Search results for Aldosterone

844 hits were found for Aldosterone

# Family MCID Name MIFTS Score
1
c HYP731 Hyperaldosteronism, Familial, Type I 60 7.878
2
CRT039 Corticosterone Methyloxidase Type I Deficiency 45 5.461
3
CNN003 Conn's Syndrome 79 5.399
4
ALD013 Aldosterone-Producing Adenoma 39 5.128
5
PRM183 Primary Aldosteronism, Seizures, and Neurologic Abnormalities 26 4.693
6
CRT064 Corticosterone Methyloxidase Deficiency 20 3.759
7
P BRT004 Bartter Disease 52 3.361
8
ADR035 Adrenocortical Carcinoma with Pure Aldosterone Hypersecretion 28 3.301
9
TNG006 Tunglang Savage Bellman Syndrome 13 3.259
10
P FML156 Familial Hyperaldosteronism 39 3.033
11
CRT040 Corticosterone Methyloxidase Type Ii Deficiency 28 2.843
12
c HYP708 Hyperaldosteronism, Familial, Type Iv 30 2.731
13
ECT055 Ectopic Aldosterone-Producing Tumor 11 2.692
14
ANG049 Angioedema Induced by Ace Inhibitors 40 2.649
15
RRN011 Rare Non Surgically Correctable Form of Primary Aldosteronism 3 1.925
16
RRS009 Rare Surgically Correctable Form of Primary Aldosteronism 3 1.925
17
c ERL059 Early-Onset Familial Hypoaldosteronism 12 1.911
18
c LTN026 Late-Onset Familial Hypoaldosteronism 12 1.911
19
c RRP004 Rare Primary Hyperaldosteronism 9 1.911
20
ADN018 Adenoma 59 0.862
21
c HYP595 Hypertension, Essential 84 0.845
22
HYP005 Hypokalemia 55 0.597
23
CNG034 Congestive Heart Failure 69 0.491
24
P KDN018 Kidney Disease 72 0.414
25
ADR008 Adrenal Adenoma 55 0.401
26
P HRT032 Heart Disease 75 0.400
27
c CHR684 Chronic Kidney Disease 70 0.385
28
ADR041 Adrenal Cortical Adenoma 43 0.275
29
c MCR113 Microvascular Complications of Diabetes 3 52 0.269
30
c MCR120 Microvascular Complications of Diabetes 7 47 0.268
31
c MCR130 Microvascular Complications of Diabetes 6 41 0.268
32
c MCR133 Microvascular Complications of Diabetes 4 41 0.268
33
P HYP120 Hypoaldosteronism 36 0.259
34
LVR012 Liver Cirrhosis 62 0.254
35
ADR016 Adrenal Cortical Carcinoma 48 0.231
36
END086 End Stage Renal Disease 51 0.229
37
c PRC016 Pre-Eclampsia 63 0.219
38
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.218
39
ADR004 Adrenal Cortical Adenocarcinoma 39 0.216
40
P RNV001 Renovascular Hypertension 48 0.211
41
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.202
42
P MYC007 Myocardial Infarction 70 0.200
43
P ATR011 Atrial Fibrillation 66 0.199
44
P HYP069 Hyperparathyroidism 63 0.197
45
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.194
46
P PHC003 Pheochromocytoma 71 0.188
47
ADR040 Adrenal Gland Pheochromocytoma 46 0.187
48
P DBT009 Diabetes Mellitus 64 0.185
49
P CRD246 Cardiovascular System Disease 57 0.179
50
P VSC007 Vascular Disease 63 0.178
51
P GLM007 Glomerulonephritis 57 0.178
52
P SLP006 Sleep Apnea 69 0.174
53
c MLG069 Malignant Hypertension 47 0.166
54
P PSD003 Pseudohypoaldosteronism 44 0.166
55
SYS003 Systolic Heart Failure 49 0.160
56
ADR005 Adrenal Carcinoma 58 0.158
57
c ACT075 Acute Myocardial Infarction 57 0.156
58
GYN001 Gynecomastia 49 0.156
59
P RNL015 Renal Hypertension 47 0.156
60
RNL077 Renal Fibrosis 47 0.156
61
INF021 Infant Gynecomastia 31 0.156
62
P NPH012 Nephrotic Syndrome 60 0.154
63
MTB004 Metabolic Acidosis 50 0.152
64
PPL001 Papillary Adenoma 44 0.150
65
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.147
66
CRD132 Cardiac Conduction Defect 58 0.143
67
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.143
68
CVD001 Covid-19 44 0.143
69
c PRM005 Primary Hyperparathyroidism 58 0.140
70
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.138
71
c ATR087 Atrial Standstill 1 75 0.136
72
P HYP086 Hypothyroidism 69 0.133
73
LPD008 Lipid Metabolism Disorder 62 0.133
74
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.133
75
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.133
76
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.133
77
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.133
78
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.133
79
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.133
80
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.133
81
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.133
82
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.133
83
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.133
84
ATH013 Atherosclerosis Susceptibility 65 0.131
85
P HYP076 Hyperthyroidism 55 0.131
86
P DBT005 Diabetes Insipidus 55 0.131
87
P PLY014 Polycystic Kidney Disease 62 0.128
88
APP015 Apparent Mineralocorticoid Excess 58 0.126
89
c SCN007 Secondary Hyperparathyroidism 51 0.126
90
HYP056 Hypoglycemia 66 0.123
91
HYP066 Hyperglycemia 61 0.123
92
HYP266 Hypoxia 57 0.123
93
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.123
94
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.120
95
HYP006 Hypertensive Heart Disease 49 0.120
96
c DLT002 Dilated Cardiomyopathy 79 0.118
97
P LVR013 Liver Disease 68 0.118
98
CRB039 Cerebrovascular Disease 67 0.118
