Search results for "amyloidosis cerebral"

The MalaCard for "amyloidosis cerebral" has been retired.
Searching MalaCards for entries containing "amyloidosis cerebral"

590 hits were found for 'amyloidosis cerebral'

# Family MCID Name MIFTS Score
1
CRB096 Cerebral Amyloid Angiopathy, Dutch, Italian, Iowa, Flemish, Arctic Variants 32 8.782
2
P CRB019 Cerebral Amyloid Angiopathy 56 8.498
3
GRS011 Gerstmann-Straussler Disease 44 3.907
4
DMN032 Dementia, Familial British 36 3.637
5
DMN004 Dementia, Familial Danish 27 3.588
6
c HRD084 Hereditary Cerebral Amyloid Angiopathy 14 2.919
7
CRB009 Cerebritis 36 1.091
8
P AMY004 Amyloidosis 63 0.991
9
CRB085 Cerebral Hemorrhage 40 0.277
10
ANR040 Aneurysm 56 0.267
11
SPS057 Spasticity 41 0.238
12
MLR004 Malaria 80 0.228
13
NRN002 Neuronitis 40 0.201
14
P ENC018 Encephalopathy 59 0.198
15
BRN071 Brain Injury 51 0.197
16
P LYM118 Lymphoma 68 0.196
17
P MYL007 Myeloma 52 0.193
18
P ART022 Arthritis 73 0.185
19
P PRM001 Primary Cutaneous Amyloidosis 54 0.178
20
DMN002 Dementia 62 0.176
21
P HPT021 Hepatitis 74 0.173
22
P NRP001 Neuropathy 57 0.169
23
P AMY084 Amyloidosis, Finnish Type 45 0.165
24
P RHM011 Rheumatoid Arthritis 87 0.163
25
END072 Endotheliitis 41 0.163
26
P PLY019 Polyneuropathy 53 0.151
27
P CRD011 Cardiomyopathy 66 0.149
28
P NPH012 Nephrotic Syndrome 55 0.147
29
ATH003 Atherosclerosis 63 0.146
30
PRP027 Peripheral Vascular Disease 69 0.145
31
FCT003 Factor X Deficiency 62 0.136
32
AMY002 Amyloid Tumor 37 0.133
33
NTR005 Nutritional Deficiency Disease 51 0.128
34
ALR002 Al-Raqad Syndrome 36 0.128
35
NRM005 Neuromuscular Disease 56 0.126
36
ALP043 Alpha-2-Plasmin Inhibitor Deficiency 35 0.126
37
CRB031 Cerebral Arterial Disease 31 0.126
38
CDS001 Cadasil 50 0.122
39
P ALZ034 Alzheimer Disease 92 0.118
40
VSC006 Vascular Cancer 51 0.117
41
P LKM002 Leukemia 70 0.116
42
P MNN013 Meningitis 66 0.115
43
VSC011 Vasculitis 62 0.114
44
VSC008 Vascular Hemostatic Disease 30 0.113
45
P BLD051 Blood Coagulation Disease 44 0.112
46
BLD054 Blood Protein Disease 38 0.112
47
LGH004 Light Chain Deposition Disease 43 0.112
48
ATN002 Autonomic Nervous System Disease 46 0.110
49
P THY032 Thyroiditis 57 0.109
50
P SPS003 Spastic Diplegia 49 0.108
51
P EPL164 Epilepsy 60 0.108
52
HDC001 Headache 52 0.108
53
GLC077 Glucocorticoid Therapy, Response to 17 0.105
54
RTN023 Retinitis 49 0.105
55
P GLM007 Glomerulonephritis 56 0.105
56
PLS011 Plasmacytoma 57 0.101
57
TNP003 Tn Polyagglutination Syndrome, Somatic 30 0.101
58
HMT018 Hematopoietic Stem Cell Transplantation 39 0.101
59
SPN041 Spinal Cord Disease 50 0.100
60
P LRY019 Laryngitis 55 0.100
61
GRW007 Growth Hormone Deficiency 49 0.099
62
PRP019 Peripheral Nervous System Disease 52 0.099
63
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.098
64
VSC007 Vascular Disease 51 0.097
65
CLT003 Colitis 56 0.097
66
ATR060 Atrial Standstill, Digenic 51 0.097
67
TBR010 Tuberculosis 70 0.097
68
P NRV006 Nervous System Cancer 62 0.097
69
HPT074 Hepatic Adenoma, Somatic 35 0.096
70
PLS010 Plasma Protein Metabolism Disease 37 0.095
71
PRP021 Peripheral Nervous System Neoplasm 49 0.095
72
P DRR001 Diarrhea 60 0.095
73
c INH020 Inherited Metabolic Disorder 49 0.094
