Search results for "amyloidosis cerebral"

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

608 hits were found for 'amyloidosis cerebral'

# Family MCID Name MIFTS Score
1
CRB096 Cerebral Amyloid Angiopathy, Dutch, Italian, Iowa, Flemish, Arctic Variants 30 9.015
2
P CRB019 Cerebral Amyloid Angiopathy 58 8.479
3
DMN004 Dementia, Familial Danish 32 4.085
4
GRS011 Gerstmann-Straussler Disease 42 3.778
5
DMN032 Dementia, Familial British 36 3.657
6
c HRD084 Hereditary Cerebral Amyloid Angiopathy 15 2.928
7
CRB009 Cerebritis 38 1.092
8
P AMY004 Amyloidosis 64 0.981
9
CRB085 Cerebral Hemorrhage 43 0.276
10
ANR040 Aneurysm 57 0.260
11
SPS057 Spasticity 42 0.233
12
MLR004 Malaria 79 0.223
13
P ENC018 Encephalopathy 59 0.195
14
NRN002 Neuronitis 42 0.195
15
BRN071 Brain Injury 52 0.193
16
P LYM118 Lymphoma 70 0.185
17
P ART022 Arthritis 75 0.174
18
P HPT021 Hepatitis 70 0.167
19
DMN002 Dementia 64 0.166
20
STR067 Stroke, Ischemic 77 0.159
21
P NRP001 Neuropathy 60 0.156
22
P AMY084 Amyloidosis, Finnish Type 43 0.155
23
END072 Endotheliitis 42 0.154
24
P RHM011 Rheumatoid Arthritis 88 0.154
25
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.151
26
PRP027 Peripheral Vascular Disease 69 0.144
27
P CRD011 Cardiomyopathy 67 0.141
28
ATH003 Atherosclerosis 62 0.140
29
NTR005 Nutritional Deficiency Disease 39 0.138
30
P PLY019 Polyneuropathy 54 0.137
31
P AMY060 Amyloidosis, Primary Localized Cutaneous, 1 47 0.129
32
AMY002 Amyloid Tumor 37 0.129
33
CRB031 Cerebral Arterial Disease 31 0.128
34
FCT003 Factor X Deficiency 62 0.128
35
P HMR003 Hemorrhagic Disease 57 0.124
36
VSC006 Vascular Cancer 54 0.119
37
CDS001 Cadasil 50 0.115
38
CRD118 Cardiovascular Cancer 47 0.113
39
VSC008 Vascular Hemostatic Disease 33 0.113
40
P ALZ034 Alzheimer Disease 93 0.113
41
NRM005 Neuromuscular Disease 57 0.111
42
P BLD051 Blood Coagulation Disease 45 0.110
43
BLD054 Blood Protein Disease 40 0.108
44
VSC011 Vasculitis 62 0.108
45
P SPS003 Spastic Diplegia 53 0.107
46
GLC077 Glucocorticoid Therapy, Response to 19 0.107
47
P PRP019 Peripheral Nervous System Disease 54 0.106
48
LGH004 Light Chain Deposition Disease 42 0.106
49
P LKM002 Leukemia 70 0.106
50
ATN002 Autonomic Nervous System Disease 47 0.105
51
HDC001 Headache 54 0.100
52
P THY032 Thyroiditis 54 0.100
53
P HRT032 Heart Disease 76 0.099
54
P NRV007 Nervous System Disease 71 0.098
55
GRW007 Growth Hormone Deficiency 48 0.097
56
RTN023 Retinitis 49 0.097
57
P GLM007 Glomerulonephritis 56 0.097
58
PRP021 Peripheral Nervous System Neoplasm 50 0.097
59
P EPL164 Epilepsy 66 0.096
60
HMT018 Hematopoietic Stem Cell Transplantation 41 0.096
61
ATR060 Atrial Standstill, Digenic 53 0.095
62
PLS011 Plasmacytoma 56 0.095
63
GLT021 Glutaricaciduria, Type I 48 0.095
64
c INH020 Inherited Metabolic Disorder 49 0.094
65
PLS010 Plasma Protein Metabolism Disease 38 0.094
66
P MYP004 Myopathy 67 0.092
67
P NRV006 Nervous System Cancer 62 0.091
68
P LRY019 Laryngitis 55 0.089
69
CLT003 Colitis 59 0.088
70
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 38 0.088
71
PRT014 Protein S Deficiency 52 0.087
72
TBR010 Tuberculosis 69 0.087
73
BRT030 Birth Defects 43 0.087
74
ACR041 Acromelic Frontonasal Dysostosis 46 0.086
75
ATN003 Autonomic Nervous System Neoplasm 43 0.084
76
IMM127 Immune System Cancer 42 0.084
77
P CRN178 Coronary Heart Disease 6 24 0.084
