Search results for "alzheimer disease familial"

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

736 hits were found for 'alzheimer disease familial'

# Family MCID Name MIFTS Score
1
P ALZ034 Alzheimer Disease 92 11.733
2
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 41 5.837
3
c ALZ036 Alzheimer Disease, Type 3 49 5.657
4
c ERL006 Early-Onset Familial Alzheimer Disease 36 3.079
5
c LTN003 Late-Onset Familial Alzheimer Disease 34 2.923
6
FML202 Familial Alzheimer-Like Prion Disease 5 1.633
7
DMN002 Dementia 62 0.755
8
P ENC018 Encephalopathy 59 0.524
9
TPT001 Tauopathy 51 0.520
10
c CNT035 Central Nervous System Disease 60 0.513
11
P NRV007 Nervous System Disease 71 0.441
12
NRN002 Neuronitis 40 0.417
13
CRB009 Cerebritis 36 0.338
14
DSS008 Disease of Mental Health 48 0.333
15
P AMY004 Amyloidosis 63 0.318
16
PHY002 Physical Disorder 43 0.318
17
VSC002 Vascular Dementia 41 0.283
18
DRG001 Drug Psychosis 39 0.264
19
CND002 Conduct Disorder 54 0.259
20
c ALZ012 Alzheimer Disease 12 19 0.252
21
PSY004 Psychotic Disorder 62 0.248
22
MTH009 Mouth Disease 63 0.204
23
LRN003 Learning Disability 49 0.203
24
c ALZ032 Alzheimer Disease 18 23 0.187
25
P BRS047 Breast Cancer 100 0.185
26
P CRB019 Cerebral Amyloid Angiopathy 56 0.184
27
PRP019 Peripheral Nervous System Disease 52 0.180
28
c HYP163 Hyperlipidemia Type 3 52 0.177
29
DWN001 Down Syndrome 65 0.175
30
c ALZ037 Alzheimer Disease-2 36 0.174
31
END072 Endotheliitis 41 0.169
32
P HRT032 Heart Disease 64 0.169
33
ALR002 Al-Raqad Syndrome 36 0.168
34
PCK002 Pick Disease 66 0.167
35
GLT021 Glutaricaciduria, Type I 47 0.167
36
P SCH015 Schizophrenia 78 0.164
37
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 42 0.164
38
ART111 Artery Disease 56 0.162
39
CRB039 Cerebrovascular Disease 49 0.162
40
P THY032 Thyroiditis 57 0.157
41
P CRN211 Coronary Artery Disease 74 0.156
42
P LTR001 Lateral Sclerosis 50 0.154
43
P OBS005 Obesity 91 0.154
44
MDD011 Mood Disorder 60 0.151
45
ATH003 Atherosclerosis 63 0.150
46
VSC007 Vascular Disease 51 0.149
47
SPS057 Spasticity 41 0.148
48
SPC010 Speech and Communication Disorders 42 0.148
49
ATN002 Autonomic Nervous System Disease 46 0.146
50
RTN023 Retinitis 49 0.144
51
P EPL164 Epilepsy 60 0.143
52
ALN001 Aland Island Eye Disease 45 0.143
53
NTR005 Nutritional Deficiency Disease 51 0.142
54
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 28 0.139
55
SMN008 Semantic Dementia 43 0.137
56
P LKM002 Leukemia 70 0.133
57
P CRT072 Creutzfeldt-Jakob Disease 62 0.133
58
GLC008 Glucose Metabolism Disease 44 0.131
59
P ATX004 Ataxia 53 0.131
60
P CRB088 Cerebral Atrophy 40 0.131
61
P NRB001 Neuroblastoma 70 0.129
62
SLP005 Sleep Disorder 52 0.129
63
APH002 Aphasia 52 0.129
64
P CLR023 Colorectal Cancer 96 0.127
65
P KDN018 Kidney Disease 64 0.126
66
ANS006 Anosognosia 36 0.125
67
c CNG401 Congenital Heart Disease 67 0.124
68
P MYP004 Myopathy 67 0.123
69
BLD054 Blood Protein Disease 38 0.122
70
MNT002 Mental Depression 52 0.122
71
MVM001 Movement Disease 45 0.121
72
END040 Endogenous Depression 51 0.120
73
P HPT021 Hepatitis 74 0.120
74
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.120
75
ANX002 Anxiety Disorder 67 0.120
76
PRN023 Prion Disease 44 0.119
77
ART021 Arteriosclerosis 59 0.116
78
P NRP001 Neuropathy 57 0.116
79
P HYD006 Hydrocephalus 68 0.116
80
SPS019 Spastic Paraparesis 34 0.116
81
P PNC044 Pancreatitis 62 0.114
82
PRS047 Prostatitis 56 0.114
83
P CTR002 Cataract 57 0.114
84
ACD009 Acid-Labile Subunit, Deficiency of 37 0.114
85
MLN008 Melanoma 61 0.113
86
P ART022 Arthritis 73 0.113
87
BRT030 Birth Defects 44 0.113
88
PRP027 Peripheral Vascular Disease 69 0.112
89
ACR041 Acromelic Frontonasal Dysostosis 45 0.111
90
P SPS003 Spastic Diplegia 49 0.110
91
BRN071 Brain Injury 51 0.106
92
ISC004 Ischemia 56 0.105
93
PST086 Posterior Cortical Atrophy 33 0.105
94
PRD011 Proud Syndrome 42 0.104
95
CRB033 Cerebral Degeneration 45 0.104
96
LPD008 Lipid Metabolism Disorder 42 0.104
