Search results for Methylcobalamin

487 hits were found for Methylcobalamin

# Family MCID Name MIFTS Score
1
HMC033 Homocystinuria-Megaloblastic Anemia, Cblg Complementation Type 36 6.508
2
MTH056 Methylmalonic Aciduria and Homocystinuria, Cblf Type 37 3.807
3
MTH055 Methylmalonic Aciduria and Homocystinuria, Cbld Type 38 3.796
4
HMC042 Homocystinuria-Megaloblastic Anemia, Cble Complementation Type 26 3.796
5
MTH079 Methylmalonic Acidemia and Homocysteinemia, Cblx Type 30 3.041
6
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 49 2.258
7
MTH051 Methylmalonic Aciduria and Homocystinuria, Cblj Type 26 2.231
8
HMC036 Homocystinuria Without Methylmalonic Aciduria 19 2.216
9
MTH021 Methylmalonic Acidemia with Homocystinuria 46 2.177
10
MTH067 Methylmalonic Acidemia with Homocystinuria Type Cblj 9 2.150
11
P NRP001 Neuropathy 57 0.188
12
P PRP019 Peripheral Nervous System Disease 64 0.160
13
DBT010 Diabetic Neuropathy 56 0.103
14
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.098
15
P LTR001 Lateral Sclerosis 56 0.098
16
VTM002 Vitamin B12 Deficiency 48 0.092
17
P ATS364 Autism 68 0.086
18
P HMC002 Homocystinuria 52 0.080
19
PRS063 Paresthesia 46 0.073
20
SLW005 Slowed Nerve Conduction Velocity, Autosomal Dominant 32 0.073
21
P MTR014 Motor Neuron Disease 66 0.065
22
P EXN002 Exanthem 58 0.065
23
HMC014 Homocysteinemia 54 0.065
24
INT002 Intermittent Claudication 60 0.057
25
P INF032 Infertility 60 0.057
26
P MLN007 Male Infertility 57 0.057
27
P MGL001 Megaloblastic Anemia 54 0.057
28
c PRM092 Primary Lateral Sclerosis, Adult, 1 54 0.057
29
AZS001 Azoospermia 51 0.057
30
P MTH008 Methylmalonic Acidemia 50 0.057
31
BCK006 Back Pain 44 0.057
32
ATN004 Autonomic Neuropathy 43 0.057
33
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.046
34
P ALZ034 Alzheimer Disease 90 0.046
35
MYL069 Myeloma, Multiple 85 0.046
36
DFC004 Deficiency Anemia 77 0.046
37
P HYP086 Hypothyroidism 70 0.046
38
HYP056 Hypoglycemia 68 0.046
39
P ADN016 Adenocarcinoma 65 0.046
40
P BRS044 Breast Adenocarcinoma 59 0.046
41
SPN027 Spinal Stenosis 58 0.046
42
HYP266 Hypoxia 58 0.046
43
P SLP005 Sleep Disorder 58 0.046
44
ERY029 Erythermalgia, Primary 58 0.046
45
P INF037 Inflammatory Bowel Disease 57 0.046
46
c CNT035 Central Nervous System Disease 56 0.046
47
P ART021 Arteriosclerosis 56 0.046
48
P PLY019 Polyneuropathy 55 0.046
49
P MSC003 Muscular Atrophy 52 0.046
50
BLL003 Bell's Palsy 50 0.046
51
DBT004 Diabetic Polyneuropathy 48 0.046
52
CYT002 Cytokine Deficiency 46 0.046
53
DBT002 Diabetic Autonomic Neuropathy 45 0.046
54
PST053 Postherpetic Neuralgia 43 0.046
55
WLL004 Wallerian Degeneration 40 0.046
56
NRD037 Neurodevelopmental Disorder with Dysmorphic Facies and Distal Limb Anomalies 34 0.046
57
ISL099 Isolated Methylmalonic Acidemia 30 0.046
58
CMB083 Combined Immunodeficiency and Megaloblastic Anemia with or Without Hyperhomocysteinemia 23 0.046
59
P CLR023 Colorectal Cancer 100 0.033
60
P HPT023 Hepatocellular Carcinoma 99 0.033
61
P BRS047 Breast Cancer 99 0.033
62
P PRS040 Prostate Cancer 97 0.033
63
P OVR042 Ovarian Cancer 89 0.033
64
c HYP595 Hypertension, Essential 87 0.033
65
P GST053 Gastric Cancer 85 0.033
66
c LKM061 Leukemia, Acute Myeloid 84 0.033
67
