Search results for Hydrochlorothiazide

632 hits were found for Hydrochlorothiazide

# Family MCID Name MIFTS Score
1
c HYP595 Hypertension, Essential 85 45.324
2
HYP005 Hypokalemia 55 18.740
3
P DBT005 Diabetes Insipidus 54 10.085
4
c TYP009 Type 2 Diabetes Mellitus 92 9.873
5
P DBT009 Diabetes Mellitus 67 9.245
6
HYP540 Hypertension, Diastolic 37 8.321
7
NPH009 Nephrolithiasis 54 8.238
8
HYP014 Hyperuricemia 51 7.933
9
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 7.761
10
PRT251 Proteinuria, Chronic Benign 57 7.420
11
P SKN015 Skin Carcinoma 71 7.394
12
PLM010 Pulmonary Edema 55 6.911
13
CNG034 Congestive Heart Failure 69 6.786
14
c CHR684 Chronic Kidney Disease 69 6.303
15
c MCR113 Microvascular Complications of Diabetes 3 52 6.224
16
IDP073 Idiopathic Hypercalciuria 40 5.890
17
P KDN018 Kidney Disease 72 5.887
18
c MCR130 Microvascular Complications of Diabetes 6 41 5.769
19
c MCR120 Microvascular Complications of Diabetes 7 47 5.769
20
c MCR133 Microvascular Complications of Diabetes 4 41 5.769
21
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 5.759
22
NPH091 Nephrolithiasis, Calcium Oxalate 61 5.690
23
PRT058 Pure Autonomic Failure 58 5.621
24
P HYP069 Hyperparathyroidism 62 5.502
25
c ACT071 Acute Kidney Failure 60 5.461
26
IMP005 Impotence 52 5.330
27
P MLN008 Melanoma 76 5.213
28
P EXN002 Exanthem 58 5.013
29
48X005 48,xyyy 39 4.750
30
c BSL007 Basal Cell Carcinoma 68 4.714
31
P NPH012 Nephrotic Syndrome 60 4.691
32
P HYP024 Hypoparathyroidism 55 4.639
33
c HYP836 Hypercholesterolemia, Familial, 1 73 4.539
34
c BLD140 Blood Group, I System 46 4.530
35
URL001 Urolithiasis 46 4.320
36
LPD008 Lipid Metabolism Disorder 62 4.305
37
P RNV001 Renovascular Hypertension 49 4.281
38
GT001 Gout 64 4.215
39
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 63 4.200
40
GLC003 Glucose Intolerance 54 4.111
41
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 4.110
42
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 4.110
43
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 4.110
44
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 4.110
45
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 4.110
46
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 4.110
47
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 4.110
48
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 4.110
49
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 4.110
50
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 4.110
51
CRD132 Cardiac Conduction Defect 60 4.030
52
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 3.965
53
ATH013 Atherosclerosis Susceptibility 63 3.951
54
MSC007 Muscle Hypertrophy 64 3.929
55
RHB024 Rhabdomyosarcoma 2 67 3.906
56
P LPC002 Lip Cancer 46 3.848
57
P SLP006 Sleep Apnea 69 3.794
58
c SCN007 Secondary Hyperparathyroidism 51 3.772
59
P HRT032 Heart Disease 81 3.756
60
NPH003 Nephrocalcinosis 49 3.683
61
P CRD246 Cardiovascular System Disease 56 3.677
62
SKN019 Skin Melanoma 71 3.629
63
P ANG015 Angioedema 56 3.540
64
P VSC007 Vascular Disease 63 3.532
65
GTL001 Gitelman Syndrome 65 3.457
66
ANT039 Antisynthetase Syndrome 55 3.390
67
SXL003 Sexual Disorder 49 3.364
68
RCK004 Rickets 68 3.355
69
NTR005 Nutritional Deficiency Disease 61 3.334
70
BNR002 Bone Resorption Disease 47 3.298
71
CRB039 Cerebrovascular Disease 66 3.280
72
P HYP733 Hypercalciuria, Absorptive, 2 45 3.273
73
P ANR048 Aniridia 1 64 3.266
74
LPP008 Lipoprotein Quantitative Trait Locus 65 3.263
75
ADL002 Adult Syndrome 70 3.245
