Search results for Hydroxocobalamin

588 hits were found for Hydroxocobalamin

# Family MCID Name MIFTS Score
1
CYN003 Cyanide Poisoning 24 0.225
2
VTM002 Vitamin B12 Deficiency 48 0.088
3
PRN011 Pernicious Anemia 53 0.078
4
MTB004 Metabolic Acidosis 50 0.078
5
DFC004 Deficiency Anemia 70 0.068
6
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.068
7
OCL069 Ocular Motor Apraxia 51 0.068
8
P MTH008 Methylmalonic Acidemia 50 0.068
9
P HMC002 Homocystinuria 53 0.062
10
P KDN018 Kidney Disease 72 0.055
11
P CRD119 Cardiac Arrest 67 0.055
12
P EXN002 Exanthem 57 0.055
13
DBT010 Diabetic Neuropathy 54 0.055
14
HMC014 Homocysteinemia 53 0.055
15
MGL001 Megaloblastic Anemia 51 0.055
16
END086 End Stage Renal Disease 51 0.055
17
DBT002 Diabetic Autonomic Neuropathy 41 0.055
18
ULC004 Ulcerative Colitis 73 0.048
19
P MLT020 Multiple Sclerosis 72 0.048
20
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.048
21
c INF071 Inflammatory Bowel Disease 1 67 0.048
22
c MCR129 Microvascular Complications of Diabetes 1 66 0.048
23
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.048
24
CLT003 Colitis 62 0.048
25
TXC005 Toxic Shock Syndrome 62 0.048
26
GLS018 Glass Syndrome 57 0.048
27
P NRP001 Neuropathy 56 0.048
28
P INF037 Inflammatory Bowel Disease 54 0.048
29
P MTH007 Methemoglobinemia 46 0.048
30
TRN022 Transcobalamin Ii Deficiency 45 0.048
31
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.048
32
DSR002 Disorders of Intracellular Cobalamin Metabolism 31 0.048
33
ISL099 Isolated Methylmalonic Acidemia 29 0.048
34
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.048
35
P PNC035 Pancreatic Cancer 84 0.039
36
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.039
37
LPT014 Leptin Deficiency or Dysfunction 74 0.039
38
c THR092 Thrombophilia Due to Thrombin Defect 73 0.039
39
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.039
40
P LVR013 Liver Disease 68 0.039
41
PNC129 Pancreatic Adenocarcinoma 68 0.039
42
P ADN016 Adenocarcinoma 64 0.039
43
P CRN300 Coronary Heart Disease 1 63 0.039
44
LPP008 Lipoprotein Quantitative Trait Locus 62 0.039
45
c ACT071 Acute Kidney Failure 60 0.039
46
P MCR010 Microcephaly 59 0.039
47
PLM033 Pulmonary Embolism 59 0.039
48
P URT039 Urticaria 58 0.039
49
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 54 0.039
50
NNL006 Non-Alcoholic Steatohepatitis 54 0.039
51
HRT012 Heart Valve Disease 53 0.039
52
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.039
53
ART140 Arteries, Anomalies of 52 0.039
54
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.039
55
P LCT001 Lactic Acidosis 51 0.039
56
HYP781 Hypoascorbemia 51 0.039
57
DYS073 Dysphagia 50 0.039
58
AMB002 Amblyopia 49 0.039
59
LPT006 Leptin Receptor Deficiency 48 0.039
60
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.039
61
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.039
62
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.039
63
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.039
64
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.039
65
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.039
66
CVD001 Covid-19 44 0.039
67
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.039
68
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.039
69
P HYP265 Hypotonia 43 0.039
70
SPP007 Suppression Amblyopia 39 0.039
71