78
MRC001 Marchiafava Bignami Disease 50 0.083
79
P DRR001 Diarrhea 51 0.083
80
P BCL006 B-Cell Lymphomas 64 0.082
81
MRG013 Mirage Syndrome 26 0.082
82
ALR002 Al-Raqad Syndrome 36 0.082
83
ATN004 Autonomic Neuropathy 44 0.081
84
PCK002 Pick Disease 67 0.081
85
P CRV039 Cervicitis 44 0.079
86
ULC004 Ulcerative Colitis 75 0.079
87
P LPS004 Lupus Erythematosus 63 0.078
88
P ATR011 Atrial Fibrillation 64 0.078
89
IMM025 Immunoglobulin a Deficiency 2 27 0.078
90
CNT010 Central Nervous System Hematologic Cancer 21 0.077
91
DFC004 Deficiency Anemia 65 0.077
92
PRT011 Protein C Deficiency 51 0.077
93
c CRN214 Coronary Heart Disease 5 23 0.075
94
P SDR002 Siderosis 44 0.075
95
FCT006 Factor V Deficiency 60 0.075
96
P PNM007 Pneumonia 66 0.074
97
CRN025 Corneal Dystrophy 41 0.074
98
CRH001 Crohn's Disease 76 0.074
99
P END033 Endocarditis 52 0.073
100
P PNC044 Pancreatitis 60 0.073
101
TNP003 Tn Polyagglutination Syndrome, Somatic 44 0.073
102
BNS002 Bone Structure Disease 36 0.073
103
c SYS001 Systemic Lupus Erythematosus 87 0.073
104
HRT007 Heart Cancer 50 0.072
105
HPT074 Hepatic Adenoma, Somatic 51 0.072
106
PRD011 Proud Syndrome 42 0.071
107
P CRN035 Cranial Nerve Palsy 43 0.071
108
SPR066 Superficial Siderosis 33 0.071
109
SPN051 Spondylitis 50 0.071
110
BLD053 Blood Platelet Disease 46 0.071
111
P ATX004 Ataxia 53 0.070
112
P HRT017 Heart Tumor 35 0.070
113
c ADL079 Adult Heart Tumor 19 0.070
114
P LVR013 Liver Disease 72 0.069
115
P MYC007 Myocardial Infarction 79 0.068
116
END030 End Stage Renal Failure 52 0.068
117
ALN001 Aland Island Eye Disease 45 0.068
118
AND005 Androgen Insensitivity Syndrome, Mild 16 0.068
119
P LTT001 Lattice Corneal Dystrophy 32 0.068
120
ART017 Aortic Disease 58 0.067
121
c THR092 Thrombophilia Due to Thrombin Defect 56 0.067
122
CRD119 Cardiac Arrest 63 0.067
123
INC021 Incontinentia Pigmenti 60 0.067
124
c ACT134 Acute Liver Failure 50 0.067
125
P DBT005 Diabetes Insipidus 53 0.067
126
SCK003 Sickle Cell Anemia 68 0.067
127
P PYL005 Pyelonephritis 52 0.067
128
PRT036 Peritonitis 62 0.066
129
GTR002 Goiter 54 0.066
130
HYP037 Hyperhomocysteinemia 50 0.066
131
P MSC005 Muscular Dystrophy 64 0.066
132
NRM002 Normal Pressure Hydrocephalus 50 0.065
133
PRP080 Peripheral Artery Disease 36 0.065
134
WLL006 Wells Syndrome 56 0.065
135
PHY002 Physical Disorder 44 0.064
136
VND001 Vein Disease 52 0.064
137
c CRN173 Coronary Heart Disease 8 20 0.064
138
XNT001 Xanthogranulomatous Pyelonephritis 30 0.064
139
P SNS014 Sinusitis 60 0.063
140
c CRN172 Coronary Heart Disease 3 21 0.063
141
P FML161 Familial Mediterranean Fever, Ar 63 0.063
142
CRN106 Corneal Dystrophy, Gelatinous Drop-Like 29 0.063
143
P OBS005 Obesity 93 0.062
144
IRN001 Iron Deficiency Anemia 51 0.062
145
RHM027 Rheumatic Disease 57 0.062
146
OCL009 Ocular Cancer 62 0.061
147
BNM001 Bone Marrow Cancer 52 0.061
148
BNC003 Bone Cancer 45 0.061
149
P ASP006 Aspergillosis 60 0.061
150
PRP030 Purpura 59 0.061
151
ADN018 Adenoma 59 0.060
152
ATN005 Autonomic Dysfunction 45 0.060
153
PRP016 Paraplegia 49 0.059
154
PRT019 Protein-Losing Enteropathy 41 0.059
155
c CRN176 Coronary Heart Disease 9 20 0.059
156
SPN186 Spinal Cord Injury 62 0.059
157
MTR014 Motor Neuron Disease 59 0.059
158
P LPR003 Leprosy 68 0.059
159
c NPH055 Nephrotic Syndrome, Type 1 59 0.059
160
