1012 hits were found for 'WAS'

# ++ Fam MCID Name MIFTS Score
1
P WSK001 Wiskott-Aldrich Syndrome 76 23.400
2
WSR001 Was-Related Disorders 22 13.922
3
P XLN068 X-Linked Thrombocytopenia 38 5.411
4
c THR014 Thrombocytopenia 66 4.890
5
THR065 Thrombocytopenia, X-Linked, Intermittent 4 4.192
6
c NTR004 Neutropenia 59 3.444
7
INT051 Intussusception 57 3.434
8
P SVR003 Severe Congenital Neutropenia 55 3.434
9
ULC004 Ulcerative Colitis 71 2.470
10
P PNC035 Pancreatic Cancer 82 2.448
11
HMT018 Hematopoietic Stem Cell Transplantation 41 2.448
12
PRT014 Protein S Deficiency 67 2.435
13
P AGM001 Agammaglobulinemia 58 2.435
14
c PNC044 Pancreatitis 58 2.435
15
P INF037 Inflammatory Bowel Disease 44 2.435
16
BRK003 Burkitt's Lymphoma 71 2.420
17
TNS005 Tonsillitis 57 2.420
18
SHG001 Shigellosis 57 2.420
19
END072 Endotheliitis 51 2.420
20
VCC001 Vaccinia 47 2.420
21
NRN002 Neuronitis 47 2.420
22
PRM097 Primary Immunodeficiency Disease 46 2.420
23
SVR014 Severe Congenital Neutropenia X-Linked 16 2.420
24
TBR010 Tuberculosis 82 1.759
25
GT001 Gout 66 1.759
26
PRP030 Purpura 60 1.759
27
c THR005 Thrombotic Thrombocytopenic Purpura 55 1.746
28
c MYL007 Myeloma 53 1.746
29
P MLT019 Multiple Myeloma 76 1.731
30
c DRR001 Diarrhea 49 1.731
31
CRB009 Cerebritis 46 1.711
32
HV1006 Hiv-1 42 1.711
33
P HYP163 Hyperlipidemia Type 3 22 0.214
34
LKM002 Leukemia 70 0.086
35
NSY001 N Syndrome 57 0.083
36
CYT018 Cytochrome P450 2d6 Variant 12 0.083
37
P ADN016 Adenocarcinoma 60 0.079
38
c HPT021 Hepatitis 65 0.076
39
P HPT001 Hepatitis C 66 0.072
40
P BRS047 Breast Cancer 85 0.068
41
P ART022 Arthritis 75 0.068
42
c NPH019 Nephronophthisis 1 20 0.068
43
P AST005 Asthma 86 0.063
44
P HYP075 Hypertension 76 0.063
45
ESP021 Esophageal Cancer 68 0.063
46
ACT073 Acute Leukemia 62 0.063
47
c HPT003 Hepatitis a 57 0.063
48
P OPT015 Optic Atrophy Type 1 38 0.063
49
P CLR023 Colorectal Cancer 66 0.059
50
LNG032 Lung Cancer 61 0.059
51
SML019 Smallpox 41 0.059
52
c LBR005 Leber Congenital Amaurosis 10 19 0.059
53
CRV058 Cervicofacial Lymphatic Malformation 8 0.059
54
P SCH015 Schizophrenia 69 0.054
55
P PNM007 Pneumonia 67 0.054
56
ADN018 Adenoma 67 0.054
57
LYM017 Lyme Disease 62 0.054
58
RFT001 Rift Valley Fever 46 0.054
59
WST005 West Nile Virus 46 0.054
60
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 25 0.054
61
P SYS001 Systemic Lupus Erythematosus 83 0.048
62
ATX002 Ataxia Telangiectasia 81 0.048
63
ACR007 Acromegaly 75 0.048
64
P DLT002 Dilated Cardiomyopathy 74 0.048
65
HPT023 Hepatocellular Carcinoma 69 0.048
66
c DBT009 Diabetes Mellitus 68 0.048
67
c LPS004 Lupus Erythematosus 65 0.048
68
MYL006 Myeloid Leukemia 64 0.048
69
P INF038 Influenza 63 0.048
70
HMN010 Hemangioma 62 0.048
71
MYS005 Myositis 61 0.048
72
HDC001 Headache 58 0.048
73
P MLN008 Melanoma 56 0.048
74
P MMP001 Mumps 56 0.048
75
SRC014 Sarcoma 54 0.048
76
P LRY019 Laryngitis 53 0.048
77
c HPT007 Hepatitis E 52 0.048
78
c SCK002 Sick Sinus Syndrome 50 0.048
79
CRT002 Cartilage-Hair Hypoplasia 50 0.048
80
NPH021 Nephropathic Cystinosis 47 0.048
81
CHN016 Cohen Syndrome 44 0.048
82
c HPT073 Hepatitis C Virus 43 0.048
83
VRL002 Variola Minor 21 0.048
84
KRN005 Kuru Encephalopathy 19 0.048
85
THY020 Thyroid Hyalinizing Trabecular Adenoma 16 0.048
86
VRL003 Variola Major 16 0.048
87
P ALZ001 Alzheimer's Disease 93 0.041
88
ACT019 Acute Myeloid Leukemia 87 0.041
89
P RHM011 Rheumatoid Arthritis 83 0.041
90
P MYC007 Myocardial Infarction 82 0.041
91
P OBS005 Obesity 79 0.041
92
P MLT020 Multiple Sclerosis 75 0.041
93
CNG034 Congestive Heart Failure 74 0.041
94
PHC003 Pheochromocytoma 71 0.041
95
P OST018 Osteosarcoma 70 0.041
96
OLV001 Olivopontocerebellar Atrophy 70 0.041
97
DCH001 Duchenne Muscular Dystrophy 70 0.041
98
P RTN024 Retinoblastoma 70 0.041
99
VSC007 Vascular Disease 69 0.041
100
SPS077 Sepsis 67 0.041
101
PRT036 Peritonitis 67 0.041
102
CLN016 Colon Cancer 66 0.041
103
P PRM005 Primary Hyperparathyroidism 66 0.041
104
c MNN013 Meningitis 62 0.041
105
ADL030 Adult-Onset Still's Disease 61 0.041
106
P DMN002 Dementia 61 0.041
107
P HYD006 Hydrocephalus 60 0.041
108
SQM006 Squamous Cell Carcinoma 58 0.041
109
PHR003 Pharyngitis 57 0.041
110
ISC004 Ischemia 57 0.041
111
c HYP069 Hyperparathyroidism 57 0.041
112
c ATX004 Ataxia 56 0.041
113
CRV035 Cervical Cancer 54 0.041
114
c MYL014 Myeloproliferative Disorder 54 0.041
115
NRP001 Neuropathy 54 0.041
116
c TRT010 Teratoma 53 0.041
117
PSR002 Psoriasis 51 0.041
118
c CNG018 Congenital Heart Block 50 0.041
119
ENC006 Encephalomyelitis 49 0.041
120
P MCL015 Mucolipidosis Ii 48 0.041
121
RLP002 Relapsing-Remitting Multiple Sclerosis 48 0.041
122
CVR006 Cavernous Hemangioma 47 0.041
123
IMP005 Impotence 47 0.041
124
GST045 Gastroenteritis 46 0.041
125
c VRN002 Variant Creutzfeldt-Jakob Disease 45 0.041
126
P MBS002 Moebius Syndrome 45 0.041
127
LNG029 Lung Adenocarcinoma 42 0.041
128
BTN004 Biotin Deficiency 40 0.041
129
MNK002 Monkeypox 39 0.041
130
NNT008 Neonatal Abstinence Syndrome 35 0.041
131
OCH001 Ochronosis 33 0.041
132
c MCL046 Mucolipidosis Iii Alpha/beta 32 0.041
133
P CHR269 Chromosome 9p Deletion 32 0.041
134
TXC020 Toxic Oil Syndrome 32 0.041
135
HMP014 Hemophagocytic Lymphohistiocytosis, Familial, 4 30 0.041
136
MTG001 Metagonimiasis 21 0.041
137
MYC021 Mycobacterium Xenopi 20 0.041
138
HRD009 Hereditary Wilms' Tumor 19 0.041
139
RMB001 Rombo Syndrome 17 0.041
