Search results for "alzheimer disease familial"

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

812 hits were found for 'alzheimer disease familial'

# Family MCID Name MIFTS Score
1
P ALZ034 Alzheimer Disease 92 12.860
2
c ALZ036 Alzheimer Disease, Type 3 53 6.778
3
c ALZ037 Alzheimer Disease-2 52 6.586
4
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 39 5.693
5
c ALZ035 Alzheimer Disease-4 45 4.868
6
c ALZ012 Alzheimer Disease 12 32 4.084
7
c ALZ002 Alzheimer Disease Type 1 21 3.625
8
c ALZ039 Alzheimer's Disease 7 26 3.609
9
c ERL006 Early-Onset Familial Alzheimer Disease 37 2.979
10
FML202 Familial Alzheimer-Like Prion Disease 9 1.583
11
DMN002 Dementia 65 0.746
12
NRN002 Neuronitis 41 0.402
13
P ENC018 Encephalopathy 59 0.333
14
CRB009 Cerebritis 39 0.328
15
PHY002 Physical Disorder 43 0.320
16
P AMY004 Amyloidosis 65 0.315
17
VSC002 Vascular Dementia 54 0.277
18
c CNT035 Central Nervous System Disease 60 0.266
19
CND002 Conduct Disorder 54 0.235
20
DSS008 Disease of Mental Health 52 0.232
21
MTH009 Mouth Disease 61 0.202
22
LRN003 Learning Disability 49 0.195
23
c ALZ032 Alzheimer Disease 18 35 0.192
24
P CRB019 Cerebral Amyloid Angiopathy 58 0.181
25
PRP019 Peripheral Nervous System Disease 55 0.179
26
P HRT032 Heart Disease 75 0.177
27
P BRS047 Breast Cancer 100 0.176
28
GLT021 Glutaricaciduria, Type I 46 0.174
29
DWN001 Down Syndrome 66 0.170
30
c ALZ043 Alzheimer's Disease 15 32 0.167
31
PCK002 Pick Disease 68 0.166
32
CRB039 Cerebrovascular Disease 63 0.164
33
END072 Endotheliitis 42 0.163
34
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 41 0.162
35
MDD011 Mood Disorder 61 0.160
36
P SCH015 Schizophrenia 77 0.160
37
P NRV007 Nervous System Disease 71 0.155
38
ART111 Artery Disease 55 0.155
39
P LTR001 Lateral Sclerosis 53 0.153
40
DRG001 Drug Psychosis 38 0.153
41
P THY032 Thyroiditis 54 0.151
42
P CRN211 Coronary Artery Disease 74 0.149
43
SPC010 Speech and Communication Disorders 41 0.149
44
ATN002 Autonomic Nervous System Disease 48 0.145
45
NTR005 Nutritional Deficiency Disease 36 0.145
46
P OBS005 Obesity 92 0.144
47
ATH003 Atherosclerosis 65 0.141
48
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 27 0.141
49
SMN008 Semantic Dementia 44 0.140
50
SPS057 Spasticity 42 0.138
51
ALR002 Al-Raqad Syndrome 36 0.138
52
RTN023 Retinitis 50 0.137
53
PSY004 Psychotic Disorder 67 0.137
54
ALN001 Aland Island Eye Disease 45 0.136
55
AMN003 Amnestic Disorder 43 0.135
56
c ALZ042 Alzheimer's Disease 14 40 0.135
57
SLP005 Sleep Disorder 53 0.134
58
P EPL164 Epilepsy 66 0.133
59
GLC008 Glucose Metabolism Disease 42 0.133
60
MVM001 Movement Disease 49 0.130
61
P CRT072 Creutzfeldt-Jakob Disease 61 0.130
62
VSC007 Vascular Disease 67 0.129
63
APH002 Aphasia 54 0.128
64
P ATX004 Ataxia 53 0.125
65
P CRB088 Cerebral Atrophy 43 0.124
66
BLD054 Blood Protein Disease 37 0.124
67
P MYP004 Myopathy 67 0.122
68
P LKM002 Leukemia 71 0.121
69
P NRB001 Neuroblastoma 70 0.120
70
P CLR023 Colorectal Cancer 97 0.120
71
MNT002 Mental Depression 53 0.120
72
P KDN018 Kidney Disease 66 0.119
73
SPN369 Spinal Disease 39 0.119
74
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.118
75
P NRP001 Neuropathy 59 0.116
76
P HPT021 Hepatitis 69 0.115
77
ANX002 Anxiety Disorder 67 0.114
78
P PRK057 Parkinson Disease, Late-Onset 70 0.114
79
P HYD006 Hydrocephalus 66 0.114
80
PRN023 Prion Disease 48 0.111
81
BRT030 Birth Defects 43 0.111
82
LPD008 Lipid Metabolism Disorder 58 0.111
83
P ART022 Arthritis 75 0.110
84
ACR041 Acromelic Frontonasal Dysostosis 45 0.110
85
P PNC044 Pancreatitis 61 0.109
86
PRD011 Proud Syndrome 42 0.108
87
END040 Endogenous Depression 53 0.108
88
P CTR002 Cataract 58 0.107
89
PRP027 Peripheral Vascular Disease 69 0.107
90
PRS047 Prostatitis 56 0.106
91
ART021 Arteriosclerosis 58 0.106
92
SPS019 Spastic Paraparesis 41 0.106
93
P SPS003 Spastic Diplegia 52 0.104
94
ISC004 Ischemia 61 0.104
95
CRB033 Cerebral Degeneration 44 0.104
96
BRN071 Brain Injury 52 0.104
97
PST086 Posterior Cortical Atrophy 32 0.103
98
P GRV001 Graves' Disease 59 0.103
99
ADR009 Adrenal Cortex Disease 39 0.102
100
APR001 Apraxia 51 0.102
101
P LVR013 Liver Disease 75 0.101
102
P CRT033 Corticobasal Degeneration 47 0.100
103
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.100
104
EYD002 Eye Disease 61 0.099
105
MLN008 Melanoma 62 0.098
106
MLT021 Multiple System Atrophy 70 0.098
107
CRH001 Crohn's Disease 75 0.096
108
