Search results for was

1359 hits were found for was

# Family MCID Name MIFTS Score
1
P WSK001 Wiskott-Aldrich Syndrome 74 19.599
2
WSR001 Was-Related Disorders 13 9.140
3
NTR036 Neutropenia, Severe Congenital, X-Linked 30 5.608
4
P THR014 Thrombocytopenia 63 5.258
5
THR042 Thrombocytopenia, X-Linked 43 4.918
6
P NTR004 Neutropenia 58 4.811
7
PRM097 Primary Immunodeficiency Disease 64 3.442
8
c SVR003 Severe Congenital Neutropenia 56 3.402
9
P AGM005 Agammaglobulinemia, X-Linked 1 56 3.391
10
P XLN007 X-Linked Disease 34 2.802
11
BRL010 Buruli Ulcer 46 2.792
12
c NRD016 Neurodegeneration with Brain Iron Accumulation 6 37 2.769
13
c SPN366 Spinocerebellar Ataxia with Axonal Neuropathy Type 2 33 2.769
14
DDN009 Duodenal Obstruction 31 2.769
15
TXC008 Toxic Optic Neuropathy 29 2.769
16
P HMR003 Hemorrhagic Disease 55 2.039
17
BLD053 Blood Platelet Disease 46 2.008
18
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 53 0.140
19
P ADN016 Adenocarcinoma 69 0.103
20
P LKM002 Leukemia 72 0.101
21
P BRS047 Breast Cancer 100 0.099
22
P LYM118 Lymphoma 69 0.090
23
P HPT021 Hepatitis 68 0.086
24
P LNG032 Lung Cancer 94 0.083
25
P CLR023 Colorectal Cancer 95 0.081
26
P ESP024 Esophagitis 59 0.078
27
PLM129 Pulmonary Disease, Chronic Obstructive 62 0.076
28
P PRS040 Prostate Cancer 88 0.067
29
P RNL014 Renal Cell Carcinoma 80 0.064
30
ESP021 Esophageal Cancer 74 0.064
31
P ART022 Arthritis 72 0.064
32
P HPT023 Hepatocellular Carcinoma 89 0.061
33
HMT002 Hematologic Cancer 62 0.061
34
P PNC044 Pancreatitis 60 0.061
35
HMT018 Hematopoietic Stem Cell Transplantation 40 0.061
36
P CRD011 Cardiomyopathy 67 0.057
37
P MYL006 Myeloid Leukemia 64 0.057
38
LYM027 Lymphopenia 54 0.057
39
SQM006 Squamous Cell Carcinoma 69 0.054
40
P BCL006 B-Cell Lymphomas 64 0.054
41
CHL071 Child Syndrome 59 0.054
42
ADN018 Adenoma 58 0.054
43
KDS001 Kid Syndrome 57 0.054
44
ADL002 Adult Syndrome 57 0.054
45
PRS047 Prostatitis 55 0.054
46
PHR003 Pharyngitis 53 0.054
47
ANG054 Angina Pectoris 49 0.054
48
END072 Endotheliitis 41 0.054
49
c WSK002 Wiskott-Aldrich Syndrome 2 28 0.054
50
P OBS005 Obesity 91 0.050
51
P AST005 Asthma 81 0.050
52
HDG012 Hodgkin Lymphoma 73 0.050
53
P SCH015 Schizophrenia 71 0.050
54
P PNM007 Pneumonia 66 0.050
55
c HYP595 Hypertension, Essential 66 0.050
56
SRC014 Sarcoma 66 0.050
57
ACR007 Acromegaly 66 0.050
58
P KDN017 Kidney Cancer 65 0.050
59
P LPS004 Lupus Erythematosus 63 0.050
60
PRT036 Peritonitis 60 0.050
61
P GLM045 Glioma 59 0.050
62
RTN018 Retinal Disease 51 0.050
63
P CRV039 Cervicitis 45 0.050
64
NLL002 Null Syndrome 26 0.050
65
c SYS001 Systemic Lupus Erythematosus 86 0.045
66
HV1006 Hiv-1 80 0.045
67
P INF038 Influenza 71 0.045
68
BRN024 Bronchitis 62 0.045
69
P GST049 Gastrointestinal System Cancer 59 0.045
70
CLT003 Colitis 58 0.045
71
OCL009 Ocular Cancer 58 0.045
72
CRT002 Cartilage-Hair Hypoplasia 58 0.045
73
P THY032 Thyroiditis 53 0.045
74
HDC001 Headache 53 0.045
75
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 46 0.045
76
NRN002 Neuronitis 39 0.045
77
MRG013 Mirage Syndrome 36 0.045
78
MNK002 Monkeypox 35 0.045
79
P RHM011 Rheumatoid Arthritis 87 0.040
80
P PNC035 Pancreatic Cancer 84 0.040
81
P MLT019 Multiple Myeloma 82 0.040
82
P MYC007 Myocardial Infarction 77 0.040
83
P RTN024 Retinoblastoma 75 0.040
84
P HRT032 Heart Disease 75 0.040
85
c CHR090 Chronic Lymphocytic Leukemia 75 0.040
86
ULC004 Ulcerative Colitis 72 0.040
87
CNG034 Congestive Heart Failure 70 0.040
88
MLN008 Melanoma 70 0.040
89
TBR010 Tuberculosis 69 0.040
90
P MNN013 Meningitis 65 0.040
91
OTT002 Otitis Media 65 0.040
92
P LKM068 Leukemia, Chronic Myeloid, Somatic 64 0.040
93
c HPT001 Hepatitis C 62 0.040
94
