Search results for "WAS"

963 hits were found for 'WAS'

# Family MCID Name MIFTS Score
1
P WSK001 Wiskott-Aldrich Syndrome 78 21.947
2
WSR001 Was-Related Disorders 6 15.289
3
THR065 Thrombocytopenia, X-Linked, Intermittent 9 7.091
4
c THR014 Thrombocytopenia 70 5.292
5
XLN068 X-Linked Thrombocytopenia 52 4.832
6
c NTR004 Neutropenia 64 4.298
7
SVR014 Severe Congenital Neutropenia X-Linked 24 3.703
8
c THR005 Thrombotic Thrombocytopenic Purpura 58 3.052
9
P SVR003 Severe Congenital Neutropenia 50 3.039
10
INT051 Intussusception 58 3.024
11
PRM097 Primary Immunodeficiency Disease 46 3.024
12
P HYP163 Hyperlipidemia Type 3 27 0.214
13
c HPT021 Hepatitis 64 0.095
14
P LKM002 Leukemia 77 0.083
15
P HYP075 Hypertension 85 0.075
16
P ESP024 Esophagitis 63 0.075
17
P ADN016 Adenocarcinoma 58 0.075
18
P ART022 Arthritis 75 0.068
19
P BRS047 Breast Cancer 100 0.063
20
c PNC044 Pancreatitis 69 0.063
21
P AST005 Asthma 88 0.058
22
ESP021 Esophageal Cancer 80 0.058
23
P LNG032 Lung Cancer 72 0.058
24
PRS047 Prostatitis 60 0.058
25
SML019 Smallpox 42 0.058
26
CRV058 Cervicofacial Lymphatic Malformation 13 0.058
27
P SCH015 Schizophrenia 82 0.053
28
P PNM007 Pneumonia 76 0.053
29
P CLR023 Colorectal Cancer 73 0.053
30
ADN018 Adenoma 64 0.053
31
P CRV039 Cervicitis 57 0.053
32
END072 Endotheliitis 50 0.053
33
WST005 West Nile Virus 42 0.053
34
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 33 0.053
35
P SYS001 Systemic Lupus Erythematosus 85 0.048
36
HPT023 Hepatocellular Carcinoma 79 0.048
37
ACR007 Acromegaly 79 0.048
38
c DBT009 Diabetes Mellitus 78 0.048
39
c LPS004 Lupus Erythematosus 72 0.048
40
c MYL006 Myeloid Leukemia 72 0.048
41
P HMN010 Hemangioma 70 0.048
42
SRC014 Sarcoma 69 0.048
43
P INF038 Influenza 68 0.048
44
c HPT016 Hepatitis B 68 0.048
45
DMN002 Dementia 66 0.048
46
P HPT001 Hepatitis C 66 0.048
47
MYS005 Myositis 66 0.048
48
P LRY019 Laryngitis 65 0.048
49
ULC004 Ulcerative Colitis 63 0.048
50
P MLN008 Melanoma 63 0.048
51
P MMP001 Mumps 59 0.048
52
HDC001 Headache 58 0.048
53
c SCK002 Sick Sinus Syndrome 56 0.048
54
CRT002 Cartilage-Hair Hypoplasia 56 0.048
55
CHN016 Cohen Syndrome 50 0.048
56
NRN002 Neuronitis 43 0.048
57
KR002 Kuru 43 0.048
58
VRL002 Variola Minor 24 0.048
59
VRL003 Variola Major 18 0.048
60
P ALZ001 Alzheimer's Disease 97 0.041
61
P RHM011 Rheumatoid Arthritis 93 0.041
62
P ACT019 Acute Myeloid Leukemia 92 0.041
63
P MYC007 Myocardial Infarction 92 0.041
64
P OBS005 Obesity 89 0.041
65
TBR010 Tuberculosis 83 0.041
66
P RTN024 Retinoblastoma 81 0.041
67
P OST018 Osteosarcoma 79 0.041
68
OLV001 Olivopontocerebellar Atrophy 79 0.041
69
P PHC003 Pheochromocytoma 78 0.041
70
P CLN016 Colon Cancer 78 0.041
71
CNG034 Congestive Heart Failure 78 0.041
72
P HMP004 Hemophilia B 77 0.041
73
PRT036 Peritonitis 71 0.041
74
P CHR071 Charcot-Marie-Tooth Disease 70 0.041
75
SPS077 Sepsis 70 0.041
76
P FRN006 Frontotemporal Dementia 70 0.041
77
P MLT020 Multiple Sclerosis 69 0.041
78
P HYD006 Hydrocephalus 68 0.041
79
c MNN013 Meningitis 68 0.041
80
P GT001 Gout 65 0.041
81
PHR003 Pharyngitis 65 0.041
82
PRP030 Purpura 64 0.041
83
P MCL015 Mucolipidosis Ii 64 0.041
84
P FML020 Familial Combined Hyperlipidemia 63 0.041
85
ISC004 Ischemia 63 0.041
86
PSR002 Psoriasis 63 0.041
87
P CRT072 Creutzfeldt-Jakob Disease 62 0.041
88
VGN023 Vaginitis 62 0.041
89
ADL030 Adult-Onset Still's Disease 61 0.041
90
HV1006 Hiv-1 61 0.041
91
NRP001 Neuropathy 61 0.041
92
P CRV035 Cervical Cancer 60 0.041
93
CVR006 Cavernous Hemangioma 58 0.041
94
c ATX004 Ataxia 58 0.041
95
c VRN002 Variant Creutzfeldt-Jakob Disease 58 0.041
96
BRN056 Bronchopulmonary Dysplasia 57 0.041
97
IMP005 Impotence 55 0.041
98
c TRT010 Teratoma 55 0.041
99
MBS002 Moebius Syndrome 53 0.041
100
GST045 Gastroenteritis 53 0.041
101
ENC006 Encephalomyelitis 52 0.041
102
c MYL014 Myeloproliferative Disorder 52 0.041
103
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 51 0.041
104
c CNG018 Congenital Heart Block 49 0.041
105
RLP002 Relapsing-Remitting Multiple Sclerosis 46 0.041
106
c MCL046 Mucolipidosis Iii Alpha/beta 41 0.041
107
NNT008 Neonatal Abstinence Syndrome 41 0.041
108
MNK002 Monkeypox 40 0.041
109
c HMP014 Hemophagocytic Lymphohistiocytosis, Familial, 4 38 0.041
110
OCH001 Ochronosis 37 0.041
111
MYC021 Mycobacterium Xenopi 26 0.041
112
PRD013 Periodic Fever, Familial, Autosomal Dominant 24 0.041
113
LNR007 Linear and Whorled Nevoid Hypermelanosis 23 0.041
114
SPN151 Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy 22 0.041
115
RMB001 Rombo Syndrome 21 0.041
116
MTG001 Metagonimiasis 20 0.041
117
DTH005 Diethylstilbestrol Syndrome 14 0.041
118
AML003 Amelia Cleft Lip Palate Hydrocephalus Iris Coloboma 2 0.041
119
c TYP009 Type 2 Diabetes Mellitus 95 0.034
120
P PRK002 Parkinson's Disease 92 0.034
121
P PNC035 Pancreatic Cancer 91 0.034
122
P PRS040 Prostate Cancer 87 0.034
123
CDS001 Cadasil 84 0.034
124
CRN211 Coronary Artery Disease 84 0.034
125
P SMT004 Smith-Lemli-Opitz Syndrome 82 0.034
126
P GST019 Gastrointestinal Stromal Tumor 82 0.034
127
P DLT002 Dilated Cardiomyopathy 82 0.034
128
P OVR042 Ovarian Cancer 81 0.034
129