74
GLT021 Glutaricaciduria, Type I 47 0.094
75
P BCL006 B-Cell Lymphomas 64 0.093
76
P ATR011 Atrial Fibrillation 63 0.093
77
P MYP004 Myopathy 67 0.092
78
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.091
79
PRT014 Protein S Deficiency 54 0.090
80
ATN004 Autonomic Neuropathy 44 0.090
81
ULC004 Ulcerative Colitis 74 0.089
82
PCK002 Pick Disease 66 0.088
83
P CRV039 Cervicitis 45 0.088
84
BRT030 Birth Defects 44 0.087
85
IMM127 Immune System Cancer 41 0.087
86
P NRV007 Nervous System Disease 71 0.087
87
P CRN178 Coronary Heart Disease 6 22 0.086
88
P LPS004 Lupus Erythematosus 63 0.085
89
P HRT032 Heart Disease 64 0.085
90
P SDR002 Siderosis 44 0.085
91
P PNM007 Pneumonia 67 0.084
92
c CNG401 Congenital Heart Disease 67 0.084
93
ACR041 Acromelic Frontonasal Dysostosis 45 0.084
94
CRN025 Corneal Dystrophy 40 0.083
95
DFC004 Deficiency Anemia 64 0.083
96
MRC001 Marchiafava Bignami Disease 33 0.083
97
INC021 Incontinentia Pigmenti 57 0.082
98
FCT006 Factor V Deficiency 62 0.082
99
ATN003 Autonomic Nervous System Neoplasm 43 0.082
100
P PNC044 Pancreatitis 62 0.082
101
c CLD010 Cold-Induced Sweating Syndrome 1 43 0.082
102
P END033 Endocarditis 52 0.081
103
SPR066 Superficial Siderosis 33 0.081
104
c SYS001 Systemic Lupus Erythematosus 87 0.080
105
c THR092 Thrombophilia Due to Thrombin Defect 56 0.080
106
P ORG009 Organ System Cancer 45 0.080
107
PRT011 Protein C Deficiency 52 0.079
108
c CRN214 Coronary Heart Disease 5 22 0.078
109
P CRN035 Cranial Nerve Palsy 44 0.078
110
P LTT001 Lattice Corneal Dystrophy 33 0.078
111
P ATX004 Ataxia 53 0.078
112
KHL003 Kohlschutter-Tonz Syndrome 35 0.077
113
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 27 0.076
114
CNT010 Central Nervous System Hematologic Cancer 20 0.076
115
PRT036 Peritonitis 65 0.076
116
P PYL005 Pyelonephritis 52 0.076
117
P FML161 Familial Mediterranean Fever, Ar 64 0.076
118
SPN051 Spondylitis 50 0.076
119
CRH001 Crohn's Disease 76 0.076
120
P LVR013 Liver Disease 76 0.075
121
TPT001 Tauopathy 51 0.075
122
DRM006 Dermatitis 58 0.075
123
GTR002 Goiter 54 0.075
124
c ACT134 Acute Liver Failure 46 0.075
125
CRD119 Cardiac Arrest 63 0.075
126
ALN001 Aland Island Eye Disease 45 0.075
127
P SNS014 Sinusitis 66 0.074
128
P MYC007 Myocardial Infarction 80 0.074
129
HYP037 Hyperhomocysteinemia 49 0.074
130
P KDN018 Kidney Disease 64 0.073
131
NRM002 Normal Pressure Hydrocephalus 47 0.073
132
END030 End Stage Renal Failure 53 0.073
133
P MSC005 Muscular Dystrophy 64 0.072
134
IRN001 Iron Deficiency Anemia 51 0.072
135
SCK003 Sickle Cell Anemia 72 0.072
136
P OBS005 Obesity 91 0.071
137
SVN001 Sveinsson Choreoretinal Atrophy 28 0.070
138
PRD011 Proud Syndrome 42 0.070
139
MTR014 Motor Neuron Disease 57 0.070
140
PRP030 Purpura 60 0.070
141
CRN106 Corneal Dystrophy, Gelatinous Drop-Like 32 0.069
142
P AGM001 Agammaglobulinemia 63 0.069
143
BNS002 Bone Structure Disease 37 0.069
144
P INT063 Intellectual Disability 46 0.069
145
XNT001 Xanthogranulomatous Pyelonephritis 32 0.069
146
ART017 Aortic Disease 57 0.069
147
P HYP086 Hypothyroidism 63 0.068
148
SRC014 Sarcoma 66 0.068
149
DSS009 Disseminated Intravascular Coagulation 52 0.068
150
ADN018 Adenoma 59 0.068
151
