Search results for Hydroxocobalamin

538 hits were found for Hydroxocobalamin

# Family MCID Name MIFTS Score
1
CYN003 Cyanide Poisoning 24 0.236
2
VTM002 Vitamin B12 Deficiency 48 0.105
3
PRN011 Pernicious Anemia 51 0.088
4
MTB004 Metabolic Acidosis 48 0.077
5
DFC004 Deficiency Anemia 77 0.072
6
P CRD119 Cardiac Arrest 71 0.065
7
OCL069 Ocular Motor Apraxia 53 0.065
8
P HMC002 Homocystinuria 52 0.065
9
P MTH008 Methylmalonic Acidemia 50 0.065
10
P KDN018 Kidney Disease 73 0.059
11
END030 End Stage Renal Failure 60 0.059
12
DBT010 Diabetic Neuropathy 56 0.059
13
P MGL001 Megaloblastic Anemia 54 0.059
14
DBT002 Diabetic Autonomic Neuropathy 45 0.059
15
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.051
16
P MLT020 Multiple Sclerosis 73 0.051
17
P CRN018 Coronary Artery Anomaly 67 0.051
18
c MCR129 Microvascular Complications of Diabetes 1 67 0.051
19
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 64 0.051
20
TXC005 Toxic Shock Syndrome 63 0.051
21
ISC004 Ischemia 62 0.051
22
ART140 Arteries, Anomalies of 60 0.051
23
P CRN300 Coronary Heart Disease 1 59 0.051
24
P EXN002 Exanthem 58 0.051
25
P NRP001 Neuropathy 57 0.051
26
HRT012 Heart Valve Disease 56 0.051
27
HMC014 Homocysteinemia 54 0.051
28
GLS018 Glass Syndrome 51 0.051
29
TRN022 Transcobalamin Ii Deficiency 50 0.051
30
P MTH007 Methemoglobinemia 47 0.051
31
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.051
32
DSR002 Disorders of Intracellular Cobalamin Metabolism 32 0.051
33
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.051
34
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.041
35
LPT014 Leptin Deficiency or Dysfunction 72 0.041
36
P URT039 Urticaria 61 0.041
37
c ACT071 Acute Kidney Failure 60 0.041
38
P LYM031 Lymphocytic Leukemia 56 0.041
39
P MCR010 Microcephaly 56 0.041
40
DYS073 Dysphagia 52 0.041
41
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.041
42
AMB002 Amblyopia 51 0.041
43
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.041
44
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 49 0.041
45
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.041
46
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.041
47
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.041
48
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.041
49
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.041
50
LPT006 Leptin Receptor Deficiency 47 0.041
51
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.041
52
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.041
53
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.041
54
SPP007 Suppression Amblyopia 37 0.041
55
HMC033 Homocystinuria-Megaloblastic Anemia, Cblg Complementation Type 36 0.041
56
ALC011 Alcoholic Neuropathy 35 0.041
57
c ACQ047 Acquired Methemoglobinemia 33 0.041
58
ISL099 Isolated Methylmalonic Acidemia 30 0.041
59
TRN059 Transcobalamin Deficiency 21 0.041
60
P CLR023 Colorectal Cancer 100 0.029
61
P HPT023 Hepatocellular Carcinoma 99 0.029
62
P BRS047 Breast Cancer 99 0.029
63
P PRS040 Prostate Cancer 97 0.029