HMC033 Homocystinuria-Megaloblastic Anemia, Cblg Complementation Type 36 0.039
72
ALC011 Alcoholic Neuropathy 34 0.039
73
c ACQ047 Acquired Methemoglobinemia 34 0.039
74
TRN059 Transcobalamin Deficiency 23 0.039
75
P HPT023 Hepatocellular Carcinoma 100 0.028
76
P CLR023 Colorectal Cancer 99 0.028
77
P PRS040 Prostate Cancer 97 0.028
78
P BRS047 Breast Cancer 97 0.028
79
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.028
80
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.028
81
P OVR042 Ovarian Cancer 88 0.028
82
P ALZ034 Alzheimer Disease 88 0.028
83
c SYS001 Systemic Lupus Erythematosus 86 0.028
84
MYL069 Myeloma, Multiple 85 0.028
85
c LKM061 Leukemia, Acute Myeloid 84 0.028
86
c HYP595 Hypertension, Essential 84 0.028
87
P GST053 Gastric Cancer 83 0.028
88
NRL016 Neural Tube Defects 82 0.028
89
MLR004 Malaria 81 0.028
90
CYS001 Cystic Fibrosis 81 0.028
91
P GLM040 Glioma Susceptibility 1 81 0.028
92
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.028
93
STR067 Stroke, Ischemic 81 0.028
94
P RHM011 Rheumatoid Arthritis 80 0.028
95
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.028
96
c NRF023 Neurofibromatosis, Type Ii 80 0.028
97
P BLD134 Bladder Cancer 79 0.028
98
IMM167 Immune Deficiency Disease 78 0.028
99
P LNG064 Lung Cancer Susceptibility 3 78 0.028
100
P PRK057 Parkinson Disease, Late-Onset 78 0.028
101
AST005 Asthma 76 0.028
102
P HRT032 Heart Disease 75 0.028
103
PHN003 Phenylketonuria 75 0.028
104
GLB015 Glioblastoma Multiforme 75 0.028
105
c ATR087 Atrial Standstill 1 75 0.028
106
P RSP003 Respiratory Failure 74 0.028
107
BRN028 Brain Cancer 74 0.028
108
P SCH015 Schizophrenia 74 0.028
109
P OST002 Osteoporosis 74 0.028
110
c HYP836 Hypercholesterolemia, Familial, 1 73 0.028
111
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.028
112
P CNR004 Cone-Rod Dystrophy 2 73 0.028
113
ANX010 Anxiety 73 0.028
114
MSC157 Muscular Dystrophy, Duchenne Type 72 0.028
115
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.028
116
c HPT073 Hepatitis C Virus 72 0.028
117
HMN044 Human Immunodeficiency Virus Type 1 71 0.028
118
PRP027 Peripheral Vascular Disease 71 0.028
119
BHC003 Behcet Syndrome 71 0.028
120
P EPL164 Epilepsy 71 0.028
121
P SRC025 Sarcoidosis 1 70 0.028
122
P ATS364 Autism 70 0.028
123
P MYC007 Myocardial Infarction 70 0.028
124
MYL009 Myelodysplastic Syndrome 70 0.028
125
LGH007 Leigh Syndrome 70 0.028
126
c CHR684 Chronic Kidney Disease 70 0.028
127
ADL002 Adult Syndrome 70 0.028
128
CNG034 Congestive Heart Failure 69 0.028
129
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.028
130
PLM001 Pulmonary Tuberculosis 69 0.028
131
P MLN008 Melanoma 69 0.028
132
P ART022 Arthritis 69 0.028
133
ACR008 Acrocallosal Syndrome 69 0.028
134
CRB037 Cerebral Palsy 69 0.028
135
LYM133 Lymphoma, Hodgkin, Classic 69 0.028
136
P OCL013 Oculodentodigital Dysplasia 69 0.028
137
P HYP086 Hypothyroidism 69 0.028
138
P ANG001 Angelman Syndrome 69 0.028
139
P LKM062 Leukemia, Acute Lymphoblastic 69 0.028
140
P LYM118 Lymphoma 68 0.028
141
P PNM007 Pneumonia 68 0.028
142
P MYC084 Mycobacterium Tuberculosis 1 68 0.028
143
P LKM002 Leukemia 68 0.028
144
SKN019 Skin Melanoma 68 0.028
145
PCK003 Pick Disease of Brain 68 0.028
146
P INF038 Influenza 68 0.028
147
RCK004 Rickets 68 0.028
148
P MJR001 Major Depressive Disorder 68 0.028
149
