Search results for Dextromethorphan

524 hits were found for Dextromethorphan

# Family MCID Name MIFTS Score
1
PSD088 Pseudobulbar Affect 33 11.336
2
PNG002 Pain Agnosia 51 9.964
3
c AMY091 Amyotrophic Lateral Sclerosis 1 88 8.829
4
P LTR001 Lateral Sclerosis 58 8.829
5
DBT010 Diabetic Neuropathy 54 6.501
6
CYT018 Cytochrome P450 2d6 Variant 26 6.412
7
P CHR345 Chronic Pain 50 6.367
8
P DMN002 Dementia 66 6.292
9
P ALZ034 Alzheimer Disease 87 6.172
10
MNT002 Mental Depression 57 6.106
11
DPR016 Depression 65 5.793
12
SRT004 Serotonin Syndrome 54 5.781
13
P MJR001 Major Depressive Disorder 68 5.697
14
P SZR006 Seizure Disorder 70 5.672
15
CMM005 Common Cold 56 5.547
16
P NRP001 Neuropathy 60 5.339
17
P PRP019 Peripheral Nervous System Disease 58 5.045
18
OPD006 Opioid Addiction 48 4.890
19
P SBS003 Substance Abuse 54 4.704
20
c MJR022 Major Affective Disorder 8 38 4.644
21
c MJR024 Major Affective Disorder 9 41 4.644
22
P BPL003 Bipolar Disorder 56 4.644
23
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 4.498
24
OPT003 Opiate Dependence 49 4.286
25
P SCH015 Schizophrenia 74 4.154
26
P ATT013 Attention Deficit-Hyperactivity Disorder 64 4.115
27
P MLT020 Multiple Sclerosis 79 4.069
28
P RTT002 Rett Syndrome 79 4.047
29
TRM010 Traumatic Brain Injury 51 4.046
30
SPN186 Spinal Cord Injury 61 3.992
31
P PRK039 Parkinsonism 55 3.824
32
FBR047 Fibromyalgia 58 3.814
33
c TYP009 Type 2 Diabetes Mellitus 92 3.797
34
P HNT016 Huntington Disease 73 3.661
35
P PRK057 Parkinson Disease, Late-Onset 80 3.650
36
PTH003 Pathologic Nystagmus 52 3.525
37
WTH001 Withdrawal Disorder 48 3.477
38
PLM129 Pulmonary Disease, Chronic Obstructive 74 3.357
39
GLY010 Glycine Encephalopathy 57 3.357
40
P DBT009 Diabetes Mellitus 67 3.341
41
BRN071 Brain Injury 50 3.253
42
c DNT047 Dentinogenesis Imperfecta Type 2 35 3.219
43
PST053 Postherpetic Neuralgia 40 3.187
44
P MYC033 Myoclonus 47 3.165
45
c CHR684 Chronic Kidney Disease 69 3.161
46
P EXN002 Exanthem 58 3.131
47
DWN001 Down Syndrome 70 3.084
48
RTN003 Retinal Ischemia 49 3.041
49
48X005 48,xyyy 39 3.041
50
OCL069 Ocular Motor Apraxia 57 2.952
51
END040 Endogenous Depression 55 2.906
52
OPD001 Opioid Abuse 44 2.904
53
P DYS154 Dystonia 64 2.890
54
TRG002 Trigeminal Neuralgia 61 2.870
55
P URN019 Urinary Tract Infection 49 2.825
56
TXC005 Toxic Shock Syndrome 62 2.758
57
P LKM002 Leukemia 67 2.745
58
c MGR028 Migraine with or Without Aura 1 64 2.725
59
ATH013 Atherosclerosis Susceptibility 63 2.709
60
P KDN018 Kidney Disease 72 2.709
61
DBT006 Diabetic Macular Edema 48 2.709
62
MCL006 Macular Retinal Edema 57 2.709
63
c PNS012 Paine Syndrome 60 2.664
64
c EPS039 Episodic Pain Syndrome, Familial, 1 42 2.664
65
ADL002 Adult Syndrome 70 2.655
66
P ENC018 Encephalopathy 62 2.646
67
P BRS047 Breast Cancer 98 2.645
68
P TRM003 Tremor 48 2.615
69
MDD011 Mood Disorder 62 2.615
70
STR067 Stroke, Ischemic 80 2.608
71
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.575
72
SBC016 Subacute Delirium 43 2.539
73
P TRN020 Turner Syndrome 67 2.522
74
BRN024 Bronchitis 67 2.463
75
PSY004 Psychotic Disorder 66 2.436
76
AMN003 Amnestic Disorder 54 2.436
77
P ATS364 Autism 69 2.374
78
ALL029 Allergic Disease 59 2.366
79
P RHM011 Rheumatoid Arthritis 82 2.347
80
P ART022 Arthritis 71 2.347
81
P HYP265 Hypotonia 42 2.346
82
