Search results for memory impairment

827 hits were found for memory impairment

# Family MCID Name MIFTS Score
1
P ALZ034 Alzheimer Disease 95 0.400
2
DMN002 Dementia 68 0.370
3
AGN016 Aging 65 0.346
4
PSY004 Psychotic Disorder 72 0.247
5
P SCH015 Schizophrenia 71 0.246
6
P ENC018 Encephalopathy 58 0.233
7
P EPL164 Epilepsy 70 0.224
8
NRN002 Neuronitis 43 0.216
9
CRB009 Cerebritis 41 0.216
10
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 42 0.215
11
c CNT035 Central Nervous System Disease 65 0.211
12
ANX010 Anxiety 72 0.193
13
P NRV007 Nervous System Disease 75 0.183
14
P HPT021 Hepatitis 75 0.183
15
ISC004 Ischemia 66 0.175
16
P MLT020 Multiple Sclerosis 85 0.170
17
BRN071 Brain Injury 54 0.162
18
MNT002 Mental Depression 60 0.162
19
SMN008 Semantic Dementia 41 0.158
20
END072 Endotheliitis 46 0.156
21
TMP001 Temporal Lobe Epilepsy 54 0.153
22
RTR001 Retrograde Amnesia 40 0.146
23
P LKM002 Leukemia 75 0.142
24
P ATT013 Attention Deficit-Hyperactivity Disorder 67 0.140
25
VSC002 Vascular Dementia 58 0.138
26
P DBT009 Diabetes Mellitus 72 0.136
27
TRM010 Traumatic Brain Injury 54 0.135
28
P LVR013 Liver Disease 76 0.135
29
PST028 Post-Traumatic Stress Disorder 59 0.134
30
c BLD140 Blood Group, I System 37 0.134
31
TRN012 Transient Global Amnesia 40 0.129
32
P KDN018 Kidney Disease 69 0.129
33
P ART022 Arthritis 77 0.127
34
P SPC019 Specific Language Impairment 30 0.126
35
DYS182 Dysphasia, Familial Developmental 29 0.125
36
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.124
37
P DYS005 Dyslexia 39 0.123
38
P ATS364 Autism 70 0.123
39
URN009 Urinary System Disease 58 0.123
40
P PRS038 Personality Disorder 65 0.118
41
HYP266 Hypoxia 61 0.118
42
P LYM118 Lymphoma 71 0.117
43
P BRS047 Breast Cancer 100 0.117
44
FRN006 Frontotemporal Dementia 70 0.114
45
APH002 Aphasia 58 0.114
46
P ENC004 Encephalitis 66 0.113
47
CRB039 Cerebrovascular Disease 68 0.111
48
P RHM011 Rheumatoid Arthritis 91 0.106
49
P PRS013 Prosopagnosia 34 0.106
50
P PRK057 Parkinson Disease, Late-Onset 78 0.105
51
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.105
52
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.105
53
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.105
54
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.105
55
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.105
56
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.105
57
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.105
58
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.105
59
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.105
60
HDN002 Head Injury 48 0.104
61
c ATS007 Autism Spectrum Disorder 68 0.104
62
AST005 Asthma 83 0.103
63
P MYC084 Mycobacterium Tuberculosis 1 69 0.100
64
WLL001 Williams-Beuren Syndrome 63 0.100
65
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.099
66
c HPT003 Hepatitis a 63 0.099
67
MVM001 Movement Disease 40 0.099
68
ACQ007 Acquired Immunodeficiency Syndrome 65 0.098
69
c HPT001 Hepatitis C 73 0.098
70
ATM095 Autoimmune Disease 66 0.098
71
VRL011 Viral Infectious Disease 64 0.097
72
MDD011 Mood Disorder 64 0.097
73
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.096
74
P BPL003 Bipolar Disorder 61 0.096
75
BSL008 Basal Ganglia Disease 44 0.095
76
P LPS004 Lupus Erythematosus 69 0.094
77
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.094
78
c HPT016 Hepatitis B 68 0.094
79
P NRP001 Neuropathy 63 0.094
80
DWN001 Down Syndrome 70 0.094
81
c SYS001 Systemic Lupus Erythematosus 86 0.092
82
ANT019 Anterograde Amnesia 29 0.091
83
P MJR001 Major Depressive Disorder 70 0.091
84
P MNN013 Meningitis 71 0.091
85
ART140 Arteries, Anomalies of 51 0.090
86
HYP066 Hyperglycemia 64 0.090
87
SLP005 Sleep Disorder 59 0.090
88
ANS006 Anosognosia 27 0.090
89
FRN051 Frontotemporal Lobar Degeneration with Tdp43 Inclusions, Grn-Related 42 0.090
90
c HPT073 Hepatitis C Virus 73 0.088
91
CMM004 Common Variable Immunodeficiency 71 0.088
92
GLC008 Glucose Metabolism Disease 38 0.087
93
P INF038 Influenza 77 0.087
94
LRN003 Learning Disability 49 0.087
95
SPS003 Spastic Diplegia 55 0.086
96
TRN015 Transient Cerebral Ischemia 58 0.086
97
P AMY004 Amyloidosis 69 0.084
98
P GRF003 Graft-Versus-Host Disease 72 0.084
99
DMY004 Demyelinating Disease 58 0.082
100
P MYL006 Myeloid Leukemia 69 0.081
101
MLR004 Malaria 86 0.081
102
P HYP086 Hypothyroidism 62 0.081
103
P AGN002 Agnosia 61 0.081
104
SPC010 Speech and Communication Disorders 40 0.080
105
DVL001 Developmental Coordination Disorder 37 0.080
106
P CRB088 Cerebral Atrophy 38 0.079