CYS001 Cystic Fibrosis 84 0.033
68
NRL016 Neural Tube Defects 83 0.033
69
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.033
70
MLR004 Malaria 82 0.033
71
STR067 Stroke, Ischemic 82 0.033
72
P RHM011 Rheumatoid Arthritis 82 0.033
73
SQM013 Squamous Cell Carcinoma, Head and Neck 81 0.033
74
IMM167 Immune Deficiency Disease 79 0.033
75
P OST002 Osteoporosis 79 0.033
76
P BLD134 Bladder Cancer 79 0.033
77
P LNG064 Lung Cancer Susceptibility 3 79 0.033
78
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.033
79
P HRT032 Heart Disease 78 0.033
80
P PRK057 Parkinson Disease, Late-Onset 77 0.033
81
P SCH015 Schizophrenia 76 0.033
82
c ATR087 Atrial Standstill 1 76 0.033
83
P RSP003 Respiratory Failure 75 0.033
84
BRN028 Brain Cancer 75 0.033
85
ANX010 Anxiety 75 0.033
86
c THR092 Thrombophilia Due to Thrombin Defect 74 0.033
87
GLB002 Glioblastoma 74 0.033
88
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.033
89
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.033
90
P MYC007 Myocardial Infarction 74 0.033
91
c HPT073 Hepatitis C Virus 74 0.033
92
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.033
93
HMN044 Human Immunodeficiency Virus Type 1 73 0.033
94
P MLT020 Multiple Sclerosis 73 0.033
95
P KDN018 Kidney Disease 73 0.033
96
PRP027 Peripheral Vascular Disease 72 0.033
97
P CNR004 Cone-Rod Dystrophy 2 72 0.033
98
PLM001 Pulmonary Tuberculosis 72 0.033
99
P SRC025 Sarcoidosis 1 72 0.033
100
MYL009 Myelodysplastic Syndrome 72 0.033
101
LPT014 Leptin Deficiency or Dysfunction 72 0.033
102
P ART022 Arthritis 71 0.033
103
P PNM007 Pneumonia 71 0.033
104
P LVR013 Liver Disease 71 0.033
105
CRB039 Cerebrovascular Disease 71 0.033
106
MSC157 Muscular Dystrophy, Duchenne Type 70 0.033
107
RCK004 Rickets 70 0.033
108
LYM133 Lymphoma, Hodgkin, Classic 70 0.033
109
BHC003 Behcet Syndrome 70 0.033
110
P LYM118 Lymphoma 70 0.033
111
c ATS007 Autism Spectrum Disorder 69 0.033
112
CRB037 Cerebral Palsy 69 0.033
113
P MYC084 Mycobacterium Tuberculosis 1 69 0.033
114
P INF038 Influenza 69 0.033
115
P HPT021 Hepatitis 69 0.033
116
LGH007 Leigh Syndrome 69 0.033
117
CNG034 Congestive Heart Failure 69 0.033
118
P MJR001 Major Depressive Disorder 69 0.033
119
P LKM002 Leukemia 69 0.033
120
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.033
121
c CHR684 Chronic Kidney Disease 68 0.033
122
P DMN002 Dementia 68 0.033
123
P HYD006 Hydrocephalus 68 0.033
124
ALC007 Alcohol Dependence 68 0.033
125
P LKM062 Leukemia, Acute Lymphoblastic 68 0.033
126
ATH013 Atherosclerosis Susceptibility 68 0.033
127
PSY004 Psychotic Disorder 68 0.033
128
P GLM040 Glioma Susceptibility 1 68 0.033
129
P MSC005 Muscular Dystrophy 68 0.033
130
P NRV007 Nervous System Disease 68 0.033
131
CRP001 Carpal Tunnel Syndrome 68 0.033
132
P DRM053 Dermatitis, Atopic 68 0.033
133
c FML001 Familial Atrial Fibrillation 67 0.033
134
P MCR115 Microvascular Complications of Diabetes 5 67 0.033
135
P CRN018 Coronary Artery Anomaly 67 0.033
136
P NSP012 Nasopharyngeal Carcinoma 67 0.033
137
P ATR011 Atrial Fibrillation 67 0.033
138
P OLG002 Oligodendroglioma 67 0.033
139
c MCR129 Microvascular Complications of Diabetes 1 67 0.033
140
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.033
141
P THR014 Thrombocytopenia 67 0.033
