Search results for Bradykinin

410 hits were found for Bradykinin

# Family MCID Name MIFTS Score
1
c HRD002 Hereditary Angioedema 60 3.103
2
ANG049 Angioedema Induced by Ace Inhibitors 40 2.652
3
NNH013 Non-Histaminic Angioedema 29 2.652
4
P ANG015 Angioedema 57 0.390
5
PRT037 Pertussis 65 0.389
6
P NRB001 Neuroblastoma 72 0.281
7
P GLM045 Glioma 63 0.281
8
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.279
9
GLL048 Glial Tumor 45 0.265
10
ISC004 Ischemia 58 0.228
11
AST005 Asthma 76 0.225
12
BRN004 Brain Edema 56 0.215
13
CHL014 Cholera 59 0.193
14
P RHN004 Rhinitis 57 0.193
15
c HYP595 Hypertension, Essential 84 0.190
16
C1N001 C1 Inhibitor Deficiency 39 0.184
17
P HRT032 Heart Disease 75 0.178
18
CMP040 Complement Component 4, Partial Deficiency of 33 0.168
19
P PHC003 Pheochromocytoma 71 0.161
20
LPP008 Lipoprotein Quantitative Trait Locus 62 0.161
21
c ACT027 Acute Pancreatitis 60 0.161
22
ADR040 Adrenal Gland Pheochromocytoma 46 0.161
23
P CHR345 Chronic Pain 44 0.154
24
c MCR113 Microvascular Complications of Diabetes 3 52 0.150
25
c MCR120 Microvascular Complications of Diabetes 7 47 0.150
26
c MCR130 Microvascular Complications of Diabetes 6 41 0.150
27
c MCR133 Microvascular Complications of Diabetes 4 41 0.150
28
48X005 48,xyyy 39 0.150
29
ALL003 Allergic Rhinitis 67 0.146
30
ALL026 Allergic Hypersensitivity Disease 62 0.143
31
CNG034 Congestive Heart Failure 69 0.139
32
P VSC007 Vascular Disease 63 0.139
33
P PNC044 Pancreatitis 61 0.139
34
P CRD246 Cardiovascular System Disease 57 0.139
35
OST012 Osteoarthritis 78 0.134
36
TXC005 Toxic Shock Syndrome 62 0.134
37
P CRN300 Coronary Heart Disease 1 63 0.130
38
PLR008 Pleurisy 50 0.130
39
BNB002 Bainbridge-Ropers Syndrome 42 0.130
40
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.126
41
P URT039 Urticaria 58 0.126
42
BNR002 Bone Resorption Disease 48 0.126
43
P RNV001 Renovascular Hypertension 48 0.126
44
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.121
45
P MYC007 Myocardial Infarction 70 0.121
46
HYP066 Hyperglycemia 61 0.121
47
ART140 Arteries, Anomalies of 52 0.121
48
P KDN018 Kidney Disease 72 0.111
49
PNG002 Pain Agnosia 51 0.111
50
CYT002 Cytokine Deficiency 42 0.111
51
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.106
52
TRM010 Traumatic Brain Injury 51 0.106
53
BRN071 Brain Injury 49 0.106
54
c ACQ012 Acquired Angioedema 38 0.106
55
P PRS040 Prostate Cancer 97 0.101
56
P HYP098 Hypereosinophilic Syndrome 67 0.095
57
P PRD008 Periodontitis 64 0.095
58
LVR012 Liver Cirrhosis 62 0.095
59
LNG099 Lung Disease 60 0.095
60
P AST007 Astrocytoma 51 0.095
61
HLX001 Helix Syndrome 47 0.095
62
CRB004 Cerebral Artery Occlusion 45 0.095
63
c DLT002 Dilated Cardiomyopathy 79 0.089
64
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.089
65
c PRC016 Pre-Eclampsia 63 0.089
66
P CYS018 Cystitis 59 0.089
67
THR024 Thrombosis 57 0.089
68
HYP266 Hypoxia 57 0.089
69
ALL006 Allergic Asthma 56 0.089
70
P NRP001 Neuropathy 56 0.089
71
HYP060 Hyperinsulinism 54 0.089
72
DBT010 Diabetic Neuropathy 54 0.089
73
RNL077 Renal Fibrosis 47 0.089
74
P LNG032 Lung Cancer 98 0.082
75
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.082
76
c HYP836 Hypercholesterolemia, Familial, 1 73 0.082
77
OST159 Osteogenic Sarcoma 66 0.082
78
P MCR115 Microvascular Complications of Diabetes 5 66 0.082
79
P NTR004 Neutropenia 63 0.082
80
CRC006 Carcinoid Syndrome 55 0.082
81
SYN007 Synovitis 54 0.082
82
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.082
83