140
LNR007 Linear and Whorled Nevoid Hypermelanosis 17 0.041
141
PRD013 Periodic Fever, Familial, Autosomal Dominant 14 0.041
142
DTH005 Diethylstilbestrol Syndrome 13 0.041
143
AML003 Amelia Cleft Lip Palate Hydrocephalus Iris Coloboma 1 0.041
144
CDS001 Cadasil 80 0.034
145
P CSH001 Cushing's Syndrome 78 0.034
146
P PRS040 Prostate Cancer 76 0.034
147
P GST019 Gastrointestinal Stromal Tumor 75 0.034
148
OVR042 Ovarian Cancer 73 0.034
149
P SMT004 Smith-Lemli-Opitz Syndrome 72 0.034
150
P PRM006 Primary Biliary Cirrhosis 69 0.034
151
HYP004 Hypercalcemia 69 0.034
152
STR067 Stroke, Ischemic 69 0.034
153
CRN211 Coronary Artery Disease, 68 0.034
154
P MYL005 Myelofibrosis 67 0.034
155
P MLR004 Malaria 66 0.034
156
CRB011 Cerebrotendinous Xanthomatosis 66 0.034
157
P FRN006 Frontotemporal Dementia 66 0.034
158
P PLY011 Polycystic Ovary Syndrome 66 0.034
159
P HMP004 Hemophilia B 66 0.034
160
DBT011 Diabetic Retinopathy 66 0.034
161
HYP056 Hypoglycemia 66 0.034
162
P AMY004 Amyloidosis 65 0.034
163
VSC011 Vasculitis 65 0.034
164
c HYP095 Hypercholesterolemia 65 0.034
165
SKN016 Skin Disease 64 0.034
166
THR079 Thromboembolism 63 0.034
167
P HYP117 Hypertriglyceridemia 63 0.034
168
MSL001 Measles 62 0.034
169
P BCK002 Beckwith-Wiedemann Syndrome 62 0.034
170
P CHR071 Charcot-Marie-Tooth Disease 61 0.034
171
RHM001 Rheumatic Fever 60 0.034
172
P GLM007 Glomerulonephritis 60 0.034
173
MXD005 Mixed Connective Tissue Disease 60 0.034
174
P CLF002 Cleft Palate 60 0.034
175
P GST044 Gastritis 59 0.034
176
P EPD003 Epidermolysis Bullosa Simplex 59 0.034
177
DSS009 Disseminated Intravascular Coagulation 59 0.034
178
c HYP086 Hypothyroidism 59 0.034
179
PRT011 Protein C Deficiency 59 0.034
180
P SYN007 Synovitis 58 0.034
181
P CST002 Castleman's Disease 58 0.034
182
ANG020 Angiosarcoma 58 0.034
183
CRM001 Crimean-Congo Hemorrhagic Fever 58 0.034
184
HLY001 Hailey-Hailey Disease 57 0.034
185
P PRS038 Personality Disorder 56 0.034
186
c PRP029 Porphyria 56 0.034
187
ACT049 Acute Disseminated Encephalomyelitis 56 0.034
188
URT001 Urethritis 56 0.034
189
BRN056 Bronchopulmonary Dysplasia 55 0.034
190
c RBL001 Rubella 55 0.034
191
CRN017 Coronary Thrombosis 55 0.034
192
VSC002 Vascular Dementia 55 0.034
193
c HYP076 Hyperthyroidism 55 0.034
194
BTN003 Biotinidase Deficiency 54 0.034
195
DPH001 Diphtheria 54 0.034
196
ACN011 Acne 54 0.034
197
PRV004 Periventricular Leukomalacia 54 0.034
198
TTH006 Tooth Disease 54 0.034
199
PRT037 Pertussis 54 0.034
200
P SNS014 Sinusitis 54 0.034
201
P ANG015 Angioedema 54 0.034
202
INT075 Intracranial Hypertension 53 0.034
203
HRD057 Hereditary Pancreatitis 53 0.034
204
ACR008 Acrocallosal Syndrome 53 0.034
205
c EPD016 Epidermolysis Bullosa 53 0.034
206
PRG009 Progressive Multifocal Leukoencephalopathy 53 0.034
207
P MMB001 Membranoproliferative Glomerulonephritis 52 0.034
208
MMR004 Memory Impairment 52 0.034
209
c MYP004 Myopathy 52 0.034
210
CHR074 Choriocarcinoma 52 0.034
211
HPY002 H. Pylori Infection 52 0.034
212
MCK005 Mckusick-Kaufman Syndrome 52 0.034
213
CHC001 Chickenpox 51 0.034
214
P SPH001 Sapho Syndrome 51 0.034
215
P ESP024 Esophagitis 51 0.034
216
c MNT147 Mental Retardation 51 0.034
217
END031 Endometrial Stromal Sarcoma 51 0.034
218
OBS001 Obstructive Jaundice 50 0.034
219
CRT013 Carotid Stenosis 50 0.034
220
PLM010 Pulmonary Edema 50 0.034
221
HYP068 Hyperostosis 50 0.034
222
P TRN001 Transthyretin Amyloidosis 49 0.034
223
VLV010 Vulvovaginitis 49 0.034
224
NCR004 Nocardiosis 49 0.034
225
SYN036 Syncope 49 0.034
226
P PRT029 Parathyroid Adenoma 49 0.034
227
HMR003 Hemorrhagic Disease 49 0.034
228
P GLC007 Glaucoma 49 0.034
229
HDN002 Head Injury 49 0.034
230
PRC013 Pericarditis 48 0.034
231
PHC013 Phaeochromocytoma 48 0.034
232
FLT006 Floating-Harbor Syndrome 47 0.034
233
P LMB024 Limbic Encephalitis 47 0.034
234
LDP002 Lead Poisoning 47 0.034
235
HLC001 Holocarboxylase Synthetase Deficiency 47 0.034
236
PRC012 Pericardial Effusion 47 0.034
237
SLY001 Sly Syndrome 47 0.034
238
PLG002 Plague 46 0.034
239
P KRN004 Kernicterus 46 0.034
240
P CNG052 Congenital Amegakaryocytic Thrombocytopenia 45 0.034
241
LKM006 Leukomalacia 45 0.034
242
CYS014 Cystadenocarcinoma 45 0.034
243
FCL012 Facial Paralysis 44 0.034
244
c FTL001 Fetal Alcohol Syndrome 44 0.034
245
ASP007 Aspiration Pneumonia 43 0.034
246
CHR101 Char Syndrome 42 0.034
247
BRL002 Buruli Ulcer Disease 42 0.034
248
WGN003 Wagner Syndrome 42 0.034
249
BRS064 Bursitis 41 0.034
250
BTN002 Boutonneuse Fever 40 0.034
251
CHL039 Choledocholithiasis 40 0.034
252
FGS001 Fg Syndrome 39 0.034
253
CTS011 Cutis Marmorata Telangiectatica Congenita 37 0.034
254
SCR011 Scrapie 37 0.034
255
TMR004 Tumor Necrosis Factor Receptor-Associated Periodic Syndrome 37 0.034
256
c PTR004 Pterygium 36 0.034
257
AMN003 Amnestic Disorder 35 0.034
258
STR080 Stroke, Hemorrhagic 34 0.034
259
MTR010 Mature Teratoma 34 0.034
260
INP001 Inappropriate Adh Syndrome 34 0.034
261
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 33 0.034
262
SPR066 Superficial Siderosis 33 0.034
263
EPM005 Epimerase Deficiency Galactosemia 33 0.034
264
AKN002 Akinetic Mutism 33 0.034
265
DNN002 Donnai-Barrow Syndrome 33 0.034
266
P CTR098 Cataract 1, Multiple Types 32 0.034
267
ELP001 Elephantiasis 32 0.034
268
VLV032 Vulva Cancer 31 0.034
269
ADN032 Adenosine Monophosphate Deaminase Deficiency 30 0.034
270
