Search results for Cobalamin

478 hits were found for Cobalamin

# Family MCID Name MIFTS Score
1
MTH056 Methylmalonic Aciduria and Homocystinuria, Cblf Type 29 5.546
2
HMC042 Homocystinuria-Megaloblastic Anemia, Cble Complementation Type 22 5.123
3
c MGL018 Megaloblastic Anemia 1 42 4.649
4
DSR002 Disorders of Intracellular Cobalamin Metabolism 19 4.199
5
TRN067 Transcobalamin I Deficiency 19 4.175
6
VTM002 Vitamin B12 Deficiency 47 3.855
7
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 51 3.691
8
MTH055 Methylmalonic Aciduria and Homocystinuria, Cbld Type 34 3.648
9
HMC033 Homocystinuria-Megaloblastic Anemia, Cblg Complementation Type 29 3.648
10
MTH051 Methylmalonic Aciduria and Homocystinuria, Cblj Type 24 2.119
11
MTH067 Methylmalonic Acidemia with Homocystinuria Type Cblj 7 2.073
12
PRN011 Pernicious Anemia 50 0.152
13
P HMC002 Homocystinuria 50 0.148
14
MTH078 Methylmalonic Aciduria, Cblb Type 61 0.126
15
P MGL001 Megaloblastic Anemia 51 0.118
16
P GST044 Gastritis 60 0.110
17
P ATR005 Atrophic Gastritis 48 0.095
18
AGN016 Aging 64 0.089
19
TRN059 Transcobalamin Deficiency 23 0.089
20
DMN002 Dementia 68 0.077
21
TRN022 Transcobalamin Ii Deficiency 46 0.077
22
P LKM002 Leukemia 72 0.071
23
P NRP001 Neuropathy 63 0.071
24
P HML001 Hemolytic-Uremic Syndrome 50 0.071
25
NRL016 Neural Tube Defects 78 0.063
26
P MLT020 Multiple Sclerosis 78 0.063
27
IRN002 Iron Metabolism Disease 55 0.063
28
P GLM045 Glioma 54 0.063
29
HMC014 Homocysteinemia 48 0.063
30
P ADN016 Adenocarcinoma 70 0.055
31
P PNC044 Pancreatitis 64 0.055
32
HLC007 Helicobacter Pylori Infection 63 0.055
33
P PLY011 Polycystic Ovary Syndrome 63 0.055
34
P ENC018 Encephalopathy 62 0.055
35
HYD012 Hydrops Fetalis 51 0.055
36
AMN002 Amino Acid Metabolic Disorder 47 0.055
37
NRL018 Neural Tube Defects, Folate-Sensitive 44 0.055
38
EXC002 Exocrine Pancreatic Insufficiency 43 0.055
39
HYD059 Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect 37 0.055
40
VTM024 Vitamin B12-Responsive Methylmalonic Acidemia 26 0.055
41
MTH077 Methylmalonic Aciduria, Cbla Type 26 0.055
42
FTL016 Fetal Edema 25 0.055
43
MTH079 Methylmalonic Acidemia and Homocysteinemia, Cblx Type 22 0.055
44
c SYS001 Systemic Lupus Erythematosus 86 0.045
45
CYS001 Cystic Fibrosis 84 0.045
46
GST053 Gastric Cancer 77 0.045
47
P LVR013 Liver Disease 75 0.045
48
P NRV007 Nervous System Disease 73 0.045
49
ACR006 Aceruloplasminemia 73 0.045
50
DPR016 Depression 72 0.045
51
c LKM063 Leukemia, Chronic Myeloid 70 0.045
52
P LPS004 Lupus Erythematosus 68 0.045
53
P KDN018 Kidney Disease 68 0.045
54
P DRM053 Dermatitis, Atopic 67 0.045
55
c PLM164 Pulmonary Hypertension, Primary, 1 66 0.045
56
DRM006 Dermatitis 66 0.045
57
CNN005 Connective Tissue Disease 64 0.045
58
P DBT009 Diabetes Mellitus 64 0.045
59
P THR014 Thrombocytopenia 64 0.045
60
APH001 Aphthous Stomatitis 63 0.045
61
THR100 Thrombocytopenic Purpura, Autoimmune 62 0.045
62
