Search results for fibromyalgia

519 hits were found for fibromyalgia

# Family MCID Name MIFTS Score
1
MYF002 Myofascial Pain Syndrome 39 3.995
2
P MYP004 Myopathy 67 0.569
3
c PND001 Pain Disorder 54 0.569
4
NRM005 Neuromuscular Disease 56 0.567
5
P MSC033 Muscle Disorders 52 0.567
6
RHM027 Rheumatic Disease 58 0.535
7
P CLL015 Collagen Disease 50 0.522
8
c CNT068 Central Pain Syndrome 29 0.396
9
EXF001 Exfoliation Syndrome 57 0.359
10
P PLN008 Peeling Skin Syndrome 45 0.359
11
P CHR345 Chronic Pain 50 0.327
12
CHR066 Chronic Fatigue Syndrome 64 0.308
13
SLP005 Sleep Disorder 53 0.281
14
P SHR029 Short Syndrome 58 0.275
15
c PLN017 Peeling Skin Syndrome 1 34 0.270
16
c PLN018 Peeling Skin Syndrome 2 40 0.269
17
c PLN021 Peeling Skin Syndrome 3 29 0.248
18
P GNR027 Generalized Peeling Skin Syndrome 19 0.236
19
WLL006 Wells Syndrome 59 0.228
20
GDS001 Good Syndrome 44 0.228
21
GNR004 Generalized Anxiety Disorder 51 0.215
22
CSY001 C Syndrome 50 0.211
23
P ART022 Arthritis 75 0.201
24
ANX002 Anxiety Disorder 67 0.201
25
SRT004 Serotonin Syndrome 49 0.199
26
ADL002 Adult Syndrome 52 0.188
27
MSC004 Muscle Tissue Disease 34 0.188
28
WST001 West Syndrome 57 0.181
29
MNT002 Mental Depression 53 0.167
30
NSY001 N Syndrome 36 0.164
31
MDD011 Mood Disorder 61 0.153
32
END040 Endogenous Depression 53 0.148
33
LRN003 Learning Disability 49 0.145
34
DSS008 Disease of Mental Health 52 0.139
35
RHM028 Rheumatic Heart Disease 50 0.139
36
SKN016 Skin Disease 66 0.136
37
SKN027 Skin Conditions 43 0.136
38
BCK006 Back Pain 43 0.136
39
WSC001 Wisconsin Syndrome 14 0.133
40
P RHM011 Rheumatoid Arthritis 89 0.123
41
ATN005 Autonomic Dysfunction 49 0.123
42
MVM001 Movement Disease 49 0.120
43
CPM001 Cap Myopathy 30 0.120
44
P MYL005 Myelofibrosis 67 0.112
45
CHL071 Child Syndrome 58 0.112
46
HDC001 Headache 54 0.112
47
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 53 0.112
48
KDS001 Kid Syndrome 53 0.112
49
ADR009 Adrenal Cortex Disease 39 0.112
50
ATN002 Autonomic Nervous System Disease 48 0.108
51
NVD002 Nevada Syndrome 14 0.108
52
IRR002 Irritable Bowel Syndrome 58 0.105
53
P NRP001 Neuropathy 59 0.100
54
SLP001 Sleeping Sickness 48 0.100
55
P DYS021 Dysautonomia 44 0.100
56
PCK002 Pick Disease 68 0.096
57
SKN023 Skin Tag 44 0.096
58
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.096
59
RDN001 Reading Disorder 34 0.096
60
RDC010 Reducing Body Myopathy 31 0.096
61
CND002 Conduct Disorder 54 0.092
62
CNN005 Connective Tissue Disease 62 0.087
63
PRP019 Peripheral Nervous System Disease 55 0.087
64
INS024 Insulin-Like Growth Factor I 75 0.082
65
INC002 Inclusion Body Myositis 66 0.082
66
DWN001 Down Syndrome 66 0.082
67
RBR001 Roberts Syndrome 60 0.082
68
OLV001 Olivopontocerebellar Atrophy 53 0.082
69