P FRN006 Frontotemporal Dementia 68 0.028
150
P THR014 Thrombocytopenia 67 0.028
151
P HPT021 Hepatitis 67 0.028
152
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.028
153
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.028
154
FCT007 Factor Vii Deficiency 67 0.028
155
P OLG002 Oligodendroglioma 67 0.028
156
CRB039 Cerebrovascular Disease 67 0.028
157
PSY004 Psychotic Disorder 67 0.028
158
P TRN020 Turner Syndrome 67 0.028
159
FLL027 Fallopian Tube Carcinoma 67 0.028
160
c ATS007 Autism Spectrum Disorder 67 0.028
161
CRP001 Carpal Tunnel Syndrome 67 0.028
162
c MGR028 Migraine with or Without Aura 1 67 0.028
163
c RHB024 Rhabdomyosarcoma 2 67 0.028
164
MYC006 Mycosis Fungoides 66 0.028
165
P CLC063 Celiac Disease 1 66 0.028
166
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.028
167
ALC007 Alcohol Dependence 66 0.028
168
ANG054 Angina Pectoris 66 0.028
169
P DMN002 Dementia 66 0.028
170
P MSC005 Muscular Dystrophy 66 0.028
171
P NSP012 Nasopharyngeal Carcinoma 66 0.028
172
P MCR115 Microvascular Complications of Diabetes 5 66 0.028
173
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.028
174
HYP056 Hypoglycemia 66 0.028
175
P ATR011 Atrial Fibrillation 66 0.028
176
P HYD006 Hydrocephalus 66 0.028
177
P MNN013 Meningitis 66 0.028
178
P DRM053 Dermatitis, Atopic 66 0.028
179
MYL031 Myeloproliferative Neoplasm 66 0.028
180
P NRV007 Nervous System Disease 66 0.028
181
c SML038 Small Cell Cancer of the Lung 65 0.028
182
KHL003 Kohlschutter-Tonz Syndrome 65 0.028
183
P PLM036 Pulmonary Fibrosis 65 0.028
184
TTN003 Tetanus 65 0.028
185
c FML001 Familial Atrial Fibrillation 65 0.028
186
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.028
187
P DYS154 Dystonia 65 0.028
188
DMN031 Dementia, Lewy Body 65 0.028
189
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 65 0.028
190
PPL049 Papillon-Lefevre Syndrome 65 0.028
191
P MTR014 Motor Neuron Disease 65 0.028
192
PRP001 Propionic Acidemia 65 0.028
193
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.028
194
PND002 Pendred Syndrome 65 0.028
195
c ART101 Aortic Valve Disease 2 65 0.028
196
PRT037 Pertussis 65 0.028
197
ATH013 Atherosclerosis Susceptibility 65 0.028
198
P PRS038 Personality Disorder 65 0.028
199
c DBT099 Diabetes Mellitus, Type I 65 0.028
200
P ADL010 Adult Respiratory Distress Syndrome 65 0.028
201
LYS012 Lysosomal Acid Lipase Deficiency 65 0.028
202
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.028
203
P DBT009 Diabetes Mellitus 64 0.028
204
NRM005 Neuromuscular Disease 64 0.028
205
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.028
206
CLR108 Colorectal Adenoma 64 0.028
207
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.028
208
PLM031 Poliomyelitis 64 0.028
209
P GLM045 Glioma 63 0.028
210
c PRC016 Pre-Eclampsia 63 0.028
211
P NTR004 Neutropenia 63 0.028
212
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.028
213
P VSC007 Vascular Disease 63 0.028
214
CNT061 Conotruncal Heart Malformations 63 0.028
215
SKN016 Skin Disease 63 0.028
216
CHN016 Cohen Syndrome 63 0.028
217
P MVM001 Movement Disease 63 0.028
218
DPR016 Depression 63 0.028
219
c ALP101 Alpha-Thalassemia 62 0.028
220
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.028
221
HMT002 Hematologic Cancer 62 0.028
222
LPD008 Lipid Metabolism Disorder 62 0.028
223
c FNC043 Fanconi Anemia, Complementation Group E 62 0.028
