Search results for carbamide peroxide

617 hits were found for carbamide peroxide

# Family MCID Name MIFTS Score
1
c NRF023 Neurofibromatosis, Type Ii 80 0.314
2
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.269
3
P NRB001 Neuroblastoma 72 0.148
4
ATH013 Atherosclerosis Susceptibility 65 0.132
5
48X005 48,xyyy 39 0.132
6
P LVR013 Liver Disease 68 0.129
7
c FNC043 Fanconi Anemia, Complementation Group E 62 0.126
8
P CTR002 Cataract 60 0.125
9
HMS001 Hemosiderosis 54 0.125
10
P RRH023 Rare Hereditary Hemochromatosis 41 0.125
11
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.125
12
DRM006 Dermatitis 61 0.122
13
P PRD008 Periodontitis 64 0.122
14
ISC004 Ischemia 58 0.118
15
HRW001 Hair Whorl 36 0.116
16
HYP066 Hyperglycemia 61 0.116
17
P VSC007 Vascular Disease 63 0.114
18
P ALZ034 Alzheimer Disease 88 0.110
19
FTT001 Fatty Liver Disease 61 0.110
20
P DBT009 Diabetes Mellitus 64 0.109
21
P KDN018 Kidney Disease 72 0.109
22
ALL026 Allergic Hypersensitivity Disease 62 0.109
23
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.104
24
P GLM045 Glioma 63 0.099
25
GLL048 Glial Tumor 45 0.099
26
GNG013 Gingivitis 59 0.099
28
P CLR023 Colorectal Cancer 99 0.095
29
SKN016 Skin Disease 63 0.094
30
AGN016 Aging 56 0.094
31
PRT036 Peritonitis 64 0.091
32
c ACT027 Acute Pancreatitis 60 0.091
33
P DNT007 Dentin Sensitivity 36 0.091
34
P HPT023 Hepatocellular Carcinoma 100 0.090
35
IRN002 Iron Metabolism Disease 57 0.090
36
CLT003 Colitis 62 0.089
37
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.088
38
LVR012 Liver Cirrhosis 62 0.088
39
P BRS047 Breast Cancer 97 0.085
40
P INF032 Infertility 57 0.085
41
P GST044 Gastritis 56 0.083
42
GNG003 Gingival Recession 44 0.081
43
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.081
44
VSL002 Visual Epilepsy 59 0.081
45
P GLM007 Glomerulonephritis 57 0.081
46
P SZR006 Seizure Disorder 56 0.081
47
P ECL001 Eclampsia 50 0.081
48
KRT009 Keratosis 51 0.080
49
c HYP595 Hypertension, Essential 84 0.080
50
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.079
51
P MCR115 Microvascular Complications of Diabetes 5 66 0.079
52
P PNC044 Pancreatitis 61 0.079
53
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.079
54
DWN001 Down Syndrome 70 0.078
55
P ENC018 Encephalopathy 61 0.078
56
c ACT075 Acute Myocardial Infarction 57 0.078
57
P OCL013 Oculodentodigital Dysplasia 69 0.077
58
P TRN020 Turner Syndrome 67 0.077
59
GLB015 Glioblastoma Multiforme 75 0.076
60
DFC004 Deficiency Anemia 70 0.076
61
P BCL017 B-Cell Lymphoma 58 0.076
62
NNL006 Non-Alcoholic Steatohepatitis 54 0.076
63
c MCR113 Microvascular Complications of Diabetes 3 52 0.076
64
c MCR120 Microvascular Complications of Diabetes 7 47 0.076
65
c MCR130 Microvascular Complications of Diabetes 6 41 0.076
66
c MCR133 Microvascular Complications of Diabetes 4 41 0.076
67
P PNC035 Pancreatic Cancer 84 0.075
68
PLM001 Pulmonary Tuberculosis 69 0.075
69
ATM095 Autoimmune Disease 62 0.075
70
TXC005 Toxic Shock Syndrome 62 0.075
71
P THL005 Thalassemia 60 0.075
72
P INF037 Inflammatory Bowel Disease 54 0.075
73
CYT002 Cytokine Deficiency 42 0.075
74
P RSP003 Respiratory Failure 74 0.074
75
P LNG032 Lung Cancer 98 0.074
76
CYS001 Cystic Fibrosis 81 0.074
77
P PNM007 Pneumonia 68 0.074
78
P CRD119 Cardiac Arrest 67 0.074
79
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.074
80
c ACT071 Acute Kidney Failure 60 0.072
81
KRT013 Keratolytic Winter Erythema 46 0.072
82
URM002 Uremia 49 0.071
83
c CHR684 Chronic Kidney Disease 70 0.071
84
