Search results for "alzheimer disease familial"

The MalaCard for "alzheimer disease familial" has been retired.
Searching MalaCards for entries containing "alzheimer disease familial"

720 hits were found for 'alzheimer disease familial'

# Family MCID Name MIFTS Score
1
P ALZ034 Alzheimer Disease 93 12.582
2
c ALZ036 Alzheimer Disease, Type 3 51 6.640
3
c ALZ037 Alzheimer Disease-2 54 6.432
4
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 42 5.701
5
c ALZ035 Alzheimer Disease-4 38 4.677
6
c ALZ012 Alzheimer Disease 12 25 3.846
7
c ALZ002 Alzheimer Disease Type 1 22 3.624
8
c ALZ039 Alzheimer's Disease 7 21 3.332
9
c ERL006 Early-Onset Familial Alzheimer Disease 42 2.988
10
FML202 Familial Alzheimer-Like Prion Disease 4 1.584
11
DMN002 Dementia 64 0.768
12
NRN002 Neuronitis 42 0.418
13
P ENC018 Encephalopathy 59 0.343
14
CRB009 Cerebritis 38 0.340
15
PHY002 Physical Disorder 44 0.334
16
P AMY004 Amyloidosis 64 0.325
17
VSC002 Vascular Dementia 54 0.288
18
c CNT035 Central Nervous System Disease 59 0.283
19
CND002 Conduct Disorder 56 0.244
20
DSS008 Disease of Mental Health 55 0.240
21
MTH009 Mouth Disease 63 0.214
22
LRN003 Learning Disability 51 0.200
23
c ALZ032 Alzheimer Disease 18 26 0.195
24
P BRS047 Breast Cancer 100 0.191
25
P CRB019 Cerebral Amyloid Angiopathy 58 0.186
26
P PRP019 Peripheral Nervous System Disease 54 0.183
27
P HRT032 Heart Disease 76 0.182
28
c HYP163 Hyperlipidemia Type 3 34 0.176
29
GLT021 Glutaricaciduria, Type I 48 0.175
30
DWN001 Down Syndrome 65 0.175
31
PCK002 Pick Disease 67 0.171
32
c ALZ043 Alzheimer's Disease 15 21 0.169
33
END072 Endotheliitis 42 0.169
34
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 44 0.164
35
P SCH015 Schizophrenia 76 0.164
36
DRG001 Drug Psychosis 40 0.161
37
ART111 Artery Disease 57 0.158
38
P LTR001 Lateral Sclerosis 52 0.158
39
P THY032 Thyroiditis 54 0.157
40
MDD011 Mood Disorder 61 0.156
41
P NRV007 Nervous System Disease 71 0.156
42
P OBS005 Obesity 93 0.153
43
SPC010 Speech and Communication Disorders 46 0.152
44
P CRN211 Coronary Artery Disease 75 0.152
45
ATN002 Autonomic Nervous System Disease 47 0.147
46
ATH003 Atherosclerosis 62 0.147
47
NTR005 Nutritional Deficiency Disease 39 0.147
48
SPS057 Spasticity 42 0.144
49
SMN008 Semantic Dementia 44 0.143
50
RTN023 Retinitis 49 0.142
51
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 29 0.142
52
ALN001 Aland Island Eye Disease 45 0.141
53
PSY004 Psychotic Disorder 67 0.141
54
P EPL164 Epilepsy 66 0.139
55
VSC007 Vascular Disease 67 0.136
56
ALR002 Al-Raqad Syndrome 36 0.136
57
P CRT072 Creutzfeldt-Jakob Disease 63 0.135
58
c ALZ042 Alzheimer's Disease 14 37 0.134
59
GLC008 Glucose Metabolism Disease 47 0.134
60
SLP005 Sleep Disorder 53 0.133
61
P CRB088 Cerebral Atrophy 42 0.131
62
APH002 Aphasia 53 0.131
63
P ATX004 Ataxia 53 0.130
64
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 60 0.130
65
MVM001 Movement Disease 54 0.129
66
P CLR023 Colorectal Cancer 97 0.128
67
BLD054 Blood Protein Disease 40 0.126
68
P LKM002 Leukemia 70 0.126
69
MNT002 Mental Depression 54 0.125
70
SPN369 Spinal Disease 41 0.124
71
P NRB001 Neuroblastoma 69 0.124
72
P MYP004 Myopathy 67 0.123
73
SCR035 Sacral Agenesis with Vertebral Anomalies 33 0.122
74
STR067 Stroke, Ischemic 77 0.122
75
P HPT021 Hepatitis 70 0.119
76
P HYD006 Hydrocephalus 67 0.118
77
BRT030 Birth Defects 43 0.117
78
ACR041 Acromelic Frontonasal Dysostosis 46 0.115
79
PRN023 Prion Disease 48 0.115
80
ANX002 Anxiety Disorder 69 0.115
81
P NRP001 Neuropathy 60 0.114
82
P PNC044 Pancreatitis 60 0.113
83
P ART022 Arthritis 75 0.113
84
PRP027 Peripheral Vascular Disease 69 0.112
85
P CTR002 Cataract 57 0.112
86
ART021 Arteriosclerosis 59 0.111
87
SPS019 Spastic Paraparesis 34 0.111
88
PRS047 Prostatitis 56 0.111
89
LPD008 Lipid Metabolism Disorder 58 0.109
90
P SPS003 Spastic Diplegia 53 0.109
91
P PRK057 Parkinson Disease, Late-Onset 72 0.108