99
LPP008 Lipoprotein Quantitative Trait Locus 62 0.118
100
ISC004 Ischemia 58 0.118
101
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 0.118
102
DST006 Diastolic Heart Failure 45 0.118
103
c HYP438 Hyperaldosteronism, Familial, Type Iii 35 0.118
104
ACR007 Acromegaly 71 0.115
105
c ACT071 Acute Kidney Failure 60 0.115
106
HYP060 Hyperinsulinism 54 0.115
107
GLC003 Glucose Intolerance 54 0.115
108
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.112
109
STR067 Stroke, Ischemic 81 0.112
110
P LDD007 Liddle Syndrome 1 59 0.112
111
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.109
112
P PRD021 Periodic Paralysis 45 0.109
113
IDP033 Idiopathic Edema 44 0.109
114
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.106
115
P CRN300 Coronary Heart Disease 1 63 0.106
116
ART140 Arteries, Anomalies of 52 0.106
117
c HYP600 Hyperaldosteronism, Familial, Type Ii 32 0.106
118
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.103
119
P HYP061 Hypertrophic Cardiomyopathy 70 0.103
120
P MYP004 Myopathy 70 0.103
121
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.103
122
c BNG021 Benign Essential Hypertension 26 0.103
123
P MCR115 Microvascular Complications of Diabetes 5 66 0.099
124
PRT037 Pertussis 65 0.099
125
IMP005 Impotence 52 0.099
126
MSC007 Muscle Hypertrophy 64 0.096
127
c SVR001 Severe Acute Respiratory Syndrome 62 0.096
128
PRT013 Portal Hypertension 59 0.096
129
PRT058 Pure Autonomic Failure 59 0.096
130
NPH010 Nephrosclerosis 50 0.096
131
c FML275 Familial Hypoaldosteronism 19 0.096
132
RCK004 Rickets 68 0.092
133
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.092
134
P KDN017 Kidney Cancer 60 0.092
135
P ART021 Arteriosclerosis 54 0.092
136
P HYP083 Hypopituitarism 53 0.092
137
P ECL001 Eclampsia 50 0.092
138
CYS001 Cystic Fibrosis 81 0.089
139
P CRD119 Cardiac Arrest 67 0.089
140
ANG054 Angina Pectoris 66 0.089
141
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.089
142
P PYL005 Pyelonephritis 56 0.089
143
P MLT074 Multiple Endocrine Neoplasia 56 0.089
144
P ACT105 Acute Mountain Sickness 52 0.089
145
P RNL007 Renal Tubular Acidosis 51 0.089
146
IGG001 Iga Glomerulonephritis 48 0.089
147
P FML187 Familial Hypertension 37 0.089
148
RRC029 Rare Cause of Hypertension 17 0.089
149
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.085
150
AGN016 Aging 56 0.085
151
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.081
152
c FML001 Familial Atrial Fibrillation 65 0.081
153
DPR016 Depression 63 0.081
154
CHL014 Cholera 59 0.081
155
c PSD114 Pseudohypoaldosteronism, Type I, Autosomal Recessive 59 0.081
156
PLM010 Pulmonary Edema 54 0.081
157
47X002 47,xyy 49 0.081
158
URM002 Uremia 49 0.081
159
c PRM093 Premature Ovarian Failure 7 47 0.081
160
ADR051 Adrenal Hyperplasia, Congenital, Due to Steroid 11-Beta-Hydroxylase Deficiency 41 0.081
161
HYP780 Hypoadrenocorticism, Familial 63 0.077
162
ATM095 Autoimmune Disease 62 0.077
163
TXC005 Toxic Shock Syndrome 62 0.077
164
CRD223 Cardiac Arrhythmia 60 0.077
165
ANR040 Aneurysm 59 0.077
166
FML063 Familial Glucocorticoid Deficiency 58 0.077
167
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.077
168
48X005 48,xyyy 39 0.077
169
ADR048 Adrenal Hyperplasia, Congenital, Due to 3-Beta-Hydroxysteroid Dehydrogenase 2 Deficiency 37 0.077
170
ADR057 Adrenogenital Syndrome 32 0.077
171
c HYP836 Hypercholesterolemia, Familial, 1 73 0.073
172
P PLM037 Pulmonary Hypertension 67 0.073
173
P ORT004 Orthostatic Intolerance 62 0.073
174
P MYC008 Myocarditis 59 0.073
175
MNT002 Mental Depression 58 0.073
176
ATN004 Autonomic Neuropathy 45 0.073
177
P OST002 Osteoporosis 74 0.068
178
ANX010 Anxiety 73 0.068
179
P MJR001 Major Depressive Disorder 68 0.068
180
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.068
181
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.068
182
ART002 Arts Syndrome 64 0.068
183
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.068
184
P PLY011 Polycystic Ovary Syndrome 56 0.068
185
NPH003 Nephrocalcinosis 51 0.068
186
PRT029 Parathyroid Adenoma 50 0.068
187
ATS010 Autosomal Recessive Disease 48 0.068
188
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.068
189
c PSD112 Pseudohypoaldosteronism, Type I, Autosomal Dominant 48 0.068
190
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.068
191
PRM020 Premenstrual Tension 40 0.068
192
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.068
193
INS024 Insulin-Like Growth Factor I 79 0.063
194
MSC157 Muscular Dystrophy, Duchenne Type 72 0.063
195
P TTR001 Tetralogy of Fallot 70 0.063
196
P MSC005 Muscular Dystrophy 66 0.063
197
c MCR129 Microvascular Complications of Diabetes 1 66 0.063
198
HYP020 Hyperprolactinemia 64 0.063
199
ANR007 Anorexia Nervosa 63 0.063
200
FTT001 Fatty Liver Disease 61 0.063
201
P NRP001 Neuropathy 56 0.063
202
ADR056 Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete 56 0.063
203