142
LVR012 Liver Cirrhosis 67 0.033
143
c SML038 Small Cell Cancer of the Lung 67 0.033
144
MYC006 Mycosis Fungoides 67 0.033
145
P DBT009 Diabetes Mellitus 66 0.033
146
P CLC063 Celiac Disease 1 66 0.033
147
P BLD124 Bleeding Disorder, Platelet-Type, 11 66 0.033
148
PRT037 Pertussis 66 0.033
149
ACR008 Acrocallosal Syndrome 66 0.033
150
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.033
151
P PRS038 Personality Disorder 66 0.033
152
MYL031 Myeloproliferative Neoplasm 66 0.033
153
DSS008 Disease of Mental Health 66 0.033
154
ANG054 Angina Pectoris 66 0.033
155
P TRN020 Turner Syndrome 66 0.033
156
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.033
157
P VSC007 Vascular Disease 65 0.033
158
P DYS154 Dystonia 65 0.033
159
P OCL013 Oculodentodigital Dysplasia 65 0.033
160
P ANG001 Angelman Syndrome 65 0.033
161
ALL026 Allergic Hypersensitivity Disease 65 0.033
162
FCT007 Factor Vii Deficiency 65 0.033
163
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.033
164
DPR016 Depression 64 0.033
165
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.033
166
CLR108 Colorectal Adenoma 64 0.033
167
c RHB024 Rhabdomyosarcoma 2 64 0.033
168
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 64 0.033
169
SKN016 Skin Disease 64 0.033
170
CNT061 Conotruncal Heart Malformations 64 0.033
171
FLL027 Fallopian Tube Carcinoma 64 0.033
172
c FNC043 Fanconi Anemia, Complementation Group E 64 0.033
173
LPD008 Lipid Metabolism Disorder 64 0.033
174
P ENC018 Encephalopathy 64 0.033
175
P NTR004 Neutropenia 64 0.033
176
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.033
177
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 63 0.033
178
DRM006 Dermatitis 63 0.033
179
KHL003 Kohlschutter-Tonz Syndrome 63 0.033
180
P PSR002 Psoriasis 63 0.033
181
c HPT016 Hepatitis B 63 0.033
182
c PRC016 Pre-Eclampsia 63 0.033
183
PRP001 Propionic Acidemia 63 0.033
184
P MVM001 Movement Disease 63 0.033
185
PPL049 Papillon-Lefevre Syndrome 63 0.033
186
TXC005 Toxic Shock Syndrome 63 0.033
187
LYS012 Lysosomal Acid Lipase Deficiency 63 0.033
188
HYP066 Hyperglycemia 63 0.033
189
MDD011 Mood Disorder 62 0.033
190
ADL002 Adult Syndrome 62 0.033
191
BLD131 Bladder Urothelial Carcinoma 62 0.033
192
LYM012 Lymphoplasmacytic Lymphoma 62 0.033
193
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.033
194
NRM005 Neuromuscular Disease 62 0.033
195
VRL011 Viral Infectious Disease 62 0.033
196
TTN003 Tetanus 62 0.033
197
ISC004 Ischemia 62 0.033
198
P LYM033 Lymphoproliferative Syndrome 62 0.033
199
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.033
200
c HPT001 Hepatitis C 62 0.033
201
CRC021 Carcinosarcoma 62 0.033
202
P ANP001 Anaplastic Large Cell Lymphoma 62 0.033
203
c PNS012 Paine Syndrome 61 0.033
204
PRT013 Portal Hypertension 61 0.033
205
P ART023 Arthropathy 61 0.033
206
CRY035 Cryptorchidism, Unilateral or Bilateral 61 0.033
207
LBR030 Leber Optic Atrophy 61 0.033
208
ACQ007 Acquired Immunodeficiency Syndrome 61 0.033
209
P BCL017 B-Cell Lymphoma 61 0.033
210
P MYL006 Myeloid Leukemia 61 0.033
211
NTR005 Nutritional Deficiency Disease 61 0.033
212
P PNC044 Pancreatitis 61 0.033
213
THR100 Thrombocytopenic Purpura, Autoimmune 61 0.033
214