92
CRB033 Cerebral Degeneration 46 0.108
93
PRD011 Proud Syndrome 42 0.107
94
ISC004 Ischemia 59 0.105
95
PST086 Posterior Cortical Atrophy 35 0.105
96
BRN071 Brain Injury 52 0.105
97
APR001 Apraxia 48 0.105
98
P HYP607 Hypercholesterolemia, Familial 77 0.105
99
EYD002 Eye Disease 63 0.103
100
P CRT033 Corticobasal Degeneration 46 0.103
101
P LVR013 Liver Disease 72 0.102
102
ADR009 Adrenal Cortex Disease 41 0.102
103
P PRS040 Prostate Cancer 89 0.100
104
MLT021 Multiple System Atrophy 71 0.099
105
NRM002 Normal Pressure Hydrocephalus 50 0.098
106
CRH001 Crohn's Disease 76 0.097
107
TTH006 Tooth Disease 52 0.097
108
P GRV001 Graves' Disease 61 0.097
109
RSP006 Respiratory System Disease 62 0.097
110
P DMN033 Dementia, Frontotemporal 63 0.096
111
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.095
112
P DYS021 Dysautonomia 47 0.095
113
LNG099 Lung Disease 62 0.095
114
ADJ001 Adjustment Disorder 38 0.094
115
GLB003 Globe Disease 35 0.094
116
c ALZ008 Alzheimer Disease Risk Factor 19 0.094
117
BSL008 Basal Ganglia Disease 43 0.093
118
SPC003 Specific Developmental Disorder 40 0.093
119
P RHM011 Rheumatoid Arthritis 88 0.093
120
ACD009 Acid-Labile Subunit, Deficiency of 48 0.093
121
SPC005 Speech Disorder 43 0.092
122
P CRN178 Coronary Heart Disease 6 24 0.092
123
BNS002 Bone Structure Disease 36 0.092
124
P TRM003 Tremor 54 0.092
125
P MSC005 Muscular Dystrophy 64 0.092
126
c CRN214 Coronary Heart Disease 5 23 0.090
127
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 57 0.090
128
CRB031 Cerebral Arterial Disease 31 0.089
129
NWC001 Newcastle Disease 54 0.088
130
OPT006 Optic Nerve Disease 51 0.087
131
ADN018 Adenoma 59 0.087
132
P MYC007 Myocardial Infarction 79 0.087
133
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 39 0.086
134
P AST005 Asthma 82 0.086
135
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 60 0.085
136
FST001 Foster-Kennedy Syndrome 34 0.085
137
BRN028 Brain Cancer 70 0.085
138
WTH001 Withdrawal Disorder 41 0.084
139
HYP266 Hypoxia 55 0.084
140
P MYS005 Myositis 56 0.083
141
LPD004 Lipoid Nephrosis 48 0.083
142
CRB085 Cerebral Hemorrhage 43 0.082
143
ISC006 Ischemic Heart Disease 68 0.082
144
ETH011 Ethylmalonic Encephalopathy 59 0.082
145
RTN018 Retinal Disease 56 0.082
146
GNR004 Generalized Anxiety Disorder 51 0.082
147
P AMY084 Amyloidosis, Finnish Type 43 0.081
148
P DYS154 Dystonia 64 0.081
149
P HNT016 Huntington Disease 80 0.081
150
c INH020 Inherited Metabolic Disorder 49 0.081
151
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.080
152
P HMC003 Hemochromatosis 72 0.080
153
P FML035 Familial Hyperlipidemia 50 0.079
154
HYP037 Hyperhomocysteinemia 50 0.079
155
P HRP006 Herpes Simplex 65 0.079
156
c GRN014 Grn-Related Frontotemporal Dementia 43 0.079
157
P OST002 Osteoporosis 64 0.079
158
DMN031 Dementia, Lewy Body 60 0.078
159
P PNM007 Pneumonia 66 0.078
160
c TRC078 Trichohepatoenteric Syndrome 2 31 0.078
161
WLS001 Wilson Disease 72 0.078
162
KWS002 Kawasaki Disease 70 0.078
163
LPP001 Lipoprotein Lipase Deficiency 65 0.077
164
CNT098 Central Core Disease 66 0.077
165
RDN001 Reading Disorder 39 0.077
166
MTR014 Motor Neuron Disease 59 0.076
167
FRN030 Frontotemporal Dementia with Parkinsonism-17 31 0.076
168
BLD053 Blood Platelet Disease 46 0.076
169
MSC004 Muscle Tissue Disease 36 0.076
170
SKN016 Skin Disease 68 0.075
171
c ESS001 Essential Tremor 61 0.075
172
TRM010 Traumatic Brain Injury 52 0.075
173
CNG034 Congestive Heart Failure 71 0.075
174
EXF001 Exfoliation Syndrome 57 0.075
175
ADT003 Auditory System Disease 51 0.075
176
AYM001 Ayme-Gripp Syndrome 45 0.074
177
P MSC033 Muscle Disorders 52 0.074
178
INC002 Inclusion Body Myositis 63 0.074
179
HMZ003 Homozygous Familial Hypercholesterolemia 44 0.074
180
P HYP071 Hypersensitivity Reaction Type Ii Disease 51 0.074
181
P ALX003 Alexander Disease 64 0.074
182
WLL006 Wells Syndrome 56 0.074
