Search results for Zinc

2244 hits were found for Zinc

# Family MCID Name MIFTS Score
1
ZNC004 Zinc Deficiency, Transient Neonatal 25 8.492
2
ACR056 Acrodermatitis Enteropathica, Zinc-Deficiency Type 54 6.159
3
ZNC006 Zinc, Elevated Plasma 20 4.064
4
ZNC005 Zinc-Responsive Necrolytic Acral Erythema 18 2.394
5
HYP803 Hyperzincemia with Functional Zinc Depletion 11 2.372
6
DSR029 Disorder of Zinc Metabolism and Transport 4 2.349
7
P DRR001 Diarrhea 55 0.361
8
IRN002 Iron Metabolism Disease 58 0.296
9
ACR005 Acrodermatitis 35 0.288
10
ENT007 Enteropathica 27 0.275
11
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.220
12
DFC004 Deficiency Anemia 77 0.213
13
LVR012 Liver Cirrhosis 67 0.198
14
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.184
15
P LTR001 Lateral Sclerosis 56 0.184
16
DRM006 Dermatitis 63 0.180
17
HLX001 Helix Syndrome 46 0.179
18
P ALP008 Alopecia 58 0.174
19
CMM005 Common Cold 57 0.169
20
c ACT004 Acute Diarrhea 38 0.169
21
IRN001 Iron Deficiency Anemia 59 0.163
22
NTR005 Nutritional Deficiency Disease 61 0.161
23
P NRF023 Neurofibromatosis, Type Ii 77 0.160
24
P DBT009 Diabetes Mellitus 66 0.159
25
P PNM007 Pneumonia 71 0.156
26
HMN044 Human Immunodeficiency Virus Type 1 73 0.155
27
KRT002 Keratomalacia 47 0.155
28
P LVR013 Liver Disease 71 0.152
30
CHL079 Children's Interstitial Lung Disease 27 0.149
31
HYP066 Hyperglycemia 63 0.146
32
P ALZ034 Alzheimer Disease 90 0.145
33
HRW001 Hair Whorl 36 0.141
34
HYP080 Hypogonadism 51 0.138
35
HYP064 Hypogonadotropism 40 0.137
36
48X005 48,xyyy 37 0.135
37
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.131
38
CRH001 Crohn's Disease 75 0.128
39
P PRS040 Prostate Cancer 97 0.125
40
WLS001 Wilson Disease 69 0.125
41
P PSR002 Psoriasis 63 0.125
42
P THL005 Thalassemia 62 0.125
43
PST011 Pustulosis of Palm and Sole 51 0.125
44
INS024 Insulin-Like Growth Factor I 79 0.124
45
ALC007 Alcohol Dependence 68 0.123
46
P SCK005 Sickle Cell Disease 53 0.121
47
c DNT047 Dentinogenesis Imperfecta Type 2 34 0.121
48
IMM167 Immune Deficiency Disease 79 0.120
49
P KDN018 Kidney Disease 73 0.120
50
ESP021 Esophageal Cancer 90 0.118
51
P LKM002 Leukemia 69 0.118
52
P NRB010 Neuroblastoma 1 66 0.118
53
P INF032 Infertility 60 0.118
54
BNR002 Bone Resorption Disease 51 0.118
55
CYT002 Cytokine Deficiency 46 0.117
56
PPL052 Papillomatosis, Confluent and Reticulated 34 0.117
57
P HYP086 Hypothyroidism 70 0.116
58
P HRP006 Herpes Simplex 66 0.116
59
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 41 0.115
60
P CLR023 Colorectal Cancer 100 0.114
61
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 55 0.114
62
c PCH010 Pachyonychia Congenita 3 43 0.114
63
P ENC018 Encephalopathy 64 0.113
64
LSH001 Leishmaniasis 64 0.113
65
P KLZ004 Kala-Azar 1 43 0.113
66
ALL026 Allergic Hypersensitivity Disease 65 0.112
67
DWN001 Down Syndrome 70 0.111
68
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.109
69
HYP056 Hypoglycemia 68 0.109
70
SCK003 Sickle Cell Anemia 74 0.108
71
ISC004 Ischemia 62 0.108
72
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.107
73
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.107
74
P CTR002 Cataract 62 0.106
75
TRM010 Traumatic Brain Injury 54 0.106
76
BRN071 Brain Injury 51 0.106
77
P OST002 Osteoporosis 79 0.103
78
P RTN024 Retinoblastoma 74 0.103
79
SKN016 Skin Disease 64 0.103
80
c FML008 Familial Retinoblastoma 46 0.103
81
ANR007 Anorexia Nervosa 64 0.102
82
P SZR006 Seizure Disorder 59 0.102
83
P INF037 Inflammatory Bowel Disease 57 0.102
84
P MLN007 Male Infertility 57 0.102
85
PRT038 Protein-Energy Malnutrition 56 0.102
86
HPT004 Hepatic Coma 42 0.102
87
CYS001 Cystic Fibrosis 84 0.101
88
HPT019 Hepatic Encephalopathy 60 0.101
89
VSL002 Visual Epilepsy 58 0.101
90
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.101
91
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.101
92
P HPT023 Hepatocellular Carcinoma 99 0.100
93
P ATS364 Autism 68 0.100
94
NRL016 Neural Tube Defects 83 0.099
95
AGN016 Aging 58 0.099
96
47X002 47,xyy 49 0.099
97
P PNC035 Pancreatic Cancer 86 0.098
98
c PRC016 Pre-Eclampsia 63 0.098
99
GNG013 Gingivitis 60 0.098
100
DYS015 Dysentery 45 0.098
101
P BRS047 Breast Cancer 99 0.097
102
INS001 Insulinoma 60 0.097
103
P EXN002 Exanthem 58 0.097
104
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.095
105
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.095
106
GST023 Gastric Ulcer 53 0.095
107
c BTT014 Beta-Thalassemia 73 0.094
108
PLM001 Pulmonary Tuberculosis 72 0.094
109
DPR016 Depression 64 0.094
110
LYM027 Lymphopenia 58 0.094
111
P NRP001 Neuropathy 57 0.094
112
P MYC007 Myocardial Infarction 74 0.093
113
ATH013 Atherosclerosis Susceptibility 68 0.093
114
P PNC044 Pancreatitis 61 0.093
115
GST045 Gastroenteritis 60 0.093
116
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.093
117
URM002 Uremia 50 0.093
118
ATX019 Ataxia with Vitamin E Deficiency 46 0.093
119
c CHR684 Chronic Kidney Disease 68 0.092
120
P PRD008 Periodontitis 66 0.092
121
ATM095 Autoimmune Disease 62 0.092
122
CHL014 Cholera 58 0.092
123
P VSC007 Vascular Disease 65 0.091
124
ACQ007 Acquired Immunodeficiency Syndrome 61 0.091
125
END030 End Stage Renal Failure 60 0.091
126
CNT047 Contact Dermatitis 58 0.091
127
DNT012 Dental Caries 52 0.091
128
ATS010 Autosomal Recessive Disease 49 0.091
129
MLR004 Malaria 82 0.089
130
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.089
131
P RHM011 Rheumatoid Arthritis 82 0.088
132
HYP266 Hypoxia 58 0.088
133
BCT022 Bacterial Infectious Disease 57 0.088
134
PRS045 Prostatic Hypertrophy 55 0.088
135
HMS001 Hemosiderosis 54 0.088
136
P RRH023 Rare Hereditary Hemochromatosis 41 0.088
137
P GST053 Gastric Cancer 85 0.087
138
P GLM045 Glioma 64 0.087
139
ACT119 Acute Promyelocytic Leukemia 63 0.087
140
PRS047 Prostatitis 57 0.087
141
GLL048 Glial Tumor 48 0.087
142
RCK004 Rickets 70 0.085
143