97
APR001 Apraxia 50 0.104
98
P LVR013 Liver Disease 76 0.103
99
P HYP607 Hypercholesterolemia, Familial 77 0.102
100
P CRT033 Corticobasal Degeneration 44 0.102
101
MLT021 Multiple System Atrophy 71 0.100
102
P PRK057 Parkinson Disease, Late-Onset 72 0.100
103
RSP006 Respiratory System Disease 61 0.100
104
P RHM011 Rheumatoid Arthritis 87 0.098
105
P PRS040 Prostate Cancer 89 0.098
106
TTH006 Tooth Disease 52 0.098
107
CRH001 Crohn's Disease 76 0.098
108
NRM002 Normal Pressure Hydrocephalus 47 0.097
109
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 41 0.097
110
ADR009 Adrenal Cortex Disease 40 0.097
111
EYD002 Eye Disease 62 0.097
112
P MSC005 Muscular Dystrophy 64 0.097
113
LNG099 Lung Disease 63 0.095
114
P TRM003 Tremor 54 0.095
115
P DYS021 Dysautonomia 47 0.094
116
BNS002 Bone Structure Disease 37 0.094
117
P HNT016 Huntington Disease 80 0.093
118
ADJ001 Adjustment Disorder 38 0.092
119
SPC003 Specific Developmental Disorder 39 0.092
120
P GRV001 Graves' Disease 62 0.091
121
P DMN033 Dementia, Frontotemporal 63 0.091
122
P MYC007 Myocardial Infarction 80 0.091
123
P LYM118 Lymphoma 68 0.090
124
c ALZ008 Alzheimer Disease Risk Factor 17 0.090
125
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 59 0.090
126
KHL003 Kohlschutter-Tonz Syndrome 35 0.090
127
GLB003 Globe Disease 34 0.090
128
SPC005 Speech Disorder 41 0.089
129
P AST005 Asthma 80 0.088
130
HYP266 Hypoxia 55 0.088
131
BSL008 Basal Ganglia Disease 40 0.088
132
ADN018 Adenoma 59 0.088
133
CRB031 Cerebral Arterial Disease 31 0.088
134
c PND001 Pain Disorder 53 0.087
135
NWC001 Newcastle Disease 51 0.087
136
P MYS005 Myositis 57 0.086
137
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 55 0.085
138
WTH001 Withdrawal Disorder 36 0.084
139
OPT006 Optic Nerve Disease 47 0.084
140
BRN028 Brain Cancer 69 0.084
141
P FML035 Familial Hyperlipidemia 49 0.084
142
STR067 Stroke, Ischemic 74 0.084
143
c GRN014 Grn-Related Frontotemporal Dementia 36 0.083
144
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 38 0.083
145
CRB085 Cerebral Hemorrhage 40 0.083
146
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 59 0.083
147
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 77 0.083
148
P HMC003 Hemochromatosis 71 0.082
149
SPN041 Spinal Cord Disease 50 0.082
150
P DYS154 Dystonia 62 0.082
151
FST001 Foster-Kennedy Syndrome 31 0.082
152
GNR004 Generalized Anxiety Disorder 49 0.081
153
c INH020 Inherited Metabolic Disorder 49 0.081
154
P OST002 Osteoporosis 63 0.081
155
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 56 0.080
156
RTN018 Retinal Disease 55 0.080
157
c CRN214 Coronary Heart Disease 5 22 0.080
158
P PNM007 Pneumonia 67 0.080
159
BLD053 Blood Platelet Disease 44 0.080
160
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.080
161
LPD004 Lipoid Nephrosis 49 0.080
162
P CRN178 Coronary Heart Disease 6 22 0.079
163
P HRP006 Herpes Simplex 65 0.079
164
AYM001 Ayme-Gripp Syndrome 40 0.079
165
HYP037 Hyperhomocysteinemia 49 0.079
166
CNG034 Congestive Heart Failure 72 0.079
167
HMZ003 Homozygous Familial Hypercholesterolemia 43 0.079
168
SKN016 Skin Disease 69 0.077
169
CHR008 Choroiditis 43 0.077
170
KWS002 Kawasaki Disease 70 0.077
171
INC002 Inclusion Body Myositis 64 0.077
172
DMN031 Dementia, Lewy Body 58 0.077
173
c ESS001 Essential Tremor 58 0.077
174
P AMY084 Amyloidosis, Finnish Type 45 0.077
175
P LKD001 Leukodystrophy 58 0.076
176
TRM010 Traumatic Brain Injury 52 0.076
177
MYC033 Myoclonus 41 0.076
178
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.076
179
MTR014 Motor Neuron Disease 57 0.076
180
EXF001 Exfoliation Syndrome 56 0.076
181
ETH011 Ethylmalonic Encephalopathy 57 0.076
182
P MSC033 Muscle Disorders 52 0.076
183
MSC004 Muscle Tissue Disease 35 0.076
184
RDN001 Reading Disorder 39 0.075
185
WLS001 Wilson Disease 72 0.075
186
c TRC078 Trichohepatoenteric Syndrome 2 30 0.075
187
ACT049 Acute Disseminated Encephalomyelitis 50 0.074
188
P HYP086 Hypothyroidism 63 0.074