P LKM002 Leukemia 68 0.071
85
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.069
86
c DBT099 Diabetes Mellitus, Type I 65 0.069
87
P PSR002 Psoriasis 62 0.069
88
P PYL005 Pyelonephritis 56 0.069
89
PST011 Pustulosis of Palm and Sole 52 0.069
90
END086 End Stage Renal Disease 51 0.069
91
RTR008 Root Resorption 45 0.069
92
PLP001 Pulpitis 49 0.068
93
P PRS040 Prostate Cancer 97 0.068
94
P PRK057 Parkinson Disease, Late-Onset 78 0.068
95
OST159 Osteogenic Sarcoma 66 0.068
96
SQM006 Squamous Cell Carcinoma 60 0.068
97
P ALC033 Alcohol Use Disorder 58 0.068
98
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.068
99
ORL015 Oral Squamous Cell Carcinoma 43 0.068
100
c SYS001 Systemic Lupus Erythematosus 86 0.066
101
MLR004 Malaria 81 0.066
102
P MYC007 Myocardial Infarction 70 0.066
103
P ADL010 Adult Respiratory Distress Syndrome 65 0.066
104
ALC006 Alcoholic Hepatitis 61 0.066
105
P DRR001 Diarrhea 55 0.066
106
PLM010 Pulmonary Edema 54 0.066
107
P RHM011 Rheumatoid Arthritis 80 0.065
108
CRB039 Cerebrovascular Disease 67 0.065
109
P MSC005 Muscular Dystrophy 66 0.065
110
c HPT001 Hepatitis C 62 0.065
111
P SCK005 Sickle Cell Disease 50 0.065
112
c CHR098 Chronic Pyelonephritis 38 0.065
113
c PCH010 Pachyonychia Congenita 3 44 0.064
114
AST005 Asthma 76 0.063
115
ULC004 Ulcerative Colitis 73 0.063
116
BCT022 Bacterial Infectious Disease 56 0.063
117
NPH009 Nephrolithiasis 55 0.063
118
MTB004 Metabolic Acidosis 50 0.063
119
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.063
120
CRV035 Cervical Cancer 76 0.061
121
c HMC039 Hemochromatosis, Type 1 74 0.061
122
c BTT014 Beta-Thalassemia 74 0.061
123
P MLN008 Melanoma 69 0.061
124
P LPS004 Lupus Erythematosus 61 0.061
125
HLC007 Helicobacter Pylori Infection 59 0.061
126
HYP005 Hypokalemia 55 0.060
127
STR067 Stroke, Ischemic 81 0.060
128
P MLT020 Multiple Sclerosis 72 0.060
129
ALC007 Alcohol Dependence 66 0.060
130
GST023 Gastric Ulcer 53 0.060
131
DNT012 Dental Caries 53 0.060
132
OCL069 Ocular Motor Apraxia 51 0.060
133
c RHB024 Rhabdomyosarcoma 2 67 0.059
134
SCK003 Sickle Cell Anemia 74 0.058
135
CRH001 Crohn's Disease 74 0.058
136
PRP027 Peripheral Vascular Disease 71 0.058
137
PLM033 Pulmonary Embolism 59 0.058
138
ADN018 Adenoma 59 0.058
139
P PNM006 Pneumoconiosis 56 0.058
140
P RTN018 Retinal Disease 53 0.058
141
PRS021 Prostatic Adenoma 51 0.058
142
ANT018 Anthracosis 48 0.058
143
P EPL164 Epilepsy 71 0.057
144
P DRM053 Dermatitis, Atopic 66 0.057
145
P ART022 Arthritis 69 0.056
146
RTN017 Retinal Detachment 61 0.056
147
P MYL006 Myeloid Leukemia 60 0.056
148
STT001 Status Epilepticus 60 0.056
149
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.056
150
P NRP001 Neuropathy 56 0.056
151
CHR100 Chronic Ulcer of Skin 55 0.056
152
PST092 Posttransplant Acute Limbic Encephalitis 29 0.056
153
BRX001 Bruxism 50 0.054
154
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.054
155
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.054
156
P LKM062 Leukemia, Acute Lymphoblastic 69 0.054
157
P SYS005 Systemic Scleroderma 68 0.054
158
LSH001 Leishmaniasis 63 0.054
159
DPR016 Depression 63 0.054
160
P VSC011 Vasculitis 62 0.054
161
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.054
162
PRN019 Perinatal Necrotizing Enterocolitis 59 0.054
163
PRS045 Prostatic Hypertrophy 53 0.054
164
P ACT008 Actinic Keratosis 53 0.054
165
ENT011 Enterocolitis 51 0.054
166
P OVR082 Overgrowth Syndrome 50 0.054
167
PRS129 Prostatic Hyperplasia, Benign 49 0.054
168
CLS016 Clostridium Difficile Colitis 48 0.054