TST025 Testicular Microlithiasis 29 0.034
271
BDY001 Body Dysmorphic Disorder 29 0.034
272
WNC001 Winchester Syndrome 29 0.034
273
FNC027 Fanconi Anemia, Complementation Group a 29 0.034
274
c LBR004 Leber Congenital Amaurosis 1 25 0.034
275
SNL010 Senile Systemic Amyloidosis 24 0.034
276
UNC001 Uncombable Hair Syndrome 24 0.034
277
FCT008 Factitious Disorder 22 0.034
278
P SPN205 Spinal Muscular Atrophy, X-Linked 2, Infantile 21 0.034
279
MNT006 Manitoba Oculotrichoanal Syndrome 21 0.034
280
c CTR096 Cataract 6, Multiple Types 20 0.034
281
CRN046 Corneal Fleck Dystrophy 20 0.034
282
MMS001 Momo Syndrome 18 0.034
283
OPH001 Ophthalmomyiasis 18 0.034
284
PRD003 Periodontosis 18 0.034
285
SHR004 Sharp Syndrome 16 0.034
286
c CTR132 Cataract 3, Multiple Types 15 0.034
287
MLT011 Multiple Mucosal Neuroma 12 0.034
288
CNT057 Central Centrifugal Cicatricial Alopecia 11 0.034
289
UND003 Undifferentiated Connective Tissue Syndrome 11 0.034
290
c MLT076 Multiple System Atrophy with Orthostatic Hypotension 9 0.034
291
HND010 Handigodu Disease 9 0.034
292
KRK002 Karak Syndrome 7 0.034
293
YSH001 Yusho Disease 7 0.034
294
BTH003 Bothriocephalosis 5 0.034
295
ABS002 Absence of Gluteal Muscle 4 0.034
296
c CTR102 Cataract 2, Multiple Types 4 0.034
297
LYM053 Lymphomatous Thyroiditis 4 0.034
298
P AMY001 Amyotrophic Lateral Sclerosis 87 0.024
299
P FML011 Familial Adenomatous Polyposis 80 0.024
300
HDG007 Hodgkin's Lymphoma 80 0.024
301
CRH001 Crohn's Disease 78 0.024
302
ACH004 Achondroplasia 77 0.024
303
APL001 Aplastic Anemia 77 0.024
304
P FML021 Familial Hypercholesterolemia 76 0.024
305
AND002 Androgen Insensitivity Syndrome 75 0.024
306
P PRM021 Primary Pulmonary Hypertension 74 0.024
307
HRD008 Hereditary Hemorrhagic Telangiectasia 74 0.024
308
BLM001 Bloom Syndrome 74 0.024
309
P HMC003 Hemochromatosis 73 0.024
310
P OST002 Osteoporosis 73 0.024
311
P OST012 Osteoarthritis 72 0.024
312
P NMN002 Niemann-Pick Disease 72 0.024
313
PRP027 Peripheral Vascular Disease 71 0.024
314
BRN024 Bronchitis 71 0.024
315
ADR007 Adrenoleukodystrophy 70 0.024
316
P MCP002 Mucopolysaccharidosis I 70 0.024
317
P PRD006 Prader-Willi Syndrome 69 0.024
318
THL005 Thalassemia 69 0.024
319
LVR012 Liver Cirrhosis 69 0.024
320
ALP006 Alpha Thalassemia 68 0.024
321
WRN001 Werner Syndrome 68 0.024
322
RNL002 Renal Agenesis 68 0.024
323
P PRP003 Porphyria Cutanea Tarda 68 0.024
324
MYC006 Mycosis Fungoides 68 0.024
325
LSC001 Lesch-Nyhan Syndrome 68 0.024
326
LYM007 Lymphangioleiomyomatosis 67 0.024
327
P WGN002 Wegener's Granulomatosis 67 0.024
328
CHR065 Chronic Myeloid Leukemia 67 0.024
329
P ANG001 Angelman Syndrome 67 0.024
330
P LPR003 Leprosy 67 0.024
331
P UVT001 Uveitis 66 0.024
332
KLN001 Klinefelter's Syndrome 66 0.024
333
MLG056 Malignant Hyperthermia 66 0.024
334
DFC004 Deficiency Anemia 65 0.024
335
P THR015 Thrombophilia 65 0.024
336
P ART023 Arthropathy 65 0.024
337
P RCK004 Rickets 65 0.024
338
P ATP001 Atopic Dermatitis 64 0.024
339
ACT119 Acute Promyelocytic Leukemia 64 0.024
340
ART019 Aortic Valve Stenosis 64 0.024
341
c HMP007 Hemophilia 64 0.024
342
P GRF002 Graft Versus Host Disease 64 0.024
343
P THY023 Thymoma 63 0.024
344
CHR066 Chronic Fatigue Syndrome 63 0.024
345
SPN038 Spina Bifida 63 0.024
346
PRT010 Parathyroid Carcinoma 63 0.024
347
CCC001 Coccidioidomycosis 63 0.024
348
LYN001 Lynch Syndrome 63 0.024
349
P GRV001 Graves' Disease 63 0.024
350
P LVR013 Liver Disease 62 0.024
351
c HPT016 Hepatitis B 62 0.024
352
c CRN037 Craniosynostosis 62 0.024
353
PLY017 Polyarteritis Nodosa 62 0.024
354
SML001 Small Cell Carcinoma 62 0.024
355
PLM001 Pulmonary Tuberculosis 62 0.024
356
SPT013 Septic Shock 62 0.024
357
ACQ007 Acquired Immunodeficiency Syndrome 62 0.024
358
GLC003 Glucose Intolerance 62 0.024
359
HMP002 Hemophagocytic Lymphohistiocytosis 62 0.024
360
P MGR002 Migraine 61 0.024
361
THR004 Thrombocytosis 61 0.024
362
HYD012 Hydrops Fetalis 61 0.024
363
PLY041 Polymyositis 61 0.024
364
CHL065 Cholangiocarcinoma 61 0.024
365
P END044 Endometriosis 61 0.024
366
BRN002 Bronchiolitis 60 0.024
367
P OST009 Osteochondritis Dissecans 60 0.024
368
MLD001 Melioidosis 60 0.024
369
P DGR001 Digeorge Syndrome 60 0.024
370
KLP002 Klippel-Trenaunay Syndrome 60 0.024
371
PMP001 Pemphigus 60 0.024
372
P PRN023 Prion Disease 60 0.024
373
TTN003 Tetanus 60 0.024
374
BRN029 Brain Disease 60 0.024
375
P RSP003 Respiratory Failure 60 0.024
376
DRM006 Dermatitis 60 0.024
377
PPL022 Papilloma 60 0.024
378
CRY004 Cryoglobulinemia 59 0.024
379
P DRM010 Dermatomyositis 59 0.024
380
c HPT015 Hepatitis D 59 0.024
381
P ATS007 Autism Spectrum Disorder 59 0.024
382
c ACT075 Acute Myocardial Infarction 59 0.024
383
WRM001 Wermer Syndrome 59 0.024
384
DRM014 Dermatofibrosarcoma Protuberans 59 0.024
385
SCH014 Schistosomiasis 59 0.024
386
P ESS001 Essential Tremor 59 0.024
387
P VCT001 Vacterl Association 59 0.024
388
ANR002 Aniridia 59 0.024
389
P FML020 Familial Combined Hyperlipidemia 59 0.024
390
INS001 Insulinoma 59 0.024
391
P MCH002 Machado-Joseph Disease 59 0.024
392
ACT009 Acute Monocytic Leukemia 59 0.024
393
P FCS002 Fucosidosis 59 0.024
394
c TXP001 Toxoplasmosis 59 0.024
395
RCT015 Reactive Arthritis 58 0.024
396
CLR003 Clear Cell Adenocarcinoma 58 0.024
397
HYP014 Hyperuricemia 58 0.024
398
CNT009 Central Core Myopathy 58 0.024
399
P MJR001 Major Depressive Disorder 58 0.024
400
