphoblastic Leukemia/lymphoma |
47 |
0.065 |
|
747 |
|
P
|
LYM033 |
Lymphoproliferative Syndrome |
59 |
0.064 |
|
748 |
|
P
|
MYS005 |
Myositis |
56 |
0.064 |
|
749 |
|
P
|
PTY003 |
Pityriasis Rubra Pilaris |
58 |
0.064 |
|
750 |
|
P
|
NRN021 |
Neuronal Ceroid Lipofuscinosis |
64 |
0.064 |
|
751 |
|
|
CRT013 |
Carotid Stenosis |
50 |
0.064 |
|
752 |
|
c
|
ATM006 |
Autoimmune Lymphoproliferative Syndrome |
74 |
0.064 |
|
753 |
|
c
|
DNT047 |
Dentinogenesis Imperfecta Type 2 |
31 |
0.064 |
|
754 |
|
c
|
PLY105 |
Polycystic Ovary Syndrome 1 |
38 |
0.064 |
|
755 |
|
c
|
CHR682 |
Chronic Bilirubin Encephalopathy |
39 |
0.064 |
|
756 |
|
c
|
PSR032 |
Psoriasis 11 |
47 |
0.064 |
|
757 |
|
c
|
PSR028 |
Psoriasis 7 |
42 |
0.064 |
|
758 |
|
c
|
PSR018 |
Psoriasis 13 |
41 |
0.064 |
|
759 |
|
P
|
PTT014 |
Pitt-Hopkins Syndrome |
63 |
0.064 |
|
760 |
|
c
|
HYP864 |
Hypoparathyroidism, Familial Isolated, 1 |
48 |
0.064 |
|
761 |
|
|
LMY014 |
Leiomyoma, Uterine |
56 |
0.063 |
|
762 |
|
c
|
PRD013 |
Periodic Fever, Familial, Autosomal Dominant |
67 |
0.063 |
|
763 |
|
|
PRT029 |
Parathyroid Adenoma |
50 |
0.063 |
|
764 |
|
c
|
BLC008 |
Bile Acid Synthesis Defect, Congenital, 2 |
50 |
0.063 |
|
765 |
|
|
GLS007 |
Glossitis |
47 |
0.063 |
|
766 |
|
|
HYP636 |
Hypocalcemic Vitamin D-Dependent Rickets |
39 |
0.063 |
|
767 |
|
|
ORT008 |
Orotic Aciduria |
55 |
0.063 |
|
768 |
|
P
|
MCR010 |
Microcephaly |
59 |
0.063 |
|
769 |
|
P
|
NRF002 |
Neurofibromatosis |
56 |
0.063 |
|
770 |
|
c
|
ART101 |
Aortic Valve Disease 2 |
65 |
0.063 |
|
771 |
|
c
|
INF145 |
Infantile Liver Failure Syndrome 1 |
50 |
0.063 |
|
772 |
|
|
WGN007 |
Wagner Vitreoretinopathy |
38 |
0.063 |
|
773 |
|
|
WGN003 |
Wagner Syndrome |
36 |
0.063 |
|
774 |
|
c
|
PSD066 |
Pseudohypoparathyroidism, Type Ib |
55 |
0.063 |
|
775 |
|
P
|
PYL005 |
Pyelonephritis |
56 |
0.063 |
|
776 |
|
|
MYF001 |
Myofibroma |
45 |
0.063 |
|
777 |
|
|
GYR004 |
Gyrate Atrophy of Choroid and Retina |
57 |
0.063 |
|
778 |
|
|
ATN005 |
Autonomic Dysfunction |
46 |
0.063 |
|
779 |
|
c
|
JVN010 |
Juvenile Rheumatoid Arthritis |
64 |
0.063 |
|
780 |
|
|
RNL078 |
Renal Dysplasia |
50 |
0.063 |
|
781 |
|
|
RTN020 |
Retinal Vascular Disease |
46 |
0.063 |
|
782 |
|
c
|
CHL119 |
Cholangitis, Primary Sclerosing |
57 |
0.063 |
|
783 |
|
P
|
BRD002 |
Bardet-Biedl Syndrome |
66 |
0.063 |
|
784 |
|
P
|
HYP035 |
Hypophosphatasia |
61 |
0.063 |
|
785 |
|
P
|
CRB101 |
Cerebrooculofacioskeletal Syndrome 1 |
60 |
0.062 |
|
786 |
|
|
PTZ001 |
Peutz-Jeghers Syndrome |
70 |