189
P HYP071 Hypersensitivity Reaction Type Ii Disease 46 0.074
190
WLL006 Wells Syndrome 57 0.074
191
P HYP004 Hypercalcemia 54 0.073
192
FRN030 Frontotemporal Dementia with Parkinsonism-17 30 0.073
193
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 35 0.073
194
c HYP595 Hypertension, Essential 69 0.073
195
P HYP117 Hypertriglyceridemia 65 0.073
196
CNT098 Central Core Disease 68 0.072
197
P CLC005 Celiac Disease 67 0.072
198
P HYP027 Hypobetalipoproteinemia 52 0.072
199
BRN080 Brain Ischemia 42 0.071
200
P PRD008 Periodontitis 46 0.071
201
FML026 Familial Lipoprotein Lipase Deficiency 51 0.071
202
c CRN172 Coronary Heart Disease 3 19 0.071
203
P ALX003 Alexander Disease 64 0.071
204
P PSR002 Psoriasis 63 0.071
205
P MTC003 Metachromatic Leukodystrophy 71 0.071
206
P INT063 Intellectual Disability 46 0.071
207
ADT003 Auditory System Disease 49 0.070
208
CLT003 Colitis 56 0.070
209
ATS008 Autosomal Dominant Disease 41 0.070
210
P OPN001 Open-Angle Glaucoma 47 0.070
211
BNS003 Binswanger's Disease 30 0.070
212
OBS015 Obesity, Hyperphagia, and Developmental Delay 35 0.070
213
INC022 Inclusion-Cell Disease 46 0.069
214
HDC001 Headache 52 0.069
215
RPR002 Reproductive System Disease 45 0.069
216
NRM005 Neuromuscular Disease 56 0.069
217
HPT074 Hepatic Adenoma, Somatic 35 0.069
218
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.069
219
MYC002 Mycobacterium Avium Complex Disease 52 0.069
220
C3D001 C3 Deficiency 50 0.068
221
P RTN016 Retinal Degeneration 50 0.068
222
P GT001 Gout 58 0.068
223
CTS003 Coats Disease 57 0.068
224
VND001 Vein Disease 51 0.068
225
c ALZ035 Alzheimer Disease-4 35 0.068
226
PRP080 Peripheral Artery Disease 35 0.068
227
CDS001 Cadasil 50 0.068
228
P LYN001 Lynch Syndrome 69 0.068
229
GDS001 Good Syndrome 46 0.068
230
DFC001 Defective Apolipoprotein B-100 29 0.068
231
ATN005 Autonomic Dysfunction 44 0.068
232
P PRP029 Porphyria 56 0.067
233
FTT001 Fatty Liver Disease 60 0.067
234
ETN001 Eating Disorder 59 0.067
235
CNV002 Conversion Disorder 45 0.067
236
LKC003 Leukocyte Disease 45 0.067
237
P BPL003 Bipolar Disorder 58 0.067
238
CSY001 C Syndrome 49 0.067
239
ALZ029 Alzheimer Disease Mitochondrial 25 0.067
240
P INF038 Influenza 71 0.066
241
HPT023 Hepatocellular Carcinoma 90 0.066
242
DRG003 Drug Dependence 53 0.066
243
P RCK004 Rickets 59 0.066
244
P CRB042 Cerebellar Ataxia 64 0.066
245
c CHR579 Chiari Malformation Type Ii 38 0.066
246
BHV002 Behavioral Variant of Frontotemporal Dementia 37 0.066
247
CLN019 Colonic Disease 50 0.065
248
P GLM045 Glioma 53 0.065
249
OTP003 Oto-Palatal-Digital Syndrome 14 0.065
250
P NRV006 Nervous System Cancer 62 0.065
251
CHL071 Child Syndrome 58 0.065
252
KDS001 Kid Syndrome 53 0.065
253
PRP016 Paraplegia 49 0.065
254
TNG002 Tangier Disease 61 0.065
255
ULC004 Ulcerative Colitis 74 0.064
256
P PLN008 Peeling Skin Syndrome 45 0.064
257
P MCR010 Microcephaly 60 0.064
258
INS024 Insulin-Like Growth Factor I 75 0.064
259
CYS001 Cystic Fibrosis 87 0.064
260
BRN118 Brain Small Vessel Disease with or Without Ocular Anomalies 42 0.064
261
P CRV039 Cervicitis 45 0.063
262
LPP001 Lipoprotein Lipase Deficiency 63 0.063
263
P SLP006 Sleep Apnea 60 0.063
264
VNW007 Von Willebrand Disease 57 0.063
265
ADL002 Adult Syndrome 53 0.063
266
AND015 Androgen Insensitivity 64 0.062
267
c MTR002 Mitral Valve Insufficiency 42 0.062
268
LGP003 Logopenic Progressive Aphasia 21 0.062
269
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.062
270
P ENC004 Encephalitis 60 0.062
271
CRB004 Cerebral Artery Occlusion 39 0.062
272
P MYL007 Myeloma 52 0.061
273
BRC012 Brucellosis 66 0.061
274
P SZR006 Seizure Disorder 56 0.061
275
P MYL006 Myeloid Leukemia 67 0.061
276
ATS009 Autosomal Genetic Disease 38 0.061
277
BRN106 Burns 52 0.061
278
CRT016 Carotid Artery Disease 54 0.061
279
c PRK031 Parkinson Disease 1 54 0.061
280
CRB087 Cerebral Arteriosclerosis 23 0.061
281
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.060
282