c HYP073 Hypersensitivity Reaction Type Iv Disease 45 0.059
161
BCL002 B Cell Deficiency 50 0.058
162
c DLT001 Delta Chain Disease 16 0.058
163
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 42 0.058
164
P INF032 Infertility 61 0.058
165
DRM006 Dermatitis 61 0.058
166
SRC014 Sarcoma 66 0.058
167
P ADN016 Adenocarcinoma 69 0.058
168
P HYP086 Hypothyroidism 65 0.057
169
P ALX003 Alexander Disease 64 0.057
170
PMS001 Poems Syndrome 55 0.057
171
P INT063 Intellectual Disability 53 0.057
172
P TMP003 Temporal Arteritis 60 0.056
173
P CTS001 Cutis Laxa 59 0.056
174
P SCK002 Sick Sinus Syndrome 50 0.056
175
P RPD001 Rapidly Progressive Glomerulonephritis 44 0.056
176
P AGM001 Agammaglobulinemia 64 0.056
177
c CRN175 Coronary Heart Disease 4 21 0.056
178
PRD019 Periodic Fever, Familial 50 0.056
179
TBR011 Tuberculous Meningitis 46 0.056
180
DWN001 Down Syndrome 65 0.056
181
ADJ001 Adjustment Disorder 38 0.056
182
P PLM037 Pulmonary Hypertension 79 0.055
183
DSS009 Disseminated Intravascular Coagulation 51 0.055
184
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.055
185
c HPT001 Hepatitis C 68 0.055
186
ADL030 Adult-Onset Still's Disease 57 0.055
187
HRT012 Heart Valve Disease 41 0.055
188
KHL003 Kohlschutter-Tonz Syndrome 37 0.055
189
HYP056 Hypoglycemia 61 0.055
190
P LYM026 Lymphoblastic Leukemia 60 0.055
191
P PLY017 Polyarteritis Nodosa 55 0.054
192
CHR008 Choroiditis 43 0.054
193
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 34 0.054
194
CNG034 Congestive Heart Failure 71 0.053
195
CMM004 Common Variable Immunodeficiency 67 0.053
196
P KDN017 Kidney Cancer 67 0.053
197
CRN030 Coronary Stenosis 50 0.053
198
c DLT002 Dilated Cardiomyopathy 75 0.053
199
c CHR089 Chronic Kidney Failure 66 0.053
200
TRN018 Transitional Cell Carcinoma 54 0.053
201
MND006 Mondor Disease 21 0.053
202
WTH001 Withdrawal Disorder 41 0.053
203
HYD057 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 44 0.053
204
HNM002 Hinman Syndrome 25 0.052
205
c CRN177 Coronary Heart Disease 7 22 0.052
206
c ART101 Aortic Valve Disease 2 55 0.052
207
MNN009 Meningoencephalitis 45 0.052
208
LNG099 Lung Disease 62 0.051
209
SVN001 Sveinsson Choreoretinal Atrophy 26 0.051
210
FBR012 Fabry Disease 69 0.051
211
TXC002 Toxic Encephalopathy 51 0.051
212
P THR014 Thrombocytopenia 64 0.051
213
ISC006 Ischemic Heart Disease 68 0.051
214
c ACT210 Acute Respiratory Distress Syndrome 57 0.051
215
P CHL066 Cholangitis 49 0.050
216
MTR007 Motor Peripheral Neuropathy 43 0.050
217
GST039 Gastroduodenitis 31 0.050
218
CNN005 Connective Tissue Disease 61 0.050
219
HYP088 Hyper-Igd Syndrome 43 0.050
220
ATN001 Autonomic Peripheral Neuropathy 20 0.050
221
DSS008 Disease of Mental Health 55 0.050
222
SNG003 Single Ventricular Heart 24 0.050
223
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.050
224
P HYP083 Hypopituitarism 52 0.050
225
SYN036 Syncope 47 0.050
226
P CHR071 Charcot-Marie-Tooth Disease 66 0.049
227
P HST010 Histiocytosis 55 0.049
228
P ART023 Arthropathy 63 0.049
229
P LTR001 Lateral Sclerosis 52 0.049
230
P PHC003 Pheochromocytoma 71 0.048
231
P PRP029 Porphyria 58 0.048
232
SLP005 Sleep Disorder 53 0.048
233
ECH003 Echinococcosis 53 0.048
234
LPD004 Lipoid Nephrosis 48 0.048
235
CRN031 Cranial Nerve Disease 40 0.048
236
FCL012 Facial Paralysis 50 0.048
237
CST005 Castleman Disease 38 0.048
