# |
|
Family |
MCID |
Name |
MIFTS |
Score |
1 |
|
P
|
FTL069 |
Fetal Akinesia Deformation Sequence 1 |
63 |
34.333 |
|
2 |
|
c
|
ERL029 |
Early-Onset, Autosomal Dominant Alzheimer Disease |
59 |
19.896 |
|
3 |
|
P
|
ALZ034 |
Alzheimer Disease |
87 |
15.045 |
|
4 |
|
|
MLT118 |
Multiple Acyl-Coa Dehydrogenase Deficiency |
65 |
14.550 |
|
5 |
|
c
|
FTL070 |
Fetal Akinesia Deformation Sequence 2 |
36 |
11.689 |
|
6 |
|
c
|
FTL071 |
Fetal Akinesia Deformation Sequence 3 |
30 |
6.602 |
|
7 |
|
|
RBF001 |
Riboflavin Deficiency |
49 |
5.732 |
|
8 |
|
P
|
CHR012 |
Chronic Granulomatous Disease |
69 |
4.861 |
|
9 |
|
|
HLX001 |
Helix Syndrome |
48 |
4.786 |
|
10 |
|
|
DRM006 |
Dermatitis |
62 |
4.772 |
|
11 |
|
|
CNG506 |
Congenital Amyoplasia |
27 |
4.604 |
|
12 |
|
|
DWN001 |
Down Syndrome |
70 |
4.480 |
|
13 |
|
P
|
NRB001 |
Neuroblastoma |
66 |
4.303 |
|
14 |
|
|
ETN001 |
Eating Disorder |
59 |
4.063 |
|
15 |
|
P
|
MYP004 |
Myopathy |
67 |
4.061 |
|
16 |
|
|
ACY011 |
Acyl-Coa Dehydrogenase Deficiency |
30 |
4.010 |
|
17 |
|
P
|
DMN002 |
Dementia |
66 |
3.886 |
|
18 |
|
c
|
CRB172 |
Cerebral Amyloid Angiopathy, Cst3-Related |
65 |
3.683 |
|
19 |
|
P
|
AMY004 |
Amyloidosis |
70 |
3.657 |
|
20 |
|
P
|
MYC033 |
Myoclonus |
47 |
3.657 |
|
21 |
|
P
|
DST002 |
Distal Arthrogryposis |
65 |
3.425 |
|
22 |
|
c
|
ALZ056 |
Alzheimer Disease 3 |
55 |
3.351 |
|
23 |
|
|
MLD018 |
Mild Cognitive Impairment |
48 |
3.262 |
|
24 |
|
|
CHR178 |
Chromosomal Triplication |
34 |
3.219 |
|
25 |
|
P
|
DRM053 |
Dermatitis, Atopic |
65 |
3.205 |
|
26 |
|
|
CLF027 |
Cleft Palate, Isolated |
64 |
3.196 |
|
27 |
|
P
|
MJR001 |
Major Depressive Disorder |
68 |
3.042 |
|
28 |
|
|
MNT002 |
Mental Depression |
57 |
3.009 |
|
29 |
|
|
AGN016 |
Aging |
54 |
2.912 |
|
30 |
|
P
|
CNG001 |
Congenital Myasthenic Syndrome |
68 |
2.906 |
|
31 |
|
|
IRN002 |
Iron Metabolism Disease |
57 |
2.873 |
|
32 |
|
|
SPS019 |
Spastic Paraparesis |
38 |
2.871 |
|
33 |
|
|
PRT037 |
Pertussis |
65 |
2.871 |
|
34 |
|
|
ATX038 |
Ataxia and Polyneuropathy, Adult-Onset |
46 |
2.834 |
|
35 |
|
P
|
MTH007 |
Methemoglobinemia |
46 |
2.763 |
|
36 |
|
|
ATS010 |
Autosomal Recessive Disease |
42 |
2.753 |
|
37 |
|
|
FRN006 |
Frontotemporal Dementia |
68 |
2.751 |
|
38 |
|
|
SKN016 |
Skin Disease |
63 |
2.726 |
|
39 |
|
|
ART140 |
Arteries, Anomalies of |
53 |
2.705 |
|
40 |
|
|
LPP008 |
Lipoprotein Quantitative Trait Locus |
65 |
2.705 |
|
41 |
|
|
DPR016 |
Depression |
65 |
2.688 |
|
42 |
|
c
|
ALZ063 |
Alzheimer's Disease 1 |
31 |
2.628 |
|
43 |
|
|
APH002 |
Aphasia |
56 |
2.610 |
|
44 |
|
c
|
MJR022 |
Major Affective Disorder 8 |
38 |
2.569 |
|
45 |
|
c
|
MJR024 |
Major Affective Disorder 9 |
41 |
2.569 |
|
46 |
|
P
|
PRK039 |
Parkinsonism |
55 |
2.569 |
|
47 |
|
P
|
BPL003 |
Bipolar Disorder |
56 |
2.569 |
|
48 |
|
|
PLY012 |
Polyhydramnios |
46 |
2.560 |
|
49 |
|
|
NNL005 |
Non-Alcoholic Fatty Liver Disease |
63 |
2.534 |
|
50 |
|
|
ISC004 |
Ischemia |
61 |
2.444 |
|
51 |
|
|
NRL016 |
Neural Tube Defects |
81 |
2.433 |
|
52 |
|
|
HYP266 |
Hypoxia |
57 |
2.433 |
|
53 |
|
c
|
INH020 |
Inherited Metabolic Disorder |
48 |
2.400 |
|
54 |
|
|
RPD005 |
Rapidly Involuting Congenital Hemangioma |
46 |
2.388 |
|
55 |
|
c
|
DLT002 |
Dilated Cardiomyopathy |
78 |
2.388 |
|
56 |
|
|
LPD008 |
Lipid Metabolism Disorder |
62 |
2.337 |
|
57 |
|
|
CHL014 |
Cholera |
62 |
2.309 |
|
58 |
|
|
CHG001 |
Chagas Disease |
66 |
2.283 |
|
59 |
|
P
|
MYC008 |
Myocarditis |
59 |
2.283 |
|
60 |
|
c
|
2HY001 |
2-Hydroxyglutaric Aciduria |
38 |
2.262 |
|
61 |
|
P
|
ATT013 |
Attention Deficit-Hyperactivity Disorder |
64 |
2.262 |
|
62 |
|
P
|
CTR002 |
Cataract |
60 |
2.228 |
|
63 |
|
|
HMC014 |
Homocysteinemia |
52 |
2.214 |
|
64 |
|
P
|
HNT016 |
Huntington Disease |
73 |
2.214 |
|
65 |
|
|
CRN048 |
Craniofacial-Deafness-Hand Syndrome |
52 |
2.214 |
|
66 |
|
|
47X002 |
47,xyy |
48 |
2.214 |
|
67 |
|
P
|
SYP003 |
Syphilis |
59 |
2.214 |
|
68 |
|
|
HYP060 |
Hyperinsulinism |
54 |
2.214 |
|
69 |
|
|
FTT001 |
Fatty Liver Disease |
62 |
2.171 |
|
70 |
|
P
|
ENC018 |
Encephalopathy |
62 |
2.171 |
|
71 |
|
c
|
BDY010 |
Body Mass Index Quantitative Trait Locus 4 |
46 |
2.164 |
|
72 |
|
c
|
BDY011 |
Body Mass Index Quantitative Trait Locus 10 |
45 |
2.164 |
|
73 |
|
c
|
BDY005 |
Body Mass Index Quantitative Trait Locus 9 |
47 |
2.164 |
|
74 |
|
c
|
BDY012 |
Body Mass Index Quantitative Trait Locus 7 |
44 |
2.164 |
|
75 |
|
P
|
BDY004 |
Body Mass Index Quantitative Trait Locus 11 |
83 |
2.164 |
|
76 |
|
c
|
BDY006 |
Body Mass Index Quantitative Trait Locus 8 |
44 |
2.164 |
|
77 |
|
c
|
BDY017 |
Body Mass Index Quantitative Trait Locus 14 |
45 |
2.164 |
|
78 |
|
c
|
BDY020 |
Body Mass Index Quantitative Trait Locus 19 |
52 |
2.164 |
|
79 |
|
c
|
BDY015 |
Body Mass Index Quantitative Trait Locus 12 |
46 |
2.164 |
|
80 |
|
c
|
BDY019 |
Body Mass Index Quantitative Trait Locus 18 |
47 |
2.164 |
|
81 |
|
|
PPL052 |
Papillomatosis, Confluent and Reticulated |
34 |
2.112 |
|
82 |
|
c
|
CNG223 |
Congenital Methemoglobinemia |
39 |
2.112 |
|
83 |
|
P
|
PSR002 |
Psoriasis |
63 |
2.111 |
|
84 |
|
|
PST011 |
Pustulosis of Palm and Sole |
52 |
2.111 |
|
85 |
|
|
IRR002 |
Irritable Bowel Syndrome |
65 |
2.085 |
|
86 |
|
|
BCK006 |
Back Pain |
47 |
2.076 |
|
87 |
|
|
MLT163 |
Multiple Pterygium Syndrome, Escobar Variant |
64 |
2.068 |
|
88 |
|
c
|
ATS307 |
Autosomal Recessive Cerebellar Ataxia |
39 |
2.059 |
|
89 |
|
|
ARG004 |
Argyria |
26 |
2.059 |
|
90 |
|
|
GLB002 |
Glioblastoma |
67 |
2.059 |
|
91 |
|
|
RST011 |
Restrictive Dermopathy, Lethal |
51 |
2.059 |
|
92 |
|
c
|
L2H001 |
L-2-Hydroxyglutaric Aciduria |
49 |
2.004 |
|
93 |
|
|
LPD042 |
Lipid Storage Myopathy Due to Flavin Adenine Dinucleotide Synthetase Deficiency |
22 |
2.004 |
|
94 |
|
P
|
MSC003 |
Muscular Atrophy |
52 |
2.004 |
|
95 |
|
|
ALL014 |
Allergic Encephalomyelitis |
34 |
2.004 |
|
96 |
|
|
ALL029 |
Allergic Disease |
59 |
1.987 |
|
97 |
|
c
|
ATR087 |
Atrial Standstill 1 |
74 |
1.982 |
|
98 |
|
|
CNG065 |
Congenital Contractures |
25 |
1.982 |
|
99 |
|
|
MTB004 |
Metabolic Acidosis |
48 |
1.946 |
|
100 |
|
P
|
FTT008 |
Fatty Liver Disease, Nonalcoholic 1 |
48 |
1.946 |
|
101 |
|
|
MLR009 |
Miliaria |
33 |
1.946 |
|
102 |
|
|
GLC009 |
Glucosephosphate Dehydrogenase Deficiency |
53 |
1.946 |
|
103 |
|
|
MLR001 |
Miliaria Rubra |
32 |
1.946 |
|
104 |
|
|
NRN004 |
Neuroendocrine Tumor |
59 |
1.946 |
|
105 |
|
|
CRC006 |
Carcinoid Syndrome |
55 |
1.946 |
|
106 |
|
c
|
ALZ054 |
Alzheimer Disease 4 |
43 |
1.945 |
|
107 |
|
|
TRM010 |
Traumatic Brain Injury |
51 |
1.945 |
|
108 |
|
|
PRN009 |
Paranoid Schizophrenia |
49 |
1.945 |
|
109 |
|
P
|
AST005 |
Asthma |
76 |
1.913 |
|
110 |
|
|
CND006 |
Candida Glabrata |
30 |
1.913 |
|
111 |
|
|
MLT134 |