183
P HYP086 Hypothyroidism 65 0.073
184
c PND001 Pain Disorder 55 0.073
185
CHR008 Choroiditis 43 0.073
186
P CLC005 Celiac Disease 67 0.073
187
HPT074 Hepatic Adenoma, Somatic 51 0.072
188
BRN080 Brain Ischemia 41 0.072
189
CNV002 Conversion Disorder 42 0.072
190
P PRD008 Periodontitis 46 0.072
191
ETN001 Eating Disorder 60 0.072
192
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 38 0.072
193
OBS015 Obesity, Hyperphagia, and Developmental Delay 46 0.072
194
P BPL003 Bipolar Disorder 62 0.071
195
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.071
196
MYC033 Myoclonus 41 0.071
197
P INT063 Intellectual Disability 53 0.071
198
P DNT015 Dent Disease 61 0.070
199
P OPN001 Open-Angle Glaucoma 48 0.070
200
CLT003 Colitis 59 0.070
201
P LKD001 Leukodystrophy 58 0.070
202
NRM005 Neuromuscular Disease 57 0.069
203
MYC002 Mycobacterium Avium Complex Disease 51 0.069
204
c CRN173 Coronary Heart Disease 8 20 0.069
205
c PRK031 Parkinson Disease 1 55 0.069
206
ATS008 Autosomal Dominant Disease 42 0.069
207
DRG003 Drug Dependence 53 0.069
208
CTS003 Coats Disease 57 0.069
209
GDS001 Good Syndrome 45 0.069
210
PRP080 Peripheral Artery Disease 36 0.069
211
c CRN175 Coronary Heart Disease 4 21 0.069
212
c HYP595 Hypertension, Essential 69 0.069
213
ALC007 Alcohol Dependence 65 0.069
214
CYS001 Cystic Fibrosis 86 0.068
215
c CRN172 Coronary Heart Disease 3 21 0.068
216
CSY001 C Syndrome 49 0.068
217
HNM002 Hinman Syndrome 25 0.068
218
ATN005 Autonomic Dysfunction 45 0.068
219
P GT001 Gout 58 0.068
220
VND001 Vein Disease 52 0.067
221
LKC003 Leukocyte Disease 47 0.067
222
FTT001 Fatty Liver Disease 60 0.067
223
c MCL062 Mucolipidosis Ii Alpha/beta 60 0.067
224
P PRP029 Porphyria 58 0.067
225
P MTC003 Metachromatic Leukodystrophy 71 0.067
226
P LYN001 Lynch Syndrome 69 0.067
227
BRN118 Brain Small Vessel Disease with or Without Ocular Anomalies 42 0.067
228
C3D001 C3 Deficiency 53 0.067
229
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 76 0.067
230
c CHR579 Chiari Malformation Type Ii 38 0.067
231
BNS003 Binswanger's Disease 41 0.067
232
HPT023 Hepatocellular Carcinoma 91 0.066
233
IMM136 Immune System Disease 50 0.066
234
KDS001 Kid Syndrome 53 0.066
235
P PLN008 Peeling Skin Syndrome 47 0.066
236
P HYP027 Hypobetalipoproteinemia 52 0.066
237
P RCK004 Rickets 59 0.066
238
CHL071 Child Syndrome 58 0.066
239
P RTN016 Retinal Degeneration 54 0.066
240
P CRB042 Cerebellar Ataxia 64 0.066
241
CLN019 Colonic Disease 50 0.065
242
HDC001 Headache 54 0.065
243
P HYP117 Hypertriglyceridemia 65 0.065
244
SNS001 Sensorineural Hearing Loss 57 0.065
245
c AMY091 Amyotrophic Lateral Sclerosis 1 78 0.065
246
P GLM045 Glioma 58 0.065
247
PRP016 Paraplegia 49 0.064
248
c HMG001 Hemoglobin C Disease 47 0.064
249
P PRS038 Personality Disorder 61 0.064
250
ALZ029 Alzheimer Disease Mitochondrial 29 0.064
251
INS024 Insulin-Like Growth Factor I 74 0.063
252
HYD057 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 44 0.063
253
ULC004 Ulcerative Colitis 75 0.063
254
CDS001 Cadasil 50 0.063
255
ALL026 Allergic Hypersensitivity Disease 53 0.063
256
CRB004 Cerebral Artery Occlusion 46 0.062
257
P CRV039 Cervicitis 44 0.062
258
BHV002 Behavioral Variant of Frontotemporal Dementia 38 0.062
259
P SLP006 Sleep Apnea 61 0.062
260
HV1006 Hiv-1 82 0.062
261
P MYL006 Myeloid Leukemia 67 0.062
262
ATS009 Autosomal Genetic Disease 39 0.062
263
DFC001 Defective Apolipoprotein B-100 29 0.062
264
MRG013 Mirage Syndrome 26 0.061
265
P TYS001 Tay-Sachs Disease 71 0.061
266
LGP003 Logopenic Progressive Aphasia 22 0.061
267
CRB087 Cerebral Arteriosclerosis 24 0.061
268
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 26 0.061
269
c MTR002 Mitral Valve Insufficiency 44 0.061
270
KHL003 Kohlschutter-Tonz Syndrome 37 0.061
271
c PRK030 Parkinson Disease 4 39 0.061
272
P FML187 Familial Hypertension 41 0.061
273
GST050 Gastrointestinal System Disease 54 0.061