PMS001 Poems Syndrome 56 0.068
152
WLL006 Wells Syndrome 57 0.068
153
P CTS001 Cutis Laxa 57 0.067
154
P ASP006 Aspergillosis 61 0.067
155
PRP016 Paraplegia 49 0.067
156
ATN005 Autonomic Dysfunction 44 0.067
157
P ART023 Arthropathy 63 0.066
158
HRT007 Heart Cancer 51 0.066
159
P HRT017 Heart Tumor 34 0.066
160
c ADL079 Adult Heart Tumor 17 0.066
161
c ART101 Aortic Valve Disease 2 56 0.066
162
c CRN172 Coronary Heart Disease 3 19 0.066
163
P TMP003 Temporal Arteritis 61 0.066
164
BLD053 Blood Platelet Disease 44 0.066
165
PRP080 Peripheral Artery Disease 35 0.066
166
P PLM037 Pulmonary Hypertension 78 0.066
167
PHY002 Physical Disorder 43 0.066
168
SPN186 Spinal Cord Injury 62 0.066
169
BCL002 B Cell Deficiency 50 0.065
170
RHM027 Rheumatic Disease 55 0.065
171
P RPD001 Rapidly Progressive Glomerulonephritis 43 0.065
172
PRT019 Protein-Losing Enteropathy 42 0.065
173
HYP056 Hypoglycemia 60 0.064
174
P LYM026 Lymphoblastic Leukemia 60 0.064
175
RLP001 Relapsing Polychondritis 52 0.064
176
c CRN175 Coronary Heart Disease 4 19 0.064
177
c CRN173 Coronary Heart Disease 8 19 0.064
178
TBR011 Tuberculous Meningitis 46 0.064
179
P LPR003 Leprosy 70 0.064
180
BNM001 Bone Marrow Cancer 56 0.064
181
P DBT005 Diabetes Insipidus 53 0.064
182
c HPT001 Hepatitis C 68 0.064
183
PRD019 Periodic Fever, Familial 48 0.062
184
BNC003 Bone Cancer 44 0.062
185
P SCK002 Sick Sinus Syndrome 49 0.062
186
DWN001 Down Syndrome 65 0.062
187
CHR008 Choroiditis 43 0.062
188
P INF032 Infertility 61 0.062
189
OCL009 Ocular Cancer 61 0.062
190
ACQ007 Acquired Immunodeficiency Syndrome 60 0.062
191
VND001 Vein Disease 51 0.062
192
c ACT210 Acute Respiratory Distress Syndrome 55 0.062
193
c DLT002 Dilated Cardiomyopathy 75 0.061
194
c JVN010 Juvenile Rheumatoid Arthritis 65 0.060
195
CNG034 Congestive Heart Failure 72 0.059
196
CMM004 Common Variable Immunodeficiency 68 0.059
197
LYM012 Lymphoplasmacytic Lymphoma 46 0.059
198
P CHL066 Cholangitis 48 0.059
199
GST039 Gastroduodenitis 32 0.059
200
MNN009 Meningoencephalitis 42 0.059
201
c INF071 Inflammatory Bowel Disease 1 51 0.059
202
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 30 0.059
203
UND005 Undifferentiated Pleomorphic Sarcoma 39 0.059
204
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 41 0.059
205
MYC033 Myoclonus 41 0.059
206
FCL012 Facial Paralysis 50 0.058
207
LNG099 Lung Disease 63 0.058
208
TRN018 Transitional Cell Carcinoma 56 0.058
209
P PHC003 Pheochromocytoma 72 0.058
210
SYN036 Syncope 45 0.058
211
FBR012 Fabry Disease 68 0.058
212
P ALX003 Alexander Disease 64 0.057
213
P LTR001 Lateral Sclerosis 50 0.057
214
P DRM010 Dermatomyositis 59 0.057
215
PRR002 Pure Red-Cell Aplasia 47 0.057
216
AND015 Androgen Insensitivity 64 0.057
217
AMS002 Amish Infantile Epilepsy Syndrome 34 0.057
218
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.057
219
P PLY017 Polyarteritis Nodosa 54 0.057
220
c HPT073 Hepatitis C Virus 72 0.057
221
P KDN017 Kidney Cancer 67 0.057
222
ARS001 Aarskog-Scott Syndrome 52 0.057
223
HYP088 Hyper-Igd Syndrome 41 0.057
224
c CRN176 Coronary Heart Disease 9 19 0.056
225
c DLT001 Delta Chain Disease 14 0.056
226
OST017 Osteomyelitis 60 0.056
227
LFT009 Left Ventricular Outflow Tract Obstruction 43 0.056