76
MTB004 Metabolic Acidosis 48 3.170
77
P CRD119 Cardiac Arrest 67 3.120
78
CNN003 Conn's Syndrome 79 3.071
79
DBT092 Diabetes Insipidus, Nephrogenic, X-Linked 38 3.049
80
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 3.001
81
PRP027 Peripheral Vascular Disease 71 2.998
82
END086 End Stage Renal Disease 52 2.949
83
ART140 Arteries, Anomalies of 53 2.930
84
P NTR004 Neutropenia 63 2.926
85
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 2.924
86
P URN019 Urinary Tract Infection 49 2.906
87
P CTN003 Cutaneous Lupus Erythematosus 52 2.873
88
RST023 Resting Heart Rate, Variation in 40 2.862
89
P DNT020 Dent Disease 1 63 2.826
90
c SBC035 Subacute Cutaneous Lupus Erythematosus 34 2.812
91
P HYP750 Hypertriglyceridemia, Familial 62 2.788
92
ANG054 Angina Pectoris 66 2.773
93
P CRN300 Coronary Heart Disease 1 73 2.757
94
P MYC007 Myocardial Infarction 70 2.729
95
P TRN020 Turner Syndrome 67 2.715
96
NSP002 Nasopharyngitis 45 2.686
97
P PRK057 Parkinson Disease, Late-Onset 80 2.653
98
P RNL015 Renal Hypertension 45 2.604
99
INT067 Interstitial Nephritis 46 2.603
100
HYP066 Hyperglycemia 61 2.549
101
c PRC016 Pre-Eclampsia 65 2.534
102
P PNC044 Pancreatitis 61 2.492
103
HMP001 Hemopericardium 47 2.479
104
NPH010 Nephrosclerosis 50 2.479
105
P PRC012 Pericardial Effusion 50 2.479
106
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 2.478
107
P BND020 Bone Disease 59 2.445
108
P ECL001 Eclampsia 52 2.438
109
HYD002 Hydronephrosis 58 2.437
110
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 2.420
111
P HYP802 Hypocalcemia, Autosomal Dominant 1 68 2.414
112
HMC014 Homocysteinemia 52 2.397
113
P RSP003 Respiratory Failure 74 2.372
114
P TRM003 Tremor 48 2.344
115
47X002 47,xyy 48 2.344
116
ALL029 Allergic Disease 59 2.344
117
P PRD021 Periodic Paralysis 41 2.309
118
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 2.295
119
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 2.290
120
SYN036 Syncope 45 2.258
121
P ALC033 Alcohol Use Disorder 61 2.219
122
FML035 Familial Hyperlipidemia 55 2.219
123
c ACT027 Acute Pancreatitis 60 2.212
124
P RNL007 Renal Tubular Acidosis 50 2.194
125
HYP025 Hyperphosphatemia 48 2.174
126
P PSD003 Pseudohypoaldosteronism 44 2.151
127
HYP056 Hypoglycemia 65 2.151
128
TXC005 Toxic Shock Syndrome 62 2.112
129
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 2.104
130
LPT014 Leptin Deficiency or Dysfunction 78 2.102
131
c BRN108 Branchiootic Syndrome 1 62 2.088
132
AGN016 Aging 54 2.067
133
PMP014 Pemphigoid 51 2.024
134
INT007 Intermediate Coronary Syndrome 54 2.024
135
BLL006 Bullous Pemphigoid 61 2.024
136
PRP030 Purpura 54 2.024
137
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 2.022
138
P DRR001 Diarrhea 55 2.022
139
P FNG006 Feingold Syndrome 1 62 1.995
140
P PLY014 Polycystic Kidney Disease 69 1.992
141
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 1.992
142
P ATR011 Atrial Fibrillation 66 1.988
143
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 1.956
144
c ACT068 Acute Cystitis 61 1.952
145
c MLG069 Malignant Hypertension 46 1.952
146
P HDC001 Headache 57 1.952
147
BRN056 Bronchopulmonary Dysplasia 56 1.952
148
OCL069 Ocular Motor Apraxia 57 1.942
149
c PRM005 Primary Hyperparathyroidism 59 1.942
150
c BNG021 Benign Essential Hypertension 35 1.942
151
P ENC018 Encephalopathy 62 1.942
152
P ADL010 Adult Respiratory Distress Syndrome 71 1.928
153
END072 Endotheliitis 36 1.926
154
HYP006 Hypertensive Heart Disease 49 1.886
155