MLT074 Multiple Endocrine Neoplasia 58 0.024
401
PSD007 Pseudomyxoma Peritonei 58 0.024
402
ANR008 Aneurysm Disease 57 0.024
403
P CMP010 Complex Regional Pain Syndrome 57 0.024
404
P VLC001 Velocardiofacial Syndrome 57 0.024
405
PRN009 Paranoid Schizophrenia 57 0.024
406
P PMP005 Pemphigus Vulgaris 57 0.024
407
P HRP006 Herpes Simplex 57 0.024
408
DNT005 Dentatorubral-Pallidoluysian Atrophy 57 0.024
409
BRN071 Brain Injury 57 0.024
410
SLP006 Sleep Apnea 57 0.024
411
MYM001 Myoma 56 0.024
412
P DBT005 Diabetes Insipidus 56 0.024
413
P MMB002 Membranous Glomerulonephritis 56 0.024
414
c NRN021 Neuronal Ceroid Lipofuscinosis 56 0.024
415
CHR001 Churg-Strauss Syndrome 56 0.024
416
P FML032 Familial Hypertrophic Cardiomyopathy 56 0.024
417
c OCL002 Oculocutaneous Albinism 56 0.024
418
c ENC004 Encephalitis 56 0.024
419
MYX005 Myxoid Liposarcoma 56 0.024
420
MLB002 Male Breast Cancer 56 0.024
421
MTR014 Motor Neuron Disease 56 0.024
422
MDD011 Mood Disorder 56 0.024
423
CHR090 Chronic Lymphocytic Leukemia 56 0.024
424
CHL014 Cholera 56 0.024
425
P PSR001 Psoriatic Arthritis 56 0.024
426
P ANP001 Anaplastic Large Cell Lymphoma 56 0.024
427
ALV005 Alveolar Soft Part Sarcoma 56 0.024
428
P GTR002 Goiter 55 0.024
429
P INF032 Infertility 55 0.024
430
c ACT135 Acute Graft Versus Host Disease 55 0.024
431
P SHR029 Short Syndrome 55 0.024
432
c HRM001 Hermansky-Pudlak Syndrome 55 0.024
433
NRN001 Neuroendocrine Carcinoma 55 0.024
434
SCR008 Scrub Typhus 55 0.024
435
P PLY006 Polydactyly 55 0.024
436
P HYP055 Hypoplastic Left Heart Syndrome 55 0.024
437
THY022 Thymic Carcinoma 55 0.024
438
CMM005 Common Cold 55 0.024
439
P PRT008 Proteus Syndrome 55 0.024
440
NPH051 Nephritis 55 0.024
441
P CND004 Candidiasis 55 0.024
442
STR008 Strongyloidiasis 55 0.024
443
PSD012 Pseudoachondroplasia 55 0.024
444
DRV001 Dravet Syndrome 55 0.024
445
LPS007 Lupus Nephritis 55 0.024
446
c SYP003 Syphilis 55 0.024
447
P PLM006 Pulmonary Alveolar Proteinosis 55 0.024
448
FLT001 Felty's Syndrome 54 0.024
449
P MTR005 Mitral Valve Prolapse 54 0.024
450
APP008 Appendicitis 54 0.024
451
HST011 Histoplasmosis 54 0.024
452
NRM002 Normal Pressure Hydrocephalus 54 0.024
453
SRS001 Serous Cystadenocarcinoma 54 0.024
454
c VNT002 Ventricular Septal Defect 54 0.024
455
ALS001 Alstrom Syndrome 54 0.024
456
VNS010 Venous Thromboembolism 54 0.024
457
MCR004 Macroglobulinemia 54 0.024
458
ALK013 Alkaptonuria 54 0.024
459
AVN001 Avian Influenza 54 0.024
460
P LPS002 Liposarcoma 54 0.024
461
c MSC005 Muscular Dystrophy 54 0.024
462
SCH012 Schizoaffective Disorder 54 0.024
463
LYM040 Lymphoblastic Lymphoma 54 0.024
464
TTR011 Tetraploidy 54 0.024
465
LYM009 Lymphocytic Choriomeningitis 54 0.024
466
PLM034 Pulmonary Emphysema 53 0.024
467
RTN017 Retinal Detachment 53 0.024
468
CLL003 Cellulitis 53 0.024
469
CHR103 Charge Syndrome 53 0.024
470
c FML035 Familial Hyperlipidemia 53 0.024
471
ORL005 Oral Candidiasis 53 0.024
472
CHL067 Cholecystitis 53 0.024
473
c MLG069 Malignant Hypertension 53 0.024
474
P OMP004 Omphalocele 53 0.024
475
ANN002 Anencephaly 53 0.024
476
NRL004 Neuroleptic Malignant Syndrome 53 0.024
477
CRT033 Corticobasal Degeneration 53 0.024
478
CHR285 Chronic Myelomonocytic Leukemia 53 0.024
479
P HYP083 Hypopituitarism 53 0.024
480
TYP011 Typhus 53 0.024
481
RSC001 Rosacea 53 0.024
482
OST017 Osteomyelitis 53 0.024
483
PLY023 Polycystic Liver Disease 53 0.024
484
NWC001 Newcastle Disease 53 0.024
485
c SCL016 Scleroderma 53 0.024
486
P FNC004 Fanconi Syndrome 52 0.024
487
P ESN001 Eosinophilic Esophagitis 52 0.024
488
GNR005 Gonorrhea 52 0.024
489
STT002 Status Asthmaticus 52 0.024
490
c BCT007 Bacterial Meningitis 52 0.024
491
ECH003 Echinococcosis 52 0.024
492
BCT015 Bacteremia 52 0.024
493
FBR047 Fibromyalgia 52 0.024
494
P CYS010 Cystinosis 51 0.024
495
MCS003 Mucous Membrane Pemphigoid 51 0.024
496
PRM126 Primary Peritoneal Carcinoma 51 0.024
497
KLB001 Klebsiella 51 0.024
498
BCT004 Bacteriuria 51 0.024
499
P WVR001 Weaver Syndrome 51 0.024
500
EPT020 Epithelioid Hemangioendothelioma 51 0.024
501
LYM027 Lymphopenia 51 0.024
502
c SPN049 Spinocerebellar Ataxia 51 0.024
503
MYL001 Myelitis 51 0.024
504
c PRM010 Primary Open Angle Glaucoma 51 0.024
505
RNL014 Renal Cell Carcinoma 51 0.024
506
DRM004 Dermatofibrosarcoma 51 0.024
507
RBS001 Rabies 51 0.024
508
P HMN013 Hemangiopericytoma 51 0.024
509
SPT005 Spotted Fever 51 0.024
510
HYP006 Hypertensive Heart Disease 51 0.024
511
MNC007 Monocytic Leukemia 51 0.024
512
c ATM024 Autoimmune Pancreatitis 51 0.024
513
P OPN001 Open-Angle Glaucoma 51 0.024
514
CLS010 Cluster Headache 51 0.024
515
P MYC008 Myocarditis 51 0.024
516
SSN001 Seasonal Affective Disorder 51 0.024
517
P INT068 Intestinal Disease 51 0.024
518
P SCL015 Scleritis 50 0.024
519
SBC001 Subacute Sclerosing Panencephalitis 50 0.024
520
LYM021 Lymphadenitis 50 0.024
521
MTN003 Motion Sickness 50 0.024
522
VGN023 Vaginitis 50 0.024
523
CYS009 Cystadenoma 50 0.024
524
c WLM002 Wilms Tumor 50 0.024
525
ALB002 Albinism 50 0.024
526
NPH018 Nephrogenic Systemic Fibrosis 50 0.024
527
NNS002 Nonspecific Interstitial Pneumonia 50 0.024
528
TCK001 Tick-Borne Encephalitis 50 0.024
529
ECT026 Ectopic Pregnancy 50 0.024
530
DRG003 Drug Dependence 50 0.024
531
DST006 Diastolic Heart Failure 50 0.024
532
ORL011 Oral Cancer 50 0.024
533
ADL002 Adult Syndrome 50 0.024
534
c DNT011 Dentinogenesis Imperfecta 50 0.024