274
FML039 Female Reproductive System Disease 48 0.061
275
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.060
276
P HYP060 Hyperinsulinism 59 0.060
277
P PSR002 Psoriasis 63 0.060
278
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.060
279
ADR007 Adrenoleukodystrophy 71 0.060
280
P MCR010 Microcephaly 58 0.060
281
SBC016 Subacute Delirium 27 0.060
282
P ENC004 Encephalitis 61 0.060
283
P SZR006 Seizure Disorder 57 0.060
284
AND015 Androgen Insensitivity 63 0.059
285
ATP002 Atopy 63 0.059
286
SPN041 Spinal Cord Disease 48 0.059
287
AND005 Androgen Insensitivity Syndrome, Mild 16 0.059
288
P KDN017 Kidney Cancer 67 0.059
289
ART017 Aortic Disease 58 0.059
290
c HRD039 Hereditary Amyloidosis 44 0.059
291
P AGN002 Agnosia 56 0.058
292
P CRN035 Cranial Nerve Palsy 43 0.058
293
TNG002 Tangier Disease 61 0.058
294
CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 43 0.058
295
BRC012 Brucellosis 65 0.058
296
BRN106 Burns 52 0.058
297
SXL003 Sexual Disorder 47 0.058
298
c CRN174 Coronary Heart Disease 2 22 0.058
299
CRD118 Cardiovascular Cancer 47 0.058
300
c CRN177 Coronary Heart Disease 7 22 0.057
301
P MSC003 Muscular Atrophy 51 0.057
302
ADL002 Adult Syndrome 53 0.057
303
DVL001 Developmental Coordination Disorder 37 0.057
304
ATT013 Attention Deficit-Hyperactivity Disorder 68 0.057
305
CRB027 Cerebellar Disease 47 0.057
306
DMN032 Dementia, Familial British 36 0.056
307
CRN031 Cranial Nerve Disease 40 0.056
308
PLM129 Pulmonary Disease, Chronic Obstructive 62 0.056
309
PHN003 Phenylketonuria 73 0.055
310
P MLT019 Multiple Myeloma 80 0.055
311
P NMN002 Niemann-Pick Disease 63 0.055
312
OBS061 Obstructive Sleep Apnea 66 0.055
313
SKN023 Skin Tag 46 0.055
314
P MNN013 Meningitis 65 0.055
315
PRD007 Periodontal Disease 43 0.055
316
OVR063 Overnutrition 49 0.055
317
FCL011 Facial Nerve Disease 38 0.055
318
GNC005 Geniculate Ganglionitis 31 0.055
319
CRT016 Carotid Artery Disease 55 0.055
320
BRN004 Brain Edema 51 0.055
321
VNW001 Von Willebrand's Disease 61 0.054
322
HMT018 Hematopoietic Stem Cell Transplantation 41 0.054
323
DLS001 Delusional Disorder 41 0.054
324
GLC003 Glucose Intolerance 55 0.054
325
P ALC004 Alcohol Abuse 60 0.054
326
AMY002 Amyloid Tumor 37 0.054
327
LNS003 Lens Disease 38 0.053
328
P SPR098 Supranuclear Palsy, Progressive 58 0.053
329
P INF038 Influenza 74 0.053
330
c FML303 Familial/multiple Cancer 16 0.053
331
IRS003 Iris Disease 32 0.053
332
INT074 Intracranial Arteriosclerosis 14 0.053
333
EYC003 Eye Accommodation Disease 26 0.053
334
YNG002 Young Syndrome 26 0.053
335
MDY003 Mody, Type Ii 38 0.052
336
SCR011 Scrapie 39 0.052
337
P NRV006 Nervous System Cancer 62 0.052
338
P THR014 Thrombocytopenia 64 0.052
339
HYP121 Hypoalphalipoproteinemia 61 0.052
340
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 24 0.052
341
PRP030 Purpura 59 0.052
342
CRB008 Cerebral Atherosclerosis 43 0.052
343
P INF032 Infertility 61 0.052
344
DFC004 Deficiency Anemia 65 0.052
345
P ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 60 0.052
346
c HMG004 Hemoglobin D Disease 33 0.052
347
c SCH051 Schizophrenia 4 31 0.052
348
P MTC069 Mitochondrial Disorders 52 0.051
349
P LYM026 Lymphoblastic Leukemia 60 0.051
350
c INF071 Inflammatory Bowel Disease 1 51 0.051
351
OCL011 Ocular Motility Disease 38 0.051
352
PRT011 Protein C Deficiency 51 0.051
353
MTR031 Motor Neuro-Ophthalmic Disorders 23 0.051
354
TMP001 Temporal Lobe Epilepsy 51 0.051
355
P WSK001 Wiskott-Aldrich Syndrome 72 0.050
356
IMP003 Impaired Renal Function Disease 37 0.050
357
HDN002 Head Injury 45 0.050
358
ACT084 Acute Stress Disorder 40 0.050
359
P DRR001 Diarrhea 51 0.050
360
XNT003 Xanthomatosis 47 0.050
361
GLB001 Gilbert Syndrome 61 0.049
362
NSD001 Nose Disease 52 0.049
363
c HMG003 Hemoglobin E Disease 44 0.049
364
P EXN002 Exanthem 57 0.049
365
DYS073 Dysphagia 49 0.049
366
MLR007 Male Reproductive System Disease 37 0.049