c TYP008 Type 1 Diabetes Mellitus 70 1.880
156
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.880
157
P OST002 Osteoporosis 76 1.854
158
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.854
159
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 1.854
160
INT323 Intraocular Pressure Quantitative Trait Locus 64 1.854
161
CHL067 Cholecystitis 60 1.854
162
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 1.854
163
APN008 Apnea, Obstructive Sleep 67 1.842
164
CYS010 Cystinosis 62 1.822
165
ISC004 Ischemia 61 1.805
166
HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 1.803
167
P FML187 Familial Hypertension 34 1.803
168
MNT002 Mental Depression 57 1.758
169
PLM129 Pulmonary Disease, Chronic Obstructive 74 1.721
170
P VSC011 Vasculitis 61 1.721
171
P HYP098 Hypereosinophilic Syndrome 66 1.721
172
MRK001 Merkel Cell Carcinoma 64 1.721
173
BRN024 Bronchitis 67 1.721
174
GRN017 Granulocytopenia 42 1.721
175
KDN013 Kidney Hypertrophy 34 1.721
176
ORL011 Oral Cancer 60 1.721
177
RYN005 Raynaud Phenomenon 45 1.721
178
P ORL007 Oral Cavity Cancer 51 1.721
179
SQM006 Squamous Cell Carcinoma 60 1.703
180
CRT013 Carotid Stenosis 51 1.702
181
P RHN004 Rhinitis 57 1.702
182
TRN015 Transient Cerebral Ischemia 63 1.678
183
HYP060 Hyperinsulinism 54 1.678
184
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 46 1.654
185
LPT006 Leptin Receptor Deficiency 50 1.654
186
AMD002 Amed Syndrome, Digenic 37 1.654
187
PRD004 Prediabetes Syndrome 52 1.654
188
c HNT011 Huntington Disease-Like 3 34 1.653
189
c HNT004 Huntington Disease-Like 2 52 1.653
190
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 1.633
191
c MGR028 Migraine with or Without Aura 1 64 1.633
192
P SRC025 Sarcoidosis 1 71 1.633
193
THY029 Thyroid Carcinoma 51 1.633
194
DFF036 Differentiated Thyroid Carcinoma 51 1.633
195
c MLG039 Malignant Essential Hypertension 23 1.633
196
VSC002 Vascular Dementia 60 1.633
197
P HRD221 Hereditary Nephrogenic Diabetes Insipidus 17 1.633
198
PRP080 Peripheral Artery Disease 54 1.624
199
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.624
200
c PSD092 Pseudohypoaldosteronism, Type Iie 48 1.615
201
P MYP006 Myopia 56 1.560
202
ANX010 Anxiety 70 1.542
203
c SYS001 Systemic Lupus Erythematosus 87 1.537
204
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 1.537
205
P LPS004 Lupus Erythematosus 61 1.537
206
ANR004 Anuria 44 1.537
207
PRC013 Pericarditis 53 1.537
208
CRD001 Cardiac Tamponade 43 1.537
209
GST045 Gastroenteritis 58 1.537
210
P HML002 Hemolytic Anemia 62 1.532
211
P THR014 Thrombocytopenia 66 1.532
212
CNS004 Constipation 56 1.487
213
P PRC031 Preeclampsia/eclampsia 1 43 1.436
214
P PHT010 Photoparoxysmal Response 1 46 1.436
215
CRH001 Crohn's Disease 80 1.436
216
PHT003 Phototoxic Dermatitis 28 1.436
217
SKN013 Skin Benign Neoplasm 50 1.436
218
CTS005 Catastrophic Antiphospholipid Syndrome 43 1.436
219
CRY008 Cryopyrin-Associated Periodic Syndrome 48 1.436
220
CRT084 Creatinine Clearance Quantitative Trait Locus 25 1.431
221
DRG013 Drug-Induced Lupus Erythematosus 49 1.431
222
P PLY017 Polyarteritis Nodosa 60 1.431
223
P GST044 Gastritis 55 1.431
224
CHL004 Cholelithiasis 49 1.431
225
P PRM002 Primary Hyperoxaluria 65 1.431
226
FML327 Familial Primary Hypomagnesemia with Hypercalciuria and Nephrocalcinosis 18 1.431
227
P HYP077 Hypertrichosis 46 1.418
228
P ACT028 Acute Closed-Angle Glaucoma 32 1.390
229
AND005 Androgen Insensitivity Syndrome, Mild 21 1.361
230
STR067 Stroke, Ischemic 80 1.356
231
ALC007 Alcohol Dependence 66 1.356