INT007 Intermediate Coronary Syndrome 50 0.082
70
SHH001 Sheehan Syndrome 44 0.082
71
ADJ001 Adjustment Disorder 38 0.082
72
ALX002 Alexithymia 37 0.082
73
P OBS005 Obesity 92 0.077
74
P ART023 Arthropathy 64 0.077
75
WLL001 Williams-Beuren Syndrome 60 0.077
76
JNT002 Joint Disorders 55 0.077
77
ALL026 Allergic Hypersensitivity Disease 52 0.077
78
SPC010 Speech and Communication Disorders 41 0.077
79
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 41 0.077
80
SPN369 Spinal Disease 39 0.077
81
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.077
82
c SYS001 Systemic Lupus Erythematosus 86 0.071
83
P NRV007 Nervous System Disease 71 0.071
84
P LPS004 Lupus Erythematosus 64 0.071
85
P SPN052 Spondyloarthropathy 60 0.071
86
CHN016 Cohen Syndrome 54 0.071
87
PLN006 Poland Syndrome 54 0.071
88
P SPS003 Spastic Diplegia 52 0.071
89
LPD004 Lipoid Nephrosis 48 0.071
90
P CRN035 Cranial Nerve Palsy 46 0.071
91
ACR041 Acromelic Frontonasal Dysostosis 45 0.071
92
PHY002 Physical Disorder 43 0.071
93
BRT030 Birth Defects 43 0.071
94
MLT001 Multiple Chemical Sensitivity 43 0.071
95
SMT001 Somatization Disorder 42 0.071
96
PRD011 Proud Syndrome 42 0.071
97
CRN031 Cranial Nerve Disease 40 0.071
98
P HYP265 Hypotonia 38 0.071
99
WHP002 Whiplash 36 0.071
100
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 35 0.071
101
VSL004 Visual Cortex Disease 28 0.071
102
c CRN214 Coronary Heart Disease 5 22 0.071
103
c CRN173 Coronary Heart Disease 8 18 0.071
104
PSR001 Psoriatic Arthritis 64 0.065
105
P OST002 Osteoporosis 64 0.065
106
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 43 0.065
107
ESN002 Eosinophilia-Myalgia Syndrome 42 0.065
108
SPC005 Speech Disorder 41 0.065
109
ADT003 Auditory System Disease 40 0.065
110
NTR005 Nutritional Deficiency Disease 36 0.065
111
c DYS033 Dysautonomia Like Disorder 16 0.065
112
PRP027 Peripheral Vascular Disease 68 0.058
113
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.058
114
DFC004 Deficiency Anemia 64 0.058
115
P ALX003 Alexander Disease 63 0.058
116
ISC004 Ischemia 61 0.058
117
c RHM021 Rheumatoid Arthritis, Systemic Juvenile 59 0.058
118
ETN001 Eating Disorder 58 0.058
119
RSP006 Respiratory System Disease 58 0.058
120
P FNC043 Fanconi Anemia, Complementation Group E 55 0.058
121
CMP010 Complex Regional Pain Syndrome 54 0.058
122
FDL002 Food Allergy 53 0.058
123
PRV006 Pervasive Developmental Disorder 53 0.058
124
ART002 Arts Syndrome 51 0.058
125
GRW007 Growth Hormone Deficiency 50 0.058
126
SMT006 Somatoform Disorder 50 0.058
127
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.058
128
PTT009 Pituitary Gland Disease 47 0.058
129
HYP085 Hypothalamic Disease 44 0.058
130
SXL003 Sexual Disorder 42 0.058
131
AYM001 Ayme-Gripp Syndrome 41 0.058
132
