Search results for Levothyroxine

931 hits were found for Levothyroxine

# Family MCID Name MIFTS Score
1
P HYP086 Hypothyroidism 69 26.358
2
P THY032 Thyroiditis 56 12.512
3
GTR002 Goiter 52 10.036
4
THY029 Thyroid Carcinoma 54 9.698
5
P HYP076 Hyperthyroidism 53 8.007
6
c CNG006 Congenital Hypothyroidism 63 7.599
7
HSH003 Hashimoto Thyroiditis 60 6.654
8
c GRV008 Graves Disease 1 54 6.033
9
THY030 Thyroid Gland Disease 50 5.991
10
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 5.391
11
P GRV001 Graves' Disease 54 4.525
12
DFF036 Differentiated Thyroid Carcinoma 51 4.085
13
NDL007 Nodular Goiter 48 4.011
14
MYX004 Myxedema 43 3.509
15
CNG034 Congestive Heart Failure 69 3.439
16
PST014 Postsurgical Hypothyroidism 28 3.301
17
P HRT032 Heart Disease 84 3.168
18
THY122 Thyroid Gland Cancer 59 3.132
19
LPD008 Lipid Metabolism Disorder 61 2.926
20
LYM053 Lymphomatous Thyroiditis 22 2.925
21
P MLT008 Multinodular Goiter 42 2.865
22
P OST002 Osteoporosis 77 2.849
23
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 2.849
24
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 2.849
25
DWN001 Down Syndrome 70 2.781
26
P DBT009 Diabetes Mellitus 67 2.691
27
P MYC007 Myocardial Infarction 69 2.679
28
c MJR024 Major Affective Disorder 9 40 2.677
29
c MJR022 Major Affective Disorder 8 37 2.677
30
P BPL003 Bipolar Disorder 56 2.677
31
c TYP009 Type 2 Diabetes Mellitus 92 2.673
32
P CRN300 Coronary Heart Disease 1 73 2.466
33
c THY109 Thyroid Cancer, Nonmedullary, 1 55 2.355
34
OCL069 Ocular Motor Apraxia 57 2.323
35
LPP008 Lipoprotein Quantitative Trait Locus 65 2.230
36
P CLC063 Celiac Disease 1 66 2.143
37
SYS003 Systolic Heart Failure 49 2.125
38
P KDN018 Kidney Disease 72 2.123
39
DPR016 Depression 65 2.119
40
c HYP836 Hypercholesterolemia, Familial, 1 73 2.095
41
NNL005 Non-Alcoholic Fatty Liver Disease 63 2.089
42
P LVR013 Liver Disease 68 2.089
43
FTT001 Fatty Liver Disease 61 2.089
44
P INF032 Infertility 60 2.086
45
ATH013 Atherosclerosis Susceptibility 63 2.083
46
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 2.038
47
ALC007 Alcohol Dependence 65 2.038
48
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 2.018
49
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 2.018
50
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 2.018
51
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 2.018
52
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 2.018
53
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 2.018
54
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 2.018
55
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 2.018
56
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 2.018
57
ATH010 Athyreosis 34 2.010
58
P ATR011 Atrial Fibrillation 66 2.002
59
P GST044 Gastritis 55 1.990
60
CHR178 Chromosomal Triplication 34 1.933
61
ANG054 Angina Pectoris 65 1.930
62
ETH004 Euthyroid Sick Syndrome 38 1.902
63
c HYP795 Hypothyroidism, Congenital, Nongoitrous, 4 47 1.900
64
DFC004 Deficiency Anemia 74 1.889
65
MNT002 Mental Depression 56 1.872
66
MDD011 Mood Disorder 62 1.844
67
P URT039 Urticaria 57 1.827
68
BRN028 Brain Cancer 73 1.821
69
CNS004 Constipation 56 1.809
70
P HYP083 Hypopituitarism 52 1.790
71
NNL006 Non-Alcoholic Steatohepatitis 54 1.780
72
PLC008 Placenta Disease 49 1.779
73
P HYP024 Hypoparathyroidism 55 1.761
74
P LCT002 Lactose Intolerance 52 1.752
75
GST050 Gastrointestinal System Disease 55 1.752
76
P MJR007 Major Affective Disorder 1 42 1.747
77
AGN016 Aging 54 1.729
78
PPL002 Papillary Carcinoma 46 1.725
79
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 1.695
80
P NPH012 Nephrotic Syndrome 62 1.691
81
P HDC001 Headache 56 1.647
82
BNR002 Bone Resorption Disease 47 1.644
83
c CHR684 Chronic Kidney Disease 74 1.633
84
c ACT075 Acute Myocardial Infarction 55 1.633
85
CRH001 Crohn's Disease 80 1.633
86
NNT010 Nontoxic Goiter 32 1.599
87
c TRN047 Transient Congenital Hypothyroidism 22 1.595
88
c PRC016 Pre-Eclampsia 64 1.592
89
c TYP008 Type 1 Diabetes Mellitus 77 1.563
90
ANT039 Antisynthetase Syndrome 55 1.560
91
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.539
92
P TRM003 Tremor 50 1.523
93
GST037 Gastroparesis 52 1.495
94
IRN002 Iron Metabolism Disease 56 1.452
95
HYP020 Hyperprolactinemia 63 1.446
96
AMN001 Amenorrhea 53 1.446
97
IRN001 Iron Deficiency Anemia 58 1.428
98
GST019 Gastrointestinal Stromal Tumor 78 1.422
99
48X005 48,xyyy 39 1.422
100
c CHR708 Chronic Urticaria 42 1.407
101
GLC096 Galactorrhea 40 1.376
102
GRD001 Giardiasis 46 1.364
103
PRT251 Proteinuria, Chronic Benign 58 1.343
104
P LPS004 Lupus Erythematosus 61 1.332
105
HYP029 Hyperthyroxinemia 32 1.331
106
P ECL001 Eclampsia 52 1.323
107
c ATR087 Atrial Standstill 1 74 1.319
108
FCT008 Factitious Disorder 34 1.319
109
c SYS001 Systemic Lupus Erythematosus 86 1.315
110
P ATR005 Atrophic Gastritis 50 1.297
111
END028 Endemic Goiter 36 1.281
112
THY123 Thyroid Gland Follicular Carcinoma 53 1.270
113
P HMN010 Hemangioma 61 1.268
114
ADN018 Adenoma 58 1.265
115
47X002 47,xyy 48 1.254
116
LVR012 Liver Cirrhosis 62 1.239
117