P CSH001 Cushing's Syndrome 80 0.034
130
CRB011 Cerebrotendinous Xanthomatosis 75 0.034
131
SKN016 Skin Disease 75 0.034
132
P MLR004 Malaria 75 0.034
133
DCH001 Duchenne Muscular Dystrophy 74 0.034
134
P PRM006 Primary Biliary Cirrhosis 72 0.034
135
P MYL005 Myelofibrosis 72 0.034
136
DBT011 Diabetic Retinopathy 70 0.034
137
c HYP095 Hypercholesterolemia 70 0.034
138
CCC001 Coccidioidomycosis 70 0.034
139
c HYP086 Hypothyroidism 69 0.034
140
P GLM007 Glomerulonephritis 68 0.034
141
MSL001 Measles 67 0.034
142
P BCK002 Beckwith-Wiedemann Syndrome 67 0.034
143
P GST044 Gastritis 66 0.034
144
c THY032 Thyroiditis 66 0.034
145
VSC011 Vasculitis 66 0.034
146
P HYP117 Hypertriglyceridemia 65 0.034
147
LYM017 Lyme Disease 64 0.034
148
c HYP069 Hyperparathyroidism 64 0.034
149
P HRD057 Hereditary Pancreatitis 64 0.034
150
THR079 Thromboembolism 64 0.034
151
ALK013 Alkaptonuria 63 0.034
152
MXD005 Mixed Connective Tissue Disease 63 0.034
153
ACT049 Acute Disseminated Encephalomyelitis 63 0.034
154
HYP056 Hypoglycemia 63 0.034
155
LYM009 Lymphocytic Choriomeningitis 63 0.034
156
RHM001 Rheumatic Fever 62 0.034
157
c EPD003 Epidermolysis Bullosa Simplex 62 0.034
158
DSS009 Disseminated Intravascular Coagulation 62 0.034
159
c HYP076 Hyperthyroidism 62 0.034
160
BTN003 Biotinidase Deficiency 62 0.034
161
P RBL001 Rubella 62 0.034
162
c MYP004 Myopathy 62 0.034
163
c PRP029 Porphyria 61 0.034
164
PRT037 Pertussis 61 0.034
165
c MYL007 Myeloma 61 0.034
166
ART111 Artery Disease 60 0.034
167
P GLC007 Glaucoma 60 0.034
168
ANG020 Angiosarcoma 60 0.034
169
CHC001 Chickenpox 60 0.034
170
P SYN007 Synovitis 59 0.034
171
CHR074 Choriocarcinoma 59 0.034
172
CRN017 Coronary Thrombosis 59 0.034
173
VSC002 Vascular Dementia 59 0.034
174
SLY001 Sly Syndrome 58 0.034
175
P PRS038 Personality Disorder 58 0.034
176
PRC012 Pericardial Effusion 58 0.034
177
DPH001 Diphtheria 58 0.034
178
P QFV001 Q Fever 57 0.034
179
P VRL012 Viral Meningitis 57 0.034
180
P SNS014 Sinusitis 57 0.034
181
c ANG015 Angioedema 57 0.034
182
ACN011 Acne 57 0.034
183
EPD016 Epidermolysis Bullosa 56 0.034
184
LDP002 Lead Poisoning 56 0.034
185
CRD002 Cri-Du-Chat Syndrome 56 0.034
186
PLG002 Plague 56 0.034
187
NCR004 Nocardiosis 56 0.034
188
c SPN049 Spinocerebellar Ataxia 56 0.034
189
P CNG052 Congenital Amegakaryocytic Thrombocytopenia 55 0.034
190
TTH006 Tooth Disease 55 0.034
191
URT001 Urethritis 54 0.034
192
CYS014 Cystadenocarcinoma 54 0.034
193
CRM001 Crimean-Congo Hemorrhagic Fever 54 0.034
194
END031 Endometrial Stromal Sarcoma 53 0.034
195
LMB024 Limbic Encephalitis 53 0.034
196
PRC013 Pericarditis 53 0.034
197
PRG009 Progressive Multifocal Leukoencephalopathy 52 0.034
198
PRT029 Parathyroid Adenoma 52 0.034
199
c KRN004 Kernicterus 52 0.034
200
P CLF002 Cleft Palate 52 0.034
201
BRS064 Bursitis 52 0.034
202
INT075 Intracranial Hypertension 51 0.034
203
MNT147 Mental Retardation 51 0.034
204
TRG005 Torg Winchester Syndrome 51 0.034
205
P CST002 Castleman's Disease 50 0.034
206
OBS001 Obstructive Jaundice 50 0.034
207
MMR004 Memory Impairment 50 0.034
208
HYP068 Hyperostosis 50 0.034
209
ACT099 Acute Fatty Liver of Pregnancy 49 0.034
210
CRT013 Carotid Stenosis 49 0.034
211
WGN003 Wagner Syndrome 48 0.034
212
BRL002 Buruli Ulcer Disease 48 0.034
213
ASP007 Aspiration Pneumonia 48 0.034
214
MLN003 Melancholia 48 0.034
215
PLM010 Pulmonary Edema 48 0.034
216
HDN002 Head Injury 48 0.034
217
MMB001 Membranoproliferative Glomerulonephritis 47 0.034
218
CHL039 Choledocholithiasis 47 0.034
219
VLV010 Vulvovaginitis 47 0.034
220
PRV004 Periventricular Leukomalacia 46 0.034
221
c HPT073 Hepatitis C Virus 45 0.034
222
c FTL001 Fetal Alcohol Syndrome 45 0.034
223
ANR040 Aneurysm 44 0.034
224
c CLR108 Colorectal Adenoma 44 0.034
225
CTS011 Cutis Marmorata Telangiectatica Congenita 44 0.034
226
SYN036 Syncope 44 0.034
227
c PTR004 Pterygium 43 0.034
228
EPM005 Epimerase Deficiency Galactosemia 43 0.034
229
LNG029 Lung Adenocarcinoma 42 0.034
230
PHC013 Phaeochromocytoma 42 0.034
231
KSH001 Keshan Disease 42 0.034
232
AMN003 Amnestic Disorder 41 0.034
233
c CTR098 Cataract 1, Multiple Types 41 0.034
234
HMT018 Hematopoietic Stem Cell Transplantation 40 0.034
235
FCL012 Facial Paralysis 40 0.034
236
INP001 Inappropriate Adh Syndrome 40 0.034
237
P FNC027 Fanconi Anemia, Complementation Group a 39 0.034
238
CRB009 Cerebritis 39 0.034
239
DNN002 Donnai-Barrow Syndrome 38 0.034
240
ELP001 Elephantiasis 38 0.034
241
SPR066 Superficial Siderosis 38 0.034
242
AKN002 Akinetic Mutism 36 0.034
243
MYP071 Myopathy Due to Myoadenylate Deaminase Deficiency 33 0.034
244
KYS001 Kyasanur Forest Disease 33 0.034
245
LKM006 Leukomalacia 33 0.034
246
TST025 Testicular Microlithiasis 32 0.034
247
BDY001 Body Dysmorphic Disorder 32 0.034
248
c CTR096 Cataract 6, Multiple Types 29 0.034
249
UNC001 Uncombable Hair Syndrome 28 0.034
250
c LBR004 Leber Congenital Amaurosis 1 27 0.034
251
NRC003 Narcissistic Personality Disorder 27 0.034
252
MNT006 Manitoba Oculotrichoanal Syndrome 27 0.034
253
P SPN205 Spinal Muscular Atrophy, X-Linked 2, Infantile 26 0.034
254
CHR158 Charles Bonnet Syndrome 26 0.034
255
MMS001 Momo Syndrome 25 0.034