SPC003 Specific Developmental Disorder 38 0.058
133
TMP012 Temple Syndrome 38 0.058
134
FCL011 Facial Nerve Disease 36 0.058
135
WRT001 Worth's Syndrome 34 0.058
136
c TRC078 Trichohepatoenteric Syndrome 2 29 0.058
137
GNC005 Geniculate Ganglionitis 27 0.058
138
c ATM007 Autoimmune Disease of Central Nervous System 25 0.058
139
ATM052 Autoimmune Disease 1 25 0.058
140
EYC003 Eye Accommodation Disease 24 0.058
141
SCL044 Scalp Syndrome 15 0.058
142
NVS004 Nova Syndrome 13 0.058
143
TSY001 Tau Syndrome 10 0.058
144
P OST012 Osteoarthritis 83 0.050
145
P INF038 Influenza 72 0.050
146
BRN028 Brain Cancer 70 0.050
147
P INT068 Intestinal Disease 60 0.050
148
P RHN004 Rhinitis 60 0.050
149
GLB001 Gilbert Syndrome 60 0.050
150
P GRV001 Graves' Disease 59 0.050
151
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.050
152
PST028 Post-Traumatic Stress Disorder 57 0.050
153
CTS003 Coats Disease 57 0.050
154
P EXN002 Exanthem 57 0.050
155
P PLY019 Polyneuropathy 56 0.050
156
DBT010 Diabetic Neuropathy 55 0.050
157
P THY032 Thyroiditis 54 0.050
158
NWC001 Newcastle Disease 54 0.050
159
SCT005 Scott Syndrome 53 0.050
160
OPT006 Optic Nerve Disease 52 0.050
161
IRN001 Iron Deficiency Anemia 52 0.050
162
CRS005 Crest Syndrome 51 0.050
163
IMG001 Image Syndrome 50 0.050
164
MSC072 Muscle Cancer 49 0.050
165
MSS002 Mass Syndrome 48 0.050
166
MGR028 Migraine with or Without Aura 1 47 0.050
167
ADR038 Adermatoglyphia 46 0.050
168
P CRV039 Cervicitis 45 0.050
169
c GRV008 Graves Disease 1 44 0.050
170
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.050
171
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.050
172
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.050
173
GRW004 Growth Retardation with Deafness and Mental Retardation Due to Igf1 Deficiency 39 0.050
174
c CHR579 Chiari Malformation Type Ii 37 0.050
175
WTH001 Withdrawal Disorder 37 0.050
176
P ADV001 Advanced Sleep Phase Syndrome 37 0.050
177
c DGT005 Digital Arthropathy-Brachydactyly, Familial 33 0.050
178
FST001 Foster-Kennedy Syndrome 31 0.050
179
WDS002 Woods Syndrome 27 0.050
180
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 27 0.050
181
TYL001 Taylor's Syndrome 26 0.050
182
c MJR007 Major Affective Disorder 1 24 0.050
183
CNT017 Central Nervous System Origin Vertigo 24 0.050
184
PRS011 Persian Gulf Syndrome 23 0.050
185
NLL002 Null Syndrome 20 0.050
186
BKS002 Book Syndrome 19 0.050
187
c MJR008 Major Affective Disorder 2 19 0.050
188
c CRN176 Coronary Heart Disease 9 18 0.050
189
c GRV009 Graves Disease 2 16 0.050
190
ATM054 Autoimmune Disease 3 15 0.050
191
c ADV005 Advanced Sleep Phase Syndrome 3 15 0.050
192
ATM055 Autoimmune Disease 4 15 0.050
193
P BRS047 Breast Cancer 100 0.041
194
P HNT016 Huntington Disease 80 0.041