ANT039 Antisynthetase Syndrome 55 2.320
83
SBS005 Substance-Induced Psychosis 30 2.280
84
P LKM062 Leukemia, Acute Lymphoblastic 69 2.203
85
CNS004 Constipation 56 2.203
86
P CRD119 Cardiac Arrest 67 2.203
87
SBS004 Substance Dependence 47 2.195
88
CRB004 Cerebral Artery Occlusion 45 2.186
89
RHB024 Rhabdomyosarcoma 2 67 2.175
90
P ANR048 Aniridia 1 64 2.172
91
HRP004 Herpes Zoster 61 2.146
92
IRR002 Irritable Bowel Syndrome 65 2.131
93
PRC051 Paracetamol Poisoning 29 2.105
94
ALC007 Alcohol Dependence 66 2.073
95
NRT001 Neurotic Disorder 56 2.050
96
GST092 Gastroesophageal Reflux 61 2.007
97
TRN015 Transient Cerebral Ischemia 63 2.007
98
DBT002 Diabetic Autonomic Neuropathy 41 1.977
99
MTH086 Methotrexate Toxicity 32 1.962
100
c MCR130 Microvascular Complications of Diabetes 6 41 1.962
101
c MCR120 Microvascular Complications of Diabetes 7 47 1.962
102
P SCL018 Scoliosis 57 1.962
103
c MCR113 Microvascular Complications of Diabetes 3 52 1.962
104
c MCR133 Microvascular Complications of Diabetes 4 41 1.962
105
IDP070 Idiopathic Scoliosis 42 1.962
106
CCN001 Cocaine Dependence 48 1.962
107
P ALC033 Alcohol Use Disorder 61 1.956
108
VSC002 Vascular Dementia 60 1.956
109
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 1.930
110
IMM167 Immune Deficiency Disease 78 1.929
111
SVR001 Severe Acute Respiratory Syndrome 67 1.902
112
MNN017 Mononeuropathy 41 1.902
113
c MJR006 Major Affective Disorder 5 32 1.902
114
c MJR023 Major Affective Disorder 7 33 1.902
115
c MJR004 Major Affective Disorder 4 28 1.902
116
c MJR003 Major Affective Disorder 6 32 1.902
117
c MJR008 Major Affective Disorder 2 34 1.902
118
P MJR007 Major Affective Disorder 1 42 1.902
119
GRW007 Growth Hormone Deficiency 46 1.880
120
BRN004 Brain Edema 54 1.880
121
URM002 Uremia 47 1.871
122
BRN014 Bronchopneumonia 53 1.871
123
PLM010 Pulmonary Edema 55 1.871
124
P INF038 Influenza 68 1.860
125
TBC004 Tobacco Addiction 63 1.824
126
CRB039 Cerebrovascular Disease 66 1.812
127
P CNR004 Cone-Rod Dystrophy 2 74 1.789
128
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 1.789
129
c BLD140 Blood Group, I System 46 1.789
130
c PRM092 Primary Lateral Sclerosis, Adult, 1 38 1.789
131
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 63 1.789
132
INT002 Intermittent Claudication 61 1.789
133
RSP027 Respiratory Papillomatosis, Juvenile Recurrent, Congenital 47 1.789
134
P MTR014 Motor Neuron Disease 65 1.784
135
NRL016 Neural Tube Defects 81 1.774
136
MRP001 Morphine Dependence 42 1.774
137
P PSR002 Psoriasis 63 1.680
138
PST011 Pustulosis of Palm and Sole 52 1.680
139
c DVL034 Developmental and Epileptic Encephalopathy 3 44 1.669
140
P RHN004 Rhinitis 57 1.669
141
ERL001 Early Myoclonic Encephalopathy 62 1.669
142
DRM006 Dermatitis 62 1.669
143
P HDC001 Headache 57 1.669
144
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 1.656
145
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.653
146
SNS003 Sensory Peripheral Neuropathy 52 1.653
147
HMP005 Hemiplegia 54 1.653
148
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 1.596
149
ATX019 Ataxia with Vitamin E Deficiency 44 1.596
150
URT010 Ureteral Obstruction 45 1.552
151
ADG002 Audiogenic Seizures 25 1.552
152
PRX097 Paroxysmal Dystonia 32 1.552
153
DMP001 Dumping Syndrome 43 1.552
154
GNR004 Generalized Anxiety Disorder 55 1.552