238
ERD001 Erdheim-Chester Disease 51 0.047
239
CHR001 Churg-Strauss Syndrome 49 0.047
240
MYC002 Mycobacterium Avium Complex Disease 51 0.047
241
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 0.047
242
17B002 17-Beta-Hydroxysteroid Dehydrogenase X Deficiency 34 0.047
243
GST053 Gastric Cancer 77 0.047
244
PRC013 Pericarditis 52 0.047
245
P PRT013 Portal Hypertension 59 0.047
246
PRS047 Prostatitis 56 0.047
247
P LYM033 Lymphoproliferative Syndrome 53 0.047
248
P PRD008 Periodontitis 46 0.047
249
LFT009 Left Ventricular Outflow Tract Obstruction 44 0.047
250
PRD007 Periodontal Disease 43 0.047
251
HNS001 Hansen's Disease 29 0.047
252
c HPT073 Hepatitis C Virus 72 0.047
253
P ESP024 Esophagitis 62 0.047
254
MCR088 Microscopic Polyangiitis 48 0.047
255
DDN006 Duodenitis 44 0.047
256
PST055 Postural Hypotension 37 0.047
257
RLP001 Relapsing Polychondritis 49 0.046
258
HMS001 Hemosiderosis 45 0.046
259
BLS002 Blastomycosis 42 0.046
260
P RNL014 Renal Cell Carcinoma 81 0.046
261
BRC012 Brucellosis 65 0.046
262
PRR002 Pure Red-Cell Aplasia 46 0.046
263
MNN017 Mononeuropathy 40 0.046
264
DMY004 Demyelinating Disease 55 0.045
265
SPC010 Speech and Communication Disorders 46 0.045
266
MYC033 Myoclonus 41 0.045
267
ARC002 Arachnoiditis 38 0.045
268
P APL001 Aplastic Anemia 73 0.045
269
P HYP076 Hyperthyroidism 56 0.045
270
ALP008 Alopecia 55 0.045
271
PPL002 Papillary Carcinoma 49 0.045
272
ACR007 Acromegaly 65 0.045
273
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.045
274
ADL002 Adult Syndrome 53 0.045
275
TTH006 Tooth Disease 52 0.045
276
ART004 Aortic Atherosclerosis 46 0.045
277
HYP189 Hypoadrenalism 40 0.045
278
MTC056 Mitochondrial Dna Depletion Syndrome 4a 43 0.044
279
P MYL005 Myelofibrosis 67 0.044
280
CRP017 Carpal Tunnel Syndrome, Familial 44 0.044
281
HRD059 Hereditary Peripheral Nervous Disorder 14 0.044
282
P ALG002 Alagille Syndrome 72 0.043
283
P PSD087 Pseudoxanthoma Elasticum 67 0.043
284
P NMN002 Niemann-Pick Disease 63 0.043
285
DFF005 Diffuse Large B-Cell Lymphoma 56 0.043
286
P MYS005 Myositis 56 0.043
287
P SYP003 Syphilis 53 0.043
288
HYP006 Hypertensive Heart Disease 50 0.043
289
NRM004 Neuroma 48 0.043
290
P ESN007 Eosinophilia 61 0.043
291
GST050 Gastrointestinal System Disease 54 0.043
292
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 44 0.043
293
c MCL062 Mucolipidosis Ii Alpha/beta 60 0.043
294
OST017 Osteomyelitis 59 0.043
295
DST006 Diastolic Heart Failure 46 0.043
296
P CNN004 Connective Tissue Cancer 45 0.043
297
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 39 0.043
298
RTR011 Retroperitoneal Fibrosis 38 0.043
299
CLL021 Collagenous Colitis 38 0.043
300
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.043
301
CRN017 Coronary Thrombosis 48 0.043
302
CHR005 Chorioamnionitis 48 0.043
303
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 76 0.042
304
c CRN174 Coronary Heart Disease 2 22 0.042
305
c HPT016 Hepatitis B 64 0.042
306
SNS001 Sensorineural Hearing Loss 57 0.042
307
URM002 Uremia 50 0.042
308
ACD009 Acid-Labile Subunit, Deficiency of 48 0.042
309
P DYS021 Dysautonomia 47 0.042
310
BRN014 Bronchopneumonia 45 0.042
311
CHR012 Chronic Granulomatous Disease 65 0.041
312
HRY003 Hairy Cell Leukemia 60 0.041
313
P DRM010 Dermatomyositis 58 0.041
314
c INF071 Inflammatory Bowel Disease 1 51 0.041