169
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.054
170
P KLZ004 Kala-Azar 1 41 0.054
171
P OVR042 Ovarian Cancer 88 0.051
172
MYL069 Myeloma, Multiple 85 0.051
173
HMN044 Human Immunodeficiency Virus Type 1 71 0.051
174
SRC014 Sarcoma 65 0.051
175
c SCL052 Scleroderma, Familial Progressive 61 0.051
176
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.051
177
MNT002 Mental Depression 58 0.051
178
CNS004 Constipation 58 0.051
179
P CND004 Candidiasis 58 0.051
180
P CRD246 Cardiovascular System Disease 57 0.051
181
SPN035 Spindle Cell Sarcoma 53 0.051
182
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.051
183
CVD001 Covid-19 44 0.051
184
ESP021 Esophageal Cancer 90 0.049
185
c LKM061 Leukemia, Acute Myeloid 84 0.049
186
ANX010 Anxiety 73 0.049
187
P ATS364 Autism 70 0.049
188
P HPT021 Hepatitis 67 0.049
189
c MGR028 Migraine with or Without Aura 1 67 0.049
190
c SML038 Small Cell Cancer of the Lung 65 0.049
191
OST017 Osteomyelitis 64 0.049
192
NTR005 Nutritional Deficiency Disease 62 0.049
193
P INT143 Interstitial Cystitis 61 0.049
194
c HPT016 Hepatitis B 59 0.049
195
P ANP001 Anaplastic Large Cell Lymphoma 58 0.049
196
P END033 Endocarditis 57 0.049
197
DBT010 Diabetic Neuropathy 54 0.049
198
INF034 Infective Endocarditis 53 0.049
199
CRD137 Cardiogenic Shock 47 0.049
200
c DRR009 Diarrhea 6 46 0.049
201
49X006 49, Xxxxy Syndrome 41 0.049
202
PRP030 Purpura 54 0.048
203
P GLM040 Glioma Susceptibility 1 81 0.046
204
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.046
205
c ATR087 Atrial Standstill 1 75 0.046
206
c SPN225 Spondyloarthropathy 1 73 0.046
207
MSC157 Muscular Dystrophy, Duchenne Type 72 0.046
208
ADL002 Adult Syndrome 70 0.046
209
CRB037 Cerebral Palsy 69 0.046
210
P THR014 Thrombocytopenia 67 0.046
211
P NSP012 Nasopharyngeal Carcinoma 66 0.046
212
c MCR129 Microvascular Complications of Diabetes 1 66 0.046
213
c HPT003 Hepatitis a 62 0.046
214
VRL011 Viral Infectious Disease 61 0.046
215
P KDN017 Kidney Cancer 60 0.046
216
P PRP019 Peripheral Nervous System Disease 58 0.046
217
THR024 Thrombosis 57 0.046
218
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.046
219
c ACT134 Acute Liver Failure 56 0.046
220
P VNS003 Venous Insufficiency 55 0.046
221
CRH005 Crohn's Colitis 53 0.046
222
INT075 Intracranial Hypertension 53 0.046
223
ALC009 Alcoholic Liver Cirrhosis 53 0.046
224
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.046
225
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.046
226
ILS001 Ileus 51 0.046
227
STM007 Stomatitis 50 0.046
228
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.046
229
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.046
230
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.046
231
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.046
232
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.046
233
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.046
234
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.046
235
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.046
236
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.046
237
c MCR112 Microvascular Complications of Diabetes 2 41 0.046
238
c LKM005 Leukemia, T-Cell, Chronic 34 0.046
239
IMM167 Immune Deficiency Disease 78 0.044
240
c THR092 Thrombophilia Due to Thrombin Defect 73 0.044
241
P AMY004 Amyloidosis 70 0.044
242
P MYC084 Mycobacterium Tuberculosis 1 68 0.044
243
P INF038 Influenza 68 0.044
244
P DMN002 Dementia 66 0.044
245
P RHB003 Rhabdomyosarcoma 63 0.044