107
MLN008 Melanoma 72 0.078
108
DRM006 Dermatitis 67 0.077
109
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.076
110
VCC001 Vaccinia 50 0.076
111
AMS001 Amusia 25 0.076
112
SPS057 Spasticity 41 0.075
113
P SLP006 Sleep Apnea 65 0.075
114
P FRG001 Fragile X Syndrome 69 0.075
115
P SZR006 Seizure Disorder 55 0.074
116
P THY032 Thyroiditis 56 0.074
117
LYM009 Lymphocytic Choriomeningitis 46 0.074
118
P PNM007 Pneumonia 70 0.074
119
IMM136 Immune System Disease 57 0.074
120
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.074
121
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.073
122
VSC007 Vascular Disease 71 0.073
123
ANR040 Aneurysm 61 0.073
124
c BLM008 Bulimia Nervosa 2 53 0.073
125
P PNC044 Pancreatitis 64 0.072
126
MCS002 Mucositis 61 0.072
127
WRN002 Wernicke-Korsakoff Syndrome 52 0.072
128
c CHR089 Chronic Kidney Failure 72 0.072
129
SCH011 Schizotypal Personality Disorder 36 0.072
130
PRS047 Prostatitis 59 0.071
131
P HRP006 Herpes Simplex 70 0.071
132
P ASP001 Asperger Syndrome 51 0.071
133
APN008 Apnea, Obstructive Sleep 67 0.071
134
P MYP006 Myopia 56 0.071
135
ALC007 Alcohol Dependence 65 0.070
136
END030 End Stage Renal Failure 59 0.070
137
OBS002 Obsessive-Compulsive Disorder 68 0.070
138
LNG099 Lung Disease 67 0.070
139
SCL003 Social Phobia 50 0.070
140
c LKM061 Leukemia, Acute Myeloid 81 0.069
141
DYS004 Dyscalculia 30 0.069
142
CRB037 Cerebral Palsy 70 0.069
143
LMB024 Limbic Encephalitis 42 0.069
144
P LYM026 Lymphoblastic Leukemia 66 0.068
145
TTN003 Tetanus 65 0.068
146
LYM027 Lymphopenia 56 0.068
147
FCL014 Focal Epilepsy 56 0.068
148
P DRM053 Dermatitis, Atopic 68 0.068
149
NRM005 Neuromuscular Disease 60 0.068
150
RLP002 Relapsing-Remitting Multiple Sclerosis 59 0.068
151
P INF032 Infertility 59 0.068
152
P MYP004 Myopathy 69 0.067
153
DMN031 Dementia, Lewy Body 66 0.067
154
c CHR417 Chronic Graft Versus Host Disease 65 0.067
155
BRN080 Brain Ischemia 45 0.067
156
APR001 Apraxia 52 0.066
157
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.066
158
RTN023 Retinitis 52 0.065
159
SCH012 Schizoaffective Disorder 51 0.065
160
GLB002 Glioblastoma 74 0.064
161
P HRT032 Heart Disease 80 0.064
162
HMT018 Hematopoietic Stem Cell Transplantation 58 0.063
163
P CHR345 Chronic Pain 52 0.063
164
P ART021 Arteriosclerosis 62 0.063
165
P TRM003 Tremor 54 0.063
166
P CRN018 Coronary Artery Anomaly 69 0.062
167
P LTR001 Lateral Sclerosis 58 0.061
168
MYL009 Myelodysplastic Syndrome 75 0.061
169
P PNC025 Panic Disorder 57 0.061
170
CYT008 Cytomegalovirus Infection 57 0.061
171
LVR012 Liver Cirrhosis 73 0.060
172
HPT019 Hepatic Encephalopathy 59 0.060
173
P LNG032 Lung Cancer 99 0.060
174
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 63 0.059
175
P HNT016 Huntington Disease 78 0.059
176
P PSR002 Psoriasis 65 0.059
177
CLT003 Colitis 63 0.059
178
P HYD006 Hydrocephalus 68 0.059
179
RDN001 Reading Disorder 36 0.059
180
P HPT023 Hepatocellular Carcinoma 94 0.058
181
CYS001 Cystic Fibrosis 85 0.058
182
P SPR120 Supranuclear Palsy, Progressive, 1 70 0.058
183
c BPL002 Bipolar I Disorder 50 0.058
184
P PRS040 Prostate Cancer 88 0.058
185
GNR004 Generalized Anxiety Disorder 53 0.057
186
RMS001 Rem Sleep Behavior Disorder 42 0.057
187
P FBR031 Febrile Seizures 52 0.057
188
LYM024 Lymphatic System Disease 45 0.057
189
ETN001 Eating Disorder 61 0.057
190
CNG034 Congestive Heart Failure 74 0.056
191
P CRN300 Coronary Heart Disease 1 57 0.056
192
NRL016 Neural Tube Defects 79 0.056
193
VSL003 Visual Agnosia 33 0.056
194
P BCL006 B-Cell Lymphomas 70 0.056
195
P SBS003 Substance Abuse 57 0.056
196
P MYC007 Myocardial Infarction 81 0.056
197
PRT037 Pertussis 70 0.056
198
DRG003 Drug Dependence 51 0.055
199
ACT084 Acute Stress Disorder 35 0.055
200
ISC006 Ischemic Heart Disease 73 0.055
201
P GLM045 Glioma 61 0.055
202
P FTL001 Fetal Alcohol Syndrome 59 0.055
203
c PNS012 Paine Syndrome 52 0.055
204
PST011 Pustulosis of Palm and Sole 47 0.055
205
CRH001 Crohn's Disease 80 0.055
206
BRD004 Borderline Personality Disorder 50 0.054
207
PCK003 Pick Disease of Brain 66 0.054
208
STR067 Stroke, Ischemic 84 0.054
209
P CRV039 Cervicitis 49 0.054
210
BRS051 Breast Disease 67 0.054
211
c HYP805 Hypercholesterolemia, Autosomal Dominant, 3 47 0.053
212
SKN016 Skin Disease 68 0.053
213
RHM027 Rheumatic Disease 62 0.053
214
HPD002 Hepadnavirus Infection 14 0.053
215
CRT072 Creutzfeldt-Jakob Disease 65 0.053
216
P CHR012 Chronic Granulomatous Disease 69 0.052
217
ANX004 Anoxia 49 0.052
218
ENT004 Enthesopathy 38 0.052
219