535
SPL018 Splenomegaly 50 0.024
536
P MLS001 Melas Syndrome 50 0.024
537
CYS008 Cystic Echinococcosis 50 0.024
538
EYD002 Eye Disease 50 0.024
539
LYM026 Lymphoblastic Leukemia 49 0.024
540
CWP001 Cowpox 49 0.024
541
P PRM100 Primary Spontaneous Pneumothorax 49 0.024
542
JCB001 Jacobsen Syndrome 49 0.024
543
PLY012 Polyhydramnios 49 0.024
544
EXS001 Exostosis 49 0.024
545
EPD037 Epidermal Nevus 49 0.024
546
c SPN016 Spondylocostal Dysostosis 49 0.024
547
P BTM001 Beta-Mannosidosis 49 0.024
548
c PRG013 Paraganglioma 49 0.024
549
MYL003 Myeloid Sarcoma 49 0.024
550
MCR037 Macroglossia 49 0.024
551
MDS022 Mediastinitis 49 0.024
552
BRN018 Borna Disease 49 0.024
553
SYS003 Systolic Heart Failure 48 0.024
554
PRM052 Primary Progressive Aphasia 48 0.024
555
P CLR017 Clear Cell Sarcoma 48 0.024
556
BRS051 Breast Disease 48 0.024
557
CLL021 Collagenous Colitis 48 0.024
558
ORC001 Orchitis 48 0.024
559
c CTR002 Cataract 48 0.024
560
PLM020 Pleomorphic Xanthoastrocytoma 48 0.024
561
BLS002 Blastomycosis 48 0.024
562
P ATR005 Atrophic Gastritis 48 0.024
563
CLL002 Collecting Duct Carcinoma 48 0.024
564
c BRC006 Brachydactyly 48 0.024
565
MCL002 Macular Corneal Dystrophy 48 0.024
566
c ACT078 Acute Porphyria 48 0.024
567
MTB004 Metabolic Acidosis 48 0.024
568
SPL004 Splenic Marginal Zone Lymphoma 48 0.024
569
P DFF019 Diffuse Gastric Cancer 47 0.024
570
CNR004 Cone-Rod Dystrophy 2 47 0.024
571
CLF001 Cleft Lip 47 0.024
572
ANR018 Anorchia 47 0.024
573
P GND004 Gonadal Dysgenesis 47 0.024
574
ADN020 Adenosarcoma 47 0.024
575
c KBK001 Kabuki Syndrome 47 0.024
576
P RBN002 Robinow Syndrome 47 0.024
577
ANG011 Angiodysplasia 47 0.024
578
c ENC008 Encephalocele 47 0.024
579
GLM008 Glomus Tumor 46 0.024
580
NSP001 Nasopharynx Carcinoma 46 0.024
581
STN007 Stenotrophomonas Maltophilia 46 0.024
582
END041 Endometrial Adenocarcinoma 46 0.024
583
MMM001 Mammary Paget's Disease 46 0.024
584
P CHR104 Chorea 46 0.024
585
CHL061 Childhood Leukemia 46 0.024
586
P DYS026 Dysfibrinogenemia 46 0.024
587
P CNG119 Congenital Porphyria 46 0.024
588
PRP023 Peripheral Neuropathy 46 0.024
589
RDC002 Radiculopathy 46 0.024
590
EST003 Eastern Equine Encephalitis 46 0.024
591
DBT006 Diabetic Macular Edema 46 0.024
592
CRN012 Craniometaphyseal Dysplasia 46 0.024
593
MTS001 Mutism 45 0.024
594
BRS081 Breast Cancer Susceptibility 45 0.024
595
c MCP004 Mucopolysaccharidosis Iv 45 0.024
596
ACR005 Acrodermatitis 45 0.024
597
TND004 Tendinopathy 45 0.024
598
LPM005 Lipomatosis 45 0.024
599
OLG003 Oligohydramnios 45 0.024
600
PLS025 Plasmablastic Lymphoma 45 0.024
601
FLL013 Follicular Dendritic Cell Sarcoma 45 0.024
602
P BRS044 Breast Adenocarcinoma 45 0.024
603
END028 Endemic Goiter 45 0.024
604
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 45 0.024
605
SCB001 Scabies 45 0.024
606
OST097 Osteoporotic Fracture 44 0.024
607
FRN002 Frontal Lobe Epilepsy 44 0.024
608
RSD004 Rosai-Dorfman Disease 44 0.024
609
GST029 Gastric Cardia Adenocarcinoma 44 0.024
610
P OVR046 Ovarian Cyst 44 0.024
611
MYC013 Mycobacterium Abscessus 44 0.024
612
P AZS001 Azoospermia 44 0.024
613
NDL021 Nodular Lymphocyte Predominant Hodgkin Lymphoma 44 0.024
614
CHK001 Chikungunya 44 0.024
615
MCN008 Mucinous Cystadenocarcinoma 44 0.024
616
VRY001 Very Long-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 44 0.024
617
PPL018 Papillary Adenocarcinoma 44 0.024
618
ASC002 Ascariasis 44 0.024
619
P OCL017 Oculocutaneous Albinism Type 1 44 0.024
620
ALC010 Alcoholic Cardiomyopathy 44 0.024
621
CTS005 Catastrophic Antiphospholipid Syndrome 43 0.024
622
GND002 Gender Identity Disorder 43 0.024
623
FRM007 Freeman Sheldon Syndrome 43 0.024
624
CHL052 Choledochal Cyst 43 0.024
625
ACT087 Acth Deficiency 43 0.024
626
c STC001 Stickler Syndrome 43 0.024
627
P MLT075 Multifocal Motor Neuropathy 43 0.024
628
CTY001 Cat Eye Syndrome 43 0.024
629
MTC027 Mitochondrial Trifunctional Protein Deficiency 42 0.024
630
LGS001 Legius Syndrome 42 0.024
631
TKT001 Tako-Tsubo Cardiomyopathy 42 0.024
632
DYS073 Dysphagia 42 0.024
633
RTR011 Retroperitoneal Fibrosis 42 0.024
634
HRT012 Heart Valve Disease 42 0.024
635
HRD039 Hereditary Amyloidosis 42 0.024
636
c ANT034 Anterior Uveitis 42 0.024
637
SMN007 Seminoma 42 0.024
638
BLR015 Blue Rubber Bleb Nevus Syndrome 42 0.024
639
CHR276 Chronic Active Epstein-Barr Virus Infection 42 0.024
640
INT063 Intellectual Disability 42 0.024
641
LPD006 Lipoid Proteinosis 42 0.024
642
MYS001 Myositis Ossificans 42 0.024
643
P LSS005 Lissencephaly 1 42 0.024
644
DBW001 Dubowitz Syndrome 42 0.024
645
CRD053 Cardiovascular Disease Risk Factor 42 0.024
646
PRS039 Prostate Adenocarcinoma 41 0.024
647
P MWT001 Mowat-Wilson Syndrome 41 0.024
648
CRY001 Cryptogenic Organizing Pneumonia 41 0.024
649
PYR014 Pyridoxine-Dependent Epilepsy 41 0.024
650
P CYS017 Cystic Teratoma 41 0.024
651
ETH011 Ethylmalonic Encephalopathy 41 0.024
652
DNR001 Duane Retraction Syndrome 41 0.024
653
GND001 Gonadoblastoma 41 0.024
654
PTY003 Pityriasis Rubra Pilaris 41 0.024
655
FCL022 Focal Dystonia 41 0.024
656
P ORF002 Orofacial Cleft 41 0.024
657
GST040 Gastric Adenocarcinoma 41 0.024
658
BRN013 Bronchiolitis Obliterans Organizing Pneumonia 41 0.024
659
CHY006 Chylous Ascites 40 0.024
660
MNN014 Mononeuritis 40 0.024
661
BRB001 Beriberi 40 0.024
662
MXD032 Mixed Germ Cell Tumor 40 0.024
663
c PRN026 Porencephaly 40 0.024
