Search results for Cyanocobalamin

606 hits were found for Cyanocobalamin

# Family MCID Name MIFTS Score
1
VTM002 Vitamin B12 Deficiency 48 0.147
2
DFC004 Deficiency Anemia 70 0.106
3
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.102
4
PRN011 Pernicious Anemia 53 0.102
5
P LVR013 Liver Disease 68 0.067
6
MGL001 Megaloblastic Anemia 51 0.067
7
P MYC007 Myocardial Infarction 70 0.061
8
P NRP001 Neuropathy 56 0.061
9
CYN003 Cyanide Poisoning 24 0.061
10
STR067 Stroke, Ischemic 81 0.055
11
CRB039 Cerebrovascular Disease 67 0.055
12
NTR005 Nutritional Deficiency Disease 62 0.055
13
P CRD246 Cardiovascular System Disease 57 0.055
14
HMC014 Homocysteinemia 53 0.055
15
NRL016 Neural Tube Defects 82 0.047
16
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.047
17
P KDN018 Kidney Disease 72 0.047
18
ANG054 Angina Pectoris 66 0.047
19
ATH013 Atherosclerosis Susceptibility 65 0.047
20
P VSC007 Vascular Disease 63 0.047
21
P CRN300 Coronary Heart Disease 1 63 0.047
22
LPP008 Lipoprotein Quantitative Trait Locus 62 0.047
23
ISC004 Ischemia 58 0.047
24
c ACT075 Acute Myocardial Infarction 57 0.047
25
INT007 Intermediate Coronary Syndrome 55 0.047
26
P INF037 Inflammatory Bowel Disease 54 0.047
27
PRP080 Peripheral Artery Disease 53 0.047
28
ART140 Arteries, Anomalies of 52 0.047
29
END086 End Stage Renal Disease 51 0.047
30
P MTH008 Methylmalonic Acidemia 50 0.047
31
NRL018 Neural Tube Defects, Folate-Sensitive 48 0.047
32
PRS063 Paresthesia 41 0.047
33
P CRN133 Coronary Artery Disease, Autosomal Dominant, 1 32 0.047
34
ISL099 Isolated Methylmalonic Acidemia 29 0.047
35
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.039
36
AST005 Asthma 76 0.039
37
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.039
38
c THR092 Thrombophilia Due to Thrombin Defect 73 0.039
39
c CHR684 Chronic Kidney Disease 70 0.039
40
CNG034 Congestive Heart Failure 69 0.039
41
P MJR001 Major Depressive Disorder 68 0.039
42
c RHB024 Rhabdomyosarcoma 2 67 0.039
43
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.039
44
P MCR115 Microvascular Complications of Diabetes 5 66 0.039
45
P NRV007 Nervous System Disease 66 0.039
46
P PLM036 Pulmonary Fibrosis 65 0.039
47
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.039
48
P DBT009 Diabetes Mellitus 64 0.039
49
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.039
50
LPD008 Lipid Metabolism Disorder 62 0.039
51
ALL026 Allergic Hypersensitivity Disease 62 0.039
52
TXC005 Toxic Shock Syndrome 62 0.039
53
P ENC018 Encephalopathy 61 0.039
54
CHR066 Chronic Fatigue Syndrome 61 0.039
55
PLM033 Pulmonary Embolism 59 0.039
56
P URT039 Urticaria 58 0.039
57
P PRP019 Peripheral Nervous System Disease 58 0.039
58
IRN002 Iron Metabolism Disease 57 0.039
59
THR024 Thrombosis 57 0.039
60
P PLY019 Polyneuropathy 56 0.039
61
P DRR001 Diarrhea 55 0.039
62
GLC003 Glucose Intolerance 54 0.039
63
AMN001 Amenorrhea 54 0.039
64
PNC001 Pancytopenia 54 0.039
65
P HMC002 Homocystinuria 53 0.039
66
NRT004 Neuritis 52 0.039
67
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.039
68
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.039
69
HYP781 Hypoascorbemia 51 0.039
70
P ECL001 Eclampsia 50 0.039
71
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.039
72
PRD004 Prediabetes Syndrome 47 0.039
73
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.039
74
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.039
75