END086 End Stage Renal Disease 54 1.239
118
P PTT006 Pituitary Adenoma 55 1.237
119
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 1.236
120
MLD018 Mild Cognitive Impairment 48 1.236
121
c BLD140 Blood Group, I System 47 1.236
122
ATX019 Ataxia with Vitamin E Deficiency 44 1.236
123
LPT014 Leptin Deficiency or Dysfunction 77 1.232
124
PPL035 Papillary Thyroid Microcarcinoma 39 1.210
125
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 1.206
126
c HYP724 Hyperlipoproteinemia, Type Iii 66 1.206
127
PLY012 Polyhydramnios 46 1.199
128
ALL029 Allergic Disease 61 1.190
129
HLC007 Helicobacter Pylori Infection 67 1.188
130
CHR710 Chronic Spontaneous Urticaria 45 1.188
131
SXL003 Sexual Disorder 49 1.176
132
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.174
133
c MGR028 Migraine with or Without Aura 1 64 1.172
134
P CRD246 Cardiovascular System Disease 55 1.158
135
c ATM101 Autoimmune Gastritis 40 1.153
136
c ATM011 Autoimmune Hepatitis 62 1.153
137
HMP001 Hemopericardium 47 1.132
138
P PRC012 Pericardial Effusion 50 1.132
139
P OVR046 Ovarian Cyst 44 1.115
140
P THR014 Thrombocytopenia 66 1.115
141
CYT002 Cytokine Deficiency 43 1.115
142
HYP080 Hypogonadism 49 1.106
143
P DMN002 Dementia 65 1.101
144
P HYP069 Hyperparathyroidism 62 1.101
145
P SLP005 Sleep Disorder 62 1.101
146
PRM315 Permanent Congenital Hypothyroidism 26 1.101
147
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.085
148
HYP025 Hyperphosphatemia 47 1.072
149
P INT068 Intestinal Disease 53 1.072
150
SCH012 Schizoaffective Disorder 49 1.072
151
DYS073 Dysphagia 53 1.071
152
ANX010 Anxiety 70 1.041
153
P HYP760 Hypothyroidism, Congenital, Nongoitrous, 2 54 1.033
154
HYP056 Hypoglycemia 65 1.033
155
ADL002 Adult Syndrome 69 1.032
156
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 1.032
157
P PRG092 Pregnancy Loss, Recurrent 1 42 1.032
158
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 1.032
159
c SYS043 Systemic Lupus Erythematosus 1 38 1.032
160
LPT006 Leptin Receptor Deficiency 50 1.032
161
P ALC033 Alcohol Use Disorder 67 1.032
162
END072 Endotheliitis 36 1.032
163
IDP031 Idiopathic Hypersomnia 39 1.024
164
P HYP263 Hypersomnia 40 1.024
165
IMM003 Immunoglobulin Alpha Deficiency 44 1.005
166
PTT037 Pituitary Tumors 44 1.003
167
P ENC018 Encephalopathy 62 0.992
168
c SBC007 Subacute Thyroiditis 43 0.992
169
EXP004 Exophthalmos 50 0.992
170
GRW007 Growth Hormone Deficiency 47 0.992
171
P SHR001 Short Bowel Syndrome 53 0.986
172
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.986
173
c PRM340 Primary Adrenal Insufficiency 37 0.986
174
RHB024 Rhabdomyosarcoma 2 65 0.985
175
CRB039 Cerebrovascular Disease 65 0.971
176
c PRM093 Premature Ovarian Failure 7 47 0.964
177
c ACT150 Acute Adrenal Insufficiency 48 0.964
178
PLC007 Placental Abruption 47 0.948
179
P ALZ034 Alzheimer Disease 87 0.941
180
INT303 Intracranial Hypertension, Idiopathic 56 0.941
181
ULC004 Ulcerative Colitis 74 0.941
182
P ANG015 Angioedema 56 0.936
183
P VNW001 Von Willebrand's Disease 64 0.936
184
P SLP006 Sleep Apnea 69 0.924
185
HYP005 Hypokalemia 55 0.924
186
GST033 Gestational Diabetes 61 0.911
187
c ACT071 Acute Kidney Failure 60 0.898
188
c VRL010 Viral Hepatitis 52 0.884
189
ISC004 Ischemia 61 0.884
190
P CRP001 Carpal Tunnel Syndrome 66 0.882
191
P SNS001 Sensorineural Hearing Loss 59 0.870
192
P EXN002 Exanthem 58 0.870
193
P RSP003 Respiratory Failure 74 0.870
194
ATM061 Autoimmune Polyglandular Syndrome Type 3 28 0.870
195
SBC016 Subacute Delirium 42 0.870
196
P ALP008 Alopecia 53 0.870
197
SHH001 Sheehan Syndrome 44 0.870
198
c PRM316 Primary Congenital Hypothyroidism 31 0.870
199
THY111 Thyroid Carcinoma, Familial Medullary 67 0.855
200
P HYP750 Hypertriglyceridemia, Familial 62 0.855
201
P DRR001 Diarrhea 55 0.855
202
THY125 Thyroid Gland Medullary Carcinoma 48 0.855
203
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.840
204
CRD223 Cardiac Arrhythmia 63 0.840
205
P OVR082 Overgrowth Syndrome 42 0.824
206
c FML297 Familial Thyroid Dyshormonogenesis 47 0.807
207
P HPT021 Hepatitis 68 0.807
208
PLM011 Plummer's Disease 34 0.807
209
INT075 Intracranial Hypertension 52 0.807
210
GST092 Gastroesophageal Reflux 60 0.788
211
c LKM063 Leukemia, Chronic Myeloid 71 0.788
212
FML037 Female Breast Cancer 51 0.788
213
PRN011 Pernicious Anemia 52 0.788
214
c HPT016 Hepatitis B 62 0.788
215
P SKN015 Skin Carcinoma 71 0.788
216
RST023 Resting Heart Rate, Variation in 40 0.788
217
IRR002 Irritable Bowel Syndrome 65 0.788
218
P PRD021 Periodic Paralysis 42 0.788
219
PRP107 Peripheral Hypothyroidism 16 0.788
220
CRD137 Cardiogenic Shock 56 0.788
221
HMC014 Homocysteinemia 52 0.769
222
c HNT004 Huntington Disease-Like 2 51 0.769
223
c HNT011 Huntington Disease-Like 3 33 0.769
224
OVR029 Ovarian Hyperstimulation Syndrome 63 0.769
225
RRM016 Rare Movement Disorder 15 0.769
227
c MCR133 Microvascular Complications of Diabetes 4 41 0.747
228
RCK004 Rickets 65 0.747
229
P RHM011 Rheumatoid Arthritis 81 0.747
230
c MCR113 Microvascular Complications of Diabetes 3 52 0.747
231