HLC007 Helicobacter Pylori Infection 61 0.033
215
DPH001 Diphtheria 61 0.033
216
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.033
217
GLB015 Glioblastoma Multiforme 60 0.033
218
SQM006 Squamous Cell Carcinoma 60 0.033
219
P CRB101 Cerebrooculofacioskeletal Syndrome 1 60 0.033
220
CHR072 Chordoma 60 0.033
221
c ACT071 Acute Kidney Failure 60 0.033
222
MNT002 Mental Depression 60 0.033
223
PLM033 Pulmonary Embolism 60 0.033
224
ART140 Arteries, Anomalies of 60 0.033
225
END030 End Stage Renal Failure 60 0.033
226
c HPT003 Hepatitis a 60 0.033
227
ADN018 Adenoma 60 0.033
228
P CRN300 Coronary Heart Disease 1 59 0.033
229
RNL024 Renal Glucosuria 59 0.033
230
GRD007 Grade Iii Astrocytoma 59 0.033
231
P SZR006 Seizure Disorder 59 0.033
232
SZR001 Sezary's Disease 59 0.033
233
NRN004 Neuroendocrine Tumor 59 0.033
234
P BPL003 Bipolar Disorder 59 0.033
235
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 59 0.033
236
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.033
237
c ACT075 Acute Myocardial Infarction 59 0.033
238
IRN001 Iron Deficiency Anemia 59 0.033
239
c MST023 Mesothelioma, Malignant 59 0.033
240
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 58 0.033
241
VSL002 Visual Epilepsy 58 0.033
242
P PRV006 Pervasive Developmental Disorder 58 0.033
243
P PLY011 Polycystic Ovary Syndrome 58 0.033
244
GST033 Gestational Diabetes 58 0.033
245
TRD006 Tardive Dyskinesia 58 0.033
246
P ALC033 Alcohol Use Disorder 58 0.033
247
HRP004 Herpes Zoster 58 0.033
248
IRN002 Iron Metabolism Disease 58 0.033
249
THR024 Thrombosis 58 0.033
250
AGN016 Aging 58 0.033
251
GLB001 Gilbert Syndrome 58 0.033
252
INT007 Intermediate Coronary Syndrome 58 0.033
253
P GST044 Gastritis 58 0.033
254
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 57 0.033
255
BCT022 Bacterial Infectious Disease 57 0.033
256
GST050 Gastrointestinal System Disease 57 0.033
257
LMY014 Leiomyoma, Uterine 57 0.033
258
P MMP001 Mumps 57 0.033
259
TRN018 Transitional Cell Carcinoma 57 0.033
260
VSC002 Vascular Dementia 57 0.033
261
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.033
262
BRN004 Brain Edema 57 0.033
263
PRP030 Purpura 56 0.033
264
APH001 Aphthous Stomatitis 56 0.033
265
P LYM031 Lymphocytic Leukemia 56 0.033
266
P MCR010 Microcephaly 56 0.033
267
HMN014 Human Immunodeficiency Virus Infectious Disease 56 0.033
268
P RTN016 Retinal Degeneration 56 0.033
269
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.033
270
MCS002 Mucositis 56 0.033
271
P ANT006 Antiphospholipid Syndrome 56 0.033
272
GLS001 Gliosarcoma 56 0.033
273
PPL022 Papilloma 56 0.033
274
PRT038 Protein-Energy Malnutrition 56 0.033
275
c FML035 Familial Hyperlipidemia 56 0.033
276
HRT012 Heart Valve Disease 56 0.033
277
SNS003 Sensory Peripheral Neuropathy 56 0.033
278
P SBS003 Substance Abuse 56 0.033
279
c CNG216 Congenital Hydrocephalus 55 0.033
280
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 55 0.033
281
ACD008 Acid-Labile Subunit Deficiency 55 0.033
282
AMN003 Amnestic Disorder 55 0.033
283
HYP060 Hyperinsulinism 55 0.033
284
END040 Endogenous Depression 55 0.033
285
HYP005 Hypokalemia 55 0.033
286
P DRR001 Diarrhea 55 0.033
287
MSS001 Masa Syndrome 55 0.033
288
c PSR017 Psoriasis 2 55 0.033
289
P TRM003 Tremor 55 0.033