664
ANS003 Anisakiasis 40 0.024
665
NCR007 Necrotizing Fasciitis 40 0.024
666
OVR012 Ovarian Serous Cystadenocarcinoma 40 0.024
667
TLR001 Tularemia 40 0.024
668
ALT001 Alternating Hemiplegia of Childhood 40 0.024
669
P TRN034 Transverse Myelitis 40 0.024
670
PSD010 Pseudogout 40 0.024
671
TBR008 Tuberculous Peritonitis 40 0.024
672
ANX004 Anoxia 40 0.024
673
EPC002 Epicondylitis 40 0.024
674
CND006 Candida Glabrata 39 0.024
675
ESP028 Esophageal Squamous Cell Carcinoma 39 0.024
676
AND003 Andersen-Tawil Syndrome 39 0.024
677
STC004 Stachybotrys Chartarum 39 0.024
678
ANT024 Anthrax Disease 39 0.024
679
P SLL003 Salla Disease 39 0.024
680
ISL005 Isolated Acth Deficiency 39 0.024
681
OBS004 Obstructive Hydrocephalus 39 0.024
682
EPD029 Epidermolysis Bullosa Simplex, Generalized 39 0.024
683
FNT004 Fainting 39 0.024
684
BLP005 Blepharitis 39 0.024
685
END060 Endolymphatic Hydrops 38 0.024
686
P ACH020 Achromatopsia 2 38 0.024
687
DCB001 Decubitus Ulcer 38 0.024
688
PRS045 Prostatic Hypertrophy 38 0.024
689
BRN038 Bronchial Disease 38 0.024
690
ZYG002 Zygomycosis 38 0.024
691
BRS050 Breast Cyst 38 0.024
692
PRN014 Paronychia 38 0.024
693
DNR002 Duane-Radial Ray Syndrome 38 0.024
694
EPS026 Epispadias 38 0.024
695
INF013 Inferior Myocardial Infarction 37 0.024
696
HRP002 Herpes Gestationis 37 0.024
697
c 3Q2003 3q29 Microdeletion Syndrome 37 0.024
698
ANG037 Angiomatosis 37 0.024
699
NCR002 Necrobiosis Lipoidica 37 0.024
700
ACL001 Acalculous Cholecystitis 37 0.024
701
BLK001 Balkan Nephropathy 37 0.024
702
CTS002 Cat-Scratch Disease 37 0.024
703
THN006 Thin Basement Membrane Nephropathy 37 0.024
704
P SCL025 Scleromyxedema 37 0.024
705
c DMN027 Dominant Optic Atrophy 37 0.024
706
RPP001 Rapp-Hodgkin Syndrome 37 0.024
707
TRF001 Trifunctional Protein Deficiency 37 0.024
708
MYC019 Mycobacterium Marinum 37 0.024
709
MTR003 Mitral Valve Stenosis 37 0.024
710
LNG039 Lung Squamous Cell Carcinoma 37 0.024
711
THM001 Thomsen Disease 37 0.024
712
PLN006 Poland Syndrome 36 0.024
713
PRM018 Primary Hypertrophic Osteoarthropathy 36 0.024
714
WHP002 Whiplash 36 0.024
715
HPT063 Hepatitis B Virus Infection 36 0.024
716
c ALV006 Alveolar Capillary Dysplasia 36 0.024
717
MGS001 Megaesophagus 36 0.024
718
HST006 Histidinemia 36 0.024
719
OCL025 Ocular Toxoplasmosis 36 0.024
720
P CHR288 Chronic Recurrent Multifocal Osteomyelitis 36 0.024
721
P DYS005 Dyslexia 36 0.024
722
P FNN001 Finnish Type Amyloidosis 36 0.024
723
VGN017 Vaginal Cancer 36 0.024
724
EPD046 Epididymitis 35 0.024
725
PMP002 Pemphigoid Gestationis 35 0.024
726
MYC017 Mycobacterium Kansasii 35 0.024
727
GLD002 Goldberg-Shprintzen Megacolon Syndrome 35 0.024
728
CRD002 Cri-Du-Chat Syndrome 35 0.024
729
RTR001 Retrograde Amnesia 34 0.024
730
EMN001 Emanuel Syndrome 34 0.024
731
P ICH047 Ichthyosis, Congenital, Autosomal Recessive 1 34 0.024
732
c ACT004 Acute Diarrhea 34 0.024
733
P SPR035 Superior Vena Cava Syndrome 34 0.024
734
TNC003 Tinea Corporis 34 0.024
735
YNG002 Young Syndrome 34 0.024
736
LPB001 Lipoblastoma 34 0.024
737
TST021 Testicular Germ Cell Tumor 34 0.024
738
ADR021 Adrenocorticotropic Hormone Deficiency 34 0.024
739
INT079 Intrahepatic Cholangiocarcinoma 34 0.024
740
KKC001 Kikuchi Disease 34 0.024
741
LCK001 Locked-in Syndrome 33 0.024
742
TTZ002 Tietz Syndrome 33 0.024
743
LNG030 Lung Adenoma 33 0.024
744
CRP002 Croup 33 0.024
745
TBS001 Tabes Dorsalis 33 0.024
746
BRN055 Bronchogenic Cyst 33 0.024
747
SPR009 Sporadic Breast Cancer 33 0.024
748
c LTT001 Lattice Corneal Dystrophy 33 0.024
749
NPH016 Nephropathy-Hypertension 33 0.024
750
BSL033 Basal Ganglia Cancification, Idiopathic, 1 32 0.024
751
MTH044 Mthfr Gene Mutation 32 0.024
752
PST086 Posterior Cortical Atrophy 32 0.024
753
DYS036 Dysequilibrium Syndrome 32 0.024
754
PNC041 Pancreatic Ductal Adenocarcinoma 32 0.024
755
P HMR005 Hemorrhoid 32 0.024
756
CGN002 Cogan's Syndrome 32 0.024
757
UNV001 Unverricht-Lundborg Syndrome 32 0.024
758
LYM020 Lymph Node Cancer 32 0.024
759
TYP013 Type 1 Von Willebrand Disease 32 0.024
760
P XNT005 Xanthinuria Type 1 32 0.024
761
ACT099 Acute Fatty Liver of Pregnancy 32 0.024
762
HNS001 Hansen's Disease 32 0.024
763
c PPL025 Popliteal Pterygium Syndrome 31 0.024
764
MNN002 Mononeuritis Multiplex 31 0.024
765
TNC001 Tinea Cruris 31 0.024
766
MNN032 Meningococcal Meningitis 31 0.024
767
TRN021 Transaldolase Deficiency 31 0.024
768
SPP009 Sepiapterin Reductase Deficiency 31 0.024
769
c ICH049 Ichthyosis, Congenital, Autosomal Recessive 2 31 0.024
770
PRS064 Persistent Vegetative State 31 0.024
771
SPN028 Spondyloepimetaphyseal Dysplasia, Strudwick Type 31 0.024
772
INT020 Intravenous Leiomyomatosis 31 0.024
773
P GLM006 Glomangioma 31 0.024
774
SLL001 Sialolithiasis 30 0.024
775
HYP034 Hypertensive Encephalopathy 30 0.024
776
HRP001 Herpangina 30 0.024
777
PYR011 Pyropoikilocytosis 30 0.024
778
c USH006 Usher Syndrome, Type 1b 30 0.024
779
VGN019 Vaginal Discharge 30 0.024
780
DSQ001 Desquamative Interstitial Pneumonia 30 0.024
781
MYC018 Mycobacterium Malmoense 30 0.024
782
c CTR103 Cataract 4, Multiple Types 30 0.024
783
MLK004 Malakoplakia 30 0.024
784
c TRP015 Triphalangeal Thumb 30 0.024
785
c CHR130 Charcot-Marie-Tooth Disease Type 1b 29 0.024
786
GST052 Gestational Choriocarcinoma 29 0.024
787
EHL012 Ehlers-Danlos Syndrome Dermatosparaxis Type 29 0.024
788
EXS013 Exstrophy-Epispadias Complex 29 0.024