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.082
84
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.082
85
P RNL015 Renal Hypertension 47 0.082
86
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.082
87
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.082
88
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.082
89
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.082
90
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.082
91
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.082
92
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.082
93
PLC002 Plica Syndrome 36 0.082
94
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.082
95
P ALZ034 Alzheimer Disease 88 0.075
96
STR067 Stroke, Ischemic 81 0.075
97
c CHR684 Chronic Kidney Disease 70 0.075
98
P PLM037 Pulmonary Hypertension 67 0.075
99
CHG001 Chagas Disease 66 0.075
100
ATH013 Atherosclerosis Susceptibility 65 0.075
101
P DBT009 Diabetes Mellitus 64 0.075
102
PRT013 Portal Hypertension 59 0.075
103
P FBR017 Fibrosarcoma 56 0.075
104
GLC003 Glucose Intolerance 54 0.075
105
PLM010 Pulmonary Edema 54 0.075
106
END086 End Stage Renal Disease 51 0.075
107
NTR046 Neutrophil Migration 50 0.075
108
ATX019 Ataxia with Vitamin E Deficiency 42 0.075
109
CYS001 Cystic Fibrosis 81 0.067
110
c ATR087 Atrial Standstill 1 75 0.067
111
BRN028 Brain Cancer 74 0.067
112
c MGR028 Migraine with or Without Aura 1 67 0.067
113
c RHB024 Rhabdomyosarcoma 2 67 0.067
114
P MSC005 Muscular Dystrophy 66 0.067
115
c SML038 Small Cell Cancer of the Lung 65 0.067
116
c FNC043 Fanconi Anemia, Complementation Group E 62 0.067
117
CHL067 Cholecystitis 57 0.067
118
P INF037 Inflammatory Bowel Disease 54 0.067
119
CRN030 Coronary Stenosis 50 0.067
120
MTB004 Metabolic Acidosis 50 0.067
121
RTN020 Retinal Vascular Disease 46 0.067
122
MYC005 Myocardial Stunning 46 0.067
123
c MLG068 Malignant Glioma 46 0.067
124
BRN032 Brain Glioma 45 0.067
125
DMP001 Dumping Syndrome 44 0.067
126
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.067
127
P FML187 Familial Hypertension 37 0.067
128
GLB015 Glioblastoma Multiforme 75 0.058
129
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.058
130
MSC157 Muscular Dystrophy, Duchenne Type 72 0.058
131
DWN001 Down Syndrome 70 0.058
132
P ART022 Arthritis 69 0.058
133
BRN024 Bronchitis 68 0.058
134
ANG054 Angina Pectoris 66 0.058
135
P DRM053 Dermatitis, Atopic 66 0.058
136
PRT036 Peritonitis 64 0.058
137
MSC007 Muscle Hypertrophy 64 0.058
138
P END044 Endometriosis 63 0.058
139
LPD008 Lipid Metabolism Disorder 62 0.058
140
c SVR001 Severe Acute Respiratory Syndrome 62 0.058
141
P ART023 Arthropathy 62 0.058
142
ATM095 Autoimmune Disease 62 0.058
143
CRD223 Cardiac Arrhythmia 60 0.058
144
IGR001 Ige Responsiveness, Atopic 59 0.058
145
GNG013 Gingivitis 59 0.058
146
P EXN002 Exanthem 57 0.058
147
DSS009 Disseminated Intravascular Coagulation 57 0.058
148
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.058
149
CMM005 Common Cold 57 0.058
150
c ANG068 Angioedema, Hereditary, Type I 57 0.058
151
HYP005 Hypokalemia 55 0.058
152
OCL069 Ocular Motor Apraxia 51 0.058
153
47X002 47,xyy 49 0.058
154
PLL012 Pollen Allergy 46 0.058
155
HDN002 Head Injury 46 0.058
156
URT010 Ureteral Obstruction 45 0.058
157
CYT018 Cytochrome P450 2d6 Variant 27 0.058
158
P CLR023 Colorectal Cancer 99 0.048
159
P BRS047 Breast Cancer 97 0.048
160
c SYS001 Systemic Lupus Erythematosus 86 0.048
161
P GST053 Gastric Cancer 83 0.048
162
P BLD134 Bladder Cancer 79 0.048
