Search results for Desmopressin

747 hits were found for Desmopressin

# Family MCID Name MIFTS Score
1
P DBT005 Diabetes Insipidus 54 11.768
2
P VNW001 Von Willebrand's Disease 64 11.343
3
P HMP007 Hemophilia 52 6.544
4
c HMP029 Hemophilia a 69 5.887
5
FCT001 Factor Viii Deficiency 61 5.803
6
P BLD124 Bleeding Disorder, Platelet-Type, 11 68 3.710
7
BLD053 Blood Platelet Disease 51 3.608
8
c ACQ017 Acquired Von Willebrand Syndrome 48 3.471
9
URM002 Uremia 47 3.447
10
LWC001 Low Compliance Bladder 44 3.385
11
DBT087 Diabetes Insipidus, Neurohypophyseal 58 3.203
12
CNN003 Conn's Syndrome 77 2.960
13
ADL002 Adult Syndrome 69 2.830
14
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 2.682
15
P SCL018 Scoliosis 57 2.600
16
P THR014 Thrombocytopenia 66 2.560
17
LVR012 Liver Cirrhosis 62 2.511
18
OCL069 Ocular Motor Apraxia 57 2.467
19
PRS045 Prostatic Hypertrophy 53 2.419
20
P PTT006 Pituitary Adenoma 55 2.411
21
PRS129 Prostatic Hyperplasia, Benign 48 2.393
22
PRS021 Prostatic Adenoma 43 2.393
23
SCK003 Sickle Cell Anemia 74 2.342
24
ADN018 Adenoma 58 2.281
25
DFC004 Deficiency Anemia 74 2.280
26
c ART101 Aortic Valve Disease 2 65 2.222
27
LPT001 Leptospirosis 65 2.205
28
THR024 Thrombosis 56 2.189
29
P SLP006 Sleep Apnea 69 2.138
30
STR067 Stroke, Ischemic 79 2.068
31
P SZR006 Seizure Disorder 69 2.014
32
ACT058 Active Peptic Ulcer Disease 55 1.982
33
CNS004 Constipation 56 1.965
34
P DBT009 Diabetes Mellitus 67 1.949
35
P HYP086 Hypothyroidism 68 1.948
36
AGN016 Aging 53 1.928
37
P PRS040 Prostate Cancer 95 1.876
38
TRM010 Traumatic Brain Injury 50 1.829
39
IDP070 Idiopathic Scoliosis 41 1.814
40
FCT002 Factor Xi Deficiency 61 1.807
41
P SCK005 Sickle Cell Disease 56 1.774
42
URL001 Urolithiasis 45 1.767
43
P FNG006 Feingold Syndrome 1 61 1.760
44
P ATT013 Attention Deficit-Hyperactivity Disorder 65 1.749
45
P RHN004 Rhinitis 56 1.749
46
c VNW005 Von Willebrand Disease, Type 1 46 1.703
47
P HMR003 Hemorrhagic Disease 59 1.680
48
P CLR023 Colorectal Cancer 100 1.664
49
BLD051 Blood Coagulation Disease 52 1.621
50
47X002 47,xyy 47 1.609
51
SPR126 Superior Semicircular Canal Dehiscence 41 1.590
52
c HMG029 Hemoglobin Se Disease 41 1.590
53
P URN019 Urinary Tract Infection 48 1.570
54
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.553
55
ACQ007 Acquired Immunodeficiency Syndrome 58 1.534
56
BRN071 Brain Injury 50 1.516
57
INF118 Inflammatory Myopathy with Abundant Macrophages 27 1.503
58
c THR092 Thrombophilia Due to Thrombin Defect 74 1.408
59
THR035 Thrombasthenia 48 1.408
60
P HYP083 Hypopituitarism 51 1.407
61
DSS025 Dissociative Seizures 26 1.370
62
HST010 Histiocytosis 49 1.362
63
APN008 Apnea, Obstructive Sleep 66 1.362
64
PRS047 Prostatitis 57 1.345
65
CRB039 Cerebrovascular Disease 65 1.345
66
P NNT058 Neonatal Diabetes 52 1.338
67
PTT037 Pituitary Tumors 44 1.334
68
P HYD006 Hydrocephalus 62 1.331
69
PRP030 Purpura 54 1.316
70
P PLY014 Polycystic Kidney Disease 71 1.301
71
48X005 48,xyyy 39 1.269
72
P EHL001 Ehlers-Danlos Syndrome 57 1.252
73
GRM004 Germinoma 40 1.248
74
P ENC018 Encephalopathy 62 1.215
75
CLF001 Cleft Lip 54 1.194
76
CLF004 Cleft Lip/palate 56 1.194
77
TXC005 Toxic Shock Syndrome 61 1.187
78
c ACQ014 Acquired Hemophilia 45 1.187
79
P MLT020 Multiple Sclerosis 79 1.173
80
NPH009 Nephrolithiasis 54 1.173
81
SPN186 Spinal Cord Injury 60 1.173
82
PTT046 Pituitary Hormone Deficiency, Combined, 2 62 1.166
83
PTT003 Pituitary-Dependent Cushing's Disease 39 1.159
84
P NJM001 Nijmegen Breakage Syndrome 75 1.125
85
c PNS012 Paine Syndrome 60 1.125
86
P BRS047 Breast Cancer 97 1.125
87
c PRS130 Prostate Cancer, Hereditary, 8 32 1.125
88
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 1.125
89
c EPS039 Episodic Pain Syndrome, Familial, 1 42 1.125
90
c PRS136 Prostate Cancer, Hereditary, 6 33 1.125
91
P TRN020 Turner Syndrome 67 1.125
92
CHL079 Children's Interstitial Lung Disease 25 1.125
93
CNT025 Central Pontine Myelinolysis 42 1.114
94
P HRD221 Hereditary Nephrogenic Diabetes Insipidus 18 1.098
95
P HYP076 Hyperthyroidism 53 1.098
96
P RSP003 Respiratory Failure 73 1.081
97