224
c HPT001 Hepatitis C 62 0.028
225
P PSR002 Psoriasis 62 0.028
226
c HPT003 Hepatitis a 62 0.028
227
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.028
228
c SVR001 Severe Acute Respiratory Syndrome 62 0.028
229
P HYP750 Hypertriglyceridemia, Familial 62 0.028
230
P ART023 Arthropathy 62 0.028
231
PHL006 Phelan-Mcdermid Syndrome 62 0.028
232
ATM095 Autoimmune Disease 62 0.028
233
ALL026 Allergic Hypersensitivity Disease 62 0.028
234
MDD011 Mood Disorder 62 0.028
235
MSS001 Masa Syndrome 62 0.028
236
LVR012 Liver Cirrhosis 62 0.028
237
BLD131 Bladder Urothelial Carcinoma 62 0.028
238
MSL001 Measles 62 0.028
239
NTR005 Nutritional Deficiency Disease 62 0.028
240
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.028
241
HYP066 Hyperglycemia 61 0.028
242
FTT001 Fatty Liver Disease 61 0.028
243
INT002 Intermittent Claudication 61 0.028
244
DRM006 Dermatitis 61 0.028
245
c PNS012 Paine Syndrome 61 0.028
246
CHR066 Chronic Fatigue Syndrome 61 0.028
247
WLD007 Waldenstroem's Macroglobulinemia 61 0.028
248
P PNC044 Pancreatitis 61 0.028
249
P SJG008 Sjogren Syndrome 61 0.028
250
GST033 Gestational Diabetes 61 0.028
251
VRL011 Viral Infectious Disease 61 0.028
252
P LPS004 Lupus Erythematosus 61 0.028
253
P MYL006 Myeloid Leukemia 60 0.028
254
SPN186 Spinal Cord Injury 60 0.028
255
PTN001 Patent Foramen Ovale 60 0.028
256
SZR001 Sezary's Disease 60 0.028
257
P CRB101 Cerebrooculofacioskeletal Syndrome 1 60 0.028
258
DRR016 Diarrhea 2, with Microvillus Atrophy 60 0.028
259
DPH001 Diphtheria 60 0.028
260
P SCL018 Scoliosis 60 0.028
261
c ACT027 Acute Pancreatitis 60 0.028
262
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.028
263
ACQ007 Acquired Immunodeficiency Syndrome 60 0.028
264
LNG099 Lung Disease 60 0.028
265
SQM006 Squamous Cell Carcinoma 60 0.028
266
c HYP260 Hypophosphatemic Rickets, Autosomal Dominant 60 0.028
267
LBR030 Leber Optic Atrophy 60 0.028
268
CHC001 Chickenpox 60 0.028
269
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.028
270
P THL005 Thalassemia 60 0.028
271
P RBL001 Rubella 59 0.028
272
PRT013 Portal Hypertension 59 0.028
273
IDP011 Idiopathic Interstitial Pneumonia 59 0.028
274
c HPT016 Hepatitis B 59 0.028
275
P SLP005 Sleep Disorder 59 0.028
276
P LYM033 Lymphoproliferative Syndrome 59 0.028
277
VSL002 Visual Epilepsy 59 0.028
278
c LTN004 Late-Onset Retinal Degeneration 59 0.028
279
GRD007 Grade Iii Astrocytoma 59 0.028
280
IRN001 Iron Deficiency Anemia 59 0.028
281
ADN018 Adenoma 59 0.028
282
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.028
283
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 59 0.028
284
HLC007 Helicobacter Pylori Infection 59 0.028
285
RNL024 Renal Glucosuria 58 0.028
286
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.028
287
P ANP001 Anaplastic Large Cell Lymphoma 58 0.028
288
GLB001 Gilbert Syndrome 58 0.028
289
ISC004 Ischemia 58 0.028
290
RBS001 Rabies 58 0.028
291
ERY029 Erythermalgia, Primary 58 0.028
292
P BCL017 B-Cell Lymphoma 58 0.028
293
CHR072 Chordoma 58 0.028
294
P ALC033 Alcohol Use Disorder 58 0.028
295
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.028
296
DSS008 Disease of Mental Health 58 0.028
297
P MMP001 Mumps 58 0.028
298
MNT002 Mental Depression 58 0.028
299
CNS004 Constipation 58 0.028
300
LYM027 Lymphopenia 58 0.028
301