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.039
76
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.039
77
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.039
78
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.039
79
P CHR345 Chronic Pain 44 0.039
80
c PRM038 Primary Agammaglobulinemia 44 0.039
81
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.039
82
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.039
83
CYT002 Cytokine Deficiency 42 0.039
84
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.039
85
BCK006 Back Pain 42 0.039
86
ATX019 Ataxia with Vitamin E Deficiency 42 0.039
87
MTH056 Methylmalonic Aciduria and Homocystinuria, Cblf Type 38 0.039
88
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.039
89
P HPT023 Hepatocellular Carcinoma 100 0.027
90
P CLR023 Colorectal Cancer 99 0.027
91
P PRS040 Prostate Cancer 97 0.027
92
P BRS047 Breast Cancer 97 0.027
93
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.027
94
P OVR042 Ovarian Cancer 88 0.027
95
P ALZ034 Alzheimer Disease 88 0.027
96
c SYS001 Systemic Lupus Erythematosus 86 0.027
97
MYL069 Myeloma, Multiple 85 0.027
99
c LKM061 Leukemia, Acute Myeloid 84 0.027
100
c HYP595 Hypertension, Essential 84 0.027
101
P PNC035 Pancreatic Cancer 84 0.027
102
P GST053 Gastric Cancer 83 0.027
103
MLR004 Malaria 81 0.027
104
CYS001 Cystic Fibrosis 81 0.027
105
P GLM040 Glioma Susceptibility 1 81 0.027
106
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.027
107
P RHM011 Rheumatoid Arthritis 80 0.027
108
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.027
109
c NRF023 Neurofibromatosis, Type Ii 80 0.027
110
P BLD134 Bladder Cancer 79 0.027
111
IMM167 Immune Deficiency Disease 78 0.027
112
P LNG064 Lung Cancer Susceptibility 3 78 0.027
113
P PRK057 Parkinson Disease, Late-Onset 78 0.027
114
P HRT032 Heart Disease 75 0.027
115
PHN003 Phenylketonuria 75 0.027
116
GLB015 Glioblastoma Multiforme 75 0.027
117
c ATR087 Atrial Standstill 1 75 0.027
118
P RSP003 Respiratory Failure 74 0.027
119
BRN028 Brain Cancer 74 0.027
120
LPT014 Leptin Deficiency or Dysfunction 74 0.027
121
P SCH015 Schizophrenia 74 0.027
122
P OST002 Osteoporosis 74 0.027
123
CRH001 Crohn's Disease 74 0.027
124
c HYP836 Hypercholesterolemia, Familial, 1 73 0.027
125
ULC004 Ulcerative Colitis 73 0.027
126
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.027
127
P CNR004 Cone-Rod Dystrophy 2 73 0.027
128
ANX010 Anxiety 73 0.027
129
MSC157 Muscular Dystrophy, Duchenne Type 72 0.027
130
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.027
131
P MLT020 Multiple Sclerosis 72 0.027
132
c HPT073 Hepatitis C Virus 72 0.027
133
c LKM063 Leukemia, Chronic Myeloid 72 0.027
134
HMN044 Human Immunodeficiency Virus Type 1 71 0.027
135
PRP027 Peripheral Vascular Disease 71 0.027
136
BHC003 Behcet Syndrome 71 0.027
137
P EPL164 Epilepsy 71 0.027
138
P SRC025 Sarcoidosis 1 70 0.027
139
P ATS364 Autism 70 0.027
140
MYL009 Myelodysplastic Syndrome 70 0.027
141
DWN001 Down Syndrome 70 0.027
142
LGH007 Leigh Syndrome 70 0.027
143
ADL002 Adult Syndrome 70 0.027
144
CRT072 Creutzfeldt-Jakob Disease 70 0.027
145
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.027
146
PLM001 Pulmonary Tuberculosis 69 0.027
147
P MLN008 Melanoma 69 0.027
148
P ART022 Arthritis 69 0.027
149
ACR008 Acrocallosal Syndrome 69 0.027
150
CRB037 Cerebral Palsy 69 0.027
151
LYM133 Lymphoma, Hodgkin, Classic 69 0.027
152