RSP006 Respiratory System Disease 58 0.095
109
TTH006 Tooth Disease 52 0.095
110
P HYP607 Hypercholesterolemia, Familial 76 0.094
111
NRM002 Normal Pressure Hydrocephalus 50 0.094
112
LNG099 Lung Disease 64 0.094
113
c ALZ008 Alzheimer Disease Risk Factor 18 0.094
114
SPC005 Speech Disorder 41 0.093
115
ADJ001 Adjustment Disorder 38 0.093
116
c CRN214 Coronary Heart Disease 5 22 0.093
117
SPC003 Specific Developmental Disorder 38 0.092
118
P PRS040 Prostate Cancer 90 0.092
119
P DMN033 Dementia, Frontotemporal 62 0.092
120
P CRN178 Coronary Heart Disease 6 21 0.092
121
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.091
122
GLB003 Globe Disease 32 0.091
123
P RHM011 Rheumatoid Arthritis 89 0.091
124
P DYS021 Dysautonomia 44 0.090
125
BSL008 Basal Ganglia Disease 40 0.090
126
BNS002 Bone Structure Disease 37 0.090
127
ACD009 Acid-Labile Subunit, Deficiency of 45 0.089
128
P TRM003 Tremor 54 0.089
129
P MSC005 Muscular Dystrophy 65 0.088
130
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 36 0.088
131
KWS002 Kawasaki Disease 70 0.087
132
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 54 0.087
133
NWC001 Newcastle Disease 54 0.086
134
BRN028 Brain Cancer 70 0.085
135
OPT006 Optic Nerve Disease 52 0.085
136
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 59 0.085
137
CRB031 Cerebral Arterial Disease 27 0.084
138
P MYC007 Myocardial Infarction 79 0.084
139
STR067 Stroke, Ischemic 75 0.084
140
ADN018 Adenoma 58 0.084
141
P HNT016 Huntington Disease 80 0.083
142
P AST005 Asthma 82 0.083
143
FST001 Foster-Kennedy Syndrome 31 0.083
144
CNT098 Central Core Disease 65 0.082
145
GNR004 Generalized Anxiety Disorder 51 0.082
146
LPD004 Lipoid Nephrosis 48 0.082
147
WTH001 Withdrawal Disorder 37 0.081
148
P OST002 Osteoporosis 64 0.081
149
HYP266 Hypoxia 56 0.081
150
P MYS005 Myositis 57 0.080
151
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 53 0.080
152
DMN031 Dementia, Lewy Body 58 0.079
153
c TRC078 Trichohepatoenteric Syndrome 2 29 0.079
154
RTN018 Retinal Disease 53 0.079
155
CRB085 Cerebral Hemorrhage 46 0.079
156
c INH020 Inherited Metabolic Disorder 49 0.078
157
c GRN014 Grn-Related Frontotemporal Dementia 40 0.078
158
MSC004 Muscle Tissue Disease 34 0.078
159
c PRK031 Parkinson Disease 1 51 0.078
160
P DYS154 Dystonia 65 0.078
161
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.077
162
P AMY084 Amyloidosis, Finnish Type 42 0.077
163
P FML035 Familial Hyperlipidemia 48 0.077
164
HPT074 Hepatic Adenoma, Somatic 50 0.077
165
P PNM007 Pneumonia 68 0.076
166
ETH011 Ethylmalonic Encephalopathy 56 0.076
167
HYP037 Hyperhomocysteinemia 50 0.076
168
P HRP006 Herpes Simplex 65 0.076
169
P ALX003 Alexander Disease 63 0.076
170
FRN030 Frontotemporal Dementia with Parkinsonism-17 29 0.075
171
P MSC033 Muscle Disorders 52 0.075
172
P HMC003 Hemochromatosis 72 0.075
173
CNG034 Congestive Heart Failure 72 0.075
174
MTR014 Motor Neuron Disease 58 0.075
175
SKN016 Skin Disease 66 0.074
176
DRG003 Drug Dependence 50 0.074
177
ETN001 Eating Disorder 58 0.074
178
HNM002 Hinman Syndrome 25 0.073
179
WLS001 Wilson Disease 72 0.073
180
THR024 Thrombosis 57 0.073
181
EXF001 Exfoliation Syndrome 57 0.073
182
P BPL003 Bipolar Disorder 62 0.073
183
c ESS001 Essential Tremor 59 0.072
184
INC002 Inclusion Body Myositis 66 0.072
185
BLD053 Blood Platelet Disease 46 0.072
186
WLL006 Wells Syndrome 59 0.072
187
OBS015 Obesity, Hyperphagia, and Developmental Delay 41 0.072
188
P PRD008 Periodontitis 63 0.072
189
TRM010 Traumatic Brain Injury 52 0.072
190
P CLC005 Celiac Disease 68 0.072
191
ADT003 Auditory System Disease 40 0.071
192
INC022 Inclusion-Cell Disease 46 0.071
193
MYC033 Myoclonus 42 0.071
194
P HYP086 Hypothyroidism 64 0.071
195
RDN001 Reading Disorder 34 0.070
196
HMZ003 Homozygous Familial Hypercholesterolemia 47 0.070
197
c PND001 Pain Disorder 54 0.070
198
CHR008 Choroiditis 44 0.070
199
BRN080 Brain Ischemia 41 0.070
200
c PRK030 Parkinson Disease 4 38 0.070
201
c CRN175 Coronary Heart Disease 4 19 0.070
202
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.069
203
P DNT015 Dent Disease 61 0.069
204
MYC002 Mycobacterium Avium Complex Disease 52 0.069
205
CNV002 Conversion Disorder 41 0.069
206
CLT003 Colitis 60 0.069
207
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.069
208
CSY001 C Syndrome 50 0.069
209
c HYP595 Hypertension, Essential 69 0.068
210
c CRN173 Coronary Heart Disease 8 18 0.068