64
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.029
65
P ALZ034 Alzheimer Disease 90 0.029
66
P OVR042 Ovarian Cancer 89 0.029
67
c SYS001 Systemic Lupus Erythematosus 88 0.029
68
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.029
69
c HYP595 Hypertension, Essential 87 0.029
70
P GST053 Gastric Cancer 85 0.029
71
MYL069 Myeloma, Multiple 85 0.029
72
c LKM061 Leukemia, Acute Myeloid 84 0.029
73
CYS001 Cystic Fibrosis 84 0.029
74
NRL016 Neural Tube Defects 83 0.029
75
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.029
76
MLR004 Malaria 82 0.029
77
STR067 Stroke, Ischemic 82 0.029
78
P RHM011 Rheumatoid Arthritis 82 0.029
79
SQM013 Squamous Cell Carcinoma, Head and Neck 81 0.029
80
AST005 Asthma 80 0.029
81
IMM167 Immune Deficiency Disease 79 0.029
82
P OST002 Osteoporosis 79 0.029
83
P BLD134 Bladder Cancer 79 0.029
84
P LNG064 Lung Cancer Susceptibility 3 79 0.029
85
P HRT032 Heart Disease 78 0.029
86
P PRK057 Parkinson Disease, Late-Onset 77 0.029
87
P SCH015 Schizophrenia 76 0.029
88
c ATR087 Atrial Standstill 1 76 0.029
89
P RSP003 Respiratory Failure 75 0.029
90
BRN028 Brain Cancer 75 0.029
91
ANX010 Anxiety 75 0.029
92
c THR092 Thrombophilia Due to Thrombin Defect 74 0.029
93
GLB002 Glioblastoma 74 0.029
94
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.029
95
P MYC007 Myocardial Infarction 74 0.029
96
c HPT073 Hepatitis C Virus 74 0.029
97
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.029
98
P EPL164 Epilepsy 73 0.029
99
HMN044 Human Immunodeficiency Virus Type 1 73 0.029
100
PRP027 Peripheral Vascular Disease 72 0.029
101
P CNR004 Cone-Rod Dystrophy 2 72 0.029
102
PLM001 Pulmonary Tuberculosis 72 0.029
103
P SRC025 Sarcoidosis 1 72 0.029
104
MYL009 Myelodysplastic Syndrome 72 0.029
105
P ART022 Arthritis 71 0.029
106
P PNM007 Pneumonia 71 0.029
107
P LVR013 Liver Disease 71 0.029
108
CRB039 Cerebrovascular Disease 71 0.029
109
c MGR028 Migraine with or Without Aura 1 70 0.029
110
MSC157 Muscular Dystrophy, Duchenne Type 70 0.029
111
P HYP086 Hypothyroidism 70 0.029
112
RCK004 Rickets 70 0.029
113
FRN006 Frontotemporal Dementia 70 0.029
114
LYM133 Lymphoma, Hodgkin, Classic 70 0.029
115
BHC003 Behcet Syndrome 70 0.029
116
P LYM118 Lymphoma 70 0.029
117
c ATS007 Autism Spectrum Disorder 69 0.029
118
CRB037 Cerebral Palsy 69 0.029
119
P MYC084 Mycobacterium Tuberculosis 1 69 0.029
120
P INF038 Influenza 69 0.029
121
P HPT021 Hepatitis 69 0.029
122
LGH007 Leigh Syndrome 69 0.029
123
CNG034 Congestive Heart Failure 69 0.029
124
P MJR001 Major Depressive Disorder 69 0.029
125
P LKM002 Leukemia 69 0.029
126
P ATS364 Autism 68 0.029
127
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.029
128
c CHR684 Chronic Kidney Disease 68 0.029
129
P DMN002 Dementia 68 0.029
130
P HYD006 Hydrocephalus 68 0.029
131
ALC007 Alcohol Dependence 68 0.029
132
HYP056 Hypoglycemia 68 0.029
133
P LKM062 Leukemia, Acute Lymphoblastic 68 0.029
134
ATH013 Atherosclerosis Susceptibility 68 0.029
135
PSY004 Psychotic Disorder 68 0.029
136
P GLM040 Glioma Susceptibility 1 68 0.029