163
INS024 Insulin-Like Growth Factor I 79 0.048
164
IMM167 Immune Deficiency Disease 78 0.048
165
CRV035 Cervical Cancer 76 0.048
166
P RSP003 Respiratory Failure 74 0.048
167
ULC004 Ulcerative Colitis 73 0.048
168
P RTN024 Retinoblastoma 73 0.048
169
ANX010 Anxiety 73 0.048
170
P SRC025 Sarcoidosis 1 70 0.048
171
P AMY004 Amyloidosis 70 0.048
172
c PNC108 Pancreatitis, Hereditary 70 0.048
173
P MLN008 Melanoma 69 0.048
174
P PNM007 Pneumonia 68 0.048
175
P SYS005 Systemic Scleroderma 68 0.048
176
P CRD119 Cardiac Arrest 67 0.048
177
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.048
178
P DMN002 Dementia 66 0.048
179
P ADL010 Adult Respiratory Distress Syndrome 65 0.048
180
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.048
181
SKN016 Skin Disease 63 0.048
182
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.048
183
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.048
184
CLT003 Colitis 62 0.048
185
P PSR002 Psoriasis 62 0.048
186
P HYP750 Hypertriglyceridemia, Familial 62 0.048
187
c SCL052 Scleroderma, Familial Progressive 61 0.048
188
VRL011 Viral Infectious Disease 61 0.048
189
P LPS004 Lupus Erythematosus 61 0.048
190
TRG002 Trigeminal Neuralgia 60 0.048
191
PRT058 Pure Autonomic Failure 59 0.048
192
ADN018 Adenoma 59 0.048
193
BRG013 Buerger Disease 58 0.048
194
P PRP019 Peripheral Nervous System Disease 58 0.048
195
P MTC069 Mitochondrial Disorders 56 0.048
196
BCT022 Bacterial Infectious Disease 56 0.048
197
c FML035 Familial Hyperlipidemia 55 0.048
198
MCL006 Macular Retinal Edema 55 0.048
199
P DRR001 Diarrhea 55 0.048
200
CPL003 Capillary Leak Syndrome 55 0.048
201
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.048
202
P ART021 Arteriosclerosis 54 0.048
203
OCL006 Ocular Hypertension 53 0.048
204
HMC014 Homocysteinemia 53 0.048
205
PRP080 Peripheral Artery Disease 53 0.048
206
c FML008 Familial Retinoblastoma 53 0.048
207
PST011 Pustulosis of Palm and Sole 52 0.048
208
IMP005 Impotence 52 0.048
209
P ECL001 Eclampsia 50 0.048
210
RNL078 Renal Dysplasia 50 0.048
211
P OPN001 Open-Angle Glaucoma 49 0.048
212
MTC005 Mitochondrial Metabolism Disease 49 0.048
213
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.048
214
TNP001 Tinea Pedis 46 0.048
215
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.048
216
IMM136 Immune System Disease 45 0.048
217
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.048
218
c PCH010 Pachyonychia Congenita 3 44 0.048
219
c SPR086 Spermatogenic Failure 3 44 0.048
220
CVD001 Covid-19 44 0.048
221
TRP009 Triple X Syndrome 42 0.048
222
HGH020 High Molecular Weight Kininogen Deficiency 41 0.048
223
ANX004 Anoxia 40 0.048
224
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.048
225
NRD001 Neurodermatitis 35 0.048
226
MST020 Mast Cell Activation Syndrome 26 0.048
227
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.048
228
VSC009 Vascular Skin Disease 21 0.048
229
P HPT023 Hepatocellular Carcinoma 100 0.034
230
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.034
231
P OVR042 Ovarian Cancer 88 0.034
232
MLR004 Malaria 81 0.034
233
P GLM040 Glioma Susceptibility 1 81 0.034
234
P RHM011 Rheumatoid Arthritis 80 0.034
235
P LNG064 Lung Cancer Susceptibility 3 78 0.034
236
P MDL005 Medulloblastoma 77 0.034
237
c TBR025 Tuberous Sclerosis 1 77 0.034
238
END057 Endometrial Cancer 74 0.034
239
LPT014 Leptin Deficiency or Dysfunction 74 0.034
240
P OST002 Osteoporosis 74 0.034
241
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.034
242