789
P D2H001 D-2-Hydroxyglutaric Aciduria 29 0.024
790
SBD001 Subdural Empyema 28 0.024
791
INT003 Intracranial Hypotension 28 0.024
792
RMS001 Rem Sleep Behavior Disorder 28 0.024
793
CHR028 Chronic Wasting Disease 28 0.024
794
c CNG224 Congenital Disorder of Glycosylation Type 1a 28 0.024
795
P FRN036 Frontonasal Dysplasia 1 28 0.024
796
CTN013 Cutaneous Anthrax 28 0.024
797
TTZ001 Tietze's Syndrome 28 0.024
798
MNR012 M�ni�re Disease 28 0.024
799
CLC010 Calcifying Epithelial Odontogenic Tumor 28 0.024
800
MDL006 Madelung Disease 28 0.024
801
CYC008 Cyclic Vomiting Syndrome 28 0.024
802
ADG002 Audiogenic Seizures 28 0.024
803
SPL007 Splenic Abscess 27 0.024
804
MNT003 Mental Retardation in Cri-Du-Chat Syndrome 27 0.024
805
CRN061 Corneal Dystrophy Avellino Type 27 0.024
806
P CMM008 Communicating Hydrocephalus 27 0.024
807
RDT005 Radiation Induced Cancer 27 0.024
808
END014 Endemic Typhus 27 0.024
809
BRK004 Barakat Syndrome 27 0.024
810
CRB079 Cerebrospinal Fluid Leak 27 0.024
811
PLC009 Placenta Praevia 27 0.024
812
DFN222 Deafness-Dystonia-Optic Neuronopathy Syndrome 27 0.024
813
ANH001 Ainhum 27 0.024
814
NRS005 Neurosarcoidosis 27 0.024
815
VBR003 Vibrio Vulnificus Infection 27 0.024
816
c OST039 Osteogenesis Imperfecta Type 5 27 0.024
817
NRC001 Neurocirculatory Asthenia 27 0.024
818
IMM039 Immune Hydrops Fetalis 26 0.024
819
TRL003 Toriello Carey Syndrome 26 0.024
820
ANS006 Anosognosia 26 0.024
821
c LYM063 Lymphoma, Diffuse Large Cell 26 0.024
822
RHB022 Rhabdoid Tumors, Somatic 25 0.024
823
INN003 Iniencephaly 25 0.024
824
P OPT051 Opitz Gbbb Syndrome, Type I 25 0.024
825
FMR003 Femoral Neuropathy 25 0.024
826
TYL002 Tylosis with Esophageal Cancer 25 0.024
827
CHR158 Charles Bonnet Syndrome 25 0.024
828
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 24 0.024
829
HYP160 Hyperkeratosis Lenticularis Perstans 24 0.024
830
c PST061 Posterior Polymorphous Corneal Dystrophy 24 0.024
831
INT011 Interstitial Emphysema 24 0.024
832
NRC003 Narcissistic Personality Disorder 24 0.024
833
STY001 Satoyoshi Syndrome 24 0.024
834
PRS051 Parastremmatic Dwarfism 24 0.024
835
JPN001 Japanese Spotted Fever 24 0.024
836
PDT027 Pediatric Ulcerative Colitis 24 0.024
837
PNM003 Pneumatosis Cystoides Intestinalis 24 0.024
838
IDM001 Ideomotor Apraxia 24 0.024
839
CYT004 Cytomegalic Inclusion Disease 24 0.024
840
MYC014 Mycobacterium Chelonae 24 0.024
841
DYS009 Dysthymic Disorder 24 0.024
842
BRS061 Breast Sarcoma 23 0.024
843
OVR059 Ovary Adenocarcinoma 23 0.024
844
P SVR013 Severe Congenital Neutropenia Autosomal Recessive 3 23 0.024
845
P MNT061 Mental Retardation-Hypotonic Facies Syndrome, X-Linked 23 0.024
846
c ICH041 Ichthyosis, Autosomal Recessive 4b 23 0.024
847
BLN002 Balanitis Xerotica Obliterans 23 0.024
848
TRT003 Tertiary Syphilis 23 0.024
849
HST001 Histrionic Personality Disorder 23 0.024
850
TRN028 Transient Acantholytic Dermatosis 23 0.024
851
NRM009 Normokalemic Periodic Paralysis 22 0.024
852
c CHR057 Chronic Laryngitis 22 0.024
853
c OCL035 Oculocutaneous Albinism Type 1b 22 0.024
854
SCL022 Scleredema 22 0.024
855
P ELL007 Elliptocytosis-1 22 0.024
856
c LSS006 Lissencephaly 2 22 0.024
857
SML008 Small Intestine Lymphoma 22 0.024
858
AMY012 Amyloidosis Cerebral 22 0.024
859
PNT006 Pentosuria 22 0.024
860
c ACT072 Acute Laryngitis 21 0.024
861
ATY013 Atypical Rett Syndrome 21 0.024
862
MSN002 Mesenteric Lymphadenitis 21 0.024
863
HRD052 Hereditary Mucoepithelial Dysplasia 21 0.024
864
ADT001 Auditory Agnosia 21 0.024
865
BNT002 Bantu Siderosis 21 0.024
866
c OBS047 Obesity, Early-Onset 20 0.024
867
OVR047 Ovarian Cystadenocarcinoma 20 0.024
868
c ORF007 Orofaciodigital Syndrome 2 20 0.024
869
c LMB018 Limb-Girdle Muscular Dystrophy, Type 1a 20 0.024
870
ATM021 Autoimmune Inner Ear Disease 20 0.024
871
CRT009 Critical Illness Polyneuropathy 20 0.024
872
CNR008 Cone-Rod Dystrophy Amelogenesis Imperfecta 20 0.024
873
c CHR247 Chromosome 4p Deletion 20 0.024
874
HRT003 Heart Lymphoma 20 0.024
875
PRT056 Protein R Deficiency 20 0.024
876
LYM056 Lymphoma, Somatic 19 0.024
877
CYC002 Cyclosporiasis 19 0.024
878
HRL002 Harlequin Syndrome 19 0.024
879
OVR098 Ovarian Fibroma 19 0.024
880
OMS001 Omsk Hemorrhagic Fever 19 0.024
881
c ACT059 Acute Maxillary Sinusitis 19 0.024
882
SKN012 Skin Carcinoma in Situ 19 0.024
883
ISS001 Isosporiasis 18 0.024
884
FMR012 Femur-Fibula-Ulna Complex 18 0.024
885
c AMY008 Amyotrophic Lateral Sclerosis Type 2 18 0.024
886
P HYD015 Hydroa Vacciniforme 18 0.024
887
c CLR079 Colorectal Cancer 2 18 0.024
888
HMC012 Hemicrania Continua 18 0.024
889
RCT017 Rectal Disease 18 0.024
890
HYP440 Hyperphosphatasia with Mental Retardation Syndrome 18 0.024
891
c CTS012 Cutis Verticis Gyrata 18 0.024
892
THN005 Thunderclap Headache 17 0.024
893
CNG049 Congenital Stromal Corneal Dystrophy 17 0.024
894
CNT067 Central Cord Syndrome 17 0.024
895
LJH001 Lujo Hemorrhagic Fever 17 0.024
896
P CTR101 Cataract 39, Multiple Types, Autosomal Dominant 17 0.024
897
TRS006 Triose Phosphate-Isomerase Deficiency 17 0.024
898
c TTR013 Tetrasomy X 17 0.024
899
P ANN010 Anonychia-Onychodystrophy with Hypoplasia or Absence of Distal Phalanges 17 0.024
900
PSD078 Pseudofolliculitis Barbae 17 0.024
901
MRZ001 Mirizzi Syndrome 17 0.024
902
PRN010 Paranoid Personality Disorder 17 0.024
903
PLM015 Pulmonary Systemic Sclerosis 17 0.024
904