P THR005 Thrombotic Thrombocytopenic Purpura 64 1.081
98
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 1.081
99
P CYS018 Cystitis 58 1.062
100
P THY032 Thyroiditis 56 1.062
101
NRG002 Neurogenic Bladder 54 1.048
102
P AMY004 Amyloidosis 69 1.043
103
c ACT068 Acute Cystitis 60 1.036
104
LNG108 Langerhans Cell Histiocytosis 57 1.025
105
c VNW010 Von Willebrand Disease, Type 2 50 1.001
106
P ATR010 Atrial Heart Septal Defect 58 1.000
107
HRT011 Heart Septal Defect 49 1.000
108
P HRM001 Hermansky-Pudlak Syndrome 65 0.989
109
HDN002 Head Injury 44 0.989
110
c HMP004 Hemophilia B 68 0.976
111
GRY002 Gray Platelet Syndrome 57 0.975
112
PLM033 Pulmonary Embolism 58 0.975
113
ALL003 Allergic Rhinitis 66 0.963
114
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.950
115
P CRD119 Cardiac Arrest 68 0.936
116
AMN001 Amenorrhea 53 0.936
117
PHR003 Pharyngitis 57 0.921
118
c ACT071 Acute Kidney Failure 60 0.921
119
END086 End Stage Renal Disease 54 0.921
120
PTT041 Pituitary Stalk Interruption Syndrome 54 0.921
121
c RRH015 Rare Hemorrhagic Disorder 22 0.921
122
P HDC001 Headache 56 0.921
123
PRT058 Pure Autonomic Failure 58 0.915
124
c ACT075 Acute Myocardial Infarction 55 0.913
125
DSS009 Disseminated Intravascular Coagulation 56 0.906
126
P KDN018 Kidney Disease 71 0.906
127
DTR001 Detrusor Sphincter Dyssynergia 37 0.906
128
P SLP005 Sleep Disorder 61 0.906
129
MYL009 Myelodysplastic Syndrome 67 0.891
130
P BRN019 Bernard-Soulier Syndrome 61 0.891
131
HYP780 Hypoadrenocorticism, Familial 61 0.891
132
DPS001 Dipsogenic Diabetes Insipidus 21 0.874
133
INT075 Intracranial Hypertension 52 0.874
134
PRS063 Paresthesia 39 0.874
135
CYS001 Cystic Fibrosis 77 0.869
136
AMN003 Amnestic Disorder 53 0.869
137
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.857
138
NRL016 Neural Tube Defects 80 0.857
139
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.857
140
P HYP069 Hyperparathyroidism 62 0.857
141
ALC007 Alcohol Dependence 65 0.839
142
c GRV008 Graves Disease 1 54 0.839
143
MLT157 Multiple System Atrophy 1 69 0.839
144
c ATS347 Autosomal Dominant Polycystic Kidney Disease 64 0.839
145
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.820
146
c PSD048 Pseudo-Von Willebrand Disease 40 0.820
147
SPT006 Septooptic Dysplasia 62 0.820
148
ACR007 Acromegaly 70 0.820
149
P MTR003 Mitral Valve Stenosis 53 0.820
150
MRP001 Morphine Dependence 41 0.820
151
P HLP001 Holoprosencephaly 68 0.820
152
SBC016 Subacute Delirium 42 0.820
153
P PRD006 Prader-Willi Syndrome 60 0.799
154
CRC014 Carcinoid Tumors, Intestinal 46 0.799
155
P MYC007 Myocardial Infarction 69 0.799
156
P PYL005 Pyelonephritis 56 0.799
157
SBP001 Subependymal Giant Cell Astrocytoma 45 0.799
158
P GRV001 Graves' Disease 54 0.799
159
c PRM005 Primary Hyperparathyroidism 59 0.799
160
TLN003 Telangiectasis 51 0.799
161
P RHM011 Rheumatoid Arthritis 81 0.776
162
CHR072 Chordoma 56 0.776
163
MNN043 Meningioma, Familial 79 0.776
164
P THR015 Thrombophilia 51 0.776
165
BLD129 Bladder Exstrophy-Epispadias-Cloacal Exstrophy Complex 41 0.776
166
BLD130 Bladder Exstrophy 44 0.776
167
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.776
168
BRN004 Brain Edema 54 0.776
169
DRY001 Dry Eye Syndrome 49 0.776
170
ANR004 Anuria 44 0.776
171
HMG005 Hemoglobinopathy 55 0.776
172
SCR001 Secretory Meningioma 40 0.776
173
P HRD008 Hereditary Hemorrhagic Telangiectasia 64 0.776
174
INT395 Intracranial Meningioma 47 0.776
175
LNG099 Lung Disease 62 0.776
176
CHC001 Chickenpox 56 0.776
177
c ACQ042 Acquired Hemophilia a 37 0.776
178
CNT060 Central Serous Chorioretinopathy 38 0.776
179
HYP706 Hypermobile Ehlers-Danlos Syndrome 54 0.776
180
CYN002 Cyanosis, Transient Neonatal 43 0.751
181
P ORT004 Orthostatic Intolerance 61 0.751
182
P BND020 Bone Disease 60 0.751
183
NRN004 Neuroendocrine Tumor 55 0.751
184
URT010 Ureteral Obstruction 44 0.751
185
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.751
186
P ART005 Arteriovenous Malformation 64 0.751
187
BCT004 Bacteriuria 48 0.751
188
c HYP595 Hypertension, Essential 84 0.745
189
P PTN014 Patent Ductus Arteriosus 1 59 0.723