228
PRS047 Prostatitis 56 0.056
229
P HYP083 Hypopituitarism 50 0.056
230
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 32 0.056
231
P CRN211 Coronary Artery Disease 74 0.056
232
P PRP029 Porphyria 56 0.056
233
P ALG002 Alagille Syndrome 70 0.055
234
P CHR071 Charcot-Marie-Tooth Disease 66 0.055
235
P HYP076 Hyperthyroidism 59 0.055
236
P HST010 Histiocytosis 56 0.055
237
CST005 Castleman Disease 42 0.055
238
KRT004 Keratitis 70 0.055
239
PRR008 Periarteritis Nodosa 28 0.055
240
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 77 0.055
241
ECH003 Echinococcosis 53 0.055
242
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 32 0.054
243
DDN006 Duodenitis 44 0.054
244
MCR088 Microscopic Polyangiitis 47 0.054
245
MVD001 Moved to 60 0.054
246
DSS008 Disease of Mental Health 48 0.054
247
ARC002 Arachnoiditis 38 0.054
248
DMY004 Demyelinating Disease 52 0.054
249
HRT012 Heart Valve Disease 39 0.054
250
CHR005 Chorioamnionitis 47 0.054
251
ACR007 Acromegaly 66 0.054
252
ERD001 Erdheim-Chester Disease 51 0.054
253
TXC002 Toxic Encephalopathy 52 0.054
254
HMS001 Hemosiderosis 42 0.054
255
ISC006 Ischemic Heart Disease 54 0.054
256
PRC013 Pericarditis 52 0.054
257
P NMN002 Niemann-Pick Disease 63 0.054
258
ADL030 Adult-Onset Still's Disease 57 0.054
259
DFF005 Diffuse Large B-Cell Lymphoma 57 0.054
260
NRM004 Neuroma 47 0.054
261
c PND001 Pain Disorder 53 0.054
262
P THR014 Thrombocytopenia 63 0.054
263
CNN005 Connective Tissue Disease 60 0.054
264
c CHR089 Chronic Kidney Failure 67 0.053
265
BRC012 Brucellosis 66 0.053
266
C3D001 C3 Deficiency 50 0.053
267
MTR007 Motor Peripheral Neuropathy 44 0.053
268
PRD007 Periodontal Disease 42 0.053
269
P PRD008 Periodontitis 46 0.053
270
RTR011 Retroperitoneal Fibrosis 40 0.053
271
CLL021 Collagenous Colitis 36 0.053
272
HNS001 Hansen's Disease 30 0.053
273
MND006 Mondor Disease 20 0.053
274
MTC056 Mitochondrial Dna Depletion Syndrome 4a 45 0.053
275
MYC002 Mycobacterium Avium Complex Disease 52 0.053
276
CRN030 Coronary Stenosis 50 0.053
277
ALP008 Alopecia 56 0.053
278
P ESP024 Esophagitis 62 0.053
279
WTH001 Withdrawal Disorder 36 0.053
280
PST055 Postural Hypotension 36 0.053
281
BLS002 Blastomycosis 42 0.053
282
P ADN016 Adenocarcinoma 69 0.053
283
c CRN177 Coronary Heart Disease 7 21 0.053
284
CHR001 Churg-Strauss Syndrome 48 0.053
285
ADJ001 Adjustment Disorder 38 0.052
286
P RNL014 Renal Cell Carcinoma 80 0.052
287
HRY003 Hairy Cell Leukemia 56 0.052
288
P MYC008 Myocarditis 56 0.052
289
MNN017 Mononeuropathy 37 0.052
290
EPT020 Epithelioid Hemangioendothelioma 46 0.052
291
CRD137 Cardiogenic Shock 44 0.052
292
P APL001 Aplastic Anemia 74 0.052
293
P MYS033 Miyoshi Muscular Dystrophy 1 40 0.052
294
P MYS005 Myositis 57 0.052
295
HYP006 Hypertensive Heart Disease 49 0.052
296
P ESN007 Eosinophilia 61 0.051
297
TTH006 Tooth Disease 52 0.051
298
HYP189 Hypoadrenalism 39 0.051
299
BRN014 Bronchopneumonia 45 0.051
300
ART004 Aortic Atherosclerosis 46 0.051
301
SCH014 Schistosomiasis 59 0.051
302
CRP017 Carpal Tunnel Syndrome, Familial 44 0.051
303
P PRT013 Portal Hypertension 61 0.051
304
ATN001 Autonomic Peripheral Neuropathy 19 0.051
305
c HPT016 Hepatitis B 61 0.050