P OCL013 Oculodentodigital Dysplasia 69 0.027
153
P HYP086 Hypothyroidism 69 0.027
154
P ANG001 Angelman Syndrome 69 0.027
155
P LKM062 Leukemia, Acute Lymphoblastic 69 0.027
156
P LYM118 Lymphoma 68 0.027
157
P PNM007 Pneumonia 68 0.027
158
P MYC084 Mycobacterium Tuberculosis 1 68 0.027
159
P LKM002 Leukemia 68 0.027
160
SKN019 Skin Melanoma 68 0.027
161
PCK003 Pick Disease of Brain 68 0.027
162
P INF038 Influenza 68 0.027
163
RCK004 Rickets 68 0.027
164
P FRN006 Frontotemporal Dementia 68 0.027
165
PNC129 Pancreatic Adenocarcinoma 68 0.027
166
P THR014 Thrombocytopenia 67 0.027
167
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.027
168
P HPT021 Hepatitis 67 0.027
169
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.027
170
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.027
171
c INF071 Inflammatory Bowel Disease 1 67 0.027
172
FCT007 Factor Vii Deficiency 67 0.027
173
P OLG002 Oligodendroglioma 67 0.027
174
PSY004 Psychotic Disorder 67 0.027
175
P PRP003 Porphyria Cutanea Tarda 67 0.027
176
P TRN020 Turner Syndrome 67 0.027
177
FLL027 Fallopian Tube Carcinoma 67 0.027
178
c ATS007 Autism Spectrum Disorder 67 0.027
179
CRP001 Carpal Tunnel Syndrome 67 0.027
180
MYC006 Mycosis Fungoides 66 0.027
181
P CLC063 Celiac Disease 1 66 0.027
182
ALC007 Alcohol Dependence 66 0.027
183
P DMN002 Dementia 66 0.027
184
P MSC005 Muscular Dystrophy 66 0.027
185
P NSP012 Nasopharyngeal Carcinoma 66 0.027
186
c MCR129 Microvascular Complications of Diabetes 1 66 0.027
187
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.027
188
HYP056 Hypoglycemia 66 0.027
189
P ATR011 Atrial Fibrillation 66 0.027
190
CHG001 Chagas Disease 66 0.027
191
P HYD006 Hydrocephalus 66 0.027
192
P MNN013 Meningitis 66 0.027
193
P DRM053 Dermatitis, Atopic 66 0.027
194
MYL031 Myeloproliferative Neoplasm 66 0.027
195
c SML038 Small Cell Cancer of the Lung 65 0.027
196
KHL003 Kohlschutter-Tonz Syndrome 65 0.027
197
TTN003 Tetanus 65 0.027
198
c FML001 Familial Atrial Fibrillation 65 0.027
199
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.027
200
P DYS154 Dystonia 65 0.027
201
DMN031 Dementia, Lewy Body 65 0.027
202
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 65 0.027
203
PPL049 Papillon-Lefevre Syndrome 65 0.027
204
P MTR014 Motor Neuron Disease 65 0.027
205
PRP001 Propionic Acidemia 65 0.027
206
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.027
207
PND002 Pendred Syndrome 65 0.027
208
c ART101 Aortic Valve Disease 2 65 0.027
209
PRT037 Pertussis 65 0.027
210
P PRS038 Personality Disorder 65 0.027
211
c DBT099 Diabetes Mellitus, Type I 65 0.027
212
P ADL010 Adult Respiratory Distress Syndrome 65 0.027
213
LYS012 Lysosomal Acid Lipase Deficiency 65 0.027
214
NRM005 Neuromuscular Disease 64 0.027
215
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.027
216
CLR108 Colorectal Adenoma 64 0.027
217
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.027
218
PLM031 Poliomyelitis 64 0.027
219
P ADN016 Adenocarcinoma 64 0.027
220
P GLM045 Glioma 63 0.027
221
c PRC016 Pre-Eclampsia 63 0.027
222
P NTR004 Neutropenia 63 0.027
223
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.027
224
CNT061 Conotruncal Heart Malformations 63 0.027
225
SKN016 Skin Disease 63 0.027
226
CHN016 Cohen Syndrome 63 0.027
227
P MVM001 Movement Disease 63 0.027
228
DPR016 Depression 63 0.027
229
c ALP101 Alpha-Thalassemia 62 0.027
230
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.027