315
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 49 0.041
316
SNS003 Sensory Peripheral Neuropathy 47 0.041
317
CRD137 Cardiogenic Shock 46 0.041
318
GRN017 Granulocytopenia 42 0.041
319
P INF038 Influenza 74 0.041
320
CHL071 Child Syndrome 58 0.041
321
ALL026 Allergic Hypersensitivity Disease 53 0.041
322
KDS001 Kid Syndrome 53 0.041
323
CYT008 Cytomegalovirus Infection 51 0.041
324
MYL001 Myelitis 48 0.041
325
RDN001 Reading Disorder 39 0.041
326
INS024 Insulin-Like Growth Factor I 74 0.040
327
AND015 Androgen Insensitivity 63 0.040
328
OVR029 Ovarian Hyperstimulation Syndrome 60 0.040
329
c AFB002 Afibrinogenemia, Congenital 54 0.040
330
c CHR417 Chronic Graft Versus Host Disease 50 0.040
331
CRY004 Cryoglobulinemia 47 0.040
332
ISC002 Ischemic Optic Neuropathy 46 0.040
333
NSH001 Nasu-Hakola Disease 45 0.040
334
AMS002 Amish Infantile Epilepsy Syndrome 35 0.040
335
KRT004 Keratitis 70 0.040
336
P ALP009 Alopecia Areata 61 0.040
337
P GST044 Gastritis 58 0.040
338
ARS001 Aarskog-Scott Syndrome 52 0.040
339
P SCL009 Sclerosing Cholangitis 47 0.040
340
c HRD088 Hereditary Neuropathies 41 0.040
341
CRY008 Cryopyrin-Associated Periodic Syndrome 34 0.040
342
P NRM001 Neuromyelitis Optica 59 0.039
343
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.039
344
GNR004 Generalized Anxiety Disorder 51 0.039
345
MDL002 Medulloepithelioma 43 0.039
346
STR079 Sturge-Weber Syndrome, Somatic, Mosaic 40 0.039
347
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 37 0.039
348
CYS001 Cystic Fibrosis 86 0.039
349
c CHR090 Chronic Lymphocytic Leukemia 74 0.039
350
GST019 Gastrointestinal Stromal Tumor 72 0.039
351
P INT070 Intestinal Obstruction 56 0.039
352
P LMY004 Leiomyosarcoma 53 0.039
353
P PLM006 Pulmonary Alveolar Proteinosis 48 0.039
354
MGL016 Megaloblastic Anemia-1, Finnish Type 46 0.039
355
PLV005 Pelviureteric Junction Obstruction 45 0.039
356
DBT002 Diabetic Autonomic Neuropathy 42 0.039
357
GNG013 Gingivitis 60 0.038
358
KRT009 Keratosis 50 0.038
359
CLC006 Calcinosis 49 0.038
360
WHP001 Whipple Disease 48 0.038
361
UND005 Undifferentiated Pleomorphic Sarcoma 43 0.038
362
IMP003 Impaired Renal Function Disease 37 0.038
363
ADP007 Adie Pupil 34 0.038
364
P CRB059 Cerebellar Degeneration 32 0.038
365
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 31 0.038
366
KRN002 Kearns-Sayre Syndrome 59 0.038
367
MCR013 Microphthalmia 59 0.038
368
GLB003 Globe Disease 35 0.038
369
P MCR129 Microvascular Complications of Diabetes 1 57 0.037
370
c VRL007 Viral Encephalitis 54 0.037
371
NWC001 Newcastle Disease 54 0.037
372
LMB062 Limb Ischemia 48 0.037
373
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.037
374
HDG012 Hodgkin Lymphoma 73 0.036
375
P MYC008 Myocarditis 54 0.036
376
ANG054 Angina Pectoris 51 0.036
377
PRG009 Progressive Multifocal Leukoencephalopathy 50 0.036
378
P CLL015 Collagen Disease 49 0.036
379
ATR057 Atrioventricular Block 49 0.036
380
CLL003 Cellulitis 49 0.036
381
RTC005 Reticulosarcoma 48 0.036
382
NTR003 Natural Killer Cell Leukemia 47 0.036
383
KRT008 Keratopathy 46 0.036
384
EPT020 Epithelioid Hemangioendothelioma 45 0.036
385
CHR286 Chronic Neutrophilic Leukemia 44 0.036
386
P CHR102 Charcot-Marie-Tooth Neuropathy 43 0.036
387
P MYS033 Miyoshi Muscular Dystrophy 1 42 0.036
388
RSD004 Rosai-Dorfman Disease 39 0.036
