Home
User Guide
What's in a MalaCard Search Guide Our Sources
Analysis Tools
GeneCards GeneAnalytics GeneAlaCart PathCards VarElect
News and Views Disease Lists/Categories
About
About MalaCards Datasets Our Publications Weizmann Institute LifeMap Discovery® Terms of Use MalaCards Team

Search results for Memantine

563 hits were found for Memantine

# Family MCID Name MIFTS Score
1
P ALZ034 Alzheimer Disease 87 27.330
2
P DMN002 Dementia 66 21.859
3
VSC002 Vascular Dementia 60 14.497
4
P SCH015 Schizophrenia 74 12.011
5
c MJR022 Major Affective Disorder 8 38 11.265
6
c MJR024 Major Affective Disorder 9 41 11.265
7
P BPL003 Bipolar Disorder 56 11.265
8
DPR016 Depression 65 10.502
9
MNT002 Mental Depression 57 10.481
10
ALC007 Alcohol Dependence 66 10.047
11
P MJR001 Major Depressive Disorder 68 10.024
12
OBS002 Obsessive-Compulsive Disorder 68 9.843
13
MLD018 Mild Cognitive Impairment 48 9.490
14
FRN006 Frontotemporal Dementia 68 8.910
15
c ATS007 Autism Spectrum Disorder 72 8.721
16
P ATS364 Autism 69 8.652
17
P TRM003 Tremor 48 8.300
18
BRN071 Brain Injury 50 8.068
19
P PRK039 Parkinsonism 55 7.948
20
DWN001 Down Syndrome 70 7.852
21
PTH003 Pathologic Nystagmus 52 7.743
22
P HNT016 Huntington Disease 73 7.742
23
P LTR001 Lateral Sclerosis 58 7.550
24
OPT003 Opiate Dependence 49 7.544
25
c AMY091 Amyotrophic Lateral Sclerosis 1 88 7.521
26
INT323 Intraocular Pressure Quantitative Trait Locus 64 7.418
27
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 7.169
28
P SZR006 Seizure Disorder 70 6.878
29
ISC004 Ischemia 61 6.766
30
P MLT020 Multiple Sclerosis 79 6.750
31
DMN031 Dementia, Lewy Body 65 6.724
32
SPS057 Spasticity 42 6.703
33
TRM010 Traumatic Brain Injury 51 6.646
34
P ATT013 Attention Deficit-Hyperactivity Disorder 64 6.591
35
APH002 Aphasia 56 6.471
36
P HDC001 Headache 57 6.462
37
PNG002 Pain Agnosia 51 6.242
38
c MGR028 Migraine with or Without Aura 1 64 6.211
39
ETN001 Eating Disorder 59 6.172
40
P PRK057 Parkinson Disease, Late-Onset 80 5.967
41
P PRV006 Pervasive Developmental Disorder 52 5.953
42
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 5.842
43
ANX010 Anxiety 70 5.777
44
FBR047 Fibromyalgia 58 5.721
45
CRB004 Cerebral Artery Occlusion 45 5.662
46
48X005 48,xyyy 39 5.450
47
P EPL164 Epilepsy 68 5.414
48
OPD001 Opioid Abuse 44 5.131
49
P ALC033 Alcohol Use Disorder 61 5.084
50
MDD011 Mood Disorder 62 5.039
51
P ENC018 Encephalopathy 62 5.039
52
CRB039 Cerebrovascular Disease 66 4.947
53
P NRB001 Neuroblastoma 66 4.929
54
OPD006 Opioid Addiction 48 4.914
55
PSY004 Psychotic Disorder 66 4.909
56
KHL003 Kohlschutter-Tonz Syndrome 59 4.895
57
GNR004 Generalized Anxiety Disorder 55 4.890
58
SBC016 Subacute Delirium 43 4.867
59
SPN186 Spinal Cord Injury 61 4.842
60
PST028 Post-Traumatic Stress Disorder 59 4.841
61
END040 Endogenous Depression 55 4.726
62
NRT001 Neurotic Disorder 56 4.660
63
GLB002 Glioblastoma 67 4.629
64
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 44 4.532
65
CMP010 Complex Regional Pain Syndrome 60 4.528
66
STR067 Stroke, Ischemic 80 4.509
67
FRG010 Fragile X Tremor/ataxia Syndrome 44 4.394