PRV006 Pervasive Developmental Disorder 56 0.052
220
PNM013 Pneumococcal Meningitis 40 0.052
221
P CTR002 Cataract 60 0.052
222
BRN028 Brain Cancer 72 0.052
223
GRS011 Gerstmann-Straussler Disease 48 0.052
224
c LKM071 Leukemia, Chronic Lymphocytic 75 0.051
225
SKN027 Skin Conditions 48 0.051
226
NRV006 Nervous System Cancer 61 0.051
227
INS024 Insulin-Like Growth Factor I 83 0.051
228
P TBR001 Tuberous Sclerosis 69 0.051
229
SRC014 Sarcoma 68 0.051
230
P MCR115 Microvascular Complications of Diabetes 5 66 0.051
231
P ALC004 Alcohol Abuse 63 0.051
232
c LKM004 Leukemia, B-Cell, Chronic 37 0.051
233
P RTT002 Rett Syndrome 82 0.050
234
LYM019 Lymphosarcoma 58 0.050
235
ALX002 Alexithymia 40 0.050
236
SML019 Smallpox 57 0.050
237
WLF001 Wolff-Parkinson-White Syndrome 57 0.050
238
AMN003 Amnestic Disorder 45 0.050
239
P ANG001 Angelman Syndrome 61 0.050
240
c CHR579 Chiari Malformation Type Ii 42 0.050
241
P GRM010 Germ Cells Tumors 37 0.050
242
SYN041 Synesthesia 25 0.050
243
LYM143 Lymphoma, Non-Hodgkin, Familial 71 0.050
244
c CNG006 Congenital Hypothyroidism 62 0.050
245
c ERL020 Early-Onset Schizophrenia 51 0.050
246
CRB090 Cerebral Hypoxia 47 0.050
247
P DYS154 Dystonia 61 0.049
248
CNN005 Connective Tissue Disease 65 0.049
249
CRT033 Corticobasal Degeneration 51 0.049
250
LSH001 Leishmaniasis 71 0.049
251
MSC033 Muscle Disorders 53 0.049
252
CCN001 Cocaine Dependence 52 0.049
253
SPC005 Speech Disorder 44 0.049
254
PLY082 Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy 40 0.049
255
MSC004 Muscle Tissue Disease 39 0.049
256
P KLZ004 Kala-Azar 1 31 0.049
257
ACR006 Aceruloplasminemia 65 0.049
258
P CRG003 Crigler-Najjar Syndrome, Type I 62 0.049
259
DYS003 Dysgraphia 29 0.049
260
P ART023 Arthropathy 68 0.049
261
ALL026 Allergic Hypersensitivity Disease 59 0.049
262
ACT118 Acute Non Lymphoblastic Leukemia 32 0.048
263
P FRD012 Friedreich Ataxia 1 58 0.048
264
GST053 Gastric Cancer 84 0.048
265
NRF026 Neurofibromatosis, Type Iv, of Riccardi 72 0.048
266
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 55 0.048
267
P CLL015 Collagen Disease 53 0.048
268
VTM002 Vitamin B12 Deficiency 46 0.048
269
HMN044 Human Immunodeficiency Virus Type 1 71 0.047
270
PST086 Posterior Cortical Atrophy 38 0.047
271
MYL069 Myeloma, Multiple 86 0.047
272
c ACT135 Acute Graft Versus Host Disease 57 0.047
273
c FTL006 Fetal Alcohol Spectrum Disorder 48 0.047
274
ANT011 Antisocial Personality Disorder 51 0.047
275
LYM067 Lymphoid Leukemia 43 0.047
276
CHL068 Cholestasis 60 0.046
277
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.046
278
THR024 Thrombosis 61 0.046
279
P PLY019 Polyneuropathy 58 0.046
280
P HRP009 Herpes Simplex Encephalitis 50 0.045
281
JPN002 Japanese Encephalitis 59 0.045
282
P CLR023 Colorectal Cancer 98 0.045
283
P OVR042 Ovarian Cancer 82 0.045
284
CNN003 Conn's Syndrome 70 0.044
285
CRB172 Cerebral Amyloid Angiopathy, Cst3-Related 58 0.044
286
CHR066 Chronic Fatigue Syndrome 67 0.044
287
P NRM001 Neuromyelitis Optica 67 0.044
288
RSP006 Respiratory System Disease 63 0.044
289
CRT016 Carotid Artery Disease 58 0.044
290
BNF002 Bone Fracture 56 0.044
291
PRV004 Periventricular Leukomalacia 53 0.044
292
LKM006 Leukomalacia 46 0.044
293
MYL020 Myelomeningocele 54 0.044
294
RMN001 Rumination Disorder 39 0.044
295
MSL004 Mesial Temporal Lobe Epilepsy with Hippocampal Sclerosis 18 0.044
296
ALL006 Allergic Asthma 60 0.044
297
CHL014 Cholera 56 0.044
298
CHL061 Childhood Leukemia 50 0.044
299
PRN009 Paranoid Schizophrenia 49 0.044
300
SPS019 Spastic Paraparesis 33 0.044
301
ATN004 Autonomic Neuropathy 46 0.044
302
c TBR025 Tuberous Sclerosis 1 63 0.043
303
P BLM007 Bulimia Nervosa 1 53 0.043
304
DPH001 Diphtheria 63 0.043
305
c SVR001 Severe Acute Respiratory Syndrome 58 0.043
306
AST054 Australia Antigen 26 0.043
307
BRN106 Burns 57 0.043
308
LKN001 Leukoencephalopathy with Vanishing White Matter 56 0.043
309
LYM133 Lymphoma, Hodgkin, Classic 78 0.043
310
P MDL005 Medulloblastoma 76 0.043
311
P NTR004 Neutropenia 60 0.043
312
JNT002 Joint Disorders 60 0.043
313
P ANT006 Antiphospholipid Syndrome 59 0.043
314
CRT015 Carotid Artery Occlusion 42 0.043
315
P ADN016 Adenocarcinoma 71 0.042
316
P ATR011 Atrial Fibrillation 68 0.042
317
c SML038 Small Cell Cancer of the Lung 67 0.042
318
P ACT074 Acute Lymphocytic Leukemia 61 0.042
319
P SDR002 Siderosis 48 0.042
320
TCL003 T Cell Deficiency 43 0.042
321
ENC039 Encephalopathy, Familial, with Neuroserpin Inclusion Bodies 42 0.042
322
SPR066 Superficial Siderosis 40 0.042
323
MXD001 Mixed Cerebral Palsy 20 0.042
324
