Search results for "WAS"

978 hits were found for 'WAS'

# Family MCID Name MIFTS Score
1
P WSK001 Wiskott-Aldrich Syndrome 79 22.954
2
WSR001 Was-Related Disorders 6 15.191
3
THR065 Thrombocytopenia, X-Linked, Intermittent 9 7.293
4
c THR014 Thrombocytopenia 71 5.225
5
XLN068 X-Linked Thrombocytopenia 51 5.218
6
c NTR004 Neutropenia 64 4.232
7
SVR014 Severe Congenital Neutropenia X-Linked 25 4.211
8
c THR005 Thrombotic Thrombocytopenic Purpura 59 3.005
9
P SVR003 Severe Congenital Neutropenia 53 2.993
10
INT051 Intussusception 59 2.977
11
PRM097 Primary Immunodeficiency Disease 46 2.977
12
c THR037 Thrombocytopenia 2 34 2.105
13
P HYP163 Hyperlipidemia Type 3 28 0.213
14
c HPT021 Hepatitis 64 0.098
15
P LKM002 Leukemia 77 0.092
16
P ADN016 Adenocarcinoma 59 0.079
17
P HYP075 Hypertension 87 0.075
18
P ESP024 Esophagitis 64 0.075
19
P ART022 Arthritis 75 0.071
20
c PNC044 Pancreatitis 69 0.067
21
P BRS047 Breast Cancer 86 0.063
22
P CLR023 Colorectal Cancer 77 0.063
23
GST053 Gastric Cancer 38 0.063
24
P AST005 Asthma 89 0.058
25
ESP021 Esophageal Cancer 80 0.058
26
P LNG032 Lung Cancer 79 0.058
27
c DBT009 Diabetes Mellitus 74 0.058
28
PRS047 Prostatitis 60 0.058
29
SML019 Smallpox 42 0.058
30
CRV058 Cervicofacial Lymphatic Malformation 12 0.058
31
P SYS001 Systemic Lupus Erythematosus 88 0.053
32
P SCH015 Schizophrenia 82 0.053
33
P PNM007 Pneumonia 78 0.053
34
c LPS004 Lupus Erythematosus 77 0.053
35
P INF038 Influenza 68 0.053
36
ADN018 Adenoma 66 0.053
37
CLT003 Colitis 64 0.053
38
P CRV039 Cervicitis 58 0.053
39
HPT023 Hepatocellular Carcinoma 54 0.053
40
END072 Endotheliitis 51 0.053
41
WST005 West Nile Virus 46 0.053
42
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 34 0.053
43
c TYP009 Type 2 Diabetes Mellitus 100 0.048
44
P OBS005 Obesity 91 0.048
45
ACR007 Acromegaly 80 0.048
46
c MYL006 Myeloid Leukemia 75 0.048
47
PRT036 Peritonitis 72 0.048
48
P HMN010 Hemangioma 71 0.048
49
SRC014 Sarcoma 70 0.048
50
c HPT016 Hepatitis B 70 0.048
51
P HPT001 Hepatitis C 67 0.048
52
ULC004 Ulcerative Colitis 65 0.048
53
P MLN008 Melanoma 65 0.048
54
P LRY019 Laryngitis 65 0.048
55
P MMP001 Mumps 60 0.048
56
CRT002 Cartilage-Hair Hypoplasia 60 0.048
57
HDC001 Headache 58 0.048
58
c SCK002 Sick Sinus Syndrome 58 0.048
59
CHN016 Cohen Syndrome 50 0.048
60
KR002 Kuru 47 0.048
61
NRN002 Neuronitis 44 0.048
62
HMP009 Haemophilus Influenzae 41 0.048
63
VRL002 Variola Minor 24 0.048
64
VRL003 Variola Major 17 0.048
65
P RHM011 Rheumatoid Arthritis 94 0.041
66
P MYC007 Myocardial Infarction 93 0.041
67
P ACT019 Acute Myeloid Leukemia 93 0.041
68
TBR010 Tuberculosis 87 0.041
69
P MLT020 Multiple Sclerosis 85 0.041
70
P RTN024 Retinoblastoma 82 0.041
71
P OST018 Osteosarcoma 82 0.041
72
OLV001 Olivopontocerebellar Atrophy 80 0.041
73
P PHC003 Pheochromocytoma 80 0.041
74
CNG034 Congestive Heart Failure 78 0.041
75
P HMP004 Hemophilia B 78 0.041
76
P CHR071 Charcot-Marie-Tooth Disease 72 0.041
77
SPS077 Sepsis 70 0.041
78
P MYS005 Myositis 70 0.041
79
P GLM007 Glomerulonephritis 69 0.041
80
P HYD006 Hydrocephalus 68 0.041
81
c MNN013 Meningitis 68 0.041
82
DMN002 Dementia 67 0.041
83
P GT001 Gout 66 0.041
84
PRP030 Purpura 66 0.041
85
PHR003 Pharyngitis 66 0.041
86
P MCL015 Mucolipidosis Ii 66 0.041
87
P FML020 Familial Combined Hyperlipidemia 66 0.041
88
P CLN016 Colon Cancer 65 0.041
89
c HYP069 Hyperparathyroidism 65 0.041
90
P CRT072 Creutzfeldt-Jakob Disease 64 0.041
91
ISC004 Ischemia 63 0.041
92
PSR002 Psoriasis 63 0.041
93
VGN023 Vaginitis 63 0.041
94
ADL030 Adult-Onset Still's Disease 62 0.041
95
NRP001 Neuropathy 62 0.041
96
P CRV035 Cervical Cancer 61 0.041
97
P SYN007 Synovitis 60 0.041
98
c TRT010 Teratoma 59 0.041
99
CVR006 Cavernous Hemangioma 59 0.041
100
c ATX004 Ataxia 59 0.041
101
c VRN002 Variant Creutzfeldt-Jakob Disease 58 0.041
102
ACN011 Acne 58 0.041
103
BRN056 Bronchopulmonary Dysplasia 57 0.041
104
IMP005 Impotence 55 0.041
105
CRM001 Crimean-Congo Hemorrhagic Fever 54 0.041
106
GST045 Gastroenteritis 54 0.041
107
MBS002 Moebius Syndrome 53 0.041
108
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 51 0.041
109
HYP068 Hyperostosis 50 0.041
110
c CNG018 Congenital Heart Block 48 0.041
111
AML029 Ameloblastoma 48 0.041
112
RLP002 Relapsing-Remitting Multiple Sclerosis 47 0.041
113
c MCL046 Mucolipidosis Iii Alpha/beta 42 0.041
114
HMT018 Hematopoietic Stem Cell Transplantation 41 0.041
115
MNK002 Monkeypox 41 0.041
116
NNT008 Neonatal Abstinence Syndrome 40 0.041
117
P HMP014 Hemophagocytic Lymphohistiocytosis, Familial, 4 39 0.041
118
OCH001 Ochronosis 38 0.041
119
MYC021 Mycobacterium Xenopi 26 0.041
120
PRD013 Periodic Fever, Familial, Autosomal Dominant 24 0.041
121
SPN151 Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy 24 0.041
122
LNR007 Linear and Whorled Nevoid Hypermelanosis 23 0.041
123
RMB001 Rombo Syndrome 21 0.041
124
MTG001 Metagonimiasis 20 0.041
125
AML003 Amelia Cleft Lip Palate Hydrocephalus Iris Coloboma 2 0.041
126
P ALZ001 Alzheimer's Disease 100 0.034
127
P PRS040 Prostate Cancer 98 0.034
128
P PRK002 Parkinson's Disease 93 0.034
129
P PNC035 Pancreatic Cancer 93 0.034
130
P DLT002 Dilated Cardiomyopathy 88 0.034
131
P OVR042 Ovarian Cancer 85 0.034
132