68
AMN003 Amnestic Disorder 54 4.378
69
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 4.334
70
P NRP001 Neuropathy 60 4.319
71
P OPN001 Open-Angle Glaucoma 55 4.272
72
GLL048 Glial Tumor 52 4.219
73
GLM045 Glioma 63 4.219
74
P PRS038 Personality Disorder 65 4.210
75
STT001 Status Epilepticus 59 4.207
76
ACT084 Acute Stress Disorder 54 4.191
77
HMN044 Human Immunodeficiency Virus Type 1 78 4.162
78
P SBS003 Substance Abuse 54 4.137
79
CNS004 Constipation 56 4.119
80
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 38 4.088
81
P PRP019 Peripheral Nervous System Disease 58 4.031
82
SYN036 Syncope 45 3.976
83
HMC014 Homocysteinemia 52 3.951
84
PTH002 Pathological Gambling 48 3.917
85
RLP002 Relapsing-Remitting Multiple Sclerosis 56 3.917
86
PRV004 Periventricular Leukomalacia 52 3.896
87
WTH001 Withdrawal Disorder 48 3.867
88
P MVM001 Movement Disease 61 3.867
89
P BRS047 Breast Cancer 98 3.814
90
TBC004 Tobacco Addiction 63 3.814
91
HYP266 Hypoxia 57 3.769
92
OCL006 Ocular Hypertension 53 3.745
93
BRN004 Brain Edema 54 3.660
94
BNS003 Binswanger's Disease 41 3.660
95
DRG003 Drug Dependence 46 3.616
96
ADS004 Aids Dementia Complex 40 3.610
97
c BPL002 Bipolar I Disorder 47 3.584
98
P HYD006 Hydrocephalus 61 3.572
99
P GLM040 Glioma Susceptibility 1 71 3.551
100
P MYC033 Myoclonus 47 3.544
101
CCN001 Cocaine Dependence 48 3.542
102
BRN028 Brain Cancer 74 3.524
103
c ESS001 Essential Tremor 57 3.394
104
LRN003 Learning Disability 49 3.370
105
SMN008 Semantic Dementia 47 3.359
106
P MTR014 Motor Neuron Disease 65 3.351
107
P CHR345 Chronic Pain 50 3.279
108
c SYS001 Systemic Lupus Erythematosus 87 3.180
109
P LPS004 Lupus Erythematosus 61 3.180
110
OCL069 Ocular Motor Apraxia 57 3.113
111
NRT004 Neuritis 53 3.103
112
PRP016 Paraplegia 52 3.077
113
PSD088 Pseudobulbar Affect 33 3.077
114
AGN016 Aging 54 3.070
116
P NRV007 Nervous System Disease 67 3.034
117
ALL014 Allergic Encephalomyelitis 34 3.026
118
HGH043 High Grade Glioma 45 3.016
119
CCN002 Cocaine Abuse 49 3.016
120
c TYP009 Type 2 Diabetes Mellitus 92 2.975
121
HYP056 Hypoglycemia 65 2.975
122
MRP001 Morphine Dependence 42 2.962
123
P ENC004 Encephalitis 61 2.951
124
RHB024 Rhabdomyosarcoma 2 67 2.927
125
P PRS040 Prostate Cancer 95 2.925
126
DBT010 Diabetic Neuropathy 54 2.904
127
GRN059 Grn Frontotemporal Dementia 16 2.893
128
RCK004 Rickets 68 2.884
129
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 2.868
130
DYS073 Dysphagia 53 2.863
131
GLS001 Gliosarcoma 64 2.825
132
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 2.818
133
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 2.818
134
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 2.818
135
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 2.818
136
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 2.818
137
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 2.818
138
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 2.818
139
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 2.818
140
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 2.818
141