0.062 |
|
787 |
|
c
|
MCL062 |
Mucolipidosis Ii Alpha/beta |
68 |
0.062 |
|
788 |
|
|
PRS063 |
Paresthesia |
41 |
0.062 |
|
789 |
|
|
PRT014 |
Protein S Deficiency |
44 |
0.062 |
|
790 |
|
|
OMN001 |
Omenn Syndrome |
67 |
0.062 |
|
791 |
|
c
|
HMG029 |
Hemoglobin Se Disease |
39 |
0.062 |
|
792 |
|
P
|
SPN429 |
Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy 2 |
52 |
0.062 |
|
793 |
|
|
INS001 |
Insulinoma |
60 |
0.062 |
|
794 |
|
c
|
GLY060 |
Glycogen Storage Disease Ia |
63 |
0.062 |
|
795 |
|
|
FDB001 |
Foodborne Botulism |
55 |
0.062 |
|
796 |
|
|
HLC001 |
Holocarboxylase Synthetase Deficiency |
48 |
0.062 |
|
797 |
|
|
PGM030 |
Pigmentation Anomaly of the Skin |
26 |
0.062 |
|
798 |
|
c
|
CHR064 |
Chronic Monocytic Leukemia |
33 |
0.062 |
|
799 |
|
|
ACN002 |
Acanthosis Nigricans |
60 |
0.062 |
|
800 |
|
|
FLT009 |
Folate Malabsorption, Hereditary |
50 |
0.062 |
|
801 |
|
P
|
MTC003 |
Metachromatic Leukodystrophy |
70 |
0.062 |
|
802 |
|
|
BRN004 |
Brain Edema |
56 |
0.062 |
|
803 |
|
|
BTN003 |
Biotinidase Deficiency |
60 |
0.062 |
|
804 |
|
|
BNN003 |
Bone Inflammation Disease |
48 |
0.062 |
|
805 |
|
|
AMN001 |
Amenorrhea |
54 |
0.061 |
|
806 |
|
|
ALL010 |
Allergic Contact Dermatitis |
56 |
0.061 |
|
807 |
|
P
|
PLY169 |
Polycystic Liver Disease 1 with or Without Kidney Cysts |
60 |
0.061 |
|
808 |
|
P
|
CNJ013 |
Conjunctivitis |
65 |
0.061 |
|
809 |
|
P
|
FCL005 |
Focal Segmental Glomerulosclerosis |
57 |
0.061 |
|
810 |
|
P
|
RST001 |
Restless Legs Syndrome |
54 |
0.061 |
|
811 |
|
c
|
BCT007 |
Bacterial Meningitis |
55 |
0.061 |
|
812 |
|
c
|
MLG068 |
Malignant Glioma |
46 |
0.061 |
|
813 |
|
|
PFF001 |
Pfeiffer Syndrome |
79 |
0.061 |
|
814 |
|
P
|
RBL001 |
Rubella |
59 |
0.061 |
|
815 |
|
P
|
SNS001 |
Sensorineural Hearing Loss |
60 |
0.061 |
|
816 |
|
|
BCT002 |
Bacterial Vaginosis |
53 |
0.061 |
|
817 |
|
|
EMB004 |
Embryonal Carcinoma |
56 |
0.061 |
|
818 |
|
P
|
MTC133 |
Mitochondrial Myopathy |
49 |
0.061 |
|
819 |
|
|
CHL067 |
Cholecystitis |
57 |
0.061 |
|
820 |
|
|
KRN002 |
Kearns-Sayre Syndrome |
63 |
0.061 |
|
821 |
|
P
|
MTR014 |
Motor Neuron Disease |
65 |
0.061 |
|
822 |
|
|
CHD001 |
Chediak-Higashi Syndrome |
66 |
0.061 |
|
823 |
|
|
GLY010 |
Glycine Encephalopathy |
62 |
0.061 |
|
824 |
|
c
|
MLT160 |
Multiple Endocrine Neoplasia, Type Iia |
70 |
0.061 |
|
825 |
|
|
GLC106 |
Glucocorticoid Resistance, Generalized |
48 |
0.061 |
|
826 |
|
c
|
HPT007 |
Hepatitis E |
53 |
0.061 |
|
827 |
|
|
ART001 |
Arterial Tortuosity Syndrome |
66 |
0.060 |
|