367
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.048
368
c ADV003 Advanced Sleep Phase Syndrome, Familial, 1 28 0.048
369
c CNG031 Congenital Nervous System Abnormality 39 0.048
370
P TRC086 Trichohepatoenteric Syndrome 1 46 0.048
371
P MYL005 Myelofibrosis 67 0.048
372
ATM053 Autoimmune Disease 2 19 0.048
373
P ALG002 Alagille Syndrome 72 0.048
374
P SPC019 Specific Language Impairment 29 0.048
375
SBS004 Substance Dependence 50 0.048
376
ADS004 Aids Dementia Complex 39 0.048
377
CRD119 Cardiac Arrest 63 0.047
378
P ATX030 Ataxia-Telangiectasia 76 0.047
379
PST028 Post-Traumatic Stress Disorder 57 0.047
380
ADP007 Adie Pupil 34 0.047
381
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 36 0.047
382
GRF001 Graft-Versus-Host Disease, Protection Against 54 0.047
383
CYS039 Cystic Kidney Disease 52 0.047
384
CRB037 Cerebral Palsy 54 0.047
385
ACT049 Acute Disseminated Encephalomyelitis 49 0.047
386
P CHR084 Chromosomal Disease 37 0.047
387
c GRV009 Graves Disease 2 19 0.047
388
P FML056 Familial Deafness 20 0.047
389
P AMY082 Amyloidosis, Familial Visceral 46 0.047
390
ADM013 Adamantinoma of Long Bones 59 0.046
391
P NRC002 Narcolepsy 62 0.046
392
c GRV008 Graves Disease 1 45 0.046
393
CPL007 Capillary Malformation-Arteriovenous Malformation 41 0.046
394
HMT002 Hematologic Cancer 64 0.046
395
c HPT016 Hepatitis B 64 0.046
396
OBS002 Obsessive-Compulsive Disorder 66 0.046
397
ATM052 Autoimmune Disease 1 28 0.046
398
ANS012 Anus Disease 32 0.046
399
VRL011 Viral Infectious Disease 59 0.046
400
c AST039 Asthma 2 31 0.045
401
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.045
402
MLG108 Malignant Melanoma, Somatic 67 0.045
403
VSC047 Vascular Malformation 45 0.045
404
VTM002 Vitamin B12 Deficiency 44 0.045
405
PLS010 Plasma Protein Metabolism Disease 38 0.045
406
17B002 17-Beta-Hydroxysteroid Dehydrogenase X Deficiency 34 0.045
407
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 41 0.045
408
NSY001 N Syndrome 39 0.045
409
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 23 0.044
410
HML018 Homologous Wasting Disease 17 0.044
411
P ANG001 Angelman Syndrome 61 0.044
412
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 0.044
413
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 56 0.044
414
HYP080 Hypogonadism 54 0.044
415
P IDP010 Idiopathic Generalized Epilepsy 61 0.044
416
ABT001 Abetalipoproteinemia 60 0.044
417
NRL016 Neural Tube Defects 76 0.044
418
P GLL020 Gallbladder Disease 59 0.044
419
P LKN019 Leukoencephalopathy, Diffuse Hereditary, with Spheroids 48 0.044
420
SYN058 Synucleinopathy 39 0.044
421
OCL009 Ocular Cancer 62 0.044
422
c CRN176 Coronary Heart Disease 9 20 0.043
423
HRT007 Heart Cancer 50 0.043
424
c CLR079 Colorectal Cancer 2 31 0.043
425
CRN030 Coronary Stenosis 50 0.043
426
FXF002 Fox-Fordyce Disease 39 0.043
427
LVR012 Liver Cirrhosis 67 0.043
428
STM006 Stomach Disease 50 0.043
429
MYC026 Myoclonus Epilepsy 33 0.043
430
VSC008 Vascular Hemostatic Disease 33 0.042
431
P HRT017 Heart Tumor 35 0.042
432
SYN036 Syncope 47 0.042
433
CRB025 Carbohydrate Metabolic Disorder 47 0.042
434
P HYP614 Hyperlipidemia, Familial Combined 51 0.042
435
P BLD051 Blood Coagulation Disease 45 0.042
436
PPL023 Pupil Disease 23 0.042
437
HNS001 Hansen's Disease 29 0.042
438
RST001 Restless Legs Syndrome 54 0.042
439
FML330 Familial Lcat Deficiency 32 0.042
440
DMY004 Demyelinating Disease 55 0.042
441
c BRN108 Branchiootic Syndrome 1 36 0.042
442
NNL002 Nonalcoholic Steatohepatitis 53 0.042
443
P END044 Endometriosis 53 0.042
444
HRD059 Hereditary Peripheral Nervous Disorder 14 0.041
445
HYP006 Hypertensive Heart Disease 50 0.041
446
FSH001 Fish-Eye Disease 43 0.041
447
VSC006 Vascular Cancer 54 0.041
448
P SDR002 Siderosis 44 0.041
449
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 34 0.041
450
TTR011 Tetraploidy 41 0.041
451