P PRP019 Peripheral Nervous System Disease 58 0.028
302
P INF032 Infertility 57 0.028
303
P OPT009 Optic Neuritis 57 0.028
304
IRN002 Iron Metabolism Disease 57 0.028
305
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.028
306
c ACT075 Acute Myocardial Infarction 57 0.028
307
THR024 Thrombosis 57 0.028
308
c MST023 Mesothelioma, Malignant 57 0.028
309
APH001 Aphthous Stomatitis 57 0.028
310
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.028
311
P PRV006 Pervasive Developmental Disorder 57 0.028
312
APH002 Aphasia 57 0.028
313
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.028
314
P CRD246 Cardiovascular System Disease 57 0.028
315
VSC002 Vascular Dementia 57 0.028
316
HMR039 Hemorrhage, Intracerebral 57 0.028
317
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.028
318
HYP266 Hypoxia 57 0.028
319
P BPL003 Bipolar Disorder 56 0.028
320
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.028
321
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 56 0.028
322
CMR002 Coumarin Resistance 56 0.028
323
P PLY011 Polycystic Ovary Syndrome 56 0.028
324
TRN018 Transitional Cell Carcinoma 56 0.028
325
LMY014 Leiomyoma, Uterine 56 0.028
326
P MTC069 Mitochondrial Disorders 56 0.028
327
BCT022 Bacterial Infectious Disease 56 0.028
328
P SZR006 Seizure Disorder 56 0.028
329
SCH003 Schizophreniform Disorder 56 0.028
330
HMG005 Hemoglobinopathy 56 0.028
331
GST050 Gastrointestinal System Disease 56 0.028
332
MCS002 Mucositis 56 0.028
333
BRN004 Brain Edema 56 0.028
334
P PLY019 Polyneuropathy 56 0.028
335
AGN016 Aging 56 0.028
336
P GST044 Gastritis 56 0.028
337
c FML035 Familial Hyperlipidemia 55 0.028
338
HYP005 Hypokalemia 55 0.028
339
NRN004 Neuroendocrine Tumor 55 0.028
340
MCL006 Macular Retinal Edema 55 0.028
341
P MLN007 Male Infertility 55 0.028
342
P DRR001 Diarrhea 55 0.028
343
P ANT006 Antiphospholipid Syndrome 55 0.028
344
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.028
345
P SBS003 Substance Abuse 55 0.028
347
BRN045 Brunner Syndrome 55 0.028
348
END040 Endogenous Depression 55 0.028
349
INT007 Intermediate Coronary Syndrome 55 0.028
350
HYP060 Hyperinsulinism 54 0.028
351
PRP030 Purpura 54 0.028
352
TRD006 Tardive Dyskinesia 54 0.028
353
GLS001 Gliosarcoma 54 0.028
354
ACD008 Acid-Labile Subunit Deficiency 54 0.028
355
MNN032 Meningococcal Meningitis 54 0.028
356
AMN003 Amnestic Disorder 54 0.028
357
GLC003 Glucose Intolerance 54 0.028
358
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.028
359
PRT038 Protein-Energy Malnutrition 54 0.028
360
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.028
361
P ART021 Arteriosclerosis 54 0.028
362
AMN001 Amenorrhea 54 0.028
363
P LTR001 Lateral Sclerosis 54 0.028
364
LYM040 Lymphoblastic Lymphoma 54 0.028
365
PPL022 Papilloma 54 0.028
366
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.028
367
SNS003 Sensory Peripheral Neuropathy 54 0.028
368
P TRM003 Tremor 54 0.028
369
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.028
370
PRP036 Peripheral T-Cell Lymphoma 53 0.028
371
P RTN016 Retinal Degeneration 53 0.028
372
P PLM006 Pulmonary Alveolar Proteinosis 53 0.028
373
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.028
374
P HMR003 Hemorrhagic Disease 53 0.028
375
FNG017 Fungal Infectious Disease 53 0.028
376
GTR002 Goiter 53 0.028
377
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.028