232
IDP033 Idiopathic Edema 41 1.356
233
P CHR345 Chronic Pain 50 1.356
234
PLY100 Polyploidy 36 1.345
235
CRD223 Cardiac Arrhythmia 63 1.345
236
P HYP086 Hypothyroidism 69 1.345
237
P SZR006 Seizure Disorder 70 1.311
238
P BRS047 Breast Cancer 98 1.311
239
P PMP001 Pemphigus 55 1.311
240
P NRP001 Neuropathy 60 1.311
241
P FNC004 Fanconi Syndrome 60 1.311
242
P LBY004 Labyrinthitis 43 1.311
243
MYT011 Myotonia 39 1.311
244
P HYP263 Hypersomnia 41 1.311
245
HYP017 Hypophosphatemia 49 1.268
246
ATR057 Atrioventricular Block 54 1.268
247
c HYP272 Hypercholesterolemia, Familial, 3 45 1.241
248
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 1.239
249
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 70 1.239
250
c MCR115 Microvascular Complications of Diabetes 5 65 1.233
251
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 1.232
252
MNR012 Meniere Disease 56 1.204
253
P CTN015 Cutaneous T Cell Lymphoma 48 1.204
254
P HYP076 Hyperthyroidism 53 1.204
255
P NJM001 Nijmegen Breakage Syndrome 76 1.201
256
EPT021 Epithelial Recurrent Erosion Dystrophy 46 1.201
257
ATS010 Autosomal Recessive Disease 42 1.186
258
c FNC043 Fanconi Anemia, Complementation Group E 62 1.171
259
ACT167 Acute Generalized Exanthematous Pustulosis 38 1.169
260
MYC006 Mycosis Fungoides 65 1.169
261
PRM057 Paramyotonia Congenita of Von Eulenburg 59 1.169
262
NRM009 Normokalemic Periodic Paralysis 28 1.169
263
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.169
264
P LYM118 Lymphoma 67 1.169
265
PMP006 Pemphigus Vulgaris, Familial 58 1.169
266
P LCH002 Lichen Planus 54 1.169
267
PST092 Posttransplant Acute Limbic Encephalitis 28 1.169
268
DBT010 Diabetic Neuropathy 54 1.169
269
INT002 Intermittent Claudication 61 1.169
270
c VRL010 Viral Hepatitis 53 1.169
271
P PSD015 Pseudohypoparathyroidism 55 1.169
272
P MGR001 Migraine Without Aura 49 1.169
273
CLN015 Colon Adenocarcinoma 65 1.169
274
P PYL005 Pyelonephritis 57 1.169
275
LVR012 Liver Cirrhosis 63 1.169
276
RTR011 Retroperitoneal Fibrosis 47 1.169
277
P PLM037 Pulmonary Hypertension 72 1.098
278
c ART120 Arthrogryposis, Distal, Type 3 49 1.098
279
ENH001 Enhanced S-Cone Syndrome 58 1.097
280
ATM100 Autoimmune Optic Neuritis 28 1.097
281
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.097
282
P OPT009 Optic Neuritis 57 1.097
283
NRT004 Neuritis 53 1.097
284
DMY004 Demyelinating Disease 50 1.097
286
GLC008 Glucose Metabolism Disease 40 1.096
287
ART016 Aortic Aneurysm 68 1.089
288
P PRK039 Parkinsonism 55 1.003
289
GST023 Gastric Ulcer 52 1.003
290
P MYC008 Myocarditis 59 1.003
291
P RNL115 Renal Tubular Acidosis, Proximal 32 0.983
292
c DWL002 Dowling-Degos Disease 1 58 0.983
293
TLM001 Telomere Length, Mean Leukocyte 16 0.983
294
P APL001 Aplastic Anemia 73 0.983
295
MYL020 Myelomeningocele 51 0.983
296
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.983
297
P ORT004 Orthostatic Intolerance 63 0.983
298
c HYP243 Hyperparathyroidism 1 47 0.983
299
DRG024 Drug Allergy 40 0.983
300
ACT003 Acute Kidney Tubular Necrosis 46 0.983
301
P PSR002 Psoriasis 63 0.983
302
P HRP006 Herpes Simplex 65 0.983
303
CNT025 Central Pontine Myelinolysis 43 0.983
304
P ACN011 Acne 57 0.983
305
ADN018 Adenoma 59 0.983
306
PST011 Pustulosis of Palm and Sole 52 0.983
307
P INT070 Intestinal Obstruction 57 0.983
309
LWC001 Low Compliance Bladder 45 0.983
310
ATN004 Autonomic Neuropathy 42 0.983
311
INP001 Inappropriate Adh Syndrome 48 0.983
312
HYD005 Hydrocele 46 0.983
313
SPL018 Splenomegaly 49 0.983
314