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 47 0.041
452
c HPT003 Hepatitis a 59 0.041
453
VTM003 Vitamin Metabolic Disorder 33 0.041
454
c ADL079 Adult Heart Tumor 19 0.041
455
HDR003 Hidradenitis 46 0.041
456
MNK001 Menkes Disease 61 0.041
457
CYT008 Cytomegalovirus Infection 51 0.041
458
DRG011 Drug Addiction 51 0.041
459
MLR004 Malaria 79 0.041
460
ABL002 Ablepharon-Macrostomia Syndrome 57 0.040
461
PLS009 Plasma Cell Neoplasm 48 0.040
462
PSD029 Pseudocholinesterase Deficiency 40 0.040
463
THY030 Thyroid Gland Disease 51 0.040
464
KR002 Kuru 36 0.040
465
c CNT015 Central Sleep Apnea 44 0.040
466
DGN001 Degenerative Disc Disease 53 0.040
467
ACN011 Acne 63 0.040
468
c ATM007 Autoimmune Disease of Central Nervous System 28 0.040
469
PRD004 Prediabetes Syndrome 43 0.040
470
P MSC007 Muscle Hypertrophy 59 0.040
471
CHL123 Chlamydia 59 0.039
472
SPR066 Superficial Siderosis 33 0.039
473
P SHR029 Short Syndrome 60 0.039
474
P PRM006 Primary Biliary Cirrhosis 52 0.039
475
P HRD018 Hair Disease 50 0.039
476
P FRG001 Fragile X Syndrome 68 0.039
477
P LCT001 Lactic Acidosis 52 0.039
478
P SCK002 Sick Sinus Syndrome 50 0.039
479
ATM012 Autoimmune Disease of Blood 37 0.039
480
P CNJ013 Conjunctivitis 65 0.039
481
CRN024 Corneal Disease 44 0.039
482
MXD023 Mixed Cell Type Cancer 47 0.039
483
P ATX010 Ataxia Neuropathy Spectrum 28 0.039
484
SXD001 Sex Differentiation Disease 40 0.039
485
APH001 Aphthous Stomatitis 62 0.039
486
ATM054 Autoimmune Disease 3 18 0.039
487
FDL002 Food Allergy 54 0.038
488
MNN009 Meningoencephalitis 45 0.038
489
CRB150 Cerebral Creatine Deficiency Syndrome 2 48 0.038
490
CHN016 Cohen Syndrome 55 0.038
491
VSL004 Visual Cortex Disease 29 0.038
492
c AMY009 Amyloidosis Aa 39 0.038
493
WLL001 Williams-Beuren Syndrome 61 0.038
494
P GNR027 Generalized Peeling Skin Syndrome 22 0.038
495
ADR038 Adermatoglyphia 48 0.038
496
HRN022 Hearing Loss/deafness 25 0.038
497
c ATS308 Autosomal Dominant Cerebellar Ataxia 49 0.038
498
ART004 Aortic Atherosclerosis 46 0.038
499
P HYP090 Hyperalphalipoproteinemia 46 0.038
500
P GLB002 Glioblastoma 66 0.037
501
BWN006 Bowen's Disease 31 0.037
502
KRT002 Keratomalacia 54 0.037
503
ART005 Arteriovenous Malformation 65 0.037
504
ACN018 Acne Inversa, Familial, 1 45 0.037
505
HYP085 Hypothalamic Disease 44 0.037
506
P ADV001 Advanced Sleep Phase Syndrome 41 0.037
507
CRD144 Cardiovascular Disease Risk Factor ) 40 0.037
508
P ENC011 Encephalomyopathy 34 0.037
509
BLM001 Bloom Syndrome 62 0.037
510
P ECL001 Eclampsia 54 0.036
511
INT007 Intermediate Coronary Syndrome 52 0.036
512
HYP066 Hyperglycemia 60 0.036
513
P TXP001 Toxoplasmosis 60 0.036
514
c ART101 Aortic Valve Disease 2 55 0.036
515
c MCL042 Macular Degeneration, Age-Related, 1 71 0.036
516
ATM059 Autoimmune Disease 6 26 0.036
517
P MRT001 Muir-Torre Syndrome 58 0.036
518
c SCH064 Schizophrenia 10 22 0.036
519
SRT004 Serotonin Syndrome 49 0.036
520
FRB001 Farber Lipogranulomatosis 51 0.036
521
P GLY010 Glycine Encephalopathy 52 0.036
522
HYP064 Hypogonadotropism 38 0.036
523
c MYC058 Myocardial Infarction 2 29 0.036
524
P CRB059 Cerebellar Degeneration 32 0.036
525
c DLT001 Delta Chain Disease 16 0.036
526
EYD001 Eye Degenerative Disease 31 0.035
527
P SYR001 Syringomyelia 47 0.035
528
BLL006 Bullous Pemphigoid 58 0.035
529
CHR103 Charge Syndrome 64 0.035
530
P MTC004 Mitochondrial Encephalomyopathy 40 0.035
531
MLT001 Multiple Chemical Sensitivity 43 0.035
532
c MJR007 Major Affective Disorder 1 28 0.035
533
P HRP009 Herpes Simplex Encephalitis 46 0.035
534
OLF001 Olfactory Nerve Disease 21 0.035
535
P SPS008 Spastic Ataxia 32 0.035
536
CRR007 Cirrhosis, Cryptogenic 44 0.035
537
CNT017 Central Nervous System Origin Vertigo 28 0.035
538
P CSH001 Cushing's Syndrome 64 0.035
539
OCL006 Ocular Hypertension 48 0.035
540
P RNL015 Renal Hypertension 47 0.035
541
CRV043 Cervical Dystonia 44 0.035
542
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 45 0.035