378
NRT001 Neurotic Disorder 53 0.028
379
TXC002 Toxic Encephalopathy 53 0.028
380
PRP080 Peripheral Artery Disease 53 0.028
381
c PSR017 Psoriasis 2 53 0.028
382
P RTN018 Retinal Disease 53 0.028
383
c CNT035 Central Nervous System Disease 52 0.028
384
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.028
385
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.028
386
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.028
387
ACR041 Acromelic Frontonasal Dysostosis 52 0.028
388
NRT004 Neuritis 52 0.028
389
PST011 Pustulosis of Palm and Sole 52 0.028
390
MRG003 Marginal Zone B-Cell Lymphoma 52 0.028
391
THY030 Thyroid Gland Disease 52 0.028
392
P MSC003 Muscular Atrophy 52 0.028
393
NRP045 Neuropathy, Ataxia, and Retinitis Pigmentosa 52 0.028
394
c PSR023 Psoriasis 1 52 0.028
395
BWN001 Bowen-Conradi Syndrome 52 0.028
396
PTH003 Pathologic Nystagmus 52 0.028
397
HYP014 Hyperuricemia 52 0.028
398
LMY002 Leiomyoma 52 0.028
399
PNG002 Pain Agnosia 51 0.028
400
SPS003 Spastic Diplegia 51 0.028
401
MTH078 Methylmalonic Aciduria, Cblb Type 51 0.028
402
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.028
403
FDL002 Food Allergy 51 0.028
404
PLS009 Plasma Cell Neoplasm 51 0.028
405
c PRM108 Primary Progressive Multiple Sclerosis 51 0.028
406
LNG031 Lung Benign Neoplasm 51 0.028
407
TRM010 Traumatic Brain Injury 51 0.028
408
P THR015 Thrombophilia 51 0.028
409
P AST007 Astrocytoma 51 0.028
410
PNN001 Panniculitis 51 0.028
411
HYP081 Hypolipoproteinemia 51 0.028
412
GNT002 Giant Cell Glioblastoma 50 0.028
413
SCH012 Schizoaffective Disorder 50 0.028
414
PRS034 Parasitic Helminthiasis Infectious Disease 50 0.028
415
P OVR082 Overgrowth Syndrome 50 0.028
416
P ECL001 Eclampsia 50 0.028
417
PST021 Postpartum Depression 50 0.028
418
BRN009 Burning Mouth Syndrome 50 0.028
419
AZS001 Azoospermia 50 0.028
420
STM007 Stomatitis 50 0.028
421
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.028
422
PLC008 Placenta Disease 50 0.028
423
LNG015 Lingual-Facial-Buccal Dyskinesia 50 0.028
424
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.028
425
P ATR005 Atrophic Gastritis 50 0.028
426
DBT004 Diabetic Polyneuropathy 49 0.028
427
VRC001 Varicocele 49 0.028
428
47X002 47,xyy 49 0.028
429
MCR004 Macroglobulinemia 49 0.028
430
BKR002 Baker-Gordon Syndrome 49 0.028
431
BRN071 Brain Injury 49 0.028
432
PTH002 Pathological Gambling 49 0.028
433
P CTN015 Cutaneous T Cell Lymphoma 49 0.028
434
NRL018 Neural Tube Defects, Folate-Sensitive 48 0.028
435
DFN270 Deafness, Dystonia, and Cerebral Hypomyelination 48 0.028
436
VTM033 Vitamin K Deficiency Bleeding 48 0.028
437
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.028
438
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.028
439
DBT006 Diabetic Macular Edema 48 0.028
440
SPL018 Splenomegaly 48 0.028
441
HPR003 Heparin-Induced Thrombocytopenia 48 0.028
442
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.028
443
PRD004 Prediabetes Syndrome 47 0.028
444
c PSR032 Psoriasis 11 47 0.028
445
c MCR120 Microvascular Complications of Diabetes 7 47 0.028
446
c OPT050 Opitz Gbbb Syndrome, Type Ii 47 0.028
447
KRT002 Keratomalacia 47 0.028
448
GLS007 Glossitis 47 0.028
449
RTC005 Reticulosarcoma 47 0.028
450
LYM012 Lymphoplasmacytic Lymphoma 47 0.028
451
c INH020 Inherited Metabolic Disorder 47 0.028
452