231
HMT002 Hematologic Cancer 62 0.027
232
CLT003 Colitis 62 0.027
233
c FNC043 Fanconi Anemia, Complementation Group E 62 0.027
234
c HPT001 Hepatitis C 62 0.027
235
P PSR002 Psoriasis 62 0.027
236
c HPT003 Hepatitis a 62 0.027
237
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.027
238
c SVR001 Severe Acute Respiratory Syndrome 62 0.027
239
P HYP750 Hypertriglyceridemia, Familial 62 0.027
240
P ART023 Arthropathy 62 0.027
241
PHL006 Phelan-Mcdermid Syndrome 62 0.027
242
ATM095 Autoimmune Disease 62 0.027
243
CRC021 Carcinosarcoma 62 0.027
244
MDD011 Mood Disorder 62 0.027
245
MSS001 Masa Syndrome 62 0.027
246
LVR012 Liver Cirrhosis 62 0.027
247
BLD131 Bladder Urothelial Carcinoma 62 0.027
248
MSL001 Measles 62 0.027
249
P PRP029 Porphyria 62 0.027
250
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.027
251
PSR001 Psoriatic Arthritis 61 0.027
252
HYP066 Hyperglycemia 61 0.027
253
FTT001 Fatty Liver Disease 61 0.027
254
INT002 Intermittent Claudication 61 0.027
255
DRM006 Dermatitis 61 0.027
256
c PNS012 Paine Syndrome 61 0.027
257
WLD007 Waldenstroem's Macroglobulinemia 61 0.027
258
P PNC044 Pancreatitis 61 0.027
259
P SJG008 Sjogren Syndrome 61 0.027
260
GST033 Gestational Diabetes 61 0.027
261
VRL011 Viral Infectious Disease 61 0.027
262
P LPS004 Lupus Erythematosus 61 0.027
263
P MYL006 Myeloid Leukemia 60 0.027
264
SPN186 Spinal Cord Injury 60 0.027
265
HRP004 Herpes Zoster 60 0.027
266
SZR001 Sezary's Disease 60 0.027
267
P CRB101 Cerebrooculofacioskeletal Syndrome 1 60 0.027
268
DRR016 Diarrhea 2, with Microvillus Atrophy 60 0.027
269
DPH001 Diphtheria 60 0.027
270
P SCL018 Scoliosis 60 0.027
271
c ACT027 Acute Pancreatitis 60 0.027
272
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.027
273
ACQ007 Acquired Immunodeficiency Syndrome 60 0.027
274
LNG099 Lung Disease 60 0.027
275
SQM006 Squamous Cell Carcinoma 60 0.027
276
c HYP260 Hypophosphatemic Rickets, Autosomal Dominant 60 0.027
277
LBR030 Leber Optic Atrophy 60 0.027
278
CHC001 Chickenpox 60 0.027
279
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.027
280
c ACT071 Acute Kidney Failure 60 0.027
281
P THL005 Thalassemia 60 0.027
282
P HRD011 Hereditary Spherocytosis 60 0.027
283
P OPT006 Optic Nerve Disease 60 0.027
284
P RBL001 Rubella 59 0.027
285
PRT013 Portal Hypertension 59 0.027
286
P MCR010 Microcephaly 59 0.027
287
IDP011 Idiopathic Interstitial Pneumonia 59 0.027
288
c HPT016 Hepatitis B 59 0.027
289
P SLP005 Sleep Disorder 59 0.027
290
P LYM033 Lymphoproliferative Syndrome 59 0.027
291
VSL002 Visual Epilepsy 59 0.027
292
c LTN004 Late-Onset Retinal Degeneration 59 0.027
293
GRD007 Grade Iii Astrocytoma 59 0.027
294
IRN001 Iron Deficiency Anemia 59 0.027
295
ADN018 Adenoma 59 0.027
296
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.027
297
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 59 0.027
298
HLC007 Helicobacter Pylori Infection 59 0.027
299
PPT005 Peptic Ulcer Disease 59 0.027
300
RNL024 Renal Glucosuria 58 0.027
301
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.027
302
P ANP001 Anaplastic Large Cell Lymphoma 58 0.027
303
GLB001 Gilbert Syndrome 58 0.027
304
ERY029 Erythermalgia, Primary 58 0.027
305
P BCL017 B-Cell Lymphoma 58 0.027
306
CHR072 Chordoma 58 0.027
307
P ALC033 Alcohol Use Disorder 58 0.027
308
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.027
309
DSS008 Disease of Mental Health 58 0.027