256
CRN046 Corneal Fleck Dystrophy 24 0.034
257
c CTR132 Cataract 3, Multiple Types 24 0.034
258
OPH001 Ophthalmomyiasis 22 0.034
259
PRD003 Periodontosis 21 0.034
260
MLT011 Multiple Mucosal Neuroma 16 0.034
261
c CTR102 Cataract 2, Multiple Types 12 0.034
262
CNT057 Central Centrifugal Cicatricial Alopecia 12 0.034
263
UND003 Undifferentiated Connective Tissue Syndrome 12 0.034
264
MLT076 Multiple System Atrophy with Orthostatic Hypotension 12 0.034
265
YSH001 Yusho Disease 10 0.034
266
SHR004 Sharp Syndrome 10 0.034
267
ERB002 Erb's Palsy 10 0.034
268
HND010 Handigodu Disease 10 0.034
269
KRK002 Karak Syndrome 7 0.034
270
LYM053 Lymphomatous Thyroiditis 7 0.034
271
ABS002 Absence of Gluteal Muscle 6 0.034
272
BTH003 Bothriocephalosis 6 0.034
273
NDD001 Nodding Syndrome 6 0.034
274
P AMY001 Amyotrophic Lateral Sclerosis 98 0.024
275
HDG007 Hodgkin's Lymphoma 92 0.024
276
P FML021 Familial Hypercholesterolemia 85 0.024
277
P FML011 Familial Adenomatous Polyposis 85 0.024
278
AGR001 Age Related Macular Degeneration 83 0.024
279
P MLT019 Multiple Myeloma 82 0.024
280
P PRM021 Primary Pulmonary Hypertension 82 0.024
281
P APL001 Aplastic Anemia 82 0.024
282
P HRD008 Hereditary Hemorrhagic Telangiectasia 81 0.024
283
P NMN002 Niemann-Pick Disease 81 0.024
284
AND002 Androgen Insensitivity Syndrome 80 0.024
285
VNH001 Von Hippel-Lindau Disease 80 0.024
286
P HMC003 Hemochromatosis 78 0.024
287
ADR007 Adrenoleukodystrophy 77 0.024
288
BRK003 Burkitt's Lymphoma 77 0.024
289
P NRL016 Neural Tube Defects 77 0.024
290
LSC001 Lesch-Nyhan Syndrome 77 0.024
291
P OST012 Osteoarthritis 75 0.024
292
P PRP003 Porphyria Cutanea Tarda 75 0.024
293
P OST002 Osteoporosis 75 0.024
294
BLM001 Bloom Syndrome 74 0.024
295
CRH001 Crohn's Disease 74 0.024
296
P LYM007 Lymphangioleiomyomatosis 73 0.024
297
HST011 Histoplasmosis 73 0.024
298
c THL005 Thalassemia 72 0.024
299
P FCL005 Focal Segmental Glomerulosclerosis 72 0.024
300
P PRD006 Prader-Willi Syndrome 71 0.024
301
c CHR065 Chronic Myeloid Leukemia 71 0.024
302
P WGN002 Wegener's Granulomatosis 71 0.024
303
P ANG001 Angelman Syndrome 70 0.024
304
VSC007 Vascular Disease 70 0.024
305
SCH014 Schistosomiasis 70 0.024
306
P LYN001 Lynch Syndrome 70 0.024
307
c CRN037 Craniosynostosis 70 0.024
308
PLY017 Polyarteritis Nodosa 69 0.024
309
P END044 Endometriosis 69 0.024
310
BRN024 Bronchitis 69 0.024
311
P MGR002 Migraine 69 0.024
312
P LVR013 Liver Disease 69 0.024
313
CHL065 Cholangiocarcinoma 69 0.024
314
P DRV001 Dravet Syndrome 69 0.024
315
DRM006 Dermatitis 69 0.024
316
P RSP003 Respiratory Failure 68 0.024
317
P PRM005 Primary Hyperparathyroidism 68 0.024
318
P ADD001 Addison's Disease 68 0.024
319
GNT003 Genital Herpes 68 0.024
320
SCR008 Scrub Typhus 68 0.024
321
P DRM010 Dermatomyositis 68 0.024
322
KLP002 Klippel-Trenaunay Syndrome 67 0.024
323
c CHR090 Chronic Lymphocytic Leukemia 67 0.024
324
PRP027 Peripheral Vascular Disease 67 0.024
325
PSD007 Pseudomyxoma Peritonei 67 0.024
326
P AMY004 Amyloidosis 67 0.024
327
c HMP007 Hemophilia 67 0.024
328
P FCS002 Fucosidosis 67 0.024
329
TRG002 Trigeminal Neuralgia 67 0.024
330
P DGR001 Digeorge Syndrome 67 0.024
331
SPN038 Spina Bifida 67 0.024
332
P OST009 Osteochondritis Dissecans 67 0.024
333
MYC006 Mycosis Fungoides 66 0.024
334
ACT119 Acute Promyelocytic Leukemia 66 0.024
335
P THY023 Thymoma 66 0.024
336
HLY001 Hailey-Hailey Disease 66 0.024
337
P PLY011 Polycystic Ovary Syndrome 66 0.024
338
P HRP006 Herpes Simplex 66 0.024
339
P THR015 Thrombophilia 66 0.024
340
P ESS001 Essential Tremor 65 0.024
341
c TXP001 Toxoplasmosis 65 0.024
342
HYP004 Hypercalcemia 65 0.024
343
c UVT001 Uveitis 65 0.024
344
PPL022 Papilloma 65 0.024
345
P FML032 Familial Hypertrophic Cardiomyopathy 65 0.024
346
c ENC004 Encephalitis 65 0.024
347
ANR002 Aniridia 65 0.024
348
P RCK004 Rickets 64 0.024
349
c SCL016 Scleroderma 64 0.024
350
CYS008 Cystic Echinococcosis 64 0.024
351
DRM014 Dermatofibrosarcoma Protuberans 64 0.024
352
MLG056 Malignant Hyperthermia 64 0.024
353
c NRN021 Neuronal Ceroid Lipofuscinosis 64 0.024
354
P MCP004 Mucopolysaccharidosis Iv 64 0.024
355
P ATP001 Atopic Dermatitis 64 0.024
356
ALL003 Allergic Rhinitis 64 0.024
357
c SML001 Small Cell Carcinoma 64 0.024
358
ART019 Aortic Valve Stenosis 64 0.024
359
P GRV001 Graves' Disease 64 0.024
360
CHR066 Chronic Fatigue Syndrome 64 0.024
361
STR008 Strongyloidiasis 64 0.024
362
FLT001 Felty's Syndrome 63 0.024
363
CHR103 Charge Syndrome 63 0.024
364
CMM005 Common Cold 63 0.024
365
P HMP002 Hemophagocytic Lymphohistiocytosis 63 0.024
366
c MLG069 Malignant Hypertension 63 0.024
367
ALV006 Alveolar Capillary Dysplasia 63 0.024
368
P ART023 Arthropathy 63 0.024
369
P VLC001 Velocardiofacial Syndrome 63 0.024
370
TTN003 Tetanus 63 0.024
371
DFC004 Deficiency Anemia 62 0.024
372
P RNL014 Renal Cell Carcinoma 62 0.024
373
c MSC005 Muscular Dystrophy 62 0.024
374
NSP001 Nasopharynx Carcinoma 62 0.024
375
P HYP055 Hypoplastic Left Heart Syndrome 62 0.024
376
P ANP001 Anaplastic Large Cell Lymphoma 62 0.024
377
P GTR002 Goiter 62 0.024
378
CNT009 Central Core Myopathy 61 0.024
379