290
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 55 0.033
291
P NRV006 Nervous System Cancer 55 0.033
292
MRG003 Marginal Zone B-Cell Lymphoma 55 0.033
293
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 54 0.033
294
DRR016 Diarrhea 2, with Microvillus Atrophy 54 0.033
295
HMT018 Hematopoietic Stem Cell Transplantation 54 0.033
296
GTR002 Goiter 54 0.033
297
LYM040 Lymphoblastic Lymphoma 54 0.033
298
TXC002 Toxic Encephalopathy 54 0.033
299
AMN001 Amenorrhea 54 0.033
300
PRP036 Peripheral T-Cell Lymphoma 53 0.033
301
IMP005 Impotence 53 0.033
302
c LRG017 Large Intestine Cancer 53 0.033
303
P ECL001 Eclampsia 53 0.033
304
P RTN018 Retinal Disease 53 0.033
305
THY030 Thyroid Gland Disease 53 0.033
306
NRT001 Neurotic Disorder 53 0.033
307
SPS003 Spastic Diplegia 53 0.033
308
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.033
309
DYS073 Dysphagia 52 0.033
310
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 52 0.033
311
HYP014 Hyperuricemia 52 0.033
312
LMY002 Leiomyoma 52 0.033
313
LNG031 Lung Benign Neoplasm 52 0.033
314
PNG002 Pain Agnosia 52 0.033
315
GNT002 Giant Cell Glioblastoma 52 0.033
316
P CTN015 Cutaneous T Cell Lymphoma 52 0.033
317
P CHR345 Chronic Pain 52 0.033
318
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.033
319
P AST007 Astrocytoma 52 0.033
320
c CNT033 Central Nervous System Cancer 51 0.033
321
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.033
322
PLC008 Placenta Disease 51 0.033
323
P THR015 Thrombophilia 51 0.033
324
STM007 Stomatitis 51 0.033
325
PRN011 Pernicious Anemia 51 0.033
326
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.033
327
c INH020 Inherited Metabolic Disorder 51 0.033
328
OVR082 Overgrowth Syndrome 51 0.033
329
HYP081 Hypolipoproteinemia 51 0.033
330
PRP080 Peripheral Artery Disease 51 0.033
331
PST021 Postpartum Depression 51 0.033
332
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.033
333
GLS018 Glass Syndrome 51 0.033
334
PST011 Pustulosis of Palm and Sole 51 0.033
335
URM002 Uremia 50 0.033
336
P PLM006 Pulmonary Alveolar Proteinosis 50 0.033
337
SCH012 Schizoaffective Disorder 50 0.033
338
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.033
339
MNC006 Monoclonal Gammopathy of Uncertain Significance 50 0.033
340
ACR041 Acromelic Frontonasal Dysostosis 50 0.033
341
c PSR023 Psoriasis 1 50 0.033
342
c HMN021 Human T-Cell Leukemia Virus Type 1 50 0.033
343
MCR004 Macroglobulinemia 50 0.033
344
NRL018 Neural Tube Defects, Folate-Sensitive 50 0.033
345
SCH003 Schizophreniform Disorder 49 0.033
346
TST044 Testicular Torsion 49 0.033
347
ANG046 Angioimmunoblastic T-Cell Lymphoma 49 0.033
348
P ATR005 Atrophic Gastritis 49 0.033
349
c LTN004 Late-Onset Retinal Degeneration 49 0.033
350
SQM002 Squamous Cell Papilloma 49 0.033
351
47X002 47,xyy 49 0.033
352
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.033
353
BWN001 Bowen-Conradi Syndrome 49 0.033
354
HPR003 Heparin-Induced Thrombocytopenia 49 0.033
355
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.033
356
SPL018 Splenomegaly 48 0.033
357
c MCR120 Microvascular Complications of Diabetes 7 48 0.033
358
HYP781 Hypoascorbemia 48 0.033
359
PTH002 Pathological Gambling 48 0.033
360