DYS073 Dysphagia 53 0.983
315
P PLM064 Pulmonary Sequestration 22 0.983
316
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.983
317
KRT002 Keratomalacia 55 0.983
318
RDN001 Reading Disorder 40 0.980
319
c PNS012 Paine Syndrome 60 0.908
320
ANG049 Angioedema Induced by Ace Inhibitors 40 0.908
321
P CNR004 Cone-Rod Dystrophy 2 74 0.908
322
DFC004 Deficiency Anemia 74 0.908
323
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 0.908
324
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 54 0.908
325
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.908
326
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 43 0.908
327
c HYP724 Hyperlipoproteinemia, Type Iii 67 0.908
328
HYP555 Hypertriglyceridemia, Transient Infantile 38 0.908
329
SCN001 Secondary Hyperparathyroidism of Renal Origin 24 0.908
330
P END084 Endocrine System Disease 44 0.908
331
CRB009 Cerebritis 43 0.908
332
HYP052 Hyperkalemic Periodic Paralysis 63 0.897
333
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.897
334
ATM095 Autoimmune Disease 61 0.897
335
c MJR022 Major Affective Disorder 8 38 0.897
336
MLD018 Mild Cognitive Impairment 48 0.897
337
c MJR024 Major Affective Disorder 9 41 0.897
338
SVR097 Severe Cutaneous Adverse Reaction 69 0.897
339
c PSD090 Pseudohypoaldosteronism, Type Iia 32 0.897
340
P ANT061 Antenatal Bartter Syndrome 36 0.897
341
GYN001 Gynecomastia 47 0.897
342
c ACT075 Acute Myocardial Infarction 56 0.897
343
HYP034 Hypertensive Encephalopathy 43 0.897
344
P BPL003 Bipolar Disorder 56 0.897
345
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.897
346
ERY003 Erythema Multiforme 56 0.897
347
PRS045 Prostatic Hypertrophy 53 0.897
348
HYP008 Hypertensive Retinopathy 39 0.897
349
INF021 Infant Gynecomastia 30 0.897
350
P BRT004 Bartter Disease 58 0.897
351
P DST107 Distal Renal Tubular Acidosis 48 0.897
352
MDL009 Medullary Sponge Kidney 39 0.897
353
P MCR129 Microvascular Complications of Diabetes 1 68 0.784
354
c MCR112 Microvascular Complications of Diabetes 2 42 0.784
355
P PHC003 Pheochromocytoma 69 0.777
356
c ATR087 Atrial Standstill 1 74 0.777
358
RNL114 Renal Cell Carcinoma, Nonpapillary 80 0.777
359
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 51 0.777
360
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 53 0.777
361
ADR040 Adrenal Gland Pheochromocytoma 46 0.777
362
CHR431 Chronic Venous Insufficiency 48 0.777
363
ERY066 Erythema Multiforme Major 29 0.777
364
PTY001 Pityriasis Rosea 44 0.777
365
IGG001 Iga Glomerulonephritis 50 0.777
366
INS001 Insulinoma 59 0.777
367
LNG099 Lung Disease 62 0.777
368
P VNS003 Venous Insufficiency 55 0.777
369
c DLT002 Dilated Cardiomyopathy 78 0.777
370
RTN020 Retinal Vascular Disease 46 0.777
371
ADR008 Adrenal Adenoma 55 0.777
372
P KDN017 Kidney Cancer 61 0.777
373
P MTR003 Mitral Valve Stenosis 53 0.777
374
PLM033 Pulmonary Embolism 58 0.777
375
P HYP265 Hypotonia 42 0.777
376
DWR001 Dwarfism 44 0.777
377
GRW007 Growth Hormone Deficiency 46 0.634
378
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 0.634
379
P ALZ034 Alzheimer Disease 87 0.634
380
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 0.634
381
PRS129 Prostatic Hyperplasia, Benign 49 0.634
382
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 0.634
383
FBR032 Fibromuscular Dysplasia 48 0.634
384
GST092 Gastroesophageal Reflux 61 0.634
385
CMP034 Complete Androgen Insensitivity Syndrome 55 0.634
386
APP015 Apparent Mineralocorticoid Excess 57 0.634
387
SZR026 Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance 57 0.634
