Search results for Zinc

2344 hits were found for Zinc

# Family MCID Name MIFTS Score
1
ZNC004 Zinc Deficiency, Transient Neonatal 25 7.598
2
ACR056 Acrodermatitis Enteropathica, Zinc-Deficiency Type 57 5.538
3
ZNC006 Zinc, Elevated Plasma 20 3.634
4
P ZNC008 Zinc Finger Protein 1 22 3.111
5
c ZNC011 Zinc Finger Protein 106 13 2.966
6
c ZNC010 Zinc Finger Protein 105 8 2.961
7
c ZNC009 Zinc Finger Protein 103 6 2.956
8
c ZNC012 Zinc Finger Protein 109 5 2.956
9
ZNC005 Zinc-Responsive Necrolytic Acral Erythema 17 2.148
10
HYP803 Hyperzincemia with Functional Zinc Depletion 12 2.123
11
DSR029 Disorder of Zinc Metabolism and Transport 4 2.101
12
P DRR001 Diarrhea 55 0.352
13
IRN002 Iron Metabolism Disease 57 0.289
14
ACR005 Acrodermatitis 38 0.279
15
ENT007 Enteropathica 26 0.266
16
DFC004 Deficiency Anemia 70 0.207
17
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.202
18
LVR012 Liver Cirrhosis 62 0.194
19
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.181
20
P LTR001 Lateral Sclerosis 54 0.181
21
P ALP008 Alopecia 54 0.171
22
DRM006 Dermatitis 61 0.170
23
CMM005 Common Cold 57 0.167
24
HLX001 Helix Syndrome 47 0.167
25
c ACT004 Acute Diarrhea 39 0.163
26
IRN001 Iron Deficiency Anemia 59 0.159
27
c DRR009 Diarrhea 6 46 0.159
28
NTR005 Nutritional Deficiency Disease 62 0.158
29
c NRF023 Neurofibromatosis, Type Ii 80 0.155
30
P PNM007 Pneumonia 68 0.154
31
P LVR013 Liver Disease 68 0.153
32
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.153
33
P DBT009 Diabetes Mellitus 64 0.153
34
KRT002 Keratomalacia 47 0.152
35
HMN044 Human Immunodeficiency Virus Type 1 71 0.151
36
CHL079 Children's Interstitial Lung Disease 26 0.151
38
P ALZ034 Alzheimer Disease 88 0.140
39
HRW001 Hair Whorl 36 0.137
40
HYP080 Hypogonadism 50 0.135
41
HYP066 Hyperglycemia 61 0.129
42
48X005 48,xyyy 39 0.129
43
P PRS040 Prostate Cancer 97 0.128
44
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.125
45
CRH001 Crohn's Disease 74 0.124
46
INS024 Insulin-Like Growth Factor I 79 0.123
47
P PSR002 Psoriasis 62 0.123
48
P THL005 Thalassemia 60 0.123
49
PST011 Pustulosis of Palm and Sole 52 0.123
50
WLS001 Wilson Disease 71 0.122
51
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.121
52
P SCK005 Sickle Cell Disease 50 0.120
53
ALC007 Alcohol Dependence 66 0.118
54
ESP021 Esophageal Cancer 90 0.117
55
P LKM002 Leukemia 68 0.117
56
P KDN018 Kidney Disease 72 0.117
57
PPL052 Papillomatosis, Confluent and Reticulated 33 0.117
58
P NRB001 Neuroblastoma 72 0.116
59
BNR002 Bone Resorption Disease 48 0.116
60
IMM167 Immune Deficiency Disease 78 0.114
61
DWN001 Down Syndrome 70 0.113
62
P INF032 Infertility 57 0.113
63
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.113
64
CYT002 Cytokine Deficiency 42 0.113
65
P HYP086 Hypothyroidism 69 0.112
66
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.112
67
c PCH010 Pachyonychia Congenita 3 44 0.111
68
P HRP006 Herpes Simplex 65 0.110
69
P ENC018 Encephalopathy 61 0.110
70
ISC004 Ischemia 58 0.110
71
LSH001 Leishmaniasis 63 0.109
72
P KLZ004 Kala-Azar 1 41 0.109
73
P CLR023 Colorectal Cancer 99 0.108
74
SCK003 Sickle Cell Anemia 74 0.108
75
HYP056 Hypoglycemia 66 0.106
76
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.105
77
ALL026 Allergic Hypersensitivity Disease 62 0.104
78
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.103
79
P RTN024 Retinoblastoma 73 0.103
80
SKN016 Skin Disease 63 0.103
81
c FML008 Familial Retinoblastoma 53 0.103
82
ANR007 Anorexia Nervosa 63 0.102
83
P CTR002 Cataract 60 0.101
84
HPT004 Hepatic Coma 45 0.101
85
P OST002 Osteoporosis 74 0.100
86
P ATS364 Autism 70 0.100
87
HPT019 Hepatic Encephalopathy 60 0.100
88
P SZR006 Seizure Disorder 56 0.100
89
P MLN007 Male Infertility 55 0.100
90
TRM010 Traumatic Brain Injury 51 0.100
91
P HPT023 Hepatocellular Carcinoma 100 0.099
92
VSL002 Visual Epilepsy 59 0.099
93
PRT038 Protein-Energy Malnutrition 54 0.099
94
P INF037 Inflammatory Bowel Disease 54 0.099
95
BRN071 Brain Injury 49 0.099
96
CYS001 Cystic Fibrosis 81 0.098
97
DYS015 Dysentery 52 0.098
98
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.098
99
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.098
100
c PRC016 Pre-Eclampsia 63 0.097
101
P BRS047 Breast Cancer 97 0.095
102
P PNC035 Pancreatic Cancer 84 0.095
103
NRL016 Neural Tube Defects 82 0.095
104
RCK004 Rickets 68 0.095
105
INS001 Insulinoma 60 0.095
106
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.094
107
DPR016 Depression 63 0.094
108
ATM095 Autoimmune Disease 62 0.094
109
GNG013 Gingivitis 59 0.094
110
47X002 47,xyy 49 0.094
111
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.093
112
P EXN002 Exanthem 57 0.093
113
c BTT014 Beta-Thalassemia 74 0.092
114
LYM027 Lymphopenia 58 0.092
115
P NRP001 Neuropathy 56 0.092
116
GST023 Gastric Ulcer 53 0.092
117
ATX019 Ataxia with Vitamin E Deficiency 42 0.092
118
PLM001 Pulmonary Tuberculosis 69 0.091
119
AGN016 Aging 56 0.091
120
P MYC007 Myocardial Infarction 70 0.090
121
GST045 Gastroenteritis 59 0.090
122
URM002 Uremia 49 0.090
123
c CHR684 Chronic Kidney Disease 70 0.089
124
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.089
125
P PRD008 Periodontitis 64 0.089
126
P PNC044 Pancreatitis 61 0.089
127
CHL014 Cholera 59 0.089
128
BCT022 Bacterial Infectious Disease 56 0.089
129
DNT012 Dental Caries 53 0.089
130
MLR004 Malaria 81 0.087
131
ATH013 Atherosclerosis Susceptibility 65 0.087
132
P VSC007 Vascular Disease 63 0.087
133
ACQ007 Acquired Immunodeficiency Syndrome 60 0.087
134
CNT047 Contact Dermatitis 58 0.087
135
MCS002 Mucositis 56 0.087
136
HMS001 Hemosiderosis 54 0.087
137
ATS010 Autosomal Recessive Disease 48 0.087
138
P RRH023 Rare Hereditary Hemochromatosis 41 0.087
139
P GST053 Gastric Cancer 83 0.086
140
c ATS007 Autism Spectrum Disorder 67 0.086
141
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.086
142