137
ADR054 Adrenocortical Carcinoma, Hereditary 68 0.029
138
P MSC005 Muscular Dystrophy 68 0.029
139
P NRV007 Nervous System Disease 68 0.029
140
CRP001 Carpal Tunnel Syndrome 68 0.029
141
P DRM053 Dermatitis, Atopic 68 0.029
142
c FML001 Familial Atrial Fibrillation 67 0.029
143
P MCR115 Microvascular Complications of Diabetes 5 67 0.029
144
P NSP012 Nasopharyngeal Carcinoma 67 0.029
145
P ATR011 Atrial Fibrillation 67 0.029
146
P OLG002 Oligodendroglioma 67 0.029
147
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.029
148
P THR014 Thrombocytopenia 67 0.029
149
LVR012 Liver Cirrhosis 67 0.029
150
P MNN013 Meningitis 67 0.029
151
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.029
152
c SML038 Small Cell Cancer of the Lung 67 0.029
153
MYC006 Mycosis Fungoides 67 0.029
154
P DBT009 Diabetes Mellitus 66 0.029
155
P CLC063 Celiac Disease 1 66 0.029
156
P BLD124 Bleeding Disorder, Platelet-Type, 11 66 0.029
157
PRT037 Pertussis 66 0.029
158
ACR008 Acrocallosal Syndrome 66 0.029
159
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.029
160
P PRS038 Personality Disorder 66 0.029
161
MYL031 Myeloproliferative Neoplasm 66 0.029
162
DSS008 Disease of Mental Health 66 0.029
163
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.029
164
ANG054 Angina Pectoris 66 0.029
165
P TRN020 Turner Syndrome 66 0.029
166
DMN031 Dementia, Lewy Body 66 0.029
167
P MTR014 Motor Neuron Disease 66 0.029
168
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.029
169
P VSC007 Vascular Disease 65 0.029
170
P DYS154 Dystonia 65 0.029
171
P OCL013 Oculodentodigital Dysplasia 65 0.029
172
P ANG001 Angelman Syndrome 65 0.029
173
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 65 0.029
174
P ADN016 Adenocarcinoma 65 0.029
175
ALL026 Allergic Hypersensitivity Disease 65 0.029
176
FCT007 Factor Vii Deficiency 65 0.029
177
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.029
178
DPR016 Depression 64 0.029
179
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.029
180
P PRP019 Peripheral Nervous System Disease 64 0.029
181
CLR108 Colorectal Adenoma 64 0.029
182
c RHB024 Rhabdomyosarcoma 2 64 0.029
183
SKN016 Skin Disease 64 0.029
184
CNT061 Conotruncal Heart Malformations 64 0.029
185
FLL027 Fallopian Tube Carcinoma 64 0.029
186
c FNC043 Fanconi Anemia, Complementation Group E 64 0.029
187
LPD008 Lipid Metabolism Disorder 64 0.029
188
P NTR004 Neutropenia 64 0.029
189
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.029
190
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 63 0.029
191
DRM006 Dermatitis 63 0.029
192
KHL003 Kohlschutter-Tonz Syndrome 63 0.029
193
P PSR002 Psoriasis 63 0.029
194
c HPT016 Hepatitis B 63 0.029
195
c PRC016 Pre-Eclampsia 63 0.029
196
PRP001 Propionic Acidemia 63 0.029
197
c ALP101 Alpha-Thalassemia 63 0.029
198
P MVM001 Movement Disease 63 0.029
199
PCK003 Pick Disease of Brain 63 0.029
200
PPL049 Papillon-Lefevre Syndrome 63 0.029
201
LYS012 Lysosomal Acid Lipase Deficiency 63 0.029
202
HYP066 Hyperglycemia 63 0.029
203