155
HYP056 Hypoglycemia 65 1.552
156
P HYP263 Hypersomnia 41 1.552
157
ACT167 Acute Generalized Exanthematous Pustulosis 38 1.496
158
STR077 Streptococcal Toxic-Shock Syndrome 35 1.496
159
SXL003 Sexual Disorder 49 1.496
160
HRN029 Hearing Loss, Noise-Induced 37 1.496
161
NCR007 Necrotizing Fasciitis 49 1.496
162
FSC004 Fasciitis 49 1.496
163
c LKM061 Leukemia, Acute Myeloid 83 1.483
164
P MCR129 Microvascular Complications of Diabetes 1 68 1.483
165
GLS018 Glass Syndrome 61 1.463
166
c PRS136 Prostate Cancer, Hereditary, 6 33 1.463
167
P PRS040 Prostate Cancer 95 1.463
168
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 1.463
169
c PRS130 Prostate Cancer, Hereditary, 8 32 1.463
170
PRS047 Prostatitis 58 1.463
171
ACT055 Actinomycosis 55 1.463
172
HNT002 Hantavirus Pulmonary Syndrome 55 1.463
173
VTM033 Vitamin K Deficiency Bleeding 48 1.463
174
KRT002 Keratomalacia 55 1.463
175
CRB009 Cerebritis 43 1.463
176
CTS005 Catastrophic Antiphospholipid Syndrome 43 1.463
177
AND005 Androgen Insensitivity Syndrome, Mild 21 1.463
178
CRY008 Cryopyrin-Associated Periodic Syndrome 48 1.463
179
c MCR115 Microvascular Complications of Diabetes 5 65 1.420
180
P PRV006 Pervasive Developmental Disorder 52 1.420
181
P HYP098 Hypereosinophilic Syndrome 66 1.420
182
SYN036 Syncope 45 1.420
183
ACT191 Acute Encephalopathy with Biphasic Seizures and Late Reduced Diffusion 19 1.420
184
NPH009 Nephrolithiasis 54 1.420
185
FCL014 Focal Epilepsy 53 1.420
186
ART004 Aortic Atherosclerosis 47 1.420
187
c ACT071 Acute Kidney Failure 60 1.420
188
CHL068 Cholestasis 61 1.420
189
P FBR031 Febrile Seizures 52 1.420
190
HMN044 Human Immunodeficiency Virus Type 1 78 1.318
191
P SLP006 Sleep Apnea 69 1.318
192
ACQ007 Acquired Immunodeficiency Syndrome 59 1.318
193
c BCT007 Bacterial Meningitis 55 1.291
194
P MNN013 Meningitis 65 1.291
195
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 1.290
196
END072 Endotheliitis 36 1.290
197
MCL027 Macular Dystrophy, Dominant Cystoid 51 1.290
198
c THR090 Thrombocythemia 1 50 1.290
199
P ANP001 Anaplastic Large Cell Lymphoma 61 1.290
200
SPL004 Splenic Marginal Zone Lymphoma 50 1.290
201
MYL009 Myelodysplastic Syndrome 67 1.290
202
PRT251 Proteinuria, Chronic Benign 57 1.290
203
CHR563 Chronic Eosinophilic Leukemia 48 1.290
204
P LYM118 Lymphoma 67 1.290
205
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 38 1.290
206
MYL005 Myelofibrosis 71 1.290
207
MYL069 Myeloma, Multiple 77 1.290
208
PLY001 Polycythemia Vera 69 1.290
209
P CMP005 Campomelic Dysplasia 65 1.290
210
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 58 1.290
211
CHR286 Chronic Neutrophilic Leukemia 43 1.290
212
P CHR285 Chronic Myelomonocytic Leukemia 60 1.290
213
c ACT073 Acute Leukemia 58 1.290
214
INT253 Intestinal Benign Neoplasm 46 1.290
215
BNM001 Bone Marrow Cancer 46 1.290
216
TXC002 Toxic Encephalopathy 52 1.290
217
EXT010 Extramedullary Plasmacytoma 46 1.290
218
P AGN002 Agnosia 54 1.290
219
MNC006 Monoclonal Gammopathy of Uncertain Significance 47 1.290
220
P PLY018 Polycythemia 56 1.290
221
MYF002 Myofascial Pain Syndrome 46 1.290
222
PRL017 Prolymphocytic Leukemia 47 1.290
223
SML008 Small Intestine Lymphoma 33 1.290
224
P ESS003 Essential Thrombocythemia 69 1.290
225
MYL031 Myeloproliferative Neoplasm 66 1.290
226