P RHM011 Rheumatoid Arthritis 80 0.085
143
ACT119 Acute Promyelocytic Leukemia 63 0.085
144
FTT001 Fatty Liver Disease 61 0.085
145
PRS047 Prostatitis 56 0.085
146
PRS045 Prostatic Hypertrophy 53 0.085
147
OST159 Osteogenic Sarcoma 66 0.084
148
HYP266 Hypoxia 57 0.084
149
c DBT099 Diabetes Mellitus, Type I 65 0.082
150
P GLM045 Glioma 63 0.082
151
P NTR004 Neutropenia 63 0.082
152
CTN007 Cutaneous Leishmaniasis 62 0.082
153
c WLM018 Wilms Tumor 5 61 0.082
154
MNT002 Mental Depression 58 0.082
155
END086 End Stage Renal Disease 51 0.082
156
GLL048 Glial Tumor 45 0.082
157
c LKM061 Leukemia, Acute Myeloid 84 0.081
158
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.081
159
P DRM053 Dermatitis, Atopic 66 0.081
160
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.081
161
BLR008 Bilirubin Metabolic Disorder 57 0.081
162
STM007 Stomatitis 50 0.081
163
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.081
164
HVY002 Heavy Metal Poisoning 22 0.081
165
GLB015 Glioblastoma Multiforme 75 0.080
166
CLT003 Colitis 62 0.080
167
SQM006 Squamous Cell Carcinoma 60 0.080
168
P BCL017 B-Cell Lymphoma 58 0.080
169
EYD002 Eye Disease 58 0.080
170
c ACT075 Acute Myocardial Infarction 57 0.080
171
P HRT032 Heart Disease 75 0.078
172
P ADN016 Adenocarcinoma 64 0.078
173
c SVR001 Severe Acute Respiratory Syndrome 62 0.078
174
GST033 Gestational Diabetes 61 0.078
175
P MYL006 Myeloid Leukemia 60 0.078
176
P LNG032 Lung Cancer 98 0.077
177
P LPR021 Leprosy 3 69 0.077
178
TTN003 Tetanus 65 0.077
179
LPP008 Lipoprotein Quantitative Trait Locus 62 0.077
180
c HPT016 Hepatitis B 59 0.077
181
P HYP076 Hyperthyroidism 55 0.077
182
PRS021 Prostatic Adenoma 51 0.077
183
HNS001 Hansen's Disease 34 0.077
184
CRV035 Cervical Cancer 76 0.076
185
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.076
186
P LKM062 Leukemia, Acute Lymphoblastic 69 0.076
187
TXC005 Toxic Shock Syndrome 62 0.076
188
P ALP009 Alopecia Areata 60 0.076
189
ADN018 Adenoma 59 0.076
190
PRS129 Prostatic Hyperplasia, Benign 49 0.076
191
DWR001 Dwarfism 44 0.076
192
CVD001 Covid-19 44 0.076
193
c HYP595 Hypertension, Essential 84 0.074
194
ULC004 Ulcerative Colitis 73 0.074
195
CNG034 Congestive Heart Failure 69 0.074
196
MDD011 Mood Disorder 62 0.074
197
P OVR042 Ovarian Cancer 88 0.073
198
P LYM118 Lymphoma 68 0.073
199
c HPT001 Hepatitis C 62 0.073
200
c ACT027 Acute Pancreatitis 60 0.073
201
P PRP019 Peripheral Nervous System Disease 58 0.073
202
GLC003 Glucose Intolerance 54 0.073
203
HYP781 Hypoascorbemia 51 0.073
204
c MCR120 Microvascular Complications of Diabetes 7 47 0.073
205
P MLN008 Melanoma 69 0.071
206
P ART022 Arthritis 69 0.071
207
P CLC063 Celiac Disease 1 66 0.071
208
P CRN300 Coronary Heart Disease 1 63 0.071
209
P NPH012 Nephrotic Syndrome 60 0.071
210
c MCR113 Microvascular Complications of Diabetes 3 52 0.071
211
ART140 Arteries, Anomalies of 52 0.071
212
KRT009 Keratosis 51 0.071
213
c MCR130 Microvascular Complications of Diabetes 6 41 0.071
214
c MCR133 Microvascular Complications of Diabetes 4 41 0.071
215
PPT005 Peptic Ulcer Disease 59 0.070
216
P ALC033 Alcohol Use Disorder 58 0.070
217
P FTL001 Fetal Alcohol Syndrome 57 0.070
218
P SKN015 Skin Carcinoma 66 0.068
219
P PLY011 Polycystic Ovary Syndrome 56 0.068
221
P BLD134 Bladder Cancer 79 0.067
222
P DMN002 Dementia 66 0.067
223
ORL011 Oral Cancer 60 0.067
224
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.067
225
GTR002 Goiter 53 0.067
226
P NGH001 Night Blindness 48 0.067
227
P SBR004 Seborrheic Dermatitis 45 0.067
228
KWS001 Kwashiorkor 44 0.067
229
PCD001 Pica Disease 41 0.067
230
CHR178 Chromosomal Triplication 35 0.067
231
CHL068 Cholestasis 61 0.065
232
SPN186 Spinal Cord Injury 60 0.065
233
LNG099 Lung Disease 60 0.065
234
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.065
235
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.065
236
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.065
237
MST005 Mastitis 53 0.065
238
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.065
239
ARG004 Argyria 27 0.065
240
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.063
241
c HPT073 Hepatitis C Virus 72 0.063
242
P PHC003 Pheochromocytoma 71 0.063
243
P HPT021 Hepatitis 67 0.063
244
CLN015 Colon Adenocarcinoma 65 0.063
245
LPD008 Lipid Metabolism Disorder 62 0.063
246
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.063
247
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.063
248
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.063
249
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.063
250
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.063
251
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.063
252
ADR040 Adrenal Gland Pheochromocytoma 46 0.063
253
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.063
254
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.063
255
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.063
256
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.063
257
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.063
258
P LNG064 Lung Cancer Susceptibility 3 78 0.062
259
c ATR087 Atrial Standstill 1 75 0.062
260
c HYP836 Hypercholesterolemia, Familial, 1 73 0.062
261
ANX010 Anxiety 73 0.062
262
P AMY004 Amyloidosis 70 0.062
263
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.062
264
P HML002 Hemolytic Anemia 63 0.062
265
GST050 Gastrointestinal System Disease 56 0.062
266
P GST044 Gastritis 56 0.062
267
ALC009 Alcoholic Liver Cirrhosis 53 0.062
268
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.062
269
OLG001 Oligospermia 45 0.062
270
CRB004 Cerebral Artery Occlusion 45 0.062
271
c SPR086 Spermatogenic Failure 3 44 0.062
272
HMP009 Haemophilus Influenzae 43 0.062
273
P MJR001 Major Depressive Disorder 68 0.060
274
c WLM013 Wilms Tumor 1 65 0.060
275
P EHL001 Ehlers-Danlos Syndrome 58 0.060
276
P PRN023 Prion Disease 57 0.060
277