190
ANR007 Anorexia Nervosa 59 0.723
191
HYP674 Hyperostosis Cranialis Interna 32 0.723
193
CRN019 Coronary Artery Vasospasm 47 0.723
194
BRN002 Bronchiolitis 57 0.723
195
THY030 Thyroid Gland Disease 50 0.723
196
HYD001 Hydranencephaly 42 0.723
197
INT078 Intracranial Thrombosis 50 0.723
198
MCR004 Macroglobulinemia 48 0.723
199
VRL011 Viral Infectious Disease 60 0.723
200
CHR066 Chronic Fatigue Syndrome 59 0.723
201
THY108 Thymic Neuroendocrine Tumor 32 0.723
202
P PRK039 Parkinsonism 55 0.698
203
ILC002 Ileocolitis 42 0.689
204
PTT057 Pituitary Adenoma 4, Acth-Secreting 49 0.689
205
INS024 Insulin-Like Growth Factor I 77 0.689
206
HSH003 Hashimoto Thyroiditis 60 0.689
207
c MCR115 Microvascular Complications of Diabetes 5 65 0.689
208
c SPL067 Split-Hand/foot Malformation 1 46 0.689
209
EHR002 Ehrlichiosis 39 0.689
210
P RCT021 Rectum Cancer 54 0.689
211
ACD008 Acid-Labile Subunit Deficiency 52 0.689
212
CHR048 Chronic Rhinitis 46 0.689
213
P NRF002 Neurofibromatosis 60 0.689
214
CRH001 Crohn's Disease 80 0.689
215
ISL121 Isolated Split Hand-Split Foot Malformation 42 0.689
216
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.683
217
P SCH015 Schizophrenia 74 0.645
218
c NRF024 Neurofibromatosis, Type I 76 0.645
219
FCT004 Factor Xii Deficiency 54 0.645
220
P FML018 Familial Mediterranean Fever 73 0.645
221
GST009 Gastroschisis 53 0.645
222
INT146 Intervertebral Disc Disease 61 0.645
223
P TRM004 Trimethylaminuria 45 0.645
224
LPP008 Lipoprotein Quantitative Trait Locus 65 0.645
225
MRF001 Marfan Syndrome 76 0.645
226
ECT099 Ectrodactyly-Cleft Palate Syndrome 12 0.645
227
FCT029 Factor V and Factor Viii, Combined Deficiency of, 1 33 0.645
228
P LCT002 Lactose Intolerance 51 0.645
229
CRB037 Cerebral Palsy 66 0.645
230
BRC012 Brucellosis 66 0.645
231
P GLM007 Glomerulonephritis 59 0.645
232
ENT004 Enthesopathy 51 0.645
233
ALL029 Allergic Disease 61 0.645
234
P FNC004 Fanconi Syndrome 60 0.645
235
INT007 Intermediate Coronary Syndrome 53 0.645
236
ALL014 Allergic Encephalomyelitis 34 0.645
237
ABD010 Abdominal Wall Defect 37 0.645
238
THR123 Thrombotic Microangiopathy 40 0.645
239
CHR344 Chronic Orthostatic Intolerance 13 0.645
240
HMN044 Human Immunodeficiency Virus Type 1 76 0.639
241
P PRK057 Parkinson Disease, Late-Onset 79 0.592
242
SPN092 Spinal Shock 20 0.592
243
CRN036 Craniopharyngioma 63 0.571
244
DNG001 Dengue Shock Syndrome 40 0.539
245
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.539
246
BRT054 Brittle Bone Disorder 74 0.539
247
NPH013 Nephrogenic Syndrome of Inappropriate Antidiuresis 39 0.539
248
c THR124 Thrombotic Thrombocytopenic Purpura, Hereditary 53 0.539
249
P HYP750 Hypertriglyceridemia, Familial 61 0.539
250
INT303 Intracranial Hypertension, Idiopathic 56 0.539
251
MCN017 Meconium Ileus 52 0.539
252
PRK005 Prekallikrein Deficiency 30 0.539
253
FCT008 Factitious Disorder 34 0.539
254
PLM010 Pulmonary Edema 54 0.539
255
DNG002 Dengue Hemorrhagic Fever 59 0.539
256
ILS001 Ileus 49 0.539
257
HYP034 Hypertensive Encephalopathy 43 0.539
258
OGL001 Ogilvie Syndrome 24 0.539
259
ATH013 Atherosclerosis Susceptibility 63 0.533
260
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 37 0.533
261
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.533
262
HMR039 Hemorrhage, Intracerebral 57 0.533
263
P ART021 Arteriosclerosis 53 0.533
264
CRB009 Cerebritis 43 0.533
265
INT074 Intracranial Arteriosclerosis 23 0.533
266
CRB008 Cerebral Atherosclerosis 45 0.533
267
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.533
268
HYP080 Hypogonadism 49 0.530
269
PTT009 Pituitary Gland Disease 52 0.486
270
LYM043 Lymphocytic Hypophysitis 31 0.486
271
P SRC025 Sarcoidosis 1 70 0.382
272
NRS005 Neurosarcoidosis 32 0.382
273
GRW007 Growth Hormone Deficiency 47 0.382
274
HYP056 Hypoglycemia 65 0.382
275
P OCL002 Oculocutaneous Albinism 59 0.367
276
HYD002 Hydronephrosis 58 0.367
277
ALB002 Albinism 46 0.367
278
P NTR004 Neutropenia 62 0.352
279
P ART023 Arthropathy 59 0.335
280
PTT004 Pituitary Apoplexy 46 0.335
281
PTH003 Pathologic Nystagmus 52 0.335
282
c SCN052 Secondary Adrenal Insufficiency 35 0.335