c GRV008 Graves Disease 1 56 0.063
204
BRN004 Brain Edema 56 0.063
205
P DRR001 Diarrhea 55 0.063
206
INT075 Intracranial Hypertension 53 0.063
207
P THY032 Thyroiditis 52 0.063
208
ART074 Aortic Dissection 52 0.063
209
INT067 Interstitial Nephritis 48 0.063
210
ATN005 Autonomic Dysfunction 46 0.063
211
SYN036 Syncope 45 0.063
212
c CHR098 Chronic Pyelonephritis 38 0.063
213
P BRS047 Breast Cancer 97 0.057
214
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.057
215
APN008 Apnea, Obstructive Sleep 64 0.057
216
P HYP750 Hypertriglyceridemia, Familial 62 0.057
217
ALL026 Allergic Hypersensitivity Disease 62 0.057
218
P ENC018 Encephalopathy 61 0.057
219
LNG099 Lung Disease 60 0.057
220
THY029 Thyroid Carcinoma 59 0.057
221
THR024 Thrombosis 57 0.057
222
P FCL005 Focal Segmental Glomerulosclerosis 57 0.057
223
P ACT092 Acth-Independent Macronodular Adrenal Hyperplasia 56 0.057
224
NPH009 Nephrolithiasis 55 0.057
225
GTR002 Goiter 53 0.057
226
QDR001 Quadriplegia 48 0.057
227
BNR002 Bone Resorption Disease 48 0.057
228
FBR032 Fibromuscular Dysplasia 48 0.057
229
ATX019 Ataxia with Vitamin E Deficiency 42 0.057
230
c MCR112 Microvascular Complications of Diabetes 2 41 0.057
231
HYP540 Hypertension, Diastolic 40 0.057
232
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.051
233
P RSP003 Respiratory Failure 74 0.051
234
LPT014 Leptin Deficiency or Dysfunction 74 0.051
235
c MNN043 Meningioma, Familial 74 0.051
236
c SPN225 Spondyloarthropathy 1 73 0.051
237
PRP027 Peripheral Vascular Disease 71 0.051
238
PLM001 Pulmonary Tuberculosis 69 0.051
239
CRB037 Cerebral Palsy 69 0.051
240
ART016 Aortic Aneurysm 69 0.051
241
P MYS003 Myasthenia Gravis 68 0.051
242
P HPT021 Hepatitis 67 0.051
243
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.051
244
PTT046 Pituitary Hormone Deficiency, Combined, 2 64 0.051
245
P PSR002 Psoriasis 62 0.051
246
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.051
247
MNN042 Meningioma, Radiation-Induced 62 0.051
248
NTR005 Nutritional Deficiency Disease 62 0.051
249
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.051
250
P SLP005 Sleep Disorder 59 0.051
251
P MTR012 Mitral Valve Disease 58 0.051
252
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.051
253
P ACT010 Acth-Secreting Pituitary Adenoma 55 0.051
254
P GRV001 Graves' Disease 55 0.051
255
AMN001 Amenorrhea 54 0.051
256
PST011 Pustulosis of Palm and Sole 52 0.051
257
c ART120 Arthrogryposis, Distal, Type 3 51 0.051
258
P MMB011 Membranous Nephropathy 50 0.051
259
SPN021 Spinal Meningioma 50 0.051
260
c SVR005 Severe Pre-Eclampsia 50 0.051
261
P MTR003 Mitral Valve Stenosis 50 0.051
262
P OTS001 Otosclerosis 49 0.051
263
VCC001 Vaccinia 49 0.051
264
c MTR002 Mitral Valve Insufficiency 48 0.051
265
RTN020 Retinal Vascular Disease 46 0.051
266
c BRT042 Bartter Syndrome, Type 3 46 0.051
267
PLY012 Polyhydramnios 46 0.051
268
HDN002 Head Injury 46 0.051
269
ANR004 Anuria 46 0.051
270
MSN001 Mesangial Proliferative Glomerulonephritis 45 0.051
271
P PRL003 Proliferative Glomerulonephritis 44 0.051
272
KWS001 Kwashiorkor 44 0.051
273
ADR052 Adrenal Hyperplasia, Congenital, Due to 17-Alpha-Hydroxylase Deficiency 44 0.051
274
RST023 Resting Heart Rate, Variation in 41 0.051
275
CNT060 Central Serous Chorioretinopathy 38 0.051
276
GLM044 Glomerular Disease 37 0.051
277
c PRM340 Primary Adrenal Insufficiency 36 0.051
278
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.051
279
c SYS001 Systemic Lupus Erythematosus 86 0.044
280
P FML011 Familial Adenomatous Polyposis 72 0.044
281
c EXD008 Exudative Vitreoretinopathy 1 71 0.044
282
c MGR028 Migraine with or Without Aura 1 67 0.044
283
GTL001 Gitelman Syndrome 65 0.044
284
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 0.044
285
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.044
286
c DBT099 Diabetes Mellitus, Type I 65 0.044
287
P MST009 Mastocytosis 64 0.044
288
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.044
289
P ADN016 Adenocarcinoma 64 0.044
290
SKN016 Skin Disease 63 0.044
291
TRN015 Transient Cerebral Ischemia 63 0.044
292
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.044
293
GST033 Gestational Diabetes 61 0.044
294
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.044
295
P OPT006 Optic Nerve Disease 60 0.044
296
P BND020 Bone Disease 59 0.044
297
VSL002 Visual Epilepsy 59 0.044
298
PPT005 Peptic Ulcer Disease 59 0.044
299
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.044
300
P PLY041 Polymyositis 57 0.044
301
P MYS005 Myositis 56 0.044
302
P PLY018 Polycythemia 56 0.044
303
P SZR006 Seizure Disorder 56 0.044
304
GNR004 Generalized Anxiety Disorder 56 0.044
305
INT030 Intracranial Aneurysm 56 0.044
306
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.044
307
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 0.044
308
P CYS039 Cystic Kidney Disease 54 0.044
309
ADR049 Adrenal Hypoplasia, Congenital 54 0.044