THR024 Thrombosis 61 0.045
63
DFC004 Deficiency Anemia 61 0.045
64
P NPH012 Nephrotic Syndrome 59 0.045
65
DBT010 Diabetic Neuropathy 59 0.045
66
P PLY019 Polyneuropathy 57 0.045
67
P DRR001 Diarrhea 56 0.045
68
RTN018 Retinal Disease 56 0.045
69
TRN015 Transient Cerebral Ischemia 56 0.045
70
IRN001 Iron Deficiency Anemia 55 0.045
71
SZR026 Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance 55 0.045
72
CLN015 Colon Adenocarcinoma 53 0.045
73
STM007 Stomatitis 52 0.045
74
STM006 Stomach Disease 52 0.045
75
PNC001 Pancytopenia 51 0.045
76
MCR017 Macrocytic Anemia 45 0.045
77
MTH076 Methylmalonic Aciduria Due to Methylmalonyl-Coa Mutase Deficiency 44 0.045
78
P AXN001 Axonal Neuropathy 38 0.045
79
ORG002 Organic Acidemia 38 0.045
80
P AST055 Asthma-Related Traits 1 30 0.045
81
STT009 Sutton Disease 2 29 0.045
82
c ATM060 Autoimmune Atrophic Gastritis 24 0.045
83
AMN012 Aminoacidopathies 24 0.045
84
ISL099 Isolated Methylmalonic Acidemia 23 0.045
85
INB001 Inborn Amino Acid Metabolism Disorder 16 0.045
86
P BRS047 Breast Cancer 100 0.032
87
P LNG032 Lung Cancer 98 0.032
88
P CLR023 Colorectal Cancer 97 0.032
89
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.032
90
P PRS040 Prostate Cancer 90 0.032
91
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.032
92
P ALZ034 Alzheimer Disease 87 0.032
93
MLR004 Malaria 83 0.032
94
MYL069 Myeloma, Multiple 83 0.032
95
INS024 Insulin-Like Growth Factor I 82 0.032
96
AST005 Asthma 82 0.032
97
STR067 Stroke, Ischemic 82 0.032
98
P OVR042 Ovarian Cancer 81 0.032
99
P RHM011 Rheumatoid Arthritis 80 0.032
100
P MYC007 Myocardial Infarction 79 0.032
101
SQM013 Squamous Cell Carcinoma, Head and Neck 76 0.032
102
P PRK057 Parkinson Disease, Late-Onset 76 0.032
103
P OST002 Osteoporosis 76 0.032
104
P HPT021 Hepatitis 76 0.032
105
P LNG064 Lung Cancer Susceptibility 3 76 0.032
106
P ART022 Arthritis 76 0.032
107
P INF038 Influenza 76 0.032
108
P PLM037 Pulmonary Hypertension 75 0.032
109
P HRT032 Heart Disease 74 0.032
110
P NRB001 Neuroblastoma 72 0.032
111
c CHR089 Chronic Kidney Failure 72 0.032
112
ISC006 Ischemic Heart Disease 72 0.032
113
GLB002 Glioblastoma 72 0.032
114
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.032
115
MYC006 Mycosis Fungoides 72 0.032
116
CNG034 Congestive Heart Failure 72 0.032
117
ANX010 Anxiety 72 0.032
118
c HPT073 Hepatitis C Virus 72 0.032
119
P MTC003 Metachromatic Leukodystrophy 71 0.032
120
PSY004 Psychotic Disorder 71 0.032
121
LYM133 Lymphoma, Hodgkin, Classic 71 0.032
122
PLM001 Pulmonary Tuberculosis 71 0.032
123
P MCR115 Microvascular Complications of Diabetes 5 71 0.032
124
c HPT001 Hepatitis C 71 0.032
125
PRP027 Peripheral Vascular Disease 70 0.032
126
P ATS364 Autism 70 0.032
127
P MNN013 Meningitis 70 0.032
128
P LYM118 Lymphoma 70 0.032
129
HMN044 Human Immunodeficiency Virus Type 1 70 0.032
130
P MYL005 Myelofibrosis 70 0.032
131
BRC012 Brucellosis 70 0.032
132
ART016 Aortic Aneurysm 69 0.032