388
HYP114 Hypertensive Nephropathy 36 0.634
389
c NPH055 Nephrotic Syndrome, Type 1 52 0.634
390
URT049 Urate Oxidase, Pseudogene 24 0.634
391
CRN270 Coronary Artery Dissection, Spontaneous 32 0.634
392
DSS032 Disease by Infectious Agent 55 0.634
393
RNL077 Renal Fibrosis 46 0.634
394
SPR126 Superior Semicircular Canal Dehiscence 41 0.634
395
FTT001 Fatty Liver Disease 62 0.634
396
SKN016 Skin Disease 63 0.634
397
P INN002 Inner Ear Disease 50 0.634
398
P ANT006 Antiphospholipid Syndrome 55 0.634
399
GLB002 Glioblastoma 67 0.634
400
P LCT001 Lactic Acidosis 51 0.634
401
P SYP003 Syphilis 59 0.634
402
P SYS005 Systemic Scleroderma 74 0.634
403
PPT005 Peptic Ulcer Disease 58 0.634
404
SCB001 Scabies 50 0.634
405
PLY012 Polyhydramnios 46 0.634
406
IMP004 Impetigo 48 0.634
407
P SNS001 Sensorineural Hearing Loss 59 0.634
408
OSM001 Osmotic Diarrhea 28 0.634
409
OLG003 Oligohydramnios 51 0.634
410
PRS021 Prostatic Adenoma 43 0.634
411
TST014 Testicular Cancer 52 0.634
412
GST033 Gestational Diabetes 61 0.634
413
P EYD002 Eye Disease 57 0.634
414
P PRP019 Peripheral Nervous System Disease 58 0.634
415
P GLL018 Gallbladder Cancer 53 0.634
416
MDD011 Mood Disorder 62 0.634
417
DRM006 Dermatitis 62 0.634
418
P GLM007 Glomerulonephritis 60 0.634
419
P URT039 Urticaria 58 0.634
420
GNR004 Generalized Anxiety Disorder 55 0.634
421
CLC006 Calcinosis 47 0.634
422
P INS002 in Situ Carcinoma 53 0.634
423
GST058 Gestational Diabetes Insipidus 14 0.634
424
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 46 0.634
425
P HYP120 Hypoaldosteronism 35 0.634
426
DPS001 Dipsogenic Diabetes Insipidus 22 0.634
427
MTS004 Metastatic Insulinoma 13 0.634
428
RTN017 Retinal Detachment 60 0.534
429
P MLN069 Melanoma, Uveal 61 0.534
430
c GRV008 Graves Disease 1 54 0.534
431
LWC002 Lowe Oculocerebrorenal Syndrome 68 0.534
432
MYX004 Myxedema 43 0.534
433
CHR078 Chorioretinitis 51 0.534
434
ADR009 Adrenal Cortex Disease 36 0.534
435
MCL006 Macular Retinal Edema 57 0.534
436
CRB025 Carbohydrate Metabolic Disorder 40 0.534
437
RLP003 Relapsing Fever 49 0.534
438
ADR012 Adrenal Gland Disease 44 0.534
439
HYP266 Hypoxia 57 0.534
440
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 0.455
441
P PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 0.455
442
CVD001 Covid-19 57 0.455
443
NNL006 Non-Alcoholic Steatohepatitis 54 0.455
444
c FML001 Familial Atrial Fibrillation 65 0.455
445
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 0.455
446
P PRS038 Personality Disorder 65 0.455
447
HNT002 Hantavirus Pulmonary Syndrome 55 0.455
448
ANR040 Aneurysm 61 0.455
449
P LNG032 Lung Cancer 98 0.448
450
c HLP023 Holoprosencephaly 1 56 0.448
451
c CHR686 Chronic Cutaneous Lupus Erythematosus 17 0.448
452
GRV012 Grover's Disease 29 0.448
453
PRN071 Parenteral Nutrition-Associated Cholestasis 23 0.448
454
SRT004 Serotonin Syndrome 54 0.448
455
GLM044 Glomerular Disease 35 0.448
456
ALD013 Aldosterone-Producing Adenoma 36 0.448
457
c ART115 Aortic Valve Disease 1 74 0.448
458
PLL004 Pallister W Syndrome 28 0.448
459
P RTT002 Rett Syndrome 79 0.448
460
ALL001 Allan-Herndon-Dudley Syndrome 54 0.448
461
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.448
462
ART002 Arts Syndrome 66 0.448
463
c DRM040 Dermatitis Herpetiformis, Familial 35 0.448
464
c RTN047 Retinitis Pigmentosa 18 46 0.448
465
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 0.448
466
END057 Endometrial Cancer 72 0.448
467
P MYC084 Mycobacterium Tuberculosis 1 68 0.448