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 2.818
142
PST053 Postherpetic Neuralgia 40 2.812
143
RTN003 Retinal Ischemia 49 2.811
144
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 2.792
145
P SCK005 Sickle Cell Disease 56 2.774
146
P DRR001 Diarrhea 55 2.758
147
P LNG032 Lung Cancer 98 2.756
148
P FRG001 Fragile X Syndrome 70 2.755
149
c MJR006 Major Affective Disorder 5 32 2.752
150
c MJR023 Major Affective Disorder 7 33 2.752
151
c MJR004 Major Affective Disorder 4 28 2.752
152
c MJR003 Major Affective Disorder 6 32 2.752
153
c MJR008 Major Affective Disorder 2 34 2.752
154
P MJR007 Major Affective Disorder 1 42 2.752
155
ADG002 Audiogenic Seizures 25 2.748
156
KLP001 Kleptomania 36 2.715
157
P RTN018 Retinal Disease 53 2.704
158
P CNG024 Congenital Nystagmus 36 2.696
159
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 2.665
160
P OPT009 Optic Neuritis 57 2.649
161
P DYS154 Dystonia 64 2.506
162
P BCL017 B-Cell Lymphoma 59 2.491
163
TRN015 Transient Cerebral Ischemia 63 2.471
164
DMY004 Demyelinating Disease 50 2.471
165
ACQ007 Acquired Immunodeficiency Syndrome 59 2.443
166
CHL079 Children's Interstitial Lung Disease 26 2.421
167
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 67 2.414
168
TRD006 Tardive Dyskinesia 53 2.408
169
CHR178 Chromosomal Triplication 34 2.378
170
P TRN020 Turner Syndrome 67 2.361
171
47X002 47,xyy 48 2.342
172
MTS001 Mutism 44 2.342
173
P ASP001 Asperger Syndrome 48 2.327
174
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 2.327
175
P RST001 Restless Legs Syndrome 52 2.325
176
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 2.310
177
c PRM092 Primary Lateral Sclerosis, Adult, 1 38 2.310
178
INT002 Intermittent Claudication 61 2.310
179
PLM129 Pulmonary Disease, Chronic Obstructive 74 2.273
180
CHG001 Chagas Disease 66 2.273
182
IMM167 Immune Deficiency Disease 78 2.210
183
HPT004 Hepatic Coma 43 2.201
184
HPT019 Hepatic Encephalopathy 59 2.201
185
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 2.201
186
PRT058 Pure Autonomic Failure 58 2.194
187
ATR057 Atrioventricular Block 54 2.134
188
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 2.126
189
HMN014 Human Immunodeficiency Virus Infectious Disease 54 2.126
190
CHR073 Choreatic Disease 54 2.126
191
CRB090 Cerebral Hypoxia 42 2.126
192
ADL002 Adult Syndrome 70 2.125
193
ANT039 Antisynthetase Syndrome 55 2.125
194
OBS003 Obsessive-Compulsive Personality Disorder 43 2.125
195
c PNS012 Paine Syndrome 60 2.103
196
c EPS039 Episodic Pain Syndrome, Familial, 1 42 2.103
197
P URN019 Urinary Tract Infection 49 2.060
199
FTL006 Fetal Alcohol Spectrum Disorder 43 2.046
200
P FTL001 Fetal Alcohol Syndrome 55 2.046
201
MNN017 Mononeuropathy 41 2.046
202
P CTR002 Cataract 60 1.988
203
P MGR001 Migraine Without Aura 49 1.988
204
BRD004 Borderline Personality Disorder 53 1.988
205
SCL003 Social Phobia 48 1.927
206
AMD002 Amed Syndrome, Digenic 37 1.914
207
APR001 Apraxia 52 1.912
208
SCH012 Schizoaffective Disorder 50 1.912
209
RMS001 Rem Sleep Behavior Disorder 47 1.912
210
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 1.905