CRT072 Creutzfeldt-Jakob Disease 62 0.040
95
HYP056 Hypoglycemia 60 0.040
96
P LYM026 Lymphoblastic Leukemia 60 0.040
97
ACQ007 Acquired Immunodeficiency Syndrome 60 0.040
98
P HMN010 Hemangioma 59 0.040
99
ANR040 Aneurysm 57 0.040
100
EYD002 Eye Disease 57 0.040
101
P MYS005 Myositis 56 0.040
102
TNS005 Tonsillitis 56 0.040
103
P GT001 Gout 55 0.040
104
CHN016 Cohen Syndrome 54 0.040
105
MCS002 Mucositis 54 0.040
106
P LRY019 Laryngitis 53 0.040
107
SML019 Smallpox 52 0.040
108
P SPS003 Spastic Diplegia 52 0.040
109
DMN002 Dementia 52 0.040
110
P SCK002 Sick Sinus Syndrome 50 0.040
111
RTN023 Retinitis 49 0.040
112
c CLL013 Cell Type Cancer 48 0.040
113
LKC003 Leukocyte Disease 46 0.040
114
P BLD051 Blood Coagulation Disease 43 0.040
115
TXC020 Toxic Oil Syndrome 39 0.040
116
KR002 Kuru 37 0.040
117
FXF002 Fox-Fordyce Disease 37 0.040
118
ATM052 Autoimmune Disease 1 27 0.040
119
ATM053 Autoimmune Disease 2 18 0.040
120
PRS119 Persistent Genital Arousal Disorder 13 0.040
121
c CHN017 Chondrodysplasia Punctata 1, X-Linked 12 0.040
122
YSH001 Yusho Disease 9 0.040
123
END057 Endometrial Cancer 74 0.035
124
GST019 Gastrointestinal Stromal Tumor 74 0.035
125
P CRN211 Coronary Artery Disease 73 0.035
126
c MCL042 Macular Degeneration, Age-Related, 1 72 0.035
127
P PHC003 Pheochromocytoma 72 0.035
128
SMT004 Smith-Lemli-Opitz Syndrome 69 0.035
129
THY028 Thyroid Cancer 68 0.035
130
P CHR071 Charcot-Marie-Tooth Disease 67 0.035
131
P HYD006 Hydrocephalus 66 0.035
132
P ATR011 Atrial Fibrillation 65 0.035
133
SKN016 Skin Disease 64 0.035
134
P PSR002 Psoriasis 64 0.035
135
P PLY011 Polycystic Ovary Syndrome 63 0.035
136
PRT037 Pertussis 63 0.035
137
c HPT016 Hepatitis B 62 0.035
138
VSC011 Vasculitis 62 0.035
139
LNG099 Lung Disease 61 0.035
140
P SLP006 Sleep Apnea 60 0.035
141
P HYP086 Hypothyroidism 60 0.035
142
P ATP001 Atopic Dermatitis 60 0.035
143
ADL030 Adult-Onset Still's Disease 60 0.035
144
ISC004 Ischemia 59 0.035
145
P INT068 Intestinal Disease 59 0.035
146
ACN011 Acne 59 0.035
147
P SNS014 Sinusitis 59 0.035
148
P DRR001 Diarrhea 59 0.035
149
P CLR108 Colorectal Adenoma 59 0.035
150
MSL001 Measles 58 0.035
151
GST045 Gastroenteritis 57 0.035
152
PRP030 Purpura 57 0.035
153
P CTR002 Cataract 57 0.035
154
P THR005 Thrombotic Thrombocytopenic Purpura 57 0.035
155
P NRP001 Neuropathy 57 0.035
156
P HYP069 Hyperparathyroidism 56 0.035
157
P WRD001 Waardenburg's Syndrome 56 0.035
158
c SPN294 Spinocerebellar Ataxia 1 56 0.035
159
ART111 Artery Disease 55 0.035
160
P GLM007 Glomerulonephritis 55 0.035
161
RLP002 Relapsing-Remitting Multiple Sclerosis 54 0.035
162
P HYP076 Hyperthyroidism 53 0.035
163
GST050 Gastrointestinal System Disease 53 0.035
164
KNS001 Kniest Dysplasia 53 0.035
165
IMM136 Immune System Disease 53 0.035
166
P RTN016 Retinal Degeneration 53 0.035
167
P ATX004 Ataxia 52 0.035
168
P ACT135 Acute Graft Versus Host Disease 52 0.035
169
P TRT010 Teratoma 51 0.035
170
CLN019 Colonic Disease 51 0.035
171
DCT002 Ductal Carcinoma in Situ 50 0.035
172
c CHR417 Chronic Graft Versus Host Disease 50 0.035
173
FCS012 Facioscapulohumeral Muscular Dystrophy 1 50 0.035
174
CRB045 Cerebellar Hypoplasia 50 0.035
175
CLN015 Colon Adenocarcinoma 49 0.035
176
MBS002 Moebius Syndrome 49 0.035
177
CLR109 Colorectal Adenocarcinoma 49 0.035
178
CRD002 Cri-Du-Chat Syndrome 49 0.035
179
IMP005 Impotence 49 0.035
180
c THR103 Thrombocytopenia, Congenital Amegakaryocytic 47 0.035
181
AML029 Ameloblastoma 47 0.035
182
PRN023 Prion Disease 46 0.035
183
CVR006 Cavernous Hemangioma 45 0.035
184
P KRN004 Kernicterus 45 0.035
185
CHR074 Choriocarcinoma 45 0.035
186
c LBR014 Leber Congenital Amaurosis 4 44 0.035
187
THR024 Thrombosis 43 0.035
188