306
URM002 Uremia 36 0.050
307
PPL002 Papillary Carcinoma 50 0.050
308
SNG003 Single Ventricular Heart 23 0.050
309
VHW001 Vohwinkel Syndrome 47 0.050
310
MCR013 Microphthalmia 57 0.050
311
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.050
312
P PSD087 Pseudoxanthoma Elasticum 65 0.050
313
NSH001 Nasu-Hakola Disease 46 0.050
314
P SYP003 Syphilis 51 0.050
315
GST019 Gastrointestinal Stromal Tumor 73 0.050
316
P GST044 Gastritis 64 0.050
317
P INT070 Intestinal Obstruction 55 0.050
318
c ATM003 Autoimmune Thyroiditis 59 0.050
319
P CNN004 Connective Tissue Cancer 44 0.050
320
DST006 Diastolic Heart Failure 45 0.050
321
SLP005 Sleep Disorder 52 0.049
322
KRN002 Kearns-Sayre Syndrome 60 0.049
323
P NRM001 Neuromyelitis Optica 55 0.049
324
SNS001 Sensorineural Hearing Loss 52 0.049
325
CRY004 Cryoglobulinemia 47 0.049
326
KRT009 Keratosis 50 0.049
327
ISC002 Ischemic Optic Neuropathy 45 0.049
328
LPD004 Lipoid Nephrosis 49 0.048
329
c SPN225 Spondyloarthropathy 1 62 0.048
330
CHR012 Chronic Granulomatous Disease 66 0.048
331
P AML002 Amelogenesis Imperfecta 43 0.048
332
c CHN065 Choanal Atresia, Posterior 15 0.048
333
PST086 Posterior Cortical Atrophy 33 0.048
334
ATM021 Autoimmune Inner Ear Disease 20 0.048
335
ADL086 Adolescent Idiopathic Scoliosis 36 0.048
336
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 33 0.047
337
P MYL005 Myelofibrosis 67 0.047
338
P ALP009 Alopecia Areata 62 0.047
339
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 0.047
340
P ICH001 Ichthyosis Vulgaris 44 0.047
341
ACQ017 Acquired Von Willebrand Syndrome 35 0.047
342
CRY008 Cryopyrin-Associated Periodic Syndrome 31 0.047
343
SPN119 Spondylarthropathy 46 0.047
344
SPP004 Suppurative Cholangitis 35 0.047
345
INS024 Insulin-Like Growth Factor I 75 0.047
346
OVR029 Ovarian Hyperstimulation Syndrome 59 0.047
347
GNG013 Gingivitis 61 0.047
348
P PLY014 Polycystic Kidney Disease 60 0.047
349
P PRG013 Paraganglioma 54 0.047
350
P CRB059 Cerebellar Degeneration 30 0.047
351
17B002 17-Beta-Hydroxysteroid Dehydrogenase X Deficiency 32 0.046
352
ANC002 Anca-Associated Vasculitis 43 0.046
353
CYS001 Cystic Fibrosis 87 0.046
354
c CHR090 Chronic Lymphocytic Leukemia 73 0.046
355
c AFB002 Afibrinogenemia, Congenital 51 0.046
356
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 59 0.046
357
GRF001 Graft-Versus-Host Disease, Protection Against 54 0.046
358
P PLM006 Pulmonary Alveolar Proteinosis 46 0.046
359
GRN017 Granulocytopenia 39 0.046
360
LNG024 Langerhans-Cell Histiocytosis 64 0.046
361
WHP001 Whipple Disease 49 0.046
362
ACD009 Acid-Labile Subunit, Deficiency of 37 0.046
363
LMY002 Leiomyoma 56 0.046
364
CLC006 Calcinosis 48 0.046
365
CHR286 Chronic Neutrophilic Leukemia 44 0.046
366
ATR057 Atrioventricular Block 49 0.046
367
c CHR417 Chronic Graft Versus Host Disease 50 0.046
368
P LMY004 Leiomyosarcoma 54 0.046
369
P THY023 Thymoma 57 0.046
370
KRT008 Keratopathy 49 0.046
371
CLN006 Colonic Pseudo-Obstruction 36 0.046
372
ANG054 Angina Pectoris 48 0.046
373
ANX002 Anxiety Disorder 67 0.045
374
SPC010 Speech and Communication Disorders 42 0.045
375
CRN031 Cranial Nerve Disease 39 0.045
376
c CRN174 Coronary Heart Disease 2 19 0.045