c ESS001 Essential Tremor 58 0.042
325
CRB004 Cerebral Artery Occlusion 46 0.042
326
P THR014 Thrombocytopenia 65 0.042
327
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 54 0.041
328
SND002 Sneddon Syndrome 48 0.041
329
c SPN100 Spinocerebellar Ataxia 27 44 0.041
330
CRB086 Cerebral Aneurysms 42 0.041
331
ADP001 Adiposis Dolorosa 42 0.041
332
c SPS072 Spastic Ataxia 1, Autosomal Dominant 25 0.041
333
MSL001 Measles 64 0.041
334
DFF005 Diffuse Large B-Cell Lymphoma 64 0.041
335
STT001 Status Epilepticus 60 0.041
336
PRN023 Prion Disease 51 0.041
337
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 41 0.041
338
FRG010 Fragile X Tremor/ataxia Syndrome 34 0.041
339
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.041
340
P MCR010 Microcephaly 57 0.041
341
c BRN108 Branchiootic Syndrome 1 47 0.041
342
P TCL004 T-Cell Leukemia 50 0.041
343
WHP002 Whiplash 39 0.041
344
CLS047 Classic Progressive Supranuclear Palsy Syndrome 25 0.041
345
c SPC027 Specific Language Impairment 1 16 0.041
346
P TRN020 Turner Syndrome 69 0.041
347
P DBT005 Diabetes Insipidus 54 0.041
348
OST012 Osteoarthritis 88 0.040
349
P NNN008 Noonan Syndrome 1 77 0.040
350
SVR004 Severe Combined Immunodeficiency 71 0.040
351
VLC001 Velocardiofacial Syndrome 64 0.040
352
NRT004 Neuritis 55 0.040
353
P INF037 Inflammatory Bowel Disease 52 0.040
354
BDY001 Body Dysmorphic Disorder 43 0.040
355
CHR593 Chromosome 16p13.3 Deletion Syndrome, Proximal 60 0.040
356
c MTR002 Mitral Valve Insufficiency 46 0.040
357
INT074 Intracranial Arteriosclerosis 14 0.040
358
P MSC003 Muscular Atrophy 55 0.040
359
P EXN002 Exanthem 62 0.040
360
SBS004 Substance Dependence 51 0.040
361
EWN002 Ewing's Family of Tumors 49 0.040
362
c SPN312 Spinocerebellar Ataxia 14 43 0.040
363
P PRD008 Periodontitis 67 0.039
364
VSC011 Vasculitis 66 0.039
365
P LBR001 Leber Congenital Amaurosis 65 0.039
366
IRR002 Irritable Bowel Syndrome 63 0.039
367
MGR028 Migraine with or Without Aura 1 55 0.039
368
CHR008 Choroiditis 47 0.039
369
BHV002 Behavioral Variant of Frontotemporal Dementia 41 0.039
370
P RNG031 Ring Chromosome Y Syndrome 29 0.039
371
c SPC028 Specific Language Impairment 2 13 0.039
372
P PLM037 Pulmonary Hypertension 79 0.039
373
ADR007 Adrenoleukodystrophy 72 0.039
374
HDC001 Headache 55 0.039
375
GRW007 Growth Hormone Deficiency 52 0.039
376
P FLL037 Follicular Lymphoma 76 0.039
377
P CNJ013 Conjunctivitis 67 0.039
378
CND002 Conduct Disorder 54 0.039
379
LPD016 Lipoid Proteinosis of Urbach and Wiethe 54 0.039
380
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.039
381
APL001 Aplastic Anemia 74 0.038
382
CMB081 Combined Immunodeficiency, X-Linked 64 0.038
383
MTR014 Motor Neuron Disease 62 0.038
384
DBT010 Diabetic Neuropathy 60 0.038
385
PLM175 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 48 0.038
386
P ATX030 Ataxia-Telangiectasia 80 0.038
387
SQM006 Squamous Cell Carcinoma 74 0.038
388
P GLY013 Glycogen Storage Disease 61 0.038
389
GT001 Gout 60 0.038
390
SPS007 Spastic Cerebral Palsy 46 0.038
391
c LKM063 Leukemia, Chronic Myeloid 80 0.037
392
P CRV035 Cervical Cancer 72 0.037
393
WGN006 Wegener Granulomatosis 71 0.037
394
P AGM019 Agammaglobulinemia, X-Linked 69 0.037
395
P WLD002 Waldenstrom Macroglobulinemia 65 0.037
396
c LKM062 Leukemia, Acute Lymphoblastic 64 0.037
397
P HMP007 Hemophilia 61 0.037
398
PRP019 Peripheral Nervous System Disease 53 0.037
399
PTH002 Pathological Gambling 53 0.037
400
LND001 Landau-Kleffner Syndrome 35 0.037
401
P INT030 Intracranial Aneurysm 58 0.037
402
BCL010 B-Cell Expansion with Nfkb and T-Cell Anergy 54 0.037
403
c VRL007 Viral Encephalitis 53 0.037
404
AGR002 Agoraphobia 47 0.037
405
c ALZ056 Alzheimer Disease 3 41 0.037
406
GRN014 Grn-Related Frontotemporal Dementia 34 0.037
407
FRN013 Frontotemporal Dementia, Chromosome 3-Linked 33 0.037
408
IMM103 Immunodeficiency 37 17 0.037
409
BHC003 Behcet Syndrome 68 0.037
410
LYM017 Lyme Disease 68 0.037
411
HMP009 Haemophilus Influenzae 49 0.037
412
PRG033 Progressive Non-Fluent Aphasia 48 0.037
413
DYS009 Dysthymic Disorder 42 0.037
414
BNG009 Benign Epilepsy with Centrotemporal Spikes 39 0.037
415
HNS001 Hansen's Disease 31 0.037
416
c PRC016 Pre-Eclampsia 65 0.037
417
c LKM056 Leukemia, Chronic Lymphocytic 2 35 0.037
418
P ANR048 Aniridia 1 68 0.036
419
P PRD006 Prader-Willi Syndrome 66 0.036
420
CRT013 Carotid Stenosis 52 0.036
421
P RTN024 Retinoblastoma 76 0.036
422
P AGM001 Agammaglobulinemia 70 0.036
423
P NRF023 Neurofibromatosis, Type Ii 69 0.036
424
MYL031 Myeloproliferative Neoplasm 64 0.036