SPN186 Spinal Cord Injury 63 0.029
204
MDD011 Mood Disorder 62 0.029
205
ADL002 Adult Syndrome 62 0.029
206
BLD131 Bladder Urothelial Carcinoma 62 0.029
207
P LPS004 Lupus Erythematosus 62 0.029
208
LYM012 Lymphoplasmacytic Lymphoma 62 0.029
209
P THL005 Thalassemia 62 0.029
210
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.029
211
NRM005 Neuromuscular Disease 62 0.029
212
VRL011 Viral Infectious Disease 62 0.029
213
TTN003 Tetanus 62 0.029
214
P LYM033 Lymphoproliferative Syndrome 62 0.029
215
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.029
216
c HPT001 Hepatitis C 62 0.029
217
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 62 0.029
218
ATM095 Autoimmune Disease 62 0.029
219
P ANP001 Anaplastic Large Cell Lymphoma 62 0.029
220
c PNS012 Paine Syndrome 61 0.029
221
PRT013 Portal Hypertension 61 0.029
222
P ART023 Arthropathy 61 0.029
223
CRY035 Cryptorchidism, Unilateral or Bilateral 61 0.029
224
LBR030 Leber Optic Atrophy 61 0.029
225
ACQ007 Acquired Immunodeficiency Syndrome 61 0.029
226
CHR066 Chronic Fatigue Syndrome 61 0.029
227
P BCL017 B-Cell Lymphoma 61 0.029
228
P MYL006 Myeloid Leukemia 61 0.029
229
NTR005 Nutritional Deficiency Disease 61 0.029
230
MSL001 Measles 61 0.029
231
P PNC044 Pancreatitis 61 0.029
232
THR100 Thrombocytopenic Purpura, Autoimmune 61 0.029
233
HLC007 Helicobacter Pylori Infection 61 0.029
234
DPH001 Diphtheria 61 0.029
235
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.029
236
GLB015 Glioblastoma Multiforme 60 0.029
237
SQM006 Squamous Cell Carcinoma 60 0.029
238
P CRB101 Cerebrooculofacioskeletal Syndrome 1 60 0.029
239
CHR072 Chordoma 60 0.029
240
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.029
241
MNT002 Mental Depression 60 0.029
242
INT002 Intermittent Claudication 60 0.029
243
PLM033 Pulmonary Embolism 60 0.029
244
c HPT003 Hepatitis a 60 0.029
245
ADN018 Adenoma 60 0.029
246
P INF032 Infertility 60 0.029
247
RNL024 Renal Glucosuria 59 0.029
248
GRD007 Grade Iii Astrocytoma 59 0.029
249
P SZR006 Seizure Disorder 59 0.029
250
SZR001 Sezary's Disease 59 0.029
251
NRN004 Neuroendocrine Tumor 59 0.029
252
P BPL003 Bipolar Disorder 59 0.029
253
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 59 0.029
254
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.029
255
CNS004 Constipation 59 0.029
256
c ACT075 Acute Myocardial Infarction 59 0.029
257
IRN001 Iron Deficiency Anemia 59 0.029
258
c MST023 Mesothelioma, Malignant 59 0.029
259
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 58 0.029
260
VSL002 Visual Epilepsy 58 0.029
261
P PRV006 Pervasive Developmental Disorder 58 0.029
262
P PLY011 Polycystic Ovary Syndrome 58 0.029
263
GST033 Gestational Diabetes 58 0.029
264
PLM031 Poliomyelitis 58 0.029
265
TRD006 Tardive Dyskinesia 58 0.029
266
P ALC033 Alcohol Use Disorder 58 0.029
267
HYP266 Hypoxia 58 0.029
268
IRN002 Iron Metabolism Disease 58 0.029
269
THR024 Thrombosis 58 0.029
270
AGN016 Aging 58 0.029
271
P SLP005 Sleep Disorder 58 0.029
272
GLB001 Gilbert Syndrome 58 0.029
273
ERY029 Erythermalgia, Primary 58 0.029