Multiple Pterygium Syndrome, Lethal Type |
56 |
1.902 |
|
112 |
|
|
APR001 |
Apraxia |
52 |
1.902 |
|
113 |
|
P
|
BRS053 |
Breast Fibroadenoma |
49 |
1.902 |
|
114 |
|
|
KRT009 |
Keratosis |
53 |
1.902 |
|
115 |
|
|
ANR007 |
Anorexia Nervosa |
60 |
1.859 |
|
116 |
|
P
|
HYP069 |
Hyperparathyroidism |
62 |
1.859 |
|
117 |
|
|
STN013 |
Stenotrophomonas Maltophilia Infection |
26 |
1.824 |
|
118 |
|
|
CYN002 |
Cyanosis, Transient Neonatal |
43 |
1.824 |
|
119 |
|
|
ANT003 |
Antley-Bixler Syndrome |
49 |
1.824 |
|
120 |
|
P
|
HMC002 |
Homocystinuria |
53 |
1.824 |
|
121 |
|
c
|
ALZ049 |
Alzheimer Disease 2 |
48 |
1.768 |
|
122 |
|
c
|
AMY091 |
Amyotrophic Lateral Sclerosis 1 |
88 |
1.768 |
|
123 |
|
|
ECT041 |
Ectodermal Dysplasia-Syndactyly Syndrome 2 |
36 |
1.768 |
|
124 |
|
P
|
LTR001 |
Lateral Sclerosis |
58 |
1.768 |
|
125 |
|
P
|
PRS040 |
Prostate Cancer |
95 |
1.759 |
|
126 |
|
|
PRT038 |
Protein-Energy Malnutrition |
53 |
1.758 |
|
127 |
|
|
CYS002 |
Cystic Lymphangioma |
45 |
1.758 |
|
128 |
|
|
HYP056 |
Hypoglycemia |
65 |
1.758 |
|
129 |
|
c
|
FTL072 |
Fetal Akinesia Deformation Sequence 4 |
37 |
1.749 |
|
130 |
|
|
VRG001 |
Variegate Porphyria |
56 |
1.721 |
|
131 |
|
|
TCK004 |
Tick Infestation |
30 |
1.721 |
|
132 |
|
|
PSY004 |
Psychotic Disorder |
66 |
1.721 |
|
133 |
|
P
|
PRP029 |
Porphyria |
60 |
1.721 |
|
134 |
|
c
|
MCR115 |
Microvascular Complications of Diabetes 5 |
65 |
1.689 |
|
135 |
|
c
|
TYP009 |
Type 2 Diabetes Mellitus |
92 |
1.689 |
|
136 |
|
|
BCT022 |
Bacterial Infectious Disease |
56 |
1.689 |
|
137 |
|
c
|
ACT076 |
Acute Myocarditis |
47 |
1.689 |
|
138 |
|
|
END086 |
End Stage Renal Disease |
52 |
1.689 |
|
139 |
|
P
|
SPN046 |
Spinal Muscular Atrophy |
63 |
1.689 |
|
140 |
|
P
|
SCL018 |
Scoliosis |
57 |
1.673 |
|
141 |
|
|
ADN018 |
Adenoma |
59 |
1.672 |
|
142 |
|
|
VSC002 |
Vascular Dementia |
60 |
1.672 |
|
143 |
|
|
BRN071 |
Brain Injury |
50 |
1.672 |
|
144 |
|
|
MSC193 |
Muscular Lipidosis |
22 |
1.622 |
|
145 |
|
|
PST028 |
Post-Traumatic Stress Disorder |
59 |
1.622 |
|
146 |
|
|
ACY010 |
Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of |
64 |
1.615 |
|
147 |
|
P
|
TRM004 |
Trimethylaminuria |
45 |
1.615 |
|
148 |
|
|
CRY035 |
Cryptorchidism, Unilateral or Bilateral |
58 |
1.615 |
|
149 |
|
P
|
DBT009 |
Diabetes Mellitus |
67 |
1.615 |
|
150 |
|
P
|
EPL164 |
Epilepsy |
68 |
1.615 |
|
151 |
|
|
DNT012 |
Dental Caries |
53 |
1.615 |
|
152 |
|
|
INS024 |
Insulin-Like Growth Factor I |
78 |
1.571 |
|
153 |
|
P
|
MYC084 |
Mycobacterium Tuberculosis 1 |
68 |
1.571 |
|
154 |
|
P
|
BRS047 |
Breast Cancer |
98 |
1.571 |
|
155 |
|
|
TRD008 |
Triiodothyronine Receptor Auxiliary Protein |
33 |
1.571 |
|
156 |
|
P
|
AGN002 |
Agnosia |
54 |
1.571 |
|
157 |
|
P
|
HYP265 |
Hypotonia |
42 |
1.571 |
|
158 |
|
P
|
INF037 |
Inflammatory Bowel Disease |
53 |
1.535 |
|
159 |
|
|
AMN003 |
Amnestic Disorder |
54 |
1.535 |
|
160 |
|
|
STM007 |
Stomatitis |
54 |
1.535 |
|
161 |
|
P
|
THL005 |
Thalassemia |
56 |
1.518 |
|
162 |
|
P
|
BRW001 |
Brown-Vialetto-Van Laere Syndrome |
50 |
1.518 |
|
163 |
|
|
MNC011 |
Minicore Myopathy with External Ophthalmoplegia |
37 |
1.518 |
|
164 |
|
|
CRH001 |
Crohn's Disease |
80 |
1.518 |
|
165 |
|
|
FLL031 |
Follicular Adenoma |
40 |
1.518 |
|
166 |
|
|
NRM005 |
Neuromuscular Disease |
63 |
1.518 |
|
167 |
|
P
|
LYM118 |
Lymphoma |
67 |
1.499 |
|
168 |
|
|
TCL023 |
T-Cell Lymphoma, Subcutaneous Panniculitis-Like |
50 |
1.499 |
|
169 |
|
|
LYM019 |
Lymphosarcoma |
46 |
1.499 |
|
170 |
|
P
|
RCT021 |
Rectum Cancer |
54 |
1.468 |
|
171 |
|
P
|
SCH015 |
Schizophrenia |
74 |
1.462 |
|
172 |
|
|
HLT001 |
Holt-Oram Syndrome |
66 |
1.462 |
|
173 |
|
c
|
VRL010 |
Viral Hepatitis |
53 |
1.462 |
|
174 |
|
|
GTR002 |
Goiter |
53 |
1.462 |
|
175 |
|
P
|
CRD246 |
Cardiovascular System Disease |
56 |
1.462 |
|
176 |
|
P
|
ATS364 |
Autism |
69 |
1.448 |
|
177 |
|
|
CVD001 |
Covid-19 |
57 |
1.448 |
|
178 |
|
|
CVT001 |
Cavitary Optic Disc Anomalies |
37 |
1.448 |
|
179 |
|
|
THM002 |
Thiamine-Responsive Megaloblastic Anemia Syndrome |
50 |
1.448 |
|
180 |
|
|
HMC041 |
Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity |
48 |
1.448 |
|
181 |
|
|
HYP748 |
Hypertelorism |
46 |
1.448 |
|
182 |
|
c
|
CRB175 |
Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 |
70 |
1.448 |
|
183 |
|
|
ALP089 |
Alopecia, Psychomotor Epilepsy, Pyorrhea, and Mental Subnormality |
26 |
1.448 |
|
184 |
|
|
THY029 |
Thyroid Carcinoma |
51 |
1.448 |
|
185 |
|
|
CRV002 |
Cervix Uteri Carcinoma in Situ |
47 |
1.448 |
|
186 |
|
|
GRD001 |
Giardiasis |
46 |
1.448 |
|
187 |
|
|
CRV045 |
Cervical Intraepithelial Neoplasia |
39 |
1.448 |
|
|
189 |
|
|
EPD002 |
Epidermolytic Hyperkeratosis |
56 |
1.405 |
|
190 |
|
|
HMR039 |
Hemorrhage, Intracerebral |
57 |
1.405 |
|
191 |
|
P
|
ATS411 |
Autosomal Dominant Epidermolytic Ichthyosis |
36 |
1.405 |
|
192 |
|
|
CYT014 |
Cytochrome P450 Oxidoreductase Deficiency |
34 |
1.405 |
|
193 |
|
|
48X005 |
48,xyyy |
39 |
1.405 |
|
194 |
|
P
|
CRB088 |
Cerebral Atrophy |
33 |
1.405 |
|
195 |
|
|
PSD088 |
Pseudobulbar Affect |
33 |
1.405 |
|
196 |
|
P
|
CRN300 |
Coronary Heart Disease 1 |
73 |
1.353 |
|
197 |
|
P
|
MYS003 |
Myasthenia Gravis |
68 |
1.353 |
|
198 |
|
|
HYD038 |
Hydrops Fetalis, Nonimmune |
59 |
1.353 |
|
199 |
|
|
PRT251 |
Proteinuria, Chronic Benign |
57 |
1.353 |
|
200 |
|
|
RSP021 |
Respiratory Allergy |
41 |
1.353 |
|
201 |
|
|
NPH009 |
Nephrolithiasis |
54 |
1.353 |
|
202 |
|
|
PTH002 |
Pathological Gambling |
48 |
1.353 |
|
203 |
|
|
PRM209 |
Primary Trimethylaminuria |
19 |
1.353 |
|
204 |
|
P
|
SPR120 |
Supranuclear Palsy, Progressive, 1 |
69 |
1.345 |
|
205 |
|
P
|
KLZ004 |
Kala-Azar 1 |
41 |
1.345 |
|
206 |
|
|
AVN001 |
Avian Influenza |
61 |
1.345 |
|
207 |
|
|
LSH001 |
Leishmaniasis |
64 |
1.345 |
|
208 |
|
|
DSS008 |
Disease of Mental Health |
74 |
1.345 |
|
209 |
|
P
|
HYP076 |
Hyperthyroidism |
53 |
1.345 |
|
210 |
|
|
ORL011 |
Oral Cancer |
60 |
1.345 |
|
211 |
|
|
ALP042 |
Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity |
65 |
1.339 |
|
212 |
|
|
BLM002 |
Bulimia Nervosa |
57 |
1.283 |
|
213 |
|
|
DFC004 |
Deficiency Anemia |
74 |
1.283 |
|
214 |
|
|
ORL015 |
Oral Squamous Cell Carcinoma |
43 |
1.283 |
|
215 |
|
P
|
RTN016 |
Retinal Degeneration |
52 |
1.283 |
|
216 |
|
P
|
THY032 |
Thyroiditis |
57 |
1.283 |
|
217 |
|
|
MLT028 |
Multiminicore Disease |
43 |
1.283 |
|
218 |
|
|
CRT033 |
Corticobasal Degeneration |
47 |
1.283 |
|
219 |
|
|
DBT006 |
Diabetic Macular Edema |
48 |
1.260 |
|
220 |
|
|
MCL006 |
Macular Retinal Edema |
57 |
1.260 |
|
221 |
|
|
CNG538 |
Congenital Arthrogryposis with Anterior Horn Cell Disease |
32 |
1.247 |
|
222 |
|
P
|
MTR004 |
Maturity-Onset Diabetes of the Young |
68 |
1.244 |
|