MTR014 Motor Neuron Disease 61 0.024
380
HYD012 Hydrops Fetalis 61 0.024
381
MLD001 Melioidosis 61 0.024
382
VCT001 Vacterl Association 61 0.024
383
P CND004 Candidiasis 61 0.024
384
P LPS002 Liposarcoma 61 0.024
385
TTR011 Tetraploidy 61 0.024
386
ACQ007 Acquired Immunodeficiency Syndrome 61 0.024
387
BLL003 Bell's Palsy 60 0.024
388
STT002 Status Asthmaticus 60 0.024
389
PLY023 Polycystic Liver Disease 60 0.024
390
SRS001 Serous Cystadenocarcinoma 60 0.024
391
PLM001 Pulmonary Tuberculosis 60 0.024
392
NRL004 Neuroleptic Malignant Syndrome 60 0.024
393
P DFF005 Diffuse Large B-Cell Lymphoma 60 0.024
394
P ACT009 Acute Monocytic Leukemia 60 0.024
395
PMP001 Pemphigus 60 0.024
396
BRN002 Bronchiolitis 60 0.024
397
P GRF002 Graft Versus Host Disease 60 0.024
398
CHL067 Cholecystitis 60 0.024
399
SPT013 Septic Shock 60 0.024
400
c AGM001 Agammaglobulinemia 60 0.024
401
OLG003 Oligohydramnios 59 0.024
402
INS001 Insulinoma 59 0.024
403
ACR008 Acrocallosal Syndrome 59 0.024
404
c DYS154 Dystonia 59 0.024
405
JCB001 Jacobsen Syndrome 59 0.024
406
P PRM126 Primary Peritoneal Carcinoma 59 0.024
407
GLM008 Glomus Tumor 59 0.024
408
P MLS001 Melas Syndrome 59 0.024
409
P SCL015 Scleritis 59 0.024
410
CLF001 Cleft Lip 59 0.024
411
THR004 Thrombocytosis 59 0.024
412
c ACT075 Acute Myocardial Infarction 59 0.024
413
c MLT074 Multiple Endocrine Neoplasia 59 0.024
414
P ATS007 Autism Spectrum Disorder 59 0.024
415
CHL014 Cholera 59 0.024
416
GNR005 Gonorrhea 59 0.024
417
SPH001 Sapho Syndrome 59 0.024
418
P CRT033 Corticobasal Degeneration 59 0.024
419
GLB015 Glioblastoma Multiforme 59 0.024
420
c SLP006 Sleep Apnea 59 0.024
421
P OCL017 Oculocutaneous Albinism Type 1 59 0.024
422
c HPT003 Hepatitis a 59 0.024
423
SCB001 Scabies 59 0.024
424
MCS003 Mucous Membrane Pemphigoid 58 0.024
425
P TRN001 Transthyretin Amyloidosis 58 0.024
426
P ALT001 Alternating Hemiplegia of Childhood 58 0.024
427
MYX005 Myxoid Liposarcoma 58 0.024
428
P ALP006 Alpha Thalassemia 58 0.024
429
c OCL002 Oculocutaneous Albinism 58 0.024
430
MLT022 Malt Lymphoma 58 0.024
431
c MNC007 Monocytic Leukemia 58 0.024
432
PLY041 Polymyositis 58 0.024
433
NPH018 Nephrogenic Systemic Fibrosis 58 0.024
434
P MCH002 Machado-Joseph Disease 58 0.024
435
BCT004 Bacteriuria 58 0.024
436
CLL003 Cellulitis 58 0.024
437
EPT020 Epithelioid Hemangioendothelioma 58 0.024
438
OST017 Osteomyelitis 58 0.024
439
ANN002 Anencephaly 58 0.024
440
THY019 Thyroid Hormone Resistance Syndrome 58 0.024
441
GLC003 Glucose Intolerance 58 0.024
442
CRY004 Cryoglobulinemia 57 0.024
443
c OPN001 Open-Angle Glaucoma 57 0.024
444
P DBT005 Diabetes Insipidus 57 0.024
445
P SYP003 Syphilis 57 0.024
446
PLM020 Pleomorphic Xanthoastrocytoma 57 0.024
447
ECH003 Echinococcosis 57 0.024
448
NNS002 Nonspecific Interstitial Pneumonia 57 0.024
449
PRN023 Prion Disease 57 0.024
450
P MYC008 Myocarditis 57 0.024
451
RCT015 Reactive Arthritis 57 0.024
452
PLM034 Pulmonary Emphysema 57 0.024
453
P PRT008 Proteus Syndrome 57 0.024
454
RBS001 Rabies 57 0.024
455
CHR001 Churg-Strauss Syndrome 57 0.024
456
c CTR002 Cataract 57 0.024
457
ALV005 Alveolar Soft Part Sarcoma 57 0.024
458
EGG001 Egg Allergy 57 0.024
459
P RTN012 Retinopathy of Prematurity 56 0.024
460
ORL005 Oral Candidiasis 56 0.024
461
P PLY006 Polydactyly 56 0.024
462
P WVR001 Weaver Syndrome 56 0.024
463
P HYP014 Hyperuricemia 56 0.024
464
CLL021 Collagenous Colitis 56 0.024
465
HLC001 Holocarboxylase Synthetase Deficiency 56 0.024
466
c DNT011 Dentinogenesis Imperfecta 56 0.024
467
MCL002 Macular Corneal Dystrophy 56 0.024
468
DDN006 Duodenitis 56 0.024
469
MYL003 Myeloid Sarcoma 56 0.024
470
c CHR285 Chronic Myelomonocytic Leukemia 56 0.024
471
SSN001 Seasonal Affective Disorder 56 0.024
472
P PRM052 Primary Progressive Aphasia 55 0.024
473
APP008 Appendicitis 55 0.024
474
c KBK001 Kabuki Syndrome 55 0.024
475
ANR018 Anorchia 55 0.024
476
TYP011 Typhus 55 0.024
477
PRT011 Protein C Deficiency 55 0.024
478
MMM001 Mammary Paget's Disease 55 0.024
479
RTN017 Retinal Detachment 55 0.024
480
P PMP005 Pemphigus Vulgaris 55 0.024
481
RDC002 Radiculopathy 55 0.024
482
DST006 Diastolic Heart Failure 55 0.024
483
P PSR001 Psoriatic Arthritis 55 0.024
484
ACR005 Acrodermatitis 55 0.024
485
c PRM010 Primary Open Angle Glaucoma 55 0.024
486
c BRC006 Brachydactyly 55 0.024
487
P INF032 Infertility 55 0.024
488
MDL009 Medullary Sponge Kidney 55 0.024
489
MGR001 Migraine Without Aura 55 0.024
490
P SHR029 Short Syndrome 55 0.024
491
LPM005 Lipomatosis 54 0.024
492
RFT001 Rift Valley Fever 54 0.024
493
c LYM026 Lymphoblastic Leukemia 54 0.024
494
MTN003 Motion Sickness 54 0.024
495
NPH051 Nephritis 54 0.024
496
BLS002 Blastomycosis 54 0.024
497
P HMN013 Hemangiopericytoma 54 0.024
498
c VNT002 Ventricular Septal Defect 54 0.024
499
CTY001 Cat Eye Syndrome 54 0.024
500
MYL001 Myelitis 54 0.024
501
ANG011 Angiodysplasia 54 0.024
502
PLY012 Polyhydramnios 54 0.024
503
FLT006 Floating-Harbor Syndrome 54 0.024
504
DBT006 Diabetic Macular Edema 54 0.024
505
FLL013 Follicular Dendritic Cell Sarcoma 54 0.024
506
CRN012 Craniometaphyseal Dysplasia 54 0.024
507
MCR004 Macroglobulinemia 54 0.024
508