P FML187 Familial Hypertension 35 0.060
283
P TYS001 Tay-Sachs Disease 72 0.060
284
P PRS038 Personality Disorder 60 0.060
285
HYP121 Hypoalphalipoproteinemia 61 0.060
286
P PRP003 Porphyria Cutanea Tarda 63 0.060
287
AMY002 Amyloid Tumor 37 0.060
288
c JVN024 Juvenile Hereditary Hemochromatosis 30 0.060
289
FML039 Female Reproductive System Disease 49 0.060
290
P ALC004 Alcohol Abuse 57 0.060
291
c HRD039 Hereditary Amyloidosis 43 0.059
292
ATP002 Atopy 62 0.059
293
ART017 Aortic Disease 57 0.059
294
CRB008 Cerebral Atherosclerosis 37 0.059
295
P KDN017 Kidney Cancer 67 0.059
296
HV1006 Hiv-1 80 0.059
297
c AMY091 Amyotrophic Lateral Sclerosis 1 78 0.058
298
P AGN002 Agnosia 56 0.058
299
SBC016 Subacute Delirium 23 0.058
300
c MCL042 Macular Degeneration, Age-Related, 1 71 0.058
301
P MNN013 Meningitis 66 0.058
302
SXL003 Sexual Disorder 45 0.057
303
P MSC003 Muscular Atrophy 51 0.057
304
CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 42 0.057
305
P END044 Endometriosis 53 0.057
306
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 34 0.057
307
PLM129 Pulmonary Disease, Chronic Obstructive 61 0.057
308
GLC003 Glucose Intolerance 56 0.057
309
ATT013 Attention Deficit-Hyperactivity Disorder 69 0.057
310
c CRN173 Coronary Heart Disease 8 19 0.057
311
FCL011 Facial Nerve Disease 37 0.056
312
OBS061 Obstructive Sleep Apnea 61 0.056
313
DMN032 Dementia, Familial British 36 0.056
314
GNC005 Geniculate Ganglionitis 27 0.056
315
CRB027 Cerebellar Disease 46 0.056
316
P HYP060 Hyperinsulinism 58 0.056
317
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 27 0.056
318
SNS001 Sensorineural Hearing Loss 52 0.056
319
XNT003 Xanthomatosis 45 0.056
320
DVL001 Developmental Coordination Disorder 36 0.056
321
P NMN002 Niemann-Pick Disease 63 0.056
322
P CRN035 Cranial Nerve Palsy 44 0.056
323
HMT018 Hematopoietic Stem Cell Transplantation 39 0.056
324
c MLT019 Multiple Myeloma 77 0.055
325
BRN004 Brain Edema 51 0.055
326
PRP030 Purpura 60 0.055
327
ALL026 Allergic Hypersensitivity Disease 53 0.054
328
DLS001 Delusional Disorder 40 0.054
329
ADR007 Adrenoleukodystrophy 74 0.054
330
P THR014 Thrombocytopenia 63 0.054
331
c CRN175 Coronary Heart Disease 4 19 0.054
332
P SPR098 Supranuclear Palsy, Progressive 57 0.054
333
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 42 0.054
334
P AMY082 Amyloidosis, Familial Visceral 45 0.054
335
OVR063 Overnutrition 49 0.054
336
c PRK030 Parkinson Disease 4 38 0.053
337
PRD007 Periodontal Disease 42 0.053
338
OLV001 Olivopontocerebellar Atrophy 53 0.053
339
c INF071 Inflammatory Bowel Disease 1 51 0.053
340
SCR011 Scrapie 34 0.053
341
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 21 0.053
342
PRT011 Protein C Deficiency 52 0.053
343
LNS003 Lens Disease 37 0.053
344
CRN031 Cranial Nerve Disease 39 0.052
345
P INF032 Infertility 61 0.052
346
c FML303 Familial/multiple Cancer 15 0.052
347
INT074 Intracranial Arteriosclerosis 14 0.052
348
YNG002 Young Syndrome 25 0.052
349
ABT001 Abetalipoproteinemia 60 0.052
350
EYC003 Eye Accommodation Disease 25 0.052
351
SKN023 Skin Tag 48 0.052
352
NRL016 Neural Tube Defects 76 0.051
353
DFC004 Deficiency Anemia 64 0.051
354
MDY003 Mody, Type Ii 36 0.051
355
P ALG002 Alagille Syndrome 70 0.051
356
P MTC069 Mitochondrial Disorders 51 0.051
357
DYS073 Dysphagia 51 0.051
358
P NRC002 Narcolepsy 62 0.051
359
P GLL020 Gallbladder Disease 59 0.051
360
PHN003 Phenylketonuria 71 0.051
361
MLR007 Male Reproductive System Disease 36 0.051
362
IMP003 Impaired Renal Function Disease 36 0.051
363
P LYM026 Lymphoblastic Leukemia 60 0.050
364
HDN002 Head Injury 47 0.050
365
c SCH051 Schizophrenia 4 36 0.050
366
TMP001 Temporal Lobe Epilepsy 47 0.050
367
ADS004 Aids Dementia Complex 47 0.050
368
VTM002 Vitamin B12 Deficiency 45 0.050
369
P AML002 Amelogenesis Imperfecta 43 0.050
370
HMT002 Hematologic Cancer 62 0.050
371
P DRR001 Diarrhea 60 0.050
372
P EXN002 Exanthem 57 0.050
373
IRS003 Iris Disease 32 0.049
374