223 |
|
P
|
CLR023 |
Colorectal Cancer |
100 |
1.244 |
|
224 |
|
|
ANG054 |
Angina Pectoris |
66 |
1.244 |
|
225 |
|
P
|
GST053 |
Gastric Cancer |
83 |
1.244 |
|
226 |
|
|
PHN003 |
Phenylketonuria |
76 |
1.244 |
|
227 |
|
|
NPH091 |
Nephrolithiasis, Calcium Oxalate |
61 |
1.244 |
|
228 |
|
P
|
PRS038 |
Personality Disorder |
65 |
1.244 |
|
229 |
|
P
|
LVR013 |
Liver Disease |
69 |
1.244 |
|
230 |
|
|
FDL002 |
Food Allergy |
47 |
1.244 |
|
231 |
|
|
MLT010 |
Multiple Personality Disorder |
29 |
1.244 |
|
232 |
|
|
URN010 |
Urinary Tract Obstruction |
55 |
1.244 |
|
233 |
|
|
KWS001 |
Kwashiorkor |
45 |
1.244 |
|
234 |
|
|
LPT001 |
Leptospirosis |
66 |
1.244 |
|
235 |
|
|
HYP014 |
Hyperuricemia |
51 |
1.244 |
|
236 |
|
|
MTC015 |
Mitochondrial Dna-Associated Leigh Syndrome and Narp |
17 |
1.244 |
|
237 |
|
|
NCL011 |
Nuclear Gene-Encoded Leigh Syndrome Spectrum |
21 |
1.244 |
|
238 |
|
c
|
HMC039 |
Hemochromatosis, Type 1 |
73 |
1.217 |
|
239 |
|
|
ATH013 |
Atherosclerosis Susceptibility |
63 |
1.217 |
|
240 |
|
|
NND010 |
Nondisjunction |
34 |
1.217 |
|
241 |
|
c
|
LKM061 |
Leukemia, Acute Myeloid |
83 |
1.217 |
|
242 |
|
c
|
MCL042 |
Macular Degeneration, Age-Related, 1 |
85 |
1.217 |
|
243 |
|
|
SNL009 |
Senile Plaque Formation |
29 |
1.217 |
|
244 |
|
c
|
HYP836 |
Hypercholesterolemia, Familial, 1 |
73 |
1.217 |
|
245 |
|
|
HML010 |
Hemolytic Anemia Due to Glutathione Reductase Deficiency |
21 |
1.217 |
|
246 |
|
P
|
HYP086 |
Hypothyroidism |
69 |
1.217 |
|
247 |
|
|
HMG005 |
Hemoglobinopathy |
56 |
1.217 |
|
248 |
|
|
IRN001 |
Iron Deficiency Anemia |
58 |
1.217 |
|
249 |
|
P
|
HYD006 |
Hydrocephalus |
61 |
1.217 |
|
250 |
|
c
|
PRM005 |
Primary Hyperparathyroidism |
59 |
1.217 |
|
251 |
|
P
|
NML001 |
Nemaline Myopathy |
48 |
1.217 |
|
252 |
|
P
|
CLC063 |
Celiac Disease 1 |
66 |
1.171 |
|
253 |
|
|
CHR081 |
Choroideremia |
58 |
1.171 |
|
254 |
|
c
|
TYP008 |
Type 1 Diabetes Mellitus |
70 |
1.147 |
|
255 |
|
|
WRT005 |
Warty Dyskeratoma |
16 |
1.147 |
|
256 |
|
|
MTH047 |
Methanol Poisoning |
37 |
1.147 |
|
257 |
|
c
|
MYS052 |
Myasthenic Syndrome, Congenital, 10 |
43 |
1.147 |
|
258 |
|
|
ACY009 |
Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of |
59 |
1.147 |
|
259 |
|
|
ANX010 |
Anxiety |
70 |
1.147 |
|
260 |
|
|
PRN011 |
Pernicious Anemia |
53 |
1.147 |
|
261 |
|
|
HSH003 |
Hashimoto Thyroiditis |
60 |
1.147 |
|
262 |
|
P
|
ABD014 |
Abdominal Obesity-Metabolic Syndrome 1 |
63 |
1.147 |
|
263 |
|
c
|
CRB193 |
Cerebral Amyloid Angiopathy, App-Related |
55 |
1.147 |
|
264 |
|
|
DYS004 |
Dyscalculia |
35 |
1.147 |
|
265 |
|
|
PRT019 |
Protein-Losing Enteropathy |
45 |
1.147 |
|
266 |
|
P
|
KDN018 |
Kidney Disease |
72 |
1.147 |
|
267 |
|
|
ULC004 |
Ulcerative Colitis |
74 |
1.147 |
|
268 |
|
P
|
ALP008 |
Alopecia |
54 |
1.147 |
|
269 |
|
P
|
HRM001 |
Hermansky-Pudlak Syndrome |
65 |
1.147 |
|
270 |
|
|
CNN003 |
Conn's Syndrome |
79 |
1.147 |
|
271 |
|
P
|
VSC007 |
Vascular Disease |
63 |
1.147 |
|
272 |
|
|
PPL002 |
Papillary Carcinoma |
46 |
1.147 |
|
273 |
|
|
GST033 |
Gestational Diabetes |
61 |
1.147 |
|
274 |
|
|
PLC008 |
Placenta Disease |
49 |
1.147 |
|
275 |
|
|
MCR017 |
Macrocytic Anemia |
44 |
1.147 |
|
276 |
|
|
MDM001 |
Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency |
34 |
1.147 |
|
277 |
|
|
HDN002 |
Head Injury |
44 |
1.147 |
|
278 |
|
|
CRB090 |
Cerebral Hypoxia |
42 |
1.147 |
|
279 |
|
|
ART002 |
Arts Syndrome |
66 |
1.115 |
|
280 |
|
c
|
MTR020 |
Maturity-Onset Diabetes of the Young, Type 3 |
54 |
1.115 |
|
281 |
|
c
|
ATS007 |
Autism Spectrum Disorder |
72 |
1.115 |
|
282 |
|
|
LGH007 |
Leigh Syndrome |
70 |
1.115 |
|
283 |
|
|
MYL069 |
Myeloma, Multiple |
77 |
1.115 |
|
284 |
|
c
|
HYP595 |
Hypertension, Essential |
85 |
1.115 |
|
285 |
|
c
|
MTR018 |
Maturity-Onset Diabetes of the Young, Type 1 |
63 |
1.115 |
|
286 |
|
c
|
MTR019 |
Maturity-Onset Diabetes of the Young, Type 2 |
53 |
1.115 |
|
287 |
|
P
|
PLY011 |
Polycystic Ovary Syndrome |
57 |
1.115 |
|
288 |
|
|
CNT047 |
Contact Dermatitis |
57 |
1.115 |
|
289 |
|
|
PYR012 |
Pyruvate Dehydrogenase E1-Beta Deficiency |
41 |
1.073 |
|
290 |
|
|
CLT003 |
Colitis |
63 |
1.073 |
|
291 |
|
c
|
VNT034 |
Ventricular Fibrillation, Paroxysmal Familial, 1 |
67 |
1.073 |
|
292 |
|
|
NMN001 |
Nominal Aphasia |
40 |
1.073 |
|
293 |
|
|
VSC003 |
Visceral Leishmaniasis |
55 |
1.073 |
|
294 |
|
P
|
LCT001 |
Lactic Acidosis |
51 |
1.073 |
|
295 |
|
|
DLS001 |
Delusional Disorder |
45 |
1.073 |
|
296 |
|
|
CRB004 |
Cerebral Artery Occlusion |
45 |
1.073 |
|
297 |
|
P
|
LNG064 |
Lung Cancer Susceptibility 3 |
70 |
1.073 |
|
298 |
|
|
TLN003 |
Telangiectasis |
51 |
1.073 |
|
299 |
|
|
TRN015 |
Transient Cerebral Ischemia |
63 |
1.073 |
|
300 |
|
P
|
EYD002 |
Eye Disease |
57 |
1.073 |
|
301 |
|
P
|
SBS003 |
Substance Abuse |
54 |
1.073 |
|
302 |
|
|
MDD011 |
Mood Disorder |
62 |
1.073 |
|
303 |
|
|
NDL007 |
Nodular Goiter |
48 |
1.073 |
|
304 |
|
|
GRV012 |
Grover's Disease |
29 |
0.993 |
|
305 |
|
P
|
OVR042 |
Ovarian Cancer |
88 |
0.993 |
|
306 |
|
c
|
MGR028 |
Migraine with or Without Aura 1 |
64 |
0.993 |
|
307 |
|
P
|
PTY003 |
Pityriasis Rubra Pilaris |
57 |
0.993 |
|
308 |
|
|
KRN002 |
Kearns-Sayre Syndrome |
63 |
0.993 |
|
309 |
|
c
|
ALZ050 |
Alzheimer Disease 5 |
33 |
0.993 |
|
310 |
|
P
|
CHN044 |
Chondrodysplasia Punctata Syndrome |
43 |
0.993 |
|
311 |
|
P
|
MYC007 |
Myocardial Infarction |
70 |
0.993 |
|
312 |
|
|
STR095 |
Structural Heart Defects and Renal Anomalies Syndrome |
20 |
0.993 |
|
313 |
|
|
PRM329 |
Premature Aging |
36 |
0.993 |
|
314 |
|
|
MTC004 |
Mitochondrial Encephalomyopathy |
42 |
0.993 |
|
315 |
|
|
HYP066 |
Hyperglycemia |
61 |
0.993 |
|
316 |
|
|
MTH009 |
Mouth Disease |
57 |
0.993 |
|
317 |
|
|
ACT084 |
Acute Stress Disorder |
54 |
0.993 |
|
318 |
|
|
LYM027 |
Lymphopenia |
56 |
0.993 |
|
319 |
|
c
|
ACT004 |
Acute Diarrhea |
40 |
0.993 |
|
320 |
|
c
|
PRC016 |
Pre-Eclampsia |
65 |
0.993 |
|
321 |
|
P
|
RHZ001 |
Rhizomelic Chondrodysplasia Punctata |
57 |
0.993 |
|
322 |
|
P
|
DRR001 |
Diarrhea |
55 |
0.993 |
|
323 |
|
|
SQM006 |
Squamous Cell Carcinoma |
60 |
0.993 |
|
324 |
|
|
GRN017 |
Granulocytopenia |
42 |
0.993 |
|
325 |
|
|
DYS073 |
Dysphagia |
53 |
0.993 |
|
326 |
|
c
|
DNT047 |
Dentinogenesis Imperfecta Type 2 |
35 |
0.993 |
|
327 |
|
|
HMP009 |
Haemophilus Influenzae |
41 |
0.993 |
|
328 |
|
|
YMN001 |
Yemenite Deaf-Blind Hypopigmentation Syndrome |
66 |
0.947 |
|
329 |
|
|
OTT002 |
Otitis Media |
71 |
0.947 |
|
330 |
|
P
|
EXN002 |
Exanthem |
58 |
0.947 |
|
331 |
|
c
|
SCN036 |
Secondary Progressive Multiple Sclerosis |
55 |
0.947 |
|
332 |
|
P
|
SPP010 |
Suppressor of Tumorigenicity 3 |
51 |
0.947 |
|
333 |
|
P
|
FLL037 |
Follicular Lymphoma |
74 |
0.947 |
|
334 |
|
|
OBS082 |