SMT004 Smith-Lemli-Opitz Syndrome 84 0.034
133
CDS001 Cadasil 84 0.034
134
P GST019 Gastrointestinal Stromal Tumor 83 0.034
135
CRH001 Crohn's Disease 76 0.034
136
CRB011 Cerebrotendinous Xanthomatosis 76 0.034
137
SKN016 Skin Disease 75 0.034
138
P CSH001 Cushing's Syndrome 75 0.034
139
P MLR004 Malaria 75 0.034
140
P MYL005 Myelofibrosis 75 0.034
141
DCH001 Duchenne Muscular Dystrophy 75 0.034
142
P PRM006 Primary Biliary Cirrhosis 73 0.034
143
c HYP095 Hypercholesterolemia 73 0.034
144
CCC001 Coccidioidomycosis 72 0.034
145
P PRM005 Primary Hyperparathyroidism 71 0.034
146
c HYP086 Hypothyroidism 69 0.034
147
P PLY011 Polycystic Ovary Syndrome 68 0.034
148
MSL001 Measles 68 0.034
149
ACT119 Acute Promyelocytic Leukemia 68 0.034
150
P HYP056 Hypoglycemia 67 0.034
151
ACT049 Acute Disseminated Encephalomyelitis 67 0.034
152
P HYP117 Hypertriglyceridemia 67 0.034
153
VSC011 Vasculitis 66 0.034
154
c THY032 Thyroiditis 66 0.034
155
P GST044 Gastritis 66 0.034
156
P HRD057 Hereditary Pancreatitis 66 0.034
157
RHM001 Rheumatic Fever 66 0.034
158
THR079 Thromboembolism 66 0.034
159
LYM017 Lyme Disease 65 0.034
160
HYP004 Hypercalcemia 65 0.034
161
ALK013 Alkaptonuria 65 0.034
162
MXD005 Mixed Connective Tissue Disease 64 0.034
163
HV1006 Hiv-1 64 0.034
164
c HYP076 Hyperthyroidism 64 0.034
165
LYM009 Lymphocytic Choriomeningitis 63 0.034
166
P RBL001 Rubella 63 0.034
167
BTN003 Biotinidase Deficiency 63 0.034
168
c PRP029 Porphyria 63 0.034
169
PRT037 Pertussis 62 0.034
170
P MYP004 Myopathy 62 0.034
171
DSS009 Disseminated Intravascular Coagulation 62 0.034
172
ART111 Artery Disease 62 0.034
173
SLY001 Sly Syndrome 61 0.034
174
CHR074 Choriocarcinoma 61 0.034
175
c MYL007 Myeloma 61 0.034
176
c ANG015 Angioedema 61 0.034
177
CRN017 Coronary Thrombosis 60 0.034
178
CHC001 Chickenpox 60 0.034
179
ANG020 Angiosarcoma 60 0.034
180
SPH001 Sapho Syndrome 60 0.034
181
c SLP006 Sleep Apnea 59 0.034
182
VSC002 Vascular Dementia 59 0.034
183
P PRS038 Personality Disorder 59 0.034
184
PRC012 Pericardial Effusion 58 0.034
185
DPH001 Diphtheria 58 0.034
186
EPD016 Epidermolysis Bullosa 58 0.034
187
P SNS014 Sinusitis 58 0.034
188
P QFV001 Q Fever 58 0.034
189
c EPD003 Epidermolysis Bullosa Simplex 58 0.034
190
P BCL006 B-Cell Lymphomas 57 0.034
191
LDP002 Lead Poisoning 57 0.034
192
CRD002 Cri-Du-Chat Syndrome 57 0.034
193
PLG002 Plague 56 0.034
194
TTH006 Tooth Disease 56 0.034
195
P CNG052 Congenital Amegakaryocytic Thrombocytopenia 56 0.034
196
FSH001 Fish-Eye Disease 56 0.034
197
NCR004 Nocardiosis 56 0.034
198
URT001 Urethritis 55 0.034
199
CYS014 Cystadenocarcinoma 55 0.034
200
FLT006 Floating-Harbor Syndrome 54 0.034
201
RTN023 Retinitis 54 0.034
202
END031 Endometrial Stromal Sarcoma 54 0.034
203
INT075 Intracranial Hypertension 53 0.034
204
PRC013 Pericarditis 53 0.034
205
PRT029 Parathyroid Adenoma 53 0.034
206
PRG009 Progressive Multifocal Leukoencephalopathy 53 0.034
207
BRS064 Bursitis 52 0.034
208
c KRN004 Kernicterus 52 0.034
209
P CLF002 Cleft Palate 52 0.034
210
TRG005 Torg Winchester Syndrome 52 0.034
211
AVN001 Avian Influenza 52 0.034
212
OBS001 Obstructive Jaundice 51 0.034
213
P CST002 Castleman's Disease 51 0.034
214
MMR004 Memory Impairment 51 0.034
215
ACT099 Acute Fatty Liver of Pregnancy 50 0.034
216
CRT013 Carotid Stenosis 49 0.034
217
BRL002 Buruli Ulcer Disease 49 0.034
218
LMB024 Limbic Encephalitis 49 0.034
219
WGN003 Wagner Syndrome 49 0.034
220
ASP007 Aspiration Pneumonia 49 0.034
221
MLN003 Melancholia 49 0.034
222
HDN002 Head Injury 49 0.034
223
PLM010 Pulmonary Edema 49 0.034
224
VLV010 Vulvovaginitis 48 0.034
225
CHY006 Chylous Ascites 48 0.034
226
MMB001 Membranoproliferative Glomerulonephritis 48 0.034
227
c HPT073 Hepatitis C Virus 48 0.034
228
CHL039 Choledocholithiasis 47 0.034
229
PRV004 Periventricular Leukomalacia 46 0.034
230
ANR040 Aneurysm 46 0.034
231
c CLR108 Colorectal Adenoma 46 0.034
232
MTB004 Metabolic Acidosis 45 0.034
233
c FTL001 Fetal Alcohol Syndrome 45 0.034
234
CTS011 Cutis Marmorata Telangiectatica Congenita 45 0.034
235
SCR011 Scrapie 45 0.034
236
c CTR098 Cataract 1, Multiple Types 44 0.034
237
SYN036 Syncope 44 0.034
238
LNG029 Lung Adenocarcinoma 44 0.034
239
c PTR004 Pterygium 43 0.034
240
KSH001 Keshan Disease 43 0.034
241
EPM005 Epimerase Deficiency Galactosemia 43 0.034
242
PHC013 Phaeochromocytoma 43 0.034
243
AMN003 Amnestic Disorder 43 0.034
244
c FNC027 Fanconi Anemia, Complementation Group a 41 0.034
245
OST097 Osteoporotic Fracture 41 0.034
246
INP001 Inappropriate Adh Syndrome 41 0.034
247
FCL012 Facial Paralysis 40 0.034
248
DNN002 Donnai-Barrow Syndrome 40 0.034
249
CRB009 Cerebritis 39 0.034
250
ELP001 Elephantiasis 39 0.034
251
SPR066 Superficial Siderosis 38 0.034
252
AKN002 Akinetic Mutism 37 0.034
253
MYP071 Myopathy Due to Myoadenylate Deaminase Deficiency 34 0.034
254
BDY001 Body Dysmorphic Disorder 34 0.034
255
KYS001 Kyasanur Forest Disease 33 0.034
256
LKM006 Leukomalacia 33 0.034
257
TST025 Testicular Microlithiasis 33 0.034
258
c CTR096 Cataract 6, Multiple Types 30 0.034
259
c LBR004 Leber Congenital Amaurosis 1 29 0.034
260
MNT006 Manitoba Oculotrichoanal Syndrome 28 0.034
261
UNC001 Uncombable Hair Syndrome 28 0.034
262