274
INT007 Intermediate Coronary Syndrome 58 0.029
275
P GST044 Gastritis 58 0.029
276
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 57 0.029
277
RBS001 Rabies 57 0.029
278
P INF037 Inflammatory Bowel Disease 57 0.029
279
BRN045 Brunner Syndrome 57 0.029
280
BCT022 Bacterial Infectious Disease 57 0.029
281
GST050 Gastrointestinal System Disease 57 0.029
282
LMY014 Leiomyoma, Uterine 57 0.029
283
P MMP001 Mumps 57 0.029
284
TRN018 Transitional Cell Carcinoma 57 0.029
285
HMG005 Hemoglobinopathy 57 0.029
286
P MLN007 Male Infertility 57 0.029
287
VSC002 Vascular Dementia 57 0.029
288
PTN001 Patent Foramen Ovale 57 0.029
289
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.029
290
BRN004 Brain Edema 57 0.029
291
APH002 Aphasia 56 0.029
292
PRP030 Purpura 56 0.029
293
APH001 Aphthous Stomatitis 56 0.029
294
CMR002 Coumarin Resistance 56 0.029
295
P RBL001 Rubella 56 0.029
296
HMN014 Human Immunodeficiency Virus Infectious Disease 56 0.029
297
P RTN016 Retinal Degeneration 56 0.029
298
c CNT035 Central Nervous System Disease 56 0.029
299
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.029
300
MCS002 Mucositis 56 0.029
301
P ANT006 Antiphospholipid Syndrome 56 0.029
302
GLS001 Gliosarcoma 56 0.029
303
PPL022 Papilloma 56 0.029
304
PRT038 Protein-Energy Malnutrition 56 0.029
305
P ART021 Arteriosclerosis 56 0.029
306
P LTR001 Lateral Sclerosis 56 0.029
307
c FML035 Familial Hyperlipidemia 56 0.029
308
SNS003 Sensory Peripheral Neuropathy 56 0.029
309
P SBS003 Substance Abuse 56 0.029
310
VTM027 Vitamin D-Dependent Rickets, Type 2a 56 0.029
311
c CNG216 Congenital Hydrocephalus 55 0.029
312
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 55 0.029
313
ACD008 Acid-Labile Subunit Deficiency 55 0.029
314
AMN003 Amnestic Disorder 55 0.029
315
HYP060 Hyperinsulinism 55 0.029
316
END040 Endogenous Depression 55 0.029
317
HYP005 Hypokalemia 55 0.029
318
P DRR001 Diarrhea 55 0.029
319
MSS001 Masa Syndrome 55 0.029
320
c PSR017 Psoriasis 2 55 0.029
321
P TRM003 Tremor 55 0.029
322
P PLY019 Polyneuropathy 55 0.029
323
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 55 0.029
324
P NRV006 Nervous System Cancer 55 0.029
325
P OPT009 Optic Neuritis 55 0.029
326
MRG003 Marginal Zone B-Cell Lymphoma 55 0.029
327
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 54 0.029
328
DRR016 Diarrhea 2, with Microvillus Atrophy 54 0.029
329
TRM010 Traumatic Brain Injury 54 0.029
330
HMT018 Hematopoietic Stem Cell Transplantation 54 0.029
331
GTR002 Goiter 54 0.029
332
c SCN036 Secondary Progressive Multiple Sclerosis 54 0.029
333
LYM040 Lymphoblastic Lymphoma 54 0.029
334
TXC002 Toxic Encephalopathy 54 0.029
335
AMN001 Amenorrhea 54 0.029
337
c PRM092 Primary Lateral Sclerosis, Adult, 1 54 0.029
338
P HMR003 Hemorrhagic Disease 54 0.029
339
PTH003 Pathologic Nystagmus 53 0.029
340
PRP036 Peripheral T-Cell Lymphoma 53 0.029
341
CHC001 Chickenpox 53 0.029
342
c LRG017 Large Intestine Cancer 53 0.029
343
P ECL001 Eclampsia 53 0.029
344
P RTN018 Retinal Disease 53 0.029
345