Obstructive Nephropathy |
41 |
0.947 |
|
335 |
|
P
|
LPS004 |
Lupus Erythematosus |
61 |
0.947 |
|
336 |
|
|
SKN019 |
Skin Melanoma |
71 |
0.947 |
|
337 |
|
|
ALL010 |
Allergic Contact Dermatitis |
56 |
0.947 |
|
338 |
|
P
|
ACN011 |
Acne |
57 |
0.947 |
|
339 |
|
|
MLK006 |
Milk Allergy |
47 |
0.947 |
|
340 |
|
|
MTC166 |
Mitochondrial Complex I Deficiency, Nuclear Type 19 |
23 |
0.947 |
|
341 |
|
|
STT001 |
Status Epilepticus |
59 |
0.947 |
|
342 |
|
P
|
MYT002 |
Myotonic Dystrophy |
51 |
0.947 |
|
343 |
|
P
|
CHR345 |
Chronic Pain |
50 |
0.947 |
|
344 |
|
|
FML304 |
Familial Isolated Dilated Cardiomyopathy |
49 |
0.907 |
|
345 |
|
|
ANX004 |
Anoxia |
40 |
0.907 |
|
346 |
|
|
NRM022 |
Neurometabolic Disease |
24 |
0.907 |
|
347 |
|
|
ACY005 |
Acyl-Coa Dehydrogenase, Short-Chain, Deficiency of |
55 |
0.907 |
|
348 |
|
c
|
HRM005 |
Hermansky-Pudlak Syndrome 1 |
55 |
0.907 |
|
349 |
|
P
|
RTN008 |
Retinitis Pigmentosa |
80 |
0.907 |
|
350 |
|
P
|
D2H002 |
D-2-Hydroxyglutaric Aciduria 1 |
52 |
0.907 |
|
351 |
|
|
SCH060 |
Schistosoma Mansoni Infection, Susceptibility/ |
38 |
0.907 |
|
352 |
|
P
|
MLT020 |
Multiple Sclerosis |
79 |
0.907 |
|
353 |
|
|
FZL002 |
Fazio-Londe Disease |
39 |
0.907 |
|
354 |
|
|
MND002 |
Mandibuloacral Dysplasia with Type B Lipodystrophy |
37 |
0.907 |
|
355 |
|
c
|
CRD113 |
Cardiomyopathy, Dilated, 1v |
24 |
0.907 |
|
356 |
|
|
LMB062 |
Limb Ischemia |
55 |
0.907 |
|
357 |
|
|
PLY166 |
Polyunsaturated Fatty Acids Plasma Level Quantitative Trait Locus 1 |
8 |
0.907 |
|
358 |
|
P
|
FRD001 |
Friedreich Ataxia |
61 |
0.907 |
|
359 |
|
|
GLT035 |
Glutaric Acidemia I |
57 |
0.907 |
|
360 |
|
|
ORG002 |
Organic Acidemia |
44 |
0.907 |
|
361 |
|
|
NRR001 |
Neuroretinitis |
42 |
0.907 |
|
362 |
|
|
GLC003 |
Glucose Intolerance |
54 |
0.907 |
|
363 |
|
c
|
PK3005 |
Pik3ca-Related Overgrowth Syndrome |
33 |
0.907 |
|
364 |
|
|
RTN023 |
Retinitis |
46 |
0.907 |
|
365 |
|
|
ART014 |
Articulation Disorder |
34 |
0.907 |
|
366 |
|
|
ASP007 |
Aspiration Pneumonia |
49 |
0.907 |
|
367 |
|
|
GT001 |
Gout |
64 |
0.907 |
|
368 |
|
|
SCH014 |
Schistosomiasis |
56 |
0.907 |
|
369 |
|
P
|
RSP003 |
Respiratory Failure |
74 |
0.907 |
|
370 |
|
|
CHL123 |
Chlamydia |
58 |
0.907 |
|
371 |
|
P
|
PRN023 |
Prion Disease |
60 |
0.907 |
|
372 |
|
|
SVR004 |
Severe Combined Immunodeficiency |
72 |
0.907 |
|
373 |
|
|
HRT015 |
Heritable Pulmonary Arterial Hypertension |
46 |
0.907 |
|
374 |
|
P
|
TXP001 |
Toxoplasmosis |
60 |
0.907 |
|
375 |
|
|
CCN001 |
Cocaine Dependence |
48 |
0.907 |
|
376 |
|
|
LKP003 |
Leukoplakia |
39 |
0.907 |
|
377 |
|
|
IDP022 |
Idiopathic Spinal Cord Herniation |
17 |
0.907 |
|
378 |
|
P
|
LNG032 |
Lung Cancer |
98 |
0.811 |
|
379 |
|
|
HTT002 |
Hutterite Cerebroosteonephrodysplasia Syndrome |
25 |
0.811 |
|
380 |
|
|
MLT161 |
Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly |
55 |
0.811 |
|
381 |
|
|
SMN008 |
Semantic Dementia |
47 |
0.811 |
|
382 |
|
|
SDD001 |
Sudden Infant Death Syndrome |
60 |
0.811 |
|
383 |
|
|
CMB017 |
Combined Oxidative Phosphorylation Deficiency 6 |
41 |
0.811 |
|
384 |
|
P
|
MYS005 |
Myositis |
56 |
0.811 |
|
385 |
|
|
OBS002 |
Obsessive-Compulsive Disorder |
68 |
0.811 |
|
386 |
|
P
|
ATX030 |
Ataxia-Telangiectasia |
80 |
0.811 |
|
387 |
|
|
ISV001 |
Isovaleric Acidemia |
54 |
0.811 |
|
388 |
|
|
AGN018 |
Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome |
57 |
0.811 |
|
389 |
|
|
OPP004 |
Oppositional Defiant Disorder |
49 |
0.811 |
|
390 |
|
|
DSR012 |
Disordered Steroidogenesis Due to Cytochrome P450 Oxidoreductase Deficiency |
39 |
0.811 |
|
391 |
|
P
|
ATR011 |
Atrial Fibrillation |
66 |
0.811 |
|
392 |
|
|
CRP032 |
Corpus Callosum, Agenesis of |
49 |
0.811 |
|
393 |
|
P
|
3MT016 |
3-Methylglutaconic Aciduria, Type Iii |
68 |
0.811 |
|
394 |
|
|
CNT105 |
Central Core Disease of Muscle |
59 |
0.811 |
|
395 |
|
|
IGR001 |
Ige Responsiveness, Atopic |
59 |
0.811 |
|
396 |
|
|
DMT001 |
Dimethylglycine Dehydrogenase Deficiency |
27 |
0.811 |
|
397 |
|
|
ALC028 |
Alacrima, Achalasia, and Mental Retardation Syndrome |
68 |
0.811 |
|
398 |
|
c
|
MCR312 |
Microphthalmia, Syndromic 10 |
40 |
0.811 |
|
399 |
|
|
MTH026 |
Methemoglobinemia Due to Deficiency of Methemoglobin Reductase |
35 |
0.811 |
|
400 |
|
|
OST159 |
Osteogenic Sarcoma |
66 |
0.811 |
|
401 |
|
P
|
HYP750 |
Hypertriglyceridemia, Familial |
62 |
0.811 |
|
402 |
|
|
HRW001 |
Hair Whorl |
35 |
0.811 |
|
403 |
|
c
|
CRT081 |
Cortical Dysplasia, Complex, with Other Brain Malformations 7 |
31 |
0.811 |
|
404 |
|
|
PLY183 |
Polymicrogyria with or Without Vascular-Type Ehlers-Danlos Syndrome |
41 |
0.811 |
|
405 |
|
P
|
MLG056 |
Malignant Hyperthermia |
66 |
0.811 |
|
406 |
|
P
|
MYL006 |
Myeloid Leukemia |
61 |
0.811 |
|
407 |
|
P
|
TRM003 |
Tremor |
48 |
0.811 |
|
408 |
|
|
MCR099 |
Microlissencephaly |
37 |
0.811 |
|
409 |
|
|
SVR001 |
Severe Acute Respiratory Syndrome |
67 |
0.811 |
|
410 |
|
P
|
KRT005 |
Keratoacanthoma |
47 |
0.811 |
|
411 |
|
|
OVR063 |
Overnutrition |
42 |
0.811 |
|
412 |
|
|
HYP005 |
Hypokalemia |
55 |
0.811 |
|
413 |
|
|
ANT007 |
Anterior Horn Cell Disease |
31 |
0.811 |
|
414 |
|
|
ATX031 |
Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus |
58 |
0.811 |
|
415 |
|
|
ENC067 |
Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis |
50 |
0.811 |
|
416 |
|
|
CHL004 |
Cholelithiasis |
49 |
0.811 |
|
417 |
|
|
OLG003 |
Oligohydramnios |
51 |
0.811 |
|
418 |
|
|
CRT015 |
Carotid Artery Occlusion |
45 |
0.811 |
|
419 |
|
|
PNC041 |
Pancreatic Ductal Adenocarcinoma |
51 |
0.811 |
|
420 |
|
|
PLR005 |
Pleuropneumonia |
33 |
0.811 |
|
421 |
|
|
PLS007 |
Plasmodium Falciparum Malaria |
52 |
0.811 |
|
422 |
|
P
|
ART005 |
Arteriovenous Malformation |
65 |
0.811 |
|
423 |
|
|
NNT010 |
Nontoxic Goiter |
32 |
0.811 |
|
424 |
|
|
SNL007 |
Senile Cataract |
40 |
0.811 |
|
425 |
|
|
TBL023 |
Tubulinopathies |
31 |
0.811 |
|
426 |
|
|
PLY024 |
Polymicrogyria |
47 |
0.811 |
|
427 |
|
P
|
HDC001 |
Headache |
57 |
0.811 |
|
428 |
|
P
|
HYP120 |
Hypoaldosteronism |
35 |
0.811 |
|
429 |
|
|
PRN039 |
Paraneoplastic Syndromes |
37 |
0.766 |
|
430 |
|
|
MCL027 |
Macular Dystrophy, Dominant Cystoid |
51 |
0.719 |
|
431 |
|
c
|
DRM054 |
Dermatitis, Atopic, 2 |
46 |
0.719 |
|
432 |
|
|
HYD058 |
Hydrops, Lactic Acidosis, and Sideroblastic Anemia |
60 |
0.719 |
|
433 |
|
|
MTC005 |
Mitochondrial Metabolism Disease |
45 |
0.702 |
|
434 |
|
P
|
SZR006 |
Seizure Disorder |
70 |
0.702 |
|
435 |
|
c
|
DWL002 |
Dowling-Degos Disease 1 |
58 |
0.702 |
|
436 |
|
|
DHY002 |
Dihydropyrimidine Dehydrogenase Deficiency |
57 |
0.702 |
|
437 |
|
|
MSC157 |
Muscular Dystrophy, Duchenne Type |
79 |
0.702 |
|
438 |
|
|
DSM002 |
Desmosterolosis |
39 |
0.702 |
|
439 |
|
|
ACR020 |
Acropectorovertebral Dysplasia |