133
P PNM007 Pneumonia 69 0.032
134
P BLD134 Bladder Cancer 69 0.032
135
WRN001 Werner Syndrome 69 0.032
136
P SCH015 Schizophrenia 69 0.032
137
P EPL164 Epilepsy 69 0.032
138
c LKM062 Leukemia, Acute Lymphoblastic 69 0.032
139
P ATR011 Atrial Fibrillation 68 0.032
140
LVR012 Liver Cirrhosis 68 0.032
141
P AMY004 Amyloidosis 68 0.032
142
c SML038 Small Cell Cancer of the Lung 68 0.032
143
PRT037 Pertussis 68 0.032
144
VSC007 Vascular Disease 68 0.032
145
P MYP004 Myopathy 68 0.032
146
P CRN018 Coronary Artery Anomaly 68 0.032
147
MSC157 Muscular Dystrophy, Duchenne Type 68 0.032
148
LYM017 Lyme Disease 68 0.032
149
P ART023 Arthropathy 67 0.032
150
P MCL013 Mucolipidosis Iv 67 0.032
151
P NSP012 Nasopharyngeal Carcinoma 67 0.032
152
CRB039 Cerebrovascular Disease 67 0.032
153
c THR092 Thrombophilia Due to Thrombin Defect 67 0.032
154
P FRN006 Frontotemporal Dementia 67 0.032
155
c HPT016 Hepatitis B 67 0.032
156
P HMP002 Hemophagocytic Lymphohistiocytosis 67 0.032
157
LNG099 Lung Disease 67 0.032
158
SKN016 Skin Disease 66 0.032
159
P MSC005 Muscular Dystrophy 66 0.032
160
BRS051 Breast Disease 66 0.032
161
ANG054 Angina Pectoris 66 0.032
162
OBS002 Obsessive-Compulsive Disorder 66 0.032
163
DMN031 Dementia, Lewy Body 66 0.032
164
P SLP006 Sleep Apnea 66 0.032
165
P PSR002 Psoriasis 65 0.032
166
P MJR001 Major Depressive Disorder 65 0.032
167
ART140 Arteries, Anomalies of 65 0.032
168
P DBT085 Diabetes Mellitus, Insulin-Dependent 65 0.032
169
P BCL006 B-Cell Lymphomas 65 0.032
170
PCK003 Pick Disease of Brain 65 0.032
171
ISC004 Ischemia 65 0.032
172
c CRN300 Coronary Heart Disease 1 64 0.032
173
GST050 Gastrointestinal System Disease 64 0.032
174
P LYM026 Lymphoblastic Leukemia 64 0.032
175
GST045 Gastroenteritis 64 0.032
176
P HYP086 Hypothyroidism 64 0.032
177
P THL005 Thalassemia 64 0.032
178
ATM095 Autoimmune Disease 64 0.032
179
P INT068 Intestinal Disease 64 0.032
180
GST092 Gastroesophageal Reflux 64 0.032
181
TTN003 Tetanus 64 0.032
182
c ART138 Aortic Aneurysm, Familial Abdominal, 1 64 0.032
183
MSL001 Measles 64 0.032
184
VRL011 Viral Infectious Disease 63 0.032
185
P ALP009 Alopecia Areata 63 0.032
186
MDD011 Mood Disorder 63 0.032
187
MYL031 Myeloproliferative Neoplasm 63 0.032
188
c CNT035 Central Nervous System Disease 63 0.032
189
SZR001 Sezary's Disease 63 0.032
190
HYP066 Hyperglycemia 63 0.032
191
P ALC004 Alcohol Abuse 63 0.032
192
ACQ007 Acquired Immunodeficiency Syndrome 63 0.032
193
MTH009 Mouth Disease 63 0.032
194
ADN018 Adenoma 63 0.032
195
RSP006 Respiratory System Disease 63 0.032
196
PLM033 Pulmonary Embolism 62 0.032
197
BND020 Bone Disease 62 0.032
198
FLL027 Fallopian Tube Carcinoma 62 0.032
199
c OVR114 Ovarian Cancer 1 62 0.032
200
PRP001 Propionic Acidemia 62 0.032
201
DPH001 Diphtheria 62 0.032
202
MLN008 Melanoma 62 0.032
203
HYP056 Hypoglycemia 62 0.032
204
RHM027 Rheumatic Disease 62 0.032
205
P RBL001 Rubella 62 0.032