246
c ACT068 Acute Cystitis 63 0.044
247
P PLY014 Polycystic Kidney Disease 62 0.044
248
PRT013 Portal Hypertension 59 0.044
249
c DNG003 Dengue Disease 59 0.044
250
P SLP005 Sleep Disorder 59 0.044
251
GST045 Gastroenteritis 59 0.044
252
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.044
253
P EXN002 Exanthem 57 0.044
254
P PLY011 Polycystic Ovary Syndrome 56 0.044
255
SFT003 Soft Tissue Sarcoma 56 0.044
256
LMB062 Limb Ischemia 55 0.044
257
P MSC003 Muscular Atrophy 52 0.044
258
HYP014 Hyperuricemia 52 0.044
259
SPN051 Spondylitis 51 0.044
260
c MLG068 Malignant Glioma 46 0.044
261
HPT004 Hepatic Coma 45 0.044
262
DNT001 Dental Fluorosis 43 0.044
263
INF009 Inflammatory Spondylopathy 31 0.044
264
BRN028 Brain Cancer 74 0.040
265
c MNN043 Meningioma, Familial 74 0.040
266
c LKM063 Leukemia, Chronic Myeloid 72 0.040
267
WLS001 Wilson Disease 71 0.040
268
SKN019 Skin Melanoma 68 0.040
269
BRK010 Burkitt Lymphoma 67 0.040
270
MYL031 Myeloproliferative Neoplasm 66 0.040
271
c WLM013 Wilms Tumor 1 65 0.040
272
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.040
273
MNN042 Meningioma, Radiation-Induced 62 0.040
274
P SJG008 Sjogren Syndrome 61 0.040
275
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.040
276
HPT019 Hepatic Encephalopathy 60 0.040
277
ACQ007 Acquired Immunodeficiency Syndrome 60 0.040
278
VRC005 Varicose Veins 60 0.040
279
P BND020 Bone Disease 59 0.040
280
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.040
281
PLM102 Palmoplantar Keratoderma, Epidermolytic 56 0.040
282
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.040
283
PLS011 Plasmacytoma 56 0.040
284
P SBS003 Substance Abuse 55 0.040
285
PLM136 Palmoplantar Keratoderma, Nonepidermolytic 53 0.040
286
PRP080 Peripheral Artery Disease 53 0.040
287
P INT068 Intestinal Disease 53 0.040
288
DRM011 Dermatophytosis 52 0.040
289
MCN017 Meconium Ileus 52 0.040
290
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.040
291
LNG031 Lung Benign Neoplasm 51 0.040
292
P THR015 Thrombophilia 51 0.040
293
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.040
294
HYP081 Hypolipoproteinemia 51 0.040
295
SPN021 Spinal Meningioma 50 0.040
296
c CHR431 Chronic Venous Insufficiency 49 0.040
297
ACT003 Acute Kidney Tubular Necrosis 45 0.040
298
SPP008 Suppurative Otitis Media 45 0.040
299
ATN004 Autonomic Neuropathy 45 0.040
300
PNC085 Penicillin Allergy 45 0.040
302
HYP457 Hypertrophic Scars 42 0.040
303
SCR001 Secretory Meningioma 41 0.040
304
P MLG074 Malignant Mesenchymoma 40 0.040
305
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.040
306
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.040
307
c CHR097 Chronic Purulent Otitis Media 33 0.040
308
c ATS013 Autosomal Recessive Congenital Ichthyosis 63 0.039
309
ICH001 Ichthyosis Vulgaris 55 0.039
310
P ICH004 Ichthyosis 54 0.039
311
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.036
312
P LKM071 Leukemia, Chronic Lymphocytic 79 0.036
313
ADR007 Adrenoleukodystrophy 75 0.036
314
P GRF003 Graft-Versus-Host Disease 72 0.036
315
MYL009 Myelodysplastic Syndrome 70 0.036
316
MYL005 Myelofibrosis 70 0.036
317
EWN003 Ewing Sarcoma 69 0.036
318
GST092 Gastroesophageal Reflux 67 0.036
319
c ATS007 Autism Spectrum Disorder 67 0.036
320
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.036
321
P DYS154 Dystonia 65 0.036
322
PRP001 Propionic Acidemia 65 0.036
323
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.036
324
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.036
325