THY030 Thyroid Gland Disease 53 0.029
346
NRT001 Neurotic Disorder 53 0.029
347
NNL006 Non-Alcoholic Steatohepatitis 53 0.029
348
SPS003 Spastic Diplegia 53 0.029
349
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.029
350
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 52 0.029
351
HYP014 Hyperuricemia 52 0.029
352
FDL002 Food Allergy 52 0.029
353
LMY002 Leiomyoma 52 0.029
354
LNG031 Lung Benign Neoplasm 52 0.029
355
PNG002 Pain Agnosia 52 0.029
356
GNT002 Giant Cell Glioblastoma 52 0.029
357
P CTN015 Cutaneous T Cell Lymphoma 52 0.029
358
P LCT001 Lactic Acidosis 52 0.029
359
NRT004 Neuritis 52 0.029
360
MCL006 Macular Retinal Edema 52 0.029
361
P CHR345 Chronic Pain 52 0.029
362
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.029
363
P AST007 Astrocytoma 52 0.029
364
P MSC003 Muscular Atrophy 52 0.029
365
c CNT033 Central Nervous System Cancer 51 0.029
366
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.029
367
AZS001 Azoospermia 51 0.029
368
PLC008 Placenta Disease 51 0.029
369
P THR015 Thrombophilia 51 0.029
370
STM007 Stomatitis 51 0.029
371
c INH020 Inherited Metabolic Disorder 51 0.029
372
OVR082 Overgrowth Syndrome 51 0.029
373
HYP081 Hypolipoproteinemia 51 0.029
374
PRP080 Peripheral Artery Disease 51 0.029
375
PST021 Postpartum Depression 51 0.029
376
BRN071 Brain Injury 51 0.029
377
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.029
378
BRN009 Burning Mouth Syndrome 51 0.029
379
PST011 Pustulosis of Palm and Sole 51 0.029
380
P PLM006 Pulmonary Alveolar Proteinosis 50 0.029
381
SCH012 Schizoaffective Disorder 50 0.029
382
MNC006 Monoclonal Gammopathy of Uncertain Significance 50 0.029
383
ACR041 Acromelic Frontonasal Dysostosis 50 0.029
384
c PSR023 Psoriasis 1 50 0.029
385
c HMN021 Human T-Cell Leukemia Virus Type 1 50 0.029
386
MCR004 Macroglobulinemia 50 0.029
387
NRL018 Neural Tube Defects, Folate-Sensitive 50 0.029
388
SCH003 Schizophreniform Disorder 49 0.029
389
TST044 Testicular Torsion 49 0.029
390
c PRM108 Primary Progressive Multiple Sclerosis 49 0.029
391
ANG046 Angioimmunoblastic T-Cell Lymphoma 49 0.029
392
P ATR005 Atrophic Gastritis 49 0.029
393
c LTN004 Late-Onset Retinal Degeneration 49 0.029
394
SQM002 Squamous Cell Papilloma 49 0.029
395
BHV002 Behavioral Variant of Frontotemporal Dementia 49 0.029
396
47X002 47,xyy 49 0.029
397
BWN001 Bowen-Conradi Syndrome 49 0.029
398
HPR003 Heparin-Induced Thrombocytopenia 49 0.029
399
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.029
400
SPL018 Splenomegaly 48 0.029
401
c MCR120 Microvascular Complications of Diabetes 7 48 0.029
402
HYP781 Hypoascorbemia 48 0.029
403
PTH002 Pathological Gambling 48 0.029
404
PRS034 Parasitic Helminthiasis Infectious Disease 48 0.029
405
RTC005 Reticulosarcoma 48 0.029
406
LYM019 Lymphosarcoma 48 0.029
407
LNG015 Lingual-Facial-Buccal Dyskinesia 48 0.029
408
DBT004 Diabetic Polyneuropathy 48 0.029
409
c OPT050 Opitz Gbbb Syndrome, Type Ii 48 0.029
410
ACT113 Acute Myeloblastic Leukemia with Maturation 48 0.029
411
MTH078 Methylmalonic Aciduria, Cblb Type 47 0.029