211
FCL014 Focal Epilepsy 53 1.905
212
P FNG006 Feingold Syndrome 1 62 1.895
213
PCK003 Pick Disease of Brain 69 1.895
214
SPN033 Spontaneous Ocular Nystagmus 25 1.895
215
FRN030 Frontotemporal Dementia with Parkinsonism-17 24 1.895
216
c MCR115 Microvascular Complications of Diabetes 5 65 1.869
217
P RTT002 Rett Syndrome 79 1.832
218
CRD223 Cardiac Arrhythmia 63 1.832
219
WRN002 Wernicke-Korsakoff Syndrome 50 1.832
220
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 1.832
222
c ACT073 Acute Leukemia 58 1.832
223
P INF038 Influenza 68 1.832
224
P LKM002 Leukemia 67 1.832
225
ADT003 Auditory System Disease 49 1.832
226
TTN003 Tetanus 65 1.832
227
CRT015 Carotid Artery Occlusion 45 1.832
228
CYT002 Cytokine Deficiency 43 1.832
229
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 1.810
230
c CNT035 Central Nervous System Disease 54 1.802
231
P ANR048 Aniridia 1 64 1.764
232
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 1.764
233
NRN002 Neuronitis 31 1.754
234
c OPT053 Optic Atrophy 1 62 1.747
235
P EXN002 Exanthem 58 1.747
236
P TRN034 Transverse Myelitis 47 1.747
237
c SCH073 Schizophrenia 9 25 1.747
238
NRM001 Neuromyelitis Optica 61 1.747
239
INF118 Inflammatory Myopathy with Abundant Macrophages 27 1.747
240
LYM027 Lymphopenia 56 1.747
241
MYL001 Myelitis 50 1.747
242
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.747
243
RBS001 Rabies 58 1.747
244
JPN002 Japanese Encephalitis 61 1.747
245
c ACT071 Acute Kidney Failure 60 1.747
246
P CRB088 Cerebral Atrophy 33 1.747
247
FNT004 Fainting 29 1.747
248
OCC008 Occipital Neuralgia 24 1.747
249
IMP006 Impulse Control Disorder 45 1.734
250
AND005 Androgen Insensitivity Syndrome, Mild 21 1.712
251
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 1.656
252
CLT003 Colitis 63 1.656
253
c GLC092 Glaucoma, Primary Open Angle 62 1.656
254
P RTN016 Retinal Degeneration 52 1.656
255
PPT005 Peptic Ulcer Disease 58 1.656
256
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 1.656
257
MLG169 Malignant Astrocytoma 57 1.656
258
CNG034 Congestive Heart Failure 69 1.656
259
P TMP001 Temporal Lobe Epilepsy 49 1.656
261
BLM002 Bulimia Nervosa 57 1.623
263
c SYS043 Systemic Lupus Erythematosus 1 38 1.623
264
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 38 1.623
265
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 70 1.623
266
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 58 1.623
267
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 1.623
268
SCH003 Schizophreniform Disorder 55 1.623
269
KRT002 Keratomalacia 55 1.570
270
BNG077 Benign Idiopathic Neonatal Seizures 23 1.557
271
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 63 1.557
272
c SCH085 Schizophrenia 2 27 1.557
273
c SZR022 Seizures, Benign Familial Neonatal, 1 43 1.557
274
DSS032 Disease by Infectious Agent 55 1.557
275
STT041 Stuttering 52 1.557
276
SPC005 Speech Disorder 45 1.557
277
P NRM002 Normal Pressure Hydrocephalus 49 1.557
278
CRB086 Cerebral Aneurysms 40 1.557
279
HYP264 Hypertonia 36 1.557
280
CHR158 Charles Bonnet Syndrome 23 1.557
282