c ATS007 Autism Spectrum Disorder 69 0.085
144
P NTR004 Neutropenia 64 0.085
145
c WLM018 Wilms Tumor 5 63 0.085
146
CTN007 Cutaneous Leishmaniasis 61 0.085
147
P MYL006 Myeloid Leukemia 61 0.085
148
GLB002 Glioblastoma 74 0.084
149
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.084
150
MCS002 Mucositis 56 0.084
151
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.084
152
c LKM061 Leukemia, Acute Myeloid 84 0.083
153
OST159 Osteogenic Sarcoma 67 0.083
154
GLB015 Glioblastoma Multiforme 60 0.083
155
c ACT075 Acute Myocardial Infarction 59 0.083
156
P LYM031 Lymphocytic Leukemia 56 0.083
157
HVY002 Heavy Metal Poisoning 23 0.083
158
P HRT032 Heart Disease 78 0.081
159
CLT003 Colitis 63 0.081
160
SQM006 Squamous Cell Carcinoma 60 0.081
161
MNT002 Mental Depression 60 0.081
162
EYD002 Eye Disease 59 0.081
163
P LNG032 Lung Cancer 99 0.080
164
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.080
165
P CRN018 Coronary Artery Anomaly 67 0.080
166
P LPR021 Leprosy 3 67 0.080
167
FTT001 Fatty Liver Disease 63 0.080
168
TTN003 Tetanus 62 0.080
169
ADN018 Adenoma 60 0.080
170
BLR008 Bilirubin Metabolic Disorder 58 0.080
171
P HYP076 Hyperthyroidism 55 0.080
172
PRS021 Prostatic Adenoma 52 0.080
173
HNS001 Hansen's Disease 35 0.080
174
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.078
175
P LYM118 Lymphoma 70 0.078
176
P DRM053 Dermatitis, Atopic 68 0.078
177
P ADN016 Adenocarcinoma 65 0.078
178
c HPT016 Hepatitis B 63 0.078
179
c HPT001 Hepatitis C 62 0.078
180
P ALP009 Alopecia Areata 61 0.078
181
P BCL017 B-Cell Lymphoma 61 0.078
182
PRS129 Prostatic Hyperplasia, Benign 49 0.078
183
DWR001 Dwarfism 45 0.078
184
TXC005 Toxic Shock Syndrome 63 0.077
185
MDD011 Mood Disorder 62 0.077
186
GST033 Gestational Diabetes 58 0.077
187
STM007 Stomatitis 51 0.077
188
CRV035 Cervical Cancer 77 0.075
189
ART140 Arteries, Anomalies of 60 0.075
190
c ACT210 Acute Respiratory Distress Syndrome 59 0.075
191
c HYP595 Hypertension, Essential 87 0.074
192
MLN008 Melanoma 68 0.074
193
P CLC063 Celiac Disease 1 66 0.074
194
P NPH012 Nephrotic Syndrome 65 0.074
195
P PRP019 Peripheral Nervous System Disease 64 0.074
196
GLC003 Glucose Intolerance 55 0.074
197
KRT009 Keratosis 52 0.074
198
c MCR120 Microvascular Complications of Diabetes 7 48 0.074
199
ULC004 Ulcerative Colitis 75 0.072
200
CNG034 Congestive Heart Failure 69 0.072
201
c ACT027 Acute Pancreatitis 60 0.072
202
PPT005 Peptic Ulcer Disease 60 0.072
203
HMN014 Human Immunodeficiency Virus Infectious Disease 56 0.072
204
P FTL001 Fetal Alcohol Syndrome 56 0.072
205
c MCR113 Microvascular Complications of Diabetes 3 55 0.072
206
c MCR130 Microvascular Complications of Diabetes 6 42 0.072
207
c MCR133 Microvascular Complications of Diabetes 4 42 0.072
208
P BLD134 Bladder Cancer 79 0.071
209
P SKN015 Skin Carcinoma 67 0.071
210
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.071
211
P CRN300 Coronary Heart Disease 1 59 0.071
212
HYP781 Hypoascorbemia 48 0.071
213
P SBR004 Seborrheic Dermatitis 41 0.071
215
P OVR042 Ovarian Cancer 89 0.069
216
P DMN002 Dementia 68 0.069
217
P LKM062 Leukemia, Acute Lymphoblastic 68 0.069
218
LNG099 Lung Disease 62 0.069
219
ORL011 Oral Cancer 62 0.069
220
CHL068 Cholestasis 61 0.069
221
P ALC033 Alcohol Use Disorder 58 0.069
222
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.069
223
GTR002 Goiter 54 0.069
224
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.069
225
KWS001 Kwashiorkor 46 0.069
226
CHR178 Chromosomal Triplication 36 0.069
227
PCD001 Pica Disease 33 0.069
228
P ART022 Arthritis 71 0.067
229
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 61 0.067
230
P NGH001 Night Blindness 48 0.067
231
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.067
232
ARG004 Argyria 28 0.067
233
c HPT073 Hepatitis C Virus 74 0.066
234
P PHC003 Pheochromocytoma 71 0.066
235
CLN015 Colon Adenocarcinoma 65 0.066
236
ADR040 Adrenal Gland Pheochromocytoma 51 0.066
237
OLG001 Oligospermia 44 0.066
238
c HYP836 Hypercholesterolemia, Familial, 1 74 0.064
239
P EPL164 Epilepsy 73 0.064
240
SPN186 Spinal Cord Injury 63 0.064
241
P PLY011 Polycystic Ovary Syndrome 58 0.064
242
P GST044 Gastritis 58 0.064
243
GST050 Gastrointestinal System Disease 57 0.064
244
ALC009 Alcoholic Liver Cirrhosis 53 0.064
245
HMP009 Haemophilus Influenzae 46 0.064
246
CRB004 Cerebral Artery Occlusion 38 0.064
247
OST012 Osteoarthritis 80 0.062
248
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.062
249
c ATR087 Atrial Standstill 1 76 0.062
250
P HPT021 Hepatitis 69 0.062
251
P PRN023 Prion Disease 57 0.062
252
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.062
253
HYP060 Hyperinsulinism 55 0.062
254
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.062
255
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.062
256
SXL003 Sexual Disorder 49 0.062
257
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.062
258
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.062
259
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.062
260
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.062
261
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.062
262
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.062
263
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.062
264
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.062
265
c SPR086 Spermatogenic Failure 3 41 0.062
266
MYL069 Myeloma, Multiple 85 0.060
267
AST005 Asthma 80 0.060
268
P LNG064 Lung Cancer Susceptibility 3 79 0.060
269
P RTN008 Retinitis Pigmentosa 77 0.060
270
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.060
271
c WLM013 Wilms Tumor 1 69 0.060
272
LPD008 Lipid Metabolism Disorder 64 0.060
273
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.060
274
MSL001 Measles 61 0.060
275
c ACT071 Acute Kidney Failure 60 0.060
276
c VRL010 Viral Hepatitis 56 0.060
277
PPL022 Papilloma 56 0.060
278
MST005 Mastitis 55 0.060