543
SMT004 Smith-Lemli-Opitz Syndrome 67 0.035
544
c HYP011 Hyperlipoproteinemia Type Iii 41 0.035
545
P AST007 Astrocytoma 65 0.034
546
BNF002 Bone Fracture 47 0.034
547
VSL002 Visual Epilepsy 32 0.034
548
P CMM008 Communicating Hydrocephalus 37 0.034
549
c PLN018 Peeling Skin Syndrome 2 35 0.034
550
IRN001 Iron Deficiency Anemia 51 0.034
551
DYS004 Dyscalculia 28 0.034
552
CRH005 Crohn's Colitis 52 0.034
553
MSS002 Mass Syndrome 59 0.034
554
VSC009 Vascular Skin Disease 22 0.033
555
PRN021 Paranasal Sinus Disease 50 0.033
556
LMY002 Leiomyoma 42 0.033
557
NRM003 Norum Disease 52 0.033
558
CPG001 Capgras Syndrome 22 0.033
559
ALX001 Alexia 45 0.033
560
ATX003 Ataxia with Isolated Vitamin E Deficiency 44 0.033
561
MRK002 Marek Disease 35 0.033
562
VSL003 Visual Agnosia 26 0.033
563
GND003 Gonadal Disease 43 0.033
564
SKN019 Skin Melanoma 62 0.033
565
UND005 Undifferentiated Pleomorphic Sarcoma 43 0.033
566
P STR001 Striatonigral Degeneration 27 0.033
567
ADR012 Adrenal Gland Disease 49 0.032
568
P WVR001 Weaver Syndrome 51 0.032
569
HMS001 Hemosiderosis 45 0.032
570
PRS064 Persistent Vegetative State 31 0.032
571
CHR073 Choreatic Disease 40 0.032
572
P UTR038 Uterine Disease 40 0.032
573
ATR076 Atrophic Muscular Disease 18 0.031
574
c MJR003 Major Affective Disorder 6 18 0.031
575
c ALP005 Alpha Chain Disease 37 0.031
576
KRN002 Kearns-Sayre Syndrome 59 0.031
577
P DWL002 Dowling-Degos Disease 1 51 0.031
578
c PLN021 Peeling Skin Syndrome 3 31 0.031
579
P ACH003 Achromatopsia 53 0.031
580
ALP014 Alpha-Thalassemia/mental Retardation Syndrome 53 0.031
581
BNN003 Bone Inflammation Disease 46 0.031
582
TRN015 Transient Cerebral Ischemia 56 0.031
583
P FTL009 Fetal Akinesia Deformation Sequence 49 0.031
584
CHL014 Cholera 55 0.031
585
P HYP237 Hypercalcemia, Infantile 51 0.031
586
NSL022 Nasal Cavity Disease 42 0.031
587
FNT004 Fainting 33 0.031
588
EMB004 Embryonal Carcinoma 56 0.031
589
VCC001 Vaccinia 46 0.031
590
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.031
591
c PRK007 Parkinson Disease Type 3 22 0.031
592
c PRG001 Progressive Muscular Atrophy 40 0.030
593
c MJR008 Major Affective Disorder 2 22 0.030
594
TRD006 Tardive Dyskinesia 51 0.030
595
GNG011 Gingival Disease 51 0.030
596
ASP007 Aspiration Pneumonia 46 0.030
597
P SPN301 Spinocerebellar Ataxia 2 63 0.030
598
RNL077 Renal Fibrosis 47 0.030
599
P PTT014 Pitt-Hopkins Syndrome 51 0.030
600
ART002 Arts Syndrome 53 0.030
601
P FTL001 Fetal Alcohol Syndrome 53 0.030
602
BCL002 B Cell Deficiency 50 0.030
603
RTN020 Retinal Vascular Disease 50 0.030
604
BHR001 Behr Syndrome 44 0.030
605
CRB040 Cerebrum Cancer 36 0.030
606
HYP081 Hypolipoproteinemia 41 0.030
607
MSL001 Measles 61 0.030
608
P NRX001 Neuroaxonal Dystrophy 39 0.029
609
TSY001 Tau Syndrome 12 0.029
610
PTR006 Peters Anomaly 64 0.029
611
BRD001 Brody Myopathy 49 0.029
612
WRN001 Werner Syndrome 67 0.029
613
GLB015 Glioblastoma Multiforme 62 0.029
614
STT009 Sutton Disease 2 20 0.029
615
CRN246 Cranioosteoarthropathy 31 0.029
616
HPT020 Hepatic Vascular Disease 44 0.029
617
LMB024 Limbic Encephalitis 36 0.029
618
SLP001 Sleeping Sickness 48 0.029
619
ACD004 Acdc 34 0.029
620
c OPT055 Optic Atrophy Plus Syndrome 54 0.028
621
ADL060 Adult Polyglucosan Body Disease 29 0.028
622
BSL005 Basal Ganglia Cerebrovascular Disease 11 0.028
623
PRM236 Primary Biliary Cholangitis 43 0.028
624
NSH001 Nasu-Hakola Disease 45 0.028
625
BRX001 Bruxism 51 0.028
626
CHR321 Chorea and Dementia 19 0.028
627
MTC057 Mitochondrial Recessive Ataxia Syndrome 45 0.028
628
c MJR006 Major Affective Disorder 5 18 0.028
629
PRT037 Pertussis 64 0.028
630
FML304 Familial Isolated Dilated Cardiomyopathy 30 0.028
631
c MYT020 Myotonic Dystrophy 2 55 0.028
632
CLN036 Cln11 Disease 11 0.028
633
MGL016 Megaloblastic Anemia-1, Finnish Type 46 0.028
634
WRT002 Writing Disorder 29 0.028
635