195
P HPT021 Hepatitis 69 0.041
196
P CLC005 Celiac Disease 68 0.041
197
OBS061 Obstructive Sleep Apnea 66 0.041
198
ALL003 Allergic Rhinitis 63 0.041
199
P EHL001 Ehlers-Danlos Syndrome 63 0.041
200
P BPL003 Bipolar Disorder 62 0.041
201
P SLP006 Sleep Apnea 61 0.041
202
P PNC025 Panic Disorder 60 0.041
203
SPT004 Septic Arthritis 60 0.041
204
c CNT035 Central Nervous System Disease 60 0.041
205
CNS004 Constipation 57 0.041
206
MSC077 Muscle Eye Brain Disease 57 0.041
207
P INT143 Interstitial Cystitis 57 0.041
208
RHM001 Rheumatic Fever 54 0.041
209
C3D001 C3 Deficiency 53 0.041
210
TTH006 Tooth Disease 52 0.041
211
DRG011 Drug Addiction 51 0.041
212
IMM136 Immune System Disease 51 0.041
213
SPN051 Spondylitis 51 0.041
214
CLN019 Colonic Disease 51 0.041
215
STM006 Stomach Disease 50 0.041
216
DYS014 Dyspepsia 50 0.041
217
RDC002 Radiculopathy 50 0.041
218
BRX001 Bruxism 49 0.041
219
PRT038 Protein-Energy Malnutrition 49 0.041
220
P SCL015 Scleritis 49 0.041
221
P MYT002 Myotonic Dystrophy 48 0.041
222
ADR012 Adrenal Gland Disease 48 0.041
223
NSD001 Nose Disease 48 0.041
224
RFL001 Reflex Sympathetic Dystrophy 48 0.041
225
SYN036 Syncope 47 0.041
226
NLS001 Nelson Syndrome 47 0.041
227
BRD001 Brody Myopathy 47 0.041
228
UPP004 Upper Respiratory Tract Disease 46 0.041
229
PRP021 Peripheral Nervous System Neoplasm 46 0.041
230
c MTR002 Mitral Valve Insufficiency 44 0.041
231
c ART120 Arthrogryposis, Distal, Type 3 42 0.041
232
END072 Endotheliitis 42 0.041
233
APL002 Aplasia of Lacrimal and Salivary Glands 42 0.041
234
OBS015 Obesity, Hyperphagia, and Developmental Delay 41 0.041
235
DPH021 Diaphragm Disease 41 0.041
236
CNV002 Conversion Disorder 41 0.041
237
DST004 Distal Muscular Dystrophy 40 0.041
238
ACT084 Acute Stress Disorder 40 0.041
239
GST078 Gastrointestinal Allergy 40 0.041
240
P HYP263 Hypersomnia 40 0.041
241
IMP006 Impulse Control Disorder 40 0.041
242
TNG004 Tongue Disease 39 0.041
243
PRP028 Peripheral Vertigo 38 0.041
244
ATM014 Autoimmune Disease of Endocrine System 36 0.041
245
RMN001 Rumination Disorder 34 0.041
246
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 33 0.041
247
HRZ001 Huriez Syndrome 30 0.041
248
MRG013 Mirage Syndrome 29 0.041
249
WRT002 Writing Disorder 27 0.041
250
CRB031 Cerebral Arterial Disease 27 0.041
251
PST048 Postural Orthostatic Tachycardia Syndrome 27 0.041
252
FNC005 Functional Colonic Disease 27 0.041
253
SHP003 Shapiro Syndrome 26 0.041
254
FNT003 Fountain Syndrome 26 0.041
255
PRF003 Piriformis Syndrome 26 0.041
256
GRM003 German Syndrome 22 0.041
257
ATM059 Autoimmune Disease 6 22 0.041
258
P CRN178 Coronary Heart Disease 6 21 0.041
259
c CRN172 Coronary Heart Disease 3 19 0.041
260
GLT030 Gluten Allergy 19 0.041
261