APH001 Aphthous Stomatitis 57 0.060
278
HYP005 Hypokalemia 55 0.060
279
HYP060 Hyperinsulinism 54 0.060
280
P THY032 Thyroiditis 52 0.060
281
SXL003 Sexual Disorder 47 0.060
282
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.060
283
MYL069 Myeloma, Multiple 85 0.058
284
P RTN008 Retinitis Pigmentosa 79 0.058
285
OST012 Osteoarthritis 78 0.058
286
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.058
287
P NSP012 Nasopharyngeal Carcinoma 66 0.058
288
MSL001 Measles 62 0.058
289
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.058
290
c ACT071 Acute Kidney Failure 60 0.058
291
P BND020 Bone Disease 59 0.058
292
SCH014 Schistosomiasis 57 0.058
293
PPL022 Papilloma 54 0.058
294
P MNC007 Monocytic Leukemia 53 0.058
295
c VRL010 Viral Hepatitis 52 0.058
296
P SPP010 Suppressor of Tumorigenicity 3 51 0.058
297
CCC002 Coccidiosis 51 0.058
298
PLC008 Placenta Disease 50 0.058
299
RTN023 Retinitis 46 0.058
300
GRD001 Giardiasis 45 0.058
301
ORL015 Oral Squamous Cell Carcinoma 43 0.058
302
NRR001 Neuroretinitis 42 0.058
303
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.058
304
PST092 Posttransplant Acute Limbic Encephalitis 29 0.058
305
P MLT020 Multiple Sclerosis 72 0.056
306
P MSC005 Muscular Dystrophy 66 0.056
307
c SML038 Small Cell Cancer of the Lung 65 0.056
308
P ADL010 Adult Respiratory Distress Syndrome 65 0.056
309
ETN001 Eating Disorder 60 0.056
310
THY029 Thyroid Carcinoma 59 0.056
311
c ACT073 Acute Leukemia 58 0.056
312
ANT024 Anthrax Disease 58 0.056
313
P BPL003 Bipolar Disorder 56 0.056
314
IMP005 Impotence 52 0.056
315
MTB004 Metabolic Acidosis 50 0.056
316
c MJR024 Major Affective Disorder 9 41 0.056
317
c MJR022 Major Affective Disorder 8 38 0.056
318
PLY150 Polykaryocytosis Inducer 31 0.056
319
STT009 Sutton Disease 2 30 0.056
320
AST005 Asthma 76 0.054
321
SVR004 Severe Combined Immunodeficiency 73 0.054
322
P EPL164 Epilepsy 71 0.054
323
P MYC084 Mycobacterium Tuberculosis 1 68 0.054
324
BRK010 Burkitt Lymphoma 67 0.054
325
P HYP098 Hypereosinophilic Syndrome 67 0.054
326
CHG001 Chagas Disease 66 0.054
327
c ACT068 Acute Cystitis 63 0.054
328
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.054
329
ALC006 Alcoholic Hepatitis 61 0.054
330
c DWL002 Dowling-Degos Disease 1 58 0.054
331
GLS018 Glass Syndrome 57 0.054
332
P RHN004 Rhinitis 57 0.054
333
EMB004 Embryonal Carcinoma 56 0.054
334
RSC001 Rosacea 54 0.054
335
ACD008 Acid-Labile Subunit Deficiency 54 0.054
336
P LCH002 Lichen Planus 53 0.054
337
OCL069 Ocular Motor Apraxia 51 0.054
338
ENT011 Enterocolitis 51 0.054
339
P OVR082 Overgrowth Syndrome 50 0.054
340
AZS001 Azoospermia 50 0.054
341
IMP004 Impetigo 49 0.054
342
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.054
343
NWC001 Newcastle Disease 45 0.054
344
c LKM005 Leukemia, T-Cell, Chronic 34 0.054
345
c HMC039 Hemochromatosis, Type 1 74 0.053
346
OTT002 Otitis Media 72 0.053
347
BRN024 Bronchitis 68 0.053
348
PNC129 Pancreatic Adenocarcinoma 68 0.053
349
c RHB024 Rhabdomyosarcoma 2 67 0.053
350
P MNN013 Meningitis 66 0.053
351
P MTR014 Motor Neuron Disease 65 0.053
352
PRT037 Pertussis 65 0.053
353
CLF027 Cleft Palate, Isolated 64 0.053
354
c ALP101 Alpha-Thalassemia 62 0.053
355
SHG001 Shigellosis 60 0.053
356
STT001 Status Epilepticus 60 0.053
357
P CND004 Candidiasis 58 0.053
358
P FBR017 Fibrosarcoma 56 0.053
359
ALL010 Allergic Contact Dermatitis 56 0.053
360
PLM010 Pulmonary Edema 54 0.053
361
P RTN016 Retinal Degeneration 53 0.053
362
THY030 Thyroid Gland Disease 52 0.053
363
FDL002 Food Allergy 51 0.053
364
P ECL001 Eclampsia 50 0.053
365
SQM002 Squamous Cell Papilloma 46 0.053
366
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 0.053
367
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.050
368
P PRK057 Parkinson Disease, Late-Onset 78 0.050
369
P HNT016 Huntington Disease 72 0.050
370
P MYP004 Myopathy 70 0.050
371
ART016 Aortic Aneurysm 69 0.050
372
GST092 Gastroesophageal Reflux 67 0.050
373
P PRP029 Porphyria 62 0.050
374
DCB001 Decubitus Ulcer 61 0.050
375
P OPT006 Optic Nerve Disease 60 0.050
376
P BRS044 Breast Adenocarcinoma 59 0.050
377
c ACT134 Acute Liver Failure 56 0.050
378
NPH009 Nephrolithiasis 55 0.050
379
CHR100 Chronic Ulcer of Skin 55 0.050
380
P ART021 Arteriosclerosis 54 0.050
381
P TRM003 Tremor 54 0.050
382
P FBR031 Febrile Seizures 53 0.050
383
P INT068 Intestinal Disease 53 0.050
384
TLN003 Telangiectasis 52 0.050
385
P TMP001 Temporal Lobe Epilepsy 50 0.050
386
ORL013 Oral Lichen Planus 45 0.050
387
GLC036 Glucagonoma 45 0.050
388
ALL014 Allergic Encephalomyelitis 38 0.050
389
MYL009 Myelodysplastic Syndrome 70 0.048
390
P ASP006 Aspergillosis 69 0.048
391
LYM133 Lymphoma, Hodgkin, Classic 69 0.048
392
P DYS154 Dystonia 65 0.048
393
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.048
394
PRT036 Peritonitis 64 0.048
395
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.048
396
c HPT003 Hepatitis a 62 0.048
397
c BRN108 Branchiootic Syndrome 1 62 0.048
398
P ESP024 Esophagitis 62 0.048
399
P KDN017 Kidney Cancer 60 0.048
400
DPH001 Diphtheria 60 0.048
401
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.048
402
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.048
403
PRN019 Perinatal Necrotizing Enterocolitis 59 0.048
404
BRN002 Bronchiolitis 59 0.048
405
NWB001 Newborn Respiratory Distress Syndrome 58 0.048
406
BRN056 Bronchopulmonary Dysplasia 57 0.048
407
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.048
408
HMG005 Hemoglobinopathy 56 0.048
409
ANG005 Anogenital Venereal Wart 55 0.048
410
P XRD029 Xeroderma Pigmentosum, Complementation Group a 55 0.048
411
c PRD040 Periodontitis, Chronic 53 0.048
412
P SHR001 Short Bowel Syndrome 53 0.048
413
OST011 Osteomalacia 52 0.048
414
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.048
415
P MYT002 Myotonic Dystrophy 49 0.048
416
VRC001 Varicocele 49 0.048
417
P SDR003 Sideroblastic Anemia 49 0.048