211
c HMG001 Hemoglobin C Disease 47 0.068
212
P INT063 Intellectual Disability 49 0.068
213
AYM001 Ayme-Gripp Syndrome 41 0.068
214
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 78 0.068
215
NRM005 Neuromuscular Disease 56 0.068
216
BNS003 Binswanger's Disease 42 0.068
217
P THL005 Thalassemia 64 0.068
218
CTS003 Coats Disease 57 0.068
219
IMM136 Immune System Disease 51 0.067
220
PRP080 Peripheral Artery Disease 37 0.067
221
P LKD001 Leukodystrophy 59 0.067
222
ATS008 Autosomal Dominant Disease 39 0.067
223
FTT001 Fatty Liver Disease 59 0.067
224
GDS001 Good Syndrome 44 0.067
225
P OPN001 Open-Angle Glaucoma 49 0.067
226
C3D001 C3 Deficiency 53 0.066
227
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.066
228
HDC001 Headache 54 0.066
229
LKC003 Leukocyte Disease 43 0.066
230
ATN005 Autonomic Dysfunction 49 0.066
231
ALC007 Alcohol Dependence 63 0.066
232
P CDS001 Cadasil 55 0.065
233
c CRN172 Coronary Heart Disease 3 19 0.065
234
P PRS038 Personality Disorder 62 0.065
235
VND001 Vein Disease 47 0.065
236
KDS001 Kid Syndrome 53 0.064
237
P GT001 Gout 58 0.064
238
CLN019 Colonic Disease 51 0.064
239
P PRP029 Porphyria 59 0.064
240
P PLN008 Peeling Skin Syndrome 45 0.064
241
c CHR579 Chiari Malformation Type Ii 37 0.064
242
P LYN001 Lynch Syndrome 69 0.064
243
INS024 Insulin-Like Growth Factor I 75 0.064
244
P HPT023 Hepatocellular Carcinoma 92 0.064
245
CHL071 Child Syndrome 58 0.063
246
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.063
247
P CRB042 Cerebellar Ataxia 63 0.063
248
P FML187 Familial Hypertension 38 0.063
249
P RCK004 Rickets 61 0.063
250
SNS001 Sensorineural Hearing Loss 57 0.063
251
P RTN016 Retinal Degeneration 54 0.063
252
ULC004 Ulcerative Colitis 76 0.062
253
SBC016 Subacute Delirium 24 0.062
254
P HYP060 Hyperinsulinism 58 0.062
255
P GLM045 Glioma 60 0.062
256
P HYP027 Hypobetalipoproteinemia 53 0.062
257
P SLP006 Sleep Apnea 61 0.062
258
AND005 Androgen Insensitivity Syndrome, Mild 16 0.062
259
P MTC003 Metachromatic Leukodystrophy 70 0.062
260
PRP016 Paraplegia 49 0.062
261
CYS001 Cystic Fibrosis 83 0.062
262
P HYP117 Hypertriglyceridemia 61 0.061
263
BRN118 Brain Small Vessel Disease with or Without Ocular Anomalies 40 0.061
264
GST050 Gastrointestinal System Disease 56 0.061
265
BHV002 Behavioral Variant of Frontotemporal Dementia 39 0.061
266
LGP003 Logopenic Progressive Aphasia 22 0.061
267
CRD118 Cardiovascular Cancer 44 0.061
268
MRG013 Mirage Syndrome 29 0.061
269
ALL026 Allergic Hypersensitivity Disease 52 0.061
270
P MYL006 Myeloid Leukemia 66 0.060
271
BRN106 Burns 52 0.060
272
P CRV039 Cervicitis 45 0.060
273
ATT013 Attention Deficit-Hyperactivity Disorder 69 0.060
274
c MTR002 Mitral Valve Insufficiency 44 0.060
275
DMN032 Dementia, Familial British 36 0.060
276
ATS009 Autosomal Genetic Disease 35 0.059
277
P CRN035 Cranial Nerve Palsy 46 0.059
278
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.059
279
PLM129 Pulmonary Disease, Chronic Obstructive 63 0.059
280
P TYS001 Tay-Sachs Disease 71 0.059
281
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.059
282
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.059
283
P PSR002 Psoriasis 61 0.059
284
P ENC004 Encephalitis 63 0.058
285
DFC001 Defective Apolipoprotein B-100 29 0.058
286
P ALC004 Alcohol Abuse 59 0.058
287
SPN041 Spinal Cord Disease 51 0.058
288
PRD007 Periodontal Disease 60 0.058
289
ATP002 Atopy 66 0.058
290
CRB004 Cerebral Artery Occlusion 45 0.058
291
c GRV009 Graves Disease 2 16 0.058
292
P KDN017 Kidney Cancer 65 0.057
293
BRC012 Brucellosis 66 0.057
294
LNS003 Lens Disease 33 0.057
295
IRS003 Iris Disease 31 0.057
296
P MCR010 Microcephaly 58 0.057
297
CRN031 Cranial Nerve Disease 40 0.057
298
P NRV006 Nervous System Cancer 60 0.057
299
P SZR006 Seizure Disorder 56 0.057
300
CRB087 Cerebral Arteriosclerosis 21 0.057
301
ART017 Aortic Disease 57 0.056
302
c HRD039 Hereditary Amyloidosis 46 0.056
303
SXL003 Sexual Disorder 42 0.056
304
AMY002 Amyloid Tumor 37 0.056
305
P MSC003 Muscular Atrophy 50 0.056
306
P CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 48 0.056
307
IMP003 Impaired Renal Function Disease 34 0.056
308
c CRN174 Coronary Heart Disease 2 20 0.056
309
P AGN002 Agnosia 57 0.056
310
c GRV008 Graves Disease 1 44 0.056
311
GLC003 Glucose Intolerance 55 0.055
312
CRT016 Carotid Artery Disease 57 0.055
313
BRN004 Brain Edema 52 0.055
314
DVL001 Developmental Coordination Disorder 36 0.055