279
P THY032 Thyroiditis 52 0.060
280
P MNC007 Monocytic Leukemia 52 0.060
281
PLC008 Placenta Disease 51 0.060
282
RTN023 Retinitis 46 0.060
283
NRR001 Neuroretinitis 46 0.060
284
P MLT020 Multiple Sclerosis 73 0.058
285
P MJR001 Major Depressive Disorder 69 0.058
286
P MSC005 Muscular Dystrophy 68 0.058
287
P NSP012 Nasopharyngeal Carcinoma 67 0.058
288
P HML002 Hemolytic Anemia 64 0.058
289
ETN001 Eating Disorder 61 0.058
290
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.058
291
SCH014 Schistosomiasis 57 0.058
292
ANT024 Anthrax Disease 56 0.058
293
APH001 Aphthous Stomatitis 56 0.058
294
HYP005 Hypokalemia 55 0.058
295
SPP010 Suppressor of Tumorigenicity 3 54 0.058
296
AZS001 Azoospermia 51 0.058
297
ORL015 Oral Squamous Cell Carcinoma 44 0.058
298
GRD001 Giardiasis 42 0.058
299
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 40 0.058
300
PLY150 Polykaryocytosis Inducer 31 0.058
301
STT009 Sutton Disease 2 31 0.058
302
PST092 Posttransplant Acute Limbic Encephalitis 29 0.058
303
ANX010 Anxiety 75 0.056
304
SVR004 Severe Combined Immunodeficiency 74 0.056
305
P MYC084 Mycobacterium Tuberculosis 1 69 0.056
306
BRK010 Burkitt Lymphoma 68 0.056
307
c RHB024 Rhabdomyosarcoma 2 64 0.056
308
P CND004 Candidiasis 61 0.056
309
BND020 Bone Disease 60 0.056
310
P EHL001 Ehlers-Danlos Syndrome 60 0.056
311
EMB004 Embryonal Carcinoma 57 0.056
312
P RTN016 Retinal Degeneration 56 0.056
313
ACD008 Acid-Labile Subunit Deficiency 55 0.056
314
IMP005 Impotence 53 0.056
315
OCL069 Ocular Motor Apraxia 53 0.056
316
ENT011 Enterocolitis 51 0.056
317
MTB004 Metabolic Acidosis 48 0.056
318
IMP004 Impetigo 47 0.056
319
CCC002 Coccidiosis 46 0.056
320
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.056
321
c HMC039 Hemochromatosis, Type 1 73 0.054
322
OTT002 Otitis Media 71 0.054
323
P AMY004 Amyloidosis 71 0.054
324
BRN024 Bronchitis 70 0.054
325
PNC129 Pancreatic Adenocarcinoma 69 0.054
326
CLF027 Cleft Palate, Isolated 67 0.054
327
P MNN013 Meningitis 67 0.054
328
c SML038 Small Cell Cancer of the Lung 67 0.054
329
PRT037 Pertussis 66 0.054
330
CHG001 Chagas Disease 66 0.054
331
P MTR014 Motor Neuron Disease 66 0.054
332
c ALP101 Alpha-Thalassemia 63 0.054
333
THY029 Thyroid Carcinoma 62 0.054
334
STT001 Status Epilepticus 61 0.054
335
P RHN004 Rhinitis 59 0.054
336
P BPL003 Bipolar Disorder 59 0.054
337
ENH001 Enhanced S-Cone Syndrome 56 0.054
338
ALL010 Allergic Contact Dermatitis 56 0.054
339
SHG001 Shigellosis 54 0.054
340
P ECL001 Eclampsia 53 0.054
341
THY030 Thyroid Gland Disease 53 0.054
342
FDL002 Food Allergy 52 0.054
343
OVR082 Overgrowth Syndrome 51 0.054
344
GLS018 Glass Syndrome 51 0.054
345
SQM002 Squamous Cell Papilloma 49 0.054
346
P TCL004 T-Cell Leukemia 48 0.054
347
c MJR024 Major Affective Disorder 9 42 0.054
348
c MJR022 Major Affective Disorder 8 39 0.054
349
c LKM005 Leukemia, T-Cell, Chronic 35 0.054
350
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 0.054
351
GST092 Gastroesophageal Reflux 68 0.052
352
P HYP098 Hypereosinophilic Syndrome 67 0.052
353
c ACT068 Acute Cystitis 63 0.052
354
ALC006 Alcoholic Hepatitis 60 0.052
355
P BRS044 Breast Adenocarcinoma 59 0.052
356
P PRP029 Porphyria 58 0.052
357
P FBR017 Fibrosarcoma 57 0.052
358
P ART021 Arteriosclerosis 56 0.052
359
P INT068 Intestinal Disease 56 0.052
360
PLM010 Pulmonary Edema 56 0.052
361
P TRM003 Tremor 55 0.052
362
RSC001 Rosacea 55 0.052
363
P TMP001 Temporal Lobe Epilepsy 53 0.052
364
c ACT134 Acute Liver Failure 53 0.052
365
P MYT002 Myotonic Dystrophy 52 0.052
366
ANG005 Anogenital Venereal Wart 51 0.052
367
NWC001 Newcastle Disease 45 0.052
368
GLC036 Glucagonoma 45 0.052
369
MYT026 Myotonia Atrophica 25 0.052
370
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.050
371
P PRK057 Parkinson Disease, Late-Onset 77 0.050
372
P HNT016 Huntington Disease 72 0.050
373
ART016 Aortic Aneurysm 71 0.050
374
P ASP006 Aspergillosis 67 0.050
375
PRT036 Peritonitis 66 0.050
376
P HYP750 Hypertriglyceridemia, Familial 62 0.050
377
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.050
378
P ADL010 Adult Respiratory Distress Syndrome 61 0.050
379
P KDN017 Kidney Cancer 60 0.050
380
BRN002 Bronchiolitis 60 0.050
381
c DWL002 Dowling-Degos Disease 1 59 0.050
382
c ACT073 Acute Leukemia 59 0.050
383
P OPT006 Optic Nerve Disease 59 0.050
384
HMG005 Hemoglobinopathy 57 0.050
385
c PRD040 Periodontitis, Chronic 56 0.050
386
PRN019 Perinatal Necrotizing Enterocolitis 55 0.050
387
DCB001 Decubitus Ulcer 54 0.050
388
P FBR031 Febrile Seizures 54 0.050
389
TLN003 Telangiectasis 53 0.050
390
OST011 Osteomalacia 51 0.050
391
P SHR001 Short Bowel Syndrome 50 0.050
392
SNL007 Senile Cataract 41 0.050
393
CVT001 Cavitary Optic Disc Anomalies 39 0.050
394
P ATX030 Ataxia-Telangiectasia 83 0.048
395
PRP027 Peripheral Vascular Disease 72 0.048
396
MYL009 Myelodysplastic Syndrome 72 0.048
397
LYM133 Lymphoma, Hodgkin, Classic 70 0.048
398
P DYS154 Dystonia 65 0.048
399
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.048
400
P HYP069 Hyperparathyroidism 64 0.048
401
P MYP004 Myopathy 63 0.048
402
P LPS004 Lupus Erythematosus 62 0.048
403
c BRN108 Branchiootic Syndrome 1 62 0.048
404
P ESP024 Esophagitis 62 0.048
405
c ART138 Aortic Aneurysm, Familial Abdominal, 1 62 0.048
406
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.048
407
HLC007 Helicobacter Pylori Infection 61 0.048
408
DPH001 Diphtheria 61 0.048
409
c PRT132 Protoporphyria, Erythropoietic, 1 59 0.048
410
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.048
411
BRN056 Bronchopulmonary Dysplasia 57 0.048
412
P GRV001 Graves' Disease 57 0.048
413
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.048
414
P LCH002 Lichen Planus 55 0.048
415
c GRV008 Graves Disease 1 55 0.048
416
ORL004 Oral Submucous Fibrosis 55 0.048
417
PLM017 Pulmonary Alveolar Microlithiasis 54 0.048
418
CHR100 Chronic Ulcer of Skin 53 0.048