P HNT016 Huntington Disease 72 0.034
243
P FML011 Familial Adenomatous Polyposis 72 0.034
244
P HYP061 Hypertrophic Cardiomyopathy 70 0.034
245
P TBR001 Tuberous Sclerosis 70 0.034
246
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.034
247
LYM133 Lymphoma, Hodgkin, Classic 69 0.034
248
MST024 Mastocytosis, Cutaneous 69 0.034
249
MNT001 Mantle Cell Lymphoma 69 0.034
250
P LVR013 Liver Disease 68 0.034
251
P INF038 Influenza 68 0.034
252
CRB039 Cerebrovascular Disease 67 0.034
253
P TRN020 Turner Syndrome 67 0.034
254
HYP056 Hypoglycemia 66 0.034
255
P MNN013 Meningitis 66 0.034
256
TTN003 Tetanus 65 0.034
257
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.034
258
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.034
259
P HRP006 Herpes Simplex 65 0.034
260
CLN015 Colon Adenocarcinoma 65 0.034
261
P THY023 Thymoma 65 0.034
262
P MST009 Mastocytosis 64 0.034
263
GT001 Gout 64 0.034
264
ART002 Arts Syndrome 64 0.034
265
OST017 Osteomyelitis 64 0.034
266
LSH001 Leishmaniasis 63 0.034
267
c GLC092 Glaucoma, Primary Open Angle 62 0.034
268
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.034
269
CHL068 Cholestasis 61 0.034
271
P INT143 Interstitial Cystitis 61 0.034
272
DRM006 Dermatitis 61 0.034
273
c PNS012 Paine Syndrome 61 0.034
274
GST033 Gestational Diabetes 61 0.034
275
SPN186 Spinal Cord Injury 60 0.034
276
DPH001 Diphtheria 60 0.034
277
SQM006 Squamous Cell Carcinoma 60 0.034
278
END081 Endosteal Hyperostosis, Autosomal Dominant 60 0.034
279
VRC005 Varicose Veins 60 0.034
280
P CTR002 Cataract 60 0.034
281
INS001 Insulinoma 60 0.034
282
c ACT071 Acute Kidney Failure 60 0.034
283
P OPT006 Optic Nerve Disease 60 0.034
284
P BRN022 Bronchiectasis 59 0.034
285
CHL123 Chlamydia 59 0.034
286
VSL002 Visual Epilepsy 59 0.034
287
ANR040 Aneurysm 59 0.034
288
PPT005 Peptic Ulcer Disease 59 0.034
289
ANT024 Anthrax Disease 58 0.034
290
CMP010 Complex Regional Pain Syndrome 58 0.034
291
CRD132 Cardiac Conduction Defect 58 0.034
292
P BNC003 Bone Cancer 58 0.034
293
EXT034 Extrinsic Allergic Alveolitis 58 0.034
294
P GLL018 Gallbladder Cancer 57 0.034
295
P GLL020 Gallbladder Disease 57 0.034
296
P HDC001 Headache 57 0.034
297
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.034
298
P FCL005 Focal Segmental Glomerulosclerosis 57 0.034
299
SCH014 Schistosomiasis 57 0.034
300
P MYS005 Myositis 56 0.034
301
P CHN012 Chondrosarcoma 56 0.034
302
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.034
303
LST001 Listeriosis 56 0.034
304
P SZR006 Seizure Disorder 56 0.034
305
HMG005 Hemoglobinopathy 56 0.034
306
AGN016 Aging 56 0.034
307
VSC003 Visceral Leishmaniasis 55 0.034
308
c BCT007 Bacterial Meningitis 55 0.034
309
P PLM034 Pulmonary Emphysema 55 0.034
310
P HYP076 Hyperthyroidism 55 0.034
311
P VNS003 Venous Insufficiency 55 0.034
312
P DBT005 Diabetes Insipidus 55 0.034
313
FCT004 Factor Xii Deficiency 55 0.034
314
P ALP008 Alopecia 54 0.034
315
P LTR001 Lateral Sclerosis 54 0.034
316
P TRM003 Tremor 54 0.034
317
PRS045 Prostatic Hypertrophy 53 0.034
318
P INS002 in Situ Carcinoma 53 0.034
319
HRT012 Heart Valve Disease 53 0.034
320
P FML023 Familial Hemiplegic Migraine 53 0.034
321
MST005 Mastitis 53 0.034
322
c PRD040 Periodontitis, Chronic 53 0.034
323
P HML001 Hemolytic-Uremic Syndrome 53 0.034
324
P PTS002 Ptosis 53 0.034
325
GSG001 Gas Gangrene 53 0.034
326
INT075 Intracranial Hypertension 53 0.034
327
P PNC025 Panic Disorder 53 0.034
328
P RTN018 Retinal Disease 53 0.034
329
DYS015 Dysentery 52 0.034
330
