Search results for Hydroxocobalamin

563 hits were found for Hydroxocobalamin

# Family MCID Name MIFTS Score
1
CYN003 Cyanide Poisoning 22 8.248
2
VTM002 Vitamin B12 Deficiency 48 3.963
3
PRN011 Pernicious Anemia 52 3.688
4
P MTH008 Methylmalonic Acidemia 52 3.166
5
DFC004 Deficiency Anemia 74 3.107
6
MTB004 Metabolic Acidosis 48 3.072
7
MGL001 Megaloblastic Anemia 59 2.899
8
P HMC002 Homocystinuria 52 2.733
9
P CRD119 Cardiac Arrest 68 2.470
10
HMC014 Homocysteinemia 52 2.301
11
TRN022 Transcobalamin Ii Deficiency 44 2.292
12
OCL069 Ocular Motor Apraxia 57 2.274
13
KRT002 Keratomalacia 54 2.267
14
TXC005 Toxic Shock Syndrome 61 2.193
15
ISL099 Isolated Methylmalonic Acidemia 35 2.190
16
P EXN002 Exanthem 58 2.188
17
ANT039 Antisynthetase Syndrome 55 2.067
18
END086 End Stage Renal Disease 54 2.051
19
DSR002 Disorders of Intracellular Cobalamin Metabolism 30 1.902
20
P MTH007 Methemoglobinemia 46 1.852
21
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.761
22
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 57 1.666
23
DBT002 Diabetic Autonomic Neuropathy 40 1.619
24
DBT010 Diabetic Neuropathy 54 1.619
25
P LCT001 Lactic Acidosis 50 1.608
26
CLT003 Colitis 63 1.563
27
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 1.563
28
P ANR048 Aniridia 1 66 1.563
29
c INF071 Inflammatory Bowel Disease 1 65 1.563
30
GLS018 Glass Syndrome 60 1.563
31
ULC004 Ulcerative Colitis 74 1.563
32
DYS073 Dysphagia 53 1.503
33
48X005 48,xyyy 39 1.435
34
TRN059 Transcobalamin Deficiency 24 1.424
35
PLM033 Pulmonary Embolism 58 1.409
36
P HYP265 Hypotonia 42 1.321
37
SPP007 Suppression Amblyopia 38 1.294
38
AMB002 Amblyopia 49 1.294
39
NNL006 Non-Alcoholic Steatohepatitis 54 1.281
40
c ACQ047 Acquired Methemoglobinemia 30 1.261
41
c HYP724 Hyperlipoproteinemia, Type Iii 66 1.218
42
P CRN300 Coronary Heart Disease 1 73 1.218
43
ART140 Arteries, Anomalies of 52 1.218
44
LPP008 Lipoprotein Quantitative Trait Locus 65 1.218
45
ADL002 Adult Syndrome 69 1.218
46
HRT012 Heart Valve Disease 53 1.218
47
P MCR010 Microcephaly 59 1.199
48
P URT039 Urticaria 57 1.159
49
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 1.120
50
HMC033 Homocystinuria-Megaloblastic Anemia, Cblg Complementation Type 35 1.081
51
P MLT020 Multiple Sclerosis 79 1.066
52
CYN002 Cyanosis, Transient Neonatal 43 1.064
53
ANX004 Anoxia 40 1.064
54
MTH021 Methylmalonic Acidemia with Homocystinuria 44 1.061
55
SQM006 Squamous Cell Carcinoma 59 1.038
56
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.976
57
P PNC035 Pancreatic Cancer 87 0.976
58
HYP781 Hypoascorbemia 52 0.976
59
ACT011 Acute Contagious Conjunctivitis 41 0.976
60
P CNJ013 Conjunctivitis 66 0.976
61
P ADN016 Adenocarcinoma 63 0.976
62
PNC129 Pancreatic Adenocarcinoma 64 0.976
63
P PNC044 Pancreatitis 61 0.976
64
c ACT027 Acute Pancreatitis 60 0.976
65
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.976
66
PTH003 Pathologic Nystagmus 52 0.974
67
c MGR028 Migraine with or Without Aura 1 63 0.936
68
CRY036 Cryptogenic Cirrhosis 36 0.936
69
CRB090 Cerebral Hypoxia 42 0.936
70
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 0.932
71
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.932
72
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.932