NRC003 Narcissistic Personality Disorder 27 0.034
263
P SPN205 Spinal Muscular Atrophy, X-Linked 2, Infantile 27 0.034
264
CHR158 Charles Bonnet Syndrome 26 0.034
265
c CTR102 Cataract 2, Multiple Types 25 0.034
266
MMS001 Momo Syndrome 25 0.034
267
CRN046 Corneal Fleck Dystrophy 24 0.034
268
PRD003 Periodontosis 22 0.034
269
OPH001 Ophthalmomyiasis 22 0.034
270
CGN001 Cogan-Reese Syndrome 21 0.034
271
DTH005 Diethylstilbestrol Syndrome 15 0.034
272
MNS002 Mini Stroke 15 0.034
273
HYP548 Hypogonadotropic Hypogonadism 2 with or Without Anosmia 14 0.034
274
UND003 Undifferentiated Connective Tissue Syndrome 12 0.034
275
CNT057 Central Centrifugal Cicatricial Alopecia 12 0.034
276
c CTR132 Cataract 3, Multiple Types 12 0.034
277
MLT076 Multiple System Atrophy with Orthostatic Hypotension 12 0.034
278
NDD001 Nodding Syndrome 12 0.034
279
YSH001 Yusho Disease 10 0.034
280
ERB002 Erb's Palsy 10 0.034
281
HND010 Handigodu Disease 10 0.034
282
SHR004 Sharp Syndrome 9 0.034
283
LYM053 Lymphomatous Thyroiditis 7 0.034
284
ABS002 Absence of Gluteal Muscle 6 0.034
285
BTH003 Bothriocephalosis 6 0.034
286
KRK002 Karak Syndrome 6 0.034
287
HDG007 Hodgkin's Lymphoma 93 0.024
288
P FML011 Familial Adenomatous Polyposis 89 0.024
289
P CHR090 Chronic Lymphocytic Leukemia 89 0.024
290
P MLT019 Multiple Myeloma 88 0.024
291
P FML021 Familial Hypercholesterolemia 86 0.024
292
P AGR001 Age Related Macular Degeneration 85 0.024
293
P APL001 Aplastic Anemia 83 0.024
294
P HMC003 Hemochromatosis 83 0.024
295
VNH001 Von Hippel-Lindau Disease 81 0.024
296
P ALG002 Alagille Syndrome 81 0.024
297
P NMN002 Niemann-Pick Disease 80 0.024
298
AND002 Androgen Insensitivity Syndrome 80 0.024
299
P MCP002 Mucopolysaccharidosis I 78 0.024
300
ADR007 Adrenoleukodystrophy 78 0.024
301
LSC001 Lesch-Nyhan Syndrome 78 0.024
302
BRK003 Burkitt's Lymphoma 77 0.024
303
LVR012 Liver Cirrhosis 77 0.024
304
P FML018 Familial Mediterranean Fever 76 0.024
305
P OST012 Osteoarthritis 76 0.024
306
P OST002 Osteoporosis 76 0.024
307
P PRP003 Porphyria Cutanea Tarda 75 0.024
308
P ALP006 Alpha Thalassemia 75 0.024
309
P LYM007 Lymphangioleiomyomatosis 74 0.024
310
BLM001 Bloom Syndrome 74 0.024
311
P LYN001 Lynch Syndrome 74 0.024
312
P WGN002 Wegener's Granulomatosis 74 0.024
313
CYS008 Cystic Echinococcosis 74 0.024
314
HST011 Histoplasmosis 73 0.024
315
P HRD008 Hereditary Hemorrhagic Telangiectasia 73 0.024
316
c CHR065 Chronic Myeloid Leukemia 73 0.024
317
c PLM037 Pulmonary Hypertension 73 0.024
318
ALL003 Allergic Rhinitis 73 0.024
319
c THL005 Thalassemia 72 0.024
320
P PRD006 Prader-Willi Syndrome 72 0.024
321
SCH014 Schistosomiasis 72 0.024
322
P ADD001 Addison's Disease 72 0.024
323
ACQ007 Acquired Immunodeficiency Syndrome 71 0.024
324
P DRM010 Dermatomyositis 71 0.024
325
DBT011 Diabetic Retinopathy 71 0.024
326
GNT003 Genital Herpes 70 0.024
327
P FRN006 Frontotemporal Dementia 70 0.024
328
P ANG001 Angelman Syndrome 70 0.024
329
c CRN037 Craniosynostosis 70 0.024
330
VSC007 Vascular Disease 70 0.024
331
P MGR002 Migraine 70 0.024
332
P DRV001 Dravet Syndrome 70 0.024
333
BLL006 Bullous Pemphigoid 70 0.024
334
P RSP003 Respiratory Failure 70 0.024
335
CHL065 Cholangiocarcinoma 69 0.024
336
MYC006 Mycosis Fungoides 69 0.024
337
PLY017 Polyarteritis Nodosa 69 0.024
338
KLP002 Klippel-Trenaunay Syndrome 69 0.024
339
P LVR013 Liver Disease 69 0.024
340
NRL016 Neural Tube Defects 68 0.024
341
P RCK004 Rickets 68 0.024
342
PSD007 Pseudomyxoma Peritonei 68 0.024
343
P AMY004 Amyloidosis 68 0.024
344
SCR008 Scrub Typhus 68 0.024
345
PSD012 Pseudoachondroplasia 68 0.024
346
DRM014 Dermatofibrosarcoma Protuberans 68 0.024
347
P SHR002 Short Stature 68 0.024
348
P FML032 Familial Hypertrophic Cardiomyopathy 68 0.024
349
P FCS002 Fucosidosis 68 0.024
350
P BCK002 Beckwith-Wiedemann Syndrome 68 0.024
351
P THY023 Thymoma 68 0.024
352
PRP027 Peripheral Vascular Disease 68 0.024
353
P HRP006 Herpes Simplex 68 0.024
354
SPN038 Spina Bifida 68 0.024
355
P ATP001 Atopic Dermatitis 67 0.024
356
TRG002 Trigeminal Neuralgia 67 0.024
357
BRN024 Bronchitis 67 0.024
358
HLY001 Hailey-Hailey Disease 67 0.024
359
P OST009 Osteochondritis Dissecans 67 0.024
360
P THR015 Thrombophilia 67 0.024
361
P DGR001 Digeorge Syndrome 67 0.024
362
ALV006 Alveolar Capillary Dysplasia 67 0.024
363
MLG056 Malignant Hyperthermia 66 0.024
364
STR008 Strongyloidiasis 66 0.024
365
P MCH002 Machado-Joseph Disease 66 0.024
366
CHR066 Chronic Fatigue Syndrome 66 0.024
367
c TXP001 Toxoplasmosis 66 0.024
368
c UVT001 Uveitis 66 0.024
369
DRM006 Dermatitis 66 0.024
370
PPL022 Papilloma 66 0.024
371
c ENC004 Encephalitis 66 0.024
372
CMM005 Common Cold 66 0.024
373
P GRF002 Graft Versus Host Disease 65 0.024
374
c HMP007 Hemophilia 65 0.024
375
c LNG028 Long Qt Syndrome 65 0.024
376
c SCL016 Scleroderma 65 0.024
377
CHR103 Charge Syndrome 65 0.024
378
TTN003 Tetanus 65 0.024
379
c SML001 Small Cell Carcinoma 64 0.024
380
ART019 Aortic Valve Stenosis 64 0.024
381
c ACT027 Acute Pancreatitis 64 0.024
382
FLT001 Felty's Syndrome 64 0.024
383
CHL014 Cholera 64 0.024
384
c MLG069 Malignant Hypertension 64 0.024
385
P RNL014 Renal Cell Carcinoma 64 0.024
386
P ART023 Arthropathy 64 0.024
387