310
GLC042 Glucocorticoid Deficiency 1 53 0.044
311
HRT012 Heart Valve Disease 53 0.044
312
P RTN018 Retinal Disease 53 0.044
313
c VRL010 Viral Hepatitis 52 0.044
314
P HYP730 Hypogonadotropic Hypogonadism 52 0.044
315
LMY002 Leiomyoma 52 0.044
316
PNG002 Pain Agnosia 51 0.044
317
c PTT057 Pituitary Adenoma 4, Acth-Secreting 51 0.044
318
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.044
319
HPT014 Hepatorenal Syndrome 50 0.044
320
CRN030 Coronary Stenosis 50 0.044
321
c 46X049 46,xy Sex Reversal 2 48 0.044
322
c ACT150 Acute Adrenal Insufficiency 48 0.044
323
GLC106 Glucocorticoid Resistance, Generalized 48 0.044
324
HYP025 Hyperphosphatemia 48 0.044
325
P CRC039 Coarctation of Aorta 47 0.044
326
PST048 Postural Orthostatic Tachycardia Syndrome 45 0.044
327
URT010 Ureteral Obstruction 45 0.044
328
ADR012 Adrenal Gland Disease 45 0.044
329
SCR001 Secretory Meningioma 41 0.044
330
c PSD092 Pseudohypoaldosteronism, Type Iie 39 0.044
331
CLS040 Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency 38 0.044
332
THR123 Thrombotic Microangiopathy 36 0.044
333
ADR009 Adrenal Cortex Disease 36 0.044
334
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.044
335
c LDD008 Liddle Syndrome 2 23 0.044
336
c LDD009 Liddle Syndrome 3 17 0.044
337
P HPT023 Hepatocellular Carcinoma 100 0.036
339
ULC004 Ulcerative Colitis 73 0.036
340
c THR092 Thrombophilia Due to Thrombin Defect 73 0.036
341
P CNR004 Cone-Rod Dystrophy 2 73 0.036
342
P FML018 Familial Mediterranean Fever 73 0.036
343
P RTN024 Retinoblastoma 73 0.036
344
ADL002 Adult Syndrome 70 0.036
345
P ANG001 Angelman Syndrome 69 0.036
346
P LNG028 Long Qt Syndrome 66 0.036
347
ALC007 Alcohol Dependence 66 0.036
348
P DRM053 Dermatitis, Atopic 66 0.036
349
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.036
350
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.036
351
PRT036 Peritonitis 64 0.036
352
BRC012 Brucellosis 64 0.036
353
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 0.036
354
P ANR048 Aniridia 1 63 0.036
355
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 62 0.036
356
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.036
357
CLT003 Colitis 62 0.036
358
P TRC086 Trichohepatoenteric Syndrome 1 62 0.036
359
CHR066 Chronic Fatigue Syndrome 61 0.036
360
P LPS004 Lupus Erythematosus 61 0.036
361
NRL005 Neurilemmoma 60 0.036
362
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.036
363
ACN002 Acanthosis Nigricans 60 0.036
364
P SNS001 Sensorineural Hearing Loss 60 0.036
365
VRC005 Varicose Veins 60 0.036
366
HYD002 Hydronephrosis 60 0.036
367
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.036
368
GST045 Gastroenteritis 59 0.036
369
INC002 Inclusion Body Myositis 58 0.036
370
DSS008 Disease of Mental Health 58 0.036
371
CNS004 Constipation 58 0.036
372
BRG013 Buerger Disease 58 0.036
373
P PRP019 Peripheral Nervous System Disease 58 0.036
374
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.036
375
BLR008 Bilirubin Metabolic Disorder 57 0.036
376
INT303 Intracranial Hypertension, Idiopathic 57 0.036
377
P ANG015 Angioedema 57 0.036
378
PNM008 Pneumothorax 56 0.036
379
ALL006 Allergic Asthma 56 0.036
380
c ACT134 Acute Liver Failure 56 0.036
381
P NRF002 Neurofibromatosis 56 0.036
382
P HYP024 Hypoparathyroidism 56 0.036
383
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.036
384
MCL006 Macular Retinal Edema 55 0.036
385
HMP005 Hemiplegia 55 0.036
386
INT007 Intermediate Coronary Syndrome 55 0.036
387
P ALP008 Alopecia 54 0.036
388
DBT010 Diabetic Neuropathy 54 0.036
389
PRC002 Paracoccidioidomycosis 54 0.036
390
GST023 Gastric Ulcer 53 0.036
391
P RTN022 Retinal Vein Occlusion 53 0.036
392
c FML008 Familial Retinoblastoma 53 0.036
393
P PRG013 Paraganglioma 52 0.036
394
CRT016 Carotid Artery Disease 52 0.036
395
THY030 Thyroid Gland Disease 52 0.036
396
HYP014 Hyperuricemia 52 0.036
397
SPN051 Spondylitis 51 0.036
398
OCL069 Ocular Motor Apraxia 51 0.036
399
ESP002 Esophageal Varix 51 0.036
400
DRR008 Diarrhea 1, Secretory Chloride, Congenital 51 0.036
401
HYP781 Hypoascorbemia 51 0.036
402
HYP081 Hypolipoproteinemia 51 0.036
403
c HNT004 Huntington Disease-Like 2 50 0.036
404
RTN003 Retinal Ischemia 50 0.036
405
PLC008 Placenta Disease 50 0.036
406
HRT011 Heart Septal Defect 50 0.036
407
HYP080 Hypogonadism 50 0.036
408
P IGN003 Iga Nephropathy 1 49 0.036
409
P ART018 Aortic Valve Insufficiency 49 0.036
410
P ALP061 Alopecia, Androgenetic, 1 49 0.036
411
HYP043 Hyperandrogenism 48 0.036
412
PYL006 Pyloric Stenosis 48 0.036
413
PLC007 Placental Abruption 48 0.036
414
SXL003 Sexual Disorder 47 0.036
415
PRD004 Prediabetes Syndrome 47 0.036
416
KHN001 Kuhnt-Junius Degeneration 47 0.036
417
NDL013 Nodular Regenerative Hyperplasia 47 0.036
418
CHR074 Choriocarcinoma 47 0.036
419
HYP034 Hypertensive Encephalopathy 46 0.036
420
LPD004 Lipoid Nephrosis 46 0.036
421