310
P MMP001 Mumps 58 0.027
311
MNT002 Mental Depression 58 0.027
312
CNS004 Constipation 58 0.027
313
LYM027 Lymphopenia 58 0.027
314
P INF032 Infertility 57 0.027
315
GLS018 Glass Syndrome 57 0.027
316
P OPT009 Optic Neuritis 57 0.027
317
P EXN002 Exanthem 57 0.027
318
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.027
319
c MST023 Mesothelioma, Malignant 57 0.027
320
APH001 Aphthous Stomatitis 57 0.027
321
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.027
322
P PRV006 Pervasive Developmental Disorder 57 0.027
323
APH002 Aphasia 57 0.027
324
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.027
325
VSC002 Vascular Dementia 57 0.027
326
HMR039 Hemorrhage, Intracerebral 57 0.027
327
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.027
328
HYP266 Hypoxia 57 0.027
329
P BPL003 Bipolar Disorder 56 0.027
330
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.027
331
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 56 0.027
332
CMR002 Coumarin Resistance 56 0.027
333
P PLY011 Polycystic Ovary Syndrome 56 0.027
334
TRN018 Transitional Cell Carcinoma 56 0.027
335
LMY014 Leiomyoma, Uterine 56 0.027
336
P MTC069 Mitochondrial Disorders 56 0.027
337
BCT022 Bacterial Infectious Disease 56 0.027
338
P SZR006 Seizure Disorder 56 0.027
339
SCH003 Schizophreniform Disorder 56 0.027
340
HMG005 Hemoglobinopathy 56 0.027
341
GST050 Gastrointestinal System Disease 56 0.027
342
MCS002 Mucositis 56 0.027
343
BRN004 Brain Edema 56 0.027
344
AGN016 Aging 56 0.027
345
P GST044 Gastritis 56 0.027
346
c FML035 Familial Hyperlipidemia 55 0.027
347
HYP005 Hypokalemia 55 0.027
348
NRN004 Neuroendocrine Tumor 55 0.027
349
MCL006 Macular Retinal Edema 55 0.027
350
P MLN007 Male Infertility 55 0.027
351
P ANT006 Antiphospholipid Syndrome 55 0.027
352
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.027
353
P MYP006 Myopia 55 0.027
354
P SBS003 Substance Abuse 55 0.027
356
BRN045 Brunner Syndrome 55 0.027
357
END040 Endogenous Depression 55 0.027
358
HYP060 Hyperinsulinism 54 0.027
359
PRP030 Purpura 54 0.027
360
TRD006 Tardive Dyskinesia 54 0.027
361
GLS001 Gliosarcoma 54 0.027
362
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 54 0.027
363
ACD008 Acid-Labile Subunit Deficiency 54 0.027
364
MNN032 Meningococcal Meningitis 54 0.027
365
AMN003 Amnestic Disorder 54 0.027
366
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.027
367
PRT038 Protein-Energy Malnutrition 54 0.027
368
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.027
369
P ART021 Arteriosclerosis 54 0.027
370
DBT010 Diabetic Neuropathy 54 0.027
371
P LTR001 Lateral Sclerosis 54 0.027
372
LYM040 Lymphoblastic Lymphoma 54 0.027
373
PPL022 Papilloma 54 0.027
374
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.027
375
SNS003 Sensory Peripheral Neuropathy 54 0.027
376
P TRM003 Tremor 54 0.027
377
NNL006 Non-Alcoholic Steatohepatitis 54 0.027
378
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.027
379
PRP036 Peripheral T-Cell Lymphoma 53 0.027
380
P RTN016 Retinal Degeneration 53 0.027
381
P PLM006 Pulmonary Alveolar Proteinosis 53 0.027
382
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.027
383
P HMR003 Hemorrhagic Disease 53 0.027
384
FNG017 Fungal Infectious Disease 53 0.027
385
GTR002 Goiter 53 0.027
386
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.027
387
NRT001 Neurotic Disorder 53 0.027
388
TXC002 Toxic Encephalopathy 53 0.027
389