73
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.932
74
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.932
75
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 0.932
76
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.932
77
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 35 0.932
78
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.932
79
LPT014 Leptin Deficiency or Dysfunction 77 0.932
80
LPT006 Leptin Receptor Deficiency 50 0.932
81
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 0.932
82
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.932
83
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.932
84
P MCR129 Microvascular Complications of Diabetes 1 67 0.926
85
PTN001 Patent Foramen Ovale 61 0.833
86
NRT004 Neuritis 53 0.833
87
P OPT009 Optic Neuritis 57 0.833
88
MTH055 Methylmalonic Aciduria and Homocystinuria, Cbld Type 38 0.693
89
RBS001 Rabies 57 0.693
90
SYN036 Syncope 44 0.693
91
SPN186 Spinal Cord Injury 60 0.693
92
P GST044 Gastritis 55 0.689
93
P PRP019 Peripheral Nervous System Disease 57 0.659
94
P ATR005 Atrophic Gastritis 50 0.659
95
P NRP001 Neuropathy 59 0.659
96
MCR017 Macrocytic Anemia 44 0.625
97
P NTR004 Neutropenia 62 0.625
98
P THR014 Thrombocytopenia 66 0.625
99
c INH020 Inherited Metabolic Disorder 47 0.625
100
SBC016 Subacute Delirium 42 0.588
101
ALC011 Alcoholic Neuropathy 35 0.581
102
MTH078 Methylmalonic Aciduria, Cblb Type 47 0.543
103
GLS007 Glossitis 46 0.543
104
P HYP086 Hypothyroidism 68 0.543
105
SVR001 Severe Acute Respiratory Syndrome 68 0.543
106
P MSC005 Muscular Dystrophy 66 0.543
107
P HML001 Hemolytic-Uremic Syndrome 52 0.525
108
PRP001 Propionic Acidemia 65 0.485
109
P ALZ034 Alzheimer Disease 87 0.485
110
STR067 Stroke, Ischemic 79 0.485
111
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.485
112
P MYC007 Myocardial Infarction 69 0.485
113
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.485
114
PPL022 Papilloma 53 0.485
115
P MLN007 Male Infertility 56 0.485
116
P DRR001 Diarrhea 55 0.485
117
P ALC033 Alcohol Use Disorder 67 0.485
118
BRN009 Burning Mouth Syndrome 51 0.485
119
ISC004 Ischemia 61 0.485
120
PYR009 Pyridoxine Deficiency Anemia 35 0.485
121
STM007 Stomatitis 52 0.485
122
P THY032 Thyroiditis 56 0.485
123
c CHR684 Chronic Kidney Disease 73 0.485
124
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.485
125
HYP056 Hypoglycemia 65 0.485
126
PNC001 Pancytopenia 52 0.466
127
THR123 Thrombotic Microangiopathy 40 0.421
128
P PLM037 Pulmonary Hypertension 69 0.397
129
P HYD006 Hydrocephalus 62 0.397
130
P PRV006 Pervasive Developmental Disorder 52 0.345
131
c ATS007 Autism Spectrum Disorder 71 0.345
132
ORG002 Organic Acidemia 43 0.345
133
P SCL018 Scoliosis 57 0.345
134
MLR004 Malaria 77 0.345
135
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.345
136
c MJR022 Major Affective Disorder 8 37 0.345
137
RSP027 Respiratory Papillomatosis, Juvenile Recurrent, Congenital 47 0.345
138
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.345
140
P ATR011 Atrial Fibrillation 66 0.345
141
MYL009 Myelodysplastic Syndrome 67 0.345
142
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.345
143