INF009 Inflammatory Spondylopathy 18 0.041
262
VGS001 Vagus Nerve Disease 18 0.041
263
c SPN256 Spondyloarthropathy 3 16 0.041
264
ATM053 Autoimmune Disease 2 16 0.041
265
c MJR004 Major Affective Disorder 4 16 0.041
266
c MJR003 Major Affective Disorder 6 15 0.041
267
c GNR024 Generalized Peeling Skin Syndrome Type C 12 0.041
268
BNJ001 Benjamin Syndrome 9 0.041
269
CYS001 Cystic Fibrosis 83 0.029
270
P AST005 Asthma 82 0.029
271
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 78 0.029
272
P SCH015 Schizophrenia 77 0.029
273
P HMC003 Hemochromatosis 72 0.029
274
P LKM002 Leukemia 71 0.029
275
P LGH007 Leigh Syndrome 70 0.029
276
P PRK057 Parkinson Disease, Late-Onset 70 0.029
277
P ADN016 Adenocarcinoma 69 0.029
278
P LYN001 Lynch Syndrome 69 0.029
279
c MLT136 Multiple Endocrine Neoplasia 1 69 0.029
280
c HPT001 Hepatitis C 68 0.029
281
P GLB002 Glioblastoma 68 0.029
282
WRN001 Werner Syndrome 67 0.029
283
P END044 Endometriosis 66 0.029
284
P KDN018 Kidney Disease 66 0.029
285
c CHR089 Chronic Kidney Failure 66 0.029
286
DRM006 Dermatitis 66 0.029
287
OBS002 Obsessive-Compulsive Disorder 66 0.029
288
ATP002 Atopy 66 0.029
289
P MSC005 Muscular Dystrophy 65 0.029
290
DMN002 Dementia 65 0.029
291
CNT098 Central Core Disease 65 0.029
292
P AST007 Astrocytoma 65 0.029
293
PTR006 Peters Anomaly 65 0.029
294
c HPT016 Hepatitis B 64 0.029
295
P THL005 Thalassemia 64 0.029
296
P ORT004 Orthostatic Intolerance 64 0.029
297
P HYP086 Hypothyroidism 64 0.029
298
GLB015 Glioblastoma Multiforme 63 0.029
299
P ADD001 Addison's Disease 62 0.029
300
P CRN015 Cornelia De Lange Syndrome 62 0.029
301
GST092 Gastroesophageal Reflux 62 0.029
302
APH001 Aphthous Stomatitis 62 0.029
303
P GCH001 Gaucher's Disease 62 0.029
304
c SPN225 Spondyloarthropathy 1 62 0.029
305
P DRM010 Dermatomyositis 62 0.029
306
P NRC002 Narcolepsy 62 0.029
307
CNT047 Contact Dermatitis 61 0.029
308
HYP056 Hypoglycemia 61 0.029
309
MTH009 Mouth Disease 61 0.029
310
P PNC044 Pancreatitis 61 0.029
311
CLT003 Colitis 60 0.029
312
HYP020 Hyperprolactinemia 60 0.029
313
P NRV006 Nervous System Cancer 60 0.029
314
QFV001 Q Fever 60 0.029
315
P DRR001 Diarrhea 60 0.029
316
KRT001 Keratoconjunctivitis Sicca 59 0.029
317
P ENC018 Encephalopathy 59 0.029
318
P INF032 Infertility 59 0.029
319
MRB003 Morbid Obesity 58 0.029
320
ALL006 Allergic Asthma 58 0.029
321
P AND016 Andersen Syndrome 58 0.029
322
c PNC108 Pancreatitis, Hereditary 58 0.029
323
SYN007 Synovitis 58 0.029
324
c ACT027 Acute Pancreatitis 57 0.029
325
c SVR001 Severe Acute Respiratory Syndrome 57 0.029
326
P MYS005 Myositis 57 0.029
327
STR026 Star Syndrome 57 0.029
328
P SZR006 Seizure Disorder 56 0.029
329
P SML001 Small Cell Carcinoma 56 0.029
330
HYP266 Hypoxia 56 0.029
331