283
P HYP730 Hypogonadotropic Hypogonadism 57 0.318
284
HYP005 Hypokalemia 55 0.318
285
c VSC019 Vesicoureteral Reflux 1 56 0.300
286
P ALP004 Alport Syndrome 69 0.300
287
HYP066 Hyperglycemia 60 0.300
288
GST033 Gestational Diabetes 60 0.300
289
HMR002 Hemarthrosis 43 0.300
290
FTT001 Fatty Liver Disease 61 0.300
291
c MJR022 Major Affective Disorder 8 37 0.280
292
ATS010 Autosomal Recessive Disease 42 0.280
293
c MJR024 Major Affective Disorder 9 40 0.280
294
P GLN011 Glanzmann Thrombasthenia 1 66 0.280
295
FCT007 Factor Vii Deficiency 64 0.280
296
P BPL003 Bipolar Disorder 56 0.280
297
HLL004 Hellp Syndrome 53 0.280
298
EMP001 Empty Sella Syndrome 41 0.280
299
MNC006 Monoclonal Gammopathy of Uncertain Significance 47 0.280
300
c BRN108 Branchiootic Syndrome 1 63 0.260
301
HYP020 Hyperprolactinemia 63 0.260
302
P WLF004 Wolfram Syndrome 61 0.260
303
THR004 Thrombocytosis 52 0.260
304
INP001 Inappropriate Adh Syndrome 48 0.260
305
c PRC016 Pre-Eclampsia 64 0.260
306
GST058 Gestational Diabetes Insipidus 15 0.260
307
SYN036 Syncope 44 0.260
308
INF124 Infundibulo-Neurohypophysitis 13 0.260
309
ACT245 Acth-Dependent Cushing Syndrome 22 0.260
310
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 0.237
311
PRT251 Proteinuria, Chronic Benign 58 0.237
312
DBT092 Diabetes Insipidus, Nephrogenic, X-Linked 39 0.237
313
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.237
314
P EXN002 Exanthem 58 0.237
315
MYL069 Myeloma, Multiple 76 0.237
316
c VNW008 Von Willebrand Disease, Type 3 47 0.237
317
ATM095 Autoimmune Disease 61 0.237
318
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.237
319
IMP005 Impotence 52 0.237
320
P PLM036 Pulmonary Fibrosis 65 0.237
321
MDD011 Mood Disorder 61 0.237
322
OLG003 Oligohydramnios 50 0.237
323
P BCL017 B-Cell Lymphoma 57 0.237
324
SHH001 Sheehan Syndrome 45 0.237
325
ETN001 Eating Disorder 59 0.237
326
BRN053 Bronchial Adenomas/carcinoids Childhood 21 0.237
327
PRM331 Primary Hypophysitis 18 0.237
328
c ATS007 Autism Spectrum Disorder 71 0.212
329
P PTS002 Ptosis 52 0.212
330
OPT070 Optic Nerve Hypoplasia, Bilateral 55 0.212
331
P PLV020 Pelvic Organ Prolapse 57 0.212
332
MYL031 Myeloproliferative Neoplasm 66 0.212
333
ANG011 Angiodysplasia 42 0.212
334
GLB002 Glioblastoma 67 0.212
335
P ECL001 Eclampsia 52 0.212
336
FNC007 Functioning Pituitary Adenoma 42 0.212
337
IRN002 Iron Metabolism Disease 56 0.212
338
GTR002 Goiter 52 0.212
339
c HPT003 Hepatitis a 63 0.212
340
CVD001 Covid-19 59 0.212
341
P CRD246 Cardiovascular System Disease 55 0.212
342
P TXP001 Toxoplasmosis 59 0.212
343
c CHR684 Chronic Kidney Disease 73 0.212
344
HPR003 Heparin-Induced Thrombocytopenia 47 0.212
345
ANR040 Aneurysm 60 0.212
346
c CNT101 Central Congenital Hypothyroidism 37 0.212
347
c ALM001 Al Amyloidosis 54 0.212
348
NNF007 Non-Functioning Pituitary Adenoma 39 0.212
349
PNH004 Panhypophysitis 19 0.212
350
ADN064 Adenohypophysitis 34 0.212
351
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.212
352
P PRM227 Primary Orthostatic Hypotension 24 0.212
353
THY029 Thyroid Carcinoma 55 0.212
354
P CRN300 Coronary Heart Disease 1 73 0.184
355
ING001 Inguinal Hernia 59 0.184
356
PNG002 Pain Agnosia 51 0.184
357
c TYP009 Type 2 Diabetes Mellitus 91 0.184
358
GLC096 Galactorrhea 40 0.184
359
c LKM061 Leukemia, Acute Myeloid 83 0.184
360
HYP017 Hypophosphatemia 49 0.184
361
c MCR133 Microvascular Complications of Diabetes 4 41 0.184
362
c MCR113 Microvascular Complications of Diabetes 3 52 0.184
363
c MCR130 Microvascular Complications of Diabetes 6 41 0.184
364
c MCR120 Microvascular Complications of Diabetes 7 47 0.184
365
c HYP795 Hypothyroidism, Congenital, Nongoitrous, 4 46 0.184
366
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.184
367
P GRF003 Graft-Versus-Host Disease 71 0.184
368
EPD070 Epidermoid Cysts 35 0.184
369
P GLM040 Glioma Susceptibility 1 70 0.184
370
DFF005 Diffuse Large B-Cell Lymphoma 55 0.184
371
ECT093 Ectopic Cushing Syndrome 45 0.184
372
VTM033 Vitamin K Deficiency Bleeding 49 0.184
373
ANT039 Antisynthetase Syndrome 55 0.184
374