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 0.345
144
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.345
145
c PSR028 Psoriasis 7 42 0.345
146
c DRM054 Dermatitis, Atopic, 2 47 0.345
147
APH002 Aphasia 55 0.345
148
P LYM118 Lymphoma 66 0.345
149
P CTN015 Cutaneous T Cell Lymphoma 48 0.345
150
c PSR023 Psoriasis 1 52 0.345
151
P RHM011 Rheumatoid Arthritis 81 0.345
152
P SCH015 Schizophrenia 74 0.345
153
ATH013 Atherosclerosis Susceptibility 63 0.345
154
P ATS364 Autism 72 0.345
155
P CLC063 Celiac Disease 1 65 0.345
156
CNT061 Conotruncal Heart Malformations 66 0.345
157
CHR072 Chordoma 56 0.345
158
DFN344 Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome 55 0.345
159
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 0.345
160
P TRC086 Trichohepatoenteric Syndrome 1 59 0.345
161
CYS001 Cystic Fibrosis 77 0.345
162
c SYS001 Systemic Lupus Erythematosus 85 0.345
163
P FNG006 Feingold Syndrome 1 61 0.345
164
P OST002 Osteoporosis 76 0.345
165
P OVR042 Ovarian Cancer 88 0.345
166
P MJR007 Major Affective Disorder 1 42 0.345
167
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.345
168
c TYP009 Type 2 Diabetes Mellitus 91 0.345
169
DMN031 Dementia, Lewy Body 65 0.345
170
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.345
171
P PRS040 Prostate Cancer 95 0.345
172
P SRC025 Sarcoidosis 1 70 0.345
173
NRL016 Neural Tube Defects 80 0.345
174
P PLV020 Pelvic Organ Prolapse 57 0.345
175
c SML038 Small Cell Cancer of the Lung 68 0.345
176
LYM133 Lymphoma, Hodgkin, Classic 69 0.345
177
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 0.345
178
P HMN038 Human Coronavirus Sensitivity 30 0.345
179
P NJM001 Nijmegen Breakage Syndrome 75 0.345
180
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 56 0.345
181
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 37 0.345
182
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.345
183
MSC157 Muscular Dystrophy, Duchenne Type 78 0.345
184
c MJR008 Major Affective Disorder 2 34 0.345
185
c PNS012 Paine Syndrome 60 0.345
186
ALC007 Alcohol Dependence 65 0.345
187
P BLD134 Bladder Cancer 79 0.345
188
RHB024 Rhabdomyosarcoma 2 65 0.345
189
P BRS047 Breast Cancer 97 0.345
190
P CLR023 Colorectal Cancer 100 0.345
191
SHR109 Short Stature, Auditory Canal Atresia, Mandibular Hypoplasia, and Skeletal Abnormalities 35 0.345
192
ACR041 Acromelic Frontonasal Dysostosis 53 0.345
193
P DRM053 Dermatitis, Atopic 65 0.345
194
c SYS043 Systemic Lupus Erythematosus 1 38 0.345
195
c PSR017 Psoriasis 2 53 0.345
196
c PRS130 Prostate Cancer, Hereditary, 8 32 0.345
197
TMR016 Tumor Suppressor Gene on Chromosome 11 28 0.345
198
c LKM061 Leukemia, Acute Myeloid 83 0.345
199
NRL018 Neural Tube Defects, Folate-Sensitive 46 0.345
200
ALN001 Aland Island Eye Disease 55 0.345
201
ART002 Arts Syndrome 66 0.345
202
AGN016 Aging 53 0.345
203
P NSP012 Nasopharyngeal Carcinoma 60 0.345
204
c HPT073 Hepatitis C Virus 70 0.345
205
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 49 0.345
206
LGS001 Legius Syndrome 60 0.345
207
c MJR006 Major Affective Disorder 5 32 0.345
208
c MJR023 Major Affective Disorder 7 33 0.345
209
c MJR024 Major Affective Disorder 9 40 0.345
210
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.345
211