c CRN177 Coronary Heart Disease 7 21 0.049
375
SYN036 Syncope 45 0.049
376
P HYP614 Hyperlipidemia, Familial Combined 50 0.049
377
NSD001 Nose Disease 51 0.049
378
P WSK001 Wiskott-Aldrich Syndrome 70 0.048
379
SYN058 Synucleinopathy 38 0.048
380
LYM019 Lymphosarcoma 52 0.048
381
c CNG031 Congenital Nervous System Abnormality 39 0.048
382
P FTL009 Fetal Akinesia Deformation Sequence 51 0.048
383
CYS039 Cystic Kidney Disease 49 0.048
384
c BLD124 Bleeding Disorder, Platelet-Type, 11 37 0.048
385
OCL011 Ocular Motility Disease 41 0.048
386
CRD119 Cardiac Arrest 63 0.048
387
VRL011 Viral Infectious Disease 56 0.048
388
GRF001 Graft-Versus-Host Disease, Protection Against 54 0.047
389
ATM053 Autoimmune Disease 2 16 0.047
390
MTR031 Motor Neuro-Ophthalmic Disorders 22 0.047
391
ACT084 Acute Stress Disorder 38 0.047
392
P SPC019 Specific Language Impairment 27 0.047
393
c ART101 Aortic Valve Disease 2 56 0.047
394
FSH001 Fish-Eye Disease 44 0.047
395
P MYL005 Myelofibrosis 67 0.047
396
SBS004 Substance Dependence 48 0.046
397
CRT078 Corticobasal Syndrome 36 0.046
398
P ATX030 Ataxia-Telangiectasia 78 0.046
399
OBS002 Obsessive-Compulsive Disorder 66 0.046
400
CYT008 Cytomegalovirus Infection 51 0.046
401
GTL001 Gitelman Syndrome 60 0.046
402
CRB037 Cerebral Palsy 54 0.046
403
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 35 0.046
404
P CHR084 Chromosomal Disease 37 0.046
405
ATM052 Autoimmune Disease 1 26 0.046
406
c HPT016 Hepatitis B 61 0.045
407
ADM013 Adamantinoma of Long Bones 57 0.045
408
c ADL001 Adult Lymphoma 40 0.045
409
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.045
410
P SDR002 Siderosis 44 0.045
411
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 0.045
412
c HMG001 Hemoglobin C Disease 46 0.045
413
P IDP010 Idiopathic Generalized Epilepsy 61 0.045
414
P DWL001 Dowling-Degos Disease 41 0.045
415
VSC047 Vascular Malformation 45 0.045
416
GLB001 Gilbert Syndrome 59 0.045
417
c AST039 Asthma 2 28 0.045
418
PLS010 Plasma Protein Metabolism Disease 37 0.045
419
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 60 0.045
420
PST028 Post-Traumatic Stress Disorder 55 0.044
421
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 40 0.044
422
WLL001 Williams-Beuren Syndrome 61 0.044
423
HYP080 Hypogonadism 54 0.044
424
TTR011 Tetraploidy 41 0.044
425
17B002 17-Beta-Hydroxysteroid Dehydrogenase X Deficiency 32 0.044
426
NSY001 N Syndrome 42 0.044
427
P MYC026 Myoclonus Epilepsy 33 0.044
428
P HYP090 Hyperalphalipoproteinemia 45 0.044
429
CRD144 Cardiovascular Disease Risk Factor ) 42 0.044
430
DMY004 Demyelinating Disease 52 0.044
431
P BLD051 Blood Coagulation Disease 44 0.043
432
LVR012 Liver Cirrhosis 71 0.043
433
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.043
434
P MRT001 Muir-Torre Syndrome 59 0.043
435
THY030 Thyroid Gland Disease 52 0.043
436
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 21 0.043
437
HML018 Homologous Wasting Disease 14 0.043
438
BRN018 Borna Disease 43 0.043
439
c ADV003 Advanced Sleep Phase Syndrome, Familial, 1 25 0.043
440
OCL009 Ocular Cancer 61 0.043
441
P CNJ013 Conjunctivitis 65 0.043
442
STM006 Stomach Disease 48 0.043
443
SPR066 Superficial Siderosis 33 0.043
444
MLR004 Malaria 80 0.043
445
P FML056 Familial Deafness 18 0.043
446
HRT007 Heart Cancer 51 0.043
447
c GRV009 Graves Disease 2 18 0.043
448
MVD001 Moved to 60 0.043
449
ART004 Aortic Atherosclerosis 46 0.043
450
c MTB001 Metabolic Syndrome X 61 0.042
451
HDR002 Hidradenitis Suppurativa 53 0.042
452
HYP006 Hypertensive Heart Disease 49 0.042
453
c CLR079 Colorectal Cancer 2 29 0.042
454
CHL123 Chlamydia 60 0.042
455
PSD029 Pseudocholinesterase Deficiency 40 0.042
456
HDR003 Hidradenitis 46 0.042
457
P HRT017 Heart Tumor 34 0.042
458
RST001 Restless Legs Syndrome 51 0.042
459
c HPT003 Hepatitis a 55 0.042
460
BLM001 Bloom Syndrome 63 0.042
461
HNS001 Hansen's Disease 30 0.042
462
P IGN003 Iga Nephropathy 1 31 0.042
463
c BNG076 Benign Exophthalmos Syndrome 15 0.042
464