HMN047 Human Cytomegalovirus Infection 59 0.184
375
GNG005 Gangliocytoma 54 0.184
376
MLG169 Malignant Astrocytoma 57 0.184
377
P CNT005 Central Nervous System Lymphoma 51 0.184
378
P CYS039 Cystic Kidney Disease 52 0.184
379
P BNG032 Benign Mesothelioma 53 0.184
380
CNG021 Congenital Toxoplasmosis 55 0.184
381
STT001 Status Epilepticus 58 0.184
382
P ADN016 Adenocarcinoma 63 0.184
383
MRK001 Merkel Cell Carcinoma 64 0.184
384
PSY004 Psychotic Disorder 66 0.184
385
PRT013 Portal Hypertension 59 0.184
386
P NPH005 Nephronophthisis 59 0.184
387
P UVT001 Uveitis 57 0.184
388
P MCR010 Microcephaly 59 0.184
389
ADR008 Adrenal Adenoma 55 0.184
390
PLY012 Polyhydramnios 46 0.184
391
ABS003 Absence of Septum Pellucidum 18 0.184
392
GRM010 Germ Cells Tumors 33 0.184
393
P THL005 Thalassemia 56 0.184
394
c BCT007 Bacterial Meningitis 55 0.184
395
P MNN013 Meningitis 65 0.184
396
CRC006 Carcinoid Syndrome 55 0.184
397
HYP835 Hypothalamic Obesity 38 0.184
398
DFF031 Diffuse Alveolar Hemorrhage 31 0.184
399
HMP018 Hemophilic Arthropathy 33 0.184
400
P HYP265 Hypotonia 42 0.184
401
SPS057 Spasticity 43 0.184
402
MLR004 Malaria 77 0.150
403
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.150
404
P LYM118 Lymphoma 66 0.150
405
c WLM013 Wilms Tumor 1 65 0.150
406
P ATS364 Autism 72 0.150
407
P ACT092 Acth-Independent Macronodular Adrenal Hyperplasia 56 0.150
408
c SYS001 Systemic Lupus Erythematosus 85 0.150
409
P NNN008 Noonan Syndrome 1 76 0.150
410
OTT002 Otitis Media 70 0.150
411
PLS032 Plasmodium Falciparum Blood Infection Level 21 0.150
412
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 0.150
413
P CRC039 Coarctation of Aorta 46 0.150
414
IFP003 Ifap Syndrome 2 41 0.150
415
FCT034 Factor V and Factor Viii, Combined Deficiency of, 2 41 0.150
416
c HRM009 Hermansky-Pudlak Syndrome 6 46 0.150
417
c HRM005 Hermansky-Pudlak Syndrome 1 55 0.150
418
ARC025 Arachnoid Cysts, Intracranial 37 0.150
419
c THR082 Thrombophilia Due to Activated Protein C Resistance 58 0.150
420
P MYM013 Moyamoya Disease 1 59 0.150
421
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.150
422
P LKM062 Leukemia, Acute Lymphoblastic 69 0.150
423
GRN037 Granulomatosis with Polyangiitis 66 0.150
424
c BTT014 Beta-Thalassemia 72 0.150
425
P LKM071 Leukemia, Chronic Lymphocytic 74 0.150
426
THY111 Thyroid Carcinoma, Familial Medullary 67 0.150
427
P MLN069 Melanoma, Uveal 59 0.150
428
P PHC003 Pheochromocytoma 70 0.150
429
c WLF013 Wolfram Syndrome 1 60 0.150
430
P LNG064 Lung Cancer Susceptibility 3 69 0.150
431
P LYM033 Lymphoproliferative Syndrome 59 0.150
432
SPN221 Spina Bifida Occulta 39 0.150
433
ADR040 Adrenal Gland Pheochromocytoma 45 0.150
434
P NPH012 Nephrotic Syndrome 61 0.150
435
CRY014 Cryptococcal Meningitis 48 0.150
436
INT067 Interstitial Nephritis 46 0.150
437
HYP060 Hyperinsulinism 53 0.150
438
MLT009 Multiple Cranial Nerve Palsy 25 0.150
439
PPL002 Papillary Carcinoma 46 0.150
440
P OLG002 Oligodendroglioma 66 0.150
441
HMP003 Hemopneumothorax 32 0.150
442
P HMN010 Hemangioma 61 0.150
443
BRN031 Brain Germinoma 31 0.150
444
P VSC007 Vascular Disease 62 0.150
445
P CNT037 Central Nervous System Germinoma 31 0.150
446
c ACT042 Acute Pyelonephritis 45 0.150
447
HMN009 Hemangioblastoma 53 0.150
448
LPD008 Lipid Metabolism Disorder 61 0.150
449
GST045 Gastroenteritis 58 0.150
450
c HPT001 Hepatitis C 61 0.150
451
P END033 Endocarditis 58 0.150
452
P ANT006 Antiphospholipid Syndrome 55 0.150
453
SYN007 Synovitis 54 0.150
454
DRM006 Dermatitis 61 0.150
455
ADR005 Adrenal Carcinoma 58 0.150
456
THY125 Thyroid Gland Medullary Carcinoma 48 0.150
457
P TRT010 Teratoma 50 0.150
458
ART016 Aortic Aneurysm 68 0.150
459
ASP003 Aseptic Meningitis 50 0.150
460
PLC002 Plica Syndrome 35 0.150
461
P ADL010 Adult Respiratory Distress Syndrome 70 0.150
462
GLC003 Glucose Intolerance 53 0.150
463
QDR001 Quadriplegia 49 0.150
464
P HYP024 Hypoparathyroidism 55 0.150
465
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 0.150
466
OBS004 Obstructive Hydrocephalus 44 0.150
467
P RNL007 Renal Tubular Acidosis 52 0.150
468
NPH003 Nephrocalcinosis 49 0.150
469