P MSC003 Muscular Atrophy 52 0.034
331
c THY107 Thymoma, Familial 52 0.034
332
P ACT105 Acute Mountain Sickness 52 0.034
333
HYP014 Hyperuricemia 52 0.034
334
PRS021 Prostatic Adenoma 51 0.034
335
ENT011 Enterocolitis 51 0.034
336
NRM004 Neuroma 51 0.034
337
P PRC012 Pericardial Effusion 51 0.034
338
HYP781 Hypoascorbemia 51 0.034
339
CHR005 Chorioamnionitis 51 0.034
340
P OVR082 Overgrowth Syndrome 50 0.034
341
HPT014 Hepatorenal Syndrome 50 0.034
342
CRT013 Carotid Stenosis 50 0.034
343
P TMP001 Temporal Lobe Epilepsy 50 0.034
344
c CHR431 Chronic Venous Insufficiency 49 0.034
345
PLP001 Pulpitis 49 0.034
346
PRS129 Prostatic Hyperplasia, Benign 49 0.034
347
VCC001 Vaccinia 49 0.034
348
WTH001 Withdrawal Disorder 48 0.034
349
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.034
350
DBT006 Diabetic Macular Edema 48 0.034
351
SPL018 Splenomegaly 48 0.034
352
BLD044 Bladder Disease 48 0.034
353
CHL147 Chlamydia Pneumonia 48 0.034
354
BNN003 Bone Inflammation Disease 48 0.034
355
HMP001 Hemopericardium 48 0.034
356
SXL003 Sexual Disorder 47 0.034
357
CRN017 Coronary Thrombosis 47 0.034
358
P CLB034 Coloboma, Ocular, Autosomal Dominant 47 0.034
359
SRT004 Serotonin Syndrome 47 0.034
360
P CRC039 Coarctation of Aorta 47 0.034
361
P OVR046 Ovarian Cyst 47 0.034
362
P VTR007 Vitreoretinopathy 46 0.034
363
HYP034 Hypertensive Encephalopathy 46 0.034
364
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.034
365
SMT001 Somatization Disorder 46 0.034
366
c CHR048 Chronic Rhinitis 46 0.034
367
LKS001 Leukostasis 46 0.034
368
PLC001 Placenta Accreta 46 0.034
369
MXD026 Mixed Glioma 45 0.034
370
CYN002 Cyanosis, Transient Neonatal 45 0.034
371
CRT015 Carotid Artery Occlusion 45 0.034
372
ATN004 Autonomic Neuropathy 45 0.034
373
IMM064 Immunodeficiency, Common Variable, 10 44 0.034
374
ART006 Arthus Reaction 44 0.034
375
c PRM038 Primary Agammaglobulinemia 44 0.034
376
SKN005 Skin Atrophy 43 0.034
377
PRS042 Prostate Disease 43 0.034
378
MST004 Mast Cell Neoplasm 42 0.034
379
P AVS003 Avascular Necrosis 42 0.034
380
PNM013 Pneumococcal Meningitis 42 0.034
381
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.034
382
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.034
383
P KLZ004 Kala-Azar 1 41 0.034
384
MRP001 Morphine Dependence 41 0.034
385
ART008 Arteriosclerosis Obliterans 40 0.034
386
FRM003 Farmer's Lung 39 0.034
387
c PRG020 Paragangliomas 3 39 0.034
388
ALD013 Aldosterone-Producing Adenoma 39 0.034
389
CRV045 Cervical Intraepithelial Neoplasia 39 0.034
390
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.034
391
EXT007 Extracutaneous Mastocytoma 38 0.034
392
ALL014 Allergic Encephalomyelitis 38 0.034
393
OVR094 Ovarian Epithelial Cancer 38 0.034
394
PRN039 Paraneoplastic Syndromes 38 0.034
395
CRT004 Carotid Artery Thrombosis 38 0.034
396
SCR003 Secretory Diarrhea 37 0.034
398
WHP002 Whiplash 36 0.034
399
CHR178 Chromosomal Triplication 35 0.034
400
PRM329 Premature Aging 35 0.034
401
CLD011 Cold Urticaria 35 0.034
403
DXR001 Doxorubicin Induced Cardiomyopathy 33 0.034
404
P SCL047 Sclerocornea 32 0.034
405
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.034
406
c ANG045 Angioedema, Hereditary, Type Iii 31 0.034
407
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.034
408
c CRD150 Cardiomyopathy, Familial Hypertrophic, 18 26 0.034
409
CRB041 Carboxypeptidase N Deficiency 24 0.034
410
CHR043 Chronic Inflammatory Demyelinating Polyneuritis 23 0.034
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