P VLC001 Velocardiofacial Syndrome 64 0.024
388
STT002 Status Asthmaticus 64 0.024
389
BLL003 Bell's Palsy 64 0.024
390
DFC004 Deficiency Anemia 63 0.024
391
NSP001 Nasopharynx Carcinoma 63 0.024
392
DYS026 Dysfibrinogenemia 63 0.024
393
MLT022 Malt Lymphoma 63 0.024
394
c HYP055 Hypoplastic Left Heart Syndrome 63 0.024
395
P ANP001 Anaplastic Large Cell Lymphoma 63 0.024
396
ANR002 Aniridia 62 0.024
397
c MSC005 Muscular Dystrophy 62 0.024
398
P GTR002 Goiter 62 0.024
399
TRN001 Transthyretin Amyloidosis 62 0.024
400
VCT001 Vacterl Association 62 0.024
401
MTR014 Motor Neuron Disease 62 0.024
402
MLD001 Melioidosis 62 0.024
403
LCH002 Lichen Planus 62 0.024
404
HYD012 Hydrops Fetalis 62 0.024
405
P CND004 Candidiasis 62 0.024
406
GLC003 Glucose Intolerance 62 0.024
407
CTS003 Coats Disease 62 0.024
408
P FML043 Familial Idiopathic Basal Ganglia Calcification 61 0.024
409
THR004 Thrombocytosis 61 0.024
410
CNT009 Central Core Myopathy 61 0.024
411
NRL004 Neuroleptic Malignant Syndrome 61 0.024
412
PLM001 Pulmonary Tuberculosis 61 0.024
413
c DYS154 Dystonia 61 0.024
414
SCB001 Scabies 61 0.024
415
P PRT008 Proteus Syndrome 61 0.024
416
SRS001 Serous Cystadenocarcinoma 61 0.024
417
P SCL015 Scleritis 61 0.024
418
c MLT074 Multiple Endocrine Neoplasia 61 0.024
419
PLY023 Polycystic Liver Disease 61 0.024
420
TTR011 Tetraploidy 61 0.024
421
BRN002 Bronchiolitis 61 0.024
422
c AGM001 Agammaglobulinemia 61 0.024
423
CHL067 Cholecystitis 61 0.024
424
SPT013 Septic Shock 61 0.024
425
P LPS002 Liposarcoma 60 0.024
426
OLG003 Oligohydramnios 60 0.024
427
c HMP002 Hemophagocytic Lymphohistiocytosis 60 0.024
428
JCB001 Jacobsen Syndrome 60 0.024
429
ACR008 Acrocallosal Syndrome 60 0.024
430
P PRM126 Primary Peritoneal Carcinoma 60 0.024
431
P MLS001 Melas Syndrome 60 0.024
432
PMP001 Pemphigus 60 0.024
433
MCS003 Mucous Membrane Pemphigoid 60 0.024
434
c ACT075 Acute Myocardial Infarction 60 0.024
435
CLF001 Cleft Lip 60 0.024
436
c OPN001 Open-Angle Glaucoma 60 0.024
437
c PRG013 Paraganglioma 60 0.024
438
GNR005 Gonorrhea 60 0.024
439
P ALT001 Alternating Hemiplegia of Childhood 60 0.024
440
c NRN021 Neuronal Ceroid Lipofuscinosis 59 0.024
441
c HPT003 Hepatitis a 59 0.024
442
P ATS007 Autism Spectrum Disorder 59 0.024
443
P MTR005 Mitral Valve Prolapse 59 0.024
444
P CRT033 Corticobasal Degeneration 59 0.024
445
P OCL017 Oculocutaneous Albinism Type 1 59 0.024
446
INS001 Insulinoma 59 0.024
447
ECH003 Echinococcosis 59 0.024
448
CRY004 Cryoglobulinemia 59 0.024
449
MYX005 Myxoid Liposarcoma 59 0.024
450
ANN002 Anencephaly 59 0.024
451
BCT004 Bacteriuria 59 0.024
452
CLL003 Cellulitis 59 0.024
453
PLY041 Polymyositis 59 0.024
454
OST017 Osteomyelitis 59 0.024
455
CLL021 Collagenous Colitis 58 0.024
456
P GLB002 Glioblastoma 58 0.024
457
OBS061 Obstructive Sleep Apnea 58 0.024
458
THY019 Thyroid Hormone Resistance Syndrome 58 0.024
459
NNS002 Nonspecific Interstitial Pneumonia 58 0.024
460
P MYC008 Myocarditis 58 0.024
461
P SYP003 Syphilis 58 0.024
462
ORL005 Oral Candidiasis 58 0.024
463
PLM020 Pleomorphic Xanthoastrocytoma 58 0.024
464
P CYS010 Cystinosis 58 0.024
465
P DBT005 Diabetes Insipidus 58 0.024
466
CHR001 Churg-Strauss Syndrome 58 0.024
467
P PRM100 Primary Spontaneous Pneumothorax 58 0.024
468
EPT020 Epithelioid Hemangioendothelioma 58 0.024
469
P HMR012 Hemorrhagic Fever 58 0.024
470
GLB015 Glioblastoma Multiforme 58 0.024
471
PLM034 Pulmonary Emphysema 58 0.024
472
P PSR001 Psoriatic Arthritis 58 0.024
473
NPH018 Nephrogenic Systemic Fibrosis 58 0.024
474
PRN023 Prion Disease 58 0.024
475
RBS001 Rabies 57 0.024
476
P ACT009 Acute Monocytic Leukemia 57 0.024
477
RCT015 Reactive Arthritis 57 0.024
478
c MLG002 Malignant Peritoneal Mesothelioma 57 0.024
479
c MNC007 Monocytic Leukemia 57 0.024
480
c CTR002 Cataract 57 0.024
481
ALV005 Alveolar Soft Part Sarcoma 57 0.024
482
c BRC006 Brachydactyly 57 0.024
483
EGG001 Egg Allergy 57 0.024
484
P WVR001 Weaver Syndrome 57 0.024
485
HLC001 Holocarboxylase Synthetase Deficiency 57 0.024
486
c LYM026 Lymphoblastic Leukemia 57 0.024
487
P RTN012 Retinopathy of Prematurity 57 0.024
488
P PLY006 Polydactyly 57 0.024
489
c KBK001 Kabuki Syndrome 57 0.024
490
BLS002 Blastomycosis 57 0.024
491
PRT011 Protein C Deficiency 56 0.024
492
P AMY074 Amyotrophic Lateral Sclerosis Type 14 56 0.024
493
DDN006 Duodenitis 56 0.024
494
MYL003 Myeloid Sarcoma 56 0.024
495
c OCL002 Oculocutaneous Albinism 56 0.024
496
DFF005 Diffuse Large B-Cell Lymphoma 56 0.024
497
SSN001 Seasonal Affective Disorder 56 0.024
498
c SPN049 Spinocerebellar Ataxia 56 0.024
499
LPM005 Lipomatosis 56 0.024
500
MYM001 Myoma 56 0.024
501
MCL002 Macular Corneal Dystrophy 56 0.024
502
EPD037 Epidermal Nevus 56 0.024
503
TYP011 Typhus 56 0.024
504
RTN017 Retinal Detachment 56 0.024
505
P HYP014 Hyperuricemia 56 0.024
506
RDC002 Radiculopathy 56 0.024
507
KLN001 Klinefelter's Syndrome 56 0.024
508
MMM001 Mammary Paget's Disease 56 0.024
509
c CHR285 Chronic Myelomonocytic Leukemia 56 0.024
510
DST006 Diastolic Heart Failure 55 0.024
511
CRN012 Craniometaphyseal Dysplasia 55 0.024
512
P ESN001 Eosinophilic Esophagitis 55 0.024
513
ACR005 Acrodermatitis 55 0.024
514
VNS010 Venous Thromboembolism 55 0.024
515
ANR018 Anorchia 55 0.024