23 |
0.702 |
|
440 |
|
|
ALC007 |
Alcohol Dependence |
66 |
0.702 |
|
441 |
|
P
|
PRK057 |
Parkinson Disease, Late-Onset |
80 |
0.702 |
|
442 |
|
P
|
FML011 |
Familial Adenomatous Polyposis |
71 |
0.702 |
|
443 |
|
|
MLR004 |
Malaria |
80 |
0.702 |
|
444 |
|
P
|
HYP111 |
Hyperprolinemia |
45 |
0.702 |
|
445 |
|
P
|
PLY014 |
Polycystic Kidney Disease |
69 |
0.702 |
|
446 |
|
|
HMN047 |
Human Cytomegalovirus Infection |
57 |
0.702 |
|
447 |
|
|
SBJ001 |
Subjective Cognitive Decline |
30 |
0.702 |
|
448 |
|
c
|
RHZ004 |
Rhizomelic Chondrodysplasia Punctata, Type 3 |
42 |
0.702 |
|
449 |
|
|
PRL023 |
Proliferative Vasculopathy and Hydranencephaly-Hydrocephaly Syndrome |
46 |
0.702 |
|
450 |
|
P
|
PRT133 |
Proteasome-Associated Autoinflammatory Syndrome 1 |
80 |
0.702 |
|
451 |
|
P
|
PNC035 |
Pancreatic Cancer |
86 |
0.702 |
|
452 |
|
c
|
CRB176 |
Cerebral Amyloid Angiopathy, Itm2b-Related, 1 |
43 |
0.702 |
|
453 |
|
|
KRT019 |
Keratitis, Hereditary |
66 |
0.702 |
|
454 |
|
c
|
SPN284 |
Spinocerebellar Ataxia 38 |
40 |
0.702 |
|
455 |
|
P
|
ASP006 |
Aspergillosis |
72 |
0.702 |
|
456 |
|
|
DHY010 |
Dihydrolipoamide Dehydrogenase Deficiency |
47 |
0.702 |
|
457 |
|
|
RNL114 |
Renal Cell Carcinoma, Nonpapillary |
80 |
0.702 |
|
458 |
|
|
DMN031 |
Dementia, Lewy Body |
65 |
0.702 |
|
459 |
|
|
PCK003 |
Pick Disease of Brain |
69 |
0.702 |
|
460 |
|
c
|
NMN014 |
Niemann-Pick Disease, Type C2 |
49 |
0.702 |
|
461 |
|
P
|
HRD008 |
Hereditary Hemorrhagic Telangiectasia |
65 |
0.702 |
|
462 |
|
c
|
ATS347 |
Autosomal Dominant Polycystic Kidney Disease |
66 |
0.702 |
|
463 |
|
P
|
ZLL001 |
Zellweger Syndrome |
65 |
0.702 |
|
464 |
|
P
|
BCL017 |
B-Cell Lymphoma |
59 |
0.702 |
|
465 |
|
c
|
CHR684 |
Chronic Kidney Disease |
69 |
0.702 |
|
466 |
|
|
URM002 |
Uremia |
47 |
0.702 |
|
467 |
|
P
|
HRP006 |
Herpes Simplex |
65 |
0.702 |
|
468 |
|
P
|
MSC005 |
Muscular Dystrophy |
67 |
0.702 |
|
469 |
|
P
|
MTH008 |
Methylmalonic Acidemia |
52 |
0.702 |
|
470 |
|
P
|
ALC033 |
Alcohol Use Disorder |
61 |
0.702 |
|
471 |
|
|
VCC001 |
Vaccinia |
47 |
0.702 |
|
472 |
|
|
LCL004 |
Localized Osteosarcoma |
34 |
0.702 |
|
473 |
|
P
|
SKN015 |
Skin Carcinoma |
71 |
0.702 |
|
474 |
|
|
END040 |
Endogenous Depression |
55 |
0.702 |
|
475 |
|
|
SPN035 |
Spindle Cell Sarcoma |
54 |
0.702 |
|
476 |
|
P
|
INF038 |
Influenza |
68 |
0.702 |
|
477 |
|
|
LNG099 |
Lung Disease |
62 |
0.702 |
|
478 |
|
|
TRY001 |
Trypanosomiasis |
50 |
0.702 |
|
479 |
|
P
|
DNG005 |
Dengue Virus |
56 |
0.702 |
|
480 |
|
P
|
KLP003 |
Klippel-Feil Syndrome |
47 |
0.702 |
|
481 |
|
P
|
NTR004 |
Neutropenia |
63 |
0.702 |
|
482 |
|
c
|
SCN007 |
Secondary Hyperparathyroidism |
51 |
0.702 |
|
483 |
|
c
|
ACT027 |
Acute Pancreatitis |
60 |
0.702 |
|
484 |
|
|
THY122 |
Thyroid Gland Cancer |
59 |
0.702 |
|
|
486 |
|
|
CCC002 |
Coccidiosis |
50 |
0.702 |
|
487 |
|
P
|
ECL001 |
Eclampsia |
52 |
0.702 |
|
488 |
|
|
SRC014 |
Sarcoma |
65 |
0.702 |
|
489 |
|
P
|
HYP040 |
Hypospadias |
51 |
0.702 |
|
490 |
|
P
|
HYP024 |
Hypoparathyroidism |
55 |
0.702 |
|
491 |
|
|
HYD001 |
Hydranencephaly |
43 |
0.702 |
|
492 |
|
|
PLG002 |
Plague |
58 |
0.702 |
|
493 |
|
|
CRB033 |
Cerebral Degeneration |
39 |
0.702 |
|
494 |
|
P
|
ATS308 |
Autosomal Dominant Cerebellar Ataxia |
64 |
0.702 |
|
495 |
|
|
KRT008 |
Keratopathy |
46 |
0.702 |
|
496 |
|
|
CRB037 |
Cerebral Palsy |
67 |
0.702 |
|
497 |
|
P
|
INS002 |
in Situ Carcinoma |
53 |
0.702 |
|
498 |
|
|
HRN003 |
Heroin Dependence |
44 |
0.702 |
|
499 |
|
P
|
SCK005 |
Sickle Cell Disease |
56 |
0.702 |
|
500 |
|
|
ERY069 |
Erythrokeratoderma ''en Cocardes'' |
27 |
0.702 |
|
501 |
|
|
ADR022 |
Adrenomyeloneuropathy |
39 |
0.574 |
|
502 |
|
|
PLY100 |
Polyploidy |
36 |
0.574 |
|
503 |
|
P
|
AVS003 |
Avascular Necrosis |
41 |
0.574 |
|
504 |
|
|
CHR696 |
Charcot-Marie-Tooth Disease, X-Linked Recessive, 4, with or Without Cerebellar Ataxia |
32 |
0.574 |
|
505 |
|
P
|
RTT002 |
Rett Syndrome |
79 |
0.574 |
|
506 |
|
|
ADR007 |
Adrenoleukodystrophy |
73 |
0.574 |
|
507 |
|
|
LSC001 |
Lesch-Nyhan Syndrome |
62 |
0.574 |
|
508 |
|
|
ANM045 |
Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency |
50 |
0.574 |
|
509 |
|
P
|
FRG001 |
Fragile X Syndrome |
70 |
0.574 |
|
510 |
|
|
SRC015 |
Sarcosinemia |
38 |
0.574 |
|
511 |
|
|
MYP035 |
Myopathy, Distal, with Anterior Tibial Onset |
33 |
0.574 |
|
512 |
|
c
|
CTR132 |
Cataract 3, Multiple Types |
42 |
0.574 |
|
513 |
|
|
BRT054 |
Brittle Bone Disorder |
74 |
0.574 |
|
514 |
|
|
CRV035 |
Cervical Cancer |
73 |
0.574 |
|
515 |
|
|
END057 |
Endometrial Cancer |
72 |
0.574 |
|
516 |
|
|
CRT072 |
Creutzfeldt-Jakob Disease |
68 |
0.574 |
|
517 |
|
|
GRS011 |
Gerstmann-Straussler Disease |
56 |
0.574 |
|
518 |
|
c
|
ART138 |
Aortic Aneurysm, Familial Abdominal, 1 |
61 |
0.574 |
|
519 |
|
|
CRN287 |
Carnitine Deficiency, Myopathic |
17 |
0.574 |
|
520 |
|
|
CYS001 |
Cystic Fibrosis |
78 |
0.574 |
|
521 |
|
c
|
GLY007 |
Glycogen Storage Disease Iv |
58 |
0.574 |
|
522 |
|
|
CHR100 |
Chronic Ulcer of Skin |
57 |
0.574 |
|
523 |
|
P
|
LSS002 |
Lissencephaly |
50 |
0.574 |
|
524 |
|
|
FML037 |
Female Breast Cancer |
51 |
0.574 |
|
525 |
|
|
VTM002 |
Vitamin B12 Deficiency |
48 |
0.574 |
|
526 |
|
c
|
BTT014 |
Beta-Thalassemia |
72 |
0.574 |
|
527 |
|
|
DFF005 |
Diffuse Large B-Cell Lymphoma |
54 |
0.574 |
|
528 |
|
|
NNL006 |
Non-Alcoholic Steatohepatitis |
54 |
0.574 |
|
529 |
|
|
AGR018 |
Agraphia |
37 |
0.574 |
|
530 |
|
|
SXL003 |
Sexual Disorder |
49 |
0.574 |
|
531 |
|
c
|
CNG006 |
Congenital Hypothyroidism |
63 |
0.574 |
|
532 |
|
|
CLR108 |
Colorectal Adenoma |
64 |
0.574 |
|
533 |
|
|
PYR022 |
Pyruvate Dehydrogenase E1-Alpha Deficiency |
64 |
0.574 |
|
534 |
|
|
IMM167 |
Immune Deficiency Disease |
78 |
0.574 |
|
535 |
|
c
|
GRV008 |
Graves Disease 1 |
54 |
0.574 |
|
536 |
|
|
PRN056 |
Parana Hard-Skin Syndrome |
17 |
0.574 |
|
537 |
|
c
|
SPH013 |
Spherocytosis, Type 1 |
42 |
0.574 |
|
538 |
|
|
PRS012 |
Pars Planitis |
47 |
0.574 |
|
539 |
|
c
|
BRN108 |
Branchiootic Syndrome 1 |
62 |
0.574 |
|
540 |
|
P
|
LKM062 |
Leukemia, Acute Lymphoblastic |
69 |
0.574 |
|
541 |
|
|
LPT014 |
Leptin Deficiency or Dysfunction |
78 |
0.574 |
|
542 |
|
c
|
PNT034 |
Pontocerebellar Hypoplasia, Type 2e |
52 |
0.574 |
|
543 |
|
|
CHR607 |
Chorea, Childhood-Onset, with Psychomotor Retardation |
39 |
0.574 |
|
544 |
|
|
MYP163 |
Myopathy, Mitochondrial Progressive, with Congenital Cataract and Developmental Delay |
27 |
0.574 |
|
545 |
|
P
|
DVL012 |
Developmental Dysplasia of the Hip 1 |
46 |
0.574 |
|
546 |
|
c
|
CRB098 |
Cerebrooculofacioskeletal Syndrome 2 |
30 |
0.574 |
|
547 |
|
c
|
CRB100 |
Cerebrooculofacioskeletal Syndrome 4 |
33 |
0.574 |
|
548 |
|
P
|
CRB101 |
Cerebrooculofacioskeletal Syndrome 1 |