EPD037 Epidermal Nevus 54 0.024
509
NWC001 Newcastle Disease 54 0.024
510
SCH012 Schizoaffective Disorder 54 0.024
511
BRS081 Breast Cancer Susceptibility 54 0.024
512
ASP001 Asperger Syndrome 53 0.024
513
P BTM001 Beta-Mannosidosis 53 0.024
514
RTN023 Retinitis 53 0.024
515
c HRM001 Hermansky-Pudlak Syndrome 53 0.024
516
c SPN016 Spondylocostal Dysostosis 53 0.024
517
PLS025 Plasmablastic Lymphoma 53 0.024
518
P ESN001 Eosinophilic Esophagitis 53 0.024
519
TLR001 Tularemia 53 0.024
520
VNS010 Venous Thromboembolism 53 0.024
521
MDD011 Mood Disorder 53 0.024
522
AND003 Andersen-Tawil Syndrome 53 0.024
523
PRN009 Paranoid Schizophrenia 53 0.024
524
P RBN002 Robinow Syndrome 53 0.024
525
TCK001 Tick-Borne Encephalitis 53 0.024
526
P PLM006 Pulmonary Alveolar Proteinosis 53 0.024
527
KLN001 Klinefelter's Syndrome 52 0.024
528
CLR003 Clear Cell Adenocarcinoma 52 0.024
529
LPS007 Lupus Nephritis 52 0.024
530
ADN020 Adenosarcoma 52 0.024
531
P HYP083 Hypopituitarism 52 0.024
532
STN007 Stenotrophomonas Maltophilia 52 0.024
533
MYM001 Myoma 52 0.024
534
P OMP004 Omphalocele 52 0.024
535
P DYS026 Dysfibrinogenemia 52 0.024
536
ORC001 Orchitis 52 0.024
537
P ENC008 Encephalocele 52 0.024
538
SPT005 Spotted Fever 52 0.024
539
RSD004 Rosai-Dorfman Disease 52 0.024
540
P CYS010 Cystinosis 52 0.024
541
EST003 Eastern Equine Encephalitis 52 0.024
542
DRM004 Dermatofibrosarcoma 52 0.024
543
P GND004 Gonadal Dysgenesis 52 0.024
544
c HPT007 Hepatitis E 52 0.024
545
CTS005 Catastrophic Antiphospholipid Syndrome 52 0.024
546
MMB002 Membranous Glomerulonephritis 51 0.024
547
CNR004 Cone-Rod Dystrophy 2 51 0.024
548
DYS073 Dysphagia 51 0.024
549
c PRG013 Paraganglioma 51 0.024
550
c ACT078 Acute Porphyria 51 0.024
551
P CNG119 Congenital Porphyria 51 0.024
552
SBC001 Subacute Sclerosing Panencephalitis 51 0.024
553
GND002 Gender Identity Disorder 51 0.024
554
EXS001 Exostosis 51 0.024
555
AVN001 Avian Influenza 51 0.024
556
c DRR001 Diarrhea 51 0.024
557
MCN008 Mucinous Cystadenocarcinoma 51 0.024
558
c ANT034 Anterior Uveitis 51 0.024
559
MNN014 Mononeuritis 51 0.024
560
LYM027 Lymphopenia 51 0.024
561
RSC001 Rosacea 50 0.024
562
c ATM024 Autoimmune Pancreatitis 50 0.024
563
ARR001 Arrhythmogenic Right Ventricular Dysplasia 50 0.024
564
BRN018 Borna Disease 50 0.024
565
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 50 0.024
566
CHL052 Choledochal Cyst 50 0.024
567
ANS003 Anisakiasis 50 0.024
568
CYS009 Cystadenoma 50 0.024
569
c STC001 Stickler Syndrome 50 0.024
570
CHK001 Chikungunya 50 0.024
571
c ACT135 Acute Graft Versus Host Disease 50 0.024
572
P INT063 Intellectual Disability 50 0.024
573
CLS010 Cluster Headache 50 0.024
574
P MJR001 Major Depressive Disorder 50 0.024
575
HYP006 Hypertensive Heart Disease 50 0.024
576
TYP013 Type 1 Von Willebrand Disease 50 0.024
577
DNT005 Dentatorubral-Pallidoluysian Atrophy 50 0.024
578
MYC013 Mycobacterium Abscessus 50 0.024
579
END041 Endometrial Adenocarcinoma 49 0.024
580
c BCT007 Bacterial Meningitis 49 0.024
581
P FNC004 Fanconi Syndrome 49 0.024
582
P LFR002 Lafora Disease 49 0.024
583
CWP001 Cowpox 49 0.024
584
DBW001 Dubowitz Syndrome 49 0.024
585
PYR014 Pyridoxine-Dependent Epilepsy 49 0.024
586
P MWT001 Mowat-Wilson Syndrome 49 0.024
587
P ACH020 Achromatopsia 2 49 0.024
588
FBR047 Fibromyalgia 49 0.024
589
SMN007 Seminoma 49 0.024
590
TRN044 Transposition of the Great Arteries 49 0.024
591
DRG003 Drug Dependence 49 0.024
592
TRF001 Trifunctional Protein Deficiency 49 0.024
593
CHR288 Chronic Recurrent Multifocal Osteomyelitis 49 0.024
594
P BCL006 B-Cell Lymphomas 49 0.024
595
P JRV001 Jervell-Lange Nielsen Syndrome 49 0.024
596
ALB002 Albinism 49 0.024
597
P GRM009 Germ Cell Tumors 49 0.024
598
MLT075 Multifocal Motor Neuropathy 49 0.024
599
ALC010 Alcoholic Cardiomyopathy 48 0.024
600
KLB001 Klebsiella 48 0.024
601
ACT087 Acth Deficiency 48 0.024
602
HRT012 Heart Valve Disease 48 0.024
603
RTR011 Retroperitoneal Fibrosis 48 0.024
604
ETH011 Ethylmalonic Encephalopathy 48 0.024
605
FCL022 Focal Dystonia 48 0.024
606
MTS001 Mutism 48 0.024
607
P SLL003 Salla Disease 48 0.024
608
c CHR130 Charcot-Marie-Tooth Disease Type 1b 48 0.024
609
BCT015 Bacteremia 48 0.024
610
THY022 Thymic Carcinoma 48 0.024
611
END028 Endemic Goiter 48 0.024
612
CHY006 Chylous Ascites 48 0.024
613
PPL018 Papillary Adenocarcinoma 47 0.024
614
c PRN026 Porencephaly 47 0.024
615
CRY001 Cryptogenic Organizing Pneumonia 47 0.024
616
EPD029 Epidermolysis Bullosa Simplex, Generalized 47 0.024
617
LYM021 Lymphadenitis 47 0.024
618
c ORF002 Orofacial Cleft 47 0.024
619
FRN002 Frontal Lobe Epilepsy 47 0.024
620
SPL004 Splenic Marginal Zone Lymphoma 47 0.024
621
MYS001 Myositis Ossificans 47 0.024
622
P TRN034 Transverse Myelitis 47 0.024
623
GLD002 Goldberg-Shprintzen Megacolon Syndrome 46 0.024
624
PTY003 Pityriasis Rubra Pilaris 46 0.024
625
TBR008 Tuberculous Peritonitis 46 0.024
626
SPL018 Splenomegaly 46 0.024
627
ASC002 Ascariasis 46 0.024
628
NDL021 Nodular Lymphocyte Predominant Hodgkin Lymphoma 46 0.024
629
MCR037 Macroglossia 46 0.024
630
OVR012 Ovarian Serous Cystadenocarcinoma 46 0.024
631
VTM002 Vitamin B12 Deficiency 46 0.024