389
HMN016 Hemangioendothelioma 38 0.036
390
SPL006 Splenic Infarction 35 0.036
391
ABD004 Abdominal Tuberculosis 34 0.036
392
CLN006 Colonic Pseudo-Obstruction 34 0.036
393
P WLD002 Waldenstrom Macroglobulinemia 62 0.036
394
ORL011 Oral Cancer 55 0.036
395
SPH001 Sapho Syndrome 44 0.036
396
P ICH001 Ichthyosis Vulgaris 44 0.036
397
ANT039 Antisynthetase Syndrome 37 0.036
398
ACQ017 Acquired Von Willebrand Syndrome 36 0.036
399
SPP004 Suppurative Cholangitis 33 0.036
400
KWS002 Kawasaki Disease 70 0.035
401
ANG020 Angiosarcoma 52 0.035
402
SLP001 Sleeping Sickness 48 0.035
403
P AFB001 Afibrinogenemia 46 0.035
404
BND014 Bone Development Disease 42 0.035
405
ANC002 Anca-Associated Vasculitis 41 0.035
406
ACR002 Acrocapitofemoral Dysplasia 36 0.035
407
P MYS003 Myasthenia Gravis 65 0.034
408
PSR001 Psoriatic Arthritis 64 0.034
409
GLN010 Glanzmann Thrombasthenia 63 0.034
410
c SPN225 Spondyloarthropathy 1 63 0.034
411
c EHL057 Ehlers-Danlos Syndrome, Type Iv 60 0.034
412
c ATM011 Autoimmune Hepatitis 58 0.034
413
PHR003 Pharyngitis 58 0.034
414
ADR005 Adrenal Carcinoma 56 0.034
415
PTT006 Pituitary Adenoma 55 0.034
416
GRF001 Graft-Versus-Host Disease, Protection Against 54 0.034
417
P THY023 Thymoma 53 0.034
418
END035 Endocrine Gland Cancer 52 0.034
419
HYP291 Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia 52 0.034
420
P PRM006 Primary Biliary Cirrhosis 52 0.034
421
P CTN015 Cutaneous T Cell Lymphoma 50 0.034
422
KRT010 Kartagener Syndrome 48 0.034
423
c INV001 Invasive Aspergillosis 47 0.034
424
MLT006 Multidrug-Resistant Tuberculosis 46 0.034
425
ANR004 Anuria 46 0.034
426
P ANL018 Analbuminemia 46 0.034
427
MMB001 Membranoproliferative Glomerulonephritis 45 0.034
428
LMY002 Leiomyoma 42 0.034
429
c ACT076 Acute Myocarditis 42 0.034
430
THR035 Thrombasthenia 42 0.034
431
MRT007 Martsolf Syndrome 37 0.034
432
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 36 0.034
433
FMR003 Femoral Neuropathy 34 0.034
434
c SRC023 Sarcoidosis 2 33 0.034
435
C5D001 C5 Deficiency 33 0.034
436
PNM003 Pneumatosis Cystoides Intestinalis 31 0.034
437
NCR009 Necrobiotic Xanthogranuloma 22 0.034
438
c DYS033 Dysautonomia Like Disorder 19 0.034
439
HPT023 Hepatocellular Carcinoma 91 0.033
440
P INT068 Intestinal Disease 61 0.033
441
LPM004 Lipoma 58 0.033
442
c ART115 Aortic Valve Disease 1 53 0.033
443
ALV010 Alveolar Soft-Part Sarcoma 53 0.033
444
NRT004 Neuritis 52 0.033
445
TRY001 Trypanosomiasis 52 0.033
446
MSC072 Muscle Cancer 51 0.033
447
ATY005 Atypical Teratoid Rhabdoid Tumor 49 0.033
448
P TRN034 Transverse Myelitis 48 0.033
449
SKN023 Skin Tag 46 0.033
450
P ADD001 Addison's Disease 62 0.032
451
TXC005 Toxic Shock Syndrome 61 0.032
452
CTS003 Coats Disease 57 0.032
453
P HYP071 Hypersensitivity Reaction Type Ii Disease 51 0.032
454
c INF067 Inflammatory Bowel Disease 10 51 0.032
455
END031 Endometrial Stromal Sarcoma 49 0.032
456
FSC004 Fasciitis 46 0.032
457
DPH021 Diaphragm Disease 45 0.032
458
CRR007 Cirrhosis, Cryptogenic 44 0.032
459
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 31 0.032
460
ATM052 Autoimmune Disease 1 28 0.032
461
c ALZ012 Alzheimer Disease 12 25 0.032
462
c BNG076 Benign Exophthalmos Syndrome 14 0.032
463
THY028 Thyroid Cancer 68 0.030
464
P LYM007 Lymphangioleiomyomatosis 65 0.030
465
LKC001 Leukocyte Adhesion Deficiency 65 0.030