P HYP729 Hypersensitivity Reaction Disease 43 0.035
189
TCL003 T Cell Deficiency 43 0.035
190
VGN023 Vaginitis 41 0.035
191
SYN007 Synovitis 41 0.035
192
ASP007 Aspiration Pneumonia 40 0.035
193
DNN002 Donnai-Barrow Syndrome 38 0.035
194
HYP068 Hyperostosis 38 0.035
195
RCT017 Rectal Disease 38 0.035
196
ATM012 Autoimmune Disease of Blood 37 0.035
197
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 36 0.035
198
FRN039 Frank-Ter Haar Syndrome 36 0.035
199
RDN001 Reading Disorder 36 0.035
200
c CLR080 Colorectal Cancer 5 34 0.035
201
NNT008 Neonatal Abstinence Syndrome 34 0.035
202
ENG004 Engraftment Syndrome 34 0.035
203
OCH001 Ochronosis 33 0.035
204
SPR006 Sparganosis 32 0.035
205
EYD001 Eye Degenerative Disease 32 0.035
206
c CLR079 Colorectal Cancer 2 30 0.035
207
SPN151 Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy 28 0.035
208
c ALB020 Albinism, Oculocutaneous, Type Iii 28 0.035
209
OTD001 Otodental Dysplasia 28 0.035
210
MYC021 Mycobacterium Xenopi 26 0.035
211
c HRD146 Hereditary Methemoglobinemia 25 0.035
212
DTH005 Diethylstilbestrol Syndrome 25 0.035
213
RJS001 Ruijs-Aalfs Syndrome 22 0.035
214
MTG001 Metagonimiasis 19 0.035
215
RMB001 Rombo Syndrome 18 0.035
216
SPN356 Spinocerebellar Degeneration with Macular Corneal Dystrophy, Congenital Cataracts, and Myopia 17 0.035
217
HML018 Homologous Wasting Disease 16 0.035
218
ATS012 Autosomal Dominant Partial Epilepsy with Auditory Features 14 0.035
219
MLR004 Malaria 82 0.029
220
P OST012 Osteoarthritis 79 0.029
221
DCH001 Duchenne Muscular Dystrophy 79 0.029
222
P ALZ034 Alzheimer Disease 76 0.029
223
c DLT002 Dilated Cardiomyopathy 74 0.029
224
CRH001 Crohn's Disease 73 0.029
225
P LVR013 Liver Disease 72 0.029
226
P STM004 Stomach Cancer 72 0.029
227
c HPT073 Hepatitis C Virus 70 0.029
228
P NRV007 Nervous System Disease 70 0.029
229
P MYP004 Myopathy 68 0.029
230
P RSP003 Respiratory Failure 68 0.029
231
PCK002 Pick Disease 68 0.029
232
OVR078 Ovarian Cancer, Somatic 67 0.029
233
BSL036 Basal Cell Nevus Syndrome 67 0.029
234
P ANR002 Aniridia 66 0.029
235
P CSH001 Cushing's Syndrome 65 0.029
236
OBS061 Obstructive Sleep Apnea 65 0.029
237
P EPL164 Epilepsy 65 0.029
238
OBS002 Obsessive-Compulsive Disorder 64 0.029
239
P LNG028 Long Qt Syndrome 64 0.029
240
c MCP003 Mucopolysaccharidosis Vii 63 0.029
241
ALL003 Allergic Rhinitis 63 0.029
242
P OST002 Osteoporosis 63 0.029
243
LYM115 Lymphoma, Non-Hodgkin 63 0.029
244
c LKM062 Leukemia, Acute Lymphoblastic 63 0.029
245
CRB011 Cerebrotendinous Xanthomatosis 62 0.029
246
LYM017 Lyme Disease 62 0.029
247
P INF037 Inflammatory Bowel Disease 62 0.029
248
c HMP004 Hemophilia B 62 0.029
249
P ART023 Arthropathy 62 0.029
250
PNC041 Pancreatic Ductal Adenocarcinoma 62 0.029
251
P HRP006 Herpes Simplex 62 0.029
252
P HYP117 Hypertriglyceridemia 61 0.029
253
P ENC004 Encephalitis 61 0.029
254
P PRS038 Personality Disorder 61 0.029
255
MXD005 Mixed Connective Tissue Disease 61 0.029
256
INS001 Insulinoma 60 0.029
257
P DRM010 Dermatomyositis 59 0.029
258
BLL006 Bullous Pemphigoid 59 0.029
259
P PRP029 Porphyria 59 0.029
260
VRL011 Viral Infectious Disease 59 0.029
261
P RHN004 Rhinitis 59 0.029
262
P VNT002 Ventricular Septal Defect 58 0.029
263
LYS001 Loeys-Dietz Syndrome 58 0.029
264
P BCK002 Beckwith-Wiedemann Syndrome 58 0.029
265
CTS003 Coats Disease 58 0.029
266
MYL031 Myeloproliferative Neoplasm 57 0.029
267
P UVT001 Uveitis 57 0.029
268
c PNC108 Pancreatitis, Hereditary 57 0.029
269
BTN003 Biotinidase Deficiency 57 0.029
270
c MNN043 Meningioma, Familial 56 0.029
271
P ANP001 Anaplastic Large Cell Lymphoma 56 0.029
272
EPD016 Epidermolysis Bullosa 55 0.029
273
QFV001 Q Fever 55 0.029
274