419
FDB001 Foodborne Botulism 53 0.048
420
VRC001 Varicocele 51 0.048
421
P MRC003 Mercury Poisoning 47 0.048
422
P SDR003 Sideroblastic Anemia 47 0.048
423
PRS042 Prostate Disease 42 0.048
424
ALL014 Allergic Encephalomyelitis 40 0.048
425
MRS001 Marasmus 39 0.048
426
P SCH015 Schizophrenia 76 0.045
427
END057 Endometrial Cancer 74 0.045
428
PHN003 Phenylketonuria 73 0.045
429
P PLM037 Pulmonary Hypertension 69 0.045
430
SKN019 Skin Melanoma 68 0.045
431
P MCR115 Microvascular Complications of Diabetes 5 67 0.045
432
SRC014 Sarcoma 67 0.045
433
BRR014 Barrett Esophagus 67 0.045
434
ANG054 Angina Pectoris 66 0.045
435
P END044 Endometriosis 63 0.045
436
ADL002 Adult Syndrome 62 0.045
437
P SCL018 Scoliosis 61 0.045
438
c HPT003 Hepatitis a 60 0.045
439
BRS051 Breast Disease 59 0.045
440
P GLM007 Glomerulonephritis 58 0.045
441
NWB001 Newborn Respiratory Distress Syndrome 58 0.045
442
PLM031 Poliomyelitis 58 0.045
443
P MCR010 Microcephaly 56 0.045
444
c SVR001 Severe Acute Respiratory Syndrome 56 0.045
445
PHR003 Pharyngitis 56 0.045
446
ANN002 Anencephaly 55 0.045
447
P PLY019 Polyneuropathy 55 0.045
448
P PRM006 Primary Biliary Cirrhosis 54 0.045
449
P TRT010 Teratoma 52 0.045
450
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.045
451
P ALP061 Alopecia, Androgenetic, 1 51 0.045
452
P DDN001 Duodenal Ulcer 50 0.045
453
VCC001 Vaccinia 50 0.045
454
LPR001 Lepromatous Leprosy 50 0.045
455
NNT012 Neonatal Jaundice 48 0.045
456
GRW007 Growth Hormone Deficiency 48 0.045
457
c PRM038 Primary Agammaglobulinemia 45 0.045
458
RTR008 Root Resorption 44 0.045
459
GLS007 Glossitis 44 0.045
460
GST020 Gastric Antral Vascular Ectasia 42 0.045
461
c SYS001 Systemic Lupus Erythematosus 88 0.043
462
c DLT002 Dilated Cardiomyopathy 81 0.043
463
P MDL005 Medulloblastoma 78 0.043
464
P SLP006 Sleep Apnea 71 0.043
465
P CRD119 Cardiac Arrest 71 0.043
466
P SYS005 Systemic Scleroderma 68 0.043
467
c BSL007 Basal Cell Carcinoma 68 0.043
468
DSS008 Disease of Mental Health 66 0.043
469
P HRS035 Hirschsprung Disease 1 65 0.043
470
TBC004 Tobacco Addiction 65 0.043
471
CLR108 Colorectal Adenoma 64 0.043
472
c FNC043 Fanconi Anemia, Complementation Group E 64 0.043
473
VRL011 Viral Infectious Disease 62 0.043
474
CHR066 Chronic Fatigue Syndrome 61 0.043
475
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.043
476
P MYC008 Myocarditis 60 0.043
477
P LRY044 Larynx Cancer 59 0.043
478
P MYP006 Myopia 58 0.043
479
ERY051 Erythroleukemia, Familial 58 0.043
480
PRM236 Primary Biliary Cholangitis 57 0.043
481
VSC002 Vascular Dementia 57 0.043
482
SPN035 Spindle Cell Sarcoma 57 0.043
483
VSC003 Visceral Leishmaniasis 55 0.043
484
P RTN018 Retinal Disease 53 0.043
485
CLF001 Cleft Lip 53 0.043
486
CLR109 Colorectal Adenocarcinoma 51 0.043
487
PHL006 Phelan-Mcdermid Syndrome 51 0.043
488
CRN030 Coronary Stenosis 49 0.043
489
PRM020 Premenstrual Tension 48 0.043
490
PLP001 Pulpitis 48 0.043
491
P PLL002 Pellagra 47 0.043
492
ORL013 Oral Lichen Planus 47 0.043
493
PTT037 Pituitary Tumors 47 0.043
494
P BNG032 Benign Mesothelioma 47 0.043
495
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.043
496
c MLG068 Malignant Glioma 46 0.043
497
ALV001 Alveolar Periostitis 39 0.043
498
OVR094 Ovarian Epithelial Cancer 39 0.043
499
HYP784 Hypogonadism, Male 39 0.043
500
ANP008 Anaplastic Oligoastrocytoma 31 0.043
501
SQM013 Squamous Cell Carcinoma, Head and Neck 81 0.040
502
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.040
503
P INF038 Influenza 69 0.040
504
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.040
505
P BLD124 Bleeding Disorder, Platelet-Type, 11 66 0.040
506
P PLM036 Pulmonary Fibrosis 66 0.040
507
IDP011 Idiopathic Interstitial Pneumonia 65 0.040
508
KHL003 Kohlschutter-Tonz Syndrome 63 0.040
509
HYP020 Hyperprolactinemia 62 0.040
510
RTN017 Retinal Detachment 62 0.040
511
PTT048 Pituitary Adenoma, Prolactin-Secreting 61 0.040
512
CNS004 Constipation 59 0.040
513
P PYL005 Pyelonephritis 58 0.040
514
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.040
515
TNG003 Tongue Cancer 57 0.040
516
DNY001 Denys-Drash Syndrome 57 0.040
517
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.040
518
P SBS003 Substance Abuse 56 0.040
519
P INS002 in Situ Carcinoma 55 0.040
520
GNT003 Genital Herpes 54 0.040
521
P SLM003 Salmonellosis 54 0.040
522
CHC001 Chickenpox 53 0.040
523
LMY002 Leiomyoma 52 0.040
524
RTN003 Retinal Ischemia 52 0.040
525
IMM136 Immune System Disease 52 0.040
526
P MSC003 Muscular Atrophy 52 0.040
527
CRY005 Cryptococcosis 51 0.040
528
DYS014 Dyspepsia 51 0.040
529
IMM064 Immunodeficiency, Common Variable, 10 51 0.040
530
P KRT007 Keratoconus 51 0.040
531
c SVR005 Severe Pre-Eclampsia 50 0.040
532
MWT001 Mowat-Wilson Syndrome 47 0.040
533
HDN002 Head Injury 47 0.040
534
FLL008 Folliculitis 46 0.040
535
c NGH026 Night Blindness, Congenital Stationary, Type 1a 46 0.040
536
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 46 0.040
537
CMP034 Complete Androgen Insensitivity Syndrome 46 0.040
538
TRT001 Teratocarcinoma 44 0.040
539
DMP001 Dumping Syndrome 44 0.040
540
CRT015 Carotid Artery Occlusion 44 0.040
541
EXC002 Exocrine Pancreatic Insufficiency 41 0.040
542
c PLM127 Pulmonary Hypertension, Primary, 3 33 0.040
543
HND015 Hand Skill, Relative 33 0.040
544
P RTT002 Rett Syndrome 81 0.037
545
c FNC027 Fanconi Anemia, Complementation Group a 81 0.037
546
P RSP003 Respiratory Failure 75 0.037
547
c LKM063 Leukemia, Chronic Myeloid 74 0.037
548
LPT014 Leptin Deficiency or Dysfunction 72 0.037
549
c EXD008 Exudative Vitreoretinopathy 1 69 0.037
550
CHL065 Cholangiocarcinoma 68 0.037
551
P AGM001 Agammaglobulinemia 66 0.037
552
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.037
553
P VSC011 Vasculitis 64 0.037
554
GT001 Gout 63 0.037
555
PSR001 Psoriatic Arthritis 63 0.037
556
BRS099 Breast Ductal Carcinoma 63 0.037
557