315
TNG002 Tangier Disease 62 0.055
316
OBS061 Obstructive Sleep Apnea 66 0.055
317
DLS001 Delusional Disorder 41 0.055
318
c CRN177 Coronary Heart Disease 7 20 0.055
319
P MNN013 Meningitis 67 0.055
320
ADL002 Adult Syndrome 52 0.055
321
P NMN002 Niemann-Pick Disease 65 0.054
322
CRB027 Cerebellar Disease 47 0.054
323
LPP001 Lipoprotein Lipase Deficiency 63 0.054
324
SKN023 Skin Tag 44 0.054
325
P MLT019 Multiple Myeloma 83 0.054
326
AND015 Androgen Insensitivity 64 0.054
327
OVR063 Overnutrition 50 0.054
328
HMT018 Hematopoietic Stem Cell Transplantation 41 0.053
329
DFC004 Deficiency Anemia 64 0.053
330
GNC005 Geniculate Ganglionitis 27 0.053
331
ADR007 Adrenoleukodystrophy 72 0.053
332
FCL011 Facial Nerve Disease 36 0.053
333
VNW001 Von Willebrand's Disease 61 0.053
334
P MTC069 Mitochondrial Disorders 53 0.053
335
P TRC086 Trichohepatoenteric Syndrome 1 48 0.052
336
SBS003 Substance Abuse 54 0.052
337
c INF071 Inflammatory Bowel Disease 1 51 0.052
338
CRB008 Cerebral Atherosclerosis 43 0.052
339
P THR014 Thrombocytopenia 64 0.052
340
P INF038 Influenza 72 0.051
341
P SPR098 Supranuclear Palsy, Progressive 56 0.051
342
OLV001 Olivopontocerebellar Atrophy 53 0.051
343
P LYM026 Lymphoblastic Leukemia 62 0.051
344
c FML303 Familial/multiple Cancer 14 0.051
345
P FCL005 Focal Segmental Glomerulosclerosis 60 0.051
346
c AMY091 Amyotrophic Lateral Sclerosis 1 78 0.051
347
YNG002 Young Syndrome 26 0.050
348
ANS012 Anus Disease 32 0.050
349
OCL011 Ocular Motility Disease 37 0.050
350
EYC003 Eye Accommodation Disease 24 0.050
351
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 21 0.050
352
PRP030 Purpura 58 0.050
353
IDM001 Ideomotor Apraxia 36 0.050
354
c HMG004 Hemoglobin D Disease 31 0.050
355
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.050
356
P INF032 Infertility 59 0.050
357
OBS002 Obsessive-Compulsive Disorder 66 0.050
358
MDY003 Mody, Type Ii 36 0.049
359
BNC003 Bone Cancer 58 0.049
360
HRT007 Heart Cancer 46 0.049
361
MTR031 Motor Neuro-Ophthalmic Disorders 19 0.049
362
SCK003 Sickle Cell Anemia 71 0.049
363
PRT011 Protein C Deficiency 52 0.049
364
SCR011 Scrapie 38 0.049
365
P DRR001 Diarrhea 60 0.049
366
HYP121 Hypoalphalipoproteinemia 61 0.049
367
DYS073 Dysphagia 48 0.049
368
HV1006 Hiv-1 80 0.049
369
c HYP163 Hyperlipidemia Type 3 36 0.048
370
c SCH051 Schizophrenia 4 28 0.048
371
VTM003 Vitamin Metabolic Disorder 30 0.048
372
INT074 Intracranial Arteriosclerosis 14 0.048
373
PRM243 Primary Bone Cancer 29 0.048
374
PHN003 Phenylketonuria 72 0.048
375
NSD001 Nose Disease 48 0.048
376
HDN002 Head Injury 45 0.048
377
XNT003 Xanthomatosis 46 0.048
378
FML039 Female Reproductive System Disease 48 0.048
379
TMP001 Temporal Lobe Epilepsy 50 0.048
380
ACT084 Acute Stress Disorder 40 0.048
381
CRB037 Cerebral Palsy 66 0.047
382
ATM053 Autoimmune Disease 2 16 0.047
383
P WSK001 Wiskott-Aldrich Syndrome 73 0.047
384
c HMG003 Hemoglobin E Disease 44 0.047
385
VTM002 Vitamin B12 Deficiency 45 0.047
386
P EXN002 Exanthem 57 0.047
387
P BLD051 Blood Coagulation Disease 42 0.047
388
MLR007 Male Reproductive System Disease 34 0.047
389
CRB025 Carbohydrate Metabolic Disorder 46 0.047
390
CRD119 Cardiac Arrest 61 0.047
391
ADP007 Adie Pupil 34 0.046
392
RST001 Restless Legs Syndrome 54 0.046
393
c CNG031 Congenital Nervous System Abnormality 37 0.046
394
P NRC002 Narcolepsy 62 0.046
395
HMG005 Hemoglobinopathy 52 0.046
396
c ADV003 Advanced Sleep Phase Syndrome, Familial, 1 24 0.046
397
P MYL005 Myelofibrosis 67 0.046
398
GRF001 Graft-Versus-Host Disease, Protection Against 52 0.046
399
ATN004 Autonomic Neuropathy 45 0.046
400
VRL011 Viral Infectious Disease 55 0.046
401
P SPC019 Specific Language Impairment 28 0.046
402
HMT002 Hematologic Cancer 64 0.046
403
P FML056 Familial Deafness 23 0.046
404
ADS004 Aids Dementia Complex 39 0.046
405
P ANR007 Anorexia Nervosa 61 0.046
406
CYS039 Cystic Kidney Disease 52 0.046
407
P CHR084 Chromosomal Disease 32 0.046
408
ATM052 Autoimmune Disease 1 25 0.045
409
PST028 Post-Traumatic Stress Disorder 57 0.045
410
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 43 0.045
411
c HPT016 Hepatitis B 65 0.045
412
c AST039 Asthma 2 28 0.045
413
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 34 0.045
414
SBS004 Substance Dependence 47 0.045
415
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.045
416
17B002 17-Beta-Hydroxysteroid Dehydrogenase X Deficiency 31 0.044