c MCR130 Microvascular Complications of Diabetes 6 41 0.747
232
c MCR120 Microvascular Complications of Diabetes 7 47 0.747
233
THY001 Thyroid Crisis 30 0.747
234
ADJ001 Adjustment Disorder 46 0.747
235
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 0.747
236
PPL021 Papilledema 49 0.747
237
BRK012 Broken Heart Syndrome 42 0.747
238
P ART022 Arthritis 70 0.747
239
IDP091 Idiopathic Nephrotic Syndrome 49 0.747
240
c ACT134 Acute Liver Failure 57 0.747
241
ATM095 Autoimmune Disease 61 0.747
242
P MLT020 Multiple Sclerosis 79 0.724
243
P CRD119 Cardiac Arrest 68 0.724
244
AML013 Amelogenesis Imperfecta, Hypomaturation Type, Iia1 24 0.724
245
HMN004 Hemangioma of Liver 35 0.724
246
DMY004 Demyelinating Disease 50 0.724
247
P THY054 Thyrotoxic Periodic Paralysis 51 0.724
248
P SZR006 Seizure Disorder 69 0.724
249
P CMP008 Compartment Syndrome 50 0.724
250
P SCH015 Schizophrenia 74 0.697
251
P INF037 Inflammatory Bowel Disease 53 0.697
252
SLD003 Sialadenitis 47 0.697
253
AMN015 Amenorrhea-Galactorrhea Syndrome 20 0.697
254
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 0.697
255
DSS008 Disease of Mental Health 74 0.697
256
ECT026 Ectopic Pregnancy 47 0.697
257
THR004 Thrombocytosis 52 0.697
258
c RNG013 Ring Chromosome 18 23 0.697
259
P NRC002 Narcolepsy 55 0.697
260
PRT058 Pure Autonomic Failure 58 0.697
261
P RNG032 Ring Chromosome 39 0.697
262
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.696
263
ART140 Arteries, Anomalies of 52 0.665
264
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.665
265
GST009 Gastroschisis 53 0.665
266
c ATM092 Autoimmune Polyendocrine Syndrome, Type Ii 45 0.665
267
ACT088 Acute Insulin Response 39 0.665
268
CLT003 Colitis 63 0.665
269
PRN009 Paranoid Schizophrenia 49 0.665
270
CPG001 Capgras Syndrome 26 0.665
271
c PRM005 Primary Hyperparathyroidism 59 0.665
272
CHG001 Chagas Disease 65 0.665
273
GST040 Gastric Adenocarcinoma 66 0.665
274
P CHR345 Chronic Pain 50 0.665
275
FNT004 Fainting 29 0.665
276
ABD010 Abdominal Wall Defect 39 0.665
277
PYG006 Pyogenic Granuloma 36 0.665
278
PTT046 Pituitary Hormone Deficiency, Combined, 2 62 0.639
279
c CNT101 Central Congenital Hypothyroidism 37 0.632
280
CYS001 Cystic Fibrosis 77 0.624
281
BTN003 Biotinidase Deficiency 62 0.624
282
MCS002 Mucositis 55 0.624
283
ERY003 Erythema Multiforme 56 0.624
284
SVR097 Severe Cutaneous Adverse Reaction 68 0.624
285
ANR007 Anorexia Nervosa 59 0.624
286
GLC025 Galactorrhoea-Hyperprolactinaemia 20 0.624
287
ERY066 Erythema Multiforme Major 29 0.624
288
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 0.624
289
NTR005 Nutritional Deficiency Disease 60 0.592
290
c MJR008 Major Affective Disorder 2 34 0.540
291
c MJR006 Major Affective Disorder 5 32 0.540
292
P NJM001 Nijmegen Breakage Syndrome 75 0.540
293
c MJR003 Major Affective Disorder 6 32 0.540
294
c MJR004 Major Affective Disorder 4 28 0.540
295
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 44 0.540
296
c MJR023 Major Affective Disorder 7 33 0.540
297
P END084 Endocrine System Disease 44 0.540
298
BLM002 Bulimia Nervosa 57 0.524
299
DRM006 Dermatitis 62 0.524
300
P ANR048 Aniridia 1 66 0.492
301
HYP781 Hypoascorbemia 52 0.492
302
CMP010 Complex Regional Pain Syndrome 59 0.492
303
KRT002 Keratomalacia 54 0.492
304
P LRY044 Larynx Cancer 53 0.492
305
END040 Endogenous Depression 54 0.492
306
NRT001 Neurotic Disorder 56 0.492
307
PRQ002 Paraquat Poisoning 28 0.492
308
P MYP004 Myopathy 67 0.489
309
P DBT005 Diabetes Insipidus 54 0.489
310
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.424
311
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 52 0.424
312
P LCH002 Lichen Planus 55 0.412
313
LYM043 Lymphocytic Hypophysitis 31 0.387
314
c DWL002 Dowling-Degos Disease 1 58 0.374
315
NNT003 Neonatal Thyrotoxicosis 28 0.374
316
PTT004 Pituitary Apoplexy 47 0.360
317
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.360
318
P HYP265 Hypotonia 42 0.360
319
P PRC019 Precocious Puberty 49 0.360
320
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.346
321
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.346
322
ORL013 Oral Lichen Planus 45 0.346
323
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.331
324
P STR021 Struma Ovarii 39 0.331
325
P MLN008 Melanoma 75 0.331
326
P NTR004 Neutropenia 62 0.331
327
P HYP730 Hypogonadotropic Hypogonadism 54 0.316
328
MCR037 Macroglossia 44 0.316
329
P PLY019 Polyneuropathy 53 0.316
330
c SCN052 Secondary Adrenal Insufficiency 35 0.316
331
P MYS005 Myositis 56 0.300
332
PTT009 Pituitary Gland Disease 53 0.300
333
ACR007 Acromegaly 70 0.300
334
P GND004 Gonadal Dysgenesis 46 0.300
335
P TRN020 Turner Syndrome 67 0.300
336
P TRT010 Teratoma 50 0.300
337
ENT011 Enterocolitis 55 0.282
338
UMB002 Umbilical Hernia 46 0.282
339
STT001 Status Epilepticus 58 0.282
340
P PTS002 Ptosis 52 0.282
341
c HPT001 Hepatitis C 61 0.282
342
CRD001 Cardiac Tamponade 44 0.282
343
EMP001 Empty Sella Syndrome 42 0.282
344
PRN019 Perinatal Necrotizing Enterocolitis 60 0.282
345
P NRP001 Neuropathy 59 0.282
346
P PLM037 Pulmonary Hypertension 69 0.264
347