PRS034 Parasitic Helminthiasis Infectious Disease 48 0.033
361
RTC005 Reticulosarcoma 48 0.033
362
LYM019 Lymphosarcoma 48 0.033
363
LNG015 Lingual-Facial-Buccal Dyskinesia 48 0.033
364
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.033
365
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.033
366
c OPT050 Opitz Gbbb Syndrome, Type Ii 48 0.033
367
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.033
368
ACT113 Acute Myeloblastic Leukemia with Maturation 48 0.033
369
BHR001 Behr Syndrome 47 0.033
370
MTH078 Methylmalonic Aciduria, Cblb Type 47 0.033
371
VTM033 Vitamin K Deficiency Bleeding 47 0.033
372
KRT002 Keratomalacia 47 0.033
373
c CRV002 Cervix Uteri Carcinoma in Situ 47 0.033
374
P BNG032 Benign Mesothelioma 47 0.033
375
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.033
376
PNN001 Panniculitis 47 0.033
377
LPT006 Leptin Receptor Deficiency 47 0.033
378
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.033
379
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.033
380
ATX019 Ataxia with Vitamin E Deficiency 46 0.033
381
LWC001 Low Compliance Bladder 45 0.033
382
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.033
383
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.033
384
P BCT020 Bacteremia 2 45 0.033
385
HMC041 Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity 45 0.033
386
c PRM038 Primary Agammaglobulinemia 45 0.033
387
c DRM054 Dermatitis, Atopic, 2 45 0.033
388
MYC005 Myocardial Stunning 45 0.033
389
P LYD001 Leydig Cell Tumor 45 0.033
390
PRT035 Peritoneum Cancer 45 0.033
391
c SCH085 Schizophrenia 2 45 0.033
392
CTS005 Catastrophic Antiphospholipid Syndrome 44 0.033
393
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 44 0.033
394
ANP009 Anaplastic Oligodendroglioma 44 0.033
395
P MJR007 Major Affective Disorder 1 44 0.033
396
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.033
397
DLY008 Delayed Sleep Phase Disorder 43 0.033
398
URT051 Ureter, Cancer of 43 0.033
399
c MLG079 Malignant Pleural Mesothelioma 43 0.033
400
FNT005 Fontaine Progeroid Syndrome 43 0.033
401
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.033
402
SBC016 Subacute Delirium 43 0.033
403
P RRT020 Rare Tumor 43 0.033
404
ORG002 Organic Acidemia 43 0.033
405
P PRC031 Preeclampsia/eclampsia 1 42 0.033
406
NRP045 Neuropathy, Ataxia, and Retinitis Pigmentosa 42 0.033
407
c MJR024 Major Affective Disorder 9 42 0.033
408
P HYP263 Hypersomnia 42 0.033
409
GST020 Gastric Antral Vascular Ectasia 42 0.033
410
TRP009 Triple X Syndrome 42 0.033
411
c MCR112 Microvascular Complications of Diabetes 2 42 0.033
412
AMN002 Amino Acid Metabolic Disorder 42 0.033
413
RDN001 Reading Disorder 42 0.033
414
c SPR086 Spermatogenic Failure 3 41 0.033
415
CRV045 Cervical Intraepithelial Neoplasia 41 0.033
416
MNN028 Mononeuropathy of the Median Nerve, Mild 41 0.033
417
P SBR004 Seborrheic Dermatitis 41 0.033
418
ULC007 Ulcerative Stomatitis 41 0.033
419
MCR017 Macrocytic Anemia 41 0.033
420
ORC001 Orchitis 41 0.033
421
MYF001 Myofibroma 40 0.033
422
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.033
423
P PRG092 Pregnancy Loss, Recurrent 1 40 0.033
424
c PSR028 Psoriasis 7 40 0.033
425
c PSR018 Psoriasis 13 40 0.033
426
c PSR032 Psoriasis 11 40 0.033
427