632
c USH006 Usher Syndrome, Type 1b 46 0.024
633
P HMR005 Hemorrhoid 46 0.024
634
STC004 Stachybotrys Chartarum 46 0.024
635
P ATR005 Atrophic Gastritis 46 0.024
636
BRN013 Bronchiolitis Obliterans Organizing Pneumonia 46 0.024
637
MDS022 Mediastinitis 46 0.024
638
P INF037 Inflammatory Bowel Disease 45 0.024
639
ECT026 Ectopic Pregnancy 45 0.024
640
FBR054 Fibroma 45 0.024
641
LPD006 Lipoid Proteinosis 45 0.024
642
PSD010 Pseudogout 45 0.024
643
TXC020 Toxic Oil Syndrome 45 0.024
644
P AZS001 Azoospermia 45 0.024
645
DNR001 Duane Retraction Syndrome 45 0.024
646
FRM007 Freeman Sheldon Syndrome 45 0.024
647
SPN050 Spinocerebellar Degeneration 44 0.024
648
P CLR017 Clear Cell Sarcoma 44 0.024
649
c LTT001 Lattice Corneal Dystrophy 44 0.024
650
CRP018 Cor Pulmonale 44 0.024
651
SCL025 Scleromyxedema 44 0.024
652
SCR011 Scrapie 44 0.024
653
ZYG002 Zygomycosis 44 0.024
654
P FCS001 Facioscapulohumeral Muscular Dystrophy 44 0.024
655
P CYS017 Cystic Teratoma 44 0.024
656
CHR276 Chronic Active Epstein-Barr Virus Infection 44 0.024
657
CLL002 Collecting Duct Carcinoma 44 0.024
658
THN006 Thin Basement Membrane Nephropathy 43 0.024
659
NCR002 Necrobiosis Lipoidica 43 0.024
660
c ACT004 Acute Diarrhea 43 0.024
661
MTC027 Mitochondrial Trifunctional Protein Deficiency 43 0.024
662
BLP005 Blepharitis 43 0.024
663
HRD042 Hereditary Cerebral Hemorrhage with Amyloidosis 43 0.024
664
OBS004 Obstructive Hydrocephalus 43 0.024
665
MTB004 Metabolic Acidosis 43 0.024
666
c ICH049 Ichthyosis, Congenital, Autosomal Recessive 2 43 0.024
667
RPP001 Rapp-Hodgkin Syndrome 43 0.024
668
HST006 Histidinemia 43 0.024
669
MYC019 Mycobacterium Marinum 43 0.024
670
CND006 Candida Glabrata 43 0.024
671
c CNG224 Congenital Disorder of Glycosylation Type 1a 43 0.024
672
P D2H001 D-2-Hydroxyglutaric Aciduria 43 0.024
673
P XNT005 Xanthinuria Type 1 42 0.024
674
BRB001 Beriberi 42 0.024
675
RMS001 Rem Sleep Behavior Disorder 42 0.024
676
EPS026 Epispadias 42 0.024
677
GND001 Gonadoblastoma 42 0.024
678
PRN014 Paronychia 42 0.024
679
c CHR104 Chorea 42 0.024
680
P BRS044 Breast Adenocarcinoma 42 0.024
681
P SPR035 Superior Vena Cava Syndrome 42 0.024
682
ENC017 Encephaloceles 42 0.024
683
BSL033 Basal Ganglia Cancification, Idiopathic, 1 41 0.024
684
MYC017 Mycobacterium Kansasii 41 0.024
685
WHP002 Whiplash 41 0.024
686
LPB001 Lipoblastoma 41 0.024
687
CGN002 Cogan's Syndrome 41 0.024
688
P ICH047 Ichthyosis, Congenital, Autosomal Recessive 1 41 0.024
689
PMP002 Pemphigoid Gestationis 41 0.024
690
PLN006 Poland Syndrome 41 0.024
691
OCL025 Ocular Toxoplasmosis 41 0.024
692
BLR015 Blue Rubber Bleb Nevus Syndrome 40 0.024
693
LSS003 Lassa Fever 40 0.024
694
GST052 Gestational Choriocarcinoma 40 0.024
695
ESP028 Esophageal Squamous Cell Carcinoma 40 0.024
696
MCK002 Meckel's Diverticulum 40 0.024
697
RHB022 Rhabdoid Tumors, Somatic 40 0.024
698
OST097 Osteoporotic Fracture 40 0.024
699
ACL001 Acalculous Cholecystitis 40 0.024
700
MTR010 Mature Teratoma 40 0.024
701
P VGN017 Vaginal Cancer 40 0.024
702
INF013 Inferior Myocardial Infarction 40 0.024
703
HVD003 Hiv/aids 40 0.024
704
DNR002 Duane-Radial Ray Syndrome 39 0.024
705
VRY001 Very Long-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 39 0.024
706
MGS001 Megaesophagus 39 0.024
707
P LSS005 Lissencephaly 1 39 0.024
708
INT079 Intrahepatic Cholangiocarcinoma 39 0.024
709
BTN004 Biotin Deficiency 39 0.024
710
P CTR103 Cataract 4, Multiple Types 39 0.024
711
P FNN001 Finnish Type Amyloidosis 38 0.024
712
PRM018 Primary Hypertrophic Osteoarthropathy 38 0.024
713
LGS001 Legius Syndrome 38 0.024
714
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 38 0.024
715
FNT004 Fainting 38 0.024
716
BRN055 Bronchogenic Cyst 38 0.024
717
ANG037 Angiomatosis 38 0.024
718
CRP002 Croup 38 0.024
719
MNN002 Mononeuritis Multiplex 38 0.024
720
TND004 Tendinopathy 38 0.024
721
INT020 Intravenous Leiomyomatosis 38 0.024
722
MNN032 Meningococcal Meningitis 38 0.024
723
P GLM006 Glomangioma 37 0.024
724
SYS003 Systolic Heart Failure 37 0.024
725
c DMN027 Dominant Optic Atrophy 37 0.024
726
HRP002 Herpes Gestationis 37 0.024
727
URT004 Urethral Syndrome 37 0.024
728
PST086 Posterior Cortical Atrophy 37 0.024
729
SPP009 Sepiapterin Reductase Deficiency 37 0.024
730
HPT063 Hepatitis B Virus Infection 36 0.024
731
ANX004 Anoxia 36 0.024
732
EMN001 Emanuel Syndrome 36 0.024
733
DSQ001 Desquamative Interstitial Pneumonia 36 0.024
734
MTR003 Mitral Valve Stenosis 36 0.024
735
TBS001 Tabes Dorsalis 36 0.024
736
TRN021 Transaldolase Deficiency 36 0.024
737
HNS001 Hansen's Disease 36 0.024
738
EPC002 Epicondylitis 36 0.024
739
RTR001 Retrograde Amnesia 36 0.024
740
DCB001 Decubitus Ulcer 35 0.024
741
MLK004 Malakoplakia 35 0.024
742
LNG039 Lung Squamous Cell Carcinoma 35 0.024
743
P DYS005 Dyslexia 35 0.024
744
c PPL025 Popliteal Pterygium Syndrome 35 0.024
745
NRS005 Neurosarcoidosis 35 0.024
746
TNC003 Tinea Corporis 35 0.024
747
HYP034 Hypertensive Encephalopathy 34 0.024
748
PNC041 Pancreatic Ductal Adenocarcinoma 34 0.024
749
PRS064 Persistent Vegetative State 34 0.024
750
TYL002 Tylosis with Esophageal Cancer 34 0.024