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.345
212
P GST053 Gastric Cancer 82 0.345
213
CHP002 Chops Syndrome 47 0.345
214
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.345
215
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 29 0.345
216
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.345
217
c MCR112 Microvascular Complications of Diabetes 2 42 0.345
218
SZR026 Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance 57 0.345
219
c MCR120 Microvascular Complications of Diabetes 7 47 0.345
220
MNN028 Mononeuropathy of the Median Nerve, Mild 47 0.345
221
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.345
222
AMD002 Amed Syndrome, Digenic 36 0.345
223
SPR020 Superficial Mycosis 34 0.345
224
RSP019 Respiratory Distress Syndrome in Premature Infants 52 0.345
225
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.345
226
BWN001 Bowen-Conradi Syndrome 54 0.345
227
URT051 Ureter, Cancer of 46 0.345
228
P CRP001 Carpal Tunnel Syndrome 65 0.345
229
PCK003 Pick Disease of Brain 70 0.345
230
LMY014 Leiomyoma, Uterine 55 0.345
231
MYC006 Mycosis Fungoides 64 0.345
232
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 67 0.345
233
PHN003 Phenylketonuria 76 0.345
234
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.345
235
CGN007 Cognitive Function 1, Social 27 0.345
236
MND023 Mend Syndrome 49 0.345
237
FRN006 Frontotemporal Dementia 68 0.345
238
PLY105 Polycystic Ovary Syndrome 1 39 0.345
239
c THR092 Thrombophilia Due to Thrombin Defect 74 0.345
240
P AST005 Asthma 75 0.345
241
c MCR115 Microvascular Complications of Diabetes 5 65 0.345
242
P LKM062 Leukemia, Acute Lymphoblastic 69 0.345
243
c PSR018 Psoriasis 13 40 0.345
244
P BLD124 Bleeding Disorder, Platelet-Type, 11 68 0.345
245
P MJR001 Major Depressive Disorder 68 0.345
246
SLT014 Salt and Pepper Developmental Regression Syndrome 43 0.345
247
c OVR114 Ovarian Cancer 1 60 0.345
248
P MYC084 Mycobacterium Tuberculosis 1 68 0.345
249
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 38 0.345
250
P BCT020 Bacteremia 2 43 0.345
251
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.345
252
c ART101 Aortic Valve Disease 2 65 0.345
253
c NRP036 Neuropathy, Hereditary Sensory, Type if 33 0.345
254
P OCY003 Oocyte Maturation Defect 1 46 0.345
255
c DRR009 Diarrhea 6 46 0.345
256
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.345
257
P PRG092 Pregnancy Loss, Recurrent 1 42 0.345
258
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.345
259
c CNG413 Congenital Short Bowel Syndrome 42 0.345
260
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.345
261
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 0.345
262
c ATR087 Atrial Standstill 1 74 0.345
263
P ANG001 Angelman Syndrome 64 0.345
264
c BLD140 Blood Group, I System 47 0.345
265
P PRK057 Parkinson Disease, Late-Onset 79 0.345
266
IMM162 Immunoglobulin E Concentration, Serum 28 0.345
267
c HYP595 Hypertension, Essential 84 0.345
268
MCL027 Macular Dystrophy, Dominant Cystoid 51 0.345
269
c MST023 Mesothelioma, Malignant 56 0.345
270
c PSR032 Psoriasis 11 47 0.345
271
P PRC031 Preeclampsia/eclampsia 1 43 0.345
272
c FNC043 Fanconi Anemia, Complementation Group E 62 0.345
273