468
OBS002 Obsessive-Compulsive Disorder 68 0.448
469
P LKM071 Leukemia, Chronic Lymphocytic 75 0.448
470
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.448
471
HYP789 Hypophosphatemic Rickets with Hypercalciuria, Hereditary 49 0.448
472
FRS012 First-Degree Atrioventricular Block 39 0.448
473
SCN049 Second-Degree Atrioventricular Block 33 0.448
474
MLR004 Malaria 80 0.448
475
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.448
476
MYL009 Myelodysplastic Syndrome 67 0.448
477
P INF037 Inflammatory Bowel Disease 53 0.448
478
c PRM093 Premature Ovarian Failure 7 48 0.448
479
P PRK101 Parkinsonism-Dystonia, Infantile, 1 40 0.448
480
CYN002 Cyanosis, Transient Neonatal 43 0.448
481
LYM157 Lymph Node Carcinoma 29 0.448
482
ISC015 Ischemic Colitis 43 0.448
483
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.448
484
ART074 Aortic Dissection 53 0.448
485
UMB002 Umbilical Hernia 47 0.448
486
P LYM033 Lymphoproliferative Syndrome 59 0.448
487
THR024 Thrombosis 56 0.448
488
P BRC006 Brachydactyly 51 0.448
489
PMP004 Pemphigus Foliaceus 43 0.448
490
P BRT053 Bartter Syndrome, Type 4a, Neonatal, with Sensorineural Deafness 45 0.448
491
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.448
492
c PCH010 Pachyonychia Congenita 3 43 0.448
493
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.448
494
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 0.448
495
P LDD007 Liddle Syndrome 1 57 0.448
496
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 65 0.448
497
HMH004 Hemihyperplasia, Isolated 41 0.448
498
HYP780 Hypoadrenocorticism, Familial 61 0.448
499
c HYP292 Hypophosphatasia, Infantile 55 0.448
500
RYN001 Raynaud Disease 50 0.448
501
c PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 63 0.448
502
P RNL028 Renal Tubular Dysgenesis 51 0.448
503
P CRC039 Coarctation of Aorta 46 0.448
504
LCH016 Lichen Sclerosus Et Atrophicus 42 0.448
505
MLD001 Melioidosis 67 0.448
506
BSL009 Basal Ganglia Calcification 45 0.448
507
P PTN014 Patent Ductus Arteriosus 1 59 0.448
508
CRD137 Cardiogenic Shock 56 0.448
509
c PSD094 Pseudohypoaldosteronism, Type Iib 26 0.448
510
c HPT003 Hepatitis a 63 0.448
511
LMY002 Leiomyoma 51 0.448
512
HPT004 Hepatic Coma 43 0.448
513
P HML001 Hemolytic-Uremic Syndrome 52 0.448
514
RPD005 Rapidly Involuting Congenital Hemangioma 46 0.448
515
P AMY004 Amyloidosis 70 0.448
516
CRP002 Croup 42 0.448
517
P MSC003 Muscular Atrophy 52 0.448
518
URM002 Uremia 47 0.448
519
BRN004 Brain Edema 54 0.448
520
AVN001 Avian Influenza 61 0.448
521
PRS042 Prostate Disease 42 0.448
522
CLC001 Calciphylaxis 51 0.448
523
MSN001 Mesangial Proliferative Glomerulonephritis 44 0.448
524
PLX002 Plexiform Neurofibroma 43 0.448
525
ART012 Aortitis 42 0.448
526
URT010 Ureteral Obstruction 45 0.448
527
P ART018 Aortic Valve Insufficiency 52 0.448
528
P HMC002 Homocystinuria 53 0.448
529
OCL006 Ocular Hypertension 53 0.448
530
INT075 Intracranial Hypertension 53 0.448
531
P MVM001 Movement Disease 61 0.448
532
SZR001 Sezary's Disease 60 0.448
533
ADR057 Adrenogenital Syndrome 32 0.448
534
INF118 Inflammatory Myopathy with Abundant Macrophages 27 0.448
535
SPC030 Specific Language Disorder 25 0.448
536
P MTH008 Methylmalonic Acidemia 52 0.448
537
P VNT002 Ventricular Septal Defect 58 0.448
538
CRN036 Craniopharyngioma 64 0.448
539
P LVR013 Liver Disease 69 0.448
540
ALL010 Allergic Contact Dermatitis 56 0.448
541
CHR001 Churg-Strauss Syndrome 61 0.448
542
HST010 Histiocytosis 49 0.448
543
c HRD002 Hereditary Angioedema 62 0.448