c PSR017 Psoriasis 2 53 0.027
390
P INT068 Intestinal Disease 53 0.027
391
P RTN018 Retinal Disease 53 0.027
392
c CNT035 Central Nervous System Disease 52 0.027
393
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.027
394
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.027
395
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.027
396
ACR041 Acromelic Frontonasal Dysostosis 52 0.027
397
PST011 Pustulosis of Palm and Sole 52 0.027
398
MRG003 Marginal Zone B-Cell Lymphoma 52 0.027
399
THY030 Thyroid Gland Disease 52 0.027
400
P MSC003 Muscular Atrophy 52 0.027
401
NRP045 Neuropathy, Ataxia, and Retinitis Pigmentosa 52 0.027
402
c PSR023 Psoriasis 1 52 0.027
403
BWN001 Bowen-Conradi Syndrome 52 0.027
404
HYP014 Hyperuricemia 52 0.027
405
LMY002 Leiomyoma 52 0.027
406
PNG002 Pain Agnosia 51 0.027
407
SPS003 Spastic Diplegia 51 0.027
408
MTH078 Methylmalonic Aciduria, Cblb Type 51 0.027
409
OCL069 Ocular Motor Apraxia 51 0.027
410
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.027
411
FDL002 Food Allergy 51 0.027
412
PLS009 Plasma Cell Neoplasm 51 0.027
413
c PRM108 Primary Progressive Multiple Sclerosis 51 0.027
414
LNG031 Lung Benign Neoplasm 51 0.027
415
TRM010 Traumatic Brain Injury 51 0.027
416
P THR015 Thrombophilia 51 0.027
417
BLL003 Bell's Palsy 51 0.027
418
P AST007 Astrocytoma 51 0.027
419
PNN001 Panniculitis 51 0.027
420
HYP081 Hypolipoproteinemia 51 0.027
421
GNT002 Giant Cell Glioblastoma 50 0.027
422
SCH012 Schizoaffective Disorder 50 0.027
423
PRS034 Parasitic Helminthiasis Infectious Disease 50 0.027
424
P OVR082 Overgrowth Syndrome 50 0.027
425
RDC002 Radiculopathy 50 0.027
426
PST021 Postpartum Depression 50 0.027
427
BRN009 Burning Mouth Syndrome 50 0.027
428
AZS001 Azoospermia 50 0.027
429
STM007 Stomatitis 50 0.027
430
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.027
431
PLC008 Placenta Disease 50 0.027
432
TRY001 Trypanosomiasis 50 0.027
433
LNG015 Lingual-Facial-Buccal Dyskinesia 50 0.027
434
PRN009 Paranoid Schizophrenia 50 0.027
435
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.027
436
DYS073 Dysphagia 50 0.027
437
P ATR005 Atrophic Gastritis 50 0.027
438
DBT004 Diabetic Polyneuropathy 49 0.027
439
VRC001 Varicocele 49 0.027
440
AMB002 Amblyopia 49 0.027
441
47X002 47,xyy 49 0.027
442
MCR004 Macroglobulinemia 49 0.027
443
BKR002 Baker-Gordon Syndrome 49 0.027
444
BRN071 Brain Injury 49 0.027
445
PTH002 Pathological Gambling 49 0.027
446
P CTN015 Cutaneous T Cell Lymphoma 49 0.027
447
DFN270 Deafness, Dystonia, and Cerebral Hypomyelination 48 0.027
448
VTM033 Vitamin K Deficiency Bleeding 48 0.027
449
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.027
450
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.027
451
DBT006 Diabetic Macular Edema 48 0.027
452
SPL018 Splenomegaly 48 0.027
453
LPT006 Leptin Receptor Deficiency 48 0.027
454
HPR003 Heparin-Induced Thrombocytopenia 48 0.027
455
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.027
456
c PSR032 Psoriasis 11 47 0.027
457
c MCR120 Microvascular Complications of Diabetes 7 47 0.027
458
c OPT050 Opitz Gbbb Syndrome, Type Ii 47 0.027
459
KRT002 Keratomalacia 47 0.027
460
GLS007 Glossitis 47 0.027
461
RTC005 Reticulosarcoma 47 0.027
462
LYM012 Lymphoplasmacytic Lymphoma 47 0.027
463
c INH020 Inherited Metabolic Disorder 47 0.027
464
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.027
465
c CNG216 Congenital Hydrocephalus 47 0.027