516
MCR004 Macroglobulinemia 55 0.024
517
TYP013 Type 1 Von Willebrand Disease 55 0.024
518
P PMP005 Pemphigus Vulgaris 55 0.024
519
c HRM001 Hermansky-Pudlak Syndrome 55 0.024
520
P INF032 Infertility 55 0.024
521
PRN009 Paranoid Schizophrenia 55 0.024
522
P SHR029 Short Syndrome 55 0.024
523
MGR001 Migraine Without Aura 55 0.024
524
c DNT011 Dentinogenesis Imperfecta 55 0.024
525
c PFF001 Pfeiffer Syndrome 55 0.024
526
P SPN016 Spondylocostal Dysostosis 55 0.024
527
MTN003 Motion Sickness 55 0.024
528
ASP001 Asperger Syndrome 55 0.024
529
c PRM010 Primary Open Angle Glaucoma 55 0.024
530
RFT001 Rift Valley Fever 55 0.024
531
P HMN013 Hemangiopericytoma 55 0.024
532
MYL001 Myelitis 55 0.024
533
MDL009 Medullary Sponge Kidney 55 0.024
534
ANG011 Angiodysplasia 55 0.024
535
P BTM001 Beta-Mannosidosis 55 0.024
536
NWC001 Newcastle Disease 54 0.024
537
PLY012 Polyhydramnios 54 0.024
538
FLL013 Follicular Dendritic Cell Sarcoma 54 0.024
539
CTY001 Cat Eye Syndrome 54 0.024
540
SCH012 Schizoaffective Disorder 54 0.024
541
P VNT002 Ventricular Septal Defect 54 0.024
542
TLR001 Tularemia 54 0.024
543
NPH051 Nephritis 54 0.024
544
c ANT034 Anterior Uveitis 54 0.024
545
MLT075 Multifocal Motor Neuropathy 54 0.024
546
c ACT134 Acute Liver Failure 54 0.024
547
P RBN002 Robinow Syndrome 54 0.024
548
AND003 Andersen-Tawil Syndrome 54 0.024
549
CNR004 Cone-Rod Dystrophy 2 54 0.024
550
P ENC008 Encephalocele 54 0.024
551
BRS081 Breast Cancer Susceptibility 53 0.024
552
P PLM006 Pulmonary Alveolar Proteinosis 53 0.024
553
MDD011 Mood Disorder 53 0.024
554
TCK001 Tick-Borne Encephalitis 53 0.024
555
LPS007 Lupus Nephritis 53 0.024
556
BLN003 Blindness 53 0.024
557
ADN020 Adenosarcoma 53 0.024
558
CLR003 Clear Cell Adenocarcinoma 53 0.024
559
P HYP083 Hypopituitarism 53 0.024
560
STN007 Stenotrophomonas Maltophilia 53 0.024
561
MMB002 Membranous Glomerulonephritis 53 0.024
562
TRN015 Transient Cerebral Ischemia 53 0.024
563
c HPT007 Hepatitis E 53 0.024
564
SPT005 Spotted Fever 53 0.024
565
RSD004 Rosai-Dorfman Disease 53 0.024
566
RSC001 Rosacea 52 0.024
567
ATR057 Atrioventricular Block 52 0.024
568
P OMP004 Omphalocele 52 0.024
569
c USH006 Usher Syndrome, Type 1b 52 0.024
570
P PRM052 Primary Progressive Aphasia 52 0.024
571
PLS025 Plasmablastic Lymphoma 52 0.024
572
c ACT078 Acute Porphyria 52 0.024
573
CTS005 Catastrophic Antiphospholipid Syndrome 52 0.024
574
DYS073 Dysphagia 52 0.024
575
EST003 Eastern Equine Encephalitis 52 0.024
576
HVD003 Hiv/aids 52 0.024
577
MNT147 Mental Retardation 52 0.024
578
SBC001 Subacute Sclerosing Panencephalitis 52 0.024
579
c DRR001 Diarrhea 52 0.024
580
EXS001 Exostosis 52 0.024
581
GND002 Gender Identity Disorder 51 0.024
582
MNN014 Mononeuritis 51 0.024
583
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 51 0.024
584
MCN008 Mucinous Cystadenocarcinoma 51 0.024
585
LYM027 Lymphopenia 51 0.024
586
END041 Endometrial Adenocarcinoma 51 0.024
587
ORC001 Orchitis 51 0.024
588
P GND004 Gonadal Dysgenesis 51 0.024
589
P CNG119 Congenital Porphyria 51 0.024
590
c STC001 Stickler Syndrome 51 0.024
591
P GRV001 Graves' Disease 51 0.024
592
CHL052 Choledochal Cyst 51 0.024
593
BRN018 Borna Disease 51 0.024
594
P CTR103 Cataract 4, Multiple Types 51 0.024
595
CYS009 Cystadenoma 51 0.024
596
OVR012 Ovarian Serous Cystadenocarcinoma 51 0.024
597
P FNC004 Fanconi Syndrome 50 0.024
598
CLS010 Cluster Headache 50 0.024
599
ANS003 Anisakiasis 50 0.024
600
c ATM024 Autoimmune Pancreatitis 50 0.024
601
HYP006 Hypertensive Heart Disease 50 0.024
602
P MWT001 Mowat-Wilson Syndrome 50 0.024
603
GRM009 Germ Cell Tumors 50 0.024
604
PYR014 Pyridoxine-Dependent Epilepsy 50 0.024
605
P LFR002 Lafora Disease 50 0.024
606
MYC013 Mycobacterium Abscessus 50 0.024
607
c BCT007 Bacterial Meningitis 50 0.024
608
DBW001 Dubowitz Syndrome 50 0.024
609
BCT015 Bacteremia 50 0.024
610
DNT005 Dentatorubral-Pallidoluysian Atrophy 50 0.024
611
CWP001 Cowpox 50 0.024
612
FBR047 Fibromyalgia 50 0.024
613
P PRT096 Peritoneal Mesothelioma 50 0.024
614
CHR288 Chronic Recurrent Multifocal Osteomyelitis 50 0.024
615
P ACH020 Achromatopsia 2 49 0.024
616
c ACT135 Acute Graft Versus Host Disease 49 0.024
617
DRG003 Drug Dependence 49 0.024
618
ALC010 Alcoholic Cardiomyopathy 49 0.024
619
THY022 Thymic Carcinoma 49 0.024
620
TRN044 Transposition of the Great Arteries 49 0.024
621
SMN007 Seminoma 49 0.024
622
P JRV001 Jervell-Lange Nielsen Syndrome 49 0.024
623
ETH011 Ethylmalonic Encephalopathy 49 0.024
624
ALB002 Albinism 49 0.024
625
PLS016 Plasma Cell Leukemia 49 0.024
626
KLB001 Klebsiella 49 0.024
627
P SLL003 Salla Disease 49 0.024
628
c ORF002 Orofacial Cleft 49 0.024
629
FCL022 Focal Dystonia 49 0.024
630
TRF001 Trifunctional Protein Deficiency 49 0.024
631
END028 Endemic Goiter 49 0.024
632
ACT087 Acth Deficiency 49 0.024
633
HRT012 Heart Valve Disease 49 0.024
634
GLD002 Goldberg-Shprintzen Megacolon Syndrome 49 0.024
635
MTS001 Mutism 49 0.024
636
RTR011 Retroperitoneal Fibrosis 48 0.024
637
PPL018 Papillary Adenocarcinoma 48 0.024
638
CRY001 Cryptogenic Organizing Pneumonia 48 0.024
639
c CHR130 Charcot-Marie-Tooth Disease Type 1b 48 0.024
640
LCT001 Lactic Acidosis 48 0.024
641
LGS001 Legius Syndrome 48 0.024