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.264
348
c DLT002 Dilated Cardiomyopathy 79 0.264
349
OLG003 Oligohydramnios 51 0.264
350
HYP066 Hyperglycemia 60 0.264
351
P VSC011 Vasculitis 61 0.264
352
c HYP374 Hypothyroidism, Congenital, Nongoitrous, 1 51 0.245
353
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.245
354
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.245
355
VTM002 Vitamin B12 Deficiency 48 0.245
356
MCR018 Microcytic Anemia 47 0.245
357
CHL068 Cholestasis 61 0.245
358
P ACN011 Acne 55 0.245
359
c MLG059 Malignant Struma Ovarii 31 0.245
360
P PRP019 Peripheral Nervous System Disease 57 0.245
361
TXC005 Toxic Shock Syndrome 62 0.245
362
CNN003 Conn's Syndrome 77 0.245
363
P GLM007 Glomerulonephritis 59 0.245
364
HST010 Histiocytosis 49 0.245
365
P RHN004 Rhinitis 57 0.245
366
P PSD015 Pseudohypoparathyroidism 54 0.245
367
SDD008 Sudden Sensorineural Hearing Loss 41 0.245
368
P MSC003 Muscular Atrophy 52 0.245
369
INT007 Intermediate Coronary Syndrome 53 0.245
370
ETN001 Eating Disorder 59 0.245
371
GRN017 Granulocytopenia 42 0.245
372
THY098 Thyroid Ectopia 31 0.245
373
P BLD134 Bladder Cancer 79 0.223
374
ESP021 Esophageal Cancer 84 0.223
375
LYM133 Lymphoma, Hodgkin, Classic 74 0.223
376
MYL069 Myeloma, Multiple 77 0.223
377
PRM013 Premature Menopause 57 0.223
378
P LNG032 Lung Cancer 98 0.223
379
P CTN015 Cutaneous T Cell Lymphoma 48 0.223
380
APH002 Aphasia 55 0.223
381
LNG108 Langerhans Cell Histiocytosis 57 0.223
382
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.223
383
P MJR001 Major Depressive Disorder 68 0.223
384
ATR057 Atrioventricular Block 54 0.223
385
IMP005 Impotence 52 0.223
386
MGS001 Megaesophagus 44 0.223
387
P PLY011 Polycystic Ovary Syndrome 57 0.223
388
P BRS044 Breast Adenocarcinoma 58 0.223
389
CLN015 Colon Adenocarcinoma 64 0.223
390
PST011 Pustulosis of Palm and Sole 52 0.223
392
P PSR002 Psoriasis 63 0.223
393
DWR001 Dwarfism 45 0.223
395
P BRS047 Breast Cancer 97 0.200
396
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.200
397
P MYS003 Myasthenia Gravis 68 0.200
398
ACT238 Acth Deficiency, Isolated 52 0.200
399
ESP020 Esophageal Atresia 60 0.200
400
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.200
401
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.200
402
THY069 Thyroid Hormone Resistance, Selective Pituitary 36 0.200
403
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 72 0.200
404
P STR020 Strabismus 56 0.200
405
c ACQ017 Acquired Von Willebrand Syndrome 48 0.200
406
P OMP004 Omphalocele 47 0.200
407
GYN001 Gynecomastia 48 0.200
408
PNC001 Pancytopenia 52 0.200
409
GT001 Gout 63 0.200
410
SVR001 Severe Acute Respiratory Syndrome 68 0.200
411
P LNG028 Long Qt Syndrome 63 0.200
412
CNN005 Connective Tissue Disease 66 0.200
413
P VSC007 Vascular Disease 62 0.200
414
P THR015 Thrombophilia 51 0.200
415
PRC013 Pericarditis 53 0.200
416
SBS002 Substernal Goiter 26 0.200
417
INF021 Infant Gynecomastia 30 0.200
418
P SYP003 Syphilis 59 0.200
419
KRN002 Kearns-Sayre Syndrome 63 0.200
420
P MYC008 Myocarditis 59 0.200
421
PRP030 Purpura 54 0.200
422
PRS063 Paresthesia 39 0.200
423
SYN036 Syncope 44 0.200
424
P EYD002 Eye Disease 57 0.200
425
MCH006 Mechanical Strabismus 40 0.200
426
DVR002 Diverticulitis 46 0.200
427
P AMY004 Amyloidosis 69 0.200
428
HSH004 Hashimoto Encephalopathy 27 0.200
429
P MNN013 Meningitis 65 0.200
430
MLG118 Malignancy Diagnosed During Pregnancy 16 0.200
431
PRM331 Primary Hypophysitis 18 0.200
432
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.173
433
INS024 Insulin-Like Growth Factor I 77 0.173
434
MYL009 Myelodysplastic Syndrome 67 0.173
435
MSC007 Muscle Hypertrophy 64 0.173
436
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 0.173
437
ATS010 Autosomal Recessive Disease 42 0.173
438
P END046 Endometritis 46 0.173
439
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.173
440
FML063 Familial Glucocorticoid Deficiency 58 0.173
441
P PLY041 Polymyositis 59 0.173
442
CVD001 Covid-19 58 0.173
443
P DRM010 Dermatomyositis 61 0.173
444
c PSD108 Pseudohypoparathyroidism, Type Ia 64 0.173
445
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 0.173
446
HYD038 Hydrops Fetalis, Nonimmune 57 0.173
447
P FML018 Familial Mediterranean Fever 73 0.173
448
c LYM150 Lymphatic Malformation 7 43 0.173
449
ALL003 Allergic Rhinitis 66 0.173
450
TRT017 Teratoma, Ovarian 28 0.173
451
c SML038 Small Cell Cancer of the Lung 69 0.173
452
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.173
453
P PRD006 Prader-Willi Syndrome 60 0.173
454
BRC012 Brucellosis 66 0.173
455
P URN019 Urinary Tract Infection 49 0.173
456
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.173
457
c SVR005 Severe Pre-Eclampsia 50 0.173
458
c PST001 Posterior Myocardial Infarction 20 0.173
459
FLL031 Follicular Adenoma 40 0.173
460
P PRL003 Proliferative Glomerulonephritis 43 0.173
461
FBR047 Fibromyalgia 58 0.173
462
OVR109 Ovarian Germ Cell Teratoma 32 0.173
463
P OVR049 Ovarian Disease 50 0.173
464
CYS009 Cystadenoma 43 0.173
465
HYP014 Hyperuricemia 51 0.173
466
CHR073 Choreatic Disease 53 0.173