NRM005 Neuromuscular Disease 64 0.036
326
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.036
327
HMT002 Hematologic Cancer 62 0.036
328
CTN007 Cutaneous Leishmaniasis 62 0.036
329
PSR001 Psoriatic Arthritis 61 0.036
330
c PNS012 Paine Syndrome 61 0.036
331
c WLM018 Wilms Tumor 5 61 0.036
332
SPP011 Suppression of Tumorigenicity 12 59 0.036
333
P SYP003 Syphilis 58 0.036
334
CRY005 Cryptococcosis 58 0.036
335
CRD132 Cardiac Conduction Defect 58 0.036
336
DSS008 Disease of Mental Health 58 0.036
337
CRV038 Cervical Squamous Cell Carcinoma 58 0.036
338
LYM027 Lymphopenia 58 0.036
339
APL002 Aplasia of Lacrimal and Salivary Glands 57 0.036
340
GLS018 Glass Syndrome 57 0.036
341
P HDC001 Headache 57 0.036
342
P MYS005 Myositis 56 0.036
343
P ADL017 Adult T-Cell Leukemia 56 0.036
344
ACT058 Active Peptic Ulcer Disease 55 0.036
345
URN010 Urinary Tract Obstruction 55 0.036
346
P CYS039 Cystic Kidney Disease 54 0.036
347
PRT038 Protein-Energy Malnutrition 54 0.036
348
PSD007 Pseudomyxoma Peritonei 54 0.036
349
AMN001 Amenorrhea 54 0.036
350
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.036
351
c PSR017 Psoriasis 2 53 0.036
352
c PSR023 Psoriasis 1 52 0.036
353
HPT014 Hepatorenal Syndrome 50 0.036
354
c ACH020 Achromatopsia 2 50 0.036
355
DFF035 Diffuse Cutaneous Systemic Sclerosis 49 0.036
356
SPT005 Spotted Fever 49 0.036
357
TRT020 Tritanopia 49 0.036
358
c BCT013 Bacterial Pneumonia 48 0.036
359
ADT003 Auditory System Disease 48 0.036
360
CLC006 Calcinosis 48 0.036
361
P CLR019 Color Blindness 48 0.036
362
SPL018 Splenomegaly 48 0.036
363
P LYM024 Lymphatic System Disease 48 0.036
364
c PSR032 Psoriasis 11 47 0.036
365
GST071 Gastrointestinal Carcinoma 47 0.036
366
TNP001 Tinea Pedis 46 0.036
367
MXD026 Mixed Glioma 45 0.036
368
c TRC022 Tricuspid Valve Insufficiency 45 0.036
369
P CHR345 Chronic Pain 44 0.036
370
SBC016 Subacute Delirium 44 0.036
371
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.036
372
P HYP265 Hypotonia 43 0.036
373
c PSR028 Psoriasis 7 42 0.036
374
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.036
375
ATX019 Ataxia with Vitamin E Deficiency 42 0.036
376
OBS082 Obstructive Nephropathy 42 0.036
377
GST020 Gastric Antral Vascular Ectasia 41 0.036
378
CLR033 Color Vision Deficiency 41 0.036
379
DFF003 Diffuse Scleroderma 41 0.036
380
c PSR018 Psoriasis 13 41 0.036
381
RDN001 Reading Disorder 40 0.036
382
c PLY105 Polycystic Ovary Syndrome 1 38 0.036
383
c WLM011 Wilms Tumor 6 37 0.036
384
ENM002 Enamel Erosion 26 0.036
385
P NJM001 Nijmegen Breakage Syndrome 74 0.031
386
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.031
387
GST040 Gastric Adenocarcinoma 70 0.031
388
c PNC108 Pancreatitis, Hereditary 70 0.031
389
PLY001 Polycythemia Vera 69 0.031
390
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.031
391
MNT001 Mantle Cell Lymphoma 69 0.031
392
P ESS003 Essential Thrombocythemia 68 0.031
393
RCK004 Rickets 68 0.031
394
c INF071 Inflammatory Bowel Disease 1 67 0.031
395
FCT007 Factor Vii Deficiency 67 0.031
396
P FLL037 Follicular Lymphoma 67 0.031
397
PSY004 Psychotic Disorder 67 0.031
398
P LNG028 Long Qt Syndrome 66 0.031
399
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.031
400
c LNG044 Long Qt Syndrome 1 66 0.031
401
P ATR011 Atrial Fibrillation 66 0.031
402
KHL003 Kohlschutter-Tonz Syndrome 65 0.031
403
c FML001 Familial Atrial Fibrillation 65 0.031
404
PPL049 Papillon-Lefevre Syndrome 65 0.031
405
P MTR004 Maturity-Onset Diabetes of the Young 65 0.031
406
P PRS038 Personality Disorder 65 0.031