ANH002 Anhidrosis 45 0.150
470
PRT037 Pertussis 49 0.150
471
P MYL006 Myeloid Leukemia 60 0.150
472
PRT029 Parathyroid Adenoma 51 0.150
473
PPT005 Peptic Ulcer Disease 58 0.150
474
P PRD008 Periodontitis 63 0.150
475
MYL080 Myalgic Encephalomyelitis/chronic Fatigue Syndrome 32 0.150
476
OLG006 Oligoastrocytoma 35 0.150
477
P LPS004 Lupus Erythematosus 61 0.150
478
ETV001 Etv6 Thrombocytopenia and Predisposition to Leukemia 31 0.150
479
GRN020 Granulomatous Hypophysitis 15 0.150
480
PST041 Posterior Urethral Valves 41 0.150
481
P HRP006 Herpes Simplex 65 0.150
482
EXP004 Exophthalmos 50 0.150
483
P ALP008 Alopecia 53 0.150
485
c PSD047 Pseudo-Turner Syndrome 52 0.150
486
XNT009 Xanthoma Disseminatum 34 0.150
487
P TRM003 Tremor 50 0.150
488
SLP010 Slipped Capital Femoral Epiphysis 38 0.150
489
INF034 Infective Endocarditis 53 0.106
490
ISC015 Ischemic Colitis 43 0.106
491
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.106
492
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.106
493
ACT119 Acute Promyelocytic Leukemia 62 0.106
494
c PTT060 Pituitary Adenoma 5, Multiple Types 40 0.106
495
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.106
496
TBL025 Tubulointerstitial Nephritis with Uveitis 30 0.106
497
SXL003 Sexual Disorder 49 0.106
498
CRB028 Cerebellar Medulloblastoma 33 0.106
499
P ATR011 Atrial Fibrillation 66 0.106
500
MCR025 Microhydranencephaly 33 0.106
501
SPL004 Splenic Marginal Zone Lymphoma 50 0.106
502
P APL001 Aplastic Anemia 72 0.106
503
c ALP101 Alpha-Thalassemia 62 0.106
504
RNL077 Renal Fibrosis 46 0.106
505
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.106
506
MST019 Mastoiditis 41 0.106
507
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 55 0.106
508
ECT026 Ectopic Pregnancy 47 0.106
509
c ATM002 Autoimmune Polyendocrine Syndrome Type 1 43 0.106
510
BHC003 Behcet Syndrome 70 0.106
511
ACT238 Acth Deficiency, Isolated 52 0.106
512
PLS030 Plasminogen Deficiency, Type I 52 0.106
513
CRP032 Corpus Callosum, Agenesis of 49 0.106
514
DWN001 Down Syndrome 70 0.106
515
VNH007 Von Hippel-Lindau Syndrome 72 0.106
516
AFB002 Afibrinogenemia, Congenital 63 0.106
517
CHD001 Chediak-Higashi Syndrome 66 0.106
518
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.106
519
P OST002 Osteoporosis 76 0.106
520
P MDL005 Medulloblastoma 75 0.106
521
P MJR007 Major Affective Disorder 1 42 0.106
522
DMN031 Dementia, Lewy Body 65 0.106
523
P PRT008 Proteus Syndrome 63 0.106
524
c SML038 Small Cell Cancer of the Lung 68 0.106
525
c HYD064 Hydrocephalus, Congenital, 1 51 0.106
526
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.106
527
CRD223 Cardiac Arrhythmia 63 0.106
528
STR089 Storage Pool Platelet Disease 46 0.106
529
CHR619 Chromosome 2q35 Duplication Syndrome 64 0.106
530
c GLY060 Glycogen Storage Disease Ia 62 0.106
531
GTL001 Gitelman Syndrome 65 0.106
532
P PLY006 Polydactyly 58 0.106
533
P MCR129 Microvascular Complications of Diabetes 1 67 0.106
534
PLT019 Platelet Disorder, Familial, with Associated Myeloid Malignancy 40 0.106
535
c ANM036 Anemia, Sideroblastic, 1 56 0.106
536
PLY183 Polymicrogyria with or Without Vascular-Type Ehlers-Danlos Syndrome 41 0.106
537
PRP027 Peripheral Vascular Disease 71 0.106
538
ANG054 Angina Pectoris 65 0.106
539
P HMP002 Hemophagocytic Lymphohistiocytosis 60 0.106
540
HYP025 Hyperphosphatemia 47 0.106
541
c HPT073 Hepatitis C Virus 70 0.106
542
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.106
543
P PLM037 Pulmonary Hypertension 69 0.106
544
c MCR112 Microvascular Complications of Diabetes 2 42 0.106
545
c PRM093 Premature Ovarian Failure 7 47 0.106
546
HYP001 Hypochromic Microcytic Anemia 36 0.106
547
P RNL028 Renal Tubular Dysgenesis 51 0.106
548
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.106
549
ANN002 Anencephaly 57 0.106
550
APP015 Apparent Mineralocorticoid Excess 57 0.106
551
c TYP008 Type 1 Diabetes Mellitus 77 0.106
552
KRT019 Keratitis, Hereditary 66 0.106
553
P CRD224 Cardiofaciocutaneous Syndrome 1 71 0.106
554
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 0.106
555
c HMC039 Hemochromatosis, Type 1 73 0.106