642
VTM002 Vitamin B12 Deficiency 48 0.024
643
LYM021 Lymphadenitis 48 0.024
644
c PRN026 Porencephaly 48 0.024
645
P TRN034 Transverse Myelitis 47 0.024
646
MYS001 Myositis Ossificans 47 0.024
647
PTY003 Pityriasis Rubra Pilaris 47 0.024
648
FRN002 Frontal Lobe Epilepsy 47 0.024
649
EPD029 Epidermolysis Bullosa Simplex, Generalized 47 0.024
650
RPP001 Rapp-Hodgkin Syndrome 47 0.024
651
FBR054 Fibroma 47 0.024
652
SPL004 Splenic Marginal Zone Lymphoma 47 0.024
653
TBR008 Tuberculous Peritonitis 47 0.024
654
SPL018 Splenomegaly 47 0.024
655
MCR037 Macroglossia 47 0.024
656
ASC002 Ascariasis 47 0.024
657
P ATR005 Atrophic Gastritis 46 0.024
658
c PRL003 Proliferative Glomerulonephritis 46 0.024
659
P HMR005 Hemorrhoid 46 0.024
660
STC004 Stachybotrys Chartarum 46 0.024
661
P HMR003 Hemorrhagic Disease 46 0.024
662
MDS022 Mediastinitis 46 0.024
663
BRN013 Bronchiolitis Obliterans Organizing Pneumonia 46 0.024
664
LPD006 Lipoid Proteinosis 46 0.024
665
PSD010 Pseudogout 46 0.024
666
NDL021 Nodular Lymphocyte Predominant Hodgkin Lymphoma 46 0.024
667
ECT026 Ectopic Pregnancy 46 0.024
668
P AZS001 Azoospermia 45 0.024
669
DNR001 Duane Retraction Syndrome 45 0.024
670
BRB001 Beriberi 45 0.024
671
P FCS001 Facioscapulohumeral Muscular Dystrophy 45 0.024
672
THN006 Thin Basement Membrane Nephropathy 45 0.024
673
P CLR017 Clear Cell Sarcoma 45 0.024
674
c LTT001 Lattice Corneal Dystrophy 45 0.024
675
CRP018 Cor Pulmonale 45 0.024
676
ZYG002 Zygomycosis 45 0.024
677
TXC020 Toxic Oil Syndrome 44 0.024
678
c ACT004 Acute Diarrhea 44 0.024
679
SCL025 Scleromyxedema 44 0.024
680
MTC027 Mitochondrial Trifunctional Protein Deficiency 44 0.024
681
CHR276 Chronic Active Epstein-Barr Virus Infection 44 0.024
682
CLL002 Collecting Duct Carcinoma 44 0.024
683
c OST039 Osteogenesis Imperfecta Type 5 44 0.024
684
NCR002 Necrobiosis Lipoidica 44 0.024
685
c CNG224 Congenital Disorder of Glycosylation Type 1a 44 0.024
686
P D2H001 D-2-Hydroxyglutaric Aciduria 43 0.024
687
P CYS017 Cystic Teratoma 43 0.024
688
BLP005 Blepharitis 43 0.024
689
HRD042 Hereditary Cerebral Hemorrhage with Amyloidosis 43 0.024
690
CND006 Candida Glabrata 43 0.024
691
RMS001 Rem Sleep Behavior Disorder 43 0.024
692
OBS004 Obstructive Hydrocephalus 43 0.024
693
MYC019 Mycobacterium Marinum 43 0.024
694
P ICH049 Ichthyosis, Congenital, Autosomal Recessive 2 43 0.024
695
HST006 Histidinemia 43 0.024
696
PRN014 Paronychia 43 0.024
697
GND001 Gonadoblastoma 43 0.024
698
P XNT005 Xanthinuria Type 1 43 0.024
699
c CHR104 Chorea 42 0.024
700
TTZ001 Tietze's Syndrome 42 0.024
701
EPS026 Epispadias 42 0.024
702
WHP002 Whiplash 42 0.024
703
MYC017 Mycobacterium Kansasii 42 0.024
704
P VGN017 Vaginal Cancer 42 0.024
705
LSS003 Lassa Fever 41 0.024
706
OCL025 Ocular Toxoplasmosis 41 0.024
707
MNT189 Mental Retardation, X-Linked 29 and Others 41 0.024
708
PMP002 Pemphigoid Gestationis 41 0.024
709
ESP028 Esophageal Squamous Cell Carcinoma 41 0.024
710
LPB001 Lipoblastoma 41 0.024
711
RBF001 Riboflavin Deficiency 41 0.024
712
ACL001 Acalculous Cholecystitis 41 0.024
713
PLN006 Poland Syndrome 41 0.024
714
BLR015 Blue Rubber Bleb Nevus Syndrome 41 0.024
715
MCK002 Meckel's Diverticulum 41 0.024
716
MTR010 Mature Teratoma 41 0.024
717
VRY001 Very Long-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 40 0.024
718
GST052 Gestational Choriocarcinoma 40 0.024
719
RHB022 Rhabdoid Tumors, Somatic 40 0.024
720
INF013 Inferior Myocardial Infarction 40 0.024
721
SWY002 Swyer Syndrome 40 0.024
722
c INF037 Inflammatory Bowel Disease 40 0.024
723
P LSS005 Lissencephaly 1 40 0.024
724
SPR035 Superior Vena Cava Syndrome 40 0.024
725
MGS001 Megaesophagus 40 0.024
726
INT079 Intrahepatic Cholangiocarcinoma 40 0.024
727
SPN028 Spondyloepimetaphyseal Dysplasia, Strudwick Type 39 0.024
728
CRB085 Cerebral Hemorrhage 39 0.024
729
HPT063 Hepatitis B Virus Infection 39 0.024
730
DNR002 Duane-Radial Ray Syndrome 39 0.024
731
CRP002 Croup 39 0.024
732
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 39 0.024
733
URT004 Urethral Syndrome 39 0.024
734
P FNN001 Finnish Type Amyloidosis 39 0.024
735
PRM018 Primary Hypertrophic Osteoarthropathy 39 0.024
736
FNT004 Fainting 39 0.024
737
MNN002 Mononeuritis Multiplex 38 0.024
738
ANG037 Angiomatosis 38 0.024
739
TND004 Tendinopathy 38 0.024
740
INT020 Intravenous Leiomyomatosis 38 0.024
741
c DMN027 Dominant Optic Atrophy 38 0.024
742
MNN032 Meningococcal Meningitis 38 0.024
743
PST086 Posterior Cortical Atrophy 38 0.024
744
P GLM006 Glomangioma 38 0.024
745
BRN055 Bronchogenic Cyst 38 0.024
746
SPP009 Sepiapterin Reductase Deficiency 38 0.024
747
HRP002 Herpes Gestationis 37 0.024
748
c ICH040 Ichthyosis, Congenital, Autosomal Recessive 4a 37 0.024
749
HNS001 Hansen's Disease 37 0.024
750
DSQ001 Desquamative Interstitial Pneumonia 37 0.024
751
TRS021 Triosephosphate Isomerase Deficiency 37 0.024
752
FTD001 Foot Drop 37 0.024
753
EMN001 Emanuel Syndrome 37 0.024
754
MTR003 Mitral Valve Stenosis 37 0.024
755
LNG039 Lung Squamous Cell Carcinoma 37 0.024
756
SPN137 Spondyloepiphyseal Dysplasia Maroteaux Type 37 0.024
757
ANX004 Anoxia 37 0.024
758
EPC002 Epicondylitis 36 0.024
759
TBS001 Tabes Dorsalis 36 0.024
760
TRN021 Transaldolase Deficiency 36 0.024