c PRM012 Primary Polycythemia 58 1.290
227
PLS009 Plasma Cell Neoplasm 64 1.290
228
RFR002 Refractory Hairy Cell Leukemia 34 1.290
230
c ALM001 Al Amyloidosis 54 1.290
231
MLD017 Mal De Debarquement Syndrome 29 1.290
232
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 1.290
233
LYM019 Lymphosarcoma 46 1.290
234
P NRV007 Nervous System Disease 67 1.290
235
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 1.290
236
BNR002 Bone Resorption Disease 47 1.262
237
CHL152 Childhood Acute Lymphocytic Leukemia 50 1.262
238
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 1.262
239
P RBL001 Rubella 58 1.262
240
P VSC011 Vasculitis 61 1.262
241
P CHL066 Cholangitis 52 1.262
242
47X002 47,xyy 48 1.262
243
CHR001 Churg-Strauss Syndrome 61 1.262
244
P EPL164 Epilepsy 68 1.262
245
c SCN007 Secondary Hyperparathyroidism 51 1.262
246
PRM236 Primary Biliary Cholangitis 60 1.262
247
P HYP069 Hyperparathyroidism 62 1.262
248
P RSP003 Respiratory Failure 74 1.262
249
ALL012 Allergic Angiitis 24 1.262
250
CNG124 Congenital Rubella 43 1.262
251
P MYC084 Mycobacterium Tuberculosis 1 68 1.261
252
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 1.220
253
KHL003 Kohlschutter-Tonz Syndrome 59 1.213
254
CLT003 Colitis 63 1.155
255
DRG003 Drug Dependence 46 1.106
256
MLD018 Mild Cognitive Impairment 48 1.104
257
PNM013 Pneumococcal Meningitis 43 1.057
258
P STR035 Streptococcal Group a Invasive Disease 24 1.057
259
CRD223 Cardiac Arrhythmia 63 1.057
260
RTN017 Retinal Detachment 60 1.057
261
P OST002 Osteoporosis 76 1.057
262
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.057
263
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 1.057
264
CVD001 Covid-19 57 1.057
265
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 1.057
266
PLT031 Platelet Membrane Fluidity 28 1.057
267
HYP020 Hyperprolactinemia 63 1.057
268
MLY001 Molybdenum Cofactor Deficiency 40 1.057
269
MDD018 Middle East Respiratory Syndrome 44 1.057
270
ILS001 Ileus 50 1.057
271
OST012 Osteoarthritis 77 1.057
272
P SNS001 Sensorineural Hearing Loss 59 1.057
273
PLR008 Pleurisy 50 1.057
274
CRT015 Carotid Artery Occlusion 45 1.057
275
CHR073 Choreatic Disease 54 1.057
276
CRB090 Cerebral Hypoxia 42 1.057
277
ALL014 Allergic Encephalomyelitis 34 1.057
278
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.989
279
CYS001 Cystic Fibrosis 78 0.989
280
ATS010 Autosomal Recessive Disease 42 0.989
281
MLR004 Malaria 80 0.989
282
P DXT004 Dextro-Looped Transposition of the Great Arteries 58 0.989
283
CHD004 Chudley-Mccullough Syndrome 48 0.989
284
PLY068 Polysubstance Abuse 41 0.989
285
P HRT032 Heart Disease 81 0.989
286
P HYP055 Hypoplastic Left Heart Syndrome 65 0.989
287
DYS073 Dysphagia 53 0.989
288
FXD003 Fixed Drug Eruption 34 0.975
289
FRN006 Frontotemporal Dementia 68 0.967
290
P LNG032 Lung Cancer 98 0.871
291
ANG049 Angioedema Induced by Ace Inhibitors 40 0.871
292
c MST023 Mesothelioma, Malignant 56 0.871
293
CRN239 Carnitine Deficiency, Systemic Primary 61 0.871
294
PRP083 Porphyria, Acute Intermittent 65 0.871
295
PRP082 Porphyria, Congenital Erythropoietic 56 0.871
296
CPR004 Coproporphyria, Hereditary 57 0.871
297
P MYL006 Myeloid Leukemia 61 0.871
298
ACT078 Acute Porphyria 49 0.871
299
P BNG032 Benign Mesothelioma 53 0.871
300
P PRP029 Porphyria 60 0.871
301
CTN011 Cutaneous Porphyria 45 0.871