407
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.031
408
CTR172 Citrullinemia, Classic 64 0.031
409
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 64 0.031
410
MSC007 Muscle Hypertrophy 64 0.031
411
RBR001 Roberts Syndrome 64 0.031
412
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.031
413
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 63 0.031
414
TYP007 Typhoid Fever 63 0.031
415
P HYP069 Hyperparathyroidism 63 0.031
416
P CRG003 Crigler-Najjar Syndrome, Type I 63 0.031
417
CHN016 Cohen Syndrome 63 0.031
418
c ALP101 Alpha-Thalassemia 62 0.031
419
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.031
420
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.031
421
WLD007 Waldenstroem's Macroglobulinemia 61 0.031
422
P ACH003 Achromatopsia 61 0.031
423
ARG002 Argininosuccinic Aciduria 61 0.031
424
HRP004 Herpes Zoster 60 0.031
425
CHR288 Chronic Recurrent Multifocal Osteomyelitis 60 0.031
426
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.031
427
c HYP260 Hypophosphatemic Rickets, Autosomal Dominant 60 0.031
428
P SNS001 Sensorineural Hearing Loss 60 0.031
429
HYD002 Hydronephrosis 60 0.031
430
P CHR285 Chronic Myelomonocytic Leukemia 60 0.031
431
ORN008 Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to 59 0.031
432
P LYM033 Lymphoproliferative Syndrome 59 0.031
433
INC002 Inclusion Body Myositis 58 0.031
434
c ACT073 Acute Leukemia 58 0.031
435
SCR008 Scrub Typhus 58 0.031
436
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 58 0.031
437
c CHR417 Chronic Graft Versus Host Disease 57 0.031
438
ARG007 Argininemia 57 0.031
439
P CTR177 Citrullinemia, Type Ii, Adult-Onset 57 0.031
440
GLT035 Glutaric Acidemia I 57 0.031
441
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.031
442
AYM001 Ayme-Gripp Syndrome 57 0.031
443
P PLY018 Polycythemia 56 0.031
444
CMR002 Coumarin Resistance 56 0.031
445
HPT046 Hepatic Veno-Occlusive Disease 56 0.031
446
P MTC069 Mitochondrial Disorders 56 0.031
447
SPN041 Spinal Cord Disease 56 0.031
448
EPD002 Epidermolytic Hyperkeratosis 56 0.031
449
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.031
450
c MCR256 Microphthalmia, Syndromic 9 56 0.031
451
ORL005 Oral Candidiasis 56 0.031
452
c FML035 Familial Hyperlipidemia 55 0.031
453
DFF005 Diffuse Large B-Cell Lymphoma 55 0.031
454
ISV001 Isovaleric Acidemia 55 0.031
455
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.031
456
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 55 0.031
457
c OST163 Osteopetrosis, Autosomal Recessive 3 55 0.031
458
P CRB185 Cerebellar Ataxia, Mental Retardation, and Dysequilibrium Syndrome 1 55 0.031
459
c MTR020 Maturity-Onset Diabetes of the Young, Type 3 55 0.031
460
HRY003 Hairy Cell Leukemia 55 0.031
461
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.031
462
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.031
463
PRC013 Pericarditis 54 0.031
464
ANL018 Analbuminemia 54 0.031
465
LYM040 Lymphoblastic Lymphoma 54 0.031
466
P CNT005 Central Nervous System Lymphoma 53 0.031
467
P SHR001 Short Bowel Syndrome 53 0.031
468
P HMR003 Hemorrhagic Disease 53 0.031
469
FNG017 Fungal Infectious Disease 53 0.031
470
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.031
471
TXC002 Toxic Encephalopathy 53 0.031
472
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 53 0.031
473
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.031
474
ACR041 Acromelic Frontonasal Dysostosis 52 0.031
475
MRG003 Marginal Zone B-Cell Lymphoma 52 0.031
476