GNR003 Generalized Atherosclerosis 46 0.036
422
PSD009 Pseudohermaphroditism 46 0.036
423
AND014 Androgenic Alopecia 46 0.036
424
CRN019 Coronary Artery Vasospasm 46 0.036
425
TRT001 Teratocarcinoma 45 0.036
426
URL001 Urolithiasis 45 0.036
427
GLC036 Glucagonoma 45 0.036
428
MYF001 Myofibroma 45 0.036
429
P RRC004 Rare Cardiomyopathy 44 0.036
430
c FML036 Familial Periodic Paralysis 44 0.036
431
c PRM038 Primary Agammaglobulinemia 44 0.036
432
MYX004 Myxedema 43 0.036
433
P MLT008 Multinodular Goiter 42 0.036
434
CYT002 Cytokine Deficiency 42 0.036
436
MRS001 Marasmus 42 0.036
437
P DST107 Distal Renal Tubular Acidosis 42 0.036
438
GLC008 Glucose Metabolism Disease 40 0.036
439
c LNG057 Long Qt Syndrome 13 40 0.036
440
HYP008 Hypertensive Retinopathy 39 0.036
441
P CRN074 Coronary Artery Aneurysm 39 0.036
442
P DYS021 Dysautonomia 39 0.036
443
c CHR682 Chronic Bilirubin Encephalopathy 39 0.036
444
HYP264 Hypertonia 38 0.036
445
c HNT011 Huntington Disease-Like 3 38 0.036
446
c ACT202 Acth-Independent Macronodular Adrenal Hyperplasia 2 36 0.036
447
c SCN052 Secondary Adrenal Insufficiency 36 0.036
448
HYP114 Hypertensive Nephropathy 36 0.036
449
BRK012 Broken Heart Syndrome 35 0.036
450
GLC105 Glucocorticoid Deficiency 4 with or Without Mineralocorticoid Deficiency 35 0.036
451
ATX010 Ataxia Neuropathy Spectrum 34 0.036
453
ACT064 Acute Necrotizing Encephalitis 33 0.036
454
KDN013 Kidney Hypertrophy 32 0.036
455
c PSD090 Pseudohypoaldosteronism, Type Iia 32 0.036
456
INF009 Inflammatory Spondylopathy 31 0.036
457
SNG003 Single Ventricular Heart 30 0.036
458
MTY003 Mutyh Polyposis 30 0.036
459
GLC043 Glucocorticoid Deficiency 2 27 0.036
460
c TRN053 Transient Pseudohypoaldosteronism 25 0.036
461
c BRT049 Bartter Syndrome, Type 5, Antenatal, Transient 22 0.036
462
HYP705 Hyperadrenalism 20 0.036
463
c FML159 Familial Periodic Paralyses 16 0.036
464
BLD137 Blood Group--Ahonen 16 0.036
465
INH021 Inherited Isolated Adrenal Insufficiency Due to Partial Cyp11a1 Deficiency 15 0.036
466
PRM146 Primary Unilateral Adrenal Hyperplasia 13 0.036
467
MSN011 Mesangioproliferative Glomerulopathy 12 0.036
468
P CLR023 Colorectal Cancer 99 0.026
469
P PRS040 Prostate Cancer 97 0.026
470
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.026
471
P ALZ034 Alzheimer Disease 88 0.026
472
P GST053 Gastric Cancer 83 0.026
473
P ATX030 Ataxia-Telangiectasia 82 0.026
474
c FNC027 Fanconi Anemia, Complementation Group a 81 0.026
475
P RHM011 Rheumatoid Arthritis 80 0.026
476
c NRF023 Neurofibromatosis, Type Ii 80 0.026
477
P PRK057 Parkinson Disease, Late-Onset 78 0.026
478
MRF001 Marfan Syndrome 77 0.026
479
c NRF024 Neurofibromatosis, Type I 77 0.026
480
CRV035 Cervical Cancer 76 0.026
481
ADR007 Adrenoleukodystrophy 75 0.026
482
c BTT014 Beta-Thalassemia 74 0.026
483
CRH001 Crohn's Disease 74 0.026
484
P MLT020 Multiple Sclerosis 72 0.026
485
P LFR001 Li-Fraumeni Syndrome 72 0.026
486
c LKM063 Leukemia, Chronic Myeloid 72 0.026
487
HMN044 Human Immunodeficiency Virus Type 1 71 0.026
488
CNT097 Central Hypoventilation Syndrome, Congenital 71 0.026
489
P BRG001 Brugada Syndrome 71 0.026
490
P EPL164 Epilepsy 71 0.026
491
P SRC025 Sarcoidosis 1 70 0.026
492
P ATS364 Autism 70 0.026
493
P AMY004 Amyloidosis 70 0.026
494
DWN001 Down Syndrome 70 0.026
495
c MLT160 Multiple Endocrine Neoplasia, Type Iia 70 0.026
496
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.026
497
P PNM007 Pneumonia 68 0.026
498
P SYS005 Systemic Scleroderma 68 0.026
499
CHL065 Cholangiocarcinoma 68 0.026
500
P LKM002 Leukemia 68 0.026
501
OBS002 Obsessive-Compulsive Disorder 68 0.026
502
P INF038 Influenza 68 0.026
503
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 68 0.026
504
CNN005 Connective Tissue Disease 68 0.026
505
P ALP004 Alport Syndrome 68 0.026
506
P HLP001 Holoprosencephaly 67 0.026
507
ALL003 Allergic Rhinitis 67 0.026
508
P TRN020 Turner Syndrome 67 0.026
509
c NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 67 0.026
510
c ATS007 Autism Spectrum Disorder 67 0.026
511
CRP001 Carpal Tunnel Syndrome 67 0.026
512
c RHB024 Rhabdomyosarcoma 2 67 0.026
513
P CLC063 Celiac Disease 1 66 0.026
514
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.026
515
P DMN002 Dementia 66 0.026
516
ART001 Arterial Tortuosity Syndrome 66 0.026
517
c FML346 Familial Adenomatous Polyposis 1 66 0.026
518
AND002 Androgen Insensitivity Syndrome 66 0.026
519
c LNG044 Long Qt Syndrome 1 66 0.026
520
CHG001 Chagas Disease 66 0.026
521
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.026
522
P AGM001 Agammaglobulinemia 65 0.026
523
PPL049 Papillon-Lefevre Syndrome 65 0.026
524
BRR014 Barrett Esophagus 65 0.026
525
c ART101 Aortic Valve Disease 2 65 0.026
526
P HRP006 Herpes Simplex 65 0.026
527
P PRS038 Personality Disorder 65 0.026
528
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.026
529
P THY023 Thymoma 65 0.026
530