466
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.027
467
CNT033 Central Nervous System Cancer 47 0.027
468
TST044 Testicular Torsion 47 0.027
469
NSS002 Neisseria Meningitidis Infection 47 0.027
470
LYM019 Lymphosarcoma 46 0.027
471
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.027
472
MNN028 Mononeuropathy of the Median Nerve, Mild 46 0.027
473
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.027
474
BCK003 Background Diabetic Retinopathy 46 0.027
475
ORC001 Orchitis 46 0.027
476
MYC005 Myocardial Stunning 46 0.027
477
MNN020 Meningococcal Infection 46 0.027
478
P PLL002 Pellagra 46 0.027
479
P BNG032 Benign Mesothelioma 46 0.027
480
MTH021 Methylmalonic Acidemia with Homocystinuria 46 0.027
481
SQM002 Squamous Cell Papilloma 46 0.027
482
LKS001 Leukostasis 46 0.027
483
c DRR009 Diarrhea 6 46 0.027
484
c MLG068 Malignant Glioma 46 0.027
485
GLL048 Glial Tumor 45 0.027
486
TRN022 Transcobalamin Ii Deficiency 45 0.027
487
SYN036 Syncope 45 0.027
488
MXD026 Mixed Glioma 45 0.027
489
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.027
490
P OCY003 Oocyte Maturation Defect 1 45 0.027
491
URT051 Ureter, Cancer of 45 0.027
492
ATN004 Autonomic Neuropathy 45 0.027
493
MYF001 Myofibroma 45 0.027
494
c DRM054 Dermatitis, Atopic, 2 44 0.027
495
SBC016 Subacute Delirium 44 0.027
496
ORG002 Organic Acidemia 44 0.027
497
c GZP005 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 44 0.027
498
PRM003 Premature Ejaculation 44 0.027
499
PRT035 Peritoneum Cancer 44 0.027
500
c HYP272 Hypercholesterolemia, Familial, 3 44 0.027
501
P BCT020 Bacteremia 2 44 0.027
502
FNT005 Fontaine Progeroid Syndrome 44 0.027
503
c SPR086 Spermatogenic Failure 3 44 0.027
504
CVD001 Covid-19 44 0.027
505
P CRN024 Corneal Disease 44 0.027
506
ANP009 Anaplastic Oligodendroglioma 43 0.027
507
P IMR002 Imerslund-Grasbeck Syndrome 1 43 0.027
508
LWC001 Low Compliance Bladder 43 0.027
509
MDD018 Middle East Respiratory Syndrome 43 0.027
510
P HYP265 Hypotonia 43 0.027
511
HMP009 Haemophilus Influenzae 43 0.027
512
P MJR007 Major Affective Disorder 1 43 0.027
513
TRP009 Triple X Syndrome 42 0.027
514
c RTN047 Retinitis Pigmentosa 18 42 0.027
515
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.027
516
c PSR028 Psoriasis 7 42 0.027
517
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.027
518
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.027
519
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.027
520
c MLG079 Malignant Pleural Mesothelioma 42 0.027
521
IDP070 Idiopathic Scoliosis 42 0.027
522
GST020 Gastric Antral Vascular Ectasia 41 0.027
523
49X006 49, Xxxxy Syndrome 41 0.027
524
c ADV003 Advanced Sleep Phase Syndrome, Familial, 1 41 0.027
525
DBT002 Diabetic Autonomic Neuropathy 41 0.027
526
c PSR018 Psoriasis 13 41 0.027
527
c MJR024 Major Affective Disorder 9 41 0.027
528
P SCL057 Scoliosis, Isolated 1 41 0.027
529
P RRT020 Rare Tumor 41 0.027
530
c MCR112 Microvascular Complications of Diabetes 2 41 0.027
531
MRP001 Morphine Dependence 41 0.027
532
RDN001 Reading Disorder 40 0.027
533
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.027
534
HPR006 Heparin Cofactor Ii Deficiency 40 0.027
535
CYC005 Cyclothymic Disorder 40 0.027
536
NRV004 Nerve Compression Syndrome 40 0.027
537
P PRG092 Pregnancy Loss, Recurrent 1 40 0.027
538
AMN002 Amino Acid Metabolic Disorder 39 0.027
539
ULC007 Ulcerative Stomatitis 39 0.027
540