418
URL001 Urolithiasis 45 0.048
419
c PRM038 Primary Agammaglobulinemia 44 0.048
420
SNL007 Senile Cataract 42 0.048
421
c CHR682 Chronic Bilirubin Encephalopathy 39 0.048
422
CVT001 Cavitary Optic Disc Anomalies 38 0.048
423
P SCH015 Schizophrenia 74 0.046
424
PRP027 Peripheral Vascular Disease 71 0.046
425
ADL002 Adult Syndrome 70 0.046
426
SKN019 Skin Melanoma 68 0.046
427
P CRD119 Cardiac Arrest 67 0.046
428
P MCR115 Microvascular Complications of Diabetes 5 66 0.046
429
SRC014 Sarcoma 65 0.046
430
BRR014 Barrett Esophagus 65 0.046
431
P HYP750 Hypertriglyceridemia, Familial 62 0.046
432
VRL011 Viral Infectious Disease 61 0.046
433
c PRT132 Protoporphyria, Erythropoietic, 1 61 0.046
434
P LPS004 Lupus Erythematosus 61 0.046
435
HLC007 Helicobacter Pylori Infection 59 0.046
436
P CRD246 Cardiovascular System Disease 57 0.046
437
PHR003 Pharyngitis 57 0.046
438
c GRV008 Graves Disease 1 56 0.046
439
ORL004 Oral Submucous Fibrosis 55 0.046
440
FDB001 Foodborne Botulism 55 0.046
441
P GRV001 Graves' Disease 55 0.046
442
P MYP006 Myopia 55 0.046
443
NNT012 Neonatal Jaundice 53 0.046
444
CLR109 Colorectal Adenocarcinoma 51 0.046
445
P ALP061 Alopecia, Androgenetic, 1 49 0.046
446
P MRC003 Mercury Poisoning 48 0.046
447
GLS007 Glossitis 47 0.046
448
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.046
449
P CHR345 Chronic Pain 44 0.046
450
PRS042 Prostate Disease 43 0.046
451
MRS001 Marasmus 42 0.046
452
PHN003 Phenylketonuria 75 0.044
453
ANG054 Angina Pectoris 66 0.044
454
GT001 Gout 64 0.044
455
PLM031 Poliomyelitis 64 0.044
456
P HYP069 Hyperparathyroidism 63 0.044
457
P END044 Endometriosis 63 0.044
458
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.044
459
P TRC086 Trichohepatoenteric Syndrome 1 62 0.044
460
P SCL018 Scoliosis 60 0.044
461
P MCR010 Microcephaly 59 0.044
462
BRS051 Breast Disease 58 0.044
463
P GLM007 Glomerulonephritis 57 0.044
464
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.044
465
ERY051 Erythroleukemia, Familial 56 0.044
466
ANN002 Anencephaly 56 0.044
467
SPN035 Spindle Cell Sarcoma 53 0.044
468
P DDN001 Duodenal Ulcer 52 0.044
469
P TRT010 Teratoma 52 0.044
470
CRN030 Coronary Stenosis 50 0.044
471
P KRT007 Keratoconus 50 0.044
472
DYS073 Dysphagia 50 0.044
473
LPR001 Lepromatous Leprosy 50 0.044
474
VCC001 Vaccinia 49 0.044
475
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.044
476
GRW007 Growth Hormone Deficiency 46 0.044
477
c MLG068 Malignant Glioma 46 0.044
478
RTR008 Root Resorption 45 0.044
479
GST020 Gastric Antral Vascular Ectasia 41 0.044
480
PRM020 Premenstrual Tension 40 0.044
481
ALV001 Alveolar Periostitis 30 0.044
482
c SYS001 Systemic Lupus Erythematosus 86 0.041
483
P ATX030 Ataxia-Telangiectasia 82 0.041
484
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.041
485
c DLT002 Dilated Cardiomyopathy 79 0.041
486
P MDL005 Medulloblastoma 77 0.041
487
END057 Endometrial Cancer 74 0.041
488
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.041
489
P SLP006 Sleep Apnea 69 0.041
490
P SYS005 Systemic Scleroderma 68 0.041
491
c BSL007 Basal Cell Carcinoma 68 0.041
492
P TRN020 Turner Syndrome 67 0.041
493
P PLM037 Pulmonary Hypertension 67 0.041
494
TBC004 Tobacco Addiction 64 0.041
495
CLR108 Colorectal Adenoma 64 0.041
496
P PRM006 Primary Biliary Cirrhosis 62 0.041
497
CHR066 Chronic Fatigue Syndrome 61 0.041
498
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.041
499
P MYC008 Myocarditis 59 0.041
500
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.041
501
DSS008 Disease of Mental Health 58 0.041
502
VSC002 Vascular Dementia 57 0.041
503
P PLY019 Polyneuropathy 56 0.041
504
VSC003 Visceral Leishmaniasis 55 0.041
505
HDR002 Hidradenitis Suppurativa 55 0.041
506
P LRY044 Larynx Cancer 55 0.041
507
CLF001 Cleft Lip 53 0.041
508
P RTN018 Retinal Disease 53 0.041
509
P MSC003 Muscular Atrophy 52 0.041
510
PLP001 Pulpitis 49 0.041
511
HDR003 Hidradenitis 49 0.041
512
CMP034 Complete Androgen Insensitivity Syndrome 46 0.041
513
P PLL002 Pellagra 46 0.041
514
P BNG032 Benign Mesothelioma 46 0.041
515
PTT037 Pituitary Tumors 44 0.041
516
MDD018 Middle East Respiratory Syndrome 43 0.041
517
HYP784 Hypogonadism, Male 40 0.041
518
OVR094 Ovarian Epithelial Cancer 38 0.041
519
ANP008 Anaplastic Oligoastrocytoma 30 0.041
520
LPT014 Leptin Deficiency or Dysfunction 74 0.039
521
c LKM063 Leukemia, Chronic Myeloid 72 0.039
522
PCK003 Pick Disease of Brain 68 0.039
523
KHL003 Kohlschutter-Tonz Syndrome 65 0.039
524
P PLM036 Pulmonary Fibrosis 65 0.039
525
P HRS035 Hirschsprung Disease 1 65 0.039
526
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.039
527
HYP020 Hyperprolactinemia 64 0.039
528
P ANR048 Aniridia 1 63 0.039
529
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.039
530
c FNC043 Fanconi Anemia, Complementation Group E 62 0.039
531
PHL006 Phelan-Mcdermid Syndrome 62 0.039
532
RTN017 Retinal Detachment 61 0.039
533
CHC001 Chickenpox 60 0.039
534
P DNG005 Dengue Virus 59 0.039
535
P PLY006 Polydactyly 59 0.039
536
CRY005 Cryptococcosis 58 0.039
537
CNS004 Constipation 58 0.039
538
DNY001 Denys-Drash Syndrome 57 0.039
539
P PYL005 Pyelonephritis 56 0.039
540
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.039
541
P SBS003 Substance Abuse 55 0.039
542
P SLM003 Salmonellosis 55 0.039
543
GNT003 Genital Herpes 54 0.039
544
MWT001 Mowat-Wilson Syndrome 54 0.039
545
PNC001 Pancytopenia 54 0.039
546
P INS002 in Situ Carcinoma 53 0.039
547
c NGH026 Night Blindness, Congenital Stationary, Type 1a 52 0.039
548
HYP014 Hyperuricemia 52 0.039
549
LMY002 Leiomyoma 52 0.039
550
TNG007 Tongue Carcinoma 51 0.039
551
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.039
552
RTN003 Retinal Ischemia 50 0.039
553
PST021 Postpartum Depression 50 0.039
554
BRN009 Burning Mouth Syndrome 50 0.039
555
c SVR005 Severe Pre-Eclampsia 50 0.039
556
SPL018 Splenomegaly 48 0.039