P ACT074 Acute Lymphocytic Leukemia 55 0.029
275
HYP266 Hypoxia 55 0.029
276
NRN004 Neuroendocrine Tumor 55 0.029
277
BLD034 Bile Duct Carcinoma 55 0.029
278
P GST044 Gastritis 55 0.029
279
ALK013 Alkaptonuria 54 0.029
280
RHM001 Rheumatic Fever 54 0.029
281
GST023 Gastric Ulcer 54 0.029
282
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.029
283
P FTL001 Fetal Alcohol Syndrome 53 0.029
284
PRP019 Peripheral Nervous System Disease 53 0.029
285
P INT030 Intracranial Aneurysm 53 0.029
286
LNG039 Lung Squamous Cell Carcinoma 53 0.029
287
c SVR001 Severe Acute Respiratory Syndrome 53 0.029
288
CCC001 Coccidioidomycosis 53 0.029
289
P EPD003 Epidermolysis Bullosa Simplex 53 0.029
290
RCT018 Rectal Neoplasm 53 0.029
291
ANG020 Angiosarcoma 52 0.029
292
PLM010 Pulmonary Edema 52 0.029
293
VSC002 Vascular Dementia 52 0.029
294
THR004 Thrombocytosis 52 0.029
295
VSC006 Vascular Cancer 52 0.029
296
BRN106 Burns 52 0.029
297
c INS002 in Situ Carcinoma 51 0.029
298
WST005 West Nile Virus 51 0.029
299
TTH006 Tooth Disease 51 0.029
300
P SYP003 Syphilis 51 0.029
301
AVN001 Avian Influenza 50 0.029
302
DSS009 Disseminated Intravascular Coagulation 50 0.029
303
PLG002 Plague 50 0.029
304
PRG009 Progressive Multifocal Leukoencephalopathy 50 0.029
305
TRP002 Tropical Spastic Paraparesis 50 0.029
306
PRC012 Pericardial Effusion 50 0.029
307
P HYP614 Hyperlipidemia, Familial Combined 50 0.029
308
JCB001 Jacobsen Syndrome 50 0.029
309
PRC013 Pericarditis 50 0.029
310
P PRT096 Peritoneal Mesothelioma 50 0.029
311
URN009 Urinary System Disease 49 0.029
312
SPH001 Sapho Syndrome 49 0.029
313
PSD007 Pseudomyxoma Peritonei 49 0.029
314
ATR002 Atransferrinemia 49 0.029
315
ACR012 Aicardi Syndrome 49 0.029
316
FCL012 Facial Paralysis 49 0.029
317
PRT029 Parathyroid Adenoma 49 0.029
318
INT075 Intracranial Hypertension 48 0.029
319
PRP082 Porphyria, Congenital Erythropoietic 48 0.029
320
END031 Endometrial Stromal Sarcoma 48 0.029
321
SML033 Small Cell Cancer of the Lung, Somatic 48 0.029
322
OBS001 Obstructive Jaundice 48 0.029
323
MTB004 Metabolic Acidosis 47 0.029
324
CRN017 Coronary Thrombosis 47 0.029
325
c AMY087 Amyloidosis, Hereditary, Transthyretin-Related 47 0.029
326
P RBN002 Robinow Syndrome 47 0.029
327
ACT049 Acute Disseminated Encephalomyelitis 47 0.029
328
c MLG002 Malignant Peritoneal Mesothelioma 47 0.029
329
HRT007 Heart Cancer 46 0.029
330
c CLR085 Colorectal Cancer 1 46 0.029
331
MMM001 Mammary Paget's Disease 46 0.029
332
CYS014 Cystadenocarcinoma 46 0.029
333
MMB001 Membranoproliferative Glomerulonephritis 46 0.029
334
SDD007 Sudden Cardiac Death 45 0.029
335
HMN014 Human Immunodeficiency Virus Infectious Disease 45 0.029
336
CLL002 Collecting Duct Carcinoma 44 0.029
337
RNL011 Renal Osteodystrophy 44 0.029
338
c CLR017 Clear Cell Sarcoma 44 0.029
339
c SPN290 Spinocerebellar Ataxia 15 44 0.029
340
HDN002 Head Injury 44 0.029
341
GLC011 Galactose Epimerase Deficiency 44 0.029
342
MYC005 Myocardial Stunning 44 0.029
343
c CHR418 Chronic Leukemia 43 0.029
344
CRN024 Corneal Disease 43 0.029
345
P DNT011 Dentinogenesis Imperfecta 43 0.029
346
CHC001 Chickenpox 43 0.029
347
MNN032 Meningococcal Meningitis 42 0.029
348
c PRM225 Primary Thrombocytopenia 42 0.029
349
VRL003 Variola Major 42 0.029
350
PRD003 Periodontosis 41 0.029
351
VLV010 Vulvovaginitis 41 0.029
352
PHC013 Phaeochromocytoma 41 0.029
353
GST071 Gastrointestinal Carcinoma 40 0.029
354
P LNG035 Lung Large Cell Carcinoma 40 0.029
355
RMS001 Rem Sleep Behavior Disorder 40 0.029
356
URT001 Urethritis 40 0.029
357
MRB001 Marburg Hemorrhagic Fever 40 0.029
358
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 39 0.029
359
SMT001 Somatization Disorder 39 0.029
360