302
LNG015 Lingual-Facial-Buccal Dyskinesia 47 0.871
303
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.871
304
c CHR064 Chronic Monocytic Leukemia 36 0.871
305
LYM133 Lymphoma, Hodgkin, Classic 74 0.857
306
PRS129 Prostatic Hyperplasia, Benign 49 0.857
307
P FML018 Familial Mediterranean Fever 73 0.857
308
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.857
309
DFF005 Diffuse Large B-Cell Lymphoma 54 0.857
310
HMN047 Human Cytomegalovirus Infection 57 0.857
311
LYM143 Lymphoma, Non-Hodgkin, Familial 75 0.857
312
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.857
313
c HYP836 Hypercholesterolemia, Familial, 1 73 0.857
314
HND015 Hand Skill, Relative 30 0.857
315
P BCL017 B-Cell Lymphoma 59 0.857
316
P NRB001 Neuroblastoma 66 0.857
317
c HPT001 Hepatitis C 62 0.857
318
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 0.857
319
GT001 Gout 64 0.857
320
PRS021 Prostatic Adenoma 43 0.857
321
BRC012 Brucellosis 66 0.857
322
PRS045 Prostatic Hypertrophy 53 0.857
323
P CHN059 Chondrocalcinosis 52 0.857
324
PLC008 Placenta Disease 49 0.857
325
QDR001 Quadriplegia 50 0.857
326
PLS006 Plasmodium Vivax Malaria 51 0.857
327
CRN309 Cranial Neuralgia 21 0.823
328
MTC005 Mitochondrial Metabolism Disease 45 0.823
329
AYM001 Ayme-Gripp Syndrome 56 0.823
330
MSC007 Muscle Hypertrophy 64 0.823
331
P THR117 Three M Syndrome 1 65 0.823
332
c PSR028 Psoriasis 7 43 0.823
333
c PSR017 Psoriasis 2 53 0.823
334
c PSR018 Psoriasis 13 52 0.823
335
c PSR023 Psoriasis 1 52 0.823
336
ISL014 Isolated Growth Hormone Deficiency, Type Ia 54 0.823
337
EPT021 Epithelial Recurrent Erosion Dystrophy 46 0.823
338
APN008 Apnea, Obstructive Sleep 67 0.823
339
CRN241 Corneal Dystrophy, Congenital Stromal 49 0.823
341
ADN067 Adenoid Hypertrophy 39 0.823
342
c PSR032 Psoriasis 11 47 0.823
343
c HPT003 Hepatitis a 63 0.823
344
SKN019 Skin Melanoma 71 0.823
345
ORB013 Orbital Disease 42 0.823
346
ADN002 Adenoiditis 36 0.823
347
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.823
348
P MLN008 Melanoma 76 0.823
349
GST020 Gastric Antral Vascular Ectasia 40 0.823
350
P DDN001 Duodenal Ulcer 53 0.823
351
P HPT021 Hepatitis 69 0.823
352
FCL007 Facial Neuralgia 27 0.823
353
ISL003 Isolated Growth Hormone Deficiency 57 0.823
354
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.823
355
P MTC069 Mitochondrial Disorders 57 0.823
356
HYP266 Hypoxia 57 0.823
357
DWR001 Dwarfism 44 0.823
358
CRH001 Crohn's Disease 80 0.725
359
SPS057 Spasticity 42 0.699
360
c SYS001 Systemic Lupus Erythematosus 87 0.699
361
P ALT001 Alternating Hemiplegia of Childhood 57 0.699
362
MTB004 Metabolic Acidosis 48 0.699
363
PYR035 Pyrimidine Metabolic Disorder 25 0.699
364
LNN001 Lennox-Gastaut Syndrome 61 0.699
365
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.699
366
PRP001 Propionic Acidemia 65 0.699
368
ANT078 Antipyrine Metabolism 23 0.699
369
PRT037 Pertussis 65 0.699
370
GLL048 Glial Tumor 52 0.699
371
P HMN010 Hemangioma 62 0.699
372
NRL004 Neuroleptic Malignant Syndrome 52 0.699
373
INT066 Interstitial Lung Disease 60 0.699
374
P PLY019 Polyneuropathy 52 0.699
375
P PTS002 Ptosis 52 0.699
376
P DRR001 Diarrhea 55 0.699
378
P CRB088 Cerebral Atrophy 33 0.699
379
PRT058 Pure Autonomic Failure 58 0.699
380
GLM045 Glioma 63 0.699
381
CRH005 Crohn's Colitis 53 0.592
382