751
EXS013 Exstrophy-Epispadias Complex 33 0.024
752
c XLN110 X-Linked Charcot-Marie-Tooth Disease 33 0.024
753
THM001 Thomsen Disease 33 0.024
754
P TRP015 Triphalangeal Thumb 33 0.024
755
c HYP440 Hyperphosphatasia with Mental Retardation Syndrome 33 0.024
756
P OPT051 Opitz Gbbb Syndrome, Type I 33 0.024
757
CYC008 Cyclic Vomiting Syndrome 33 0.024
758
ATM021 Autoimmune Inner Ear Disease 32 0.024
759
CTN013 Cutaneous Anthrax 32 0.024
760
P PYR011 Pyropoikilocytosis 32 0.024
761
ADG002 Audiogenic Seizures 32 0.024
762
c OCL035 Oculocutaneous Albinism Type 1b 32 0.024
763
BRK004 Barakat Syndrome 32 0.024
764
UNV001 Unverricht-Lundborg Syndrome 32 0.024
765
MDL006 Madelung Disease 32 0.024
766
TTZ002 Tietz Syndrome 32 0.024
767
P HMR003 Hemorrhagic Disease 32 0.024
768
CNG219 Congenital Aural Atresia 31 0.024
769
TNC001 Tinea Cruris 31 0.024
770
SPR009 Sporadic Breast Cancer 31 0.024
771
TRL003 Toriello Carey Syndrome 31 0.024
772
VBR003 Vibrio Vulnificus Infection 31 0.024
773
TST021 Testicular Germ Cell Tumor 31 0.024
774
CHR028 Chronic Wasting Disease 31 0.024
775
EHL050 Ehlers–danlos Syndrome Dermatosparaxis Type 31 0.024
776
VGN019 Vaginal Discharge 30 0.024
777
PRS051 Parastremmatic Dwarfism 30 0.024
778
c PST061 Posterior Polymorphous Corneal Dystrophy 30 0.024
779
SPL007 Splenic Abscess 30 0.024
780
c LSS006 Lissencephaly 2 30 0.024
781
BLK001 Balkan Nephropathy 30 0.024
782
MNT061 Mental Retardation-Hypotonic Facies Syndrome, X-Linked 30 0.024
783
P CMM008 Communicating Hydrocephalus 30 0.024
784
INT003 Intracranial Hypotension 30 0.024
785
CRT028 Cor Triatriatum 29 0.024
786
c SPN073 Spinocerebellar Ataxia Type 12 29 0.024
787
NRC001 Neurocirculatory Asthenia 29 0.024
788
INN003 Iniencephaly 29 0.024
789
CRN061 Corneal Dystrophy Avellino Type 29 0.024
790
c LMB018 Limb-Girdle Muscular Dystrophy, Type 1a 29 0.024
791
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 29 0.024
792
c ICH041 Ichthyosis, Autosomal Recessive 4b 29 0.024
793
ANH001 Ainhum 29 0.024
794
TTZ001 Tietze's Syndrome 29 0.024
795
IDM001 Ideomotor Apraxia 29 0.024
796
SNL010 Senile Systemic Amyloidosis 29 0.024
797
P SVR013 Severe Congenital Neutropenia Autosomal Recessive 3 29 0.024
798
c CTR101 Cataract 39, Multiple Types, Autosomal Dominant 29 0.024
799
PDT027 Pediatric Ulcerative Colitis 28 0.024
800
EPD046 Epididymitis 28 0.024
801
JPN001 Japanese Spotted Fever 28 0.024
802
PLC009 Placenta Praevia 28 0.024
803
STY001 Satoyoshi Syndrome 28 0.024
804
HRP001 Herpangina 28 0.024
805
SLL001 Sialolithiasis 28 0.024
806
SBD001 Subdural Empyema 28 0.024
807
c NTR033 Neutropenia, Severe Congenital 1, Autosomal Dominant 28 0.024
808
c PRK057 Parkinson Disease, Late-Onset 28 0.024
809
c OST039 Osteogenesis Imperfecta Type 5 28 0.024
810
KKC001 Kikuchi Disease 27 0.024
811
c ORF007 Orofaciodigital Syndrome 2 27 0.024
812
HYP160 Hyperkeratosis Lenticularis Perstans 27 0.024
813
MYC014 Mycobacterium Chelonae 27 0.024
814
c CTR124 Cataract 10, Multiple Types 27 0.024
815
TRT003 Tertiary Syphilis 27 0.024
816
CWC001 Cowchock Syndrome 27 0.024
817
DND007 Dandy-Walker Like Malformation with Atrioventricular Septal Defect 26 0.024
818
3Q2001 3q29 Deletion Syndrome 26 0.024
819
DYS009 Dysthymic Disorder 26 0.024
820
CNR008 Cone-Rod Dystrophy Amelogenesis Imperfecta 26 0.024
821
HRD052 Hereditary Mucoepithelial Dysplasia 26 0.024
822
YNG002 Young Syndrome 26 0.024
823
P OTD002 Otodental Syndrome 26 0.024
824
SCL022 Scleredema 26 0.024
825
CNG049 Congenital Stromal Corneal Dystrophy 26 0.024
826
CYT004 Cytomegalic Inclusion Disease 26 0.024
827
PNT006 Pentosuria 26 0.024
828
NVS007 Nevus of Ota 26 0.024
829
GLL028 Gillespie Syndrome 26 0.024
830
TRN028 Transient Acantholytic Dermatosis 26 0.024
831
c ICH051 Ichthyosis, Congenital, Autosomal Recessive 11 26 0.024
832
c TTR013 Tetrasomy X 26 0.024
833
P DNT025 Dentinogenesis Imperfecta 1 26 0.024
834
FMR003 Femoral Neuropathy 26 0.024
835
PNM003 Pneumatosis Cystoides Intestinalis 26 0.024
836
ADT001 Auditory Agnosia 25 0.024
837
c CHR247 Chromosome 4p Deletion 25 0.024
838
CPP003 Cap Polyposis 25 0.024
839
PLN007 Plantar Fasciitis 25 0.024
840
OMS001 Omsk Hemorrhagic Fever 24 0.024
841
c RNG013 Ring Chromosome 18 24 0.024
842
NRM009 Normokalemic Periodic Paralysis 24 0.024
843
c CTS012 Cutis Verticis Gyrata 24 0.024
844
OVR098 Ovarian Fibroma 24 0.024
845
ATY013 Atypical Rett Syndrome 24 0.024
846
BLN002 Balanitis Xerotica Obliterans 23 0.024
847
MSN002 Mesenteric Lymphadenitis 23 0.024
848
P CTR133 Cataract 22, Autosomal Recessive 23 0.024
849
FMR012 Femur-Fibula-Ulna Complex 23 0.024
850
HRL002 Harlequin Syndrome 23 0.024
851
PLY031 Polydactyly Myopia Syndrome 23 0.024
852
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 23 0.024
853
P HYD015 Hydroa Vacciniforme 23 0.024
854
P SKN012 Skin Carcinoma in Situ 23 0.024
855
BNT002 Bantu Siderosis 22 0.024
856
P HYP438 Hyperaldosteronism, Familial, Type Iii 22 0.024
857
ISS001 Isosporiasis 22 0.024
858
c ACT059 Acute Maxillary Sinusitis 22 0.024
859
c CHR057 Chronic Laryngitis 22 0.024
860
CNZ006 Coenzyme Q10 Deficiency, Primary, 1 22 0.024
861
NTV001 Native American Myopathy 22 0.024