377
ADL002 Adult Syndrome 53 0.045
378
CRN017 Coronary Thrombosis 46 0.044
379
INC022 Inclusion-Cell Disease 46 0.044
380
HDG012 Hodgkin Lymphoma 75 0.044
381
GLN010 Glanzmann Thrombasthenia 64 0.044
382
PSR001 Psoriatic Arthritis 64 0.044
383
GST050 Gastrointestinal System Disease 58 0.044
384
SNS003 Sensory Peripheral Neuropathy 44 0.044
385
CLL003 Cellulitis 49 0.044
386
PRG009 Progressive Multifocal Leukoencephalopathy 52 0.044
387
RSD004 Rosai-Dorfman Disease 40 0.044
388
RTC005 Reticulosarcoma 46 0.044
389
FMR003 Femoral Neuropathy 34 0.044
390
PNM003 Pneumatosis Cystoides Intestinalis 32 0.044
391
HMN016 Hemangioendothelioma 40 0.044
392
THR035 Thrombasthenia 41 0.044
393
KWS002 Kawasaki Disease 70 0.044
394
LPM004 Lipoma 59 0.044
395
GLC003 Glucose Intolerance 56 0.044
396
c SCN036 Secondary Progressive Multiple Sclerosis 50 0.044
397
P DYS021 Dysautonomia 47 0.044
398
SPN060 Spondylocarpotarsal Synostosis Syndrome 38 0.043
399
SCT005 Scott Syndrome 51 0.043
400
MRT007 Martsolf Syndrome 39 0.043
401
FLS001 Fils Syndrome 28 0.043
402
ANT039 Antisynthetase Syndrome 36 0.043
403
LYM004 Lymphoid Interstitial Pneumonia 40 0.043
404
KDS001 Kid Syndrome 53 0.042
405
c EPL070 Epilepsy, Progressive Myoclonic 2b 53 0.042
406
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.042
407
PTY003 Pityriasis Rubra Pilaris 46 0.042
408
ALV010 Alveolar Soft-Part Sarcoma 53 0.042
409
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.042
410
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 36 0.042
411
END031 Endometrial Stromal Sarcoma 49 0.042
412
TRY001 Trypanosomiasis 51 0.042
413
ATY005 Atypical Teratoid Rhabdoid Tumor 47 0.042
414
NRT004 Neuritis 52 0.042
415
FXP001 Foxp2-Related Speech and Language Disorders 15 0.042
416
OTP003 Oto-Palatal-Digital Syndrome 14 0.042
417
c BNG076 Benign Exophthalmos Syndrome 15 0.042
418
P MYS003 Myasthenia Gravis 64 0.042
419
HYP121 Hypoalphalipoproteinemia 61 0.042
420
KRT010 Kartagener Syndrome 48 0.042
421
c ATM011 Autoimmune Hepatitis 62 0.042
422
P PRM006 Primary Biliary Cirrhosis 55 0.042
423
MMB001 Membranoproliferative Glomerulonephritis 44 0.042
424
ANR004 Anuria 46 0.042
425
P CTN015 Cutaneous T Cell Lymphoma 41 0.042
426
C5D001 C5 Deficiency 33 0.042
427
PTT006 Pituitary Adenoma 54 0.042
428
SPL006 Splenic Infarction 32 0.042
429
JNT002 Joint Disorders 55 0.042
430
NCR009 Necrobiotic Xanthogranuloma 23 0.042
431
MLT006 Multidrug-Resistant Tuberculosis 46 0.042
432
ABD004 Abdominal Tuberculosis 37 0.042
433
c ACT076 Acute Myocarditis 40 0.042
434
DBT002 Diabetic Autonomic Neuropathy 37 0.042
435
c INV001 Invasive Aspergillosis 44 0.042
436
CHL071 Child Syndrome 58 0.041
437
RDN001 Reading Disorder 39 0.041
438
c MCR129 Microvascular Complications of Diabetes 1 55 0.040
439
LYM017 Lyme Disease 64 0.040
440
SPT005 Spotted Fever 56 0.040
441
c PLY059 Polycystic Kidney Disease, Adult Type I 36 0.040
442
P INT068 Intestinal Disease 60 0.040
443
P AFB001 Afibrinogenemia 38 0.040
444
c INF067 Inflammatory Bowel Disease 10 31 0.040
445
RTC009 Reticulum Cell Sarcoma 46 0.040
446
FSC004 Fasciitis 47 0.040
447
P CHR102 Charcot-Marie-Tooth Neuropathy 43 0.040
448
P LPS002 Liposarcoma 50 0.040
449