425
GLC006 Galactosemia 64 0.036
426
PTT009 Pituitary Gland Disease 56 0.036
427
HYP458 Hyper Ige Syndrome 46 0.036
428
MYX004 Myxedema 44 0.036
429
BRN018 Borna Disease 38 0.036
430
c TRC078 Trichohepatoenteric Syndrome 2 34 0.036
431
c PSD047 Pseudo-Turner Syndrome 15 0.036
432
PRK068 Prkar1b-Related Neurodegenerative Dementia with Intermediate Filaments 13 0.036
433
P OST002 Osteoporosis 75 0.035
434
P LNG028 Long Qt Syndrome 63 0.035
435
c SCL052 Scleroderma, Familial Progressive 60 0.035
436
P ECL001 Eclampsia 57 0.035
437
P CRB059 Cerebellar Degeneration 40 0.035
438
CGN007 Cognitive Function 1, Social 27 0.035
439
IMM174 Immunodeficiency with Hyper-Igm, Type 1 64 0.035
440
P ESN008 Eosinophilic Pneumonia 55 0.035
441
PLR008 Pleurisy 52 0.035
442
CRY004 Cryoglobulinemia 49 0.035
443
P HYP263 Hypersomnia 45 0.035
444
CRB142 Cerebellar Ataxia, Deafness, and Narcolepsy, Autosomal Dominant 33 0.035
445
CHL123 Chlamydia 64 0.035
446
P GLM007 Glomerulonephritis 61 0.035
447
P CHL002 Childhood Absence Epilepsy 56 0.035
448
SCK005 Sickle Cell Disease 54 0.035
449
P PNB001 Pineoblastoma 51 0.035
450
OPP004 Oppositional Defiant Disorder 47 0.035
451
c HYP768 Hyperlipoproteinemia, Type I 44 0.035
452
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 40 0.035
453
SCR011 Scrapie 40 0.035
454
c NRP041 Neuropathy, Hereditary Sensory, Type Ie 40 0.035
455
P WSK001 Wiskott-Aldrich Syndrome 76 0.035
456
c MNN043 Meningioma, Familial 69 0.035
457
P MCP040 Mucopolysaccharidosis-Plus Syndrome 61 0.035
458
P LPR021 Leprosy 3 59 0.035
459
P HYP607 Hypercholesterolemia, Familial 81 0.034
460
P MTC003 Metachromatic Leukodystrophy 72 0.034
461
KRT019 Keratitis, Hereditary 62 0.034
462
CFF002 Coffin-Lowry Syndrome 58 0.034
463
P HYP024 Hypoparathyroidism 55 0.034
464
c HMP029 Hemophilia a 69 0.034
465
c MLG068 Malignant Glioma 66 0.034
466
P DRR001 Diarrhea 60 0.034
467
HRY003 Hairy Cell Leukemia 60 0.034
468
c CRP023 Carpenter Syndrome 1 57 0.034
469
BRN004 Brain Edema 57 0.034
470
TCK001 Tick-Borne Encephalitis 55 0.034
471
P OTS001 Otosclerosis 53 0.034
472
c SPS147 Spastic Paraplegia 4, Autosomal Dominant 48 0.034
473
CHR105 Choreoacanthocytosis 46 0.034
474
CNV002 Conversion Disorder 42 0.034
475
FXF002 Fox-Fordyce Disease 40 0.034
476
CRB193 Cerebral Amyloid Angiopathy, App-Related 36 0.034
477
c ALZ057 Alzheimer Disease 10 21 0.034
478
c BSL039 Basal Ganglia Calcification, Idiopathic, 6 20 0.034
479
ALP089 Alopecia, Psychomotor Epilepsy, Pyorrhea, and Mental Subnormality 20 0.034
480
BRC012 Brucellosis 71 0.033
481
CTN007 Cutaneous Leishmaniasis 66 0.033
482
GLL008 Gilles De La Tourette Syndrome 64 0.033
483
BLL006 Bullous Pemphigoid 64 0.033
484
P UVT001 Uveitis 61 0.033
485
TRP002 Tropical Spastic Paraparesis 58 0.033
486
KLN009 Kleine-Levin Hibernation Syndrome 48 0.033
487
EPL073 Epilepsy, Nocturnal Frontal Lobe, 1 47 0.033
488
KLV001 Kluver-Bucy Syndrome 41 0.033
489
MYL057 Myelopathy, Htlv-1-Associated 38 0.033
490
DPR002 Depersonalization Disorder 38 0.033
491
FRN030 Frontotemporal Dementia with Parkinsonism-17 22 0.033
492
PRM153 Primary Progressive Apraxia of Speech 21 0.033
493
HND015 Hand Skill, Relative 19 0.033
494
HRP008 Herpes Simiae 16 0.033
495
P MYL005 Myelofibrosis 75 0.033
496
P THL005 Thalassemia 65 0.033
497
ADN018 Adenoma 63 0.033
498
c PRM005 Primary Hyperparathyroidism 59 0.033
499
LPD008 Lipid Metabolism Disorder 59 0.033
500
c BCT007 Bacterial Meningitis 59 0.033
501
OST062 Osteoarthritis with Mild Chondrodysplasia 43 0.033
502
SCK003 Sickle Cell Anemia 73 0.032
503
CHG001 Chagas Disease 72 0.032
504
CST001 Costello Syndrome 67 0.032
505
P SNS014 Sinusitis 62 0.032
506
c EPL209 Epilepsy, Idiopathic Generalized 10 55 0.032
507
P SYP003 Syphilis 55 0.032
508
OPT003 Opiate Dependence 54 0.032
509
CHR001 Churg-Strauss Syndrome 51 0.032
510
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 50 0.032
511
PNC056 Pineocytoma 49 0.032
512
MDS022 Mediastinitis 44 0.032
513
BNS003 Binswanger's Disease 43 0.032
514
MTS001 Mutism 42 0.032
515
c ALC033 Alcohol Use Disorder 40 0.032
516
PPL050 Papillary Tumor of the Pineal Region 36 0.032
517
OBS060 Obesity Due to Sim1 Deficiency 12 0.032
518
MSC157 Muscular Dystrophy, Duchenne Type 74 0.032
519
PHN003 Phenylketonuria 73 0.032
520
P MYS003 Myasthenia Gravis 73 0.032
521
PLM001 Pulmonary Tuberculosis 72 0.032
522
CHD001 Chediak-Higashi Syndrome 67 0.032
523
RCK004 Rickets 63 0.032
524
SPN051 Spondylitis 55 0.032
525
P TRC086 Trichohepatoenteric Syndrome 1 54 0.032
526