c ADV003 Advanced Sleep Phase Syndrome, Familial, 1 43 0.345
274
P KHL003 Kohlschutter-Tonz Syndrome 57 0.345
275
FCT007 Factor Vii Deficiency 64 0.345
276
PHL006 Phelan-Mcdermid Syndrome 61 0.345
277
c PRS136 Prostate Cancer, Hereditary, 6 33 0.345
278
c MJR004 Major Affective Disorder 4 28 0.345
279
c MJR003 Major Affective Disorder 6 32 0.345
280
c PRM092 Primary Lateral Sclerosis, Adult, 1 38 0.345
281
HLC007 Helicobacter Pylori Infection 67 0.345
282
P LNG064 Lung Cancer Susceptibility 3 69 0.345
283
c FML001 Familial Atrial Fibrillation 65 0.345
284
LYM040 Lymphoblastic Lymphoma 53 0.345
285
WLD007 Waldenstroem's Macroglobulinemia 59 0.345
286
MCS002 Mucositis 55 0.345
287
P CRN024 Corneal Disease 43 0.345
288
THR024 Thrombosis 56 0.345
289
SCH003 Schizophreniform Disorder 54 0.345
290
P PRK039 Parkinsonism 55 0.345
291
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.345
292
VTM033 Vitamin K Deficiency Bleeding 49 0.345
293
MLD018 Mild Cognitive Impairment 48 0.345
294
FML035 Familial Hyperlipidemia 54 0.345
295
HYP458 Hyper Ige Syndrome 60 0.345
296
CHL159 Childhood-Onset Asthma 30 0.345
297
MNN032 Meningococcal Meningitis 52 0.345
298
AGG012 Aggressive Nk-Cell Leukemia 47 0.345
299
LYM012 Lymphoplasmacytic Lymphoma 50 0.345
300
PRP036 Peripheral T-Cell Lymphoma 52 0.345
301
END040 Endogenous Depression 54 0.345
302
PRT035 Peritoneum Cancer 45 0.345
303
HYP060 Hyperinsulinism 53 0.345
304
PRM003 Premature Ejaculation 44 0.345
305
P LKM002 Leukemia 65 0.345
306
P ART021 Arteriosclerosis 53 0.345
307
MYL031 Myeloproliferative Neoplasm 66 0.345
308
TRN018 Transitional Cell Carcinoma 56 0.345
309
GLB002 Glioblastoma 67 0.345
310
P BNG032 Benign Mesothelioma 53 0.345
311
ATY005 Atypical Teratoid Rhabdoid Tumor 69 0.345
312
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 38 0.345
313
HYP014 Hyperuricemia 51 0.345
314
FLL027 Fallopian Tube Carcinoma 66 0.345
315
P PLM006 Pulmonary Alveolar Proteinosis 53 0.345
316
BCT022 Bacterial Infectious Disease 55 0.345
317
NRN004 Neuroendocrine Tumor 55 0.345
318
ACD008 Acid-Labile Subunit Deficiency 52 0.345
319
P ECL001 Eclampsia 52 0.345
320
P MVM001 Movement Disease 61 0.345
321
LVR012 Liver Cirrhosis 62 0.345
322
BRN004 Brain Edema 54 0.345
323
NRT001 Neurotic Disorder 56 0.345
324
P TRN020 Turner Syndrome 67 0.345
325
CNT033 Central Nervous System Cancer 47 0.345
326
INT002 Intermittent Claudication 61 0.345
327
MCL006 Macular Retinal Edema 56 0.345
328
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.345
329
P MLG074 Malignant Mesenchymoma 40 0.345
330
NTR005 Nutritional Deficiency Disease 60 0.345
331
MXD026 Mixed Glioma 45 0.345
332
LPD008 Lipid Metabolism Disorder 61 0.345
333
CMP010 Complex Regional Pain Syndrome 59 0.345
334
P BPL003 Bipolar Disorder 56 0.345
335
CNG034 Congestive Heart Failure 69 0.345
336
SCH012 Schizoaffective Disorder 49 0.345
337
P PNM007 Pneumonia 64 0.345
338
P KDN018 Kidney Disease 71 0.345
339
P HPT021 Hepatitis 68 0.345
340
P LTR001 Lateral Sclerosis 57 0.345
341
P MTR014 Motor Neuron Disease 65 0.345
342
IRN002 Iron Metabolism Disease 56 0.345
343
DSS008 Disease of Mental Health 74 0.345
344
P HRT032 Heart Disease 84 0.345
345
P PLY011 Polycystic Ovary Syndrome 57 0.345
346