466
INC002 Inclusion Body Myositis 63 0.030
467
P LNG064 Lung Cancer Susceptibility 3 62 0.030
468
HYP121 Hypoalphalipoproteinemia 61 0.030
469
P LYM025 Lymphedema 61 0.030
470
MRB003 Morbid Obesity 58 0.030
471
P ORL007 Oral Cavity Cancer 58 0.030
472
P INT143 Interstitial Cystitis 57 0.030
473
NRP015 Neuropathy, Congenital Hypomyelinating 56 0.030
474
INT002 Intermittent Claudication 56 0.030
475
KRT002 Keratomalacia 54 0.030
476
RSS002 Roussy-Levy Syndrome 52 0.030
477
SCT005 Scott Syndrome 50 0.030
478
c CLL013 Cell Type Cancer 48 0.030
479
HMR002 Hemarthrosis 48 0.030
480
BNN003 Bone Inflammation Disease 46 0.030
481
FLL013 Follicular Dendritic Cell Sarcoma 41 0.030
482
ISC015 Ischemic Colitis 40 0.030
483
c SBC007 Subacute Thyroiditis 39 0.030
484
P CHR084 Chromosomal Disease 37 0.030
485
c CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 37 0.030
486
SKL001 Skeletal Tuberculosis 36 0.030
487
SPN060 Spondylocarpotarsal Synostosis Syndrome 35 0.030
488
PRS025 Presbyopia 35 0.030
489
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 32 0.030
490
GST014 Gastrointestinal Lymphoma 31 0.030
491
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 30 0.030
492
CML001 Cumulative Trauma Disorders 21 0.030
493
MTR078 Motor Neuropathy, Peripheral, with Dysautonomia 19 0.030
494
P OVR042 Ovarian Cancer 75 0.030
495
c GCH015 Gaucher Disease, Type I 66 0.030
496
LYM017 Lyme Disease 63 0.030
497
CHG001 Chagas Disease 62 0.030
498
CHR063 Chronic Mucocutaneous Candidiasis 61 0.030
499
P UVT001 Uveitis 59 0.030
500
P NTR004 Neutropenia 59 0.030
501
P CNG015 Congenital Diaphragmatic Hernia 58 0.030
502
PRG097 Paragangliomas 1, with or Without Deafness 58 0.030
503
JPN002 Japanese Encephalitis 54 0.030
504
c EPL070 Epilepsy, Progressive Myoclonic 2b 53 0.030
505
P ALT001 Alternating Hemiplegia of Childhood 52 0.030
506
NRL005 Neurilemmoma 51 0.030
507
P LPS002 Liposarcoma 50 0.030
508
c VRL012 Viral Meningitis 50 0.030
509
RTC009 Reticulum Cell Sarcoma 48 0.030
510
PTY003 Pityriasis Rubra Pilaris 46 0.030
511
RNL078 Renal Dysplasia 45 0.030
512
DRM013 Dermoid Cyst 43 0.030
513
P DYS026 Dysfibrinogenemia 41 0.030
514
CHN010 Chondroma 41 0.030
515
MYX001 Myxopapillary Ependymoma 40 0.030
516
c JVN003 Juvenile Xanthogranuloma 40 0.030
517
STR037 Stress Cardiomyopathy 36 0.030
518
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 35 0.030
519
PST086 Posterior Cortical Atrophy 35 0.030
520
ATM021 Autoimmune Inner Ear Disease 30 0.030
521
P ATX010 Ataxia Neuropathy Spectrum 28 0.030
522
FXP001 Foxp2-Related Speech and Language Disorders 15 0.030
523
ADN021 Adenomatous Polyposis Coli 76 0.027
524
P BRN009 Burning Mouth Syndrome 57 0.027
525
THY103 Thyroid Cancer, Monmedullary, 1 54 0.027
526
c MLG077 Malignant Peripheral Nerve Sheath Tumor 53 0.027
527
HPT022 Hepatoblastoma 53 0.027
528
P SJG001 Sjogren's Syndrome 53 0.027
529
RDC002 Radiculopathy 53 0.027
530
P TRC072 Treacher Collins Syndrome 1 52 0.027
531
IMP005 Impotence 50 0.027
532
CYS008 Cystic Echinococcosis 50 0.027
533
RHB001 Rhabdoid Cancer 48 0.027
534
INF058 Inflammatory Myofibroblastic Tumor 46 0.027
535
P MWT001 Mowat-Wilson Syndrome 46 0.027
536
c PST005 Posterior Uveitis 45 0.027
537
HMT008 Hematuria, Benign Familial 45 0.027
538
ACN018 Acne Inversa, Familial, 1 45 0.027
539