556
c PSD106 Pseudo-Torch Syndrome 1 46 0.106
557
P HMN036 Hemangiopericytoma, Malignant 56 0.106
558
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 0.106
559
P LPR021 Leprosy 3 71 0.106
560
P WSK001 Wiskott-Aldrich Syndrome 72 0.106
561
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.106
562
PRT130 Protein Z Deficiency 23 0.106
563
c HRM012 Hermansky-Pudlak Syndrome 9 45 0.106
564
P MYC084 Mycobacterium Tuberculosis 1 68 0.106
566
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.106
567
HRT030 Hartsfield Syndrome 46 0.106
568
LPT014 Leptin Deficiency or Dysfunction 77 0.106
569
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.106
570
c PCH010 Pachyonychia Congenita 3 43 0.106
571
c THR048 Thrombocytopenia 4 28 0.106
572
DBT084 Diabetes Mellitus, Ketosis-Prone 59 0.106
573
P ASP006 Aspergillosis 71 0.106
574
ANS021 Anisocoria 24 0.106
575
c EHL071 Ehlers-Danlos Syndrome, Periodontal Type, 1 39 0.106
576
MCR359 Macrothrombocytopenia and Granulocyte Inclusions with or Without Nephritis or Sensorineural Hearing Loss 42 0.106
577
NVS017 Nevus, Epidermal 66 0.106
578
FCT006 Factor V Deficiency 55 0.106
579
END057 Endometrial Cancer 76 0.106
580
ASP030 Aspirin Resistance 41 0.106
581
P KLZ004 Kala-Azar 1 41 0.106
582
KRN002 Kearns-Sayre Syndrome 62 0.106
583
PRM004 Primary Amebic Meningoencephalitis 27 0.106
584
P MLT008 Multinodular Goiter 41 0.106
585
c ATM024 Autoimmune Pancreatitis 52 0.106
586
DRG013 Drug-Induced Lupus Erythematosus 49 0.106
587
CHR704 Chromosome 16p11.2 Deletion Syndrome 35 0.106
588
P SNS001 Sensorineural Hearing Loss 60 0.106
589
OST003 Osteonecrosis 60 0.106
590
P MMP001 Mumps 56 0.106
591
P SPL061 Split Hand-Foot Malformation 43 0.106
592
P TRC034 Torch Syndrome 24 0.106
593
CRD001 Cardiac Tamponade 44 0.106
594
RTN001 Retinal Vasculitis 46 0.106
595
NNL006 Non-Alcoholic Steatohepatitis 54 0.106
596
MRG003 Marginal Zone B-Cell Lymphoma 52 0.106
597
GST023 Gastric Ulcer 52 0.106
598
INT030 Intracranial Aneurysm 55 0.106
599
PTN001 Patent Foramen Ovale 61 0.106
600
P LKM002 Leukemia 65 0.106
601
MNC004 Monoclonal Paraproteinemia 29 0.106
602
c ATM011 Autoimmune Hepatitis 62 0.106
603
TRN018 Transitional Cell Carcinoma 56 0.106
604
P GLY013 Glycogen Storage Disease 59 0.106
605
MLN003 Melancholia 41 0.106
606
NRT004 Neuritis 53 0.106
607
HYP085 Hypothalamic Disease 38 0.106
608
P BRD002 Bardet-Biedl Syndrome 66 0.106
609
URT001 Urethritis 52 0.106
610
CHL068 Cholestasis 61 0.106
611
PNM008 Pneumothorax 54 0.106
612
BRN014 Bronchopneumonia 52 0.106
613
BCT022 Bacterial Infectious Disease 55 0.106
614
GST071 Gastrointestinal Carcinoma 46 0.106
615
GLC106 Glucocorticoid Resistance, Generalized 47 0.106
616
c BRD011 Bardet-Biedl Syndrome 10 49 0.106
617
HMP001 Hemopericardium 47 0.106
618
P ALC033 Alcohol Use Disorder 67 0.106
619
P BNG030 Benign Ependymoma 51 0.106
620
SMN007 Seminoma 42 0.106
621
CLL010 Cellular Ependymoma 58 0.106
622
NNL001 Non-Langerhans-Cell Histiocytosis 35 0.106
623
GNG004 Ganglioglioma 53 0.106
624
URN010 Urinary Tract Obstruction 55 0.106
625
CNG034 Congestive Heart Failure 69 0.106
626
CNN005 Connective Tissue Disease 66 0.106
627
P ACN011 Acne 55 0.106
628
SCH012 Schizoaffective Disorder 49 0.106
629
P DYS154 Dystonia 64 0.106
630
P HPT021 Hepatitis 68 0.106
631
TRN015 Transient Cerebral Ischemia 62 0.106
632
GLS004 Glossopharyngeal Neuralgia 37 0.106
633
PPL021 Papilledema 49 0.106
634
P CND004 Candidiasis 57 0.106
635
P HRT032 Heart Disease 84 0.106
636
MTR002 Mitral Valve Insufficiency 51 0.106
637
FNG004 Fungal Meningitis 46 0.106
638
IRN001 Iron Deficiency Anemia 58 0.106
639
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.106
640
ART074 Aortic Dissection 53 0.106
641
P OPT006 Optic Nerve Disease 57 0.106
642
PLC009 Placenta Praevia 39 0.106
643
SVR001 Severe Acute Respiratory Syndrome 68 0.106
644
HRT012 Heart Valve Disease 53 0.106
645
P LVR013 Liver Disease 68 0.106
646
P MYP004 Myopathy 67 0.106
647
ERD001 Erdheim-Chester Disease 53 0.106
648
P SYP003 Syphilis 59 0.106
649
MTS001 Mutism 44 0.106
650
THR016 Thrombophlebitis 50 0.106