IRN001 Iron Deficiency Anemia 58 0.345
347
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.345
348
c HPT001 Hepatitis C 61 0.345
349
P PLY019 Polyneuropathy 52 0.345
350
SQM002 Squamous Cell Papilloma 45 0.345
351
P CRV039 Cervicitis 52 0.345
352
DRM006 Dermatitis 61 0.345
353
ETH004 Euthyroid Sick Syndrome 38 0.345
354
HMG005 Hemoglobinopathy 55 0.345
355
PLM001 Pulmonary Tuberculosis 69 0.345
356
CNS004 Constipation 56 0.345
357
HYP005 Hypokalemia 55 0.345
358
THY030 Thyroid Gland Disease 50 0.345
359
P LVR013 Liver Disease 68 0.345
360
SPN035 Spindle Cell Sarcoma 51 0.345
361
MYF001 Myofibroma 42 0.345
362
PST011 Pustulosis of Palm and Sole 52 0.345
363
BLD131 Bladder Urothelial Carcinoma 59 0.345
364
P NRV006 Nervous System Cancer 47 0.345
365
FNG017 Fungal Infectious Disease 54 0.345
366
PSY004 Psychotic Disorder 66 0.345
367
HMT002 Hematologic Cancer 61 0.345
368
HGH043 High Grade Glioma 46 0.345
369
P ART023 Arthropathy 59 0.345
370
CRB009 Cerebritis 43 0.345
371
ALL029 Allergic Disease 61 0.345
372
P ADL010 Adult Respiratory Distress Syndrome 70 0.345
373
ATN004 Autonomic Neuropathy 42 0.345
374
PRD004 Prediabetes Syndrome 52 0.345
375
PRT038 Protein-Energy Malnutrition 53 0.345
376
GLC003 Glucose Intolerance 53 0.345
377
AMN003 Amnestic Disorder 53 0.345
378
c HPT003 Hepatitis a 63 0.345
379
RCK004 Rickets 64 0.345
380
LMY002 Leiomyoma 51 0.345
381
NWB001 Newborn Respiratory Distress Syndrome 56 0.345
382
DBT004 Diabetic Polyneuropathy 50 0.345
383
CVD001 Covid-19 59 0.345
384
NSP002 Nasopharyngitis 45 0.345
385
c PRC016 Pre-Eclampsia 64 0.345
386
ATR073 Atrophic Glossitis 28 0.345
387
MNT002 Mental Depression 56 0.345
388
PRS047 Prostatitis 57 0.345
389
P PRS038 Personality Disorder 65 0.345
390
P CRD246 Cardiovascular System Disease 55 0.345
391
P DMN002 Dementia 65 0.345
392
BCK003 Background Diabetic Retinopathy 46 0.345
393
SRC014 Sarcoma 64 0.345
394
P ART022 Arthritis 70 0.345
395
P INF032 Infertility 60 0.345
396
P SLP005 Sleep Disorder 61 0.345
397
P RTN018 Retinal Disease 53 0.345
398
TXC002 Toxic Encephalopathy 51 0.345
399
LNG031 Lung Benign Neoplasm 51 0.345
400
CRB039 Cerebrovascular Disease 65 0.345
401
PLC008 Placenta Disease 48 0.345
402
HDG004 Hodgkin's Granuloma 22 0.345
403
P MYL006 Myeloid Leukemia 60 0.345
404
AMN002 Amino Acid Metabolic Disorder 40 0.345
405
MCR004 Macroglobulinemia 48 0.345
406
AMN012 Aminoacidopathies 19 0.345
407
ATM021 Autoimmune Inner Ear Disease 36 0.345
408
VRL011 Viral Infectious Disease 60 0.345
409
P DBT009 Diabetes Mellitus 67 0.345
410
P PSR002 Psoriasis 63 0.345
411
APH001 Aphthous Stomatitis 57 0.345
412
DBT006 Diabetic Macular Edema 48 0.345
413
ULC007 Ulcerative Stomatitis 39 0.345
414
c ACT075 Acute Myocardial Infarction 55 0.345
415
P BCL017 B-Cell Lymphoma 57 0.345
416
P MSC003 Muscular Atrophy 52 0.345
417
PRT036 Peritonitis 65 0.345
418
RTC005 Reticulosarcoma 47 0.345
419
SZR001 Sezary's Disease 60 0.345
420
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.345
421
GLM045 Glioma 62 0.345
422
LYM019 Lymphosarcoma 46 0.345
423
MNN020 Meningococcal Infection 44 0.345
424
NNN007 Non-Involuting Congenital Hemangioma 40 0.345
425
FTT001 Fatty Liver Disease 61 0.345
426
P NRV007 Nervous System Disease 65 0.345