412
NSS002 Neisseria Meningitidis Infection 47 0.029
413
P PLL002 Pellagra 47 0.029
414
VTM033 Vitamin K Deficiency Bleeding 47 0.029
415
KRT002 Keratomalacia 47 0.029
416
c CRV002 Cervix Uteri Carcinoma in Situ 47 0.029
417
P BNG032 Benign Mesothelioma 47 0.029
418
PNN001 Panniculitis 47 0.029
419
MCL027 Macular Dystrophy, Dominant Cystoid 47 0.029
420
CYT002 Cytokine Deficiency 46 0.029
421
DBT006 Diabetic Macular Edema 46 0.029
422
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.029
423
MNN020 Meningococcal Infection 46 0.029
424
HMP009 Haemophilus Influenzae 46 0.029
425
SYN036 Syncope 46 0.029
426
MTH021 Methylmalonic Acidemia with Homocystinuria 46 0.029
427
ATX019 Ataxia with Vitamin E Deficiency 46 0.029
428
LWC001 Low Compliance Bladder 45 0.029
429
P BCT020 Bacteremia 2 45 0.029
430
c PRM038 Primary Agammaglobulinemia 45 0.029
431
c DRM054 Dermatitis, Atopic, 2 45 0.029
432
MYC005 Myocardial Stunning 45 0.029
433
CRB090 Cerebral Hypoxia 45 0.029
434
PRT035 Peritoneum Cancer 45 0.029
435
CYN002 Cyanosis, Transient Neonatal 45 0.029
436
c SCH085 Schizophrenia 2 45 0.029
437
CTS005 Catastrophic Antiphospholipid Syndrome 44 0.029
438
BCK006 Back Pain 44 0.029
439
GLS007 Glossitis 44 0.029
440
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 44 0.029
441
ANP009 Anaplastic Oligodendroglioma 44 0.029
442
P MJR007 Major Affective Disorder 1 44 0.029
443
ANX004 Anoxia 44 0.029
444
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.029
445
MNN032 Meningococcal Meningitis 43 0.029
446
ATN004 Autonomic Neuropathy 43 0.029
447
URT051 Ureter, Cancer of 43 0.029
448
P HYP265 Hypotonia 43 0.029
449
c MLG079 Malignant Pleural Mesothelioma 43 0.029
450
FNT005 Fontaine Progeroid Syndrome 43 0.029
451
LKS001 Leukostasis 43 0.029
452
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.029
453
SBC016 Subacute Delirium 43 0.029
454
P RRT020 Rare Tumor 43 0.029
455
ORG002 Organic Acidemia 43 0.029
456
P PRC031 Preeclampsia/eclampsia 1 42 0.029
457
NRP045 Neuropathy, Ataxia, and Retinitis Pigmentosa 42 0.029
458
c MJR024 Major Affective Disorder 9 42 0.029
459
TRP009 Triple X Syndrome 42 0.029
460
c MCR112 Microvascular Complications of Diabetes 2 42 0.029
461
AMN002 Amino Acid Metabolic Disorder 42 0.029
462
RDN001 Reading Disorder 42 0.029
463
c SPR086 Spermatogenic Failure 3 41 0.029
464
CRV045 Cervical Intraepithelial Neoplasia 41 0.029
465
MNN028 Mononeuropathy of the Median Nerve, Mild 41 0.029
466
ULC007 Ulcerative Stomatitis 41 0.029
467
P HRD086 Hereditary Hypophosphatemic Rickets 41 0.029
468
P BRB001 Beriberi 41 0.029
469
ORC001 Orchitis 41 0.029
470
MYF001 Myofibroma 40 0.029
471
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.029
472
P PRG092 Pregnancy Loss, Recurrent 1 40 0.029
474
c PSR028 Psoriasis 7 40 0.029
475
c PSR018 Psoriasis 13 40 0.029
476
c PSR032 Psoriasis 11 40 0.029
477
c OVR114 Ovarian Cancer 1 39 0.029
478
49X002 49,xxxxy Syndrome 39 0.029
479
ETH004 Euthyroid Sick Syndrome 39 0.029
480
HPT070 Hepatosplenic T-Cell Lymphoma 39 0.029
481