c SML038 Small Cell Cancer of the Lung 69 1.472
283
DFC004 Deficiency Anemia 74 1.453
284
SCK003 Sickle Cell Anemia 74 1.453
285
SPR126 Superior Semicircular Canal Dehiscence 41 1.453
286
c HMG029 Hemoglobin Se Disease 40 1.453
287
ANX004 Anoxia 40 1.447
288
c SPN294 Spinocerebellar Ataxia 1 53 1.447
289
ULC004 Ulcerative Colitis 74 1.447
290
ASY002 Asymptomatic Neurosyphilis 41 1.447
291
PLC002 Plica Syndrome 35 1.447
292
DYS009 Dysthymic Disorder 52 1.447
293
NRG002 Neurogenic Bladder 55 1.447
294
SNS003 Sensory Peripheral Neuropathy 52 1.447
295
P DYS005 Dyslexia 41 1.447
296
SYN007 Synovitis 55 1.447
297
P PLY019 Polyneuropathy 52 1.447
298
RDN001 Reading Disorder 40 1.447
299
NRS003 Neurosyphilis 45 1.447
300
CRH001 Crohn's Disease 80 1.439
301
CNT033 Central Nervous System Cancer 47 1.439
302
LNG031 Lung Benign Neoplasm 51 1.439
303
HNT002 Hantavirus Pulmonary Syndrome 55 1.439
304
P NRV006 Nervous System Cancer 48 1.439
305
VST001 Vestibular Neuronitis 33 1.397
306
SRT004 Serotonin Syndrome 54 1.322
307
P ALT001 Alternating Hemiplegia of Childhood 57 1.322
308
P SLP006 Sleep Apnea 69 1.322
309
NRN005 Neuronal Ceroid-Lipofuscinoses 61 1.322
310
SNL009 Senile Plaque Formation 29 1.322
311
P RTN024 Retinoblastoma 73 1.322
312
P AMY004 Amyloidosis 70 1.322
313
SVR001 Severe Acute Respiratory Syndrome 67 1.322
314
P NRN021 Neuronal Ceroid Lipofuscinosis 65 1.322
315
HMP005 Hemiplegia 54 1.322
316
SVR004 Severe Combined Immunodeficiency 72 1.322
317
P LVR013 Liver Disease 69 1.317
318
P OPT006 Optic Nerve Disease 58 1.317
319
P VSC007 Vascular Disease 63 1.317
320
SDD004 Sudden Arrhythmia Death Syndrome 22 1.269
321
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 63 1.269
322
SPC010 Speech and Communication Disorders 48 1.269
323
BRN032 Brain Glioma 45 1.269
324
BDY001 Body Dysmorphic Disorder 41 1.269
325
APP015 Apparent Mineralocorticoid Excess 57 1.269
326
P SMK004 Smoking As a Quantitative Trait Locus 3 44 1.269
327
P NJM001 Nijmegen Breakage Syndrome 76 1.269
328
P EPL116 Epileptic Encephalopathy, Childhood-Onset 43 1.269
329
TXC002 Toxic Encephalopathy 52 1.269
330
CLL010 Cellular Ependymoma 57 1.269
331
CRN036 Craniopharyngioma 64 1.269
332
P BNG030 Benign Ependymoma 51 1.269
333
MYF002 Myofascial Pain Syndrome 46 1.269
334
MXD026 Mixed Glioma 45 1.269
335
CYS009 Cystadenoma 43 1.269
337
HRN003 Heroin Dependence 44 1.269
338
ATX019 Ataxia with Vitamin E Deficiency 44 1.269
341
CTS005 Catastrophic Antiphospholipid Syndrome 43 1.269
342
CRY008 Cryopyrin-Associated Periodic Syndrome 48 1.269
343
P SLP005 Sleep Disorder 61 1.232
344
CHL068 Cholestasis 61 1.195
345
c BCT007 Bacterial Meningitis 55 1.174
346
c MCR130 Microvascular Complications of Diabetes 6 41 1.174
347
CHK001 Chikungunya 60 1.174
348
NNL006 Non-Alcoholic Steatohepatitis 54 1.174
349
c MCR120 Microvascular Complications of Diabetes 7 47 1.174
350
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.174
351
P NRC002 Narcolepsy 56 1.174
352
PRX097 Paroxysmal Dystonia 32 1.174
353
c MCR113 Microvascular Complications of Diabetes 3 52 1.174
354