P THY023 Thymoma 57 0.042
465
PPL023 Pupil Disease 22 0.042
466
VSC008 Vascular Hemostatic Disease 30 0.041
467
c GRV008 Graves Disease 1 44 0.041
468
ANS012 Anus Disease 32 0.041
469
MXD023 Mixed Cell Type Cancer 45 0.041
470
ACN011 Acne 63 0.041
471
KR002 Kuru 34 0.041
472
VSL002 Visual Epilepsy 30 0.041
473
P LKN019 Leukoencephalopathy, Diffuse Hereditary, with Spheroids 38 0.041
474
P TRC086 Trichohepatoenteric Syndrome 1 46 0.041
475
c HYP011 Hyperlipoproteinemia Type Iii 34 0.041
476
P PRM001 Primary Cutaneous Amyloidosis 54 0.041
477
APH001 Aphthous Stomatitis 62 0.041
478
PLS009 Plasma Cell Neoplasm 47 0.040
479
ATM012 Autoimmune Disease of Blood 36 0.040
480
VTM003 Vitamin Metabolic Disorder 31 0.040
481
VHW001 Vohwinkel Syndrome 47 0.040
482
c ADL079 Adult Heart Tumor 17 0.040
483
DRG011 Drug Addiction 55 0.040
484
HRD059 Hereditary Peripheral Nervous Disorder 12 0.040
485
P SHR029 Short Syndrome 60 0.040
486
VSC006 Vascular Cancer 51 0.040
487
HYP081 Hypolipoproteinemia 42 0.040
488
c MYT020 Myotonic Dystrophy 2 56 0.040
489
MNK001 Menkes Disease 61 0.040
490
c MCP003 Mucopolysaccharidosis Vii 62 0.040
491
NRM003 Norum Disease 53 0.040
492
P LCT001 Lactic Acidosis 52 0.040
493
P SCK002 Sick Sinus Syndrome 49 0.040
494
P PRM006 Primary Biliary Cirrhosis 55 0.040
495
FDL002 Food Allergy 56 0.040
496
c CNT015 Central Sleep Apnea 43 0.039
497
c ATM007 Autoimmune Disease of Central Nervous System 29 0.039
498
P FRG001 Fragile X Syndrome 68 0.039
499
SXD001 Sex Differentiation Disease 39 0.039
500
P MSC007 Muscle Hypertrophy 55 0.039
501
DGN001 Degenerative Disc Disease 53 0.039
502
P HRP009 Herpes Simplex Encephalitis 46 0.039
503
HYP066 Hyperglycemia 61 0.039
504
KRT002 Keratomalacia 50 0.039
505
ABL002 Ablepharon-Macrostomia Syndrome 51 0.039
506
P HRD018 Hair Disease 48 0.039
507
ART005 Arteriovenous Malformation 63 0.039
508
P TXP001 Toxoplasmosis 61 0.039
509
SMT004 Smith-Lemli-Opitz Syndrome 66 0.039
510
c BRN108 Branchiootic Syndrome 1 36 0.039
511
OLF001 Olfactory Nerve Disease 20 0.039
512
ATM054 Autoimmune Disease 3 16 0.039
513
c HMG004 Hemoglobin D Disease 32 0.038
514
CRN024 Corneal Disease 45 0.038
515
P ECL001 Eclampsia 55 0.038
516
VSL004 Visual Cortex Disease 28 0.038
517
P FTL001 Fetal Alcohol Syndrome 53 0.038
518
P ADV001 Advanced Sleep Phase Syndrome 42 0.038
519
CRB150 Cerebral Creatine Deficiency Syndrome 2 47 0.038
520
MNN009 Meningoencephalitis 42 0.038
521
BLL006 Bullous Pemphigoid 59 0.038
522
c CRN176 Coronary Heart Disease 9 19 0.038
523
FXF002 Fox-Fordyce Disease 37 0.038
524
c ATS308 Autosomal Dominant Cerebellar Ataxia 51 0.037
525
c PRC016 Pre-Eclampsia 57 0.037
526
CHN016 Cohen Syndrome 55 0.037
527
P GNR027 Generalized Peeling Skin Syndrome 21 0.037
528
P GLB002 Glioblastoma 65 0.037
529
CNT017 Central Nervous System Origin Vertigo 27 0.037
530
CRN246 Cranioosteoarthropathy 32 0.037
531
INT007 Intermediate Coronary Syndrome 52 0.037
532
P ENC011 Encephalomyopathy 35 0.037
533
HYP085 Hypothalamic Disease 43 0.037
534
P SYR001 Syringomyelia 44 0.036
535
PRS064 Persistent Vegetative State 27 0.036
536
PRP032 Porphyria Variegata 51 0.036
537
P ACR001 Aicardi-Goutieres Syndrome 54 0.036
538
P CSH001 Cushing's Syndrome 65 0.036
539
P CRB059 Cerebellar Degeneration 30 0.036
540
P PTT014 Pitt-Hopkins Syndrome 51 0.036
541
ATM059 Autoimmune Disease 6 23 0.036
542
OCL006 Ocular Hypertension 47 0.036
543
P RNL015 Renal Hypertension 47 0.036
544
CRH005 Crohn's Colitis 50 0.036
545
FXP001 Foxp2-Related Speech and Language Disorders 15 0.036
546
HYP064 Hypogonadotropism 38 0.036
547
HTC002 Hutchinson-Gilford Progeria 51 0.036
548
P AST007 Astrocytoma 66 0.036
549
P NJM001 Nijmegen Breakage Syndrome 68 0.035
550
CRV043 Cervical Dystonia 43 0.035
551
EYD001 Eye Degenerative Disease 31 0.035
552
c MYC058 Myocardial Infarction 2 28 0.035
553
P MTC004 Mitochondrial Encephalomyopathy 39 0.035
554
WRN001 Werner Syndrome 69 0.035
555
c DLT001 Delta Chain Disease 14 0.035