c MJR004 Major Affective Disorder 4 18 0.028
636
P RTH001 Rothmund-Thomson Syndrome 57 0.028
637
PRT038 Protein-Energy Malnutrition 49 0.027
638
DMN016 Dementia, Familial, Nonspecific 23 0.027
639
RTN006 Retinal Drusen 33 0.027
640
c HYP288 Hypercholesterolemia, Due to Ligand-Defective Apo B 36 0.027
641
WGN006 Wegener Granulomatosis 62 0.027
642
P EPS030 Episodic Kinesigenic Dyskinesia 1 27 0.027
643
c SPC015 Specific Language Impairment 4 11 0.027
644
TTN003 Tetanus 61 0.027
645
c ATM093 Autoimmune Disease of Peripheral Nervous System 35 0.027
646
AMS001 Amusia 25 0.027
647
PST055 Postural Hypotension 37 0.027
648
LPD027 Lip Disease 36 0.027
649
c ERL020 Early-Onset Schizophrenia 46 0.026
650
NTR018 Neutrophilia, Hereditary 45 0.026
651
c DYS119 Dystonia 9 37 0.026
652
HMC014 Homocysteinemia 34 0.026
653
P SJG001 Sjogren's Syndrome 53 0.026
654
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 54 0.026
655
CNT018 Central Nervous System Leukemia 39 0.026
656
c BNG076 Benign Exophthalmos Syndrome 14 0.026
657
P PRM016 Primary Optic Atrophy 32 0.026
658
SMT008 Smith-Magenis Syndrome 51 0.026
659
MTC005 Mitochondrial Metabolism Disease 38 0.026
660
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 36 0.026
661
c PRM225 Primary Thrombocytopenia 42 0.026
662
ACR008 Acrocallosal Syndrome 51 0.026
663
P CNT005 Central Nervous System Lymphoma 53 0.026
664
ANX004 Anoxia 44 0.026
665
IMP006 Impulse Control Disorder 40 0.026
666
c SCH061 Schizophrenia 16 18 0.026
667
RTC008 Reticulate Acropigmentation of Kitamura 34 0.026
668
LPP002 Lipoprotein Glomerulopathy 46 0.025
669
P ARC016 Auriculocondylar Syndrome 1 44 0.025
670
FTL021 Fetal Macrosomia 41 0.025
671
DRG016 Drug Induced Dyskinesia 21 0.025
672
FXP001 Foxp2-Related Speech and Language Disorders 15 0.025
673
c PRM039 Primary Angiitis of the Central Nervous System 30 0.025
674
c BLR024 Biliary Cirrhosis, Primary, 1 18 0.025
675
ATH004 Athetosis 25 0.024
676
BRN045 Brunner Syndrome 42 0.024
677
ARC001 Arcus Senilis 35 0.024
678
AMN002 Amino Acid Metabolic Disorder 48 0.024
679
PGM003 Pigmentation Disease 42 0.024
680
TRT001 Teratocarcinoma 36 0.024
681
FRT005 Fruit Allergy 30 0.024
682
MHR001 Mohr-Tranebjaerg Syndrome 40 0.024
683
KDN013 Kidney Hypertrophy 33 0.024
684
PRP028 Peripheral Vertigo 41 0.024
685
PYL017 Pyle Disease 45 0.024
686
NVS001 Neovascular Glaucoma 43 0.024
687
SBL008 Sea-Blue Histiocyte Disease 36 0.024
688
PRX034 Peroxisome Disorders 40 0.024
689
UTR033 Uterine Corpus Cancer 50 0.024
690
PRM008 Parametritis 27 0.024
691
CRB096 Cerebral Amyloid Angiopathy, Dutch, Italian, Iowa, Flemish, Arctic Variants 30 0.023
692
c MLT124 Multiple Sclerosis 5 25 0.023
693
ADL086 Adolescent Idiopathic Scoliosis 29 0.023
694
MLT073 Multisystemic Smooth Muscle Dysfunction Syndrome 37 0.023
695
ECT026 Ectopic Pregnancy 47 0.023
696
FCL044 Fecal Incontinence 35 0.023
697
PRP026 Peripheral Retinal Degeneration 34 0.023
698
STR079 Sturge-Weber Syndrome, Somatic, Mosaic 40 0.023
699
CRC034 Carcinoma Showing Thymus-Like Differentiation 22 0.023
700
GNG004 Ganglioglioma 49 0.023
701
STR026 Star Syndrome 56 0.023
702
VRT003 Vertebrobasilar Insufficiency 39 0.022
703
ALC003 Alcoholic Psychosis 36 0.022
704
XNT009 Xanthoma Disseminatum 33 0.022
705
MTH044 Mthfr Gene Mutation 22 0.022
706
BLL001 Baller-Gerold Syndrome 51 0.022
707
CRB026 Cerebellar Astrocytoma 39 0.022
708
ATY001 Atypical Depressive Disorder 35 0.022
709
PGM005 Pigment Dispersion Syndrome 39 0.022
710
MYF001 Myofibroma 35 0.022
711
FSH003 Fish Allergy 30 0.022
712
PLY039 Polymorphic Reticulosis 19 0.022
713
EXP001 Expressive Language Disorder 29 0.021
714
OPT001 Optic Disk Drusen 28 0.021
715
BKS002 Book Syndrome 19 0.021
716
CD4001 Cd45 Deficiency 35 0.021
717
SCL044 Scalp Syndrome 17 0.021
718
DFF012 Differentiating Neuroblastoma 36 0.021
719
THN007 Thinking Seizures 11 0.021
720
DVL005 Developmental Dyspraxia 21 0.021