206
c PNS012 Paine Syndrome 62 0.032
207
P WLD002 Waldenstrom Macroglobulinemia 61 0.032
208
TRN018 Transitional Cell Carcinoma 61 0.032
209
P EXN002 Exanthem 61 0.032
210
MTR014 Motor Neuron Disease 61 0.032
211
PLC008 Placenta Disease 61 0.032
212
P CMR001 Camurati-Engelmann Disease 61 0.032
213
c ATS007 Autism Spectrum Disorder 61 0.032
214
P MMP001 Mumps 61 0.032
215
PRP030 Purpura 61 0.032
216
c MCR129 Microvascular Complications of Diabetes 1 61 0.032
217
HYP266 Hypoxia 61 0.032
218
CNT061 Conotruncal Heart Malformations 61 0.032
219
c HPT003 Hepatitis a 61 0.032
220
P ANG001 Angelman Syndrome 61 0.032
221
MRB003 Morbid Obesity 60 0.032
222
NRV006 Nervous System Cancer 60 0.032
223
P NTR004 Neutropenia 60 0.032
224
ANR040 Aneurysm 60 0.032
225
MCS002 Mucositis 60 0.032
226
P PLY014 Polycystic Kidney Disease 60 0.032
227
P ART021 Arteriosclerosis 60 0.032
228
MVM001 Movement Disease 60 0.032
229
ERY003 Erythema Multiforme 60 0.032
230
HRP004 Herpes Zoster 60 0.032
231
GRD007 Grade Iii Astrocytoma 60 0.032
232
c PRM126 Primary Peritoneal Carcinoma 60 0.032
233
GLB015 Glioblastoma Multiforme 60 0.032
234
PRP019 Peripheral Nervous System Disease 60 0.032
235
MSC152 Muscular Dystrophy, Becker Type 60 0.032
236
NRM005 Neuromuscular Disease 60 0.032
237
P HMR003 Hemorrhagic Disease 60 0.032
238
PHR003 Pharyngitis 59 0.032
239
P INF032 Infertility 59 0.032
240
P ACT074 Acute Lymphocytic Leukemia 59 0.032
241
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 0.032
242
c ALP101 Alpha-Thalassemia 59 0.032
243
P OLG002 Oligodendroglioma 59 0.032
244
JNT002 Joint Disorders 59 0.032
245
c MST023 Mesothelioma, Malignant 59 0.032
246
c 3MT016 3-Methylglutaconic Aciduria, Type Iii 59 0.032
247
P BPL003 Bipolar Disorder 59 0.032
248
P ANP001 Anaplastic Large Cell Lymphoma 59 0.032
249
HDC001 Headache 59 0.032
250
SLP005 Sleep Disorder 59 0.032
251
c VRL010 Viral Hepatitis 59 0.032
252
c PRC016 Pre-Eclampsia 59 0.032
253
P OVR049 Ovarian Disease 59 0.032
254
SQM006 Squamous Cell Carcinoma 59 0.032
255
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 59 0.032
256
NRN004 Neuroendocrine Tumor 58 0.032
257
P LTR001 Lateral Sclerosis 58 0.032
258
PST028 Post-Traumatic Stress Disorder 58 0.032
259
GLS001 Gliosarcoma 58 0.032
260
LPD008 Lipid Metabolism Disorder 58 0.032
261
APH002 Aphasia 58 0.032
262
P ALP008 Alopecia 58 0.032
263
c BCT007 Bacterial Meningitis 58 0.032
264
PLM031 Poliomyelitis 58 0.032
265
P SML001 Small Cell Carcinoma 58 0.032
266
c ACT075 Acute Myocardial Infarction 58 0.032
267
VSC002 Vascular Dementia 58 0.032
268
FBR047 Fibromyalgia 57 0.032
269
NRT004 Neuritis 57 0.032
270
DMY004 Demyelinating Disease 57 0.032
271
HMT018 Hematopoietic Stem Cell Transplantation 57 0.032
272
c CRD093 Cardiomyopathy, Dilated, 1a 57 0.032
273
PNC034 Pancreas Disease 57 0.032
274
c ALM001 Al Amyloidosis 57 0.032
275
P MCR010 Microcephaly 57 0.032
276
P LKD001 Leukodystrophy 57 0.032