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.026
531
NRM005 Neuromuscular Disease 64 0.026
532
NRF007 Neurofibroma 64 0.026
533
OVR029 Ovarian Hyperstimulation Syndrome 64 0.026
534
P FRD001 Friedreich Ataxia 64 0.026
535
PRP083 Porphyria, Acute Intermittent 64 0.026
536
RBR001 Roberts Syndrome 64 0.026
537
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.026
538
c MLG084 Malignant Fibrous Histiocytoma 63 0.026
539
P SHR029 Short Syndrome 63 0.026
540
P PTT014 Pitt-Hopkins Syndrome 63 0.026
541
c ACT068 Acute Cystitis 63 0.026
542
P LMY004 Leiomyosarcoma 63 0.026
543
P END044 Endometriosis 63 0.026
544
c OPT053 Optic Atrophy 1 63 0.026
545
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.026
546
c FNC043 Fanconi Anemia, Complementation Group E 62 0.026
547
c HPT001 Hepatitis C 62 0.026
548
c HPT003 Hepatitis a 62 0.026
549
c BRN108 Branchiootic Syndrome 1 62 0.026
550
DNH001 Donohue Syndrome 62 0.026
551
HYD038 Hydrops Fetalis, Nonimmune 62 0.026
552
P VSC011 Vasculitis 62 0.026
553
P ACR001 Aicardi-Goutieres Syndrome 62 0.026
554
HSH003 Hashimoto Thyroiditis 62 0.026
555
P PRP029 Porphyria 62 0.026
556
CHL068 Cholestasis 61 0.026
557
DRM006 Dermatitis 61 0.026
558
c PNS012 Paine Syndrome 61 0.026
559
c WLM018 Wilms Tumor 5 61 0.026
560
HYP052 Hyperkalemic Periodic Paralysis 61 0.026
561
P HMN010 Hemangioma 61 0.026
562
P MYL006 Myeloid Leukemia 60 0.026
563
RGH009 Right Atrial Isomerism 60 0.026
564
FND001 Fundus Albipunctatus 60 0.026
565
TRG002 Trigeminal Neuralgia 60 0.026
566
P VNT002 Ventricular Septal Defect 60 0.026
567
c ACT027 Acute Pancreatitis 60 0.026
568
HPT019 Hepatic Encephalopathy 60 0.026
569
ACQ007 Acquired Immunodeficiency Syndrome 60 0.026
570
P ATR010 Atrial Heart Septal Defect 60 0.026
571
P CTR002 Cataract 60 0.026
572
P GLY013 Glycogen Storage Disease 60 0.026
573
P THL005 Thalassemia 60 0.026
574
c HRD002 Hereditary Angioedema 60 0.026
575
P AXN002 Axenfeld-Rieger Syndrome 59 0.026
576
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.026
577
PNM001 Pneumocystosis 59 0.026
578
c HPT016 Hepatitis B 59 0.026
579
P LKD001 Leukodystrophy 59 0.026
580
IGR001 Ige Responsiveness, Atopic 59 0.026
581
PLM033 Pulmonary Embolism 59 0.026
582
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.026
583
CYS010 Cystinosis 59 0.026
584
P NPH005 Nephronophthisis 59 0.026
585
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.026
586
PST028 Post-Traumatic Stress Disorder 58 0.026
587
P BCL017 B-Cell Lymphoma 58 0.026
588
FBR047 Fibromyalgia 58 0.026
589
DST005 Diastrophic Dysplasia 58 0.026
590
P ALC033 Alcohol Use Disorder 58 0.026
591
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.026
592
P URT039 Urticaria 58 0.026
593
NWB001 Newborn Respiratory Distress Syndrome 58 0.026
594
c DWL002 Dowling-Degos Disease 1 58 0.026
595
P UVT001 Uveitis 57 0.026
596
IRN002 Iron Metabolism Disease 57 0.026
597
P EXN002 Exanthem 57 0.026
598
P RHN004 Rhinitis 57 0.026
599
P HDC001 Headache 57 0.026
600
DSS009 Disseminated Intravascular Coagulation 57 0.026
601
APH002 Aphasia 57 0.026
602
P FTL001 Fetal Alcohol Syndrome 57 0.026
603
PNL019 Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities 57 0.026
604
SCH014 Schistosomiasis 57 0.026
605
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.026
606
LMY014 Leiomyoma, Uterine 56 0.026
607
P PNL012 Penile Cancer 56 0.026
608
P PSD015 Pseudohypoparathyroidism 56 0.026
609
ATR057 Atrioventricular Block 55 0.026
610
MCN007 Meconium Aspiration Syndrome 55 0.026
611
NRN004 Neuroendocrine Tumor 55 0.026
612
LMB062 Limb Ischemia 55 0.026
613
c BCT007 Bacterial Meningitis 55 0.026
614
P ANT006 Antiphospholipid Syndrome 55 0.026
615
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.026
616
CRC006 Carcinoid Syndrome 55 0.026
617
EPT010 Epithelial-Myoepithelial Carcinoma 55 0.026
618
P ALP106 Alport Syndrome 1, X-Linked 55 0.026
619
MYP159 Myopathy, Proximal, with Ophthalmoplegia 55 0.026
620
END040 Endogenous Depression 55 0.026
621
P SLM003 Salmonellosis 55 0.026
622
PRP030 Purpura 54 0.026
623
P PMP001 Pemphigus 54 0.026
624
P EPS030 Episodic Kinesigenic Dyskinesia 1 54 0.026
625
PRT038 Protein-Energy Malnutrition 54 0.026
626
THR013 Thoracic Outlet Syndrome 54 0.026
627
P LTR001 Lateral Sclerosis 54 0.026
628
HLL004 Hellp Syndrome 54 0.026
629
PPL022 Papilloma 54 0.026
630
MYM001 Myoma 54 0.026
631
PTT009 Pituitary Gland Disease 54 0.026
632
NNL006 Non-Alcoholic Steatohepatitis 54 0.026
633
CLR030 Clear Cell Renal Cell Carcinoma 53 0.026
634
HYP741 Hyperparathyroidism 2 with Jaw Tumors 53 0.026
635
RHM028 Rheumatic Heart Disease 53 0.026
636
OST016 Osteochondrosis 53 0.026
637
BRN038 Bronchial Disease 53 0.026
638
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.026
639
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 53 0.026
640
P SHR001 Short Bowel Syndrome 53 0.026
641
P ALT001 Alternating Hemiplegia of Childhood 53 0.026