CHL052 Choledochal Cyst 39 0.029
361
BRS064 Bursitis 39 0.029
362
LYM009 Lymphocytic Choriomeningitis 39 0.029
363
CRB009 Cerebritis 39 0.029
364
BDY001 Body Dysmorphic Disorder 38 0.029
365
TRC077 Trichomegaly 38 0.029
366
c CTR098 Cataract 1, Multiple Types 38 0.029
367
NCR004 Nocardiosis 37 0.029
368
LMB024 Limbic Encephalitis 37 0.029
369
c THR037 Thrombocytopenia 2 37 0.029
370
ELP001 Elephantiasis 36 0.029
371
IMM078 Immunodeficiency 21 36 0.029
372
SCR011 Scrapie 36 0.029
373
PRM056 Primrose Syndrome 36 0.029
374
BNS002 Bone Structure Disease 36 0.029
375
MLN003 Melancholia 35 0.029
376
CRT013 Carotid Stenosis 35 0.029
377
WHP002 Whiplash 35 0.029
378
BTN002 Boutonneuse Fever 35 0.029
379
c CTR132 Cataract 3, Multiple Types 35 0.029
380
P HRT017 Heart Tumor 34 0.029
381
PRP026 Peripheral Retinal Degeneration 34 0.029
382
c CTR096 Cataract 6, Multiple Types 34 0.029
383
CHL039 Choledocholithiasis 34 0.029
384
c CTR102 Cataract 2, Multiple Types 34 0.029
385
SPR066 Superficial Siderosis 33 0.029
386
PNM010 Pneumothorax, Primary Spontaneous 33 0.029
387
CTS011 Cutis Marmorata Telangiectatica Congenita 32 0.029
388
c SPN200 Spinocerebellar Ataxia, Autosomal Recessive 2 32 0.029
389
SPN205 Spinal Muscular Atrophy, X-Linked 2, Infantile 32 0.029
390
KYS001 Kyasanur Forest Disease 31 0.029
391
BLC004 Blackwater Fever 31 0.029
392
MYL057 Myelopathy, Htlv-1-Associated 31 0.029
393
IMM074 Immunodeficiency 16 31 0.029
394
P UNC001 Uncombable Hair Syndrome 30 0.029
395
RCT020 Rectum Adenocarcinoma 30 0.029
396
AKN002 Akinetic Mutism 30 0.029
397
PLC009 Placenta Praevia 30 0.029
398
c CLR075 Colorectal Cancer 3 29 0.029
399
YNG002 Young Syndrome 29 0.029
400
TMT003 Temtamy Syndrome 29 0.029
401
MNT006 Manitoba Oculotrichoanal Syndrome 28 0.029
402
CHL040 Cholangiolocellular Carcinoma 28 0.029
403
PRX008 Paroxysmal Cold Hemoglobinuria 28 0.029
404
RDT005 Radiation Induced Cancer 27 0.029
405
OST097 Osteoporotic Fracture 27 0.029
406
VRL002 Variola Minor 25 0.029
407
MMS001 Momo Syndrome 24 0.029
408
TRN066 Transmitted_by 24 0.029
409
GNT033 Genetic Prion Diseases 23 0.029
410
CRT028 Cor Triatriatum 23 0.029
411
CRC034 Carcinoma Showing Thymus-Like Differentiation 22 0.029
412
c NPH067 Nephronophthisis 12 21 0.029
413
OSL001 Oslam Syndrome 21 0.029
414
OPH001 Ophthalmomyiasis 21 0.029
415
MNS002 Mini Stroke 20 0.029
416
CGN001 Cogan-Reese Syndrome 20 0.029
417
CNT057 Central Centrifugal Cicatricial Alopecia 20 0.029
418
INF048 Infantile Histiocytoid Cardiomyopathy 19 0.029
419
c PRM287 Primary Adult Heart Tumor 18 0.029
420
NDD001 Nodding Syndrome 17 0.029
421
CD4004 Cd4 Deficiency 17 0.029
422
DYS180 Dyschondrosteosis and Nephritis 17 0.029
423
SDD004 Sudden Arrhythmia Death Syndrome 16 0.029
424
KRK002 Karak Syndrome 14 0.029
425
PRP014 Peripheral Degeneration of Cornea 11 0.029
426
HND010 Handigodu Disease 8 0.029
427
MLP003 Male Pseudohermaphroditism Intellectual Disability Syndrome, Verloes Type 8 0.029
428
ERB002 Erb's Palsy 8 0.029
429
ABS002 Absence of Gluteal Muscle 8 0.029
430
RTR017 Retrovirus-Associated Myelopathy 4 0.029
431
P RTT002 Rett Syndrome 82 0.020
432
P RTN008 Retinitis Pigmentosa 80 0.020
433
c AMY091 Amyotrophic Lateral Sclerosis 1 78 0.020
434
INS024 Insulin-Like Growth Factor I 75 0.020
435
P APL001 Aplastic Anemia 74 0.020
436
WLS001 Wilson Disease 73 0.020
437
P LFR001 Li-Fraumeni Syndrome 72 0.020
438
P HMC003 Hemochromatosis 72 0.020
439
ADR007 Adrenoleukodystrophy 72 0.020
440
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.020
441
MNT001 Mantle Cell Lymphoma 72 0.020
442
P FLL037 Follicular Lymphoma 71 0.020
443
MYL009 Myelodysplastic Syndrome 71 0.020
444
P LYN001 Lynch Syndrome 71 0.020
445