c MCR133 Microvascular Complications of Diabetes 4 41 1.174
355
AMP007 Amphetamine Abuse 36 1.174
356
SBS004 Substance Dependence 47 1.174
357
P MNN013 Meningitis 65 1.174
359
c EPS035 Episodic Ataxia, Type 2 63 1.140
360
P EPS003 Episodic Ataxia 59 1.140
361
c ACT134 Acute Liver Failure 59 1.041
362
P AST005 Asthma 76 1.041
363
ZKF001 Zika Fever 52 1.041
364
GTP001 Gait Apraxia 29 1.041
365
P MCR010 Microcephaly 60 1.041
366
P PNM007 Pneumonia 67 1.041
367
MTH086 Methotrexate Toxicity 32 0.981
368
SRC015 Sarcosinemia 38 0.981
369
P ANP001 Anaplastic Large Cell Lymphoma 61 0.981
370
TRC010 Trichotillomania 50 0.981
371
P MYP004 Myopathy 67 0.981
372
GSG001 Gas Gangrene 52 0.981
373
P AGN002 Agnosia 54 0.981
374
CMM004 Common Variable Immunodeficiency 72 0.981
375
RTN020 Retinal Vascular Disease 46 0.981
376
P CRD119 Cardiac Arrest 67 0.981
377
P RSP003 Respiratory Failure 74 0.981
378
LVR012 Liver Cirrhosis 63 0.981
379
PRS129 Prostatic Hyperplasia, Benign 49 0.931
380
c HYP836 Hypercholesterolemia, Familial, 1 73 0.931
381
PRT037 Pertussis 65 0.931
382
P DBT009 Diabetes Mellitus 67 0.931
383
P GLL022 Guillain-Barre Syndrome 60 0.931
384
PRS021 Prostatic Adenoma 43 0.931
385
NRL004 Neuroleptic Malignant Syndrome 52 0.931
386
PRS045 Prostatic Hypertrophy 53 0.931
387
P PRN023 Prion Disease 60 0.931
388
WRN003 Wernicke Encephalopathy 46 0.931
389
P PTS002 Ptosis 52 0.931
390
PLM010 Pulmonary Edema 55 0.931
391
CRT033 Corticobasal Degeneration 47 0.931
392
HRP004 Herpes Zoster 61 0.878
393
P LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 52 0.857
394
VSL002 Visual Epilepsy 39 0.856
395
P CNR004 Cone-Rod Dystrophy 2 74 0.825
396
P ORT004 Orthostatic Intolerance 63 0.825
397
c CNG193 Congenital Disorder of Glycosylation, Type Ip 45 0.825
398
P HYP726 Hypercalcemia, Infantile, 1 58 0.825
399
RNL114 Renal Cell Carcinoma, Nonpapillary 80 0.825
400
SMT006 Somatoform Disorder 50 0.825
401
GST020 Gastric Antral Vascular Ectasia 40 0.825
402
SMT001 Somatization Disorder 50 0.825
404
CYT018 Cytochrome P450 2d6 Variant 26 0.825
405
P SPR120 Supranuclear Palsy, Progressive, 1 69 0.806
406
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.806
407
ANS006 Anosognosia 34 0.806
408
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.806
409
SCR011 Scrapie 39 0.806
410
P CYS018 Cystitis 59 0.806
411
HYP066 Hyperglycemia 61 0.806
412
TRT001 Teratocarcinoma 42 0.806
413
ALL029 Allergic Disease 59 0.806
414
DMN012 Dementia - Subcortical 18 0.806
415
CRB159 Cerebral Visual Impairment 34 0.658
416
DRV001 Dravet Syndrome 69 0.658
417
c PLM164 Pulmonary Hypertension, Primary, 1 76 0.658
418
P PHC003 Pheochromocytoma 69 0.658
419
PLY150 Polykaryocytosis Inducer 29 0.658
420
c PRG042 Progressive Familial Heart Block, Type Ia 66 0.658
421
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 0.658
422
c THR092 Thrombophilia Due to Thrombin Defect 74 0.658
423
MNR012 Meniere Disease 56 0.658
424
SCN049 Second-Degree Atrioventricular Block 33 0.658
425
c PRM108 Primary Progressive Multiple Sclerosis 51 0.658
426
P INF037 Inflammatory Bowel Disease 53 0.658
427