761
RTR001 Retrograde Amnesia 36 0.024
762
c PPL025 Popliteal Pterygium Syndrome 36 0.024
763
PNC041 Pancreatic Ductal Adenocarcinoma 35 0.024
764
DCB001 Decubitus Ulcer 35 0.024
765
P PYR011 Pyropoikilocytosis 35 0.024
766
NRS005 Neurosarcoidosis 35 0.024
767
P DYS005 Dyslexia 35 0.024
768
HYP034 Hypertensive Encephalopathy 35 0.024
769
THM001 Thomsen Disease 35 0.024
770
TNC003 Tinea Corporis 35 0.024
771
CGN006 Cogan Syndrome 34 0.024
772
MLK004 Malakoplakia 34 0.024
773
ATM021 Autoimmune Inner Ear Disease 34 0.024
774
EXS013 Exstrophy-Epispadias Complex 34 0.024
775
c TRP015 Triphalangeal Thumb 34 0.024
776
CYC008 Cyclic Vomiting Syndrome 34 0.024
777
c HYP440 Hyperphosphatasia with Mental Retardation Syndrome 34 0.024
778
CNG219 Congenital Aural Atresia 33 0.024
779
BRK004 Barakat Syndrome 33 0.024
780
CTN013 Cutaneous Anthrax 33 0.024
781
P OPT051 Opitz Gbbb Syndrome, Type I 33 0.024
782
ADG002 Audiogenic Seizures 33 0.024
783
UNV001 Unverricht-Lundborg Syndrome 32 0.024
784
NRM009 Normokalemic Periodic Paralysis 32 0.024
785
c OCL035 Oculocutaneous Albinism Type 1b 32 0.024
786
VBR003 Vibrio Vulnificus Infection 32 0.024
787
EHL050 Ehlers–danlos Syndrome Dermatosparaxis Type 32 0.024
788
FGS001 Fg Syndrome 32 0.024
789
TNC001 Tinea Cruris 32 0.024
790
MDL006 Madelung Disease 32 0.024
791
TST021 Testicular Germ Cell Tumor 31 0.024
792
SPR009 Sporadic Breast Cancer 31 0.024
793
CHR028 Chronic Wasting Disease 31 0.024
794
BLK001 Balkan Nephropathy 31 0.024
795
IDM001 Ideomotor Apraxia 31 0.024
796
VGN019 Vaginal Discharge 31 0.024
797
SPL007 Splenic Abscess 31 0.024
798
PDT027 Pediatric Ulcerative Colitis 30 0.024
799
TRL003 Toriello Carey Syndrome 30 0.024
800
PRS051 Parastremmatic Dwarfism 30 0.024
801
INT003 Intracranial Hypotension 30 0.024
802
P CMM008 Communicating Hydrocephalus 30 0.024
803
MTH047 Methanol Poisoning 30 0.024
804
P BRS089 Breast and Colorectal Cancer 30 0.024
805
CYT004 Cytomegalic Inclusion Disease 30 0.024
806
P CTR133 Cataract 22, Autosomal Recessive 30 0.024
807
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 30 0.024
808
ARB001 Ariboflavinosis 30 0.024
809
c MCP036 Mucopolysaccharidosis Ih/s 30 0.024
810
c SPN073 Spinocerebellar Ataxia Type 12 30 0.024
811
c PST061 Posterior Polymorphous Corneal Dystrophy 30 0.024
812
P SVR013 Severe Congenital Neutropenia Autosomal Recessive 3 29 0.024
813
c LMB018 Limb-Girdle Muscular Dystrophy, Type 1a 29 0.024
814
c LSS006 Lissencephaly 2 29 0.024
815
NRC001 Neurocirculatory Asthenia 29 0.024
816
INN003 Iniencephaly 29 0.024
817
SNL010 Senile Systemic Amyloidosis 29 0.024
818
GLL028 Gillespie Syndrome 29 0.024
819
CRN061 Corneal Dystrophy Avellino Type 29 0.024
820
STY001 Satoyoshi Syndrome 29 0.024
821
EPD046 Epididymitis 29 0.024
822
c ICH041 Ichthyosis, Autosomal Recessive 4b 29 0.024
823
JPN001 Japanese Spotted Fever 29 0.024
824
PLC009 Placenta Praevia 29 0.024
825
HRP001 Herpangina 28 0.024
826
ANH001 Ainhum 28 0.024
827
PRG074 Progressive Myoclonus Epilepsy, Lafora Type 28 0.024
828
DND007 Dandy-Walker Like Malformation with Atrioventricular Septal Defect 28 0.024
829
MYC014 Mycobacterium Chelonae 28 0.024
830
c ORF007 Orofaciodigital Syndrome 2 27 0.024
831
SLL001 Sialolithiasis 27 0.024
832
HYP160 Hyperkeratosis Lenticularis Perstans 27 0.024
833
TRT003 Tertiary Syphilis 27 0.024
834
SBD001 Subdural Empyema 27 0.024
835
c CTR124 Cataract 10, Multiple Types 27 0.024
836
KKC001 Kikuchi Disease 27 0.024
837
CRT028 Cor Triatriatum 27 0.024
838
ADT001 Auditory Agnosia 27 0.024
839
CNG049 Congenital Stromal Corneal Dystrophy 27 0.024
840
P OTD002 Otodental Syndrome 27 0.024
841
3Q2001 3q29 Deletion Syndrome 27 0.024
842
PLR006 Pleural Cancer 26 0.024
843
CNR008 Cone-Rod Dystrophy Amelogenesis Imperfecta 26 0.024
844
DYS009 Dysthymic Disorder 26 0.024
845
SCL022 Scleredema 26 0.024
846
YNG002 Young Syndrome 26 0.024
847
PNT006 Pentosuria 26 0.024
848
TRN028 Transient Acantholytic Dermatosis 26 0.024
849
c PRK057 Parkinson Disease, Late-Onset 26 0.024
850
BNT002 Bantu Siderosis 26 0.024
851
PRM056 Primrose Syndrome 25 0.024
852
CPP003 Cap Polyposis 25 0.024
853
MNT061 Mental Retardation-Hypotonic Facies Syndrome, X-Linked 25 0.024
854
P TTR013 Tetrasomy X 25 0.024
855
HRD052 Hereditary Mucoepithelial Dysplasia 25 0.024
856
c ICH051 Ichthyosis, Congenital, Autosomal Recessive 11 25 0.024
857
c CHR247 Chromosome 4p Deletion 25 0.024
858
PLN007 Plantar Fasciitis 25 0.024
859
NVS007 Nevus of Ota 25 0.024
860
PNM003 Pneumatosis Cystoides Intestinalis 25 0.024
861
DPR002 Depersonalization Disorder 25 0.024
862
FMR003 Femoral Neuropathy 25 0.024
863
LCH008 Lichen Planus Pigmentosus 25 0.024
864
P DNT025 Dentinogenesis Imperfecta 1 24 0.024
865
c RNG013 Ring Chromosome 18 24 0.024
866
OMS001 Omsk Hemorrhagic Fever 24 0.024
867
ATY013 Atypical Rett Syndrome 24 0.024
868
BLN002 Balanitis Xerotica Obliterans 24 0.024
869
ARR026 Arrhythmogenic Right Ventricular Dysplasia 1 24 0.024
870
FMR012 Femur-Fibula-Ulna Complex 24 0.024
871
HRL002 Harlequin Syndrome 23 0.024
872
P HYD015 Hydroa Vacciniforme 23 0.024
873
PLY031 Polydactyly Myopia Syndrome 23 0.024
874
P HYP438 Hyperaldosteronism, Familial, Type Iii 23 0.024
875