P TRN034 Transverse Myelitis 43 0.040
450
KRT002 Keratomalacia 50 0.040
451
P WLD002 Waldenstrom Macroglobulinemia 62 0.040
452
HRD059 Hereditary Peripheral Nervous Disorder 12 0.040
453
P INF038 Influenza 71 0.040
454
GNR004 Generalized Anxiety Disorder 49 0.040
455
c EHL057 Ehlers-Danlos Syndrome, Type Iv 59 0.039
456
P LYM007 Lymphangioleiomyomatosis 65 0.039
457
PHR003 Pharyngitis 58 0.039
458
P LYM025 Lymphedema 60 0.039
459
HMR002 Hemarthrosis 47 0.039
460
SCH002 Schnitzler Syndrome 47 0.039
461
INT002 Intermittent Claudication 56 0.039
462
DND002 Dendritic Cell Sarcoma 44 0.039
463
c SBC007 Subacute Thyroiditis 42 0.039
464
FLL013 Follicular Dendritic Cell Sarcoma 36 0.039
465
ISC015 Ischemic Colitis 38 0.039
466
PRS025 Presbyopia 33 0.039
467
c HRD088 Hereditary Neuropathies 35 0.039
468
P TRC072 Treacher Collins Syndrome 1 50 0.039
469
THY103 Thyroid Cancer, Monmedullary, 1 55 0.039
470
HMM002 Haim-Munk Syndrome 33 0.039
471
P CNG015 Congenital Diaphragmatic Hernia 58 0.039
472
CHR063 Chronic Mucocutaneous Candidiasis 61 0.039
473
CHG001 Chagas Disease 62 0.039
474
STR037 Stress Cardiomyopathy 37 0.039
475
c JVN003 Juvenile Xanthogranuloma 41 0.039
476
P HYP071 Hypersensitivity Reaction Type Ii Disease 46 0.039
477
P UVT001 Uveitis 60 0.039
478
P HMN013 Hemangiopericytoma 52 0.039
479
MYX001 Myxopapillary Ependymoma 41 0.039
480
PRC010 Pericardial Mesothelioma 37 0.039
481
PRC014 Pericardium Cancer 31 0.039
482
P GLM006 Glomangioma 37 0.039
483
EPT011 Epithelioid Leiomyosarcoma 39 0.039
484
GLB003 Globe Disease 34 0.038
485
HPT023 Hepatocellular Carcinoma 90 0.037
486
MTH009 Mouth Disease 63 0.037
487
SLP001 Sleeping Sickness 48 0.037
488
NWC001 Newcastle Disease 51 0.037
489
P OVR042 Ovarian Cancer 73 0.036
490
HYP291 Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia 40 0.036
491
IMP005 Impotence 49 0.036
492
P BRN009 Burning Mouth Syndrome 54 0.036
493
PLM001 Pulmonary Tuberculosis 69 0.036
494
c FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 28 0.036
495
HPT022 Hepatoblastoma 57 0.036
496
INF058 Inflammatory Myofibroblastic Tumor 47 0.036
497
RDC002 Radiculopathy 53 0.036
498
DPH021 Diaphragm Disease 45 0.036
499
P EPT012 Epithelioid Sarcoma 43 0.036
500
ANP006 Anaplastic Ependymoma 35 0.036
501
c PST005 Posterior Uveitis 46 0.036
502
c MLG133 Malignant Ectomesenchymoma 27 0.036
503
P ECT002 Ectomesenchymoma 35 0.036
504
P ATM020 Autoimmune Enteropathy 37 0.036
505
INC002 Inclusion Body Myositis 64 0.036
506
THY028 Thyroid Cancer 71 0.036
507
LKC001 Leukocyte Adhesion Deficiency 65 0.036
508
PLV005 Pelviureteric Junction Obstruction 43 0.036
509
ADR005 Adrenal Carcinoma 57 0.036
510
P INT143 Interstitial Cystitis 57 0.036
511
MRB003 Morbid Obesity 59 0.036
512
GST014 Gastrointestinal Lymphoma 31 0.036
513
P MWT001 Mowat-Wilson Syndrome 50 0.034
514
RSS002 Roussy-Levy Syndrome 51 0.034
515
UNV001 Unverricht-Lundborg Syndrome 41 0.034
516
P MDL022 Medullary Thyroid Carcinoma, Familial 62 0.034
517
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 37 0.034
518
CHL127 Cholangiocarcinoma, Susceptibility to 55 0.034
519
EYD002 Eye Disease 62 0.034
520
P ORL007 Oral Cavity Cancer 58 0.034
521