P PLY026 Polycystic Kidney Disease, Autosomal Dominant 45 0.027
540
IRN002 Iron Metabolism Disease 43 0.027
541
P EPT012 Epithelioid Sarcoma 42 0.027
542
ANP006 Anaplastic Ependymoma 41 0.027
543
EPT011 Epithelioid Leiomyosarcoma 39 0.027
544
P ATM020 Autoimmune Enteropathy 38 0.027
545
FRY001 Frey Syndrome 37 0.027
546
CHR466 Chronic Thromboembolic Pulmonary Hypertension 37 0.027
547
PRC010 Pericardial Mesothelioma 37 0.027
548
P ECT002 Ectomesenchymoma 35 0.027
549
CHN065 Choanal Atresia, Posterior 33 0.027
550
CVT001 Cavitary Optic Disc Anomalies 32 0.027
551
HMM002 Haim-Munk Syndrome 31 0.027
552
PRC014 Pericardium Cancer 30 0.027
553
ADL086 Adolescent Idiopathic Scoliosis 29 0.027
554
c MLG133 Malignant Ectomesenchymoma 27 0.027
555
LKM059 Leukemia, Megakaryoblastic, with or Without Down Syndrome, Somatic 26 0.027
556
c ALZ043 Alzheimer's Disease 15 21 0.027
557
c AMY091 Amyotrophic Lateral Sclerosis 1 78 0.024
558
P MDL022 Medullary Thyroid Carcinoma, Familial 63 0.024
559
EYD002 Eye Disease 63 0.024
560
P GST049 Gastrointestinal System Cancer 60 0.024
561
P MSC007 Muscle Hypertrophy 59 0.024
562
c RHM021 Rheumatoid Arthritis, Systemic Juvenile 58 0.024
563
c SVR001 Severe Acute Respiratory Syndrome 57 0.024
564
JNT002 Joint Disorders 56 0.024
565
CHL127 Cholangiocarcinoma, Susceptibility to 55 0.024
566
LYM104 Lymphoma, Malt, Somatic 54 0.024
567
BRS099 Breast Ductal Carcinoma 52 0.024
568
DCT002 Ductal Carcinoma in Situ 51 0.024
569
P PNM006 Pneumoconiosis 51 0.024
570
PST095 Post-Thrombotic Syndrome 50 0.024
571
ILT001 Ileitis 49 0.024
572
LBL001 Lobular Neoplasia 48 0.024
573
MXD023 Mixed Cell Type Cancer 47 0.024
574
P HMN036 Hemangiopericytoma, Malignant 44 0.024
575
CRB006 Cribriform Carcinoma 43 0.024
576
P EPN001 Ependymoblastoma 42 0.024
577
ANT018 Anthracosis 42 0.024
578
c EPL121 Epilepsy, Progressive Myoclonic 1a 42 0.024
579
P ACQ009 Acquired Metabolic Disease 41 0.024
580
c HYP072 Hypersensitivity Reaction Type Iii Disease 41 0.024
581
CLR096 Ciliary Dyskinesia, Primary, 1, with or Without Situs Inversus 40 0.024
582
UNV001 Unverricht-Lundborg Syndrome 40 0.024
583
RHM009 Rheumatoid Lung Disease 40 0.024
584
CTN012 Cutaneous Leiomyosarcoma 38 0.024
585
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 36 0.024
586
SCL013 Scleral Disease 35 0.024
587
LYM023 Lymphatic System Cancer 35 0.024
588
MYC026 Myoclonus Epilepsy 33 0.024
589
SYN008 Synovium Cancer 31 0.024
590
NSP003 Nasopharyngeal Disease 30 0.024
591
SPN017 Spindle Cell Liposarcoma 29 0.024
592
FLS001 Fils Syndrome 28 0.024
593
SPN331 Spondyloocular Syndrome 27 0.024
594
CHN001 Chondroid Lipoma 25 0.024
595
GRM003 German Syndrome 24 0.024
596
c ALZ014 Alzheimer Disease 16 23 0.024
597
HRD083 Hereditary Antithrombin Deficiency 22 0.024
598
PRG074 Progressive Myoclonus Epilepsy, Lafora Type 22 0.024
599
c THR110 Thrombocytopenia 6 22 0.024
600
CRC034 Carcinoma Showing Thymus-Like Differentiation 22 0.024
601
ATM053 Autoimmune Disease 2 19 0.024
602
ATM054 Autoimmune Disease 3 18 0.024
603
c FML303 Familial/multiple Cancer 16 0.024
604
ATM005 Autoimmune Disease of Musculoskeletal System 16 0.024
605
CMP052 Complication in Hemodialysis 16 0.024
606
LNR001 Leiner Disease 14 0.024
607
ERL016 Early-Onset Lafora Body Disease 12 0.024
608
IMM004 Immunoglobulin Beta Deficiency 11 0.024