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.028
453
c CNG216 Congenital Hydrocephalus 47 0.028
454
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.028
455
CNT033 Central Nervous System Cancer 47 0.028
456
TST044 Testicular Torsion 47 0.028
457
NSS002 Neisseria Meningitidis Infection 47 0.028
458
LYM019 Lymphosarcoma 46 0.028
459
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.028
460
MNN028 Mononeuropathy of the Median Nerve, Mild 46 0.028
461
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.028
462
BCK003 Background Diabetic Retinopathy 46 0.028
463
ORC001 Orchitis 46 0.028
464
MYC005 Myocardial Stunning 46 0.028
465
MNN020 Meningococcal Infection 46 0.028
466
P BNG032 Benign Mesothelioma 46 0.028
467
MTH021 Methylmalonic Acidemia with Homocystinuria 46 0.028
468
SQM002 Squamous Cell Papilloma 46 0.028
469
LKS001 Leukostasis 46 0.028
470
c DRR009 Diarrhea 6 46 0.028
471
c MLG068 Malignant Glioma 46 0.028
472
GLL048 Glial Tumor 45 0.028
473
SYN036 Syncope 45 0.028
474
MXD026 Mixed Glioma 45 0.028
475
CYN002 Cyanosis, Transient Neonatal 45 0.028
476
P OCY003 Oocyte Maturation Defect 1 45 0.028
477
URT051 Ureter, Cancer of 45 0.028
478
ATN004 Autonomic Neuropathy 45 0.028
479
MYF001 Myofibroma 45 0.028
480
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.028
481
c DRM054 Dermatitis, Atopic, 2 44 0.028
482
P CHR345 Chronic Pain 44 0.028
483
SBC016 Subacute Delirium 44 0.028
484
ORG002 Organic Acidemia 44 0.028
485
c GZP005 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 44 0.028
486
PRM003 Premature Ejaculation 44 0.028
487
PRT035 Peritoneum Cancer 44 0.028
488
c HYP272 Hypercholesterolemia, Familial, 3 44 0.028
489
P BCT020 Bacteremia 2 44 0.028
490
FNT005 Fontaine Progeroid Syndrome 44 0.028
491
c PRM038 Primary Agammaglobulinemia 44 0.028
492
c SPR086 Spermatogenic Failure 3 44 0.028
493
P CRN024 Corneal Disease 44 0.028
494
CRB090 Cerebral Hypoxia 44 0.028
495
ANP009 Anaplastic Oligodendroglioma 43 0.028
496
LWC001 Low Compliance Bladder 43 0.028
497
MDD018 Middle East Respiratory Syndrome 43 0.028
498
HMP009 Haemophilus Influenzae 43 0.028
499
P MJR007 Major Affective Disorder 1 43 0.028
500
TRP009 Triple X Syndrome 42 0.028
501
CYT002 Cytokine Deficiency 42 0.028
502
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.028
503
c PSR028 Psoriasis 7 42 0.028
504
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.028
505
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.028
506
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.028
507
BCK006 Back Pain 42 0.028
508
ATX019 Ataxia with Vitamin E Deficiency 42 0.028
509
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.028
510
c MLG079 Malignant Pleural Mesothelioma 42 0.028
511
IDP070 Idiopathic Scoliosis 42 0.028
512
GST020 Gastric Antral Vascular Ectasia 41 0.028
513
49X006 49, Xxxxy Syndrome 41 0.028
514
c ADV003 Advanced Sleep Phase Syndrome, Familial, 1 41 0.028
515
c PSR018 Psoriasis 13 41 0.028
516
c MJR024 Major Affective Disorder 9 41 0.028
517
P SCL057 Scoliosis, Isolated 1 41 0.028
518
P RRT020 Rare Tumor 41 0.028
519
c MCR112 Microvascular Complications of Diabetes 2 41 0.028
520
RDN001 Reading Disorder 40 0.028
521
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.028
522
ANX004 Anoxia 40 0.028
523
HPR006 Heparin Cofactor Ii Deficiency 40 0.028
524