P DNT011 Dentinogenesis Imperfecta 52 0.031
477
NTR018 Neutrophilia, Hereditary 52 0.031
478
c ACT135 Acute Graft Versus Host Disease 52 0.031
479
SPS003 Spastic Diplegia 51 0.031
480
NPH003 Nephrocalcinosis 51 0.031
481
MTH078 Methylmalonic Aciduria, Cblb Type 51 0.031
482
AVD001 Avoidant Personality Disorder 51 0.031
483
PLS009 Plasma Cell Neoplasm 51 0.031
484
CLC001 Calciphylaxis 51 0.031
485
CYS036 Cystinosis, Nephropathic 51 0.031
486
SPL004 Splenic Marginal Zone Lymphoma 51 0.031
487
P RNL007 Renal Tubular Acidosis 51 0.031
488
c SCN007 Secondary Hyperparathyroidism 51 0.031
489
CRD229 Cardiomyopathy, Dilated, with Hypergonadotropic Hypogonadism 51 0.031
490
URC002 Urea Cycle Disorder 51 0.031
491
c ALM001 Al Amyloidosis 50 0.031
492
c PRM012 Primary Polycythemia 50 0.031
493
P FNC004 Fanconi Syndrome 50 0.031
494
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.031
495
BRN009 Burning Mouth Syndrome 50 0.031
496
c INF145 Infantile Liver Failure Syndrome 1 50 0.031
497
P MTH008 Methylmalonic Acidemia 50 0.031
498
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.031
499
RNL011 Renal Osteodystrophy 50 0.031
500
TCL002 T-Cell Large Granular Lymphocyte Leukemia 49 0.031
501
c THR090 Thrombocythemia 1 49 0.031
502
PRN014 Paronychia 49 0.031
503
MCR004 Macroglobulinemia 49 0.031
504
GST049 Gastrointestinal System Cancer 49 0.031
505
c FLL041 Follicular Lymphoma 1 49 0.031
506
P CRV031 Cervical Adenocarcinoma 49 0.031
507
MTC005 Mitochondrial Metabolism Disease 49 0.031
508
LRN003 Learning Disability 49 0.031
509
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.031
510
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.031
511
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.031
512
HYP025 Hyperphosphatemia 48 0.031
513
c PRM226 Primary Central Nervous System Lymphoma 48 0.031
514
ADN009 Adenosquamous Carcinoma 47 0.031
515
PRL017 Prolymphocytic Leukemia 47 0.031
516
RTC005 Reticulosarcoma 47 0.031
517
KHN001 Kuhnt-Junius Degeneration 47 0.031
518
LYM012 Lymphoplasmacytic Lymphoma 47 0.031
519
c INH020 Inherited Metabolic Disorder 47 0.031
520
c ADL052 Adult Acute Lymphocytic Leukemia 47 0.031
521
PLS025 Plasmablastic Lymphoma 47 0.031
522
ANV001 Anovulation 47 0.031
523
MNC019 Monocarboxylate Transporter 1 Deficiency 47 0.031
524
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.031
525
P ART106 Arterial Calcification, Generalized, of Infancy, 1 46 0.031
526
GNR003 Generalized Atherosclerosis 46 0.031
527
MTS001 Mutism 46 0.031
528
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 46 0.031
529
ANR004 Anuria 46 0.031
530
CNT025 Central Pontine Myelinolysis 46 0.031
531
EPD015 Epidemic Typhus 45 0.031
532
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.031
533
P PRD037 Periodontal Ehlers-Danlos Syndrome 45 0.031
534
P HYP733 Hypercalciuria, Absorptive, 2 45 0.031
535
EXT010 Extramedullary Plasmacytoma 45 0.031
536
NCT003 N-Acetylglutamate Synthase Deficiency 45 0.031
537
IMM136 Immune System Disease 45 0.031
538
BLC012 Bile Acid Malabsorption, Primary 45 0.031
539
c DRM054 Dermatitis, Atopic, 2 44 0.031
540
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.031
541
APP010 Appendix Cancer 44 0.031
542
ORG002 Organic Acidemia 44 0.031
543
GST027 Gastric Lymphoma 44 0.031
544
P HYP073 Hypersensitivity Reaction Type Iv Disease 44 0.031
545
SYR002 Syringocystadenoma Papilliferum 44 0.031
546
P BCT020 Bacteremia 2 44 0.031
547
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.031
548
BNM001 Bone Marrow Cancer 43 0.031