417
HML018 Homologous Wasting Disease 13 0.044
418
P ATX030 Ataxia-Telangiectasia 77 0.044
419
HYP006 Hypertensive Heart Disease 50 0.044
420
DMY004 Demyelinating Disease 53 0.044
421
PLS010 Plasma Protein Metabolism Disease 34 0.044
422
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.044
423
VSC047 Vascular Malformation 45 0.044
424
P ALG002 Alagille Syndrome 72 0.043
425
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.043
426
ADM013 Adamantinoma of Long Bones 57 0.043
427
NSY001 N Syndrome 36 0.043
428
P IDP010 Idiopathic Generalized Epilepsy 61 0.043
429
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.043
430
LVR012 Liver Cirrhosis 67 0.043
431
OCL009 Ocular Cancer 59 0.043
432
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 21 0.043
433
PYR013 Pyruvate Kinase Deficiency 58 0.043
434
c BPL002 Bipolar I Disorder 47 0.043
435
P PSD003 Pseudohypoaldosteronism 44 0.043
436
P GLL020 Gallbladder Disease 59 0.043
437
P ATX010 Ataxia Neuropathy Spectrum 30 0.043
438
P ANG001 Angelman Syndrome 61 0.043
439
PRD004 Prediabetes Syndrome 43 0.042
440
HYP080 Hypogonadism 53 0.042
441
P HRT017 Heart Tumor 32 0.042
442
SYN036 Syncope 47 0.042
443
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.042
444
c CLR079 Colorectal Cancer 2 29 0.042
445
SYN058 Synucleinopathy 38 0.042
446
STM006 Stomach Disease 50 0.042
447
FML330 Familial Lcat Deficiency 34 0.041
448
HYP085 Hypothalamic Disease 44 0.041
449
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 43 0.041
450
NRL016 Neural Tube Defects 76 0.041
451
P LKN019 Leukoencephalopathy, Diffuse Hereditary, with Spheroids 49 0.041
452
FXF002 Fox-Fordyce Disease 36 0.041
453
ABT001 Abetalipoproteinemia 60 0.041
454
HNS001 Hansen's Disease 30 0.041
455
GLB001 Gilbert Syndrome 60 0.041
456
CYT008 Cytomegalovirus Infection 52 0.041
457
CHN016 Cohen Syndrome 54 0.041
458
KRT002 Keratomalacia 52 0.041
459
VSC006 Vascular Cancer 51 0.041
460
c ADL079 Adult Heart Tumor 16 0.041
461
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 33 0.041
462
P MYC026 Myoclonus Epilepsy 34 0.041
463
HRD059 Hereditary Peripheral Nervous Disorder 11 0.040
464
VSC008 Vascular Hemostatic Disease 30 0.040
465
PPL023 Pupil Disease 23 0.040
466
P END044 Endometriosis 66 0.040
467
ABL002 Ablepharon-Macrostomia Syndrome 57 0.040
468
c HPT003 Hepatitis a 59 0.040
469
MLR004 Malaria 83 0.040
470
c BRN108 Branchiootic Syndrome 1 34 0.040
471
P HYP614 Hyperlipidemia, Familial Combined 50 0.040
472
HDR002 Hidradenitis Suppurativa 51 0.040
473
HYP034 Hypertensive Encephalopathy 38 0.040
474
c ATM007 Autoimmune Disease of Central Nervous System 25 0.040
475
HDR003 Hidradenitis 45 0.040
476
P SDR002 Siderosis 44 0.040
477
CHL123 Chlamydia 60 0.040
478
ACT049 Acute Disseminated Encephalomyelitis 49 0.040
479
PLS009 Plasma Cell Neoplasm 48 0.039
480
P CNJ013 Conjunctivitis 64 0.039
481
TTR011 Tetraploidy 41 0.039
482
MNN009 Meningoencephalitis 47 0.039
483
DRG011 Drug Addiction 51 0.039
484
ACN011 Acne 62 0.039
485
MNK001 Menkes Disease 60 0.039
486
P TXP001 Toxoplasmosis 61 0.039
487
FSH001 Fish-Eye Disease 43 0.039
488
c CNT015 Central Sleep Apnea 44 0.039
489
RTN020 Retinal Vascular Disease 48 0.039
490
THY030 Thyroid Gland Disease 48 0.039
491
NNL002 Nonalcoholic Steatohepatitis 50 0.039
492
CRN024 Corneal Disease 44 0.039
493
DGN001 Degenerative Disc Disease 52 0.039
494
MXD023 Mixed Cell Type Cancer 45 0.039
495
P SHR029 Short Syndrome 58 0.039
496
P SCK002 Sick Sinus Syndrome 50 0.038
497
KR002 Kuru 36 0.038
498
ATM054 Autoimmune Disease 3 15 0.038
499
SRT004 Serotonin Syndrome 49 0.038
500
APH001 Aphthous Stomatitis 62 0.038
501
P PRM006 Primary Biliary Cirrhosis 51 0.038
502
P FRG001 Fragile X Syndrome 69 0.038
503
P HRD018 Hair Disease 51 0.038
504
P LCT001 Lactic Acidosis 51 0.038
505
SPR066 Superficial Siderosis 34 0.038
506
c AMY009 Amyloidosis Aa 39 0.038
507
ATM012 Autoimmune Disease of Blood 35 0.038
508
OLF001 Olfactory Nerve Disease 16 0.038
509
FDL002 Food Allergy 53 0.038
510
ART005 Arteriovenous Malformation 66 0.037
511
TYP027 Type 1 Diabetes Mellitus 10 27 0.037
512
P MSC007 Muscle Hypertrophy 58 0.037
513
GNG011 Gingival Disease 46 0.037
514
IRR002 Irritable Bowel Syndrome 58 0.037
515
CRD144 Cardiovascular Disease Risk Factor ) 40 0.037
516
c ART101 Aortic Valve Disease 2 53 0.037
517
P RNL015 Renal Hypertension 48 0.037
518
RNL097 Renal Artery Disease 43 0.037
519