467
P RNL007 Renal Tubular Acidosis 52 0.173
468
SPP005 Suppurative Thyroiditis 32 0.173
469
LYM022 Lymphangioma 54 0.173
470
P HYD006 Hydrocephalus 63 0.173
471
P PLM036 Pulmonary Fibrosis 65 0.173
472
P CRN035 Cranial Nerve Palsy 42 0.173
473
c SCN007 Secondary Hyperparathyroidism 51 0.173
474
INP001 Inappropriate Adh Syndrome 48 0.173
475
P PLY006 Polydactyly 58 0.173
476
ANR040 Aneurysm 60 0.173
477
P HRP006 Herpes Simplex 65 0.173
478
SLP010 Slipped Capital Femoral Epiphysis 38 0.173
479
P MYC033 Myoclonus 46 0.173
480
ACH005 Achalasia 54 0.173
481
PLM033 Pulmonary Embolism 58 0.173
482
HMN016 Hemangioendothelioma 35 0.173
483
GRN020 Granulomatous Hypophysitis 14 0.173
484
THY128 Thyroid Tumor 33 0.173
485
P PLY188 Polyendocrinopathy 29 0.173
486
PNH004 Panhypophysitis 20 0.173
487
P PLV020 Pelvic Organ Prolapse 58 0.141
488
P SRC025 Sarcoidosis 1 70 0.141
489
ALL001 Allan-Herndon-Dudley Syndrome 54 0.141
490
PND002 Pendred Syndrome 57 0.141
491
c THY056 Thyroid Dyshormonogenesis 3 32 0.141
492
c THY102 Thyroid Cancer, Nonmedullary, 2 54 0.141
493
c MCR115 Microvascular Complications of Diabetes 5 65 0.141
494
LYM143 Lymphoma, Non-Hodgkin, Familial 79 0.141
495
DSS032 Disease by Infectious Agent 55 0.141
496
THY009 Thyroid Lymphoma 44 0.141
497
P KRT007 Keratoconus 50 0.141
498
BCT022 Bacterial Infectious Disease 56 0.141
499
GLC003 Glucose Intolerance 53 0.141
500
P OPN001 Open-Angle Glaucoma 55 0.141
501
PRT013 Portal Hypertension 59 0.141
502
P PRK039 Parkinsonism 55 0.141
503
ART074 Aortic Dissection 53 0.141
504
ASY002 Asymptomatic Neurosyphilis 41 0.141
505
P MDL005 Medulloblastoma 75 0.141
506
P MLN069 Melanoma, Uveal 59 0.141
507
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.141
508
HYP780 Hypoadrenocorticism, Familial 61 0.141
509
HYP784 Hypogonadism, Male 43 0.141
510
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.141
511
c ATS007 Autism Spectrum Disorder 72 0.141
512
ADR040 Adrenal Gland Pheochromocytoma 45 0.141
513
MTB004 Metabolic Acidosis 48 0.141
514
IFP003 Ifap Syndrome 2 42 0.141
515
PRT010 Parathyroid Carcinoma 68 0.141
516
CHN065 Choanal Atresia, Posterior 48 0.141
517
PSR001 Psoriatic Arthritis 61 0.141
518
c HYP355 Hypothyroidism, Congenital, Nongoitrous, 3 20 0.141
519
c HPT073 Hepatitis C Virus 71 0.141
520
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.141
521
HYP748 Hypertelorism 46 0.141
522
c EXD008 Exudative Vitreoretinopathy 1 71 0.141
523
OSS012 Osseous Heteroplasia, Progressive 61 0.141
524
P PHC003 Pheochromocytoma 70 0.141
525
MCC012 Mccune-Albright Syndrome 69 0.141
526
CRD132 Cardiac Conduction Defect 59 0.141
527
CLF027 Cleft Palate, Isolated 64 0.141
528
c SCL052 Scleroderma, Familial Progressive 60 0.141
529
PSD014 Pseudopseudohypoparathyroidism 54 0.141
530
P LNG064 Lung Cancer Susceptibility 3 70 0.141
531
P ART005 Arteriovenous Malformation 65 0.141
532
ALP097 Alopecia Universalis Congenita 57 0.141
533
P HPT023 Hepatocellular Carcinoma 95 0.141
534
P OPT006 Optic Nerve Disease 57 0.141
535
SYP001 Syphilitic Meningitis 31 0.141
536
P BND020 Bone Disease 60 0.141
537
P MYG005 Myoglobinuria 40 0.141
538
P BRC006 Brachydactyly 52 0.141
539
DYS015 Dysentery 50 0.141
540
P SCK002 Sick Sinus Syndrome 55 0.141
541
P BRB001 Beriberi 44 0.141
542
P CND004 Candidiasis 57 0.141
543
KRT001 Keratoconjunctivitis Sicca 49 0.141
544
CRS001 Crescentic Glomerulonephritis 42 0.141
545
P INN002 Inner Ear Disease 50 0.141
546
HRY003 Hairy Cell Leukemia 61 0.141
547
NPH009 Nephrolithiasis 54 0.141
548
P GRW001 Growth Hormone Secreting Pituitary Adenoma 47 0.141
549
PLS009 Plasma Cell Neoplasm 64 0.141
550
P BLP003 Blepharospasm 45 0.141
551
P CNJ013 Conjunctivitis 66 0.141
552
MTR010 Mature Teratoma 40 0.141
553
CHL067 Cholecystitis 59 0.141
554
P CYS017 Cystic Teratoma 41 0.141
555
MCR017 Macrocytic Anemia 44 0.141
556
CRB037 Cerebral Palsy 67 0.141
557
NNT012 Neonatal Jaundice 53 0.141
558
P OST001 Osteopetrosis 70 0.141
559
P FCL005 Focal Segmental Glomerulosclerosis 57 0.141
560
BNG018 Benign Paroxysmal Positional Nystagmus 40 0.141
561
FCL012 Facial Paralysis 49 0.141
562
ALC009 Alcoholic Liver Cirrhosis 54 0.141
563
P ATM019 Autoimmune Polyendocrine Syndrome 46 0.141
564
EST004 Estrogen Excess 37 0.141
565
PMS001 Poems Syndrome 59 0.141
566
CNV002 Conversion Disorder 47 0.141
567
MGL001 Megaloblastic Anemia 59 0.141
568
ENP001 Enophthalmos 40 0.141
569
P MLN007 Male Infertility 56 0.141
570
PRM236 Primary Biliary Cholangitis 62 0.141
571
PLM010 Pulmonary Edema 54 0.141
572
CHL039 Choledocholithiasis 37 0.141
573
MGC001 Megacolon 48 0.141
574
HYP043 Hyperandrogenism 47 0.141
575
P CHN059 Chondrocalcinosis 51 0.141
576
PLS011 Plasmacytoma 56 0.141
577
CRN036 Craniopharyngioma 63 0.141
578
CLN006 Colonic Pseudo-Obstruction 30 0.141
579
TRN015 Transient Cerebral Ischemia 62 0.141
580
PSY004 Psychotic Disorder 66 0.141
581
P THY023 Thymoma 64 0.141
582
ART002 Arts Syndrome 66 0.141
583
OST159 Osteogenic Sarcoma 66 0.141
584
P PTN014 Patent Ductus Arteriosus 1 59 0.141
585
c THY107 Thymoma, Familial 42 0.141