557
AND014 Androgenic Alopecia 46 0.039
558
FLL008 Folliculitis 46 0.039
559
HDN002 Head Injury 46 0.039
560
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.039
561
TRT001 Teratocarcinoma 45 0.039
562
IMM136 Immune System Disease 45 0.039
563
CRT015 Carotid Artery Occlusion 45 0.039
564
P BLP003 Blepharospasm 44 0.039
565
DMP001 Dumping Syndrome 44 0.039
566
EXC002 Exocrine Pancreatic Insufficiency 42 0.039
567
c CNG498 Congenital Disorder of Glycosylation, Type Iin 40 0.039
568
c BLP048 Blepharospasm, Benign Essential 37 0.039
569
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.039
570
HND015 Hand Skill, Relative 33 0.039
571
TLG001 Telogen Effluvium 30 0.039
572
MTH071 Methane Production 26 0.039
573
c FNC027 Fanconi Anemia, Complementation Group a 81 0.036
574
P GLM040 Glioma Susceptibility 1 81 0.036
575
P RTT002 Rett Syndrome 80 0.036
576
P RSP003 Respiratory Failure 74 0.036
577
c SPN225 Spondyloarthropathy 1 73 0.036
578
P CNR004 Cone-Rod Dystrophy 2 73 0.036
579
c EXD008 Exudative Vitreoretinopathy 1 71 0.036
580
P INF038 Influenza 68 0.036
581
P AGM001 Agammaglobulinemia 65 0.036
582
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.036
583
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.036
584
P RHB003 Rhabdomyosarcoma 63 0.036
585
TYP007 Typhoid Fever 63 0.036
586
P ECT006 Ectodermal Dysplasia 62 0.036
587
P PLY014 Polycystic Kidney Disease 62 0.036
588
PSR001 Psoriatic Arthritis 61 0.036
589
P SJG008 Sjogren Syndrome 61 0.036
590
DRR016 Diarrhea 2, with Microvillus Atrophy 60 0.036
591
P TXP001 Toxoplasmosis 60 0.036
592
ACN002 Acanthosis Nigricans 60 0.036
593
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.036
594
PRT013 Portal Hypertension 59 0.036
595
P ANP001 Anaplastic Large Cell Lymphoma 58 0.036
596
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.036
597
P CHN012 Chondrosarcoma 56 0.036
598
PLS011 Plasmacytoma 56 0.036
599
BRN004 Brain Edema 56 0.036
600
HPT022 Hepatoblastoma 56 0.036
601
c FML035 Familial Hyperlipidemia 55 0.036
602
AMB001 Amebiasis 55 0.036
603
ANL018 Analbuminemia 54 0.036
604
SLP001 Sleeping Sickness 54 0.036
605
CLL003 Cellulitis 54 0.036
606
CRH005 Crohn's Colitis 53 0.036
607
DRM011 Dermatophytosis 52 0.036
608
PLS009 Plasma Cell Neoplasm 51 0.036
609
c PNC106 Pancreatic Agenesis 1 51 0.036
610
P AST007 Astrocytoma 51 0.036
611
CRV040 Cervix Carcinoma 51 0.036
612
PYD002 Pyoderma 50 0.036
613
BLR001 Biliary Atresia 50 0.036
614
PNC034 Pancreas Disease 48 0.036
615
VTM002 Vitamin B12 Deficiency 48 0.036
616
MCR018 Microcytic Anemia 47 0.036
617
CLF056 Cleft Lip with or Without Cleft Palate 47 0.036
618
c SCH079 Schizophrenia 1 46 0.036
619
ACT003 Acute Kidney Tubular Necrosis 45 0.036
620
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.036
621
P SDR002 Siderosis 44 0.036
622
P HYP265 Hypotonia 43 0.036
623
CRN322 Coronavirus Infectious Disease 40 0.036
624
LKP003 Leukoplakia 39 0.036
625
ULC007 Ulcerative Stomatitis 39 0.036
626
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.036
627
P HMF004 Hemifacial Spasm 38 0.036
628
END028 Endemic Goiter 37 0.036
629
SCR003 Secretory Diarrhea 37 0.036
630
PYR009 Pyridoxine Deficiency Anemia 34 0.036
631
c HMF011 Hemifacial Spasm, Familial 33 0.036
632
NNN007 Non-Involuting Congenital Hemangioma 33 0.036
633
P EHL083 Ehlers-Danlos Syndrome, Spondylodysplastic Type, 3 32 0.036
634
EXN003 Exencephaly 31 0.036
635
STR067 Stroke, Ischemic 81 0.033
636
KPS004 Kaposi Sarcoma 75 0.033
637
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.033
638
MSC157 Muscular Dystrophy, Duchenne Type 72 0.033
639
GST040 Gastric Adenocarcinoma 70 0.033
640
c PNC108 Pancreatitis, Hereditary 70 0.033
641
EWN003 Ewing Sarcoma 69 0.033
642
CMM004 Common Variable Immunodeficiency 68 0.033
643
CNN005 Connective Tissue Disease 68 0.033
644
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.033
645
THY111 Thyroid Carcinoma, Familial Medullary 67 0.033
646
c MCR129 Microvascular Complications of Diabetes 1 66 0.033
647
KRT019 Keratitis, Hereditary 65 0.033
648
ACR006 Aceruloplasminemia 65 0.033
649
P LPS002 Liposarcoma 65 0.033
650
MNK001 Menkes Disease 64 0.033
651
BRC012 Brucellosis 64 0.033
652
TRN015 Transient Cerebral Ischemia 63 0.033
653
BLL006 Bullous Pemphigoid 62 0.033
654
P VSC011 Vasculitis 62 0.033
655
HSH003 Hashimoto Thyroiditis 62 0.033
656
INT002 Intermittent Claudication 61 0.033
657
P ENC004 Encephalitis 61 0.033
658
SDD001 Sudden Infant Death Syndrome 61 0.033
659
DNG002 Dengue Hemorrhagic Fever 60 0.033
660
P SNS001 Sensorineural Hearing Loss 60 0.033
661
VRC005 Varicose Veins 60 0.033
662
P GLY013 Glycogen Storage Disease 60 0.033
663
SPP011 Suppression of Tumorigenicity 12 59 0.033
664
CHL123 Chlamydia 59 0.033
665
PLM033 Pulmonary Embolism 59 0.033
666
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.033
667
ANR040 Aneurysm 59 0.033
668
GLB001 Gilbert Syndrome 58 0.033
669
P INT070 Intestinal Obstruction 58 0.033
670
P URT039 Urticaria 58 0.033
671
P BNC003 Bone Cancer 58 0.033
672
THR024 Thrombosis 57 0.033
673
P PRV006 Pervasive Developmental Disorder 57 0.033
674
AYM001 Ayme-Gripp Syndrome 57 0.033
675
CMR002 Coumarin Resistance 56 0.033
676
ALL006 Allergic Asthma 56 0.033
677
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.033
678
MTH009 Mouth Disease 56 0.033
679
P PNM006 Pneumoconiosis 56 0.033
680
ORP003 Oropharynx Cancer 55 0.033
681
LMB062 Limb Ischemia 55 0.033
682
PRP030 Purpura 54 0.033
683
AMN003 Amnestic Disorder 54 0.033
684
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.033
685
P ICH004 Ichthyosis 54 0.033
686
AMN001 Amenorrhea 54 0.033
687
NNL006 Non-Alcoholic Steatohepatitis 54 0.033
688
HMC014 Homocysteinemia 53 0.033
689
TRC003 Trichomoniasis 53 0.033
690
c PSR017 Psoriasis 2 53 0.033
691
DMY004 Demyelinating Disease 52 0.033
692
P HYP730 Hypogonadotropic Hypogonadism 52 0.033
693