SPN041 Spinal Cord Disease 54 0.032
527
HMS001 Hemosiderosis 50 0.032
528
DDN006 Duodenitis 46 0.032
529
ALX001 Alexia 44 0.032
530
ADS004 Aids Dementia Complex 42 0.032
531
INF009 Inflammatory Spondylopathy 32 0.032
532
MNS002 Mini Stroke 23 0.032
533
P CRN037 Craniosynostosis 68 0.031
534
LKD001 Leukodystrophy 57 0.031
535
OVR063 Overnutrition 53 0.031
536
INT075 Intracranial Hypertension 53 0.031
537
RFL001 Reflex Sympathetic Dystrophy 51 0.031
538
TRC010 Trichotillomania 46 0.031
539
ALG001 Algoneurodystrophy 39 0.031
540
c BLR024 Biliary Cirrhosis, Primary, 1 35 0.031
541
MNT001 Mantle Cell Lymphoma 76 0.030
542
GLB015 Glioblastoma Multiforme 68 0.030
543
HRP004 Herpes Zoster 61 0.030
544
PLS007 Plasmodium Falciparum Malaria 59 0.030
545
P ACT010 Acth-Secreting Pituitary Adenoma 58 0.030
546
PRS042 Prostate Disease 56 0.030
547
END040 Endogenous Depression 53 0.030
548
MYL001 Myelitis 52 0.030
549
FCL012 Facial Paralysis 50 0.030
550
P MRC003 Mercury Poisoning 50 0.030
551
IMM102 Immunodeficiency 14 49 0.030
552
PTT037 Pituitary Tumors 49 0.030
553
c BSL038 Basal Ganglia Calcification, Idiopathic, 1 47 0.030
554
PRS129 Prostatic Hyperplasia, Benign 47 0.030
555
P BLP003 Blepharospasm 46 0.030
556
SLR001 Sialuria 44 0.030
557
SCH003 Schizophreniform Disorder 44 0.030
558
CRV045 Cervical Intraepithelial Neoplasia 43 0.030
559
CLS049 Classic Phenylketonuria 43 0.030
560
IMM105 Immunodeficiency with Hyper-Igm, Type 3 42 0.030
561
c BNG023 Benign Familial Infantile Epilepsy 42 0.030
562
DLS001 Delusional Disorder 41 0.030
563
CRT012 Cortical Blindness 34 0.030
564
PTC005 Pituicytoma 28 0.030
565
WRN001 Werner Syndrome 70 0.030
566
P NJM001 Nijmegen Breakage Syndrome 69 0.030
567
P MPL001 Maple Syrup Urine Disease 66 0.030
568
P INT068 Intestinal Disease 65 0.030
569
P RHN004 Rhinitis 62 0.030
570
P SPN052 Spondyloarthropathy 61 0.030
571
P PTT006 Pituitary Adenoma 57 0.030
572
P PRM006 Primary Biliary Cirrhosis 55 0.030
573
HMG002 Hemoglobinuria 52 0.030
574
DBT004 Diabetic Polyneuropathy 51 0.030
575
NRM004 Neuroma 51 0.030
576
URT010 Ureteral Obstruction 49 0.030
577
CRB027 Cerebellar Disease 48 0.030
578
PLC008 Placenta Disease 48 0.030
579
AMB002 Amblyopia 45 0.030
580
CRV043 Cervical Dystonia 45 0.030
581
SNS008 Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis 40 0.030
582
c BTT014 Beta-Thalassemia 70 0.028
583
ALL003 Allergic Rhinitis 68 0.028
584
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 67 0.028
585
P ASP006 Aspergillosis 65 0.028
586
MTH009 Mouth Disease 64 0.028
587
P HML002 Hemolytic Anemia 62 0.028
588
MRB003 Morbid Obesity 61 0.028
589
VNW001 Von Willebrand's Disease 61 0.028
590
CHK001 Chikungunya 61 0.028
591
PRT038 Protein-Energy Malnutrition 52 0.028
592
TRN044 Transposition of the Great Arteries 49 0.028
593
BCK006 Back Pain 46 0.028
594
P AXN001 Axonal Neuropathy 38 0.028
595
MNG003 Mungan Syndrome 34 0.028
596
c MYS011 Myasthenia Gravis Congenital 28 0.028
597
THY028 Thyroid Cancer 72 0.028
598
CNT047 Contact Dermatitis 64 0.028
599
TNS005 Tonsillitis 61 0.028
600
ALL010 Allergic Contact Dermatitis 60 0.028
601
P PRT013 Portal Hypertension 59 0.028
602
BRN038 Bronchial Disease 58 0.028
603
c HPT007 Hepatitis E 57 0.028
604
P CNT005 Central Nervous System Lymphoma 57 0.028
605
PST021 Postpartum Depression 54 0.028
606
ADR013 Adrenal Gland Hyperfunction 54 0.028
607
c PRM226 Primary Central Nervous System Lymphoma 51 0.028
608
NSS002 Neisseria Meningitidis Infection 47 0.028
609
MNN032 Meningococcal Meningitis 45 0.028
610
URT001 Urethritis 44 0.028
611
CNN002 Cannabis Abuse 40 0.028
612
P BRN120 Bronchus Cancer 39 0.028
613
P HYP111 Hyperprolinemia 36 0.028
614
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 35 0.028
615
c EPL210 Epilepsy, Progressive Myoclonic, 6 24 0.028
616
c ALZ045 Alzheimer Disease 9 22 0.028
617
FML202 Familial Alzheimer-Like Prion Disease 12 0.028
618
DMN012 Dementia - Subcortical 10 0.028
619
INT031 Integrative Agnosia 10 0.028
620
HSH003 Hashimoto Thyroiditis 67 0.027
621
P AST007 Astrocytoma 66 0.027
622
PSR001 Psoriatic Arthritis 66 0.027
623
CRD119 Cardiac Arrest 63 0.027
624
DBT087 Diabetes Insipidus, Neurohypophyseal 62 0.027
625
CHR103 Charge Syndrome 59 0.027
626
PRC002 Paracoccidioidomycosis 59 0.027
627
P EPL140 Epilepsy, Idiopathic Generalized 58 0.027
628
WST005 West Nile Virus 58 0.027
629
IGR001 Ige Responsiveness, Atopic 56 0.027
630
P SCK002 Sick Sinus Syndrome 53 0.027
631
c SCN036 Secondary Progressive Multiple Sclerosis 52 0.027
632
WHM001 Whim Syndrome 52 0.027
633