828 |
|
c
|
THY109 |
Thyroid Cancer, Nonmedullary, 1 |
56 |
0.060 |
|
829 |
|
|
IGG001 |
Iga Glomerulonephritis |
48 |
0.060 |
|
830 |
|
|
PST021 |
Postpartum Depression |
50 |
0.060 |
|
831 |
|
|
CRD223 |
Cardiac Arrhythmia |
60 |
0.060 |
|
832 |
|
c
|
HYP768 |
Hyperlipoproteinemia, Type I |
67 |
0.060 |
|
833 |
|
|
PRD004 |
Prediabetes Syndrome |
47 |
0.060 |
|
834 |
|
|
RHM001 |
Rheumatic Fever |
60 |
0.060 |
|
835 |
|
P
|
GCH001 |
Gaucher's Disease |
63 |
0.060 |
|
836 |
|
|
PRT010 |
Parathyroid Carcinoma |
67 |
0.060 |
|
837 |
|
c
|
MCP052 |
Mucopolysaccharidosis, Type Vi |
67 |
0.060 |
|
838 |
|
P
|
HYP535 |
Hypogonadotropic Hypogonadism 7 with or Without Anosmia |
59 |
0.060 |
|
839 |
|
|
IDP070 |
Idiopathic Scoliosis |
42 |
0.060 |
|
840 |
|
|
CHY002 |
Chylomicron Retention Disease |
65 |
0.060 |
|
841 |
|
c
|
HMP004 |
Hemophilia B |
68 |
0.060 |
|
842 |
|
|
RFR010 |
Refractory Anemia |
48 |
0.060 |
|
843 |
|
|
GRW007 |
Growth Hormone Deficiency |
46 |
0.060 |
|
844 |
|
|
NRM005 |
Neuromuscular Disease |
64 |
0.059 |
|
845 |
|
P
|
RNL007 |
Renal Tubular Acidosis |
51 |
0.059 |
|
846 |
|
|
CYT018 |
Cytochrome P450 2d6 Variant |
27 |
0.059 |
|
847 |
|
c
|
BLD140 |
Blood Group, I System |
32 |
0.059 |
|
848 |
|
|
ALP077 |
Alpha-Methylacetoacetic Aciduria |
55 |
0.059 |
|
849 |
|
|
SPS150 |
Spastic Ataxia, Charlevoix-Saguenay Type |
58 |
0.059 |
|
850 |
|
|
GLS018 |
Glass Syndrome |
57 |
0.059 |
|
851 |
|
c
|
JVN061 |
Juvenile Arthritis |
60 |
0.059 |
|
852 |
|
|
VNT035 |
Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy |
63 |
0.059 |
|
853 |
|
P
|
RTN022 |
Retinal Vein Occlusion |
53 |
0.059 |
|
854 |
|
|
MTH021 |
Methylmalonic Acidemia with Homocystinuria |
46 |
0.059 |
|
855 |
|
|
MNN032 |
Meningococcal Meningitis |
54 |
0.059 |
|
856 |
|
c
|
HYP369 |
Hypophosphatemic Rickets, Autosomal Recessive, 2 |
29 |
0.059 |
|
857 |
|
P
|
MMP001 |
Mumps |
58 |
0.059 |
|
858 |
|
c
|
ART138 |
Aortic Aneurysm, Familial Abdominal, 1 |
59 |
0.059 |
|
859 |
|
|
GLC086 |
Glucocorticoid-Induced Osteoporosis |
43 |
0.059 |
|
860 |
|
|
LMB062 |
Limb Ischemia |
55 |
0.059 |
|
861 |
|
P
|
MNC007 |
Monocytic Leukemia |
53 |
0.059 |
|
862 |
|
P
|
THR005 |
Thrombotic Thrombocytopenic Purpura |
61 |
0.059 |
|
863 |
|
|
MCC012 |
Mccune-Albright Syndrome |
70 |
0.059 |
|
864 |
|
P
|
FML011 |
Familial Adenomatous Polyposis |
72 |
0.059 |
|
865 |
|
P
|
PNT019 |
Pontocerebellar Hypoplasia |
46 |
0.059 |
|
866 |
|
P
|
LCT002 |
Lactose Intolerance |
53 |
0.059 |
|
867 |
|
|
BLL006 |
Bullous Pemphigoid |