CRV045 Cervical Intraepithelial Neoplasia 39 0.027
541
SPP007 Suppression Amblyopia 39 0.027
542
48X005 48,xyyy 39 0.027
543
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.027
544
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 39 0.027
545
c CHR682 Chronic Bilirubin Encephalopathy 39 0.027
546
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.027
547
ETH004 Euthyroid Sick Syndrome 38 0.027
548
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.027
549
NDL024 Nodal Marginal Zone Lymphoma 38 0.027
550
P PRC031 Preeclampsia/eclampsia 1 38 0.027
551
c PLY105 Polycystic Ovary Syndrome 1 38 0.027
552
c OVR114 Ovarian Cancer 1 38 0.027
553
c SYS043 Systemic Lupus Erythematosus 1 38 0.027
554
c MJR022 Major Affective Disorder 8 38 0.027
555
HPT070 Hepatosplenic T-Cell Lymphoma 38 0.027
556
WGN007 Wagner Vitreoretinopathy 38 0.027
557
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.027
558
ATM052 Autoimmune Disease 1 37 0.027
559
HMC033 Homocystinuria-Megaloblastic Anemia, Cblg Complementation Type 36 0.027
560
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 36 0.027
561
WGN003 Wagner Syndrome 36 0.027
562
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.027
563
c MJR008 Major Affective Disorder 2 35 0.027
564
PRM155 Primary Cutaneous Anaplastic Large Cell Lymphoma 34 0.027
565
INT088 Intrinsic Factor Deficiency 34 0.027
566
PYR009 Pyridoxine Deficiency Anemia 34 0.027
567
CNG016 Congenital Intrinsic Factor Deficiency 34 0.027
568
c MJR023 Major Affective Disorder 7 33 0.027
569
PPL052 Papillomatosis, Confluent and Reticulated 33 0.027
570
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 33 0.027
571
ENC065 Encephalitis/encephalopathy, Mild, with Reversible Myelin Vacuolization 33 0.027
572
P VSC018 Visceral Steatosis 33 0.027
573
c MJR003 Major Affective Disorder 6 33 0.027
574
c MJR006 Major Affective Disorder 5 33 0.027
575
c PRS136 Prostate Cancer, Hereditary, 6 33 0.027
576
c SCH085 Schizophrenia 2 33 0.027
577
FLC001 Folic Acid Deficiency Anemia 32 0.027
578
c PRS130 Prostate Cancer, Hereditary, 8 32 0.027
579
TQP001 Taqi Polymorphism 32 0.027
580
PST103 Postpartum Psychosis 32 0.027
581
c SCH080 Schizophrenia 3 32 0.027
582
NNS045 Non-Specific Syndromic Intellectual Disability 31 0.027
583
ATR073 Atrophic Glossitis 31 0.027
584
STT009 Sutton Disease 2 30 0.027
585
c ALZ050 Alzheimer Disease 5 30 0.027
587
PYR016 Pyridoxine Deficiency 30 0.027
588
c MJR004 Major Affective Disorder 4 28 0.027
589
TMP019 Temporomandibular Joint Anomaly 28 0.027
590
TMR016 Tumor Suppressor Gene on Chromosome 11 28 0.027
591
MTH051 Methylmalonic Aciduria and Homocystinuria, Cblj Type 28 0.027
592
PRR019 Perioral Myoclonia with Absences 27 0.027
593
MLR020 Malaria, Mild 27 0.027
594
CHL079 Children's Interstitial Lung Disease 26 0.027
595
PGM030 Pigmentation Anomaly of the Skin 26 0.027
596
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.027
597
FRN030 Frontotemporal Dementia with Parkinsonism-17 24 0.027
598
TRN059 Transcobalamin Deficiency 23 0.027
599
HDG004 Hodgkin's Granuloma 23 0.027
600
c ATM060 Autoimmune Atrophic Gastritis 22 0.027
601
HDG006 Hodgkin's Paragranuloma 22 0.027
602
c NSP009 Nasopharyngeal Carcinoma 2 22 0.027
603
c IMR003 Imerslund-Grasbeck Syndrome 2 21 0.027
604
AMN012 Aminoacidopathies 21 0.027
605
LNR001 Leiner Disease 17 0.027
606
P INB001 Inborn Amino Acid Metabolism Disorder 10 0.027
Content
Loading form....