549
PLY068 Polysubstance Abuse 43 0.031
550
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 42 0.031
551
EXC002 Exocrine Pancreatic Insufficiency 42 0.031
552
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.031
553
c CTR132 Cataract 3, Multiple Types 41 0.031
554
DBT002 Diabetic Autonomic Neuropathy 41 0.031
555
LRG008 Large Granular Lymphocyte Leukemia 41 0.031
556
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 0.031
557
MNT303 Mental Retardation, X-Linked, Syndromic, Cabezas Type 41 0.031
558
HPR006 Heparin Cofactor Ii Deficiency 40 0.031
559
c HMG001 Hemoglobin C Disease 40 0.031
560
P FNC034 Fanconi Renotubular Syndrome 2 40 0.031
561
SPR126 Superior Semicircular Canal Dehiscence 40 0.031
562
ANG049 Angioedema Induced by Ace Inhibitors 40 0.031
563
P PRG092 Pregnancy Loss, Recurrent 1 40 0.031
564
MLN079 Melanoma in Congenital Melanocytic Nevus 39 0.031
565
AMN002 Amino Acid Metabolic Disorder 39 0.031
566
c ACH038 Achromatopsia 7 39 0.031
567
c HMG029 Hemoglobin Se Disease 39 0.031
568
P OTT001 Otitis Externa 39 0.031
569
c CHR682 Chronic Bilirubin Encephalopathy 39 0.031
570
AMN006 Aminoaciduria 38 0.031
571
c OVR114 Ovarian Cancer 1 38 0.031
572
c SYS043 Systemic Lupus Erythematosus 1 38 0.031
573
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.031
574
BRN135 Branched-Chain Keto Acid Dehydrogenase Kinase Deficiency 38 0.031
575
AKN002 Akinetic Mutism 37 0.031
576
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 36 0.031
577
SPT024 Spotted Fever Rickettsiosis 36 0.031
578
ADH001 Adhesions of Uterus 36 0.031
579
P YWS001 Yaws 36 0.031
580
PPT002 Peptic Ulcer Perforation 36 0.031
581
HYP114 Hypertensive Nephropathy 36 0.031
582
TNN002 Tinea Unguium 35 0.031
583
APP003 Appendiceal Neoplasm 34 0.031
584
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.031
585
c RNL113 Renal Failure, Progressive, with Hypertension 34 0.031
586
c CHR064 Chronic Monocytic Leukemia 33 0.031
587
RFR002 Refractory Hairy Cell Leukemia 33 0.031
588
P VSC018 Visceral Steatosis 33 0.031
589
BJL001 Bejel 32 0.031
590
IMM070 Immunodeficiency 13 32 0.031
591
ASH001 Asherman's Syndrome 31 0.031
592
P RNL115 Renal Tubular Acidosis, Proximal 31 0.031
593
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.031
594
ISL099 Isolated Methylmalonic Acidemia 29 0.031
595
SYN092 Syndromic X-Linked Intellectual Disability Cabezas Type 28 0.031
596
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.031
597
P OVR096 Overlap Myositis 27 0.031
598
OTM001 Otomycosis 27 0.031
599
CLS052 Classic Hairy Cell Leukemia 27 0.031
600
END014 Endemic Typhus 27 0.031
601
IDP001 Idiopathic Cd4-Positive T-Lymphocytopenia 27 0.031
602
CYT018 Cytochrome P450 2d6 Variant 27 0.031
603
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.031
604
P PRL012 Purulent Acute Otitis Media 26 0.031
605
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.031
606
c TRN053 Transient Pseudohypoaldosteronism 25 0.031
607
WLD006 Wild Type Abeta2m Amyloidosis 25 0.031
608
OVR027 Ovarian Squamous Cell Carcinoma 22 0.031
609
HML018 Homologous Wasting Disease 22 0.031
610
GYN002 Gynatresia 21 0.031
611
AMN012 Aminoacidopathies 21 0.031
612
RCK009 Rickettsial Disease 20 0.031
613
CRT064 Corticosterone Methyloxidase Deficiency 20 0.031
614
AMY010 Amyloidosis Beta2m 18 0.031
615
TRP010 Treponema Infection 17 0.031
616
GNY003 Guanylate Cyclase 2e, Pseudogene 14 0.031
617
P INB001 Inborn Amino Acid Metabolism Disorder 10 0.031
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