P GNR027 Generalized Peeling Skin Syndrome 19 0.037
520
SXD001 Sex Differentiation Disease 38 0.037
521
VSL004 Visual Cortex Disease 28 0.037
522
PSD029 Pseudocholinesterase Deficiency 40 0.037
523
WLL001 Williams-Beuren Syndrome 60 0.037
524
P GLB002 Glioblastoma 68 0.037
525
CRB150 Cerebral Creatine Deficiency Syndrome 2 45 0.037
526
HRN022 Hearing Loss/deafness 26 0.036
527
c CRN176 Coronary Heart Disease 9 18 0.036
528
MRK002 Marek Disease 33 0.036
529
BWN006 Bowen's Disease 33 0.036
530
HYP066 Hyperglycemia 61 0.036
531
c ATS308 Autosomal Dominant Cerebellar Ataxia 48 0.036
532
ART004 Aortic Atherosclerosis 46 0.036
533
c MCL042 Macular Degeneration, Age-Related, 1 73 0.036
534
P ANT006 Antiphospholipid Syndrome 56 0.036
535
P PRM001 Primary Cutaneous Amyloidosis 50 0.036
536
INT007 Intermediate Coronary Syndrome 50 0.036
537
CRH005 Crohn's Colitis 52 0.036
538
BLL006 Bullous Pemphigoid 59 0.036
539
BNF002 Bone Fracture 50 0.036
540
P HYP090 Hyperalphalipoproteinemia 48 0.035
541
ALX001 Alexia 40 0.035
542
P ENC011 Encephalomyopathy 37 0.035
543
c PRC016 Pre-Eclampsia 56 0.035
544
ATS001 Autistic Disorder 63 0.035
545
P PNC025 Panic Disorder 60 0.035
546
P MRT001 Muir-Torre Syndrome 59 0.035
547
P ADV001 Advanced Sleep Phase Syndrome 37 0.035
548
PTH002 Pathological Gambling 51 0.035
549
ATM059 Autoimmune Disease 6 22 0.035
550
c MYC058 Myocardial Infarction 2 28 0.035
551
ADR012 Adrenal Gland Disease 48 0.035
552
CRV043 Cervical Dystonia 44 0.035
553
ATN001 Autonomic Peripheral Neuropathy 17 0.035
554
P ECL001 Eclampsia 54 0.035
555
MLT001 Multiple Chemical Sensitivity 43 0.035
556
c MLT093 Multiple Sclerosis 2 18 0.034
557
c SCH064 Schizophrenia 10 19 0.034
558
IMG001 Image Syndrome 50 0.034
559
P SYR001 Syringomyelia 47 0.034
560
FRB001 Farber Lipogranulomatosis 53 0.034
561
P CRB059 Cerebellar Degeneration 34 0.034
562
LPD009 Lipid Storage Disease 49 0.034
563
HYP064 Hypogonadotropism 37 0.034
564
c DLT001 Delta Chain Disease 13 0.034
565
P MTC004 Mitochondrial Encephalomyopathy 42 0.034
566
P CSH001 Cushing's Syndrome 65 0.034
567
PRN021 Paranasal Sinus Disease 49 0.034
568
P HRP009 Herpes Simplex Encephalitis 47 0.034
569
IRN001 Iron Deficiency Anemia 52 0.034
570
UND005 Undifferentiated Pleomorphic Sarcoma 44 0.034
571
PTR006 Peters Anomaly 65 0.034
572
VSC009 Vascular Skin Disease 19 0.034
573
P GLY010 Glycine Encephalopathy 53 0.034
574
P SPS008 Spastic Ataxia 33 0.033
575
c PLN018 Peeling Skin Syndrome 2 40 0.033
576
CNT017 Central Nervous System Origin Vertigo 24 0.033
577
P AST007 Astrocytoma 65 0.033
578
OCL006 Ocular Hypertension 48 0.033
579
BNN003 Bone Inflammation Disease 44 0.033
580
CHR066 Chronic Fatigue Syndrome 64 0.033
581
CMP005 Campomelic Dysplasia 55 0.033
582
PST021 Postpartum Depression 49 0.033
583
ACN018 Acne Inversa, Familial, 1 31 0.033
584
EYD001 Eye Degenerative Disease 30 0.033
585
c HYP011 Hyperlipoproteinemia Type Iii 42 0.033
586
CRR007 Cirrhosis, Cryptogenic 43 0.033
587
GND003 Gonadal Disease 39 0.033
588
VSL002 Visual Epilepsy 31 0.033
589
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.033
590
HPT019 Hepatic Encephalopathy 56 0.032
591
P CMM008 Communicating Hydrocephalus 36 0.032
592
SKN019 Skin Melanoma 62 0.032
593
DYS004 Dyscalculia 27 0.032
594
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 46 0.032
595
LMY002 Leiomyoma 54 0.032
596
c ERL020 Early-Onset Schizophrenia 47 0.032
597
CHR103 Charge Syndrome 62 0.032
598
HMS001 Hemosiderosis 46 0.032
599
CHR073 Choreatic Disease 37 0.032
600
AGR018 Agraphia 36 0.032
601
c ALP005 Alpha Chain Disease 37 0.032
602
CPG001 Capgras Syndrome 21 0.032
603
P WVR001 Weaver Syndrome 56 0.032
604
NSL022 Nasal Cavity Disease 38 0.031
605
P STR001 Striatonigral Degeneration 28 0.031
606
P SDD001 Sudden Infant Death Syndrome 61 0.031
607
SMT004 Smith-Lemli-Opitz Syndrome 66 0.031
608
NRM003 Norum Disease 51 0.031
609
EPL114 Epilepsy, Familial Temporal Lobe, 1 38 0.031
610
P ACH003 Achromatopsia 55 0.031
611
MSL001 Measles 61 0.031
612
P UTR038 Uterine Disease 37 0.031
613
CHL014 Cholera 53 0.031
614
c PSD092 Pseudohypoaldosteronism, Type Iie 38 0.031
615
P ACR001 Aicardi-Goutieres Syndrome 54 0.031
616
BRN045 Brunner Syndrome 46 0.031
617
PRS064 Persistent Vegetative State 30 0.030
618
ATR076 Atrophic Muscular Disease 15 0.030
619
ATX003 Ataxia with Isolated Vitamin E Deficiency 40 0.030
620
c SCN036 Secondary Progressive Multiple Sclerosis 49 0.030