PPT001 Peptic Esophagitis 52 0.033
694
PNG002 Pain Agnosia 51 0.033
695
LNG031 Lung Benign Neoplasm 51 0.033
696
DRR008 Diarrhea 1, Secretory Chloride, Congenital 51 0.033
697
c SCN007 Secondary Hyperparathyroidism 51 0.033
698
BHR001 Behr Syndrome 51 0.033
699
PRS034 Parasitic Helminthiasis Infectious Disease 50 0.033
700
HPT014 Hepatorenal Syndrome 50 0.033
701
ISL003 Isolated Growth Hormone Deficiency 49 0.033
702
P END046 Endometritis 49 0.033
703
P HYP058 Hypervitaminosis a 48 0.033
704
INT067 Interstitial Nephritis 48 0.033
705
P GND004 Gonadal Dysgenesis 48 0.033
706
ANT018 Anthracosis 48 0.033
707
RNL077 Renal Fibrosis 47 0.033
708
c INH020 Inherited Metabolic Disorder 47 0.033
709
KRT013 Keratolytic Winter Erythema 46 0.033
710
CYN002 Cyanosis, Transient Neonatal 45 0.033
711
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.033
712
CRB090 Cerebral Hypoxia 44 0.033
713
SKN005 Skin Atrophy 43 0.033
714
49X006 49, Xxxxy Syndrome 41 0.033
715
ANX004 Anoxia 40 0.033
716
SPR126 Superior Semicircular Canal Dehiscence 40 0.033
717
P TRC031 Trichorhinophalangeal Syndrome 40 0.033
718
c PRG020 Paragangliomas 3 39 0.033
719
c HMG029 Hemoglobin Se Disease 39 0.033
720
P PST059 Pustular Psoriasis 37 0.033
721
PRM329 Premature Aging 35 0.033
722
ATX010 Ataxia Neuropathy Spectrum 34 0.033
723
RTC003 Root Caries 33 0.033
724
ACT064 Acute Necrotizing Encephalitis 33 0.033
725
CMM003 Common Wart 32 0.033
726
CPP004 Copper Deficiency Myelopathy 30 0.033
727
BLD137 Blood Group--Ahonen 16 0.033
728
P LKM071 Leukemia, Chronic Lymphocytic 79 0.029
729
BRN028 Brain Cancer 74 0.029
730
P NJM001 Nijmegen Breakage Syndrome 74 0.029
731
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.029
732
P GRF003 Graft-Versus-Host Disease 72 0.029
733
P HYP061 Hypertrophic Cardiomyopathy 70 0.029
734
CRB037 Cerebral Palsy 69 0.029
735
P ANG001 Angelman Syndrome 69 0.029
736
c MYT021 Myotonic Dystrophy 1 69 0.029
737
P FRN006 Frontotemporal Dementia 68 0.029
738
P THR014 Thrombocytopenia 67 0.029
739
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.029
740
c INF071 Inflammatory Bowel Disease 1 67 0.029
741
CRB039 Cerebrovascular Disease 67 0.029
742
PSY004 Psychotic Disorder 67 0.029
743
c MCL013 Mucolipidosis Iv 66 0.029
744
PRP001 Propionic Acidemia 65 0.029
745
IRR002 Irritable Bowel Syndrome 65 0.029
746
DGR001 Digeorge Syndrome 64 0.029
747
c CNG006 Congenital Hypothyroidism 64 0.029
748
PLG002 Plague 63 0.029
749
P THR117 Three M Syndrome 1 63 0.029
750
HMT002 Hematologic Cancer 62 0.029
751
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.029
752
P ART023 Arthropathy 62 0.029
753
CHR619 Chromosome 2q35 Duplication Syndrome 62 0.029
754
CRC021 Carcinosarcoma 62 0.029
756
c PNS012 Paine Syndrome 61 0.029
757
WLL001 Williams-Beuren Syndrome 60 0.029
758
KFR001 Kufor-Rakeb Syndrome 60 0.029
759
CRD223 Cardiac Arrhythmia 60 0.029
760
c DNG003 Dengue Disease 59 0.029
761
P PRD006 Prader-Willi Syndrome 59 0.029
762
c PRM005 Primary Hyperparathyroidism 58 0.029
763
P EPD083 Epidermodysplasia Verruciformis 1 58 0.029
764
PMP006 Pemphigus Vulgaris, Familial 57 0.029
765
BLM002 Bulimia Nervosa 57 0.029
766
BRD001 Brody Myopathy 57 0.029
767
c MST023 Mesothelioma, Malignant 57 0.029
768
TNS005 Tonsillitis 57 0.029
769
CHR177 Chromophobe Renal Cell Carcinoma 57 0.029
770
JPN002 Japanese Encephalitis 57 0.029
771
TRN018 Transitional Cell Carcinoma 56 0.029
772
SFT003 Soft Tissue Sarcoma 56 0.029
773
ORL005 Oral Candidiasis 56 0.029
774
P HYP024 Hypoparathyroidism 56 0.029
775
SLC006 Silicosis 56 0.029
776
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.029
777
P DRM007 Dermatitis Herpetiformis 55 0.029
778
END040 Endogenous Depression 55 0.029
779
P PMP001 Pemphigus 54 0.029
780
CRT017 Cartilage Disease 54 0.029
781
BRN014 Bronchopneumonia 54 0.029
782
THR013 Thoracic Outlet Syndrome 54 0.029
783
DBT010 Diabetic Neuropathy 54 0.029
784
LYM040 Lymphoblastic Lymphoma 54 0.029
785
MYM001 Myoma 54 0.029
786
P LCT002 Lactose Intolerance 53 0.029
787
RHM028 Rheumatic Heart Disease 53 0.029
788
OST016 Osteochondrosis 53 0.029
789
P HYP083 Hypopituitarism 53 0.029
790
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.029
791
P ORL007 Oral Cavity Cancer 53 0.029
792
P ACT008 Actinic Keratosis 53 0.029
793
c HPT007 Hepatitis E 53 0.029
794
c PSR023 Psoriasis 1 52 0.029
795
P HMP007 Hemophilia 51 0.029
796
ILS001 Ileus 51 0.029
797
MGL001 Megaloblastic Anemia 51 0.029
798
P HYP040 Hypospadias 51 0.029
799
PLR007 Pleural Empyema 50 0.029
800
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.029
801
P BRT029 Brittle Cornea Syndrome 2 50 0.029
802
CRT013 Carotid Stenosis 50 0.029
803
THY125 Thyroid Gland Medullary Carcinoma 50 0.029
804
TRY001 Trypanosomiasis 50 0.029
805
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.029
806
VLV047 Volvulus of Midgut 49 0.029
807
IRR003 Irritant Dermatitis 49 0.029
808
LYM138 Lymphoblastic Leukemia, Acute, with Lymphomatous Features 49 0.029
809
P CTN015 Cutaneous T Cell Lymphoma 49 0.029
810
c INV001 Invasive Aspergillosis 49 0.029
811
c BCT013 Bacterial Pneumonia 48 0.029
812
WTH001 Withdrawal Disorder 48 0.029
813
c PSR032 Psoriasis 11 47 0.029
814
LYM009 Lymphocytic Choriomeningitis 47 0.029
815
KHN001 Kuhnt-Junius Degeneration 47 0.029
816
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.029
817
HYP082 Hypopharynx Cancer 47 0.029
818
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.029
819
P OVR046 Ovarian Cyst 47 0.029
820
LYM019 Lymphosarcoma 46 0.029
821
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.029
822
ATN005 Autonomic Dysfunction 46 0.029
823
TST014 Testicular Cancer 46 0.029
824
MLC004 Mulchandani-Bhoj-Conlin Syndrome 44 0.029
825
c DRM054 Dermatitis, Atopic, 2 44 0.029
826
SBC016 Subacute Delirium 44 0.029
827
IMM064 Immunodeficiency, Common Variable, 10 44 0.029
828
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.029