53 |
0.574 |
|
549 |
|
c
|
RHZ011 |
Rhizomelic Chondrodysplasia Punctata, Type 1 |
53 |
0.574 |
|
550 |
|
|
HMC042 |
Homocystinuria-Megaloblastic Anemia, Cble Complementation Type |
33 |
0.574 |
|
551 |
|
|
BTT016 |
Batten-Turner Congenital Myopathy |
53 |
0.574 |
|
552 |
|
|
MYL005 |
Myelofibrosis |
71 |
0.574 |
|
553 |
|
|
OCL069 |
Ocular Motor Apraxia |
57 |
0.574 |
|
554 |
|
|
TLC001 |
Telecanthus |
35 |
0.574 |
|
555 |
|
c
|
THY109 |
Thyroid Cancer, Nonmedullary, 1 |
55 |
0.574 |
|
556 |
|
P
|
SRC025 |
Sarcoidosis 1 |
71 |
0.574 |
|
557 |
|
P
|
SCL057 |
Scoliosis, Isolated 1 |
40 |
0.574 |
|
558 |
|
|
RFS006 |
Refsum Disease, Classic |
63 |
0.574 |
|
559 |
|
P
|
RNL100 |
Renal Hypodysplasia/aplasia 1 |
63 |
0.574 |
|
560 |
|
P
|
PTN014 |
Patent Ductus Arteriosus 1 |
59 |
0.574 |
|
561 |
|
|
OST017 |
Osteomyelitis |
63 |
0.574 |
|
562 |
|
P
|
PNT019 |
Pontocerebellar Hypoplasia |
46 |
0.574 |
|
563 |
|
P
|
NRD007 |
Neurodegeneration with Brain Iron Accumulation |
52 |
0.574 |
|
564 |
|
c
|
CHR697 |
Charcot-Marie-Tooth Disease X-Linked Recessive 4 |
31 |
0.574 |
|
565 |
|
|
DST103 |
Distal Muscular Dystrophy with Anterior Tibial Onset |
29 |
0.574 |
|
566 |
|
|
GRN051 |
Granulomatous Disease, Chronic, X-Linked |
57 |
0.574 |
|
567 |
|
|
HPT004 |
Hepatic Coma |
43 |
0.574 |
|
568 |
|
|
BLS002 |
Blastomycosis |
47 |
0.574 |
|
569 |
|
|
IDP073 |
Idiopathic Hypercalciuria |
40 |
0.574 |
|
570 |
|
|
CNG393 |
Congenital Muscular Dystrophy with Hyperlaxity |
12 |
0.574 |
|
571 |
|
|
DYS003 |
Dysgraphia |
35 |
0.574 |
|
572 |
|
|
SCH012 |
Schizoaffective Disorder |
50 |
0.574 |
|
573 |
|
P
|
DYS154 |
Dystonia |
64 |
0.574 |
|
574 |
|
|
VLK001 |
Volkmann Contracture |
23 |
0.574 |
|
575 |
|
P
|
MVM001 |
Movement Disease |
61 |
0.574 |
|
576 |
|
P
|
HML002 |
Hemolytic Anemia |
62 |
0.574 |
|
577 |
|
|
HMG002 |
Hemoglobinuria |
50 |
0.574 |
|
578 |
|
|
GLL048 |
Glial Tumor |
52 |
0.574 |
|
579 |
|
P
|
HMR005 |
Hemorrhoid |
49 |
0.574 |
|
580 |
|
|
GLY078 |
Glycogen Storage Disease Due to Glycogen Branching Enzyme Deficiency |
38 |
0.574 |
|
581 |
|
P
|
THR014 |
Thrombocytopenia |
66 |
0.574 |
|
582 |
|
P
|
BRS044 |
Breast Adenocarcinoma |
58 |
0.574 |
|
583 |
|
|
ART016 |
Aortic Aneurysm |
68 |
0.574 |
|
584 |
|
P
|
SYS005 |
Systemic Scleroderma |
74 |
0.574 |
|
585 |
|
|
MTS001 |
Mutism |
44 |
0.574 |
|
586 |
|
c
|
SBC007 |
Subacute Thyroiditis |
43 |
0.574 |
|
587 |
|
|
INH003 |
Inhibited Female Orgasm |
27 |
0.574 |
|
588 |
|
P
|
SNS001 |
Sensorineural Hearing Loss |
59 |
0.574 |
|
589 |
|
|
SLP001 |
Sleeping Sickness |
56 |
0.574 |
|
590 |
|
|
RCK004 |
Rickets |
68 |
0.574 |
|
591 |
|
|
MYP164 |
Myopathy, Congenital, with Diaphragmatic Defects, Respiratory Insufficiency, and Dysmorphic Facies |
24 |
0.574 |
|
592 |
|
P
|
UVT001 |
Uveitis |
57 |
0.574 |
|
593 |
|
|
BRN028 |
Brain Cancer |
74 |
0.574 |
|
594 |
|
|
MRS001 |
Marasmus |
42 |
0.574 |
|
595 |
|
P
|
GRV001 |
Graves' Disease |
55 |
0.574 |
|
596 |
|
|
PCD001 |
Pica Disease |
38 |
0.574 |
|
597 |
|
|
ATY001 |
Atypical Depressive Disorder |
45 |
0.574 |
|
598 |
|
P
|
GLL022 |
Guillain-Barre Syndrome |
60 |
0.574 |
|
599 |
|
|
IMP005 |
Impotence |
52 |
0.574 |
|
600 |
|
c
|
BSL007 |
Basal Cell Carcinoma |
68 |
0.574 |
|
601 |
|
|
NRT004 |
Neuritis |
53 |
0.574 |
|
602 |
|
|
NNT012 |
Neonatal Jaundice |
53 |
0.574 |
|
603 |
|
P
|
ADN016 |
Adenocarcinoma |
63 |
0.574 |
|
604 |
|
|
MGL001 |
Megaloblastic Anemia |
58 |
0.574 |
|
605 |
|
|
HYP030 |
Hypoactive Sexual Desire Disorder |
41 |
0.574 |
|
606 |
|
P
|
GLY013 |
Glycogen Storage Disease |
60 |
0.574 |
|
607 |
|
P
|
END044 |
Endometriosis |
62 |
0.574 |
|
608 |
|
P
|
HRT032 |
Heart Disease |
81 |
0.574 |
|
609 |
|
|
PRM013 |
Premature Menopause |
58 |
0.574 |
|
610 |
|
|
BRD004 |
Borderline Personality Disorder |
53 |
0.574 |
|
611 |
|
|
MNN009 |
Meningoencephalitis |
48 |
0.574 |
|
612 |
|
P
|
PNC044 |
Pancreatitis |
61 |
0.574 |
|
613 |
|
P
|
INF032 |
Infertility |
57 |
0.574 |
|
614 |
|
P
|
RTN018 |
Retinal Disease |
53 |
0.574 |
|
615 |
|
P
|
AXN001 |
Axonal Neuropathy |
35 |
0.574 |
|
616 |
|
P
|
PRM002 |
Primary Hyperoxaluria |
65 |
0.574 |
|
617 |
|
P
|
KDN017 |
Kidney Cancer |
61 |
0.574 |
|
618 |
|
P
|
MTR014 |
Motor Neuron Disease |
65 |
0.574 |
|
619 |
|
|
PHM001 |
Phimosis |
38 |
0.574 |
|
620 |
|
|
BRS051 |
Breast Disease |
58 |
0.574 |
|
621 |
|
|
DMY004 |
Demyelinating Disease |
50 |
0.574 |
|
622 |
|
|
IDP070 |
Idiopathic Scoliosis |
42 |
0.574 |
|
623 |
|
|
LST001 |
Listeriosis |
59 |
0.574 |
|
624 |
|
|
CHR073 |
Choreatic Disease |
54 |
0.574 |
|
625 |
|
P
|
HRD011 |
Hereditary Spherocytosis |
64 |
0.574 |
|
626 |
|
|
CND002 |
Conduct Disorder |
51 |
0.574 |
|
627 |
|
|
HST011 |
Histoplasmosis |
55 |
0.574 |
|
628 |
|
|
SBS004 |
Substance Dependence |
47 |
0.574 |
|
629 |
|
P
|
TRC031 |
Trichorhinophalangeal Syndrome |
38 |
0.574 |
|
630 |
|
|
DCB001 |
Decubitus Ulcer |
62 |
0.574 |
|
631 |
|
|
FSC004 |
Fasciitis |
49 |
0.574 |
|
632 |
|
|
PRL005 |
Proliferative Fasciitis |
20 |
0.574 |
|
633 |
|
|
ISC003 |
Ischemic Fasciitis |
28 |
0.574 |
|
634 |
|
|
MYP017 |
Myopathy, Mitochondrial Progressive, with Congenital Cataract, Hearing Loss, and Developmental Delay |
14 |
0.574 |
|
635 |
|
|
GB1002 |
Gbe1 Adult Polyglucosan Body Disease |
7 |
0.574 |
|
636 |
|
|
ANR040 |
Aneurysm |
61 |
0.574 |
|
637 |
|
|
BRN056 |
Bronchopulmonary Dysplasia |
56 |
0.574 |
|
638 |
|
|
MTH046 |
Methylmalonic Acidemia Without Homocystinuria |
39 |
0.574 |
|
639 |
|
|
CCC003 |
Coccygodynia |
18 |
0.574 |
|
640 |
|
|
GLM045 |
Glioma |
63 |
0.574 |
|
641 |
|
|
SPT023 |
Septate Uterus |
30 |
0.541 |
|
642 |
|
|
URM005 |
Uremic Pruritus |
45 |
0.541 |
|
643 |
|
c
|
DRM040 |
Dermatitis Herpetiformis, Familial |
35 |
0.541 |
|
644 |
|
|
ATM095 |
Autoimmune Disease |
61 |
0.541 |
|
645 |
|
P
|
RST001 |
Restless Legs Syndrome |
52 |
0.541 |
|
646 |
|
P
|
CRP001 |
Carpal Tunnel Syndrome |
66 |
0.541 |
|
647 |
|
c
|
PCH010 |
Pachyonychia Congenita 3 |
43 |
0.541 |
|
648 |
|
|
PLY105 |
Polycystic Ovary Syndrome 1 |
39 |
0.541 |
|
649 |
|
c
|
CWD006 |
Cowden Syndrome 1 |
78 |
0.541 |
|
650 |
|
P
|
VSC011 |
Vasculitis |
61 |
0.541 |
|
651 |
|
|
CHR066 |
Chronic Fatigue Syndrome |
60 |
0.541 |
|
652 |
|
|
WHT017 |
Wheat Allergy |
31 |
0.541 |
|
653 |
|
|
CHR001 |
Churg-Strauss Syndrome |
61 |
0.541 |
|
654 |
|
|
APP008 |
Appendicitis |
62 |
0.541 |
|
655 |
|
|
PPT005 |
Peptic Ulcer Disease |
58 |
0.541 |
|
656 |
|
P
|
DRM007 |
Dermatitis Herpetiformis |
54 |
0.541 |
|
657 |
|
P
|
VNS003 |
Venous Insufficiency |
55 |
0.541 |
|
658 |
|
|
GST106 |
Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets |
65 |
0.541 |
|
659 |
|
|
TBS001 |
Tabes Dorsalis |
31 |
0.541 |
|
660 |
|
|
CNS004 |
Constipation |