c INV001 Invasive Aspergillosis 51 0.027
634
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 47 0.027
635
HYP085 Hypothalamic Disease 46 0.027
636
CRN031 Cranial Nerve Disease 45 0.027
637
IRN002 Iron Metabolism Disease 45 0.027
638
ASB001 Asbestosis 45 0.027
639
MLL002 Miller Fisher Syndrome 44 0.027
640
MNN042 Meningioma, Radiation-Induced 38 0.027
641
ATM052 Autoimmune Disease 1 30 0.027
642
IMM038 Immunodeficiency, Common Variable, 1 29 0.027
643
SPC022 Specific Antibody Deficiency 22 0.027
644
ASB003 Asbestos Intoxication 19 0.027
645
DVL005 Developmental Dyspraxia 19 0.027
646
P SYS005 Systemic Scleroderma 67 0.026
647
P CLC063 Celiac Disease 1 65 0.026
648
GNG013 Gingivitis 64 0.026
649
P CHR285 Chronic Myelomonocytic Leukemia 63 0.026
650
c ADL017 Adult T-Cell Leukemia 63 0.026
651
OST003 Osteonecrosis 63 0.026
652
DFC004 Deficiency Anemia 62 0.026
653
P LPS002 Liposarcoma 61 0.026
654
GNT003 Genital Herpes 58 0.026
655
P WRD001 Waardenburg's Syndrome 57 0.026
656
P LRY019 Laryngitis 57 0.026
657
CLN019 Colonic Disease 55 0.026
658
P LYM033 Lymphoproliferative Syndrome 55 0.026
659
SPP010 Suppressor of Tumorigenicity 3 55 0.026
660
TBC004 Tobacco Addiction 55 0.026
661
MCR004 Macroglobulinemia 54 0.026
662
HYP005 Hypokalemia 53 0.026
663
MTN003 Motion Sickness 52 0.026
664
P NGH001 Night Blindness 51 0.026
665
HMC014 Homocysteinemia 49 0.026
666
P SYR001 Syringomyelia 49 0.026
667
c SPN296 Spinocerebellar Ataxia 17 46 0.026
668
SYN036 Syncope 46 0.026
669
BLR008 Bilirubin Metabolic Disorder 45 0.026
670
NRS003 Neurosyphilis 44 0.026
671
HRN003 Heroin Dependence 43 0.026
672
SPN369 Spinal Disease 42 0.026
673
IMM184 Immunodeficiency 17 42 0.026
674
LBS001 Lubs X-Linked Mental Retardation Syndrome 41 0.026
675
MLN003 Melancholia 39 0.026
676
AGR018 Agraphia 38 0.026
677
c CTR122 Cataract 5, Multiple Types 38 0.026
678
c RBN017 Robinow Syndrome, Autosomal Dominant 2 37 0.026
679
c ATM083 Autoimmune Lymphoproliferative Syndrome, Type Iii 36 0.026
680
MTH047 Methanol Poisoning 32 0.026
681
CHL109 Childhood Apraxia of Speech 31 0.026
682
OBS015 Obesity, Hyperphagia, and Developmental Delay 31 0.026
683
CRN264 Craniosynostosis with Fibular Aplasia 29 0.026
684
SHR082 Short Stature, Microcephaly, and Endocrine Dysfunction 22 0.026
685
IMM074 Immunodeficiency 16 21 0.026
686
HYP767 Hyperlexia 21 0.026
687
c PRS058 Prosopagnosia, Hereditary 20 0.026
688
IMM076 Immunodeficiency 24 18 0.026
689
P AST055 Asthma-Related Traits 1 18 0.026
690
P LYN001 Lynch Syndrome 71 0.024
691
P CRD224 Cardiofaciocutaneous Syndrome 1 65 0.024
692
LPT001 Leptospirosis 64 0.024
693
SVR066 Severe Combined Immunodeficiency, X-Linked 63 0.024
694
P RBL001 Rubella 61 0.024
695
ORL011 Oral Cancer 60 0.024
696
ORL015 Oral Squamous Cell Carcinoma 59 0.024
697
SFT003 Soft Tissue Sarcoma 58 0.024
698
LYM040 Lymphoblastic Lymphoma 58 0.024
699
ERD001 Erdheim-Chester Disease 57 0.024
700
MRG003 Marginal Zone B-Cell Lymphoma 56 0.024
701
c FNC042 Fanconi Anemia, Complementation Group D2 56 0.024
702
GST009 Gastroschisis 55 0.024
703
FDL002 Food Allergy 55 0.024
704
IRN001 Iron Deficiency Anemia 55 0.024
705
PRG009 Progressive Multifocal Leukoencephalopathy 55 0.024
706
QDR001 Quadriplegia 54 0.024
707
LPR001 Lepromatous Leprosy 53 0.024
708
STM007 Stomatitis 52 0.024
709
ENT011 Enterocolitis 52 0.024
710
ADR012 Adrenal Gland Disease 51 0.024
711
RTC009 Reticulum Cell Sarcoma 51 0.024
712
CCN002 Cocaine Abuse 50 0.024
713
RTC005 Reticulosarcoma 49 0.024
714
HYP231 Hypothalamic Hamartomas 49 0.024
715
P PLM006 Pulmonary Alveolar Proteinosis 49 0.024
716
c LKM060 Leukemia, Acute Lymphoblastic 3 49 0.024
717
P NNT009 Neonatal Diabetes Mellitus 48 0.024
718
INT038 Interdigitating Dendritic Cell Sarcoma 46 0.024
719
P PTN014 Patent Ductus Arteriosus 1 45 0.024
720
NRN008 Neuronal Intranuclear Inclusion Disease 44 0.024
721
PNN005 Panencephalitis, Subacute Sclerosing 44 0.024
722
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 43 0.024
723
c PRG001 Progressive Muscular Atrophy 41 0.024
724
PRP056 Porphyria, Acute Hepatic 41 0.024
725
CRV002 Cervix Uteri Carcinoma in Situ 40 0.024
726
ATN011 Autoinflammation with Infantile Enterocolitis 39 0.024
727
RCT017 Rectal Disease 38 0.024
728
END014 Endemic Typhus 38 0.024
729
IMM003 Immunoglobulin Alpha Deficiency 37 0.024
730
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 36 0.024
731
FNT004 Fainting 36 0.024
732
CHL078 Childhood-Onset Schizophrenia 35 0.024
733
PDP001 Pedophilia 33 0.024
734