c INF071 Inflammatory Bowel Disease 1 65 0.592
383
ULC004 Ulcerative Colitis 74 0.592
384
SGM008 Segmental Dystonia 28 0.563
385
ISC015 Ischemic Colitis 43 0.563
386
P PNB001 Pineoblastoma 49 0.563
387
c ATM011 Autoimmune Hepatitis 63 0.563
388
ANX004 Anoxia 40 0.495
389
NRM022 Neurometabolic Disease 24 0.495
390
c ACT134 Acute Liver Failure 59 0.495
391
ART140 Arteries, Anomalies of 53 0.495
392
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.495
393
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 59 0.495
394
SDD001 Sudden Infant Death Syndrome 60 0.495
395
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.495
396
ALL003 Allergic Rhinitis 67 0.495
397
P AST005 Asthma 76 0.495
398
P DRM053 Dermatitis, Atopic 65 0.495
399
OBS002 Obsessive-Compulsive Disorder 68 0.495
400
MTN003 Motion Sickness 51 0.495
401
P OVR042 Ovarian Cancer 88 0.495
402
c ATR087 Atrial Standstill 1 74 0.495
403
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.495
404
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 0.495
405
P ERL057 Early Infantile Epileptic Encephalopathy 60 0.495
406
DSR012 Disordered Steroidogenesis Due to Cytochrome P450 Oxidoreductase Deficiency 39 0.495
407
c PSR021 Psoriasis 14, Pustular 58 0.495
408
LPP008 Lipoprotein Quantitative Trait Locus 65 0.495
409
c ATS007 Autism Spectrum Disorder 72 0.495
410
P FML023 Familial Hemiplegic Migraine 53 0.495
411
EXR010 Exercise-Induced Bronchoconstriction 34 0.495
412
HLC007 Helicobacter Pylori Infection 67 0.495
413
SLF014 Sulfite Oxidase Deficiency, Isolated 53 0.495
414
OBS037 Obesity-Hypoventilation Syndrome 45 0.495
415
IGR001 Ige Responsiveness, Atopic 59 0.495
416
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.495
417
P STR092 Striatal Degeneration, Autosomal Dominant 2 47 0.495
418
c HPT073 Hepatitis C Virus 71 0.495
419
OST159 Osteogenic Sarcoma 66 0.495
420
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.495
421
MST024 Mastocytosis, Cutaneous 67 0.495
422
P MDL005 Medulloblastoma 75 0.495
423
P ANG001 Angelman Syndrome 65 0.495
424
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 51 0.495
425
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 53 0.495
426
CHL065 Cholangiocarcinoma 58 0.495
427
RNL077 Renal Fibrosis 46 0.495
428
CRD137 Cardiogenic Shock 56 0.495
429
P ISL078 Isolated Ectopia Lentis 58 0.495
431
FML063 Familial Glucocorticoid Deficiency 58 0.495
432
P MYP006 Myopia 56 0.495
433
CWP001 Cowpox 45 0.495
434
CMP010 Complex Regional Pain Syndrome 60 0.495
435
NRM001 Neuromyelitis Optica 61 0.495
436
P MLG056 Malignant Hyperthermia 66 0.495
437
P MVM001 Movement Disease 61 0.495
438
SKN016 Skin Disease 63 0.495
439
GLB002 Glioblastoma 67 0.495
440
P MST009 Mastocytosis 64 0.495
441
P PLM036 Pulmonary Fibrosis 66 0.495
442
HRT012 Heart Valve Disease 53 0.495
443
P ACN011 Acne 57 0.495
444
NRM005 Neuromuscular Disease 63 0.495
445
CHL061 Childhood Leukemia 47 0.495
446
LNG099 Lung Disease 62 0.495
447
P RTN014 Retinal Artery Occlusion 47 0.495
448
CRN019 Coronary Artery Vasospasm 47 0.495
449
PRN009 Paranoid Schizophrenia 49 0.495
450
NRG002 Neurogenic Bladder 55 0.495
451
LWC001 Low Compliance Bladder 45 0.495
452
CGH001 Cough Variant Asthma 34 0.495
453
ATY001 Atypical Depressive Disorder 45 0.495
454
CMP006 Complex Partial Epilepsy 36 0.495