642
P PNC025 Panic Disorder 53 0.026
643
PRP080 Peripheral Artery Disease 53 0.026
644
c GLL024 Gallbladder Disease 1 53 0.026
645
c FML191 Familial Long Qt Syndrome 53 0.026
646
VTM028 Vitamin E, Familial Isolated Deficiency of 52 0.026
647
ACR041 Acromelic Frontonasal Dysostosis 52 0.026
648
c ACR116 Aicardi-Goutieres Syndrome 1 52 0.026
649
c THY107 Thymoma, Familial 52 0.026
650
SPS003 Spastic Diplegia 51 0.026
651
VSC044 Visceral Myopathy 51 0.026
652
ILS001 Ileus 51 0.026
653
P LCT001 Lactic Acidosis 51 0.026
654
INT079 Intrahepatic Cholangiocarcinoma 51 0.026
655
P HYP040 Hypospadias 51 0.026
656
BHR001 Behr Syndrome 51 0.026
657
SZR026 Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance 51 0.026
658
P OVR082 Overgrowth Syndrome 50 0.026
659
CRT013 Carotid Stenosis 50 0.026
660
P SCK005 Sickle Cell Disease 50 0.026
661
c INF145 Infantile Liver Failure Syndrome 1 50 0.026
662
BLS002 Blastomycosis 50 0.026
663
RNL011 Renal Osteodystrophy 50 0.026
664
ISL003 Isolated Growth Hormone Deficiency 49 0.026
665
RBF001 Riboflavin Deficiency 49 0.026
666
ONC007 Oncocytoma 49 0.026
667
INP001 Inappropriate Adh Syndrome 49 0.026
668
PPL021 Papilledema 49 0.026
669
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.026
670
ART017 Aortic Disease 49 0.026
671
CHL004 Cholelithiasis 49 0.026
672
DYS009 Dysthymic Disorder 49 0.026
673
MNN009 Meningoencephalitis 49 0.026
674
WTH001 Withdrawal Disorder 48 0.026
675
CLC006 Calcinosis 48 0.026
676
DBT006 Diabetic Macular Edema 48 0.026
677
HLX001 Helix Syndrome 47 0.026
678
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 47 0.026
679
P BLR006 Biliary Tract Disease 47 0.026
680
ACT084 Acute Stress Disorder 47 0.026
681
c INH020 Inherited Metabolic Disorder 47 0.026
682
CRD137 Cardiogenic Shock 47 0.026
683
NSS002 Neisseria Meningitidis Infection 47 0.026
684
RYN005 Raynaud Phenomenon 47 0.026
685
P PRC019 Precocious Puberty 46 0.026
686
c ACT076 Acute Myocarditis 46 0.026
687
P THY054 Thyrotoxic Periodic Paralysis 46 0.026
688
P BRT053 Bartter Syndrome, Type 4a, Neonatal, with Sensorineural Deafness 46 0.026
689
MNN020 Meningococcal Infection 46 0.026
690
FCL012 Facial Paralysis 46 0.026
691
c ACQ010 Acquired Polycythemia 46 0.026
692
GRW007 Growth Hormone Deficiency 46 0.026
693
c BRT050 Bartter Syndrome, Type 2, Antenatal 46 0.026
694
SQM002 Squamous Cell Papilloma 46 0.026
695
LKS001 Leukostasis 46 0.026
696
P HYP733 Hypercalciuria, Absorptive, 2 45 0.026
697
TTR005 Tetrahydrobiopterin Deficiency 45 0.026
698
c TRC022 Tricuspid Valve Insufficiency 45 0.026
699
c LFR007 Li-Fraumeni Syndrome 2 45 0.026
700
ATY001 Atypical Depressive Disorder 45 0.026
701
CYN002 Cyanosis, Transient Neonatal 45 0.026
702
HPT004 Hepatic Coma 45 0.026
703
c CRN278 Craniosynostosis 1 45 0.026
704
TRC012 Trichuriasis 45 0.026
705
TWN001 Twin-to-Twin Transfusion Syndrome 45 0.026
706
MLK003 Melkersson-Rosenthal Syndrome 45 0.026
707
ACT003 Acute Kidney Tubular Necrosis 45 0.026
708
P END084 Endocrine System Disease 45 0.026
709
PLS029 Plasminogen Activator Inhibitor-1 Deficiency 45 0.026
710
END035 Endocrine Gland Cancer 45 0.026
711
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.026
712
P CHR345 Chronic Pain 44 0.026
713
HNT019 Hantavirus Hemorrhagic Fever with Renal Syndrome 44 0.026
714
P PRS062 Persistent Hyperplastic Primary Vitreous 44 0.026
715
SBC016 Subacute Delirium 44 0.026
716
DBT008 Diabetic Angiopathy 44 0.026
717
c PCH010 Pachyonychia Congenita 3 44 0.026
718
DWR001 Dwarfism 44 0.026
719
CRB008 Cerebral Atherosclerosis 44 0.026
720
OVR063 Overnutrition 44 0.026
721
HPT082 Hepatic Adenomas, Familial 44 0.026
722
CNG029 Congenital Mesoblastic Nephroma 44 0.026
723
c BRT052 Bartter Syndrome, Type 1, Antenatal 43 0.026
724
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.026
725
MRG013 Mirage Syndrome 43 0.026
726
P PRP034 Purpura Fulminans 43 0.026
727
ALC010 Alcoholic Cardiomyopathy 42 0.026
728
RNL025 Renal Hypoplasia 42 0.026
729
DRG024 Drug Allergy 42 0.026
730
BP1002 Bap1 Tumor Predisposition Syndrome 42 0.026
731
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.026
732
OBS082 Obstructive Nephropathy 42 0.026
733
BNB002 Bainbridge-Ropers Syndrome 42 0.026
734
IDP091 Idiopathic Nephrotic Syndrome 42 0.026
735
49X006 49, Xxxxy Syndrome 41 0.026
736
PRS063 Paresthesia 41 0.026
737
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 41 0.026
738
P RRT020 Rare Tumor 41 0.026
739
CRN322 Coronavirus Infectious Disease 40 0.026
740
MDL009 Medullary Sponge Kidney 40 0.026
741
ADJ001 Adjustment Disorder 40 0.026
742
ART008 Arteriosclerosis Obliterans 40 0.026
743
CRB086 Cerebral Aneurysms 40 0.026
744
c TRN038 Transposition of the Great Arteries, Dextro-Looped 1 39 0.026
745
CRN006 Coronary Aneurysm 39 0.026
746
c PRG020 Paragangliomas 3 39 0.026
747
c JVN041 Juvenile Nephronophthisis 39 0.026
748
HYP344 Hyperthyroidism, Familial Gestational 39 0.026