277
MNT002 Mental Depression 57 0.032
278
P ECL001 Eclampsia 57 0.032
279
LMY002 Leiomyoma 57 0.032
280
BRN038 Bronchial Disease 56 0.032
281
CNS004 Constipation 56 0.032
282
P SZR006 Seizure Disorder 56 0.032
283
TYP041 Type I 56 0.032
284
BRN106 Burns 56 0.032
285
HYP060 Hyperinsulinism 56 0.032
286
PRP036 Peripheral T-Cell Lymphoma 56 0.032
287
IMM136 Immune System Disease 56 0.032
288
P MYP006 Myopia 56 0.032
289
PLG002 Plague 56 0.032
290
END030 End Stage Renal Failure 56 0.032
291
EWN002 Ewing's Family of Tumors 56 0.032
292
MST005 Mastitis 55 0.032
293
P HYP014 Hyperuricemia 55 0.032
294
BNF002 Bone Fracture 55 0.032
295
URN009 Urinary System Disease 55 0.032
296
P CTN015 Cutaneous T Cell Lymphoma 55 0.032
297
LYM019 Lymphosarcoma 55 0.032
298
MYM001 Myoma 55 0.032
299
GNT002 Giant Cell Glioblastoma 55 0.032
300
P PNC025 Panic Disorder 55 0.032
301
TXC002 Toxic Encephalopathy 55 0.032
302
BRN004 Brain Edema 55 0.032
303
CHL061 Childhood Leukemia 55 0.032
304
BLD053 Blood Platelet Disease 55 0.032
305
FDL002 Food Allergy 55 0.032
306
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 55 0.032
307
PRV006 Pervasive Developmental Disorder 55 0.032
308
BLD044 Bladder Disease 55 0.032
309
P RTN016 Retinal Degeneration 54 0.032
310
P TRM003 Tremor 54 0.032
311
c HYP795 Hypothyroidism, Congenital, Nongoitrous, 4 54 0.032
312
P TRC086 Trichohepatoenteric Syndrome 1 54 0.032
313
P MSC003 Muscular Atrophy 54 0.032
314
SPS003 Spastic Diplegia 54 0.032
315
ERY029 Erythermalgia, Primary 54 0.032
316
LYM024 Lymphatic System Disease 54 0.032
317
c CRP023 Carpenter Syndrome 1 54 0.032
318
KRT002 Keratomalacia 54 0.032
319
SMN008 Semantic Dementia 54 0.032
320
DYS014 Dyspepsia 54 0.032
321
SCH012 Schizoaffective Disorder 54 0.032
322
c ACT071 Acute Kidney Failure 54 0.032
323
PRP016 Paraplegia 53 0.032
324
PST021 Postpartum Depression 53 0.032
325
P INF037 Inflammatory Bowel Disease 53 0.032
326
MCR004 Macroglobulinemia 53 0.032
327
c SVR005 Severe Pre-Eclampsia 53 0.032
328
PRP080 Peripheral Artery Disease 53 0.032
329
LMY014 Leiomyoma, Uterine 53 0.032
330
BRN071 Brain Injury 53 0.032
331
FML037 Female Breast Cancer 53 0.032
332
P BRN009 Burning Mouth Syndrome 53 0.032
333
SNS003 Sensory Peripheral Neuropathy 53 0.032
334
OVR063 Overnutrition 53 0.032
335
HMG005 Hemoglobinopathy 53 0.032
336
MLN007 Male Infertility 53 0.032
337
c HMN021 Human T-Cell Leukemia Virus Type 1 52 0.032
338
DBT084 Diabetes Mellitus, Ketosis-Prone 52 0.032
339
P CLL015 Collagen Disease 52 0.032
340
P MSC033 Muscle Disorders 52 0.032
341
FRN051 Frontotemporal Lobar Degeneration with Tdp43 Inclusions, Grn-Related 52 0.032
342
P HMG032 Hemoglobin H Disease 52 0.032
343
GLC008 Glucose Metabolism Disease 52 0.032
344
URM002 Uremia 52 0.032
345
RTC009 Reticulum Cell Sarcoma 52 0.032
346
INT007 Intermediate Coronary Syndrome 52 0.032
347
SPC010 Speech and Communication Disorders 52 0.032
348