62 |
0.059 |
|
868 |
|
c
|
CRD177 |
Ceroid Lipofuscinosis, Neuronal, 1 |
62 |
0.059 |
|
869 |
|
|
RNL077 |
Renal Fibrosis |
47 |
0.059 |
|
870 |
|
|
DNN002 |
Donnai-Barrow Syndrome |
56 |
0.058 |
|
871 |
|
c
|
HPT015 |
Hepatitis D |
49 |
0.058 |
|
872 |
|
c
|
CRD184 |
Ceroid Lipofuscinosis, Neuronal, 5 |
55 |
0.058 |
|
873 |
|
c
|
DBT091 |
Diabetes Insipidus, Nephrogenic, Autosomal |
66 |
0.058 |
|
874 |
|
c
|
CRD086 |
Cardiomyopathy, Familial Hypertrophic, 1 |
68 |
0.058 |
|
875 |
|
|
LNG039 |
Lung Squamous Cell Carcinoma |
66 |
0.058 |
|
876 |
|
|
CLF001 |
Cleft Lip |
53 |
0.058 |
|
877 |
|
|
ENC067 |
Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis |
55 |
0.058 |
|
878 |
|
P
|
PSD015 |
Pseudohypoparathyroidism |
56 |
0.058 |
|
879 |
|
|
DWR001 |
Dwarfism |
44 |
0.058 |
|
880 |
|
P
|
ALP106 |
Alport Syndrome 1, X-Linked |
55 |
0.058 |
|
881 |
|
|
TRP009 |
Triple X Syndrome |
42 |
0.058 |
|
882 |
|
|
HYP257 |
Hypoparathyroidism, Sensorineural Deafness, and Renal Disease |
59 |
0.058 |
|
883 |
|
|
PYR022 |
Pyruvate Dehydrogenase E1-Alpha Deficiency |
60 |
0.058 |
|
884 |
|
|
AZS001 |
Azoospermia |
50 |
0.058 |
|
885 |
|
|
PYR021 |
Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency |
47 |
0.058 |
|
886 |
|
|
BRS099 |
Breast Ductal Carcinoma |
62 |
0.058 |
|
887 |
|
|
MCL006 |
Macular Retinal Edema |
55 |
0.058 |
|
888 |
|
|
ATN011 |
Autoinflammation with Infantile Enterocolitis |
44 |
0.058 |
|
889 |
|
|
ALP041 |
Alopecia, Neurologic Defects, and Endocrinopathy Syndrome |
51 |
0.058 |
|
890 |
|
|
GLC009 |
Glucosephosphate Dehydrogenase Deficiency |
52 |
0.058 |
|
891 |
|
|
PLY001 |
Polycythemia Vera |
69 |
0.058 |
|
892 |
|
|
HYP741 |
Hyperparathyroidism 2 with Jaw Tumors |
53 |
0.058 |
|
893 |
|
|
THR123 |
Thrombotic Microangiopathy |
36 |
0.058 |
|
894 |
|
|
THR013 |
Thoracic Outlet Syndrome |
54 |
0.057 |
|
895 |
|
P
|
PMP001 |
Pemphigus |
54 |
0.057 |
|
896 |
|
|
PRS047 |
Prostatitis |
56 |
0.057 |
|
897 |
|
c
|
HYD046 |
Hydatidiform Mole, Recurrent, 1 |
59 |
0.057 |
|
898 |
|
c
|
ALZ056 |
Alzheimer Disease 3 |
57 |
0.057 |
|
899 |
|
|
STT009 |
Sutton Disease 2 |
30 |
0.057 |
|
900 |
|
|
PRP001 |
Propionic Acidemia |
65 |
0.057 |
|
901 |
|
|
TRN022 |
Transcobalamin Ii Deficiency |
45 |
0.057 |
|
902 |
|
|
HRP008 |
Herpes Simiae |
25 |
0.057 |
|
903 |
|
|
DBT084 |
Diabetes Mellitus, Ketosis-Prone |
60 |
0.057 |
|
904 |
|
|
CRT084 |
Creatinine Clearance Quantitative Trait Locus |
25 |
0.057 |
|
905 |
|
|
SPP011 |
Suppression of Tumorigenicity 12 |
59 |
0.057 |