P RHB003 Rhabdomyosarcoma 62 0.037
558
TRN015 Transient Cerebral Ischemia 62 0.037
559
TYP007 Typhoid Fever 61 0.037
560
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 61 0.037
561
P TXP001 Toxoplasmosis 61 0.037
562
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 58 0.037
563
HDR002 Hidradenitis Suppurativa 58 0.037
564
P PLY006 Polydactyly 58 0.037
565
ECT006 Ectodermal Dysplasia 58 0.037
566
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.037
567
THR024 Thrombosis 58 0.037
568
HPT022 Hepatoblastoma 58 0.037
569
P DNG005 Dengue Virus 57 0.037
570
PLS011 Plasmacytoma 57 0.037
571
RLP002 Relapsing-Remitting Multiple Sclerosis 57 0.037
572
BRN004 Brain Edema 57 0.037
573
CLL003 Cellulitis 56 0.037
574
DRR016 Diarrhea 2, with Microvillus Atrophy 54 0.037
575
INT079 Intrahepatic Cholangiocarcinoma 54 0.037
576
PNC001 Pancytopenia 54 0.037
577
c LRG017 Large Intestine Cancer 53 0.037
578
DYS073 Dysphagia 52 0.037
579
HYP014 Hyperuricemia 52 0.037
580
CRV040 Cervix Carcinoma 52 0.037
581
P AST007 Astrocytoma 52 0.037
582
PYD002 Pyoderma 51 0.037
583
c INH020 Inherited Metabolic Disorder 51 0.037
584
PNC034 Pancreas Disease 51 0.037
585
P ANL018 Analbuminemia 51 0.037
586
BLR001 Biliary Atresia 51 0.037
587
PST021 Postpartum Depression 51 0.037
588
BRN009 Burning Mouth Syndrome 51 0.037
589
c PNC106 Pancreatic Agenesis 1 50 0.037
590
HDR003 Hidradenitis 48 0.037
591
SLP001 Sleeping Sickness 47 0.037
592
MCR018 Microcytic Anemia 46 0.037
593
ATN011 Autoinflammation with Infantile Enterocolitis 45 0.037
594
c SCH079 Schizophrenia 1 44 0.037
595
AMB001 Amebiasis 44 0.037
596
P BLP003 Blepharospasm 43 0.037
597
P HYP265 Hypotonia 43 0.037
598
CLF056 Cleft Lip with or Without Cleft Palate 42 0.037
599
P SDR002 Siderosis 42 0.037
600
AND014 Androgenic Alopecia 41 0.037
601
ULC007 Ulcerative Stomatitis 41 0.037
602
LKP003 Leukoplakia 40 0.037
603
P HMF004 Hemifacial Spasm 40 0.037
604
STT004 Steatorrhea 39 0.037
605
c BLP048 Blepharospasm, Benign Essential 38 0.037
606
END028 Endemic Goiter 37 0.037
607
SCR003 Secretory Diarrhea 36 0.037
608
c HMF011 Hemifacial Spasm, Familial 34 0.037
609
PYR009 Pyridoxine Deficiency Anemia 32 0.037
610
NNN007 Non-Involuting Congenital Hemangioma 32 0.037
611
EXN003 Exencephaly 32 0.037
612
TLG001 Telogen Effluvium 27 0.037
613
MTH071 Methane Production 26 0.037
614
OBS168 Obsolete: Atypical Teratoid/rhabdoid Tumor 25 0.037
615
OBS532 Obsolete: Ehlers-Danlos Syndrome, Fibronectinemic Type 15 0.037
616
STR067 Stroke, Ischemic 82 0.034
617
KPS004 Kaposi Sarcoma 75 0.034
618
c SPN225 Spondyloarthropathy 1 74 0.034
619
c ATM006 Autoimmune Lymphoproliferative Syndrome 73 0.034
620
P CNR004 Cone-Rod Dystrophy 2 72 0.034
621
CRB039 Cerebrovascular Disease 71 0.034
622
MSC157 Muscular Dystrophy, Duchenne Type 70 0.034
623
c PNC108 Pancreatitis, Hereditary 70 0.034
624
CMM004 Common Variable Immunodeficiency 69 0.034
625
c MYT021 Myotonic Dystrophy 1 68 0.034
626
CNN005 Connective Tissue Disease 68 0.034
627
P CNJ013 Conjunctivitis 67 0.034
628
c MCR129 Microvascular Complications of Diabetes 1 67 0.034
629
P TRN020 Turner Syndrome 66 0.034
630
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 64 0.034
631
P ENC004 Encephalitis 64 0.034
632
P ANR048 Aniridia 1 64 0.034
633
BLL006 Bullous Pemphigoid 63 0.034
634
PCK003 Pick Disease of Brain 63 0.034
635
P LPS002 Liposarcoma 62 0.034
636
P SNS001 Sensorineural Hearing Loss 62 0.034
637
P URT039 Urticaria 61 0.034
638
PRT013 Portal Hypertension 61 0.034
639
P PLY014 Polycystic Kidney Disease 61 0.034
640
SPP011 Suppression of Tumorigenicity 12 61 0.034
641
INT002 Intermittent Claudication 60 0.034
642
c PRM005 Primary Hyperparathyroidism 60 0.034
643
P INT070 Intestinal Obstruction 60 0.034
644
P GLY013 Glycogen Storage Disease 59 0.034
645
DNG002 Dengue Hemorrhagic Fever 59 0.034
646
P PRV006 Pervasive Developmental Disorder 58 0.034
647
GLB001 Gilbert Syndrome 58 0.034
648
P SJG008 Sjogren Syndrome 57 0.034
649
P CHN012 Chondrosarcoma 57 0.034
650
RHM027 Rheumatic Disease 56 0.034
651
PRP030 Purpura 56 0.034
652
CMR002 Coumarin Resistance 56 0.034
653
MTH009 Mouth Disease 56 0.034
654
P PNM006 Pneumoconiosis 55 0.034
655
ORP003 Oropharynx Cancer 55 0.034
656
AMN003 Amnestic Disorder 55 0.034
657
P ICH004 Ichthyosis 55 0.034
658
HMT018 Hematopoietic Stem Cell Transplantation 54 0.034
659
P HYP730 Hypogonadotropic Hypogonadism 54 0.034
660
P HYP050 Hyperinsulinemic Hypoglycemia 54 0.034
661
AMN001 Amenorrhea 54 0.034
662
DMY004 Demyelinating Disease 54 0.034
663
P HYP083 Hypopituitarism 53 0.034
664
CMB003 Combined T Cell and B Cell Immunodeficiency 53 0.034
665
LNG031 Lung Benign Neoplasm 52 0.034
666
c SCN007 Secondary Hyperparathyroidism 52 0.034
667
P CHR345 Chronic Pain 52 0.034
668
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 51 0.034
669
LMB062 Limb Ischemia 50 0.034
670
ISL003 Isolated Growth Hormone Deficiency 50 0.034
671
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 49 0.034
672
BHV002 Behavioral Variant of Frontotemporal Dementia 49 0.034
673
HPT014 Hepatorenal Syndrome 49 0.034
674
P END046 Endometritis 49 0.034
675
SPL018 Splenomegaly 48 0.034
676
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 48 0.034
677
PRS034 Parasitic Helminthiasis Infectious Disease 48 0.034
678
BHR001 Behr Syndrome 47 0.034
679
P GND004 Gonadal Dysgenesis 47 0.034
680
PPT001 Peptic Esophagitis 47 0.034
681
ANT018 Anthracosis 46 0.034
682
TRC003 Trichomoniasis 46 0.034
683
P HYP058 Hypervitaminosis a 45 0.034
684
CRB090 Cerebral Hypoxia 45 0.034
685
CYN002 Cyanosis, Transient Neonatal 45 0.034
686
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.034
687
ANX004 Anoxia 44 0.034
688
ACT003 Acute Kidney Tubular Necrosis 42 0.034
689
SKN005 Skin Atrophy 41 0.034
690
P TRC031 Trichorhinophalangeal Syndrome 41 0.034
691
PRM329 Premature Aging 41 0.034
692
P PST059 Pustular Psoriasis 39 0.034