829
HYP457 Hypertrophic Scars 42 0.029
830
TRP009 Triple X Syndrome 42 0.029
832
c PSR028 Psoriasis 7 42 0.029
833
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.029
834
IDP070 Idiopathic Scoliosis 42 0.029
835
P NSL008 Nasal Cavity Cancer 41 0.029
836
DNT006 Dental Pulp Necrosis 41 0.029
837
MTL005 Metal Allergy 41 0.029
838
c PSR018 Psoriasis 13 41 0.029
839
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 41 0.029
840
KLB003 Klebsiella Pneumonia 41 0.029
841
c MCR112 Microvascular Complications of Diabetes 2 41 0.029
842
c PLM150 Pulmonary Alveolar Proteinosis, Acquired 40 0.029
843
ORL012 Oral Leukoplakia 39 0.029
844
HYP001 Hypochromic Microcytic Anemia 38 0.029
845
c CHR020 Chronic Interstitial Cystitis 37 0.029
846
HRN029 Hearing Loss, Noise-Induced 37 0.029
847
c DRM040 Dermatitis Herpetiformis, Familial 35 0.029
849
ENC065 Encephalitis/encephalopathy, Mild, with Reversible Myelin Vacuolization 33 0.029
850
c PRS136 Prostate Cancer, Hereditary, 6 33 0.029
851
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.029
852
c PRS130 Prostate Cancer, Hereditary, 8 32 0.029
853
CND006 Candida Glabrata 32 0.029
854
DMN026 Dementia Pugilistica 27 0.029
855
CYT018 Cytochrome P450 2d6 Variant 27 0.029
856
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.029
857
STN013 Stenotrophomonas Maltophilia Infection 25 0.029
858
URT049 Urate Oxidase, Pseudogene 25 0.029
859
LPN002 Lip and Oral Cavity Cancer 19 0.029
860
PRL045 Proline-Negative Auxotroph of Hamster, Complementation of 18 0.029
861
CNN003 Conn's Syndrome 79 0.025
862
P APL001 Aplastic Anemia 74 0.025
863
P FML018 Familial Mediterranean Fever 73 0.025
864
SCH036 Scheie Syndrome 72 0.025
865
ACR007 Acromegaly 71 0.025
866
P SRC025 Sarcoidosis 1 70 0.025
867
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.025
868
CHL065 Cholangiocarcinoma 68 0.025
869
OBS002 Obsessive-Compulsive Disorder 68 0.025
870
P MYS003 Myasthenia Gravis 68 0.025
871
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.025
872
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 68 0.025
873
FCT007 Factor Vii Deficiency 67 0.025
874
ALL003 Allergic Rhinitis 67 0.025
875
c HMP029 Hemophilia a 67 0.025
876
MYX005 Myxoid Liposarcoma 66 0.025
877
ART001 Arterial Tortuosity Syndrome 66 0.025
878
AND002 Androgen Insensitivity Syndrome 66 0.025
879
P ATR011 Atrial Fibrillation 66 0.025
880
P HYD006 Hydrocephalus 66 0.025
881
LNG039 Lung Squamous Cell Carcinoma 66 0.025
882
MYL031 Myeloproliferative Neoplasm 66 0.025
883
SVR066 Severe Combined Immunodeficiency, X-Linked 66 0.025
884
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.025
885
P CNJ013 Conjunctivitis 65 0.025
886
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 65 0.025
887
CHY002 Chylomicron Retention Disease 65 0.025
888
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.025
889
NRM005 Neuromuscular Disease 64 0.025
890
PRP083 Porphyria, Acute Intermittent 64 0.025
891
MSC007 Muscle Hypertrophy 64 0.025
892
SPT006 Septooptic Dysplasia 64 0.025
893
OST017 Osteomyelitis 64 0.025
894
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 63 0.025
895
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.025
896
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.025
897
P SPN046 Spinal Muscular Atrophy 62 0.025
898
P BCK002 Beckwith-Wiedemann Syndrome 62 0.025
899
BRS099 Breast Ductal Carcinoma 62 0.025
900
P KLL001 Kallmann Syndrome 61 0.025
901
YLL002 Yellow Fever 61 0.025
902
RHM001 Rheumatic Fever 60 0.025
903
ING001 Inguinal Hernia 60 0.025
904
HYD002 Hydronephrosis 60 0.025
905
P RBL001 Rubella 59 0.025
906
P AXN002 Axenfeld-Rieger Syndrome 59 0.025
907
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 59 0.025
908
P CYS018 Cystitis 59 0.025
909
P NPH005 Nephronophthisis 59 0.025
910
P SYP003 Syphilis 58 0.025
911
FBR047 Fibromyalgia 58 0.025
912
ERY003 Erythema Multiforme 58 0.025
913
P MMP001 Mumps 58 0.025
914
BRG013 Buerger Disease 58 0.025
915
P GLL018 Gallbladder Cancer 57 0.025
916
APL002 Aplasia of Lacrimal and Salivary Glands 57 0.025
917
CHL067 Cholecystitis 57 0.025
918
P HDC001 Headache 57 0.025
919
DSS009 Disseminated Intravascular Coagulation 57 0.025
920
PRL032 Perlman Syndrome 57 0.025
921
LYM021 Lymphadenitis 57 0.025
922
APH002 Aphasia 57 0.025
923
P ANG015 Angioedema 57 0.025
924
PNM008 Pneumothorax 56 0.025
925
LST001 Listeriosis 56 0.025
926
P MLT074 Multiple Endocrine Neoplasia 56 0.025
927
LMY014 Leiomyoma, Uterine 56 0.025
928
P MTC069 Mitochondrial Disorders 56 0.025
929
SML019 Smallpox 56 0.025
930
FND002 Fundus Dystrophy 55 0.025
931
ISL014 Isolated Growth Hormone Deficiency, Type Ia 55 0.025
932
P ALP106 Alport Syndrome 1, X-Linked 55 0.025
933
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.025
934
ABL002 Ablepharon-Macrostomia Syndrome 53 0.025
935
HRT012 Heart Valve Disease 53 0.025
936
PRP036 Peripheral T-Cell Lymphoma 53 0.025
937
P PTS002 Ptosis 53 0.025
938
NRT001 Neurotic Disorder 53 0.025
939
TXC002 Toxic Encephalopathy 53 0.025
940
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 53 0.025
941
PRP080 Peripheral Artery Disease 53 0.025
942
FRY006 Fryns Microphthalmia Syndrome 52 0.025
943
EXP004 Exophthalmos 52 0.025
944
CHR073 Choreatic Disease 52 0.025
945
c CRS016 Crisponi/cold-Induced Sweating Syndrome 1 52 0.025
946
NRT004 Neuritis 52 0.025
947
P CHN059 Chondrocalcinosis 52 0.025
948
P RCT021 Rectum Cancer 52 0.025
949
CRT016 Carotid Artery Disease 52 0.025
950
c TRC092 Trichorhinophalangeal Syndrome, Type I 52 0.025
951
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.025
952
LGN006 Legionnaire Disease 52 0.025
953
DSM007 Desmoplastic Small Round Cell Tumor 52 0.025
954
c INH030 Inherited Retinal Disorder 51 0.025
955
SPS003 Spastic Diplegia 51 0.025
956
NPH003 Nephrocalcinosis 51 0.025
957
THR004 Thrombocytosis 51 0.025
959