CLC006 Calcinosis 51 0.032
349
PRT038 Protein-Energy Malnutrition 51 0.032
350
SPN041 Spinal Cord Disease 51 0.032
351
THY030 Thyroid Gland Disease 51 0.032
352
P NGH001 Night Blindness 51 0.032
353
P AST007 Astrocytoma 51 0.032
354
DBT004 Diabetic Polyneuropathy 51 0.032
355
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.032
356
ATN005 Autonomic Dysfunction 50 0.032
357
RTN023 Retinitis 50 0.032
358
PLC007 Placental Abruption 50 0.032
359
P BLD051 Blood Coagulation Disease 50 0.032
360
LYM012 Lymphoplasmacytic Lymphoma 50 0.032
361
P OVR046 Ovarian Cyst 50 0.032
362
NSS002 Neisseria Meningitidis Infection 49 0.032
363
c PRM108 Primary Progressive Multiple Sclerosis 49 0.032
364
RTC005 Reticulosarcoma 49 0.032
365
PNN001 Panniculitis 49 0.032
366
ANX004 Anoxia 49 0.032
367
P BRN120 Bronchus Cancer 49 0.032
368
CHC001 Chickenpox 49 0.032
369
MTB004 Metabolic Acidosis 48 0.032
370
c INH020 Inherited Metabolic Disorder 48 0.032
371
SKN027 Skin Conditions 48 0.032
372
DBT008 Diabetic Angiopathy 47 0.032
373
HDN002 Head Injury 47 0.032
374
URT031 Ureteral Disease 47 0.032
375
MYC005 Myocardial Stunning 47 0.032
376
JHN001 Johanson-Blizzard Syndrome 47 0.032
377
ANG046 Angioimmunoblastic T-Cell Lymphoma 47 0.032
378
EPD070 Epidermoid Cysts 47 0.032
379
SYN036 Syncope 47 0.032
380
MNN020 Meningococcal Infection 47 0.032
381
SPC005 Speech Disorder 47 0.032
382
ENT004 Enthesopathy 46 0.032
383
LKC003 Leukocyte Disease 46 0.032
384
c CRD187 Cardiomyopathy, Dilated, 3b 46 0.032
385
DYS073 Dysphagia 46 0.032
386
c MLG079 Malignant Pleural Mesothelioma 46 0.032
387
ULC007 Ulcerative Stomatitis 46 0.032
388
GND003 Gonadal Disease 46 0.032
389
BSL008 Basal Ganglia Disease 46 0.032
390
P CNN004 Connective Tissue Cancer 45 0.032
391
PDT001 Pediatric Lymphoma 45 0.032
392
PRD004 Prediabetes Syndrome 45 0.032
393
END072 Endotheliitis 45 0.032
394
AZS001 Azoospermia 45 0.032
395
OCL033 Oculocerebral Syndrome with Hypopigmentation 45 0.032
396
GLS007 Glossitis 45 0.032
397
NTR003 Natural Killer Cell Leukemia 45 0.032
398
INT038 Interdigitating Dendritic Cell Sarcoma 44 0.032
399
BCK006 Back Pain 44 0.032
400
MNN032 Meningococcal Meningitis 44 0.032
401
BRN080 Brain Ischemia 44 0.032
402
PRS042 Prostate Disease 44 0.032
403
LYM067 Lymphoid Leukemia 44 0.032
404
ANP009 Anaplastic Oligodendroglioma 44 0.032
405
PST053 Postherpetic Neuralgia 44 0.032
406
DBT002 Diabetic Autonomic Neuropathy 43 0.032
407
ANG025 Angioimmunoblastic Lymphadenopathy with Dysproteinemia 43 0.032
408
HPT070 Hepatosplenic T-Cell Lymphoma 43 0.032
409
DYS015 Dysentery 43 0.032
410
MYF002 Myofascial Pain Syndrome 43 0.032
411
GRN017 Granulocytopenia 43 0.032
412
URT051 Ureter, Cancer of 42 0.032
413
P HRD012 Hereditary Elliptocytosis 42 0.032
414
PRT035 Peritoneum Cancer 42 0.032
415
ADS004 Aids Dementia Complex 41 0.032
416
BCL014 B-Cell Growth Factor 41 0.032
417
SPS057 Spasticity 41 0.032
418
P ORF002 Orofacial Cleft 41 0.032