P CRB188 Cerebral Arteriopathy, Autosomal Recessive, with Subcortical Infarcts and Leukoencephalopathy 31 0.024
735
NRS005 Neurosarcoidosis 26 0.024
736
SPR032 Superficial Siderosis of the Central Nervous System 25 0.024
737
BTD002 Beta-Adrenergic Stimulation, Response to 17 0.024
738
IMM189 Immunodeficiency, Common Variable, 14 10 0.024
739
c JVN004 Juvenile Myelomonocytic Leukemia 70 0.021
740
OMN001 Omenn Syndrome 68 0.021
741
TYP007 Typhoid Fever 67 0.021
742
P THY023 Thymoma 65 0.021
743
NRF007 Neurofibroma 65 0.021
744
P HYP098 Hypereosinophilic Syndrome 65 0.021
745
ART005 Arteriovenous Malformation 64 0.021
746
c NRF024 Neurofibromatosis, Type I 63 0.021
747
CMM005 Common Cold 62 0.021
748
STF001 Stiff-Person Syndrome 61 0.021
749
P HMN010 Hemangioma 61 0.021
750
WVR001 Weaver Syndrome 61 0.021
751
P GLL022 Guillain-Barre Syndrome 61 0.021
752
CCC001 Coccidioidomycosis 60 0.021
753
NRN004 Neuroendocrine Tumor 58 0.021
754
AND002 Androgen Insensitivity Syndrome 57 0.021
755
c ANM038 Anemia, Autoimmune Hemolytic 56 0.021
756
PRN019 Perinatal Necrotizing Enterocolitis 56 0.021
757
PLS006 Plasmodium Vivax Malaria 56 0.021
758
TRY001 Trypanosomiasis 55 0.021
759
STR008 Strongyloidiasis 54 0.021
760
c MLG079 Malignant Pleural Mesothelioma 54 0.021
761
c CWD006 Cowden Syndrome 1 54 0.021
762
FND001 Fundus Albipunctatus 54 0.021
763
c CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 53 0.021
764
P TRT010 Teratoma 53 0.021
765
GLM004 Gliomatosis Cerebri 53 0.021
766
ACT103 Acute Lymphoblastic Leukemia, Childhood 53 0.021
767
P GLM040 Glioma Susceptibility 1 51 0.021
768
PYD002 Pyoderma 51 0.021
769
WHP001 Whipple Disease 50 0.021
770
NWC001 Newcastle Disease 50 0.021
771
P CRY007 Cryoglobulinemia, Familial Mixed 49 0.021
772
GRN017 Granulocytopenia 49 0.021
773
PRP036 Peripheral T-Cell Lymphoma 48 0.021
774
EXT033 Extrapulmonary Tuberculosis 48 0.021
775
SPN119 Spondylarthropathy 46 0.021
776
EPD070 Epidermoid Cysts 46 0.021
777
P PRL003 Proliferative Glomerulonephritis 45 0.021
778
c CRD182 Ceroid Lipofuscinosis, Neuronal, 10 44 0.021
779
BCL002 B Cell Deficiency 44 0.021
780
HRM002 Hermaphroditism 42 0.021
781
c ATM075 Autoimmune Encephalitis 40 0.021
782
P CYS017 Cystic Teratoma 40 0.021
783
CRV069 Cervix Disease 39 0.021
784
ANS016 Anosmia 38 0.021
785
BLT001 Bilateral Retinoblastoma 38 0.021
786
P TRN016 Transient Hypogammaglobulinemia 37 0.021
787
ATS011 Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 37 0.021
788
c TRN009 Transient Hypogammaglobulinemia of Infancy 36 0.021
789
NMN001 Nominal Aphasia 36 0.021
790
ENC005 Encephalomalacia 36 0.021
791
HYP003 Hypermethioninemia 35 0.021
792
PHT008 Photosensitive Epilepsy 35 0.021
793
FCL011 Facial Nerve Disease 35 0.021
794
ATY001 Atypical Depressive Disorder 34 0.021
795
c THY107 Thymoma, Familial 34 0.021
796
c BLP048 Blepharospasm, Benign Essential 33 0.021
797
c MGR032 Migraine, Familial Hemiplegic, 1 32 0.021
798
SBC014 Subclavian Steal Syndrome 31 0.021
799
FCL084 Facial Dysmorphism, Immunodeficiency, Livedo, and Short Stature 30 0.021
800
IMM179 Immunodeficiency 31c 29 0.021
801
HDG004 Hodgkin's Granuloma 28 0.021
802
P SCL057 Scoliosis, Isolated 1 28 0.021
803
LMB053 Limbic Encephalitis with Lgi1 Antibodies 27 0.021
804
NNT021 Neonatal Meningitis 26 0.021
805
PPL052 Papillomatosis, Confluent and Reticulated 26 0.021
806
PRS011 Persian Gulf Syndrome 26 0.021
807
LKT001 Leukotriene C4 Synthase Deficiency 24 0.021
808
MLR020 Malaria, Mild 23 0.021
809
SPC001 Space Motion Sickness 23 0.021
810
ATN016 Autoinflammation, Antibody Deficiency, and Immune Dysregulation, Plcg2-Associated 23 0.021
811
c OGC001 Oguchi Disease 1 23 0.021
812
RDN004 Radin Blood Group Antigen 23 0.021
813
HDG006 Hodgkin's Paragranuloma 21 0.021
814
XLN224 X-Linked Non-Specific Intellectual Disability 21 0.021
815
IMM023 Immunodeficiency Without Anhidrotic Ectodermal Dysplasia 21 0.021
816
GNT033 Genetic Prion Diseases 20 0.021
817
c SPR049 Supranuclear Palsy, Progressive, 2 19 0.021
818
IMM030 Immunodeficiency, Common Variable, 3 18 0.021
819
IMM135 Immunodeficiency 46 18 0.021
820
IMM037 Immunodeficiency, Common Variable, 6 17 0.021
821
IMM088 Immunodeficiency 36 17 0.021
822
IDP081 Idiopathic Hypertrophic Pachymeningitis 17 0.021
823
BLD153 Blood Group--Swann System 17 0.021
824
IMM032 Immunodeficiency, Common Variable, 5 17 0.021
825
IMM058 Immunodeficiency, Common Variable, 7 15 0.021
826
c FRM002 Form Agnosia 15 0.021
827
CLS031 Classic Galactosemia and Clinical Variant Galactosemia 13 0.021
Content
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