544
TRC022 Tricuspid Valve Insufficiency 47 0.448
545
ACQ007 Acquired Immunodeficiency Syndrome 59 0.448
546
CNN005 Connective Tissue Disease 67 0.448
547
SPN011 Spongiotic Dermatitis 31 0.448
548
PRP016 Paraplegia 52 0.448
549
P PRD008 Periodontitis 64 0.448
550
P DRM007 Dermatitis Herpetiformis 54 0.448
551
P MMB011 Membranous Nephropathy 50 0.448
552
P GRF003 Graft-Versus-Host Disease 71 0.448
553
CHL147 Chlamydia Pneumonia 47 0.448
554
OST011 Osteomalacia 52 0.448
555
TLN003 Telangiectasis 51 0.448
556
P OTS001 Otosclerosis 49 0.448
557
CRN019 Coronary Artery Vasospasm 47 0.448
558
DYS015 Dysentery 50 0.448
559
DYS009 Dysthymic Disorder 52 0.448
560
P SPN046 Spinal Muscular Atrophy 63 0.448
561
P FCL005 Focal Segmental Glomerulosclerosis 57 0.448
562
ACR007 Acromegaly 70 0.448
563
BRN012 Bronchiolitis Obliterans 56 0.448
564
HPT019 Hepatic Encephalopathy 59 0.448
565
P HYP035 Hypophosphatasia 62 0.448
566
NRW001 Norwegian Scabies 36 0.448
567
PYR004 Pyuria 36 0.448
568
P DDN001 Duodenal Ulcer 53 0.448
569
P AML002 Amelogenesis Imperfecta 56 0.448
570
DPH001 Diphtheria 59 0.448
571
P HYD006 Hydrocephalus 61 0.448
572
c CHR098 Chronic Pyelonephritis 34 0.448
573
HMP005 Hemiplegia 54 0.448
574
RBS001 Rabies 58 0.448
575
CHL123 Chlamydia 58 0.448
576
PRS025 Presbyopia 38 0.448
577
JPN002 Japanese Encephalitis 61 0.448
578
CHL013 Cholecystolithiasis 37 0.448
579
CHL039 Choledocholithiasis 37 0.448
580
MNN009 Meningoencephalitis 48 0.448
581
PLM031 Poliomyelitis 63 0.448
582
ALC005 Alcoholic Pancreatitis 38 0.448
583
P INT068 Intestinal Disease 53 0.448
584
PRP013 Paraphimosis 28 0.448
585
NRT001 Neurotic Disorder 56 0.448
586
URN010 Urinary Tract Obstruction 55 0.448
587
PLM029 Palmoplantar Keratosis 48 0.448
588
CYS009 Cystadenoma 43 0.448
589
CNT047 Contact Dermatitis 57 0.448
590
GNG005 Gangliocytoma 55 0.448
591
PHM001 Phimosis 38 0.448
592
BRN002 Bronchiolitis 57 0.448
593
P PLY019 Polyneuropathy 52 0.448
594
P PTS002 Ptosis 52 0.448
595
P HYP050 Hyperinsulinemic Hypoglycemia 57 0.448
596
ENP001 Enophthalmos 39 0.448
597
CHL068 Cholestasis 61 0.448
598
PNN001 Panniculitis 52 0.448
599
ENT004 Enthesopathy 51 0.448
600
ISL001 Islet Cell Tumor 56 0.448
601
HYP080 Hypogonadism 50 0.448
602
P LMY004 Leiomyosarcoma 62 0.448
603
NRN004 Neuroendocrine Tumor 59 0.448
604
c SVR005 Severe Pre-Eclampsia 50 0.448
605
HYP057 Hypervitaminosis D 37 0.448
606
SPN027 Spinal Stenosis 59 0.448
607
c ALM001 Al Amyloidosis 54 0.448
608
P NRF002 Neurofibromatosis 57 0.448
609
P CLL015 Collagen Disease 48 0.448
610
GLC036 Glucagonoma 46 0.448
611
PTH003 Pathologic Nystagmus 52 0.448
612
NRF007 Neurofibroma 64 0.448
613
HRS011 Horseshoe Kidney 31 0.448
614
HDN002 Head Injury 44 0.448
615
PST053 Postherpetic Neuralgia 40 0.448
616
ATN005 Autonomic Dysfunction 46 0.448
617
PRS063 Paresthesia 39 0.448
618
P HRD086 Hereditary Hypophosphatemic Rickets 40 0.448
619
HYP264 Hypertonia 36 0.448
620
P MYC033 Myoclonus 47 0.448
621
c BRT024 Bartter Syndrome Type 4 25 0.448
622
ALL012 Allergic Angiitis 24 0.448
623
ATM021 Autoimmune Inner Ear Disease 36 0.448
624
EXF003 Exfoliative Dermatitis 22 0.448
625
AMR003 Amaurosis Fugax 33 0.448
626
CGH002 Cough Headache 16 0.448
627
CRC006 Carcinoid Syndrome 55 0.448
628
FST010 Fasting Hypoglycemia 33 0.448
629
SBC016 Subacute Delirium 43 0.448
630
LPS019 Lupus Erythematosus Tumidus 20 0.448
631
ORL013 Oral Lichen Planus 46 0.448
632
PRL021 Perilymphatic Fistula 20 0.448
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