|
906 |
|
c
|
PLM127 |
Pulmonary Hypertension, Primary, 3 |
34 |
0.057 |
|
907 |
|
|
ACR006 |
Aceruloplasminemia |
65 |
0.057 |
|
908 |
|
|
FND001 |
Fundus Albipunctatus |
60 |
0.057 |
|
909 |
|
|
MCR013 |
Microphthalmia |
57 |
0.057 |
|
910 |
|
P
|
NPH005 |
Nephronophthisis |
59 |
0.057 |
|
911 |
|
P
|
MMB011 |
Membranous Nephropathy |
50 |
0.057 |
|
912 |
|
c
|
PRX059 |
Peroxisome Biogenesis Disorder 1a |
56 |
0.057 |
|
913 |
|
P
|
AGG001 |
Aggressive Periodontitis |
50 |
0.056 |
|
914 |
|
|
APP008 |
Appendicitis |
61 |
0.056 |
|
915 |
|
|
MTC005 |
Mitochondrial Metabolism Disease |
49 |
0.056 |
|
916 |
|
c
|
GCH015 |
Gaucher Disease, Type I |
70 |
0.056 |
|
917 |
|
c
|
GLY008 |
Glycogen Storage Disease Ii |
70 |
0.056 |
|
918 |
|
|
PRT082 |
Preterm Premature Rupture of the Membranes |
54 |
0.056 |
|
919 |
|
|
EHL052 |
Ehlers-Danlos Syndrome, Vascular Type |
56 |
0.056 |
|
920 |
|
|
PHR003 |
Pharyngitis |
57 |
0.056 |
|
921 |
|
|
KRT006 |
Keratoconjunctivitis |
53 |
0.056 |
|
922 |
|
|
PRL032 |
Perlman Syndrome |
57 |
0.056 |
|
923 |
|
c
|
THR001 |
Thrombocytopenia Due to Platelet Alloimmunization |
53 |
0.056 |
|
924 |
|
|
SYN007 |
Synovitis |
54 |
0.056 |
|
925 |
|
|
PLC002 |
Plica Syndrome |
36 |
0.056 |
|
926 |
|
|
PRT018 |
Portal Vein Thrombosis |
50 |
0.056 |
|
927 |
|
|
ORL012 |
Oral Leukoplakia |
39 |
0.056 |
|
928 |
|
|
WST001 |
West Syndrome |
61 |
0.056 |
|
929 |
|
|
MTH056 |
Methylmalonic Aciduria and Homocystinuria, Cblf Type |
38 |
0.056 |
|
930 |
|
|
ANV001 |
Anovulation |
47 |
0.056 |
|
931 |
|
|
CHR005 |
Chorioamnionitis |
51 |
0.056 |
|
932 |
|
P
|
SCL057 |
Scoliosis, Isolated 1 |
41 |
0.055 |
|
933 |
|
|
LBR036 |
Leber Plus Disease |
66 |
0.055 |
|
934 |
|
|
LPD012 |
Lipoid Congenital Adrenal Hyperplasia |
70 |
0.055 |
|
935 |
|
|
THR100 |
Thrombocytopenic Purpura, Autoimmune |
60 |
0.055 |
|
936 |
|
c
|
USH036 |
Usher Syndrome, Type I |
60 |
0.055 |
|
937 |
|
P
|
OBS001 |
Obstructive Jaundice |
50 |
0.055 |
|
938 |
|
P
|
ASP006 |
Aspergillosis |
69 |
0.055 |
|
939 |
|
|
GRG001 |
Greig Cephalopolysyndactyly Syndrome |
66 |
0.055 |
|
940 |
|
|
CRT017 |
Cartilage Disease |
54 |
0.055 |
|
941 |
|
|
RDN001 |
Reading Disorder |
40 |
0.055 |
|
942 |
|
P
|
ANP001 |
Anaplastic Large Cell Lymphoma |
58 |
0.055 |
|
943 |
|
P
|
KRB001 |
Krabbe Disease |
69 |
0.055 |
|
944 |
|
|
HRT012 |
Heart Valve Disease |
53 |
0.055 |
|
945 |
|
P
|
TXP001 |
Toxoplasmosis |
60 |
0.055 |
|
946 |
|
|
GST092 |
Gastroesophageal Reflux |
67 |
0.055 |
|
947 |
|
P
|
SCL009 |