862
c ACT072 Acute Laryngitis 22 0.024
863
RDT005 Radiation Induced Cancer 21 0.024
864
ANN010 Anonychia-Onychodystrophy with Hypoplasia or Absence of Distal Phalanges 21 0.024
865
LRP001 Leri Pleonosteosis 21 0.024
866
NNN015 Noonan-Like/multiple Giant Cell Lesion Syndrome 21 0.024
867
GTP001 Gait Apraxia 21 0.024
868
MLT058 Multiple Self Healing Squamous Epithelioma 20 0.024
869
SPR063 Superior Canal Dehiscence Syndrome 20 0.024
870
HMC012 Hemicrania Continua 20 0.024
871
RGN005 Regional Odontodysplasia 20 0.024
872
MNG007 Manganese Poisoning 20 0.024
873
PLR006 Pleural Cancer 20 0.024
874
PRN010 Paranoid Personality Disorder 19 0.024
875
MRZ001 Mirizzi Syndrome 19 0.024
876
c RNP003 Renpenning Syndrome 1 19 0.024
877
DYS135 Dysphagia Lusoria 19 0.024
878
CHR084 Chromosomal Disease 19 0.024
879
PSD078 Pseudofolliculitis Barbae 19 0.024
880
c FRN036 Frontonasal Dysplasia 1 19 0.024
881
SHR027 Short Stature Wormian Bones Dextrocardia 19 0.024
882
THN005 Thunderclap Headache 19 0.024
883
TRS006 Triose Phosphate-Isomerase Deficiency 18 0.024
884
FRS004 Free Sialic Acid Storage Disorders 18 0.024
885
PRM040 Primary Basilar Impression 18 0.024
886
RBN004 Robin Sequence and Oligodactyly 18 0.024
887
FML211 Familial Papillary or Follicular Thyroid Carcinoma 18 0.024
888
CNT067 Central Cord Syndrome 18 0.024
889
PRG072 Progressive Myoclonic Epilepsy 3 with or Without Intracellular Inclusions 18 0.024
890
LJH001 Lujo Hemorrhagic Fever 18 0.024
891
MRN004 Morning Glory Disc Anomaly 18 0.024
892
HYP145 Hyperbetaalaninemia 17 0.024
893
PSD027 Pseudoaminopterin Syndrome 17 0.024
894
OSL001 Oslam Syndrome 17 0.024
895
ACC005 Accessory Pancreas 17 0.024
896
ELC001 Elective Mutism 16 0.024
897
OVR027 Ovarian Squamous Cell Carcinoma 16 0.024
898
ORP002 Oropouche Fever 16 0.024
899
ACH028 Acheiria 16 0.024
900
P ENC021 Encephalopathy, Neonatal Severe 16 0.024
901
DPH012 Diphallia 16 0.024
902
c CRD093 Cardiomyopathy, Dilated, 1a 15 0.024
903
c OTD001 Otodental Dysplasia 15 0.024
904
ARR026 Arrhythmogenic Right Ventricular Dysplasia 1 15 0.024
905
SPN092 Spinal Shock 15 0.024
906
CRN126 Corneal Dystrophy, Lisch Epithelial 15 0.024
907
INF048 Infantile Histiocytoid Cardiomyopathy 15 0.024
908
CTR010 Cataract Congenital Volkmann Type 15 0.024
909
BNG042 Benign Multicystic Peritoneal Mesothelioma 15 0.024
910
SPN187 Spinocerebellar Atrophy 15 0.024
911
SBP006 Subepithelial Mucinous Corneal Dystrophy 14 0.024
912
MNS002 Mini Stroke 14 0.024
913
c DST049 Distal Spinal Muscular Atrophy Type 3 14 0.024
914
HYP548 Hypogonadotropic Hypogonadism 2 with or Without Anosmia 14 0.024
915
c ICH048 Ichthyosis, Congenital, Autosomal Recessive 9 14 0.024
916
ALK001 Alkhurma Hemorrhagic Fever 14 0.024
917
c CTR115 Cataract 16, Multiple Types 14 0.024
918
CNG067 Congenital Cystic Eye 14 0.024
919
TRG006 Trigger Thumb 13 0.024
920
CRT056 Carotidynia 13 0.024
921
c ICH040 Ichthyosis, Congenital, Autosomal Recessive 4a 13 0.024
922
c PRD030 Periodontitis 1, Juvenile 13 0.024
923
c ICH044 Ichthyosis, Congenital, Autosomal Recessive 8 13 0.024
924
URC004 Urachal Cancer 13 0.024
925
c ICH042 Ichthyosis, Congenital, Autosomal Recessive 6 13 0.024
926
c ICH050 Ichthyosis, Congenital, Autosomal Recessive 5 13 0.024
927
c CTR118 Cataract 14, Multiple Types 13 0.024
928
c ICH039 Ichthyosis, Congenital, Autosomal Recessive 10 13 0.024
929
ORF018 Orofacial Cleft11 13 0.024
930
PRM056 Primrose Syndrome 13 0.024
931
c CTR122 Cataract 5, Multiple Types 12 0.024
932
c CTR130 Cataract 9, Multiple Types 12 0.024
933
c CTR113 Cataract 11, Multiple Types 12 0.024
934
JMP002 Jumping Frenchmen of Maine 12 0.024
935
KYR001 Kyrle Disease 12 0.024
936
AKN001 Akinetopsia 12 0.024
937
MRG007 Morgellons 12 0.024
938
HYD031 Hydroxyprolinemia 12 0.024
939
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 12 0.024
940
c ICH038 Ichthyosis, Congenital, Autosomal Recessive 3 12 0.024
941
ERY040 Erythema Palmaris Hereditarium 12 0.024
942
c MNT171 Mental Retardation, Autosomal Dominant 17 12 0.024
943
c CTR104 Cataract 18, Autosomal Recessive 11 0.024
944
c CTR129 Cataract 31, Multiple Types 11 0.024
945
c CTR131 Cataract 17, Multiple Types 11 0.024
946
ACC001 Accessory Nerve Disease 11 0.024
947
c ICH045 Ichthyosis, Congenital, Autosomal Recessive 7 11 0.024
948
BRN045 Brunner Syndrome 11 0.024
949
c PRX053 Peroxisome Biogenesis Disorder 14b 11 0.024
950
MLP004 Malpuech Facial Clefting Syndrome 10 0.024
951
PRS119 Persistent Genital Arousal Disorder 10 0.024
952
UHL001 Uhl Anomaly 10 0.024
953
c ELL007 Elliptocytosis-1 9 0.024
954
URC001 Urachus Cancer 9 0.024
955
c PRX050 Peroxisome Biogenesis Disorder 9b 9 0.024
956
CTR043 Cataract, Pulverulent or Cerulean, with or Without Microcornea 8 0.024
957
MNM003 Minimally Differentiated Acute Myeloblastic Leukemia 8 0.024
958
PRV008 Parvovirus Antenatal Infection 8 0.024
959
HYP512 Hyperproinsulinemia, Familial 7 0.024
960
PHS019 Phosphohydroxylysinuria 7 0.024
961
OBS014 Obsessive-Compulsive Disorder, Protection Against 6 0.024
962
MTR033 Motor Sensory Neuropathy Type 1 Aplasia Cutis Congenita 3 0.024
963
MCK010 Mickleson Syndrome 2 0.024