556
FRB001 Farber Lipogranulomatosis 54 0.035
557
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.035
558
P CMM008 Communicating Hydrocephalus 31 0.035
559
ALX001 Alexia 42 0.035
560
CHR073 Choreatic Disease 39 0.035
561
P GLY010 Glycine Encephalopathy 53 0.035
562
LMY002 Leiomyoma 56 0.035
563
c MJR007 Major Affective Disorder 1 27 0.035
564
c SCH064 Schizophrenia 10 21 0.035
565
VSL003 Visual Agnosia 27 0.035
566
MLT001 Multiple Chemical Sensitivity 43 0.035
567
c HYP288 Hypercholesterolemia, Due to Ligand-Defective Apo B 37 0.035
568
P SPS008 Spastic Ataxia 31 0.035
569
FNT004 Fainting 33 0.034
570
FML304 Familial Isolated Dilated Cardiomyopathy 30 0.034
571
SRT004 Serotonin Syndrome 47 0.034
572
ALP014 Alpha-Thalassemia/mental Retardation Syndrome 54 0.034
573
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 37 0.034
574
BNF002 Bone Fracture 46 0.034
575
PRD004 Prediabetes Syndrome 40 0.034
576
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 35 0.034
577
IRN001 Iron Deficiency Anemia 51 0.034
578
ACN018 Acne Inversa, Familial, 1 17 0.034
579
P STR001 Striatonigral Degeneration 32 0.034
580
PRN021 Paranasal Sinus Disease 50 0.034
581
ARC001 Arcus Senilis 36 0.034
582
CHR103 Charge Syndrome 64 0.033
583
DYS004 Dyscalculia 24 0.033
584
ACR008 Acrocallosal Syndrome 51 0.033
585
c PLN018 Peeling Skin Syndrome 2 36 0.033
586
VSC009 Vascular Skin Disease 21 0.033
587
BNN003 Bone Inflammation Disease 46 0.033
588
SKN019 Skin Melanoma 61 0.033
589
LPP002 Lipoprotein Glomerulopathy 46 0.033
590
MRK002 Marek Disease 35 0.033
591
FTL021 Fetal Macrosomia 38 0.033
592
HRN022 Hearing Loss/deafness 23 0.033
593
P RTH001 Rothmund-Thomson Syndrome 56 0.033
594
HPT019 Hepatic Encephalopathy 58 0.033
595
CPG001 Capgras Syndrome 23 0.033
596
CHL050 Cholesterol Ester Storage Disease 39 0.033
597
HMS001 Hemosiderosis 42 0.033
598
GND003 Gonadal Disease 41 0.032
599
SMT008 Smith-Magenis Syndrome 49 0.032
600
P WVR001 Weaver Syndrome 54 0.032
601
RNL077 Renal Fibrosis 48 0.032
602
P ARC016 Auriculocondylar Syndrome 1 44 0.032
603
ADR012 Adrenal Gland Disease 49 0.032
604
ASP007 Aspiration Pneumonia 46 0.032
605
AND005 Androgen Insensitivity Syndrome, Mild 14 0.032
606
c FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 28 0.032
607
c PRG011 Progressive Myoclonus Epilepsy 41 0.032
608
c ALP005 Alpha Chain Disease 36 0.032
609
STR079 Sturge-Weber Syndrome, Somatic, Mosaic 39 0.032
610
RTC008 Reticulate Acropigmentation of Kitamura 36 0.032
611
KRN002 Kearns-Sayre Syndrome 60 0.032
612
NSL022 Nasal Cavity Disease 41 0.032
613
GNG011 Gingival Disease 50 0.032
614
TTN003 Tetanus 62 0.032
615
HPT020 Hepatic Vascular Disease 43 0.032
616
MHR001 Mohr-Tranebjaerg Syndrome 43 0.032
617
BCL002 B Cell Deficiency 50 0.031
618
P UTR038 Uterine Disease 38 0.031
619
ESN015 Eosinophilic Fasciitis 46 0.031
620
ATX003 Ataxia with Isolated Vitamin E Deficiency 36 0.031
621
c MJR003 Major Affective Disorder 6 17 0.031
622
IRR002 Irritable Bowel Syndrome 58 0.031
623
PGM003 Pigmentation Disease 34 0.031
624
CHL014 Cholera 56 0.031
625
BHR001 Behr Syndrome 43 0.031
626
P ACH003 Achromatopsia 48 0.031
627
UND005 Undifferentiated Pleomorphic Sarcoma 39 0.031
628
STR026 Star Syndrome 57 0.031
629
PRT055 Prieto X-Linked Mental Retardation Syndrome 24 0.031
630
TRN015 Transient Cerebral Ischemia 57 0.031
631
VCC001 Vaccinia 46 0.031
632
c HMG003 Hemoglobin E Disease 44 0.031
633
TRD006 Tardive Dyskinesia 51 0.031
634
c PRK007 Parkinson Disease Type 3 21 0.031
635
c PRG001 Progressive Muscular Atrophy 39 0.031
636
c PLN021 Peeling Skin Syndrome 3 30 0.030
637
GLB015 Glioblastoma Multiforme 63 0.030
638
ADL086 Adolescent Idiopathic Scoliosis 36 0.030
639
MSL001 Measles 61 0.030
640
c AMY009 Amyloidosis Aa 27 0.030
641
RTN020 Retinal Vascular Disease 49 0.030
642
PLY039 Polymorphic Reticulosis 20 0.030
643
c MJR008 Major Affective Disorder 2 19 0.030
644
PRT038 Protein-Energy Malnutrition 48 0.030
645