455
BRN026 Branch Retinal Artery Occlusion 41 0.495
456
MLN003 Melancholia 41 0.495
457
FCL012 Facial Paralysis 49 0.495
458
ATN004 Autonomic Neuropathy 42 0.495
459
SPS004 Spastic Quadriplegia 40 0.495
460
PRG009 Progressive Multifocal Leukoencephalopathy 58 0.495
461
INT079 Intrahepatic Cholangiocarcinoma 51 0.495
462
P PNC044 Pancreatitis 61 0.495
463
P RTN018 Retinal Disease 53 0.495
464
GST037 Gastroparesis 52 0.495
465
P URT039 Urticaria 58 0.495
466
ENC005 Encephalomalacia 44 0.495
467
STT001 Status Epilepticus 59 0.495
468
HYP060 Hyperinsulinism 54 0.495
469
P BRN022 Bronchiectasis 60 0.495
470
GLY105 Glyt1 Encephalopathy 7 0.495
471
CYT014 Cytochrome P450 Oxidoreductase Deficiency 34 0.495
472
P ENC004 Encephalitis 61 0.495
473
STM007 Stomatitis 54 0.495
474
ATN005 Autonomic Dysfunction 46 0.495
475
OHT001 Ohtahara Syndrome 38 0.495
476
PRN039 Paraneoplastic Syndromes 37 0.495
477
PRS063 Paresthesia 39 0.495
478
HYP264 Hypertonia 36 0.495
479
BRK012 Broken Heart Syndrome 42 0.495
480
P CRB059 Cerebellar Degeneration 36 0.495
481
P HYP120 Hypoaldosteronism 35 0.495
482
NNT021 Neonatal Meningitis 22 0.495
483
PRN032 Paraneoplastic Cerebellar Degeneration 25 0.495
484
c ATM075 Autoimmune Encephalitis 40 0.495
485
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 45 0.495
486
P PST059 Pustular Psoriasis 38 0.495
487
DFC004 Deficiency Anemia 74 0.419
488
SCK003 Sickle Cell Anemia 74 0.419
489
SPR126 Superior Semicircular Canal Dehiscence 41 0.419
490
P SCK005 Sickle Cell Disease 56 0.419
491
c HMG029 Hemoglobin Se Disease 40 0.419
492
CHL079 Children's Interstitial Lung Disease 26 0.419
494
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.404
495
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.404
496
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.404
497
HMC014 Homocysteinemia 52 0.404
498
c ANG068 Angioedema, Hereditary, Type I 57 0.404
499
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.404
500
VTM002 Vitamin B12 Deficiency 48 0.404
501
C1N001 C1 Inhibitor Deficiency 43 0.404
502
APH002 Aphasia 56 0.404
503
GBM001 Gaba Aminotransferase Deficiency 29 0.404
504
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 0.404
505
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.404
506
LPT014 Leptin Deficiency or Dysfunction 78 0.404
507
LPT006 Leptin Receptor Deficiency 50 0.404
508
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.404
509
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.404
510
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.404
511
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 67 0.404
512
c HYP595 Hypertension, Essential 85 0.404
513
RNL114 Renal Cell Carcinoma, Nonpapillary 80 0.404
514
CMP040 Complement Component 4, Partial Deficiency of 34 0.404
515
DMN031 Dementia, Lewy Body 65 0.404
516
PCK003 Pick Disease of Brain 69 0.404
517
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 0.404
518
PLM001 Pulmonary Tuberculosis 69 0.404
519
c HRD002 Hereditary Angioedema 62 0.404
520
LNG031 Lung Benign Neoplasm 51 0.404
521
APP008 Appendicitis 62 0.404
522
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.404
523
P ANG015 Angioedema 56 0.404
524
FRN030 Frontotemporal Dementia with Parkinsonism-17 24 0.404
Content
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