c NTR051 Neutropenia, Severe Congenital, 2, Autosomal Dominant 27 0.658
428
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.658
429
MNT320 Mental Retardation, Autosomal Dominant 6, with or Without Seizures 30 0.658
430
ATM100 Autoimmune Optic Neuritis 28 0.658
431
c ALZ063 Alzheimer's Disease 1 31 0.658
432
P FML023 Familial Hemiplegic Migraine 53 0.658
433
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.658
434
LGH007 Leigh Syndrome 70 0.658
435
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.658
436
PLY183 Polymicrogyria with or Without Vascular-Type Ehlers-Danlos Syndrome 41 0.658
437
ADR040 Adrenal Gland Pheochromocytoma 46 0.658
438
P SKN015 Skin Carcinoma 71 0.658
439
ART016 Aortic Aneurysm 68 0.658
440
HYP005 Hypokalemia 55 0.658
441
END086 End Stage Renal Disease 52 0.658
442
c DVL053 Developmental and Epileptic Encephalopathy 27 31 0.658
443
ASP007 Aspiration Pneumonia 49 0.658
444
c SVR105 Severe Congenital Neutropenia 2 11 0.658
445
LPD008 Lipid Metabolism Disorder 62 0.658
446
P TCD001 Tic Disorder 49 0.658
447
RGH001 Right Bundle Branch Block 47 0.658
448
CRB033 Cerebral Degeneration 39 0.658
449
ALB002 Albinism 47 0.658
450
TBL023 Tubulinopathies 31 0.658
452
PLY024 Polymicrogyria 47 0.658
453
P MTC069 Mitochondrial Disorders 57 0.658
454
P HYP265 Hypotonia 42 0.658
455
P DYS021 Dysautonomia 38 0.658
456
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 0.515
457
c ATR087 Atrial Standstill 1 74 0.515
458
SVR097 Severe Cutaneous Adverse Reaction 69 0.515
459
c HRD026 Hereditary Ataxia 47 0.515
460
ERY066 Erythema Multiforme Major 29 0.515
461
ERY003 Erythema Multiforme 56 0.515
462
PRN009 Paranoid Schizophrenia 49 0.515
463
PTT037 Pituitary Tumors 44 0.515
464
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 46 0.515
465
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.466
466
DMN026 Dementia Pugilistica 27 0.466
467
PST086 Posterior Cortical Atrophy 36 0.466
468
P MCH002 Machado-Joseph Disease 62 0.466
469
P MYS003 Myasthenia Gravis 68 0.466
470
c SCH051 Schizophrenia 4 32 0.466
471
P MYC084 Mycobacterium Tuberculosis 1 68 0.466
472
MTN003 Motion Sickness 51 0.466
473
CRT072 Creutzfeldt-Jakob Disease 68 0.466
474
OTT002 Otitis Media 71 0.466
475
c SPN299 Spinocerebellar Ataxia 20 33 0.466
476
PRP027 Peripheral Vascular Disease 71 0.466
477
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.466
478
LWG006 Low Grade Glioma 41 0.466
479
CGN006 Cogan Syndrome 49 0.466
480
HYP025 Hyperphosphatemia 48 0.466
481
LMB024 Limbic Encephalitis 43 0.466
482
KRN002 Kearns-Sayre Syndrome 63 0.466
483
P SPN301 Spinocerebellar Ataxia 2 59 0.466
484
PHL006 Phelan-Mcdermid Syndrome 60 0.466
485
LPT014 Leptin Deficiency or Dysfunction 78 0.466
486
c DVL071 Developmental and Epileptic Encephalopathy 46 24 0.466
487
c SCH079 Schizophrenia 1 44 0.466
488
ALX003 Alexander Disease 61 0.466
489
P STR020 Strabismus 56 0.466
490
c TBR025 Tuberous Sclerosis 1 84 0.466
491
MLT157 Multiple System Atrophy 1 69 0.466
492
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 0.466
493
OPT070 Optic Nerve Hypoplasia, Bilateral 56 0.466