427
P LPS004 Lupus Erythematosus 61 0.345
428
HDG006 Hodgkin's Paragranuloma 22 0.345
429
VSC002 Vascular Dementia 59 0.345
430
CRH001 Crohn's Disease 80 0.345
431
ATX019 Ataxia with Vitamin E Deficiency 44 0.345
432
49X006 49, Xxxxy Syndrome 40 0.345
433
MLG079 Malignant Pleural Mesothelioma 42 0.345
434
MNC020 Monoclonal Mast Cell Activation Syndrome 20 0.345
435
BCK006 Back Pain 43 0.345
436
P MNN013 Meningitis 65 0.345
437
c PRM038 Primary Agammaglobulinemia 47 0.345
438
P VSC018 Visceral Steatosis 32 0.345
439
FRN030 Frontotemporal Dementia with Parkinsonism-17 24 0.345
441
END072 Endotheliitis 36 0.345
442
PRS034 Parasitic Helminthiasis Infectious Disease 50 0.345
443
CTS005 Catastrophic Antiphospholipid Syndrome 43 0.345
444
IRR002 Irritable Bowel Syndrome 64 0.345
445
MYC005 Myocardial Stunning 45 0.345
446
CHL079 Children's Interstitial Lung Disease 25 0.345
447
P INB001 Inborn Amino Acid Metabolism Disorder 10 0.345
448
P MRC003 Mercury Poisoning 48 0.345
449
NSS002 Neisseria Meningitidis Infection 46 0.345
451
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.345
452
AND005 Androgen Insensitivity Syndrome, Mild 21 0.345
453
PRM155 Primary Cutaneous Anaplastic Large Cell Lymphoma 34 0.345
455
CHR682 Chronic Bilirubin Encephalopathy 37 0.345
456
PYR016 Pyridoxine Deficiency 29 0.345
457
RSP007 Respiratory Distress Syndrome, Infant 41 0.345
458
SFT003 Soft Tissue Sarcoma 43 0.345
459
STT009 Sutton Disease 2 30 0.345
460
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.345
461
BRN071 Brain Injury 50 0.345
462
P TRM003 Tremor 50 0.345
463
PRR019 Perioral Myoclonia with Absences 26 0.345
464
DPR016 Depression 64 0.345
465
HYP266 Hypoxia 56 0.345
466
P BCL004 B-Cell Non-Hodgkin Lymphoma 41 0.345
467
GLL048 Glial Tumor 51 0.345
468
TMP019 Temporomandibular Joint Anomaly 28 0.345
469
MTH076 Methylmalonic Aciduria Due to Methylmalonyl-Coa Mutase Deficiency 50 0.314
470
WST001 West Syndrome 64 0.314
471
P RSP003 Respiratory Failure 73 0.314
472
P HML002 Hemolytic Anemia 62 0.314
473
P ENC018 Encephalopathy 62 0.314
474
PRT251 Proteinuria, Chronic Benign 58 0.281
475
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.281
476
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.281
477
HMC041 Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity 48 0.281
478
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.281
479
PRT019 Protein-Losing Enteropathy 44 0.281
480
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.243
481
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 50 0.243
482
HMC042 Homocystinuria-Megaloblastic Anemia, Cble Complementation Type 34 0.243
483
MTH077 Methylmalonic Aciduria, Cbla Type 45 0.243
484
PLM010 Pulmonary Edema 54 0.243
485
ADN090 Adenosylcobalamin Deficiency 35 0.243
486
P ALP008 Alopecia 53 0.243
487
MTH046 Methylmalonic Acidemia Without Homocystinuria 39 0.243
488
CMB083 Combined Immunodeficiency and Megaloblastic Anemia with or Without Hyperhomocysteinemia 28 0.199
489
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 0.199
490
HYP003 Hypermethioninemia 51 0.199
491
P HML033 Hemolytic Uremic Syndrome, Atypical 1 67 0.199
492
c BRN108 Branchiootic Syndrome 1 63 0.199
493