621
RNL077 Renal Fibrosis 47 0.030
622
c PLN021 Peeling Skin Syndrome 3 29 0.030
623
EMB004 Embryonal Carcinoma 57 0.030
624
c MJR003 Major Affective Disorder 6 15 0.030
625
c PRK007 Parkinson Disease Type 3 21 0.030
626
KRN002 Kearns-Sayre Syndrome 61 0.030
627
PRT037 Pertussis 64 0.030
628
ICH054 Ichthyosis, X-Linked 46 0.030
629
TRN015 Transient Cerebral Ischemia 56 0.030
630
FNT004 Fainting 33 0.030
631
VCC001 Vaccinia 46 0.030
632
P FTL009 Fetal Akinesia Deformation Sequence 50 0.029
633
WGN006 Wegener Granulomatosis 63 0.029
634
HYP081 Hypolipoproteinemia 42 0.029
635
BRD004 Borderline Personality Disorder 47 0.029
636
OPP004 Oppositional Defiant Disorder 43 0.029
637
c PRG001 Progressive Muscular Atrophy 39 0.029
638
MSS002 Mass Syndrome 48 0.029
639
OBS003 Obsessive-Compulsive Personality Disorder 36 0.029
640
SCL003 Social Phobia 46 0.029
641
c JVN024 Juvenile Hereditary Hemochromatosis 29 0.029
642
BHR001 Behr Syndrome 42 0.029
643
c PRG011 Progressive Myoclonus Epilepsy 39 0.029
644
TRD006 Tardive Dyskinesia 49 0.029
645
RTC003 Root Caries 37 0.029
646
TTN003 Tetanus 61 0.029
647
ART002 Arts Syndrome 51 0.029
648
P FTL001 Fetal Alcohol Syndrome 53 0.029
649
THL016 Thalassemias, Alpha- 53 0.029
650
PRM008 Parametritis 27 0.029
651
CRB040 Cerebrum Cancer 32 0.029
652
c MLT124 Multiple Sclerosis 5 23 0.029
653
c MJR008 Major Affective Disorder 2 19 0.029
654
c BNG076 Benign Exophthalmos Syndrome 15 0.028
655
BLM001 Bloom Syndrome 63 0.028
656
WRT002 Writing Disorder 27 0.028
657
c OPT055 Optic Atrophy Plus Syndrome 52 0.028
658
WSC001 Wisconsin Syndrome 14 0.028
659
TSY001 Tau Syndrome 10 0.028
660
PRN009 Paranoid Schizophrenia 47 0.028
661
PST027 Postencephalitic Parkinson Disease 26 0.028
662
P NRX001 Neuroaxonal Dystrophy 38 0.028
663
MTC005 Mitochondrial Metabolism Disease 36 0.028
664
PRT038 Protein-Energy Malnutrition 49 0.028
665
P HYP237 Hypercalcemia, Infantile 47 0.028
666
c MYT020 Myotonic Dystrophy 2 56 0.028
667
P PTT014 Pitt-Hopkins Syndrome 47 0.028
668
c MJR007 Major Affective Disorder 1 24 0.028
669
ADL060 Adult Polyglucosan Body Disease 33 0.028
670
PRM236 Primary Biliary Cholangitis 47 0.028
671
CRN246 Cranioosteoarthropathy 31 0.028
672
LMB024 Limbic Encephalitis 38 0.028
673
ACD004 Acdc 33 0.027
674
CHR321 Chorea and Dementia 16 0.027
675
P SPN301 Spinocerebellar Ataxia 2 56 0.027
676
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 42 0.027
677
ALP014 Alpha-Thalassemia/mental Retardation Syndrome 51 0.027
678
BCL002 B Cell Deficiency 49 0.027
679
NSH001 Nasu-Hakola Disease 44 0.027
680
ATM021 Autoimmune Inner Ear Disease 31 0.027
681
CCN002 Cocaine Abuse 48 0.027
682
SPR012 Separation Anxiety Disorder 33 0.027
683
PST055 Postural Hypotension 36 0.027
684
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 60 0.027
685
BRB001 Beriberi 41 0.027
686
BRD001 Brody Myopathy 47 0.027
687
LPD027 Lip Disease 28 0.027
688
BRX001 Bruxism 49 0.027
689
ATY001 Atypical Depressive Disorder 32 0.027
690
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 53 0.027
691
c MJR004 Major Affective Disorder 4 16 0.026
692
GLB015 Glioblastoma Multiforme 63 0.026
693
RTN006 Retinal Drusen 30 0.026
694
CHL078 Childhood-Onset Schizophrenia 34 0.026
695
CNT018 Central Nervous System Leukemia 37 0.026
696
PLG002 Plague 51 0.026
697
P CNT005 Central Nervous System Lymphoma 53 0.026
698
SLP001 Sleeping Sickness 48 0.026
699
P ARC016 Auriculocondylar Syndrome 1 40 0.026
700
DMN016 Dementia, Familial, Nonspecific 23 0.026
701
DYS009 Dysthymic Disorder 37 0.026
702
c MJR006 Major Affective Disorder 5 15 0.026
703
UTR039 Uterine Fibroid 57 0.026
704
c SPC015 Specific Language Impairment 4 11 0.026
705
PRX034 Peroxisome Disorders 39 0.026
706
P EPS030 Episodic Kinesigenic Dyskinesia 1 27 0.026
707
AMS001 Amusia 22 0.026
708
MTC057 Mitochondrial Recessive Ataxia Syndrome 48 0.025
709
GRV012 Grover's Disease 36 0.025
710
HMC014 Homocysteinemia 35 0.025
711
c EHL032 Ehlers-Danlos Syndrome, Type Viib 49 0.025
712
P PRM016 Primary Optic Atrophy 29 0.025
713
c DBT058 Diabetes Mellitus, Insulin-Dependent, 7 35 0.025
714
c PSD090 Pseudohypoaldosteronism, Type Iia 23 0.025
715
ACR008 Acrocallosal Syndrome 52 0.025
716
IMM039 Immune Hydrops Fetalis 33 0.025
717
IMP006 Impulse Control Disorder 40 0.025
718
SMT008 Smith-Magenis Syndrome 52 0.025
719
c DYS119 Dystonia 9 36 0.025
720
ANX004 Anoxia 43 0.025
721