Sclerosing Cholangitis |
48 |
0.055 |
|
948 |
|
|
CMM004 |
Common Variable Immunodeficiency |
68 |
0.055 |
|
949 |
|
|
LPT006 |
Leptin Receptor Deficiency |
48 |
0.055 |
|
950 |
|
|
LYS012 |
Lysosomal Acid Lipase Deficiency |
65 |
0.055 |
|
951 |
|
|
CHL004 |
Cholelithiasis |
49 |
0.055 |
|
952 |
|
|
MLT092 |
Multicentric Carpotarsal Osteolysis Syndrome |
65 |
0.055 |
|
953 |
|
|
KRT013 |
Keratolytic Winter Erythema |
46 |
0.055 |
|
954 |
|
|
HDN002 |
Head Injury |
46 |
0.055 |
|
955 |
|
|
SXL003 |
Sexual Disorder |
47 |
0.055 |
|
956 |
|
|
GST020 |
Gastric Antral Vascular Ectasia |
41 |
0.055 |
|
957 |
|
|
DRY001 |
Dry Eye Syndrome |
47 |
0.054 |
|
958 |
|
|
TYP007 |
Typhoid Fever |
63 |
0.054 |
|
959 |
|
P
|
MTR004 |
Maturity-Onset Diabetes of the Young |
65 |
0.054 |
|
960 |
|
|
ETN001 |
Eating Disorder |
60 |
0.054 |
|
961 |
|
|
DRR014 |
Darier-White Disease |
60 |
0.054 |
|
962 |
|
c
|
DSB006 |
Desbuquois Dysplasia 1 |
48 |
0.054 |
|
963 |
|
|
KWS002 |
Kawasaki Disease |
65 |
0.054 |
|
964 |
|
|
GLL008 |
Gilles De La Tourette Syndrome |
66 |
0.054 |
|
965 |
|
|
FCT034 |
Factor V and Factor Viii, Combined Deficiency of, 2 |
41 |
0.054 |
|
966 |
|
|
CYS013 |
Cystinuria |
63 |
0.054 |
|
967 |
|
|
MLT118 |
Multiple Acyl-Coa Dehydrogenase Deficiency |
68 |
0.054 |
|
968 |
|
|
CLR030 |
Clear Cell Renal Cell Carcinoma |
53 |
0.054 |
|
969 |
|
|
PLG002 |
Plague |
63 |
0.054 |
|
970 |
|
|
GRN017 |
Granulocytopenia |
44 |
0.054 |
|
971 |
|
|
ATX010 |
Ataxia Neuropathy Spectrum |
34 |
0.054 |
|
972 |
|
|
SCH012 |
Schizoaffective Disorder |
50 |
0.054 |
|
973 |
|
c
|
PSD114 |
Pseudohypoaldosteronism, Type I, Autosomal Recessive |
59 |
0.054 |
|
974 |
|
|
MYC006 |
Mycosis Fungoides |
66 |
0.054 |
|
975 |
|
|
CHL109 |
Childhood Apraxia of Speech |
44 |
0.054 |
|
976 |
|
|
INT075 |
Intracranial Hypertension |
53 |
0.053 |
|
977 |
|
|
THR016 |
Thrombophlebitis |
51 |
0.053 |
|
978 |
|
c
|
SZR007 |
Seizures, Benign Familial Infantile, 3 |
42 |
0.053 |
|
979 |
|
|
SMT004 |
Smith-Lemli-Opitz Syndrome |
70 |
0.053 |
|
980 |
|
|
ATN004 |
Autonomic Neuropathy |
45 |
0.053 |
|
981 |
|
|
PST028 |
Post-Traumatic Stress Disorder |
58 |
0.053 |
|
982 |
|
P
|
RTT002 |
Rett Syndrome |
80 |
0.053 |
|
983 |
|
|
OBS002 |
Obsessive-Compulsive Disorder |
68 |
0.053 |
|
984 |
|
|
INT303 |
Intracranial Hypertension, Idiopathic |
57 |
0.053 |
|
985 |
|
P
|
PGT001 |
Paget's Disease of Bone |
58 |
0.053 |
|
986 |
|
|
LYM040 |
Lymphoblastic Lymphoma |
54 |
0.053 |
|
987 |
|
|
INT088 |
Intrinsic Factor Deficiency |
34 |