c FNC027 Fanconi Anemia, Complementation Group a 71 0.020
446
FBR012 Fabry Disease 71 0.020
447
P PFF001 Pfeiffer Syndrome 71 0.020
448
PTZ001 Peutz-Jeghers Syndrome 70 0.020
449
P FML011 Familial Adenomatous Polyposis 69 0.020
450
P CLC005 Celiac Disease 69 0.020
451
P PRK057 Parkinson Disease, Late-Onset 68 0.020
452
TST021 Testicular Germ Cell Tumor 67 0.020
453
KPS004 Kaposi Sarcoma 67 0.020
454
KWS002 Kawasaki Disease 67 0.020
455
MYC006 Mycosis Fungoides 67 0.020
456
P LYM007 Lymphangioleiomyomatosis 66 0.020
457
P DYS007 Dyskeratosis Congenita 66 0.020
458
LVR012 Liver Cirrhosis 66 0.020
459
P GLB002 Glioblastoma 66 0.020
460
CNT098 Central Core Disease 66 0.020
461
VSC007 Vascular Disease 65 0.020
462
CHR103 Charge Syndrome 65 0.020
463
P KDN018 Kidney Disease 65 0.020
464
P MSC005 Muscular Dystrophy 65 0.020
465
PRP027 Peripheral Vascular Disease 65 0.020
466
P CRN037 Craniosynostosis 65 0.020
467
MLD001 Melioidosis 65 0.020
468
P ATS007 Autism Spectrum Disorder 65 0.020
469
ATH003 Atherosclerosis 65 0.020
470
c MCP037 Mucopolysaccharidosis is 65 0.020
471
P AGM001 Agammaglobulinemia 64 0.020
472
P HMP002 Hemophagocytic Lymphohistiocytosis 64 0.020
473
P AMY004 Amyloidosis 64 0.020
474
P BRD002 Bardet-Biedl Syndrome 64 0.020
475
EWN003 Ewing Sarcoma 64 0.020
476
P PRP003 Porphyria Cutanea Tarda 64 0.020
477
URN008 Urinary Bladder Cancer 63 0.020
478
P LPR003 Leprosy 63 0.020
479
DRM006 Dermatitis 63 0.020
480
AND015 Androgen Insensitivity 63 0.020
481
PLM001 Pulmonary Tuberculosis 63 0.020
482
PSR001 Psoriatic Arthritis 63 0.020
483
RCT015 Reactive Arthritis 63 0.020
484
P MCH002 Machado-Joseph Disease 62 0.020
485
ALC007 Alcohol Dependence 62 0.020
486
P ANG001 Angelman Syndrome 62 0.020
487
c MCP009 Mucopolysaccharidosis Ii 62 0.020
488
MTH009 Mouth Disease 62 0.020
489
P ADD001 Addison's Disease 62 0.020
490
LSC001 Lesch-Nyhan Syndrome 62 0.020
491
RNL101 Renal Cell Carcinoma, Papillary 62 0.020
492
CRY002 Cryptorchidism 61 0.020
493
P THL005 Thalassemia 61 0.020
494
GLB015 Glioblastoma Multiforme 61 0.020
495
CHR066 Chronic Fatigue Syndrome 61 0.020
496
P HYP098 Hypereosinophilic Syndrome 61 0.020
497
RBR001 Roberts Syndrome 61 0.020
498
P SHR029 Short Syndrome 61 0.020
499
BLM001 Bloom Syndrome 61 0.020
500
P HRM001 Hermansky-Pudlak Syndrome 61 0.020
501
TYP007 Typhoid Fever 61 0.020
502
P HML002 Hemolytic Anemia 61 0.020
503
BLS001 Blau Syndrome 61 0.020
504
P DYS154 Dystonia 61 0.020
505
P NRN021 Neuronal Ceroid Lipofuscinosis 61 0.020
506
P CRB171 Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy 1 61 0.020
507
P MYM002 Moyamoya Disease 60 0.020
508
DFC004 Deficiency Anemia 60 0.020
509
ADR016 Adrenal Cortical Carcinoma 60 0.020
510
BRS051 Breast Disease 60 0.020
511
c ATM010 Autoimmune Hemolytic Anemia 60 0.020
512
P TXP001 Toxoplasmosis 60 0.020
513
P WVR001 Weaver Syndrome 60 0.020
514
c CNT035 Central Nervous System Disease 60 0.020
515
TTN003 Tetanus 60 0.020
516
HYP066 Hyperglycemia 59 0.020
517
P THY023 Thymoma 59 0.020
518
c ACT075 Acute Myocardial Infarction 59 0.020
519
SCR008 Scrub Typhus 59 0.020
520
FCT007 Factor Vii Deficiency 59 0.020
521
MDD011 Mood Disorder 59 0.020
522
LPP001 Lipoprotein Lipase Deficiency 59 0.020
523
P SPR098 Supranuclear Palsy, Progressive 59 0.020
524
LGN002 Legionellosis 59 0.020
525
VLC002 Vlcad Deficiency 59 0.020
526
P NPH012 Nephrotic Syndrome 59 0.020
527
P FCS002 Fucosidosis 59 0.020
528
CRD119 Cardiac Arrest 59 0.020
529
OST017 Osteomyelitis 58 0.020
530
DFF005 Diffuse Large B-Cell Lymphoma 58 0.020
531
c NMN013 Niemann-Pick Disease, Type a 58 0.020
532
P TMT001 Timothy Syndrome 58 0.020
533
PRR007 Perry Syndrome 58 0.020
534
P THR015 Thrombophilia 58 0.020