c HYP288 Hypercholesterolemia, Due to Ligand-Defective Apo B 37 0.025
722
c PRM225 Primary Thrombocytopenia 39 0.025
723
c SCH061 Schizophrenia 16 16 0.025
724
CNT010 Central Nervous System Hematologic Cancer 18 0.025
725
NMN003 Niemann–pick Disease 26 0.025
726
NTR018 Neutrophilia, Hereditary 42 0.025
727
ATH004 Athetosis 26 0.024
728
SBL008 Sea-Blue Histiocyte Disease 36 0.024
729
TCD001 Tic Disorder 48 0.024
730
CHR079 Choroid Disease 34 0.024
731
DRG016 Drug Induced Dyskinesia 23 0.024
732
CCN001 Cocaine Dependence 49 0.024
733
HPT020 Hepatic Vascular Disease 42 0.024
734
P PRM108 Primary Progressive Multiple Sclerosis 46 0.024
735
c ART120 Arthrogryposis, Distal, Type 3 42 0.024
736
PRN033 Paraneoplastic Neurologic Disorders 25 0.024
737
LPP002 Lipoprotein Glomerulopathy 46 0.024
738
PYL017 Pyle Disease 45 0.024
739
c PRM039 Primary Angiitis of the Central Nervous System 30 0.024
740
c DBT048 Diabetes Mellitus, Insulin-Dependent, 11 36 0.024
741
c PRM226 Primary Central Nervous System Lymphoma 49 0.024
742
CRB001 Cerebral Lymphoma 33 0.024
743
c BLR024 Biliary Cirrhosis, Primary, 1 16 0.024
744
HMG025 Hemoglobin H Disease, Nondeletional 39 0.024
745
GNG004 Ganglioglioma 50 0.023
746
PRP026 Peripheral Retinal Degeneration 34 0.023
747
KDN013 Kidney Hypertrophy 31 0.023
748
TRT001 Teratocarcinoma 38 0.023
749
FRT005 Fruit Allergy 31 0.023
750
NVS001 Neovascular Glaucoma 44 0.023
751
PNN005 Panencephalitis, Subacute Sclerosing 33 0.023
752
P CFF001 Coffin-Siris Syndrome 51 0.023
753
MHR001 Mohr-Tranebjaerg Syndrome 41 0.023
754
MTH044 Mthfr Gene Mutation 21 0.023
755
ARC001 Arcus Senilis 35 0.023
756
UTR033 Uterine Corpus Cancer 49 0.023
757
c LKD015 Leukodystrophy, Hypomyelinating, 3 42 0.023
758
PRM003 Premature Ejaculation 45 0.023
759
MLN003 Melancholia 34 0.023
760
CRB026 Cerebellar Astrocytoma 37 0.023
761
CML001 Cumulative Trauma Disorders 18 0.023
762
FCL044 Fecal Incontinence 35 0.022
763
ADL086 Adolescent Idiopathic Scoliosis 30 0.022
764
ECT026 Ectopic Pregnancy 48 0.022
765
MLT073 Multisystemic Smooth Muscle Dysfunction Syndrome 37 0.022
766
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 35 0.022
767
CRC034 Carcinoma Showing Thymus-Like Differentiation 21 0.022
768
ISB001 Isobutyryl-Coa Dehydrogenase Deficiency 44 0.022
769
STR079 Sturge-Weber Syndrome, Somatic, Mosaic 42 0.022
770
KLP001 Kleptomania 38 0.022
771
RMN001 Rumination Disorder 34 0.022
772
SKL006 Skull Base Neoplasm 21 0.022
773
HYD038 Hydrops Fetalis, Nonimmune 40 0.022
774
c DBT054 Diabetes Mellitus, Insulin-Dependent, 24 34 0.022
775
ASY002 Asymptomatic Neurosyphilis 36 0.022
776
STT009 Sutton Disease 2 18 0.022
777
IMM002 Immature Cataract 27 0.022
778
EXP001 Expressive Language Disorder 29 0.022
779
CRT008 Carotid Artery Dissection 41 0.022
780
CRB096 Cerebral Amyloid Angiopathy, Dutch, Italian, Iowa, Flemish, Arctic Variants 30 0.022
781
STR026 Star Syndrome 57 0.022
782
DLY005 Delayed Sleep Phase Syndrome 37 0.021
783
CRN019 Coronary Artery Vasospasm 40 0.021
784
XNT009 Xanthoma Disseminatum 34 0.021
785
MTH064 Methemoglobinemia, Beta-Globin Type 29 0.021
786
ALP093 Alpha-Thalassemia/mental Retardation Syndrome, Chromosome 16-Related 37 0.021
787
TTH007 Tooth Erosion 33 0.021
788
PGM005 Pigment Dispersion Syndrome 44 0.021
789
PRM139 Primary Melanoma of the Central Nervous System 15 0.021
790
BSL005 Basal Ganglia Cerebrovascular Disease 9 0.021
791
P CHR573 Choroid Plexus Cancer 41 0.021
792
HNZ001 Heinz Body Anemia 39 0.021
793
MYF001 Myofibroma 37 0.021
794
ALC003 Alcoholic Psychosis 33 0.021
795
ALP094 Alpha Thalassemia-Intellectual Disability Syndrome Type 1 29 0.021
796
PLY039 Polymorphic Reticulosis 19 0.021
797
FSH003 Fish Allergy 29 0.021
798
PSY003 Psychosexual Disorder 28 0.021
799
OPT001 Optic Disk Drusen 28 0.021
800
MTN003 Motion Sickness 48 0.020
801
BKS002 Book Syndrome 19 0.020
802
SHP001 Shipyard Eye 28 0.020
803
SBS005 Substance-Induced Psychosis 28 0.020
804
SCL044 Scalp Syndrome 15 0.020
805
c ADL018 Adult Choroid Plexus Cancer 15 0.020
806
INT025 Intermittent Explosive Disorder 38 0.020
807
DFF012 Differentiating Neuroblastoma 35 0.020
808
THN007 Thinking Seizures 9 0.020
809
ISL049 Isolated Dandy-Walker Malformation Without Hydrocephalus 7 0.020
810
ISL050 Isolated Dandy-Walker Malformation with Hydrocephalus 7 0.020
811
DVL005 Developmental Dyspraxia 18 0.020
812
ALP062 Alpha-2-Macroglobulin Deficiency 22 0.019