586
GST045 Gastroenteritis 58 0.141
587
P CNG048 Congenital Hepatic Fibrosis 36 0.141
588
MST020 Mast Cell Activation Syndrome 27 0.141
589
NRS003 Neurosyphilis 45 0.141
590
RYN005 Raynaud Phenomenon 45 0.141
591
c CNT075 Central Precocious Puberty 53 0.141
593
LNG099 Lung Disease 62 0.141
594
MLT006 Multidrug-Resistant Tuberculosis 47 0.141
595
STM007 Stomatitis 52 0.141
596
RTR011 Retroperitoneal Fibrosis 47 0.141
597
ACT200 Acute Monoblastic Leukemia 40 0.141
598
TRM010 Traumatic Brain Injury 50 0.141
599
PRT036 Peritonitis 65 0.141
600
PTT001 Pituitary Hypoplasia 34 0.141
601
PRT029 Parathyroid Adenoma 51 0.141
602
P ALP009 Alopecia Areata 59 0.141
603
KRT006 Keratoconjunctivitis 53 0.141
604
FRN020 Frontal Fibrosing Alopecia 47 0.141
605
P GNR008 Generalized Resistance to Thyroid Hormone 22 0.141
606
NPH018 Nephrogenic Systemic Fibrosis 49 0.141
607
PNS014 Penis Agenesis 38 0.141
608
P DST107 Distal Renal Tubular Acidosis 48 0.141
609
FTL021 Fetal Macrosomia 40 0.141
610
HYP144 Hyperacusis 23 0.141
611
LYM116 Lymph Node Disease 42 0.141
612
P HYP098 Hypereosinophilic Syndrome 66 0.141
613
c RRH009 Rare Hypothyroidism 8 0.141
614
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.100
615
ERY029 Erythermalgia, Primary 58 0.100
616
c HMC039 Hemochromatosis, Type 1 73 0.100
617
c SMP007 Simpson-Golabi-Behmel Syndrome, Type 1 54 0.100
618
ISL014 Isolated Growth Hormone Deficiency, Type Ia 54 0.100
619
VLC001 Velocardiofacial Syndrome 57 0.100
620
ABT001 Abetalipoproteinemia 68 0.100
621
RSP019 Respiratory Distress Syndrome in Premature Infants 52 0.100
622
MYC006 Mycosis Fungoides 65 0.100
623
c PSD104 Pseudohypoparathyroidism, Type Ii 30 0.100
624
TKY002 Takayasu Arteritis 61 0.100
625
THY039 Thyrotropin-Releasing Hormone Deficiency 29 0.100
626
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 53 0.100
627
c BRN108 Branchiootic Syndrome 1 63 0.100
628
AST006 Astigmatism 46 0.100
629
KGM001 Kagami-Ogata Syndrome 54 0.100
630
c ATM057 Autoimmune Thyroid Disease 2 12 0.100
631
SLW005 Slowed Nerve Conduction Velocity, Autosomal Dominant 35 0.100
632
GRN037 Granulomatosis with Polyangiitis 67 0.100
633
MCR302 Macrostomia, Isolated 29 0.100
634
P GST053 Gastric Cancer 82 0.100
635
c NLD006 Nail Disorder, Nonsyndromic Congenital, 9 35 0.100
636
c ATM024 Autoimmune Pancreatitis 52 0.100
637
ADR016 Adrenal Cortical Carcinoma 61 0.100
638
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.100
640
P GRF003 Graft-Versus-Host Disease 71 0.100
641
DRG013 Drug-Induced Lupus Erythematosus 49 0.100
642
HRT040 Hirata Disease 38 0.100
643
P FNC004 Fanconi Syndrome 60 0.100
644
CYS010 Cystinosis 61 0.100
645
P LKD001 Leukodystrophy 58 0.100
646
P PLY014 Polycystic Kidney Disease 71 0.100
648
INT395 Intracranial Meningioma 48 0.100
649
ART004 Aortic Atherosclerosis 46 0.100
650
c VRL005 Viral Pneumonia 52 0.100
651
P THR005 Thrombotic Thrombocytopenic Purpura 64 0.100
652
MRF001 Marfan Syndrome 76 0.100
653
OBS002 Obsessive-Compulsive Disorder 68 0.100
654
APL023 Aplasia Cutis Congenita, Nonsyndromic 46 0.100
655
c FNC027 Fanconi Anemia, Complementation Group a 81 0.100
656
RNL024 Renal Glucosuria 60 0.100
657
FBR089 Fibrosclerosis, Multifocal 35 0.100
658
c GLY008 Glycogen Storage Disease Ii 72 0.100
659
IMM167 Immune Deficiency Disease 77 0.100
660
DDN011 Duodenal Atresia 48 0.100
661
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.100
662
P LYM118 Lymphoma 69 0.100
663
ISC015 Ischemic Colitis 43 0.100
664
DRG024 Drug Allergy 40 0.100
665
HYP017 Hypophosphatemia 49 0.100
666
ASP007 Aspiration Pneumonia 49 0.100
667
SCN049 Second-Degree Atrioventricular Block 34 0.100
668
c ATM002 Autoimmune Polyendocrine Syndrome Type 1 43 0.100
669
P CTN003 Cutaneous Lupus Erythematosus 52 0.100
670
P FML068 Familial Hypocalciuric Hypercalcemia 54 0.100
671
CLR109 Colorectal Adenocarcinoma 50 0.100
672
P MYC084 Mycobacterium Tuberculosis 1 68 0.100
673
CHR382 Chromosome 18q Deletion Syndrome 40 0.100
674
PRT082 Preterm Premature Rupture of the Membranes 56 0.100
675
OBS081 Obesity, Early-Onset, with Adrenal Insufficiency and Red Hair 37 0.100
676
c HYP595 Hypertension, Essential 84 0.100
677
P HRS035 Hirschsprung Disease 1 66 0.100
678
P CLR023 Colorectal Cancer 100 0.100
679
EPC005 Epicanthus 36 0.100
680
ACH004 Achondroplasia 66 0.100
681
MNR012 Meniere Disease 55 0.100
682
OPT070 Optic Nerve Hypoplasia, Bilateral 55 0.100
683
SPT006 Septooptic Dysplasia 62 0.100
684
NLP001 Nail-Patella Syndrome 63 0.100
685
c MLT159 Multiple Endocrine Neoplasia, Type Iib 60 0.100
686
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 54 0.100
687
P PLG001 Pelger-Huet Anomaly 52 0.100
688
PCK003 Pick Disease of Brain 69 0.100
689
EPD070 Epidermoid Cysts 35 0.100
690
FBR032 Fibromuscular Dysplasia 47 0.100
691
c CHL119 Cholangitis, Primary Sclerosing 57 0.100
692
P MMB011 Membranous Nephropathy 50 0.100
693
TTT001 Tatton-Brown-Rahman Syndrome 45 0.100
694
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 33 0.100
695
P FRG001 Fragile X Syndrome 70 0.100
696