749
c PLM022 Pulmonary Valve Insufficiency 39 0.026
750
DBT020 Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans 39 0.026
751
ADP007 Adie Pupil 39 0.026
752
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.026
753
ALX002 Alexithymia 38 0.026
754
ALL014 Allergic Encephalomyelitis 38 0.026
755
ADR022 Adrenomyeloneuropathy 38 0.026
756
CHL073 Cholestasis-Lymphedema Syndrome 38 0.026
757
SCR039 Scorpion Envenomation 38 0.026
758
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.026
759
CRB009 Cerebritis 37 0.026
760
CRD016 Cardiac Rupture 37 0.026
761
NPH113 Nephroma 37 0.026
762
MLN070 Melanoma-Astrocytoma Syndrome 37 0.026
763
RHM014 Rheumatoid Vasculitis 37 0.026
764
SYS071 Systemic Autoimmune Disease 37 0.026
765
ART010 Arteriolosclerosis 37 0.026
766
NPH013 Nephrogenic Syndrome of Inappropriate Antidiuresis 36 0.026
767
HYP070 Hyperpituitarism 36 0.026
768
c BRT056 Bartter Syndrome, Type 4b, Neonatal, with Sensorineural Deafness 36 0.026
769
LCH001 Leech Infestation 35 0.026
770
c ATM022 Autoimmune Myocarditis 35 0.026
771
CHR178 Chromosomal Triplication 35 0.026
772
KRN001 Korean Hemorrhagic Fever 35 0.026
773
END072 Endotheliitis 35 0.026
774
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.026
775
CHR034 Chromophobe Adenoma 34 0.026
776
c RNL113 Renal Failure, Progressive, with Hypertension 34 0.026
777
c PRG106 Progressive Muscular Dystrophy 33 0.026
778
ALR002 Al-Raqad Syndrome 33 0.026
779
ART110 Arteritic Anterior Ischemic Optic Neuropathy 33 0.026
780
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.026
781
PRN007 Perinephritis 33 0.026
782
NNT010 Nontoxic Goiter 32 0.026
783
c BLD140 Blood Group, I System 32 0.026
784
TRG019 Trigonocephaly with Short Stature and Developmental Delay 32 0.026
785
LYM043 Lymphocytic Hypophysitis 32 0.026
786
NRN002 Neuronitis 32 0.026
787
PST014 Postsurgical Hypothyroidism 32 0.026
788
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.026
789
P ALB003 Albinism-Deafness Syndrome 31 0.026
790
FTL004 Fetal Erythroblastosis 31 0.026
791
PLY150 Polykaryocytosis Inducer 31 0.026
792
STR018 Steroid Inherited Metabolic Disorder 31 0.026
793
ANR010 Aneurysm of Sinus of Valsalva 30 0.026
794
ADR001 Adrenal Rest Tumor 30 0.026
795
RTR007 Retroperitoneal Leiomyosarcoma 30 0.026
796
FNT004 Fainting 30 0.026
797
PLM013 Pulmonary Immaturity 30 0.026
798
CLF051 Cleft Larynx, Posterior 30 0.026
799
MLG163 Malignant Tumor of Penis 29 0.026
800
MYC088 Mycobacterium Avium Complex Infections 29 0.026
801
P SKL032 Skeletal Muscle Disease 29 0.026
802
PST092 Posttransplant Acute Limbic Encephalitis 29 0.026
803
TMR016 Tumor Suppressor Gene on Chromosome 11 28 0.026
804
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.026
805
SCN001 Secondary Hyperparathyroidism of Renal Origin 27 0.026
806
HNM002 Hinman Syndrome 27 0.026
807
MYL080 Myalgic Encephalomyelitis/chronic Fatigue Syndrome 27 0.026
808
LRY026 Laryngeal Cleft 27 0.026
809
c HRD219 Hereditary Distal Renal Tubular Acidosis 27 0.026
810
DFF015 Diffuse Glomerulonephritis 26 0.026
811
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 26 0.026
812
c PSD094 Pseudohypoaldosteronism, Type Iib 26 0.026
813
PLM189 Pulmonary Arterial Hypertension Associated with Connective Tissue Disease 26 0.026
814
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.026
815
LSN001 Lesion of Sciatic Nerve 25 0.026
816
PLM061 Pulmonary Edema of Mountaineers 25 0.026
817
CLR014 Clear Cell Adenoma 24 0.026
818
OGL001 Ogilvie Syndrome 24 0.026
819
BLD163 Blood Group, Dombrock System 24 0.026
820
APN006 Apnea of Prematurity 24 0.026
821
ATR024 Atrial Fibrillation and Stroke 22 0.026
822
CHF001 Chief Cell Adenoma 22 0.026
823
CRB087 Cerebral Arteriosclerosis 22 0.026
824
PSM001 Psammomatous Meningioma 21 0.026
825
GLC053 Glucocorticoid Deficiency 3 21 0.026
826
BLD165 Blood Group, Colton System 20 0.026
827
c BRT024 Bartter Syndrome Type 4 20 0.026
828
AND005 Androgen Insensitivity Syndrome, Mild 19 0.026
829
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 19 0.026
830
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.026
831
LGR001 Laugier-Hunziker Syndrome 18 0.026
832
PHS019 Phosphohydroxylysinuria 18 0.026
833
CNG491 Congenital Portosystemic Shunt 17 0.026
834
PNT023 Pontine Hemorrhage 17 0.026
835
GLC107 Glucocorticoid Deficiency 5 17 0.026
836
c RNL034 Renal Cell Carcinoma 4 16 0.026
837
HYP786 Hypokalemic Alkalosis, Familial, with Specific Renal Tubulopathy 16 0.026
838
CHR263 Chromosome 7q Duplication 15 0.026
840
PLM188 Pulmonary Arterial Hypertension Associated with Another Disease 13 0.026
841
TDD001 Todd's Paralysis 12 0.026
842
ADR055 Adrenocortical Unresponsiveness to Acth with Postreceptor Defect 10 0.026
843
HYP694 Hyperreninemic Hypoaldosteronism, Familial, 2 6 0.026
844
GNT152 Genetic Hyperaldosteronism 4 0.026
Content
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