693
49X002 49,xxxxy Syndrome 39 0.034
694
c PRG020 Paragangliomas 3 36 0.034
695
CMM003 Common Wart 32 0.034
696
CPP004 Copper Deficiency Myelopathy 28 0.034
697
c LKM071 Leukemia, Chronic Lymphocytic 81 0.030
698
BRN028 Brain Cancer 75 0.030
699
RNL065 Renal Cell Carcinoma, Papillary, 1 75 0.030
700
ACR006 Aceruloplasminemia 74 0.030
701
P SRC025 Sarcoidosis 1 72 0.030
702
P GRF003 Graft-Versus-Host Disease 71 0.030
703
CRB037 Cerebral Palsy 69 0.030
704
EWN003 Ewing Sarcoma 69 0.030
705
KRT019 Keratitis, Hereditary 69 0.030
706
P HYP061 Hypertrophic Cardiomyopathy 68 0.030
707
THY111 Thyroid Carcinoma, Familial Medullary 68 0.030
708
PSY004 Psychotic Disorder 68 0.030
709
P ATR011 Atrial Fibrillation 67 0.030
710
P THR014 Thrombocytopenia 67 0.030
711
GST040 Gastric Adenocarcinoma 67 0.030
712
c INF071 Inflammatory Bowel Disease 1 66 0.030
713
c CNG006 Congenital Hypothyroidism 65 0.030
714
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 63 0.030
715
HSH003 Hashimoto Thyroiditis 63 0.030
716
PRP001 Propionic Acidemia 63 0.030
717
MNK001 Menkes Disease 62 0.030
718
CRC021 Carcinosarcoma 62 0.030
719
ACN002 Acanthosis Nigricans 62 0.030
720
CRD223 Cardiac Arrhythmia 61 0.030
721
DGR001 Digeorge Syndrome 61 0.030
722
SDD001 Sudden Infant Death Syndrome 61 0.030
723
c DNG003 Dengue Disease 61 0.030
724
P ART023 Arthropathy 61 0.030
726
VRC005 Varicose Veins 61 0.030
727
CHR619 Chromosome 2q35 Duplication Syndrome 61 0.030
728
ANR040 Aneurysm 60 0.030
729
CHL123 Chlamydia 60 0.030
730
WLL001 Williams-Beuren Syndrome 60 0.030
731
P PRD006 Prader-Willi Syndrome 60 0.030
732
PLM033 Pulmonary Embolism 60 0.030
733
P EPD083 Epidermodysplasia Verruciformis 1 59 0.030
734
c MST023 Mesothelioma, Malignant 59 0.030
735
CHR177 Chromophobe Renal Cell Carcinoma 58 0.030
736
P THR117 Three M Syndrome 1 58 0.030
737
P HMP007 Hemophilia 58 0.030
738
TNS005 Tonsillitis 58 0.030
739
P TRC086 Trichohepatoenteric Syndrome 1 57 0.030
740
P ORL007 Oral Cavity Cancer 57 0.030
741
TRN018 Transitional Cell Carcinoma 57 0.030
742
SFT003 Soft Tissue Sarcoma 57 0.030
743
P PLY147 Polydactyly, Postaxial, Type A1 57 0.030
744
PMP006 Pemphigus Vulgaris, Familial 56 0.030
745
ORL005 Oral Candidiasis 56 0.030
746
ALL006 Allergic Asthma 56 0.030
747
P BRT029 Brittle Cornea Syndrome 2 56 0.030
748
CRH005 Crohn's Colitis 56 0.030
749
BLM002 Bulimia Nervosa 56 0.030
750
P PMP001 Pemphigus 56 0.030
751
DBT010 Diabetic Neuropathy 56 0.030
752
SLC006 Silicosis 55 0.030
753
END040 Endogenous Depression 55 0.030
754
c PSR017 Psoriasis 2 55 0.030
755
OST016 Osteochondrosis 55 0.030
756
BRD001 Brody Myopathy 55 0.030
757
RHM028 Rheumatic Heart Disease 54 0.030
758
PLG002 Plague 54 0.030
759
P RCT021 Rectum Cancer 54 0.030
760
HMC014 Homocysteinemia 54 0.030
761
LYM040 Lymphoblastic Lymphoma 54 0.030
762
c PRM092 Primary Lateral Sclerosis, Adult, 1 54 0.030
763
CRT017 Cartilage Disease 54 0.030
764
c HPT007 Hepatitis E 53 0.030
765
PNG002 Pain Agnosia 52 0.030
766
MYM001 Myoma 52 0.030
767
CLN045 Colonic Benign Neoplasm 52 0.030
768
P LCT002 Lactose Intolerance 51 0.030
769
P XRD029 Xeroderma Pigmentosum, Complementation Group a 51 0.030
770
P ACT008 Actinic Keratosis 50 0.030
771
DRR008 Diarrhea 1, Secretory Chloride, Congenital 50 0.030
772
CRT013 Carotid Stenosis 50 0.030
773
c HMN021 Human T-Cell Leukemia Virus Type 1 50 0.030
774
P DRM007 Dermatitis Herpetiformis 50 0.030
775
P CRN028 Corneal Ulcer 49 0.030
776
DRM011 Dermatophytosis 49 0.030
777
RNL077 Renal Fibrosis 49 0.030
778
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.030
779
c INV001 Invasive Aspergillosis 48 0.030
780
LYM019 Lymphosarcoma 48 0.030
781
VTM002 Vitamin B12 Deficiency 48 0.030
782
ACT113 Acute Myeloblastic Leukemia with Maturation 48 0.030
783
WTH001 Withdrawal Disorder 47 0.030
784
BRN014 Bronchopneumonia 47 0.030
785
IRR003 Irritant Dermatitis 46 0.030
786
INT067 Interstitial Nephritis 46 0.030
787
c DRM054 Dermatitis, Atopic, 2 45 0.030
788
LYM009 Lymphocytic Choriomeningitis 45 0.030
789
PLR007 Pleural Empyema 44 0.030
790
INT052 Intestinal Volvulus 44 0.030
791
HYP082 Hypopharynx Cancer 44 0.030
792
P NSL008 Nasal Cavity Cancer 43 0.030
793
SBC016 Subacute Delirium 43 0.030
794
ORL012 Oral Leukoplakia 42 0.030
796
IDP070 Idiopathic Scoliosis 39 0.030
797
c PLM150 Pulmonary Alveolar Proteinosis, Acquired 39 0.030
798
HRN029 Hearing Loss, Noise-Induced 38 0.030
799
HYP001 Hypochromic Microcytic Anemia 38 0.030
800
RTC003 Root Caries 37 0.030
801
DNT006 Dental Pulp Necrosis 37 0.030
802
KLB003 Klebsiella Pneumonia 36 0.030
803
c CHR682 Chronic Bilirubin Encephalopathy 36 0.030
804
c DRM040 Dermatitis Herpetiformis, Familial 36 0.030
805
c CHR020 Chronic Interstitial Cystitis 36 0.030
806
c LKM004 Leukemia, B-Cell, Chronic 35 0.030
807
c CNG498 Congenital Disorder of Glycosylation, Type Iin 34 0.030
808
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 34 0.030
809
MTL005 Metal Allergy 32 0.030
810
c EHL083 Ehlers-Danlos Syndrome, Spondylodysplastic Type, 3 30 0.030
811
DMN026 Dementia Pugilistica 28 0.030
812
CYT018 Cytochrome P450 2d6 Variant 28 0.030
813
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 27 0.030
814
URT049 Urate Oxidase, Pseudogene 26 0.030
815
TRY004 Trypanosomiasis, Human East-African 25 0.030
816
LPN002 Lip and Oral Cavity Cancer 19 0.030
817
PRL045 Proline-Negative Auxotroph of Hamster, Complementation of 19 0.030
818
c PLM164 Pulmonary Hypertension, Primary, 1 79 0.026
819
CNN003 Conn's Syndrome 78 0.026
820
P APL001 Aplastic Anemia 76 0.026
821
MLT157 Multiple System Atrophy 1 71 0.026
822
ACR007 Acromegaly 70 0.026
823
P FML018 Familial Mediterranean Fever 70 0.026
824
c HMP029 Hemophilia a 69 0.026
825
ALL003 Allergic Rhinitis 69 0.026
826
OBS002 Obsessive-Compulsive Disorder 69 0.026
827
P MYS003 Myasthenia Gravis 68 0.026
828
P HYD006 Hydrocephalus 68 0.026
829