CYC005 Cyclothymic Disorder 40 0.028
525
NRV004 Nerve Compression Syndrome 40 0.028
526
P PRG092 Pregnancy Loss, Recurrent 1 40 0.028
527
AMN002 Amino Acid Metabolic Disorder 39 0.028
528
ULC007 Ulcerative Stomatitis 39 0.028
529
CRV045 Cervical Intraepithelial Neoplasia 39 0.028
530
48X005 48,xyyy 39 0.028
531
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.028
532
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 39 0.028
533
c CHR682 Chronic Bilirubin Encephalopathy 39 0.028
534
ETH004 Euthyroid Sick Syndrome 38 0.028
535
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.028
536
NDL024 Nodal Marginal Zone Lymphoma 38 0.028
537
MTH055 Methylmalonic Aciduria and Homocystinuria, Cbld Type 38 0.028
538
P PRC031 Preeclampsia/eclampsia 1 38 0.028
539
c PLY105 Polycystic Ovary Syndrome 1 38 0.028
540
c OVR114 Ovarian Cancer 1 38 0.028
541
MTH056 Methylmalonic Aciduria and Homocystinuria, Cblf Type 38 0.028
542
c SYS043 Systemic Lupus Erythematosus 1 38 0.028
543
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.028
544
c MJR022 Major Affective Disorder 8 38 0.028
545
HPT070 Hepatosplenic T-Cell Lymphoma 38 0.028
546
WGN007 Wagner Vitreoretinopathy 38 0.028
547
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.028
548
ATM052 Autoimmune Disease 1 37 0.028
549
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 36 0.028
550
WGN003 Wagner Syndrome 36 0.028
551
CRY036 Cryptogenic Cirrhosis 36 0.028
552
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.028
553
c MJR008 Major Affective Disorder 2 35 0.028
554
PRM155 Primary Cutaneous Anaplastic Large Cell Lymphoma 34 0.028
555
PYR009 Pyridoxine Deficiency Anemia 34 0.028
556
c MJR023 Major Affective Disorder 7 33 0.028
557
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 33 0.028
558
ENC065 Encephalitis/encephalopathy, Mild, with Reversible Myelin Vacuolization 33 0.028
559
P VSC018 Visceral Steatosis 33 0.028
560
c MJR003 Major Affective Disorder 6 33 0.028
561
c MJR006 Major Affective Disorder 5 33 0.028
562
c PRS136 Prostate Cancer, Hereditary, 6 33 0.028
563
c SCH085 Schizophrenia 2 33 0.028
564
FLC001 Folic Acid Deficiency Anemia 32 0.028
565
c PRS130 Prostate Cancer, Hereditary, 8 32 0.028
566
TQP001 Taqi Polymorphism 32 0.028
567
P CRN133 Coronary Artery Disease, Autosomal Dominant, 1 32 0.028
568
c SCH080 Schizophrenia 3 32 0.028
569
NNS045 Non-Specific Syndromic Intellectual Disability 31 0.028
570
ATR073 Atrophic Glossitis 31 0.028
571
STT009 Sutton Disease 2 30 0.028
572
c ALZ050 Alzheimer Disease 5 30 0.028
574
PYR016 Pyridoxine Deficiency 30 0.028
575
c MJR004 Major Affective Disorder 4 28 0.028
576
TMP019 Temporomandibular Joint Anomaly 28 0.028
577
TMR016 Tumor Suppressor Gene on Chromosome 11 28 0.028
578
PRR019 Perioral Myoclonia with Absences 27 0.028
579
MLR020 Malaria, Mild 27 0.028
580
CHL079 Children's Interstitial Lung Disease 26 0.028
581
PGM030 Pigmentation Anomaly of the Skin 26 0.028
582
FRN030 Frontotemporal Dementia with Parkinsonism-17 24 0.028
583
HDG004 Hodgkin's Granuloma 23 0.028
584
c ATM060 Autoimmune Atrophic Gastritis 22 0.028
585
HDG006 Hodgkin's Paragranuloma 22 0.028
586
c NSP009 Nasopharyngeal Carcinoma 2 22 0.028
587
AMN012 Aminoacidopathies 21 0.028
588
P INB001 Inborn Amino Acid Metabolism Disorder 10 0.028
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