HYP856 Hypothyroidism, Central, with Testicular Enlargement 38 0.100
697
CHR525 Chromosome Xq26.3 Duplication Syndrome 36 0.100
698
FBR012 Fabry Disease 71 0.100
699
c KRT041 Keratoconus 4 14 0.100
700
HYP677 Hyperthyroxinemia, Familial Dysalbuminemic 27 0.100
701
SRC014 Sarcoma 64 0.100
702
HRW001 Hair Whorl 35 0.100
703
LCH016 Lichen Sclerosus Et Atrophicus 41 0.100
704
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.100
705
DGR001 Digeorge Syndrome 62 0.100
706
PTZ001 Peutz-Jeghers Syndrome 69 0.100
707
STF001 Stiff-Person Syndrome 57 0.100
708
SPR004 Supravalvular Aortic Stenosis 57 0.100
709
CHR619 Chromosome 2q35 Duplication Syndrome 64 0.100
710
c THR092 Thrombophilia Due to Thrombin Defect 74 0.100
711
IGR001 Ige Responsiveness, Atopic 59 0.100
712
URT020 Ureterocele 36 0.100
713
WLL001 Williams-Beuren Syndrome 60 0.100
714
c WLM013 Wilms Tumor 1 65 0.100
715
P ATS364 Autism 72 0.100
716
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.100
717
HMP005 Hemiplegia 53 0.100
718
SPS004 Spastic Quadriplegia 39 0.100
719
PLC009 Placenta Praevia 39 0.100
720
PTT010 Pituitary Infarct 32 0.100
721
P EPL164 Epilepsy 70 0.100
722
HYP085 Hypothalamic Disease 38 0.100
723
HYP060 Hyperinsulinism 53 0.100
724
VST001 Vestibular Neuronitis 33 0.100
725
THR024 Thrombosis 56 0.100
726
P SCK004 Seckel Syndrome 58 0.100
727
P PRG013 Paraganglioma 57 0.100
728
c HRD202 Hereditary Lymphedema I 55 0.100
729
SPC010 Speech and Communication Disorders 48 0.100
730
PRP027 Peripheral Vascular Disease 71 0.100
731
c HPT003 Hepatitis a 63 0.100
732
CRN019 Coronary Artery Vasospasm 47 0.100
733
MNN017 Mononeuropathy 41 0.100
734
BLR001 Biliary Atresia 55 0.100
735
NWB001 Newborn Respiratory Distress Syndrome 56 0.100
736
LMY002 Leiomyoma 51 0.100
737
CNT047 Contact Dermatitis 57 0.100
738
P END044 Endometriosis 62 0.100
739
PRS021 Prostatic Adenoma 43 0.100
740
PLM001 Pulmonary Tuberculosis 69 0.100
741
ANR004 Anuria 44 0.100
742
P ANT006 Antiphospholipid Syndrome 55 0.100
743
c ACT027 Acute Pancreatitis 60 0.100
744
P CYS039 Cystic Kidney Disease 52 0.100
745
ACQ007 Acquired Immunodeficiency Syndrome 58 0.100
746
P HML002 Hemolytic Anemia 62 0.100
747
LYM027 Lymphopenia 56 0.100
748
PRP016 Paraplegia 52 0.100
749
P MVM001 Movement Disease 61 0.100
750
P BNG030 Benign Ependymoma 51 0.100
751
P PNC044 Pancreatitis 61 0.100
752
SVR004 Severe Combined Immunodeficiency 71 0.100
753
ADR008 Adrenal Adenoma 55 0.100
754
LYM010 Lymph Node Tuberculosis 41 0.100
755
ART012 Aortitis 42 0.100
756
P DYS154 Dystonia 64 0.100
757
CHS002 Chiasmal Syndrome 24 0.100
758
P MCR010 Microcephaly 59 0.100
759
TRN007 Transsexualism 38 0.100
760
PRS045 Prostatic Hypertrophy 52 0.100
761
PRT030 Parathyroid Gland Disease 45 0.100
762
KRT008 Keratopathy 46 0.100
763
RCT020 Rectum Adenocarcinoma 48 0.100
764
HYP026 Hypoglycemic Coma 37 0.100
765
KRT009 Keratosis 52 0.100
766
NRN004 Neuroendocrine Tumor 55 0.100
767
MNC004 Monoclonal Paraproteinemia 29 0.100
768
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.100
769
P AGM001 Agammaglobulinemia 67 0.100
770
P RCT021 Rectum Cancer 54 0.100
771
P END039 Endodermal Sinus Tumor 42 0.100
772
PRT014 Protein S Deficiency 46 0.100
773
P KDN017 Kidney Cancer 60 0.100
774
QDR001 Quadriplegia 49 0.100
775
NRS005 Neurosarcoidosis 32 0.100
776
SQM006 Squamous Cell Carcinoma 59 0.100
777
EXC002 Exocrine Pancreatic Insufficiency 42 0.100
778
P PRR002 Pure Red-Cell Aplasia 46 0.100
779
HPT019 Hepatic Encephalopathy 59 0.100
780
ADL030 Adult-Onset Still's Disease 59 0.100
781
c ACT053 Acute Thyroiditis 28 0.100
782
c BPL002 Bipolar I Disorder 47 0.100
783
GNR004 Generalized Anxiety Disorder 55 0.100
784
46X002 46 Xx Gonadal Dysgenesis 38 0.100
785
P NMN002 Niemann-Pick Disease 60 0.100
786
P SCL009 Sclerosing Cholangitis 46 0.100
787
c HRD002 Hereditary Angioedema 61 0.100
788
NRN001 Neuroendocrine Carcinoma 47 0.100
789
DSS009 Disseminated Intravascular Coagulation 56 0.100
790
HMS001 Hemosiderosis 48 0.100
791
EHR002 Ehrlichiosis 39 0.100
792
PLR008 Pleurisy 49 0.100
793
BLP004 Blepharophimosis 36 0.100
794
FNC002 Functional Diarrhea 39 0.100
795
DPH001 Diphtheria 59 0.100
796
SKN016 Skin Disease 62 0.100
797
P LYN001 Lynch Syndrome 76 0.100
798
PLC005 Placental Insufficiency 56 0.100
799
THY124 Thyroid Gland Papillary Carcinoma 38 0.100
800
CYS002 Cystic Lymphangioma 45 0.100
801
GNG013 Gingivitis 59 0.100
802
P MLT074 Multiple Endocrine Neoplasia 58 0.100
803
GST007 Gastric Dilatation 29 0.100
804
P MST009 Mastocytosis 64 0.100
805
SYS004 Systemic Mastocytosis 62 0.100
806
BLR008 Bilirubin Metabolic Disorder 57 0.100
807
INT025 Intermittent Explosive Disorder 39 0.100
808
BNN003 Bone Inflammation Disease 47 0.100
809
BCT002 Bacterial Vaginosis 53 0.100
810
NNL001 Non-Langerhans-Cell Histiocytosis 35 0.100
811
RHS001 Rh Isoimmunization 28 0.100
812
ADR004 Adrenal Cortical Adenocarcinoma 38 0.100
813
GRM004 Germinoma 40 0.100
814
c DRM040 Dermatitis Herpetiformis, Familial 35 0.100
815
c LKM061 Leukemia, Acute Myeloid 83 0.100
816
CHY005 Chylothorax, Congenital 37 0.100
817
NTH001 Netherton Syndrome 60 0.100