P DNT025 Dentinogenesis Imperfecta 1 16 0.024
905
PLY031 Polydactyly Myopia Syndrome 16 0.024
906
GTP001 Gait Apraxia 16 0.024
907
RGN005 Regional Odontodysplasia 16 0.024
908
SML010 Simultanagnosia 16 0.024
909
c PRK057 Parkinson Disease, Late-Onset 16 0.024
910
c AST037 Asthma 1 15 0.024
911
PLR006 Pleural Cancer 15 0.024
912
SDD004 Sudden Arrhythmia Death Syndrome 15 0.024
913
c CTR124 Cataract 10, Multiple Types 15 0.024
914
PNT002 Peanut Allergic Reaction 15 0.024
915
OVR027 Ovarian Squamous Cell Carcinoma 15 0.024
916
URC001 Urachus Cancer 15 0.024
917
PRS002 Prostate Lymphoma 15 0.024
918
CNZ006 Coenzyme Q10 Deficiency, Primary, 1 14 0.024
919
SGM001 Sigmoid Disease 14 0.024
920
FML211 Familial Papillary or Follicular Thyroid Carcinoma 14 0.024
921
DYS135 Dysphagia Lusoria 14 0.024
922
LKC003 Leukocyte Disease 14 0.024
923
SCH004 Schizoid Personality Disorder 14 0.024
924
NTV001 Native American Myopathy 14 0.024
925
ORP002 Oropouche Fever 14 0.024
926
ELC001 Elective Mutism 14 0.024
927
ARR026 Arrhythmogenic Right Ventricular Dysplasia 1 14 0.024
928
FRS004 Free Sialic Acid Storage Disorders 14 0.024
929
MNS002 Mini Stroke 14 0.024
930
ACC005 Accessory Pancreas 14 0.024
931
SPN092 Spinal Shock 13 0.024
932
AMR001 American Histoplasmosis 13 0.024
933
SHR027 Short Stature Wormian Bones Dextrocardia 13 0.024
934
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 13 0.024
935
TRG006 Trigger Thumb 13 0.024
936
CTR010 Cataract Congenital Volkmann Type 13 0.024
937
INF048 Infantile Histiocytoid Cardiomyopathy 13 0.024
938
NNN015 Noonan-Like/multiple Giant Cell Lesion Syndrome 13 0.024
939
PRM040 Primary Basilar Impression 13 0.024
940
OSL001 Oslam Syndrome 13 0.024
941
RBN004 Robin Sequence and Oligodactyly 13 0.024
942
KHL001 Kohler's Disease 13 0.024
943
BNG042 Benign Multicystic Peritoneal Mesothelioma 13 0.024
944
c NTR033 Neutropenia, Severe Congenital 1, Autosomal Dominant 12 0.024
945
DPH012 Diphallia 12 0.024
946
HYP145 Hyperbetaalaninemia 12 0.024
947
RHM006 Rheumatic Aortic Valve Stenosis 12 0.024
948
c RNP003 Renpenning Syndrome 1 12 0.024
949
KYR001 Kyrle Disease 11 0.024
950
c RNG013 Ring Chromosome 18 11 0.024
951
APP004 Appendix Mucinous Cystadenocarcinoma 11 0.024
952
CRN126 Corneal Dystrophy, Lisch Epithelial 11 0.024
953
THY092 Thymic Neuroendocrine Carcinoma 11 0.024
954
c PRG072 Progressive Myoclonic Epilepsy 3 with or Without Intracellular Inclusions 11 0.024
955
AKN001 Akinetopsia 11 0.024
956
URC004 Urachal Cancer 11 0.024
957
ACT116 Acute Myeloid Leukemia, Childhood 11 0.024
958
PSD027 Pseudoaminopterin Syndrome 11 0.024
959
CRT056 Carotidynia 11 0.024
960
P ACH028 Acheiria 10 0.024
961
ENC021 Encephalopathy, Neonatal Severe 10 0.024
962
P HYP512 Hyperproinsulinemia, Familial 10 0.024
963
HYD031 Hydroxyprolinemia 10 0.024
964
MRG007 Morgellons 10 0.024
965
PRV008 Parvovirus Antenatal Infection 10 0.024
966
NVS007 Nevus of Ota 9 0.024
967
BLN017 Balint Syndrome 9 0.024
968
c DST049 Distal Spinal Muscular Atrophy Type 3 9 0.024
969
PRM056 Primrose Syndrome 9 0.024
970
UHL001 Uhl Anomaly 9 0.024
971
SBP006 Subepithelial Mucinous Corneal Dystrophy 9 0.024
972
ACC001 Accessory Nerve Disease 9 0.024
973
PRS107 Persistent Sexual Arousal Syndrome 9 0.024
974
GST005 Gastric Hemangioma 8 0.024
975
PST044 Postorgasmic Illness Syndrome 8 0.024
976
MLP004 Malpuech Facial Clefting Syndrome 8 0.024
977
BRN045 Brunner Syndrome 8 0.024
978
ERY040 Erythema Palmaris Hereditarium 8 0.024
979
JMP002 Jumping Frenchmen of Maine 7 0.024
980
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 7 0.024
981
c CRD093 Cardiomyopathy, Dilated, 1a 7 0.024
982
c CTR115 Cataract 16, Multiple Types 7 0.024
983
ORF018 Orofacial Cleft11 7 0.024
984
c ICH048 Ichthyosis, Congenital, Autosomal Recessive 9 6 0.024
985
c ICH050 Ichthyosis, Congenital, Autosomal Recessive 5 6 0.024
986
c MNT171 Mental Retardation, Autosomal Dominant 17 6 0.024
987
PHS019 Phosphohydroxylysinuria 6 0.024
988
CNG067 Congenital Cystic Eye 6 0.024
989
MYP003 Myopathy of Critical Illness 6 0.024
990
c HYP548 Hypogonadotropic Hypogonadism 2 with or Without Anosmia 5 0.024
991
c ICH038 Ichthyosis, Congenital, Autosomal Recessive 3 5 0.024
992
c ICH039 Ichthyosis, Congenital, Autosomal Recessive 10 5 0.024
993
c ICH040 Ichthyosis, Congenital, Autosomal Recessive 4a 5 0.024
994
c ICH042 Ichthyosis, Congenital, Autosomal Recessive 6 5 0.024
995
c ICH044 Ichthyosis, Congenital, Autosomal Recessive 8 5 0.024
996
c ICH045 Ichthyosis, Congenital, Autosomal Recessive 7 5 0.024
997
OBS014 Obsessive-Compulsive Disorder, Protection Against 5 0.024
998
c PRD030 Periodontitis 1, Juvenile 5 0.024
999
c PRX050 Peroxisome Biogenesis Disorder 9b 5 0.024
1000
CTR043 Cataract, Pulverulent or Cerulean, with or Without Microcornea 4 0.024
1001
c CTR104 Cataract 18, Autosomal Recessive 4 0.024
1002
c CTR113 Cataract 11, Multiple Types 4 0.024
1003
c CTR118 Cataract 14, Multiple Types 4 0.024
1004
c CTR122 Cataract 5, Multiple Types 4 0.024
1005
c CTR129 Cataract 31, Multiple Types 4 0.024
1006
c CTR130 Cataract 9, Multiple Types 4 0.024
1007
c CTR131 Cataract 17, Multiple Types 4 0.024
1008
c CTR133 Cataract 22, Autosomal Recessive 4 0.024
1009
MDY003 Mody, Type Ii 4 0.024
1010
c PRX053 Peroxisome Biogenesis Disorder 14b 4 0.024
1011
MNM003 Minimally Differentiated Acute Myeloblastic Leukemia 3 0.024
1012
MCK010 Mickleson Syndrome 1 0.024