0.053 |
|
988 |
|
c
|
ATS307 |
Autosomal Recessive Cerebellar Ataxia |
42 |
0.053 |
|
989 |
|
P
|
ALG028 |
Alagille Syndrome 1 |
73 |
0.053 |
|
990 |
|
|
SFT003 |
Soft Tissue Sarcoma |
56 |
0.053 |
|
991 |
|
|
NRP051 |
Neuropathy, Hereditary, with Liability to Pressure Palsies |
59 |
0.053 |
|
992 |
|
|
HPT022 |
Hepatoblastoma |
56 |
0.053 |
|
993 |
|
c
|
MYS033 |
Miyoshi Muscular Dystrophy 1 |
56 |
0.053 |
|
994 |
|
|
LWC001 |
Low Compliance Bladder |
43 |
0.053 |
|
995 |
|
|
RSC001 |
Rosacea |
54 |
0.053 |
|
996 |
|
c
|
MNN043 |
Meningioma, Familial |
74 |
0.053 |
|
997 |
|
c
|
ACT004 |
Acute Diarrhea |
39 |
0.052 |
|
998 |
|
c
|
HNT011 |
Huntington Disease-Like 3 |
38 |
0.052 |
|
999 |
|
|
BTT001 |
Bietti Crystalline Corneoretinal Dystrophy |
52 |
0.052 |
|
1000 |
|
c
|
CHL132 |
Cholestasis, Progressive Familial Intrahepatic, 1 |
57 |
0.052 |
|
1001 |
|
P
|
PLY041 |
Polymyositis |
57 |
0.052 |
|
1002 |
|
P
|
LRY044 |
Larynx Cancer |
55 |
0.052 |
|
1003 |
|
c
|
MST023 |
Mesothelioma, Malignant |
57 |
0.052 |
|
1004 |
|
c
|
DPH024 |
Diaphragmatic Hernia, Congenital |
63 |
0.052 |
|
1005 |
|
|
CHR103 |
Charge Syndrome |
67 |
0.052 |
|
1006 |
|
|
SPR004 |
Supravalvular Aortic Stenosis |
58 |
0.052 |
|
1007 |
|
|
GLM044 |
Glomerular Disease |
37 |
0.052 |
|
1008 |
|
c
|
OPT053 |
Optic Atrophy 1 |
63 |
0.052 |
|
1009 |
|
P
|
BRN022 |
Bronchiectasis |
59 |
0.052 |
|
1010 |
|
c
|
SYS043 |
Systemic Lupus Erythematosus 1 |
38 |
0.052 |
|
1011 |
|
|
AYM001 |
Ayme-Gripp Syndrome |
57 |
0.052 |
|
1012 |
|
P
|
KRT007 |
Keratoconus |
50 |
0.052 |
|
1013 |
|
P
|
TRC031 |
Trichorhinophalangeal Syndrome |
40 |
0.052 |
|
1014 |
|
|
GLC042 |
Glucocorticoid Deficiency 1 |
53 |
0.052 |
|
1015 |
|
|
ADN011 |
Adenoid Cystic Carcinoma |
70 |
0.052 |
|
1016 |
|
|
MYL031 |
Myeloproliferative Neoplasm |
66 |
0.052 |
|
1017 |
|
|
HMT002 |
Hematologic Cancer |
62 |
0.052 |
|
1018 |
|
|
ACT064 |
Acute Necrotizing Encephalitis |
33 |
0.052 |
|
1019 |
|
|
BLD137 |
Blood Group--Ahonen |
16 |
0.052 |
|
1020 |
|
P
|
MYS003 |
Myasthenia Gravis |
68 |
0.052 |
|
1021 |
|
P
|
SML001 |
Small Cell Carcinoma |
52 |
0.052 |
|
1022 |
|
c
|
ATS347 |
Autosomal Dominant Polycystic Kidney Disease |
65 |
0.052 |
|
1023 |
|
c
|
HYP794 |
Hyperoxaluria, Primary, Type I |
63 |
0.052 |
|
1024 |
|
|
EXC002 |
Exocrine Pancreatic Insufficiency |
42 |
0.052 |
|
1025 |
|
|
FML026 |
Familial Lipoprotein Lipase Deficiency |
51 |
0.052 |
|
1026 |
|
c
|
WLM018 |
Wilms Tumor 5 |
61 |
0.052 |
|
1027 |
|
|
CHN055 |
Chanarin-Dorfman Syndrome |