56 |
0.541 |
|
661 |
|
P
|
CWD010 |
Cowden Syndrome |
70 |
0.541 |
|
662 |
|
|
FLL008 |
Folliculitis |
46 |
0.541 |
|
663 |
|
P
|
SLP005 |
Sleep Disorder |
61 |
0.541 |
|
664 |
|
P
|
ADL010 |
Adult Respiratory Distress Syndrome |
71 |
0.541 |
|
665 |
|
|
PTL002 |
Patellofemoral Pain Syndrome |
34 |
0.541 |
|
666 |
|
|
ALL012 |
Allergic Angiitis |
24 |
0.541 |
|
667 |
|
P
|
CLS010 |
Cluster Headache |
42 |
0.541 |
|
668 |
|
|
ESN016 |
Eosinophilic Pustular Folliculitis |
24 |
0.541 |
|
669 |
|
|
MCR088 |
Microscopic Polyangiitis |
51 |
0.541 |
|
670 |
|
|
ANC002 |
Anca-Associated Vasculitis |
44 |
0.541 |
|
671 |
|
c
|
GRN062 |
Granulomatous Disease, Chronic, Autosomal Recessive, 1 |
46 |
0.406 |
|
672 |
|
|
PST021 |
Postpartum Depression |
50 |
0.406 |
|
673 |
|
|
DMN026 |
Dementia Pugilistica |
27 |
0.406 |
|
674 |
|
|
RFR010 |
Refractory Anemia |
49 |
0.406 |
|
675 |
|
|
SNK001 |
Snakebite Envenomation |
22 |
0.406 |
|
676 |
|
|
CYN003 |
Cyanide Poisoning |
22 |
0.406 |
|
677 |
|
|
OST115 |
Osteonecrosis of the Jaw |
41 |
0.406 |
|
678 |
|
|
SPS057 |
Spasticity |
42 |
0.406 |
|
679 |
|
|
ARG006 |
Aregenerative Anemia |
28 |
0.406 |
|
680 |
|
|
PRC049 |
Precursor T-Cell Acute Lymphoblastic Leukemia |
45 |
0.406 |
|
681 |
|
c
|
STC015 |
Stickler Syndrome, Type I |
51 |
0.406 |
|
682 |
|
P
|
BLD134 |
Bladder Cancer |
79 |
0.406 |
|
683 |
|
P
|
NSP012 |
Nasopharyngeal Carcinoma |
61 |
0.406 |
|
684 |
|
|
GND001 |
Gonadoblastoma |
43 |
0.406 |
|
685 |
|
|
MRD002 |
Marden-Walker Syndrome |
56 |
0.406 |
|
686 |
|
|
FRG010 |
Fragile X Tremor/ataxia Syndrome |
44 |
0.406 |
|
687 |
|
|
SQM013 |
Squamous Cell Carcinoma, Head and Neck |
73 |
0.406 |
|
688 |
|
|
MND023 |
Mend Syndrome |
49 |
0.406 |
|
689 |
|
|
MST021 |
Meester-Loeys Syndrome |
42 |
0.406 |
|
690 |
|
P
|
LPR021 |
Leprosy 3 |
71 |
0.406 |
|
691 |
|
|
MTC146 |
Mitochondrial Complex I Deficiency, Nuclear Type 1 |
61 |
0.406 |
|
692 |
|
|
ALL003 |
Allergic Rhinitis |
67 |
0.406 |
|
693 |
|
P
|
LNR013 |
Linear Skin Defects with Multiple Congenital Anomalies 1 |
52 |
0.406 |
|
694 |
|
|
STR067 |
Stroke, Ischemic |
80 |
0.406 |
|
695 |
|
c
|
PLM164 |
Pulmonary Hypertension, Primary, 1 |
76 |
0.406 |
|
696 |
|
P
|
PHC003 |
Pheochromocytoma |
69 |
0.406 |
|
697 |
|
c
|
SYS001 |
Systemic Lupus Erythematosus |
87 |
0.406 |
|
698 |
|
P
|
PRG130 |
Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 |
54 |
0.406 |
|
699 |
|
|
PLY150 |
Polykaryocytosis Inducer |
29 |
0.406 |
|
700 |
|
P
|
CNR004 |
Cone-Rod Dystrophy 2 |
74 |
0.406 |
|
701 |
|
|
CRD002 |
Cri-Du-Chat Syndrome |
49 |
0.406 |
|
702 |
|
c
|
FNC027 |
Fanconi Anemia, Complementation Group a |
81 |
0.406 |
|
703 |
|
|
HYP781 |
Hypoascorbemia |
52 |
0.406 |
|
704 |
|
|
PLL017 |
Pallister-Hall-Like Syndrome |
37 |
0.406 |
|
705 |
|
c
|
LKM063 |
Leukemia, Chronic Myeloid |
71 |
0.406 |
|
706 |
|
|
EPD015 |
Epidemic Typhus |
44 |
0.406 |
|
707 |
|
|
END014 |
Endemic Typhus |
32 |
0.406 |
|
708 |
|
|
CNZ001 |
Coenzyme Q10 Deficiency Disease |
41 |
0.406 |
|
709 |
|
c
|
FTL067 |
Fetal Hemoglobin Quantitative Trait Locus 6 |
25 |
0.406 |
|
710 |
|
|
DLY008 |
Delayed Sleep Phase Disorder |
44 |
0.406 |
|
711 |
|
|
HRS016 |
Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction |
26 |
0.406 |
|
712 |
|
|
INV001 |
Invasive Aspergillosis |
49 |
0.406 |
|
713 |
|
P
|
URN019 |
Urinary Tract Infection |
49 |
0.406 |
|
714 |
|
|
ALX002 |
Alexithymia |
37 |
0.406 |
|
715 |
|
|
ASS001 |
Associative Agnosia |
24 |
0.406 |
|
716 |
|
|
MCR191 |
Microscopic Colitis |
46 |
0.406 |
|
717 |
|
P
|
BLY001 |
B-Lymphoblastic Leukemia/lymphoma |
52 |
0.406 |
|
718 |
|
|
LWG006 |
Low Grade Glioma |
41 |
0.406 |
|
719 |
|
P
|
CTN015 |
Cutaneous T Cell Lymphoma |
48 |
0.406 |
|
720 |
|
|
CRH005 |
Crohn's Colitis |
53 |
0.406 |
|
721 |
|
|
FSR001 |
Fusariosis |
45 |
0.406 |
|
722 |
|
|
NRL018 |
Neural Tube Defects, Folate-Sensitive |
45 |
0.406 |
|
723 |
|
P
|
HYP768 |
Hyperlipoproteinemia, Type I |
67 |
0.406 |
|
724 |
|
|
GST108 |
Gist-Plus Syndrome |
22 |
0.406 |
|
725 |
|
|
HYP806 |
Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy |
32 |
0.406 |
|
726 |
|
|
PRS131 |
Prostate Cancer/brain Cancer Susceptibility |
23 |
0.406 |
|
727 |
|
|
SCK003 |
Sickle Cell Anemia |
74 |
0.406 |
|
728 |
|
|
INT323 |
Intraocular Pressure Quantitative Trait Locus |
64 |
0.406 |
|
729 |
|
|
HMM004 |
Hamamy Syndrome |
39 |
0.406 |
|
730 |
|
|
ACT119 |
Acute Promyelocytic Leukemia |
62 |
0.406 |
|
731 |
|
|
TBL029 |
Tubulin, Beta |
28 |
0.406 |
|
732 |
|
P
|
MPL001 |
Maple Syrup Urine Disease |
70 |
0.406 |
|
733 |
|
|
SPN362 |
Spondylometaphyseal Dysplasia, Sedaghatian Type |
42 |
0.406 |
|
734 |
|
|
MTC207 |
Mitochondrial Complex Ii Deficiency, Nuclear Type 1 |
55 |
0.406 |
|
735 |
|
c
|
PRG038 |
Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 |
49 |
0.406 |
|
736 |
|
c
|
CLR041 |
Colorectal Cancer, Hereditary Nonpolyposis, Type 2 |
35 |
0.406 |
|
737 |
|
c
|
HYD064 |
Hydrocephalus, Congenital, 1 |
51 |
0.406 |
|
738 |
|
c
|
HYP248 |
Hyperprolinemia, Type I |
42 |
0.406 |
|
739 |
|
|
VRC005 |
Varicose Veins |
60 |
0.406 |
|
740 |
|
|
VLC001 |
Velocardiofacial Syndrome |
57 |
0.406 |
|
741 |
|
|
RTN179 |
Retinal Arteries, Tortuosity of |
41 |
0.406 |
|
742 |
|
|
KRT071 |
Keratosis, Seborrheic |
56 |
0.406 |
|
743 |
|
P
|
STR020 |
Strabismus |
56 |
0.406 |
|
744 |
|
|
DGR001 |
Digeorge Syndrome |
62 |
0.406 |
|
745 |
|
|
CRN238 |
Corneal Dystrophy, Epithelial Basement Membrane |
32 |
0.406 |
|
746 |
|
P
|
MJR007 |
Major Affective Disorder 1 |
42 |
0.406 |
|
747 |
|
|
MLT157 |
Multiple System Atrophy 1 |
69 |
0.406 |
|
748 |
|
P
|
FTL033 |
Fetal Hemoglobin Quantitative Trait Locus 1 |
42 |
0.406 |
|
749 |
|
P
|
ANG001 |
Angelman Syndrome |
65 |
0.406 |
|
750 |
|
|
ANT078 |
Antipyrine Metabolism |
23 |
0.406 |
|
751 |
|
c
|
PRG040 |
Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 |
53 |
0.406 |
|
752 |
|
c
|
MYP118 |
Myopathy, Myofibrillar, 8 |
30 |
0.406 |
|
753 |
|
|
PNG002 |
Pain Agnosia |
51 |
0.406 |
|
754 |
|
|
GST019 |
Gastrointestinal Stromal Tumor |
78 |
0.406 |
|
755 |
|
|
CLR109 |
Colorectal Adenocarcinoma |
50 |
0.406 |
|
756 |
|
|
FRG008 |
Fragile X-Associated Tremor/ataxia Syndrome |
44 |
0.406 |
|
757 |
|
|
ADR040 |
Adrenal Gland Pheochromocytoma |
46 |
0.406 |
|
758 |
|
|
BLP004 |
Blepharophimosis |
36 |
0.406 |
|
759 |
|
P
|
LCT002 |
Lactose Intolerance |
52 |
0.406 |
|
760 |
|
|
ADN072 |
Adenoma of Pancreas |
17 |
0.406 |
|
761 |
|
c
|
CHR695 |
Chronic Primary Adrenal Insufficiency |
15 |
0.406 |
|
762 |
|
P
|
PRN026 |
Porencephaly |
55 |
0.406 |
|
763 |
|
|
MTC151 |
Mitochondrial Complex I Deficiency, Nuclear Type 20 |
36 |
0.406 |
|
764 |
|
|
PRC002 |
Paracoccidioidomycosis |
54 |
0.406 |
|
765 |
|
c
|