P MLT074 Multiple Endocrine Neoplasia 56 0.029
332
STF001 Stiff-Person Syndrome 56 0.029
333
VRL011 Viral Infectious Disease 55 0.029
334
P TMT001 Timothy Syndrome 55 0.029
335
P TRM003 Tremor 54 0.029
336
P HYP083 Hypopituitarism 54 0.029
337
P NLD001 Nail Disease 54 0.029
338
PTT046 Pituitary Hormone Deficiency, Combined, 2 54 0.029
339
RST001 Restless Legs Syndrome 54 0.029
340
P MTC069 Mitochondrial Disorders 53 0.029
341
P CYS018 Cystitis 52 0.029
342
KRT006 Keratoconjunctivitis 52 0.029
343
BRN106 Burns 52 0.029
344
ISL003 Isolated Growth Hormone Deficiency 52 0.029
345
P MGR003 Migraine with Aura 52 0.029
346
LYM024 Lymphatic System Disease 52 0.029
347
MYC002 Mycobacterium Avium Complex Disease 52 0.029
348
c PRK031 Parkinson Disease 1 51 0.029
349
P LCT001 Lactic Acidosis 51 0.029
350
ANK001 Ankylosis 51 0.029
351
VSC006 Vascular Cancer 51 0.029
352
SPN041 Spinal Cord Disease 51 0.029
353
P STS008 Sotos Syndrome 1 51 0.029
354
MST017 Mast Cell Disease 50 0.029
355
STM007 Stomatitis 50 0.029
356
OPT003 Opiate Dependence 50 0.029
357
DRY001 Dry Eye Syndrome 50 0.029
358
THR013 Thoracic Outlet Syndrome 50 0.029
359
IDP002 Idiopathic Juvenile Osteoporosis 50 0.029
360
P SHR001 Short Bowel Syndrome 49 0.029
361
PRN021 Paranasal Sinus Disease 49 0.029
362
INN002 Inner Ear Disease 49 0.029
363
ACT017 Acute Chest Syndrome 48 0.029
364
JCB001 Jacobsen Syndrome 48 0.029
365
TCD001 Tic Disorder 48 0.029
366
THY030 Thyroid Gland Disease 48 0.029
367
FML039 Female Reproductive System Disease 48 0.029
368
P MYT023 Myotonia Congenita 47 0.029
369
DWR001 Dwarfism 47 0.029
370
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.029
371
BLD053 Blood Platelet Disease 46 0.029
372
GLT021 Glutaricaciduria, Type I 46 0.029
373
ICH054 Ichthyosis, X-Linked 46 0.029
374
INC022 Inclusion-Cell Disease 46 0.029
375
c TRC092 Trichorhinophalangeal Syndrome, Type I 46 0.029
376
SNS003 Sensory Peripheral Neuropathy 45 0.029
377
CRB090 Cerebral Hypoxia 45 0.029
378
URT004 Urethral Syndrome 45 0.029
379
ALN001 Aland Island Eye Disease 45 0.029
380
ULC007 Ulcerative Stomatitis 44 0.029
381
CHR056 Chronic Tic Disorder 44 0.029
382
c HMG003 Hemoglobin E Disease 44 0.029
383
c CNT015 Central Sleep Apnea 44 0.029
384
PRM020 Premenstrual Tension 44 0.029
385
P DMY001 Demyelinating Polyneuropathy 43 0.029
386
SNS023 Sensory System Cancer 43 0.029
387
MST006 Mast Syndrome 43 0.029
388
SPN119 Spondylarthropathy 42 0.029
389
BHR001 Behr Syndrome 42 0.029
390
BRN018 Borna Disease 42 0.029
391
P MTC004 Mitochondrial Encephalomyopathy 42 0.029
392
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.029
393
FCT008 Factitious Disorder 41 0.029
394
IRN002 Iron Metabolism Disease 41 0.029
395
BRN080 Brain Ischemia 41 0.029
396
URT001 Urethritis 41 0.029
397