494
c ALZ054 Alzheimer Disease 4 43 0.466
495
c ALZ057 Alzheimer Disease 10 35 0.466
496
BSL009 Basal Ganglia Calcification 45 0.466
497
c ALZ056 Alzheimer Disease 3 55 0.466
498
GLC003 Glucose Intolerance 54 0.466
499
MTC111 Mitochondrial Neurogastrointestinal Encephalomyopathy 47 0.466
500
MLY001 Molybdenum Cofactor Deficiency 40 0.466
501
PSD001 Pseudobulbar Palsy 38 0.466
502
RPD005 Rapidly Involuting Congenital Hemangioma 46 0.466
503
c CHR684 Chronic Kidney Disease 69 0.466
504
BRN018 Borna Disease 36 0.466
505
MCH006 Mechanical Strabismus 40 0.466
506
MNG007 Manganese Poisoning 28 0.466
507
PRS047 Prostatitis 58 0.466
508
P BRS044 Breast Adenocarcinoma 58 0.466
509
PLX004 Plexopathy 29 0.466
510
NRM005 Neuromuscular Disease 63 0.466
511
PRS011 Persian Gulf Syndrome 35 0.466
512
SPR012 Separation Anxiety Disorder 41 0.466
513
HLX001 Helix Syndrome 48 0.466
514
PHN011 Phenytoin Toxicity 32 0.466
515
SPP007 Suppression Amblyopia 38 0.466
516
AMB002 Amblyopia 50 0.466
517
NSP002 Nasopharyngitis 45 0.466
518
CHL147 Chlamydia Pneumonia 47 0.466
519
P UVT001 Uveitis 57 0.466
520
GT001 Gout 64 0.466
521
c ACT068 Acute Cystitis 61 0.466
522
P BRB001 Beriberi 44 0.466
523
VST003 Vestibular Nystagmus 25 0.466
524
IMP005 Impotence 52 0.466
525
P TBR001 Tuberous Sclerosis 69 0.466
526
CHL123 Chlamydia 58 0.466
527
ASP004 Asphyxia Neonatorum 50 0.466
528
MNN009 Meningoencephalitis 48 0.466
529
BRN024 Bronchitis 67 0.466
530
MCL006 Macular Retinal Edema 57 0.466
531
ANT019 Anterograde Amnesia 38 0.466
532
INT042 Internuclear Ophthalmoplegia 32 0.466
533
P HYP076 Hyperthyroidism 53 0.466
534
PLG002 Plague 58 0.466
535
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.466
536
P GND004 Gonadal Dysgenesis 47 0.466
537
P ART005 Arteriovenous Malformation 65 0.466
538
CRB037 Cerebral Palsy 67 0.466
539
NRM004 Neuroma 49 0.466
541
RFR003 Refractive Error 41 0.466
542
HDN002 Head Injury 44 0.466
543
CRB089 Cerebral Beriberi 19 0.466
544
ATN005 Autonomic Dysfunction 46 0.466
545
P HYP263 Hypersomnia 41 0.466
546
P CLS010 Cluster Headache 42 0.466
547
HYP707 Hypertrophic Olivary Degeneration 18 0.466
548
MRC001 Marchiafava Bignami Disease 23 0.466
549
PRG033 Progressive Non-Fluent Aphasia 52 0.466
550
BRN056 Bronchopulmonary Dysplasia 56 0.466
551
P CHR342 Chiari Malformation 41 0.466
552
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 0.466
553
c ATM075 Autoimmune Encephalitis 40 0.466
554
c RST012 Restless Legs Syndrome 1 33 0.413
555
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 62 0.413
556
VTM002 Vitamin B12 Deficiency 48 0.413
557
HYP458 Hyper Ige Syndrome 60 0.413
558
P MCR129 Microvascular Complications of Diabetes 1 68 0.413
559
GLS018 Glass Syndrome 61 0.413
560
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 29 0.413
561
DSS008 Disease of Mental Health 74 0.413
562
DBT002 Diabetic Autonomic Neuropathy 41 0.413
563
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 44 0.413
The MalaCards human disease database index: 1-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Content
Loading form....