535
CHL068 Cholestasis 58 0.020
536
P MCR010 Microcephaly 58 0.020
537
WLL006 Wells Syndrome 58 0.020
538
CMP005 Campomelic Dysplasia 58 0.020
539
DRM014 Dermatofibrosarcoma Protuberans 57 0.020
540
P INF032 Infertility 57 0.020
541
INT066 Interstitial Lung Disease 57 0.020
542
P BRS044 Breast Adenocarcinoma 57 0.020
543
DPH001 Diphtheria 57 0.020
544
P ORL007 Oral Cavity Cancer 57 0.020
545
P ALC004 Alcohol Abuse 57 0.020
546
CMM005 Common Cold 57 0.020
547
P RCK004 Rickets 57 0.020
548
MLG056 Malignant Hyperthermia 57 0.020
549
P GRV001 Graves' Disease 57 0.020
550
LPD008 Lipid Metabolism Disorder 57 0.020
551
LYM021 Lymphadenitis 57 0.020
552
ING001 Inguinal Hernia 57 0.020
553
c EHL033 Ehlers-Danlos Syndrome, Classic Type 57 0.020
554
P LPS002 Liposarcoma 57 0.020
555
MTR014 Motor Neuron Disease 56 0.020
556
P STC001 Stickler Syndrome 56 0.020
557
SCH014 Schistosomiasis 56 0.020
558
c HPT003 Hepatitis a 56 0.020
559
P CND004 Candidiasis 56 0.020
560
ASP002 Aspartylglucosaminuria 56 0.020
561
P HYP055 Hypoplastic Left Heart Syndrome 56 0.020
562
ORL011 Oral Cancer 56 0.020
563
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 56 0.020
564
c ACT027 Acute Pancreatitis 56 0.020
565
LMY005 Leiomyomatosis and Renal Cell Cancer 56 0.020
566
c PRC016 Pre-Eclampsia 56 0.020
567
PNC033 Pancreas Adenocarcinoma 56 0.020
568
JNT002 Joint Disorders 55 0.020
569
ORL015 Oral Squamous Cell Carcinoma 55 0.020
570
TRF001 Trifunctional Protein Deficiency 55 0.020
571
P HMP007 Hemophilia 55 0.020
572
CRM001 Crimean-Congo Hemorrhagic Fever 55 0.020
573
ALS001 Alstrom Syndrome 55 0.020
574
VGT001 Vogt-Koyanagi-Harada Disease 55 0.020
575
INT079 Intrahepatic Cholangiocarcinoma 55 0.020
576
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 55 0.020
577
P SML001 Small Cell Carcinoma 55 0.020
578
P OCL002 Oculocutaneous Albinism 55 0.020
579
ACR008 Acrocallosal Syndrome 55 0.020
580
c PRM126 Primary Peritoneal Carcinoma 55 0.020
581
c PND001 Pain Disorder 55 0.020
582
P BRC006 Brachydactyly 55 0.020
583
END041 Endometrial Adenocarcinoma 55 0.020
584
HRY003 Hairy Cell Leukemia 55 0.020
585
CHL067 Cholecystitis 55 0.020
586
P ANT006 Antiphospholipid Syndrome 54 0.020
587
RBS001 Rabies 54 0.020
588
GLC003 Glucose Intolerance 54 0.020
589
PLN006 Poland Syndrome 54 0.020
590
P MMP001 Mumps 54 0.020
591
P PRG013 Paraganglioma 54 0.020
592
HPT022 Hepatoblastoma 54 0.020
593
P KBK002 Kabuki Syndrome 1 54 0.020
594
P MLT074 Multiple Endocrine Neoplasia 54 0.020
595
P PLY006 Polydactyly 54 0.020
596
P MNC007 Monocytic Leukemia 54 0.020
597
PPL022 Papilloma 54 0.020
598
PLM034 Pulmonary Emphysema 54 0.020
599
RTN017 Retinal Detachment 54 0.020
600
P HYP083 Hypopituitarism 54 0.020
601
P HYP027 Hypobetalipoproteinemia 54 0.020
602
FLR002 Filariasis 54 0.020
603
MYX005 Myxoid Liposarcoma 54 0.020
604
CND002 Conduct Disorder 53 0.020
605
SZR001 Sezary's Disease 53 0.020
606
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 53 0.020
607
P THY097 Thyroid Hormone Resistance 53 0.020
608
P MYC008 Myocarditis 53 0.020
609
HLY001 Hailey-Hailey Disease 53 0.020
610
c BCT007 Bacterial Meningitis 53 0.020
611
DMY004 Demyelinating Disease 53 0.020
612
ANN002 Anencephaly 53 0.020
613
CYS010 Cystinosis 53 0.020
614
CLR003 Clear Cell Adenocarcinoma 53 0.020
615
P RBL001 Rubella 53 0.020
616
MGL013 Megalencephaly 53 0.020
617
CHK001 Chikungunya 53 0.020
618
P END044 Endometriosis 53 0.020
619
GST063 Gastric Cancer Risk After H. Pylori Infection 53 0.020
620
P MGL002 Megalencephalic Leukoencephalopathy with Subcortical Cysts 53 0.020
621
RSC001 Rosacea 53 0.020
622
P ALT001 Alternating Hemiplegia of Childhood 53 0.020
623
TRN015 Transient Cerebral Ischemia 53 0.020