INT079 Intrahepatic Cholangiocarcinoma 51 0.025
960
PNM005 Pneumonic Plague 51 0.025
961
P CHL066 Cholangitis 51 0.025
962
c ACT078 Acute Porphyria 51 0.025
963
HYP081 Hypolipoproteinemia 51 0.025
964
P MMB011 Membranous Nephropathy 50 0.025
965
PLR008 Pleurisy 50 0.025
966
P PRS049 Persistent Mullerian Duct Syndrome 50 0.025
967
c HRD202 Hereditary Lymphedema I 50 0.025
968
NTR046 Neutrophil Migration 50 0.025
969
c LRG001 Large Cell Carcinoma 50 0.025
970
c PSR021 Psoriasis 14, Pustular 50 0.025
971
RNL011 Renal Osteodystrophy 50 0.025
972
c CHR418 Chronic Leukemia 49 0.025
973
PRN014 Paronychia 49 0.025
974
GST049 Gastrointestinal System Cancer 49 0.025
975
CHL004 Cholelithiasis 49 0.025
976
MTC005 Mitochondrial Metabolism Disease 49 0.025
977
INT017 Intestinal Schistosomiasis 48 0.025
978
c DSB006 Desbuquois Dysplasia 1 48 0.025
979
RFR010 Refractory Anemia 48 0.025
980
VTM033 Vitamin K Deficiency Bleeding 48 0.025
981
BNN003 Bone Inflammation Disease 48 0.025
982
CHL056 Cheilitis 48 0.025
983
HYP025 Hyperphosphatemia 48 0.025
984
c VRL012 Viral Meningitis 48 0.025
985
P PRP056 Porphyria, Acute Hepatic 48 0.025
986
DRY001 Dry Eye Syndrome 47 0.025
987
P CRN028 Corneal Ulcer 47 0.025
988
PRC003 Proctitis 47 0.025
989
P HMN032 Human Herpesvirus 8 47 0.025
990
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.025
991
TST044 Testicular Torsion 47 0.025
992
CRD137 Cardiogenic Shock 47 0.025
993
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.025
994
BCK003 Background Diabetic Retinopathy 46 0.025
995
FCL012 Facial Paralysis 46 0.025
996
CLN045 Colonic Benign Neoplasm 46 0.025
997
P HMR005 Hemorrhoid 46 0.025
998
PST048 Postural Orthostatic Tachycardia Syndrome 45 0.025
999
URT010 Ureteral Obstruction 45 0.025
1000
PLR022 Pleural Disease 45 0.025
1001
c HMG003 Hemoglobin E Disease 45 0.025
1002
c HYP513 Hypogonadotropic Hypogonadism 1 with or Without Anosmia 45 0.025
1003
P END084 Endocrine System Disease 45 0.025
1004
GRN017 Granulocytopenia 44 0.025
1005
PPL001 Papillary Adenoma 44 0.025
1006
FBR054 Fibroma 44 0.025
1007
ATR013 Atrichia with Papular Lesions 44 0.025
1008
SMN007 Seminoma 43 0.025
1009
TST015 Testicular Disease 43 0.025
1010
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.025
1011
P MJR007 Major Affective Disorder 1 43 0.025
1012
CRV043 Cervical Dystonia 42 0.025
1013
ALC010 Alcoholic Cardiomyopathy 42 0.025
1014
FTL021 Fetal Macrosomia 42 0.025
1015
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.025
1016
ACT088 Acute Insulin Response 41 0.025
1017
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.025
1018
RDN001 Reading Disorder 40 0.025
1019
P MLG074 Malignant Mesenchymoma 40 0.025
1020
CHN002 Chancroid 40 0.025
1021
P DYS005 Dyslexia 40 0.025
1022
PLY100 Polyploidy 40 0.025
1023
P DYS021 Dysautonomia 39 0.025
1024
CRV045 Cervical Intraepithelial Neoplasia 39 0.025
1025
ENT001 Enterocele 39 0.025
1026
MCC013 Mucocutaneous Ulceration, Chronic 39 0.025
1027
MNR003 Mineral Metabolism Disease 39 0.025
1028
DSS010 Dissociative Disorder 39 0.025
1029
DBT007 Diabetic Cataract 38 0.025
1030
c PLY105 Polycystic Ovary Syndrome 1 38 0.025
1031
BTN004 Biotin Deficiency 38 0.025
1032
c OVR114 Ovarian Cancer 1 38 0.025
1033
ISL109 Isolated Cleft Lip 38 0.025
1034
HPT070 Hepatosplenic T-Cell Lymphoma 38 0.025
1035
ESP025 Esophagus Adenocarcinoma 38 0.025
1036
ATM052 Autoimmune Disease 1 37 0.025
1037
P CRB088 Cerebral Atrophy 37 0.025
1038
P CRB059 Cerebellar Degeneration 37 0.025
1039
ALR002 Al-Raqad Syndrome 33 0.025
1040
c MJR003 Major Affective Disorder 6 33 0.025
1041
c MJR006 Major Affective Disorder 5 33 0.025
1042
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.025
1043
OSM001 Osmotic Diarrhea 32 0.025
1044
PRT094 Protoporphyria, Erythropoietic, X-Linked 31 0.025
1045
RSP007 Respiratory Distress Syndrome, Infant 30 0.025
1046
MTY003 Mutyh Polyposis 30 0.025
1047
BRN049 Brain Tumor, Childhood 29 0.025
1048
c PLM128 Pulmonary Hypertension, Primary, 2 29 0.025
1049
PHS025 Phosphatase, Acid, of Tissues 28 0.025
1050
DSR031 Disorder of Copper Metabolism 27 0.025
1051
DFF010 Diffuse Alopecia Areata 26 0.025
1052
BNG077 Benign Idiopathic Neonatal Seizures 26 0.025
1053
ANG061 Angular Cheilitis 26 0.025
1054
ENM002 Enamel Erosion 26 0.025
1055
HRP008 Herpes Simiae 25 0.025
1056
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.021
1057
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.021
1058
c MNN043 Meningioma, Familial 74 0.021
1059
c MCP050 Mucopolysaccharidosis, Type Ii 72 0.021
1060
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.021
1061
P FML011 Familial Adenomatous Polyposis 72 0.021
1062
P WSK001 Wiskott-Aldrich Syndrome 72 0.021
1063
BHC003 Behcet Syndrome 71 0.021
1064
MLT157 Multiple System Atrophy 1 70 0.021
1065
P FRG001 Fragile X Syndrome 70 0.021
1066
c MLT160 Multiple Endocrine Neoplasia, Type Iia 70 0.021
1067
CRT072 Creutzfeldt-Jakob Disease 70 0.021
1068
WRN001 Werner Syndrome 69 0.021
1069
P OCL013 Oculodentodigital Dysplasia 69 0.021
1070
LKC009 Leukocyte Adhesion Deficiency, Type I 69 0.021
1071
P MPL001 Maple Syrup Urine Disease 69 0.021
1072
P CRN037 Craniosynostosis 68 0.021
1073
c HMP004 Hemophilia B 68 0.021
1074
MLD001 Melioidosis 68 0.021
1075
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.021
1076
P CHR012 Chronic Granulomatous Disease 67 0.021
1077
P PRP003 Porphyria Cutanea Tarda 67 0.021
1078
CRP001 Carpal Tunnel Syndrome 67 0.021
1079
c MGR028 Migraine with or Without Aura 1 67 0.021
1080
c PRM196 Premature Ovarian Failure 1 67 0.021
1081
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.021
1082
GRG001 Greig Cephalopolysyndactyly Syndrome 66 0.021
1083
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.021
1084
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.021
1085
P BRD002 Bardet-Biedl Syndrome 66 0.021
1086
c FML001 Familial Atrial Fibrillation 65 0.021
1087
PPL049