ARC002 Arachnoiditis 41 0.029
398
c PRG106 Progressive Muscular Dystrophy 40 0.029
399
c PRK045 Parkinson Disease 5 40 0.029
400
c CHR283 Chronic Inflammatory Demyelinating Polyneuropathy 40 0.029
401
c HRD088 Hereditary Neuropathies 40 0.029
402
BND014 Bone Development Disease 40 0.029
403
CRB009 Cerebritis 39 0.029
404
TND005 Tendinitis 39 0.029
405
ORB013 Orbital Disease 39 0.029
406
THL010 Thalassemia Minor 39 0.029
407
HYP540 Hypertension, Diastolic 39 0.029
408
ACT088 Acute Insulin Response 39 0.029
409
BDY001 Body Dysmorphic Disorder 39 0.029
410
CLL021 Collagenous Colitis 39 0.029
411
EPC002 Epicondylitis 39 0.029
412
NSL022 Nasal Cavity Disease 38 0.029
413
HYP007 Hypermobility Syndrome 38 0.029
414
c PRK030 Parkinson Disease 4 38 0.029
415
SXD001 Sex Differentiation Disease 38 0.029
416
P CRN276 Corneal Endothelial Dystrophy 37 0.029
417
BLD054 Blood Protein Disease 37 0.029
418
PRP080 Peripheral Artery Disease 37 0.029
419
MTR007 Motor Peripheral Neuropathy 37 0.029
420
DLY005 Delayed Sleep Phase Syndrome 37 0.029
421
CMB021 Combined Pituitary Hormone Deficiency 37 0.029
422
P ENC011 Encephalomyopathy 37 0.029
423
BNS002 Bone Structure Disease 37 0.029
424
CPL005 Capillary Disease 36 0.029
425
EXT056 External Ear Disease 36 0.029
426
SCH072 Scheuermann Disease 36 0.029
427
c RCR002 Recurrent Hypersomnia 36 0.029
428
PRS063 Paresthesia 36 0.029
429
OBS003 Obsessive-Compulsive Personality Disorder 36 0.029
430
HMF008 Hemifacial Atrophy, Progressive 36 0.029
431
MYT011 Myotonia 36 0.029
432
ATM012 Autoimmune Disease of Blood 35 0.029
433
ENT004 Enthesopathy 35 0.029
434
FRY001 Frey Syndrome 35 0.029
435
CRB079 Cerebrospinal Fluid Leak 34 0.029
436
CSL001 Causalgia 34 0.029
437
IMP003 Impaired Renal Function Disease 34 0.029
438
CHL078 Childhood-Onset Schizophrenia 34 0.029
439
ANG049 Angioedema Induced by Ace Inhibitors 34 0.029
440
ACR002 Acrocapitofemoral Dysplasia 33 0.029
441
FNT004 Fainting 33 0.029
442
HGH001 High Pressure Neurological Syndrome 33 0.029
443
c SYS043 Systemic Lupus Erythematosus 1 33 0.029
444
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 33 0.029
445
FNC006 Functional Gastric Disease 32 0.029
446
GLB003 Globe Disease 32 0.029
447
ALG001 Algoneurodystrophy 31 0.029
448
IRS003 Iris Disease 31 0.029
449
c OST147 Osteoarthritis 1 30 0.029
450
TRG003 Trigeminal Nerve Disease 30 0.029
451
WHT017 Wheat Allergy 30 0.029
452
PTT045 Pituitary Hormone Deficiency, Combined, 1 30 0.029
453
RMN002 Ramon Syndrome 30 0.029
454
FCL003 Facial Hemiatrophy 30 0.029
455
BRW006 Brown Syndrome 29 0.029
456
ATM016 Autoimmune Disease of Skin and Connective Tissue 29 0.029
457
c DRR009 Diarrhea 6 29 0.029
458
GRN016 Grant Syndrome 29 0.029
459
c NRC009 Narcolepsy 1 29 0.029
460