c SYS043 Systemic Lupus Erythematosus 1 39 0.029
482
c MJR022 Major Affective Disorder 8 39 0.029
483
WGN007 Wagner Vitreoretinopathy 38 0.029
484
BKR002 Baker-Gordon Syndrome 38 0.029
485
MTH055 Methylmalonic Aciduria and Homocystinuria, Cbld Type 38 0.029
486
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.029
487
c PLY105 Polycystic Ovary Syndrome 1 38 0.029
488
WGN003 Wagner Syndrome 38 0.029
489
ATM052 Autoimmune Disease 1 38 0.029
490
CRY036 Cryptogenic Cirrhosis 38 0.029
491
NDL024 Nodal Marginal Zone Lymphoma 37 0.029
492
48X005 48,xyyy 37 0.029
493
BCK003 Background Diabetic Retinopathy 37 0.029
494
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 37 0.029
495
MTH056 Methylmalonic Aciduria and Homocystinuria, Cblf Type 37 0.029
496
PRM155 Primary Cutaneous Anaplastic Large Cell Lymphoma 36 0.029
497
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 36 0.029
498
c MJR008 Major Affective Disorder 2 35 0.029
499
NRV004 Nerve Compression Syndrome 35 0.029
500
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 35 0.029
501
c ALZ050 Alzheimer Disease 5 34 0.029
502
c SCH080 Schizophrenia 3 34 0.029
503
FLC001 Folic Acid Deficiency Anemia 34 0.029
504
c MJR003 Major Affective Disorder 6 34 0.029
505
c MJR006 Major Affective Disorder 5 34 0.029
506
NRD037 Neurodevelopmental Disorder with Dysmorphic Facies and Distal Limb Anomalies 34 0.029
507
c PRS136 Prostate Cancer, Hereditary, 6 34 0.029
508
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 34 0.029
509
CYC005 Cyclothymic Disorder 34 0.029
510
c MJR023 Major Affective Disorder 7 34 0.029
511
TQP001 Taqi Polymorphism 34 0.029
512
c PRS130 Prostate Cancer, Hereditary, 8 33 0.029
513
c ADV003 Advanced Sleep Phase Syndrome, Familial, 1 33 0.029
514
RRS014 Rare Surgical Neurologic Disease 33 0.029
515
PYR009 Pyridoxine Deficiency Anemia 32 0.029
516
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 32 0.029
517
ATR073 Atrophic Glossitis 32 0.029
518
PYR016 Pyridoxine Deficiency 31 0.029
519
STT009 Sutton Disease 2 31 0.029
520
c CRN133 Coronary Artery Disease, Autosomal Dominant, 1 31 0.029
521
LYM098 Lymphomatous Meningitis 31 0.029
523
c MJR004 Major Affective Disorder 4 29 0.029
524
TMR016 Tumor Suppressor Gene on Chromosome 11 29 0.029
525
TMP019 Temporomandibular Joint Anomaly 29 0.029
526
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 28 0.029
527
CHL079 Children's Interstitial Lung Disease 27 0.029
528
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 27 0.029
529
HDG004 Hodgkin's Granuloma 27 0.029
530
MLR020 Malaria, Mild 27 0.029
531
PGM030 Pigmentation Anomaly of the Skin 26 0.029
532
PRR019 Perioral Myoclonia with Absences 25 0.029
533
FRN030 Frontotemporal Dementia with Parkinsonism-17 25 0.029
534
c ATM060 Autoimmune Atrophic Gastritis 23 0.029
535
HDG006 Hodgkin's Paragranuloma 23 0.029
536
c NSP009 Nasopharyngeal Carcinoma 2 22 0.029
537
AMN012 Aminoacidopathies 22 0.029
538
P INB001 Inborn Amino Acid Metabolism Disorder 11 0.029
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