818
P NSP012 Nasopharyngeal Carcinoma 60 0.100
819
MNN043 Meningioma, Familial 79 0.100
820
NRN002 Neuronitis 31 0.100
821
SCL025 Scleromyxedema 37 0.100
822
ALD013 Aldosterone-Producing Adenoma 36 0.100
823
CRN030 Coronary Stenosis 50 0.100
824
TRC022 Tricuspid Valve Insufficiency 47 0.100
825
SPN035 Spindle Cell Sarcoma 51 0.100
826
ERD001 Erdheim-Chester Disease 53 0.100
827
SPR007 Superior Mesenteric Artery Syndrome 36 0.100
828
LTR002 Lateral Sinus Thrombosis 25 0.100
829
SPH001 Sapho Syndrome 47 0.100
830
P NRM002 Normal Pressure Hydrocephalus 49 0.100
831
CNG608 Congenital Hypopituitarism 29 0.100
832
CRT033 Corticobasal Degeneration 48 0.100
833
HRS011 Horseshoe Kidney 31 0.100
834
KCH001 Kocher-Debre-Semelaigne Syndrome 12 0.100
835
P SMP003 Simpson-Golabi-Behmel Syndrome 50 0.100
836
STT009 Sutton Disease 2 29 0.100
837
P THL005 Thalassemia 56 0.100
838
BCK006 Back Pain 43 0.100
839
EXT039 Extrapontine Myelinolysis 18 0.100
840
P ACT010 Acth-Secreting Pituitary Adenoma 60 0.100
841
ACT058 Active Peptic Ulcer Disease 55 0.100
842
P NRB001 Neuroblastoma 66 0.100
843
TBR011 Tuberculous Meningitis 48 0.100
844
c FML191 Familial Long Qt Syndrome 54 0.100
845
P RRL003 Rare Lymphatic Malformation 31 0.100
846
PRN039 Paraneoplastic Syndromes 37 0.100
847
SPS057 Spasticity 43 0.100
848
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.100
849
P CTR002 Cataract 59 0.100
850
PRP028 Peripheral Vertigo 36 0.100
851
P BRN022 Bronchiectasis 59 0.100
852
P MTR014 Motor Neuron Disease 65 0.100
853
JVN003 Juvenile Xanthogranuloma 43 0.100
854
INT042 Internuclear Ophthalmoplegia 32 0.100
855
FNC007 Functioning Pituitary Adenoma 42 0.100
856
APH001 Aphthous Stomatitis 57 0.100
857
PTH003 Pathologic Nystagmus 52 0.100
858
CLL010 Cellular Ependymoma 58 0.100
859
PYD002 Pyoderma 49 0.100
860
FLL008 Folliculitis 45 0.100
861
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.100
862
SCR001 Secretory Meningioma 40 0.100
863
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.100
864
HDN002 Head Injury 44 0.100
865
c JVN010 Juvenile Rheumatoid Arthritis 66 0.100
866
P RBL001 Rubella 58 0.100
867
P DRM007 Dermatitis Herpetiformis 54 0.100
868
c BCT006 Bacterial Conjunctivitis 42 0.100
869
c HRD088 Hereditary Neuropathies 34 0.100
870
HYP264 Hypertonia 36 0.100
871
c AMY009 Amyloidosis Aa 47 0.100
872
c ALM001 Al Amyloidosis 54 0.100
873
CHR223 Chromosome 1q Deletion 13 0.100
874
AMN006 Aminoaciduria 37 0.100
875
PRN008 Peroneal Nerve Paralysis 24 0.100
876
RSC001 Rosacea 55 0.100
877
MTC004 Mitochondrial Encephalomyopathy 43 0.100
878
P INT070 Intestinal Obstruction 57 0.100
879
SBC005 Subacute Lymphocytic Thyroiditis 27 0.100
880
SKN019 Skin Melanoma 70 0.100
881
ORP003 Oropharynx Cancer 54 0.100
882
CHR048 Chronic Rhinitis 46 0.100
883
APP008 Appendicitis 62 0.100
884
DBT010 Diabetic Neuropathy 54 0.100
885
HYD005 Hydrocele 46 0.100
886
BP1002 Bap1 Tumor Predisposition Syndrome 42 0.100
887
DST006 Diastolic Heart Failure 45 0.100
888
MLR002 Miliary Tuberculosis 47 0.100
889
P ENC004 Encephalitis 61 0.100
890
P CHL066 Cholangitis 51 0.100
891
PST021 Postpartum Depression 50 0.100
892
P CLL015 Collagen Disease 47 0.100
893
DCB001 Decubitus Ulcer 61 0.100
894
LRY028 Laryngocele 21 0.100
895
PTT041 Pituitary Stalk Interruption Syndrome 54 0.100
896
c CHR417 Chronic Graft Versus Host Disease 55 0.100
897
LCH008 Lichen Planus Pigmentosus 23 0.100
898
P OTT001 Otitis Externa 43 0.100
899
c BCT007 Bacterial Meningitis 55 0.100
900
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 46 0.100
901
HYP835 Hypothalamic Obesity 38 0.100
902
LTT006 Littoral Cell Angioma of the Spleen 18 0.100
904
MLL001 Molluscum Contagiosum 48 0.100
905
CHR078 Chorioretinitis 50 0.100
906
LRN003 Learning Disability 49 0.100
907
SWL001 Swallowing Disorders 38 0.100
908
P PST059 Pustular Psoriasis 37 0.100
909
PST092 Posttransplant Acute Limbic Encephalitis 29 0.100
910
c SBC035 Subacute Cutaneous Lupus Erythematosus 34 0.100
911
c SCN039 Secondary Central Precocious Puberty 10 0.100
912
UTR054 Uterine Hypoplasia 21 0.100
913
P BCL004 B-Cell Non-Hodgkin Lymphoma 42 0.100
914
PTC005 Pituicytoma 28 0.100
915
MSC129 Muscular Pseudohypertrophy-Hypothyroidism Syndrome 22 0.100
916
ACT167 Acute Generalized Exanthematous Pustulosis 38 0.100
917
LTN011 Late-Onset Isolated Acth Deficiency 17 0.100
918
SYS071 Systemic Autoimmune Disease 35 0.100
919
c RRH015 Rare Hemorrhagic Disorder 22 0.100
920
P RRH023 Rare Hereditary Hemochromatosis 53 0.100
921
FXD003 Fixed Drug Eruption 34 0.100
922
EXR008 Exercise-Induced Malignant Hyperthermia 20 0.100
923
HRD224 Hereditary Nonpolyposis Colon Cancer 51 0.100
924
DSC009 Discoid Lupus Erythematosus 43 0.100
925
FNC050 Functioning Gonadotropic Adenoma 26 0.100
926
ADN064 Adenohypophysitis 34 0.100
927
IDP095 Idiopathic Steroid-Resistant Nephrotic Syndrome 20 0.100
928
NNF007 Non-Functioning Pituitary Adenoma 39 0.100
929
PTR034 Paternal Uniparental Disomy 19 0.100
930
P RRT020 Rare Tumor 39 0.100
931
P SKL032 Skeletal Muscle Disease 25 0.100
Content
Loading form....