MSS002 Mass Syndrome 49 0.030
646
EMB004 Embryonal Carcinoma 55 0.030
647
ART002 Arts Syndrome 53 0.030
648
CYT018 Cytochrome P450 2d6 Variant 19 0.030
649
SLP001 Sleeping Sickness 48 0.030
650
c ATX006 Ataxia-Telangiectasia-Like Disorder 52 0.030
651
APL003 Apolipoprotein a-Ii Deficiency 13 0.030
652
DSS024 Disease of Anatomical Entity 40 0.030
653
CRB040 Cerebrum Cancer 36 0.030
654
BRD001 Brody Myopathy 49 0.030
655
P NRX001 Neuroaxonal Dystrophy 32 0.029
656
MDY005 Mody, Type I 31 0.029
657
PTR006 Peters Anomaly 64 0.029
658
STT009 Sutton Disease 2 21 0.029
659
P SJG001 Sjogren's Syndrome 55 0.029
660
TSY001 Tau Syndrome 11 0.029
661
XNT009 Xanthoma Disseminatum 34 0.029
662
PRT037 Pertussis 63 0.029
663
ADL060 Adult Polyglucosan Body Disease 30 0.029
664
BWN002 Bowen Syndrome 22 0.028
665
ACD004 Acdc 35 0.028
666
P SPN301 Spinocerebellar Ataxia 2 57 0.028
667
BLL001 Baller-Gerold Syndrome 52 0.028
668
LMB024 Limbic Encephalitis 35 0.028
669
NSH001 Nasu-Hakola Disease 46 0.028
670
BSL005 Basal Ganglia Cerebrovascular Disease 10 0.028
671
c OPT055 Optic Atrophy Plus Syndrome 55 0.028
672
c PRM225 Primary Thrombocytopenia 42 0.028
673
CHR321 Chorea and Dementia 17 0.028
674
DMN016 Dementia, Familial, Nonspecific 28 0.028
675
P ATX010 Ataxia Neuropathy Spectrum 24 0.028
676
PST055 Postural Hypotension 36 0.028
677
c MJR006 Major Affective Disorder 5 17 0.028
678
PRM236 Primary Biliary Cholangitis 23 0.028
679
RTN006 Retinal Drusen 33 0.028
680
BRB001 Beriberi 40 0.028
681
CLN036 Cln11 Disease 11 0.027
682
BRX001 Bruxism 45 0.027
683
HMC014 Homocysteinemia 32 0.027
684
c MJR004 Major Affective Disorder 4 19 0.027
685
c ERL020 Early-Onset Schizophrenia 44 0.027
686
PRP028 Peripheral Vertigo 42 0.027
687
c SPC015 Specific Language Impairment 4 10 0.027
688
MTC057 Mitochondrial Recessive Ataxia Syndrome 48 0.026
689
AMS001 Amusia 24 0.026
690
CRR007 Cirrhosis, Cryptogenic 38 0.026
691
P CNT005 Central Nervous System Lymphoma 51 0.026
692
LPD027 Lip Disease 35 0.026
693
UTR039 Uterine Fibroid 55 0.026
694
AMN002 Amino Acid Metabolic Disorder 48 0.026
695
UTR033 Uterine Corpus Cancer 50 0.026
696
ANX004 Anoxia 45 0.026
697
CNT018 Central Nervous System Leukemia 38 0.026
698
MTC005 Mitochondrial Metabolism Disease 37 0.026
699
KDN013 Kidney Hypertrophy 32 0.026
700
CRB096 Cerebral Amyloid Angiopathy, Dutch, Italian, Iowa, Flemish, Arctic Variants 32 0.025
701
c SCH061 Schizophrenia 16 17 0.025
702
IMP006 Impulse Control Disorder 40 0.025
703
P PRM016 Primary Optic Atrophy 29 0.025
704
c DYS119 Dystonia 9 39 0.025
705
DRG016 Drug Induced Dyskinesia 19 0.025
706
c BLR024 Biliary Cirrhosis, Primary, 1 17 0.024
707
c PRM039 Primary Angiitis of the Central Nervous System 30 0.024
708
ATH004 Athetosis 25 0.024
709
NVS001 Neovascular Glaucoma 38 0.024
710
TRT001 Teratocarcinoma 35 0.024
711
VRT003 Vertebrobasilar Insufficiency 38 0.024
712
PRM008 Parametritis 28 0.024
713
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 54 0.024
714
PYL017 Pyle Disease 45 0.024
715
MYF001 Myofibroma 34 0.023
716
PRX034 Peroxisome Disorders 24 0.023
717
EXP001 Expressive Language Disorder 28 0.023
718
c MLT124 Multiple Sclerosis 5 24 0.023
719
PRP026 Peripheral Retinal Degeneration 33 0.023
720
MLT073 Multisystemic Smooth Muscle Dysfunction Syndrome 36 0.023
721
GNG004 Ganglioglioma 46 0.023
722
FCL044 Fecal Incontinence 34 0.023
723
ALC003 Alcoholic Psychosis 35 0.023
724
CD4001 Cd45 Deficiency 35 0.023
725
ECT026 Ectopic Pregnancy 46 0.023
726
CRC034 Carcinoma Showing Thymus-Like Differentiation 21 0.023
727
OPT001 Optic Disk Drusen 27 0.023
728
NTR018 Neutrophilia, Hereditary 32 0.022
729
CRB026 Cerebellar Astrocytoma 39 0.022
730
BKS002 Book Syndrome 18 0.021
731
PGM005 Pigment Dispersion Syndrome 35 0.021
732
SCL044 Scalp Syndrome 17 0.021
733
DFF012 Differentiating Neuroblastoma 34 0.021
734
THN007 Thinking Seizures 10 0.021
735
DVL005 Developmental Dyspraxia 17 0.020
736
DNL001 Dna Ligase Iv Deficiency 33 0.020