SCH036 Scheie Syndrome 68 0.026
830
c MCL062 Mucolipidosis Ii Alpha/beta 67 0.026
831
P MTR004 Maturity-Onset Diabetes of the Young 66 0.026
832
MYL031 Myeloproliferative Neoplasm 66 0.026
833
P SPN046 Spinal Muscular Atrophy 65 0.026
834
P ANG001 Angelman Syndrome 65 0.026
835
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 65 0.026
836
OST017 Osteomyelitis 65 0.026
837
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 65 0.026
838
MSC007 Muscle Hypertrophy 65 0.026
839
FCT007 Factor Vii Deficiency 65 0.026
840
IRR002 Irritable Bowel Syndrome 65 0.026
841
MYX005 Myxoid Liposarcoma 64 0.026
842
P KLL001 Kallmann Syndrome 64 0.026
843
HMT002 Hematologic Cancer 64 0.026
844
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.026
845
APN008 Apnea, Obstructive Sleep 64 0.026
846
LWC002 Lowe Oculocerebrorenal Syndrome 63 0.026
847
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 63 0.026
848
CHY002 Chylomicron Retention Disease 63 0.026
849
SVR066 Severe Combined Immunodeficiency, X-Linked 62 0.026
850
NRM005 Neuromuscular Disease 62 0.026
851
PRP083 Porphyria, Acute Intermittent 62 0.026
852
BRC012 Brucellosis 62 0.026
853
P BCK002 Beckwith-Wiedemann Syndrome 62 0.026
854
P MCP040 Mucopolysaccharidosis-Plus Syndrome 62 0.026
855
c PNS012 Paine Syndrome 61 0.026
856
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 61 0.026
857
ING001 Inguinal Hernia 61 0.026
858
CHL067 Cholecystitis 60 0.026
859
SPT006 Septooptic Dysplasia 60 0.026
860
c MCL013 Mucolipidosis Iv 60 0.026
861
PST028 Post-Traumatic Stress Disorder 60 0.026
862
P NPH005 Nephronophthisis 60 0.026
863
P CYS018 Cystitis 59 0.026
864
P MLT074 Multiple Endocrine Neoplasia 59 0.026
865
P HDC001 Headache 59 0.026
866
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 59 0.026
867
P SYP003 Syphilis 59 0.026
868
HYD002 Hydronephrosis 58 0.026
869
LYM021 Lymphadenitis 58 0.026
870
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 58 0.026
871
BRG013 Buerger Disease 58 0.026
872
ISL014 Isolated Growth Hormone Deficiency, Type Ia 58 0.026
873
DSS009 Disseminated Intravascular Coagulation 58 0.026
874
YLL002 Yellow Fever 58 0.026
875
INT007 Intermediate Coronary Syndrome 58 0.026
876
P MTC069 Mitochondrial Disorders 57 0.026
877
LMY014 Leiomyoma, Uterine 57 0.026
878
P MMP001 Mumps 57 0.026
879
ERY003 Erythema Multiforme 57 0.026
880
APH002 Aphasia 56 0.026
881
P BNC003 Bone Cancer 56 0.026
882
PNM008 Pneumothorax 56 0.026
883
P RBL001 Rubella 56 0.026
884
JPN002 Japanese Encephalitis 56 0.026
885
RHM001 Rheumatic Fever 56 0.026
886
c FML035 Familial Hyperlipidemia 56 0.026
887
P HYP024 Hypoparathyroidism 56 0.026
888
c CNG216 Congenital Hydrocephalus 55 0.026
889
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 55 0.026
890
LST001 Listeriosis 55 0.026
891
FRY006 Fryns Microphthalmia Syndrome 55 0.026
892
SML019 Smallpox 55 0.026
893
ABL002 Ablepharon-Macrostomia Syndrome 54 0.026
894
PRL032 Perlman Syndrome 54 0.026
895
P LYM025 Lymphedema 54 0.026
896
P MMB011 Membranous Nephropathy 54 0.026
897
FCT001 Factor Viii Deficiency 54 0.026
898
P ANG015 Angioedema 54 0.026
899
TXC002 Toxic Encephalopathy 54 0.026
900
P MGL001 Megaloblastic Anemia 54 0.026
901
P HYP040 Hypospadias 54 0.026
902
P PTS002 Ptosis 53 0.026
903
EXP004 Exophthalmos 53 0.026
904
PRP036 Peripheral T-Cell Lymphoma 53 0.026
905
P PRS049 Persistent Mullerian Duct Syndrome 53 0.026
906
CRT016 Carotid Artery Disease 53 0.026
907
NRT001 Neurotic Disorder 53 0.026
908
NNL006 Non-Alcoholic Steatohepatitis 53 0.026
909
SPS003 Spastic Diplegia 53 0.026
910
NPH003 Nephrocalcinosis 52 0.026
911
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.026
912
THY125 Thyroid Gland Medullary Carcinoma 52 0.026
913
THR004 Thrombocytosis 52 0.026
914
FND002 Fundus Dystrophy 52 0.026
915
P CTN015 Cutaneous T Cell Lymphoma 52 0.026
916
NRT004 Neuritis 52 0.026
917
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 52 0.026
918
c CHR418 Chronic Leukemia 52 0.026
919
ILS001 Ileus 51 0.026
920
HYP081 Hypolipoproteinemia 51 0.026
921
PRP080 Peripheral Artery Disease 51 0.026
923
c CRS016 Crisponi/cold-Induced Sweating Syndrome 1 51 0.026
924
APL002 Aplasia of Lacrimal and Salivary Glands 51 0.026
925
BNN003 Bone Inflammation Disease 51 0.026
926
CHL004 Cholelithiasis 50 0.026
927
TRY001 Trypanosomiasis 50 0.026
928
c PSR023 Psoriasis 1 50 0.026
929
MTC005 Mitochondrial Metabolism Disease 50 0.026
930
DSM007 Desmoplastic Small Round Cell Tumor 50 0.026
931
P OVR046 Ovarian Cyst 50 0.026
932
PLR022 Pleural Disease 50 0.026
933
RFR010 Refractory Anemia 50 0.026
934
c PSR021 Psoriasis 14, Pustular 50 0.026
935
PLR008 Pleurisy 50 0.026
936
c INF145 Infantile Liver Failure Syndrome 1 50 0.026
937
CRD137 Cardiogenic Shock 50 0.026
938
DRY001 Dry Eye Syndrome 50 0.026
939
c MLG074 Malignant Mesenchymoma 50 0.026
940
GST049 Gastrointestinal System Cancer 49 0.026
941
TST044 Testicular Torsion 49 0.026
942
c ACT078 Acute Porphyria 49 0.026
943
INT017 Intestinal Schistosomiasis 49 0.026
944
c BCT013 Bacterial Pneumonia 49 0.026
945
RNL011 Renal Osteodystrophy 49 0.026
946
P HMN032 Human Herpesvirus 8 49 0.026
947
PST048 Postural Orthostatic Tachycardia Syndrome 49 0.026
948
THR013 Thoracic Outlet Syndrome 49 0.026
949
CRN027 Corneal Neovascularization 48 0.026
950
ATN005 Autonomic Dysfunction 48 0.026
951
LGN006 Legionnaire Disease 48 0.026
952
c INH030 Inherited Retinal Disorder 48 0.026
953
ANV001 Anovulation 47 0.026
954
P HMR005 Hemorrhoid 47 0.026
955
VTM033 Vitamin K Deficiency Bleeding 47 0.026
956
HYP025 Hyperphosphatemia 47 0.026
957
c CRV002 Cervix Uteri Carcinoma in Situ 47 0.026
958
c VRL012 Viral Meningitis 47 0.026
959
PRN014 Paronychia 47 0.026
960
URT010 Ureteral Obstruction 46 0.026
961
P PRP056 Porphyria, Acute Hepatic 46 0.026
962
GRN017 Granulocytopenia 46 0.026
963
ATR013 Atrichia with Papular Lesions 46 0.026
964