c PRG011 Progressive Myoclonus Epilepsy 41 0.034
522
CLR096 Ciliary Dyskinesia, Primary, 1, with or Without Situs Inversus 35 0.034
523
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 35 0.034
524
LYM104 Lymphoma, Malt, Somatic 44 0.034
525
CLN019 Colonic Disease 50 0.034
526
SPN331 Spondyloocular Syndrome 27 0.034
527
PST095 Post-Thrombotic Syndrome 48 0.034
528
LGP003 Logopenic Progressive Aphasia 21 0.034
529
PRG074 Progressive Myoclonus Epilepsy, Lafora Type 22 0.034
530
NDL007 Nodular Goiter 44 0.034
531
ALC006 Alcoholic Hepatitis 60 0.034
532
SCL013 Scleral Disease 35 0.034
533
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 32 0.034
534
LBL001 Lobular Neoplasia 48 0.034
535
RHM009 Rheumatoid Lung Disease 41 0.034
536
CTN012 Cutaneous Leiomyosarcoma 38 0.034
537
BNN003 Bone Inflammation Disease 46 0.034
538
P MYC026 Myoclonus Epilepsy 33 0.034
539
BRS099 Breast Ductal Carcinoma 51 0.034
540
c CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 36 0.034
541
ADN020 Adenosarcoma 37 0.034
542
P ATX010 Ataxia Neuropathy Spectrum 24 0.034
543
CRB006 Cribriform Carcinoma 42 0.034
544
P EPN001 Ependymoblastoma 38 0.034
545
ANG017 Angiolipoma 38 0.034
546
CHN001 Chondroid Lipoma 26 0.034
547
SPN017 Spindle Cell Liposarcoma 31 0.034
548
ERL016 Early-Onset Lafora Body Disease 12 0.034
549
c DYS033 Dysautonomia Like Disorder 18 0.034
550
c ART115 Aortic Valve Disease 1 53 0.034
551
P NTR004 Neutropenia 59 0.034
552
ACR002 Acrocapitofemoral Dysplasia 35 0.034
553
BND014 Bone Development Disease 40 0.034
554
P ADD001 Addison's Disease 60 0.032
555
HMT008 Hematuria, Benign Familial 44 0.032
556
CTS003 Coats Disease 57 0.032
557
ATM052 Autoimmune Disease 1 26 0.032
558
RNL078 Renal Dysplasia 48 0.032
559
c ALZ012 Alzheimer Disease 12 19 0.032
560
IMP003 Impaired Renal Function Disease 36 0.032
561
c AMY091 Amyotrophic Lateral Sclerosis 1 78 0.031
562
P URF003 Urofacial Syndrome 1 51 0.031
563
P SJG001 Sjogren's Syndrome 55 0.031
564
c SVR001 Severe Acute Respiratory Syndrome 56 0.031
565
P PLM036 Pulmonary Fibrosis 69 0.031
566
INT066 Interstitial Lung Disease 60 0.031
567
MTR078 Motor Neuropathy, Peripheral, with Dysautonomia 17 0.031
568
P CHR084 Chromosomal Disease 37 0.031
569
P PNM006 Pneumoconiosis 51 0.031
570
P ACQ009 Acquired Metabolic Disease 42 0.031
571
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 35 0.030
572
LYM019 Lymphosarcoma 52 0.030
573
SKN023 Skin Tag 48 0.030
574
P CLL015 Collagen Disease 49 0.030
575
CVT001 Cavitary Optic Disc Anomalies 25 0.030
576
ORL011 Oral Cancer 53 0.030
577
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 34 0.030
578
c ADL001 Adult Lymphoma 40 0.030
579
LYM024 Lymphatic System Disease 49 0.027
580
IRN002 Iron Metabolism Disease 38 0.027
581
MXD023 Mixed Cell Type Cancer 45 0.027
582
LYM023 Lymphatic System Cancer 35 0.027
583
P MSC007 Muscle Hypertrophy 55 0.024
584
GRM003 German Syndrome 24 0.024
585
ATM053 Autoimmune Disease 2 16 0.024
586
ATM054 Autoimmune Disease 3 16 0.024
587
c ALZ014 Alzheimer Disease 16 17 0.024
588
CRC034 Carcinoma Showing Thymus-Like Differentiation 21 0.024
589
ATM005 Autoimmune Disease of Musculoskeletal System 14 0.024
590
c FML303 Familial/multiple Cancer 15 0.024