61 |
0.052 |
|
1028 |
|
c
|
HNT004 |
Huntington Disease-Like 2 |
50 |
0.052 |
|
1029 |
|
|
INF034 |
Infective Endocarditis |
53 |
0.052 |
|
1030 |
|
c
|
GZP005 |
Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 |
44 |
0.052 |
|
1031 |
|
|
CHR661 |
Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction |
48 |
0.052 |
|
1032 |
|
|
ACT084 |
Acute Stress Disorder |
47 |
0.052 |
|
1033 |
|
|
HMR039 |
Hemorrhage, Intracerebral |
57 |
0.051 |
|
1034 |
|
|
MLT157 |
Multiple System Atrophy 1 |
70 |
0.051 |
|
1035 |
|
|
AST006 |
Astigmatism |
47 |
0.051 |
|
1036 |
|
P
|
DRM010 |
Dermatomyositis |
61 |
0.051 |
|
1037 |
|
|
PTH003 |
Pathologic Nystagmus |
52 |
0.051 |
|
1038 |
|
P
|
TCD001 |
Tic Disorder |
53 |
0.051 |
|
1039 |
|
|
YLL002 |
Yellow Fever |
61 |
0.051 |
|
1040 |
|
|
FBR012 |
Fabry Disease |
72 |
0.051 |
|
1041 |
|
|
OVR029 |
Ovarian Hyperstimulation Syndrome |
64 |
0.051 |
|
1042 |
|
|
URT010 |
Ureteral Obstruction |
45 |
0.051 |
|
1043 |
|
P
|
PRN023 |
Prion Disease |
57 |
0.051 |
|
1044 |
|
|
PRS034 |
Parasitic Helminthiasis Infectious Disease |
50 |
0.051 |
|
1045 |
|
|
MTC027 |
Mitochondrial Trifunctional Protein Deficiency |
58 |
0.051 |
|
1046 |
|
|
TNS005 |
Tonsillitis |
57 |
0.051 |
|
1047 |
|
P
|
THY023 |
Thymoma |
65 |
0.051 |
|
1048 |
|
c
|
THY107 |
Thymoma, Familial |
52 |
0.051 |
|
1049 |
|
|
MCR018 |
Microcytic Anemia |
47 |
0.051 |
|
1050 |
|
|
CHL152 |
Childhood Acute Lymphocytic Leukemia |
44 |
0.051 |
|
1051 |
|
|
RSP019 |
Respiratory Distress Syndrome in Premature Infants |
58 |
0.051 |
|
1052 |
|
P
|
PRG092 |
Pregnancy Loss, Recurrent 1 |
40 |
0.051 |
|
1053 |
|
|
SPT004 |
Septic Arthritis |
58 |
0.051 |
|
1054 |
|
|
HYP348 |
Hyperglycinuria |
41 |
0.051 |
|
1055 |
|
|
CYT008 |
Cytomegalovirus Infection |
57 |
0.051 |
|
1056 |
|
c
|
MCL013 |
Mucolipidosis Iv |
66 |
0.051 |
|
1057 |
|
P
|
MYC033 |
Myoclonus |
46 |
0.051 |
|
1058 |
|
|
RFR003 |
Refractive Error |
43 |
0.051 |
|
1059 |
|
P
|
DNT020 |
Dent Disease 1 |
62 |
0.051 |
|
1060 |
|
|
ARG004 |
Argyria |
27 |
0.051 |
|
1061 |
|
|
NRN004 |
Neuroendocrine Tumor |
55 |
0.051 |
|
1062 |
|
P
|
STR020 |
Strabismus |
55 |
0.051 |
|
1063 |
|
|
GLC098 |
Glaucoma-Related Pigment Dispersion Syndrome |
45 |
0.051 |
|
1064 |
|
|
PLL001 |
Pallister-Hall Syndrome |
64 |
0.050 |
|
1065 |
|
P
|
GLC113 |
Galactosemia I |
64 |
0.050 |
|
1066 |
|
|
ALP097 |
Alopecia Universalis Congenita |
59 |
0.050 |
|
1067 |
|
|
TRT001 |
Teratocarcinoma |
45 |
0.050 |
|
1068 |
|
|
SPS019 |
Spastic Paraparesis |
38 |
0.050 |
|