651
INT066 Interstitial Lung Disease 60 0.106
652
P ANG015 Angioedema 56 0.106
653
CHR033 Chordoid Glioma 32 0.106
654
PRT014 Protein S Deficiency 46 0.106
655
HGH043 High Grade Glioma 46 0.106
656
P CRN035 Cranial Nerve Palsy 42 0.106
657
VLV008 Vulvitis 31 0.106
658
SPP008 Suppurative Otitis Media 42 0.106
659
P PRC012 Pericardial Effusion 50 0.106
660
CRN017 Coronary Thrombosis 46 0.106
661
MNN009 Meningoencephalitis 47 0.106
662
P MNN007 Meningocele 39 0.106
663
c ACT073 Acute Leukemia 59 0.106
664
MCR018 Microcytic Anemia 46 0.106
665
LMY002 Leiomyoma 51 0.106
667
DSM004 Desmoid Tumor 65 0.106
668
P ERY036 Erythema Nodosum 49 0.106
669
CHL122 Cholesteatoma of Middle Ear 51 0.106
670
P ATM019 Autoimmune Polyendocrine Syndrome 46 0.106
671
IRT001 Iritis 45 0.106
672
CHL070 Cholesterol Embolism 39 0.106
673
P HML001 Hemolytic-Uremic Syndrome 52 0.106
674
P OPT009 Optic Neuritis 57 0.106
675
DNG003 Dengue Disease 65 0.106
676
PRC013 Pericarditis 53 0.106
677
P CTR002 Cataract 59 0.106
678
P INT070 Intestinal Obstruction 57 0.106
679
P ART018 Aortic Valve Insufficiency 52 0.106
680
P HML002 Hemolytic Anemia 62 0.106
681
P PRN023 Prion Disease 60 0.106
682
MXD005 Mixed Connective Tissue Disease 57 0.106
683
OLF005 Olfactory Neuroblastoma 46 0.106
684
P MST009 Mastocytosis 64 0.106
685
P ACT010 Acth-Secreting Pituitary Adenoma 60 0.106
686
SPN027 Spinal Stenosis 58 0.106
687
P VSC011 Vasculitis 61 0.106
688
P RBL001 Rubella 58 0.106
689
MCC002 Mucocutaneous Leishmaniasis 47 0.106
690
P BRT004 Bartter Disease 58 0.106
691
BLT006 Bilateral Breast Cancer 48 0.106
692
HYP057 Hypervitaminosis D 37 0.106
693
PLY024 Polymicrogyria 48 0.106
694
P ATS382 Autosomal Dominant Tubulointerstitial Kidney Disease 35 0.106
695
LSH001 Leishmaniasis 63 0.106
696
P ENC004 Encephalitis 61 0.106
697
P SDR003 Sideroblastic Anemia 49 0.106
698
P MSC003 Muscular Atrophy 52 0.106
699
P NRB001 Neuroblastoma 66 0.106
700
P MYC008 Myocarditis 59 0.106
701
GLM045 Glioma 62 0.106
702
HNS001 Hansen's Disease 32 0.106
703
NRF007 Neurofibroma 63 0.106
705
RNX001 Runx1 Familial Platelet Disorder with Associated Myeloid Malignancies 13 0.106
706
BRK012 Broken Heart Syndrome 42 0.106
707
CNG069 Congenital Cytomegalovirus 51 0.106
708
CNG608 Congenital Hypopituitarism 29 0.106
709
P DST107 Distal Renal Tubular Acidosis 48 0.106
710
HRP009 Herpes Simplex Encephalitis 58 0.106
711
HYP231 Hypothalamic Hamartomas 33 0.106
712
MNN021 Meningococcemia 34 0.106
713
MLL006 Mollaret Meningitis 21 0.106
714
ATN005 Autonomic Dysfunction 45 0.106
715
c CNT075 Central Precocious Puberty 53 0.106
716
CNG171 Congenital Plasminogen Deficiency 18 0.106
717
CTN007 Cutaneous Leishmaniasis 61 0.106
718
IDP034 Idiopathic Central Precocious Puberty 27 0.106
719
PTC005 Pituicytoma 28 0.106
720
ANX004 Anoxia 40 0.106
721
PCH002 Pachygyria 31 0.106
722
MNN022 Meningoencephalocele 21 0.106
723
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.106
724
ACT114 Acute Myeloblastic Leukemia Without Maturation 26 0.106
725
c ATS210 Autosomal Recessive Sideroblastic Anemia 31 0.106
727
RRC033 Rare Coagulation Disorder 12 0.106
728
P PRC019 Precocious Puberty 48 0.106
729
SNG003 Single Ventricular Heart 30 0.106
730
c ACQ034 Acquired Central Diabetes Insipidus 18 0.106
731
IDP073 Idiopathic Hypercalciuria 41 0.106
732
CLP005 Ciliopathy 40 0.106
733
P RRT020 Rare Tumor 39 0.106
734
ALB014 Alobar Holoprosencephaly 45 0.106
735
CNG418 Congenital Intrauterine Infection-Like Syndrome 23 0.106
736
DWR001 Dwarfism 44 0.106
737
GRD004 Gardner-Diamond Syndrome 20 0.106
738
IDP081 Idiopathic Hypertrophic Pachymeningitis 17 0.106
739
EXT039 Extrapontine Myelinolysis 18 0.106
740
SPL018 Splenomegaly 47 0.106
741
P CRB088 Cerebral Atrophy 32 0.106
742
HYP266 Hypoxia 56 0.106
743
GLY081 Glycogen Storage Disease Due to Glucose-6-Phosphatase Deficiency 48 0.106
744
GLL048 Glial Tumor 51 0.106
745
MDL028 Midline Cerebral Malformation 8 0.106
746
c ACT134 Acute Liver Failure 57 0.106
747
c PRM340 Primary Adrenal Insufficiency 37 0.106
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