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.199
494
MTH056 Methylmalonic Aciduria and Homocystinuria, Cblf Type 35 0.199
495
IMM167 Immune Deficiency Disease 76 0.199
496
CMB007 Combined Immunodeficiency 56 0.199
497
NNT011 Neonatal Anemia 34 0.199
498
P GCH001 Gaucher's Disease 69 0.199
499
c ACT071 Acute Kidney Failure 60 0.199
500
IMP005 Impotence 52 0.199
501
PNM008 Pneumothorax 54 0.199
502
SVR004 Severe Combined Immunodeficiency 70 0.199
503
P URN019 Urinary Tract Infection 48 0.199
504
P OPT006 Optic Nerve Disease 57 0.199
505
P PLM036 Pulmonary Fibrosis 65 0.199
506
P BRN022 Bronchiectasis 59 0.199
507
GLY010 Glycine Encephalopathy 57 0.140
508
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.140
509
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.140
510
CYS019 Cystathioninuria 46 0.140
511
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.140
512
P RNL115 Renal Tubular Acidosis, Proximal 32 0.140
513
MLN011 Malonyl-Coa Decarboxylase Deficiency 37 0.140
514
INT088 Intrinsic Factor Deficiency 34 0.140
515
FDB001 Foodborne Botulism 55 0.140
516
CNG016 Congenital Intrinsic Factor Deficiency 37 0.140
517
c PLM170 Pulmonary Venoocclusive Disease 1, Autosomal Dominant 43 0.140
518
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.140
519
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 50 0.140
520
P MYS003 Myasthenia Gravis 67 0.140
521
ATM095 Autoimmune Disease 61 0.140
522
KRN002 Kearns-Sayre Syndrome 62 0.140
523
SPN369 Spinal Disease 43 0.140
524
P NPH012 Nephrotic Syndrome 61 0.140
525
HPT046 Hepatic Veno-Occlusive Disease 54 0.140
526
c ATM011 Autoimmune Hepatitis 62 0.140
527
HYP080 Hypogonadism 49 0.140
528
P LRY044 Larynx Cancer 53 0.140
529
CNT047 Contact Dermatitis 56 0.140
530
P VSC007 Vascular Disease 62 0.140
531
P BRB001 Beriberi 44 0.140
532
c ACQ017 Acquired Von Willebrand Syndrome 48 0.140
533
HMP001 Hemopericardium 47 0.140
534
P PLM025 Pulmonary Venoocclusive Disease 44 0.140
535
P EYD002 Eye Disease 57 0.140
536
P DYS154 Dystonia 64 0.140
537
STT001 Status Epilepticus 58 0.140
538
P CNG003 Congenital Dyserythropoietic Anemia 48 0.140
539
P GLM007 Glomerulonephritis 59 0.140
540
TRC022 Tricuspid Valve Insufficiency 46 0.140
541
P MYP004 Myopathy 67 0.140
542
INT066 Interstitial Lung Disease 60 0.140
543
DMY004 Demyelinating Disease 50 0.140
544
ALL010 Allergic Contact Dermatitis 55 0.140
545
GTR002 Goiter 52 0.140
546
P PRC012 Pericardial Effusion 50 0.140
547
P VNW001 Von Willebrand's Disease 64 0.140
548
OCC016 Occupational Asthma 33 0.140
549
P RNL007 Renal Tubular Acidosis 52 0.140
550
GLY105 Glyt1 Encephalopathy 7 0.140
551
HMC030 Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency 36 0.140
552
SCT002 Scotoma 42 0.140
553
HYP034 Hypertensive Encephalopathy 43 0.140
554
P NRB001 Neuroblastoma 66 0.140
555
P RTN016 Retinal Degeneration 52 0.140
556
LNG099 Lung Disease 62 0.140
557
ATM060 Autoimmune Atrophic Gastritis 19 0.140
558
P MYC033 Myoclonus 46 0.140
559
SPS019 Spastic Paraparesis 38 0.140
560
HYP264 Hypertonia 35 0.140
561
P CRB088 Cerebral Atrophy 32 0.140
562
PRS063 Paresthesia 39 0.140
563
PST092 Posttransplant Acute Limbic Encephalitis 29 0.140
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