c AST037 Asthma 1 28 0.029
461
c AST039 Asthma 2 28 0.029
462
BLN006 Blind Loop Syndrome 28 0.029
463
NRG003 Neurogenic Arthropathy 28 0.029
464
STR086 Stromal Dystrophy 28 0.029
465
c SYS038 Systemic Lupus Erythematosus 2 27 0.029
466
c STR092 Striatal Degeneration, Autosomal Dominant 2 27 0.029
467
c SCH059 Schizophrenia 17 26 0.029
468
YNG002 Young Syndrome 26 0.029
469
c WSK002 Wiskott-Aldrich Syndrome 2 25 0.029
470
KDN001 Kidney Cortex Necrosis 25 0.029
471
P MYP095 Myopathy, Distal, 4 25 0.029
472
SNT004 Sinoatrial Node Dysfunction and Deafness 25 0.029
473
P MJR018 Major Affective Disorder-7 24 0.029
474
c MLT094 Multiple Sclerosis 3 24 0.029
475
c MLT124 Multiple Sclerosis 5 23 0.029
476
CNT067 Central Cord Syndrome 23 0.029
477
TMT006 Timothy Grass Allergy 23 0.029
478
FCL001 Facial Dermatosis 23 0.029
479
c NRC011 Narcolepsy 3 22 0.029
480
c PRK022 Parkinson Disease 12 21 0.029
481
CMB002 Combat Disorder 21 0.029
482
c SYS046 Systemic Lupus Erythematosus 3 21 0.029
483
c TRC093 Trichorhinophalangeal Syndrome, Type Iii 20 0.029
484
c CRN177 Coronary Heart Disease 7 20 0.029
485
c SYS055 Systemic Lupus Erythematosus 12 20 0.029
486
c MYP112 Myopathy, Distal, 3 20 0.029
487
c NRC010 Narcolepsy 2 19 0.029
488
PTT043 Pituitary Hormone Deficiency, Combined, 6 19 0.029
489
PRC021 Parc Syndrome 19 0.029
490
c SYS065 Systemic Lupus Erythematosus 11 19 0.029
491
c CRN175 Coronary Heart Disease 4 19 0.029
492
c SYS053 Systemic Lupus Erythematosus 5 18 0.029
493
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 18 0.029
494
c MLT093 Multiple Sclerosis 2 18 0.029
495
c SPN226 Spondyloarthropathy 2 18 0.029
496
SCL001 Scalp Dermatosis 18 0.029
497
NN2002 Non 24 Hour Sleep Wake Disorder 18 0.029
498
MTR078 Motor Neuropathy, Peripheral, with Dysautonomia 18 0.029
499
ATN001 Autonomic Peripheral Neuropathy 17 0.029
500
c NRC012 Narcolepsy 4 17 0.029
501
c NRC013 Narcolepsy 5 17 0.029
502
ACC001 Accessory Nerve Disease 17 0.029
503
LGD001 Leg Dermatosis 16 0.029
504
c MLT095 Multiple Sclerosis 4 16 0.029
505
LCH010 Lichtenstein Syndrome 15 0.029
506
c MJR006 Major Affective Disorder 5 15 0.029
507
c ALX007 Alexander Disease Type I 15 0.029
508
LVT001 Levator Syndrome 15 0.029
509
c INF136 Influenza, Severe 15 0.029
510
c JVN025 Juvenile Primary Osteoporosis 15 0.029
511
c PNC068 Panic Disorder 3 15 0.029
512
AML037 Amelia of Upper Limb 14 0.029
513
c PNC070 Panic Disorder 2 14 0.029
514
PNS017 Pens Syndrome 12 0.029
515
c SCN046 Secondary Short Bowel Syndrome 12 0.029
516
SGM003 Segmentation Syndrome 1 12 0.029
517
IDP040 Idiopathic Eosinophilic Myositis 10 0.029
518
IMP007 Impairment of Oral Perception 9 0.029
519
AML036 Amelia of Lower Limb 9 0.029
Content
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