CHL056 Cheilitis 46 0.026
965
c HYP513 Hypogonadotropic Hypogonadism 1 with or Without Anosmia 46 0.026
966
KRT013 Keratolytic Winter Erythema 45 0.026
967
MNG006 Monogenic Diabetes 45 0.026
968
c PRS128 Persistent Mullerian Duct Syndrome, Types I and Ii 45 0.026
969
c TRC092 Trichorhinophalangeal Syndrome, Type I 45 0.026
970
FBR054 Fibroma 45 0.026
971
KHN001 Kuhnt-Junius Degeneration 45 0.026
972
PRC003 Proctitis 44 0.026
973
P MJR007 Major Affective Disorder 1 44 0.026
974
HYP457 Hypertrophic Scars 44 0.026
975
ENT001 Enterocele 44 0.026
976
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.026
977
c HMG003 Hemoglobin E Disease 43 0.026
978
SMN007 Seminoma 43 0.026
979
FTL021 Fetal Macrosomia 43 0.026
980
P CRB088 Cerebral Atrophy 43 0.026
981
ACT084 Acute Stress Disorder 42 0.026
982
ACT088 Acute Insulin Response 42 0.026
983
ALC010 Alcoholic Cardiomyopathy 42 0.026
984
DBT007 Diabetic Cataract 42 0.026
985
TRP009 Triple X Syndrome 42 0.026
986
c MCR112 Microvascular Complications of Diabetes 2 42 0.026
987
PPL001 Papillary Adenoma 42 0.026
988
P DYS005 Dyslexia 42 0.026
989
CRV045 Cervical Intraepithelial Neoplasia 41 0.026
990
ADS004 Aids Dementia Complex 41 0.026
991
P DYS021 Dysautonomia 41 0.026
992
PLY100 Polyploidy 41 0.026
993
PNM005 Pneumonic Plague 40 0.026
994
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.026
995
c PSR028 Psoriasis 7 40 0.026
996
c HMG029 Hemoglobin Se Disease 40 0.026
997
c PSR018 Psoriasis 13 40 0.026
998
c PSR032 Psoriasis 11 40 0.026
999
SPR126 Superior Semicircular Canal Dehiscence 39 0.026
1000
HPT070 Hepatosplenic T-Cell Lymphoma 39 0.026
1001
ESP025 Esophagus Adenocarcinoma 39 0.026
1002
MNR003 Mineral Metabolism Disease 39 0.026
1003
MCC013 Mucocutaneous Ulceration, Chronic 39 0.026
1004
ATX010 Ataxia Neuropathy Spectrum 39 0.026
1005
P CRB059 Cerebellar Degeneration 38 0.026
1006
BTN004 Biotin Deficiency 38 0.026
1007
c PLY105 Polycystic Ovary Syndrome 1 38 0.026
1008
CRY036 Cryptogenic Cirrhosis 38 0.026
1009
BCK003 Background Diabetic Retinopathy 37 0.026
1010
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.026
1011
CHN002 Chancroid 36 0.026
1012
CHN040 Choanal Atresia and Lymphedema 36 0.026
1013
DSS010 Dissociative Disorder 35 0.026
1015
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.026
1016
ISL109 Isolated Cleft Lip 34 0.026
1017
c MJR003 Major Affective Disorder 6 34 0.026
1018
c MJR006 Major Affective Disorder 5 34 0.026
1019
c PRS136 Prostate Cancer, Hereditary, 6 34 0.026
1020
c PRS130 Prostate Cancer, Hereditary, 8 33 0.026
1021
CND006 Candida Glabrata 33 0.026
1022
PRT094 Protoporphyria, Erythropoietic, X-Linked 33 0.026
1023
RRS014 Rare Surgical Neurologic Disease 33 0.026
1024
RSP007 Respiratory Distress Syndrome, Infant 31 0.026
1025
BRN049 Brain Tumor, Childhood 30 0.026
1026
ANK010 Ankylostomiasis 30 0.026
1027
c PLM128 Pulmonary Hypertension, Primary, 2 29 0.026
1028
DSR031 Disorder of Copper Metabolism 29 0.026
1029
PHS025 Phosphatase, Acid, of Tissues 29 0.026
1030
ENM002 Enamel Erosion 28 0.026
1031
P ACT232 Acute Necrotizing Encephalopathy 28 0.026
1032
SPT019 Septo-Optic Dysplasia Spectrum 28 0.026
1033
DFF010 Diffuse Alopecia Areata 27 0.026
1034
STN013 Stenotrophomonas Maltophilia Infection 26 0.026
1035
ANG061 Angular Cheilitis 25 0.026
1036
OSM001 Osmotic Diarrhea 25 0.026
1037
OBS507 Obsolete: Small Pox 22 0.026
1038
BLD137 Blood Group--Ahonen 17 0.026
1039
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.021
1040
P NNN008 Noonan Syndrome 1 76 0.021
1041
c THR092 Thrombophilia Due to Thrombin Defect 74 0.021
1042
c MNN043 Meningioma, Familial 74 0.021
1043
P FML011 Familial Adenomatous Polyposis 73 0.021
1044
c MLT156 Multiple Endocrine Neoplasia, Type I 71 0.021
1045
P WSK001 Wiskott-Aldrich Syndrome 71 0.021
1046
LPD012 Lipoid Congenital Adrenal Hyperplasia 71 0.021
1047
c PRM196 Premature Ovarian Failure 1 70 0.021
1048
FRN006 Frontotemporal Dementia 70 0.021
1049
BHC003 Behcet Syndrome 70 0.021
1050
P CRN037 Craniosynostosis 69 0.021
1051
c MLT160 Multiple Endocrine Neoplasia, Type Iia 69 0.021
1052
P CHR012 Chronic Granulomatous Disease 69 0.021
1053
P FRG001 Fragile X Syndrome 69 0.021
1054
WRN001 Werner Syndrome 68 0.021
1055
P GLM040 Glioma Susceptibility 1 68 0.021
1056
P MPL001 Maple Syrup Urine Disease 68 0.021
1057
ADR054 Adrenocortical Carcinoma, Hereditary 68 0.021
1058
CRP001 Carpal Tunnel Syndrome 68 0.021
1059
c FML001 Familial Atrial Fibrillation 67 0.021
1060
c JVN010 Juvenile Rheumatoid Arthritis 67 0.021
1061
CRT072 Creutzfeldt-Jakob Disease 67 0.021
1062
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.021
1063
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.021
1064
c ART101 Aortic Valve Disease 2 67 0.021
1065
UND005 Undifferentiated Pleomorphic Sarcoma 66 0.021
1066
c HMP004 Hemophilia B 66 0.021
1067
P PRS038 Personality Disorder 66 0.021
1068
P PRP003 Porphyria Cutanea Tarda 66 0.021
1069
MLD001 Melioidosis 66 0.021
1070
AND002 Androgen Insensitivity Syndrome 66 0.021
1071
P BRD002 Bardet-Biedl Syndrome 66 0.021
1072
LNG039 Lung Squamous Cell Carcinoma 66 0.021
1073
MSM014 Mismatch Repair Cancer Syndrome 65 0.021
1074
P OCL013 Oculodentodigital Dysplasia 65 0.021
1075
CRN036 Craniopharyngioma 65 0.021
1076
P CHR071 Charcot-Marie-Tooth Disease 65 0.021
1077
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 0.021
1078
LYM017 Lyme Disease 64 0.021
1079
LKC009 Leukocyte Adhesion Deficiency, Type I 64 0.021
1080
P THY023 Thymoma 64 0.021
1081
MNN042 Meningioma, Radiation-Induced 64 0.021
1082
OVR029 Ovarian Hyperstimulation Syndrome 63 0.021
1083
c ATM011 Autoimmune Hepatitis 63 0.021
1084
P NRN021 Neuronal Ceroid Lipofuscinosis 63 0.021
1085
c MCP050 Mucopolysaccharidosis, Type Ii 63 0.021
1086
P MVM001 Movement Disease 63 0.021
1087
PPL049 Papillon-Lefevre Syndrome 63 0.021
1088
AND019 Andersen Cardiodysrhythmic Periodic Paralysis