P HMF004 Hemifacial Spasm 40 0.033
428
c OVR114 Ovarian Cancer 1 39 0.033
429
49X002 49,xxxxy Syndrome 39 0.033
430
ETH004 Euthyroid Sick Syndrome 39 0.033
431
HPT070 Hepatosplenic T-Cell Lymphoma 39 0.033
432
c MJR022 Major Affective Disorder 8 39 0.033
433
c HRD088 Hereditary Neuropathies 39 0.033
434
WGN007 Wagner Vitreoretinopathy 38 0.033
435
BKR002 Baker-Gordon Syndrome 38 0.033
436
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.033
437
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.033
438
c PLY105 Polycystic Ovary Syndrome 1 38 0.033
439
WGN003 Wagner Syndrome 38 0.033
440
NDL024 Nodal Marginal Zone Lymphoma 37 0.033
441
48X005 48,xyyy 37 0.033
442
BCK003 Background Diabetic Retinopathy 37 0.033
443
c RCR002 Recurrent Hypersomnia 37 0.033
444
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 37 0.033
445
PRM155 Primary Cutaneous Anaplastic Large Cell Lymphoma 36 0.033
446
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 36 0.033
447
c MJR008 Major Affective Disorder 2 35 0.033
448
NRV004 Nerve Compression Syndrome 35 0.033
449
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 35 0.033
450
c SCH080 Schizophrenia 3 34 0.033
451
FLC001 Folic Acid Deficiency Anemia 34 0.033
452
c MJR003 Major Affective Disorder 6 34 0.033
453
c MJR006 Major Affective Disorder 5 34 0.033
454
c PRS136 Prostate Cancer, Hereditary, 6 34 0.033
455
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 34 0.033
456
CYC005 Cyclothymic Disorder 34 0.033
457
c HMF011 Hemifacial Spasm, Familial 34 0.033
458
c MJR023 Major Affective Disorder 7 34 0.033
459
TQP001 Taqi Polymorphism 34 0.033
460
c PRS130 Prostate Cancer, Hereditary, 8 33 0.033
461
c ADV003 Advanced Sleep Phase Syndrome, Familial, 1 33 0.033
462
RRS014 Rare Surgical Neurologic Disease 33 0.033
463
DSR002 Disorders of Intracellular Cobalamin Metabolism 32 0.033
464
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 32 0.033
465
STT009 Sutton Disease 2 31 0.033
466
c CRN133 Coronary Artery Disease, Autosomal Dominant, 1 31 0.033
467
LYM098 Lymphomatous Meningitis 31 0.033
468
c MJR004 Major Affective Disorder 4 29 0.033
469
TMR016 Tumor Suppressor Gene on Chromosome 11 29 0.033
470
TMP019 Temporomandibular Joint Anomaly 29 0.033
471
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 28 0.033
472
CHL079 Children's Interstitial Lung Disease 27 0.033
473
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 27 0.033
474
ACT181 Acute Motor Axonal Neuropathy 27 0.033
475
HDG004 Hodgkin's Granuloma 27 0.033
476
MLR020 Malaria, Mild 27 0.033
477
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.033
478
PGM030 Pigmentation Anomaly of the Skin 26 0.033
479
MTH071 Methane Production 26 0.033
480
PRR019 Perioral Myoclonia with Absences 25 0.033
481
NN2002 Non 24 Hour Sleep Wake Disorder 24 0.033
482
HDG006 Hodgkin's Paragranuloma 23 0.033
483
c NSP009 Nasopharyngeal Carcinoma 2 22 0.033
484
AMN012 Aminoacidopathies 22 0.033
485
MTH068 Methylmalonic Aciduria, Transient, Due to Transcobalamin Receptor Defect 18 0.033
486
P INB001 Inborn Amino Acid Metabolism Disorder 11 0.033
487
c MTH069 Methylmalonic Acidemia Due to Transcobalamin Receptor Defect 7 0.033
Content
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