419
OST097 Osteoporotic Fracture 41 0.032
420
MDS022 Mediastinitis 40 0.032
421
P HYP265 Hypotonia 40 0.032
422
P CHR084 Chromosomal Disease 40 0.032
423
P ATX024 Ataxia-Oculomotor Apraxia 3 40 0.032
424
FXF002 Fox-Fordyce Disease 40 0.032
425
c ACT004 Acute Diarrhea 40 0.032
426
PHT003 Phototoxic Dermatitis 40 0.032
427
ETH004 Euthyroid Sick Syndrome 40 0.032
428
MYF001 Myofibroma 39 0.032
429
c ADL001 Adult Lymphoma 39 0.032
430
PRM155 Primary Cutaneous Anaplastic Large Cell Lymphoma 39 0.032
431
MSC004 Muscle Tissue Disease 39 0.032
432
c PRC031 Preeclampsia/eclampsia 1 39 0.032
433
c MLG068 Malignant Glioma 38 0.032
434
OVR094 Ovarian Epithelial Cancer 38 0.032
435
c ADL008 Adult Oligodendroglioma 38 0.032
436
LRY017 Laryngeal Disease 38 0.032
437
TTH004 Tethered Spinal Cord Syndrome 38 0.032
438
CHL006 Childhood Oligodendroglioma 38 0.032
439
FCL044 Fecal Incontinence 38 0.032
440
TNG004 Tongue Disease 37 0.032
441
PRS063 Paresthesia 37 0.032
442
c GRN014 Grn-Related Frontotemporal Dementia 37 0.032
443
PYR016 Pyridoxine Deficiency 36 0.032
444
MSC012 Muscular Dystrophy, Duchenne and Becker Type 36 0.032
445
VSC008 Vascular Hemostatic Disease 36 0.032
446
FNT004 Fainting 36 0.032
447
AMY005 Amyloid Neuropathy 36 0.032
448
BCK003 Background Diabetic Retinopathy 36 0.032
449
SWL001 Swallowing Disorders 36 0.032
450
MN1001 Mn1 35 0.032
451
INT088 Intrinsic Factor Deficiency 35 0.032
452
FLL029 Fallopian Tube Disease 35 0.032
453
MTH021 Methylmalonic Acidemia with Homocystinuria 34 0.032
454
c TRC078 Trichohepatoenteric Syndrome 2 34 0.032
455
NSP003 Nasopharyngeal Disease 32 0.032
456
ALC011 Alcoholic Neuropathy 31 0.032
457
FRN030 Frontotemporal Dementia with Parkinsonism-17 31 0.032
458
ATR073 Atrophic Glossitis 30 0.032
459
c PLY105 Polycystic Ovary Syndrome 1 30 0.032
460
BLN006 Blind Loop Syndrome 29 0.032
461
LYM098 Lymphomatous Meningitis 29 0.032
462
HDG004 Hodgkin's Granuloma 28 0.032
463
BDY007 Body Mass Index Quantitative Trait Locus 1 26 0.032
464
P URT040 Urethral Cancer 24 0.032
465
MNS002 Mini Stroke 23 0.032
466
PRM153 Primary Progressive Apraxia of Speech 21 0.032
467
HDG006 Hodgkin's Paragranuloma 21 0.032
468
THR116 Thrombocytopenia, Cyclic 20 0.032
469
VTM003 Vitamin Metabolic Disorder 20 0.032
470
ATR076 Atrophic Muscular Disease 18 0.032
471
MXD044 Mixed Sleep Apnea 18 0.032
472
CMB083 Combined Immunodeficiency and Megaloblastic Anemia with or Without Hyperhomocysteinemia 16 0.032
473
INT074 Intracranial Arteriosclerosis 15 0.032
474
MTH068 Methylmalonic Aciduria, Transient, Due to Transcobalamin Receptor Defect 14 0.032
475
MTH002 Methylmalonic Aciduria and Homocystinuria Type Cblg 13 0.032
476
MTH003 Methylmalonic Aciduria and Homocystinuria Type Cble 13 0.032
477
ORG003 Organic Mood Syndrome 11 0.032
478
MTH069 Methylmalonic Acidemia Due to Transcobalamin Receptor Defect 8 0.032
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