CHR095 |
Chronic Progressive External Ophthalmoplegia |
49 |
0.406 |
|
766 |
|
c
|
ACT073 |
Acute Leukemia |
58 |
0.406 |
|
767 |
|
P
|
MYP006 |
Myopia |
56 |
0.406 |
|
768 |
|
|
FSC002 |
Fascioliasis |
44 |
0.406 |
|
769 |
|
P
|
SDR003 |
Sideroblastic Anemia |
51 |
0.406 |
|
770 |
|
|
PRX001 |
Peroxisomal Disease |
46 |
0.406 |
|
771 |
|
P
|
HYP083 |
Hypopituitarism |
52 |
0.406 |
|
772 |
|
|
NTR005 |
Nutritional Deficiency Disease |
61 |
0.406 |
|
773 |
|
P
|
HRD200 |
Hereditary Breast Ovarian Cancer Syndrome |
67 |
0.406 |
|
774 |
|
|
INT075 |
Intracranial Hypertension |
53 |
0.406 |
|
775 |
|
|
GSG001 |
Gas Gangrene |
52 |
0.406 |
|
776 |
|
|
MCH006 |
Mechanical Strabismus |
40 |
0.406 |
|
777 |
|
P
|
NRP001 |
Neuropathy |
60 |
0.406 |
|
778 |
|
|
AMB001 |
Amebiasis |
57 |
0.406 |
|
779 |
|
P
|
MTC133 |
Mitochondrial Myopathy |
50 |
0.406 |
|
780 |
|
|
PST092 |
Posttransplant Acute Limbic Encephalitis |
28 |
0.406 |
|
781 |
|
|
INF118 |
Inflammatory Myopathy with Abundant Macrophages |
27 |
0.406 |
|
782 |
|
|
FWL003 |
Fowler Urethral Sphincter Dysfunction Syndrome |
22 |
0.406 |
|
783 |
|
|
YLL002 |
Yellow Fever |
61 |
0.406 |
|
784 |
|
|
HRD180 |
Hereditary Persistence of Fetal Hemoglobin-Sickle Cell Disease Syndrome |
26 |
0.406 |
|
785 |
|
|
PNC129 |
Pancreatic Adenocarcinoma |
65 |
0.406 |
|
786 |
|
c
|
HPT001 |
Hepatitis C |
62 |
0.406 |
|
787 |
|
|
SYS004 |
Systemic Mastocytosis |
63 |
0.406 |
|
788 |
|
P
|
TRN020 |
Turner Syndrome |
67 |
0.406 |
|
789 |
|
P
|
MST009 |
Mastocytosis |
64 |
0.406 |
|
790 |
|
|
AVD001 |
Avoidant Personality Disorder |
49 |
0.406 |
|
791 |
|
P
|
GST044 |
Gastritis |
55 |
0.406 |
|
792 |
|
|
ACQ007 |
Acquired Immunodeficiency Syndrome |
59 |
0.406 |
|
793 |
|
|
ILS001 |
Ileus |
50 |
0.406 |
|
794 |
|
|
CLR030 |
Clear Cell Renal Cell Carcinoma |
54 |
0.406 |
|
795 |
|
|
ANT024 |
Anthrax Disease |
58 |
0.406 |
|
796 |
|
|
CHL061 |
Childhood Leukemia |
47 |
0.406 |
|
797 |
|
P
|
PLL002 |
Pellagra |
46 |
0.406 |
|
798 |
|
P
|
ART022 |
Arthritis |
71 |
0.406 |
|
799 |
|
P
|
RTN014 |
Retinal Artery Occlusion |
47 |
0.406 |
|
800 |
|
P
|
MNC007 |
Monocytic Leukemia |
47 |
0.406 |
|
801 |
|
|
ASY002 |
Asymptomatic Neurosyphilis |
41 |
0.406 |
|
802 |
|
|
SLC006 |
Silicosis |
56 |
0.406 |
|
803 |
|
|
CMM005 |
Common Cold |
56 |
0.406 |
|
804 |
|
c
|
SPR162 |
Spermatogenic Failure 50 |
42 |
0.406 |
|
805 |
|
|
CHL147 |
Chlamydia Pneumonia |
47 |
0.406 |
|
806 |
|
|
STR103 |
Streptococcus Pneumonia |
47 |
0.406 |
|
807 |
|
|
OST003 |
Osteonecrosis |
61 |
0.406 |
|
808 |
|
|
DNG003 |
Dengue Disease |
65 |
0.406 |
|
809 |
|
P
|
MLN007 |
Male Infertility |
56 |
0.406 |
|
810 |
|
P
|
ESP024 |
Esophagitis |
60 |
0.406 |
|
811 |
|
|
SYN005 |
Synostosis |
43 |
0.406 |
|
812 |
|
P
|
LKM002 |
Leukemia |
67 |
0.406 |
|
813 |
|
|
BRN026 |
Branch Retinal Artery Occlusion |
41 |
0.406 |
|
814 |
|
|
PPL022 |
Papilloma |
53 |
0.406 |
|
815 |
|
|
BLR008 |
Bilirubin Metabolic Disorder |
57 |
0.406 |
|
816 |
|
P
|
BRB001 |
Beriberi |
44 |
0.406 |
|
817 |
|
|
SQM002 |
Squamous Cell Papilloma |
46 |
0.406 |
|
818 |
|
|
TXC005 |
Toxic Shock Syndrome |
62 |
0.406 |
|
819 |
|
P
|
MLN008 |
Melanoma |
76 |
0.406 |
|
820 |
|
|
RTN020 |
Retinal Vascular Disease |
46 |
0.406 |
|
821 |
|
P
|
NPH012 |
Nephrotic Syndrome |
60 |
0.406 |
|
822 |
|
P
|
CRN037 |
Craniosynostosis |
68 |
0.406 |
|
823 |
|
|
HPT014 |
Hepatorenal Syndrome |
49 |
0.406 |
|
824 |
|
P
|
MCR010 |
Microcephaly |
60 |
0.406 |
|
825 |
|
|
RBS001 |
Rabies |
58 |
0.406 |
|
826 |
|
|
SPT005 |
Spotted Fever |
49 |
0.406 |
|
827 |
|
|
KRT002 |
Keratomalacia |
55 |
0.406 |
|
828 |
|
|
TTN003 |
Tetanus |
65 |
0.406 |
|
829 |
|
|
HYP006 |
Hypertensive Heart Disease |
49 |
0.406 |
|
830 |
|
P
|
RHN004 |
Rhinitis |
57 |
0.406 |
|
831 |
|
|
THY030 |
Thyroid Gland Disease |
50 |
0.406 |
|
832 |
|
|
ADJ001 |
Adjustment Disorder |
47 |
0.406 |
|
833 |
|
P
|
PRP019 |
Peripheral Nervous System Disease |
58 |
0.406 |
|
834 |
|
|
PRM020 |
Premenstrual Tension |
39 |
0.406 |
|
835 |
|
|
GNG013 |
Gingivitis |
59 |
0.406 |
|
836 |
|
c
|
CNT035 |
Central Nervous System Disease |
54 |
0.406 |
|
837 |
|
|
GST045 |
Gastroenteritis |
58 |
0.406 |
|
838 |
|
P
|
ART021 |
Arteriosclerosis |
54 |
0.406 |
|
839 |
|
P
|
THR015 |
Thrombophilia |
51 |
0.406 |
|
840 |
|
c
|
FML021 |
Familial Hypercholesterolemia |
72 |
0.406 |
|
841 |
|
P
|
PLY019 |
Polyneuropathy |
52 |
0.406 |
|
842 |
|
|
TYP007 |
Typhoid Fever |
64 |
0.406 |
|
843 |
|
|
ERY004 |
Erysipelas |
47 |
0.406 |
|
844 |
|
|
CHL035 |
Cholinergic Urticaria |
29 |
0.406 |
|
845 |
|
P
|
GND004 |
Gonadal Dysgenesis |
47 |
0.406 |
|
846 |
|
|
NCR001 |
Necrotizing Ulcerative Gingivitis |
26 |
0.406 |
|
847 |
|
|
PLM010 |
Pulmonary Edema |
55 |
0.406 |
|
848 |
|
|
GNG011 |
Gingival Disease |
54 |
0.406 |
|
849 |
|
P
|
URT039 |
Urticaria |
58 |
0.406 |
|
850 |
|
|
AZS001 |
Azoospermia |
45 |
0.406 |
|
851 |
|
|
HDR002 |
Hidradenitis Suppurativa |
54 |
0.406 |
|
852 |
|
P
|
BNC003 |
Bone Cancer |
58 |
0.406 |
|
853 |
|
c
|
SVR005 |
Severe Pre-Eclampsia |
50 |
0.406 |
|
854 |
|
|
DVL001 |
Developmental Coordination Disorder |
34 |
0.406 |
|
855 |
|
P
|
MNN013 |
Meningitis |
65 |
0.406 |
|
856 |
|
|
INV005 |
Inverted Follicular Keratosis |
32 |
0.406 |
|
857 |
|
P
|
ACT105 |
Acute Mountain Sickness |
52 |
0.406 |
|
858 |
|
|
ADS004 |
Aids Dementia Complex |
40 |
0.406 |
|
859 |
|
P
|
ENC004 |
Encephalitis |
61 |
0.406 |
|
860 |
|
|
ATS301 |
Autosomal Dominant Epilepsy with Auditory Features |
36 |
0.406 |
|
861 |
|
|
HNS001 |
Hansen's Disease |
32 |
0.406 |
|
862 |
|
|
MNN020 |
Meningococcal Infection |
45 |
0.406 |
|
863 |
|
|
NNT017 |
Neonatal Adrenoleukodystrophy |
54 |
0.406 |
|
864 |
|
|
ORL012 |
Oral Leukoplakia |
36 |
0.406 |
|
865 |
|
|
WLL004 |
Wallerian Degeneration |
38 |
0.406 |
|
866 |
|
|
CHR121 |
Charcot-Marie-Tooth Neuropathy X Type 5 |
17 |
0.406 |
|
867 |
|
|
DSR002 |
Disorders of Intracellular Cobalamin Metabolism |
29 |
0.406 |
|
868 |
|
P
|
MTC069 |
Mitochondrial Disorders |
57 |
0.406 |
|
869 |
|
|
CRB086 |
Cerebral Aneurysms |
40 |
0.406 |
|
870 |
|
|
DVL005 |
Developmental Dyspraxia |
22 |
0.406 |
|
871 |
|
|
CTS005 |
Catastrophic Antiphospholipid Syndrome |
43 |
0.406 |
|
872 |
|
|
CYT002 |
Cytokine Deficiency |
43 |
0.406 |
|
873 |
|
P
|
ADT009 |
Auditory Neuropathy Spectrum Disorder |
34 |
0.406 |
|
874 |
|
|
EXR007 |
Exercise-Induced Anaphylaxis |
23 |
0.406 |
|
875 |
|
|
NRS003 |
Neurosyphilis |
45 |
0.406 |
|
876 |
|
|
PNC049 |
Pancreatic Adenoma |
14 |
0.406 |
|
877 |
|
|
PST046 |
Post-Transplant Lymphoproliferative Disease |
53 |
0.406 |
|
878 |
|
|
DWR001 |
Dwarfism |
44 |
0.406 |
|
879 |
|
|
MSL001 |
Measles |
61 |
0.406 |
|
880 |
|
P
|
NRV007 |
Nervous System Disease |
67 |
0.406 |
|