MSN002 Mesenteric Lymphadenitis 23 0.024
876
ACK001 Ackerman Syndrome 23 0.024
877
P SKN012 Skin Carcinoma in Situ 23 0.024
878
P CTS012 Cutis Verticis Gyrata 23 0.024
879
OVR098 Ovarian Fibroma 23 0.024
880
c ACT059 Acute Maxillary Sinusitis 23 0.024
881
NTV001 Native American Myopathy 22 0.024
882
ISS001 Isosporiasis 22 0.024
883
CNZ006 Coenzyme Q10 Deficiency, Primary, 1 22 0.024
884
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 22 0.024
885
ANN010 Anonychia-Onychodystrophy with Hypoplasia or Absence of Distal Phalanges 22 0.024
886
NNN015 Noonan-Like/multiple Giant Cell Lesion Syndrome 21 0.024
887
c ACT072 Acute Laryngitis 21 0.024
888
LRP001 Leri Pleonosteosis 21 0.024
889
c CHR057 Chronic Laryngitis 21 0.024
890
RDT005 Radiation Induced Cancer 21 0.024
891
MNG007 Manganese Poisoning 21 0.024
892
c ICH047 Ichthyosis, Congenital, Autosomal Recessive 1 21 0.024
893
DMN026 Dementia Pugilistica 21 0.024
894
GTP001 Gait Apraxia 21 0.024
895
SPR063 Superior Canal Dehiscence Syndrome 21 0.024
896
HMC012 Hemicrania Continua 20 0.024
897
FRS004 Free Sialic Acid Storage Disorders 20 0.024
898
THR099 Third-Degree Atrioventricular Block 20 0.024
899
PRN010 Paranoid Personality Disorder 20 0.024
900
MRZ001 Mirizzi Syndrome 19 0.024
901
c RNP003 Renpenning Syndrome 1 19 0.024
902
MLT058 Multiple Self Healing Squamous Epithelioma 19 0.024
903
PSD078 Pseudofolliculitis Barbae 19 0.024
904
SHR027 Short Stature Wormian Bones Dextrocardia 19 0.024
905
THN005 Thunderclap Headache 19 0.024
906
DYS135 Dysphagia Lusoria 19 0.024
907
CHR084 Chromosomal Disease 18 0.024
908
P FRN036 Frontonasal Dysplasia 1 18 0.024
909
PRM040 Primary Basilar Impression 18 0.024
910
OSL001 Oslam Syndrome 18 0.024
911
RBN004 Robin Sequence and Oligodactyly 18 0.024
912
LJH001 Lujo Hemorrhagic Fever 18 0.024
913
FML211 Familial Papillary or Follicular Thyroid Carcinoma 18 0.024
914
RGN005 Regional Odontodysplasia 18 0.024
915
PRG072 Progressive Myoclonic Epilepsy 3 with or Without Intracellular Inclusions 18 0.024
916
MRN004 Morning Glory Disc Anomaly 18 0.024
917
HYP145 Hyperbetaalaninemia 18 0.024
918
BRN045 Brunner Syndrome 17 0.024
919
PSD027 Pseudoaminopterin Syndrome 17 0.024
920
ACC005 Accessory Pancreas 17 0.024
921
MLP004 Malpuech Facial Clefting Syndrome 17 0.024
922
INF048 Infantile Histiocytoid Cardiomyopathy 16 0.024
923
ELC001 Elective Mutism 16 0.024
924
ORP002 Oropouche Fever 16 0.024
925
P ENC021 Encephalopathy, Neonatal Severe 16 0.024
926
c NTR033 Neutropenia, Severe Congenital 1, Autosomal Dominant 16 0.024
927
DPH012 Diphallia 16 0.024
928
c CRD093 Cardiomyopathy, Dilated, 1a 16 0.024
929
ALK001 Alkhurma Hemorrhagic Fever 15 0.024
930
BNG042 Benign Multicystic Peritoneal Mesothelioma 15 0.024
931
URC004 Urachal Cancer 15 0.024
932
SPN092 Spinal Shock 15 0.024
933
CRN126 Corneal Dystrophy, Lisch Epithelial 15 0.024
934
CNG408 Congenital Deafness with Vitiligo and Achalasia 15 0.024
935
ACH028 Acheiria 15 0.024
936
c OTD001 Otodental Dysplasia 14 0.024
937
SBP006 Subepithelial Mucinous Corneal Dystrophy 14 0.024
938
c DST049 Distal Spinal Muscular Atrophy Type 3 14 0.024
939
c ICH048 Ichthyosis, Congenital, Autosomal Recessive 9 14 0.024
940
PRS119 Persistent Genital Arousal Disorder 14 0.024
941
CNG067 Congenital Cystic Eye 14 0.024
942
TRG006 Trigger Thumb 14 0.024
943
CRT056 Carotidynia 13 0.024
944
c PRD030 Periodontitis 1, Juvenile 13 0.024
945
c ICH042 Ichthyosis, Congenital, Autosomal Recessive 6 13 0.024
946
c ICH050 Ichthyosis, Congenital, Autosomal Recessive 5 13 0.024
947
c CTR115 Cataract 16, Multiple Types 13 0.024
948
c CTR118 Cataract 14, Multiple Types 13 0.024
949
c ICH039 Ichthyosis, Congenital, Autosomal Recessive 10 13 0.024
950
ORF018 Orofacial Cleft11 13 0.024
951
c CTR122 Cataract 5, Multiple Types 12 0.024
952
c CTR130 Cataract 9, Multiple Types 12 0.024
953
MRG007 Morgellons 12 0.024
954
c CTR113 Cataract 11, Multiple Types 12 0.024
955
HYD031 Hydroxyprolinemia 12 0.024
956
c ICH044 Ichthyosis, Congenital, Autosomal Recessive 8 12 0.024
957
KYR001 Kyrle Disease 12 0.024
958
c ICH038 Ichthyosis, Congenital, Autosomal Recessive 3 12 0.024
959
ERY040 Erythema Palmaris Hereditarium 12 0.024
960
JMP002 Jumping Frenchmen of Maine 12 0.024
961
c MNT171 Mental Retardation, Autosomal Dominant 17 12 0.024
962
c CTR129 Cataract 31, Multiple Types 11 0.024
963
ACC001 Accessory Nerve Disease 11 0.024
964
c CTR131 Cataract 17, Multiple Types 11 0.024
965
c ICH045 Ichthyosis, Congenital, Autosomal Recessive 7 11 0.024
966
c CTR104 Cataract 18, Autosomal Recessive 11 0.024
967
c PRX053 Peroxisome Biogenesis Disorder 14b 11 0.024
968
c ELL007 Elliptocytosis-1 10 0.024
969
c PRX050 Peroxisome Biogenesis Disorder 9b 10 0.024
970
URC001 Urachus Cancer 9 0.024
971
UHL001 Uhl Anomaly 9 0.024
972
CTR043 Cataract, Pulverulent or Cerulean, with or Without Microcornea 8 0.024
973
MNM003 Minimally Differentiated Acute Myeloblastic Leukemia 8 0.024
974
PRV008 Parvovirus Antenatal Infection 7 0.024
975
HYP512 Hyperproinsulinemia, Familial 7 0.024
976
PHS019 Phosphohydroxylysinuria 7 0.024
977
OBS014 Obsessive-Compulsive Disorder, Protection Against 6 0.024
978
MTR033 Motor Sensory Neuropathy Type 1 Aplasia Cutis Congenita 3 0.024