624
HYP730 Hypogonadotropic Hypogonadism 52 0.020
625
WHM001 Whim Syndrome 52 0.020
626
TRN018 Transitional Cell Carcinoma 52 0.020
627
ALV010 Alveolar Soft-Part Sarcoma 52 0.020
628
P HMR012 Hemorrhagic Fever 52 0.020
629
c CNG021 Congenital Toxoplasmosis 52 0.020
630
ECH003 Echinococcosis 52 0.020
631
SBS003 Substance Abuse 52 0.020
632
P BRN009 Burning Mouth Syndrome 52 0.020
633
P PLY041 Polymyositis 52 0.020
634
BRN002 Bronchiolitis 52 0.020
635
OLG003 Oligohydramnios 52 0.020
636
APP015 Apparent Mineralocorticoid Excess 52 0.020
637
P HYP097 Hyperekplexia 52 0.020
638
P PTS002 Ptosis 52 0.020
639
P ENC018 Encephalopathy 52 0.020
640
QBC001 Quebec Platelet Disorder 52 0.020
641
c ACT009 Acute Monocytic Leukemia 52 0.020
642
P OST009 Osteochondritis Dissecans 52 0.020
643
PSD012 Pseudoachondroplasia 52 0.020
644
GTR002 Goiter 52 0.020
645
P CYS018 Cystitis 52 0.020
646
P LCH002 Lichen Planus 52 0.020
647
EPD001 Epidermodysplasia Verruciformis 52 0.020
648
CHL014 Cholera 52 0.020
649
P DBT005 Diabetes Insipidus 52 0.020
650
P PMP005 Pemphigus Vulgaris 51 0.020
651
OMP004 Omphalocele 51 0.020
652
LGS001 Legius Syndrome 51 0.020
653
NWC001 Newcastle Disease 51 0.020
654
c HPT007 Hepatitis E 51 0.020
655
BLD131 Bladder Urothelial Carcinoma 51 0.020
656
PRS042 Prostate Disease 51 0.020
657
P ECL001 Eclampsia 51 0.020
658
PRT014 Protein S Deficiency 51 0.020
659
ORL004 Oral Submucous Fibrosis 51 0.020
660
ETH011 Ethylmalonic Encephalopathy 51 0.020
661
MYM001 Myoma 51 0.020
662
URC002 Urea Cycle Disorder 51 0.020
663
HST011 Histoplasmosis 51 0.020
664
P PLY017 Polyarteritis Nodosa 51 0.020
665
P GND004 Gonadal Dysgenesis 51 0.020
666
CLR030 Clear Cell Renal Cell Carcinoma 51 0.020
667
BNM001 Bone Marrow Cancer 51 0.020
668
RPP001 Rapp-Hodgkin Syndrome 51 0.020
669
P LCT001 Lactic Acidosis 50 0.020
670
NPH018 Nephrogenic Systemic Fibrosis 50 0.020
671
RDC002 Radiculopathy 50 0.020
672
BRS099 Breast Ductal Carcinoma 50 0.020
673
FML037 Female Breast Cancer 50 0.020
674
PRR016 Pierre Robin Syndrome 50 0.020
675
P MMB011 Membranous Nephropathy 50 0.020
676
MSC072 Muscle Cancer 50 0.020
677
c LRG001 Large Cell Carcinoma 50 0.020
678
BLT006 Bilateral Breast Cancer 50 0.020
679
P HYP014 Hyperuricemia 50 0.020
680
ORT008 Orotic Aciduria 50 0.020
681
INF034 Infective Endocarditis 50 0.020
682
BLD044 Bladder Disease 50 0.020
683
SRS001 Serous Cystadenocarcinoma 50 0.020
684
STR008 Strongyloidiasis 50 0.020
685
P PRM006 Primary Biliary Cirrhosis 50 0.020
686
TMP001 Temporal Lobe Epilepsy 50 0.020
687
P PLY023 Polycystic Liver Disease 49 0.020
688
ATX029 Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia 49 0.020
689
P MSC003 Muscular Atrophy 49 0.020
690
MCN001 Mucinous Adenocarcinoma 49 0.020
691
DNR002 Duane-Radial Ray Syndrome 49 0.020
692
PMP001 Pemphigus 49 0.020
693
AMN001 Amenorrhea 49 0.020
694
LYM024 Lymphatic System Disease 49 0.020
695
SPT005 Spotted Fever 49 0.020
696
CHR288 Chronic Recurrent Multifocal Osteomyelitis 49 0.020
697
MLB001 Mulibrey Nanism 49 0.020
698
PRT011 Protein C Deficiency 49 0.020
699
OPT006 Optic Nerve Disease 49 0.020
700
ATR057 Atrioventricular Block 49 0.020
701
LPR001 Lepromatous Leprosy 49 0.020
702
CLF001 Cleft Lip 49 0.020
703
MCR004 Macroglobulinemia 48 0.020
704
CLL003 Cellulitis 48 0.020
705
c OST124 Osteogenesis Imperfecta, Type V 48 0.020
706
c ICH047 Ichthyosis, Congenital, Autosomal Recessive 1 48 0.020
707
DRG003 Drug Dependence 48 0.020
708
FML026 Familial Lipoprotein Lipase Deficiency 48 0.020
709
KRT009 Keratosis 48 0.020
710
c ACT134 Acute Liver Failure 48 0.020
711
INC021 Incontinentia Pigmenti 48 0.020
712
INT051 Intussusception 48 0.020
713
c SVR005 Severe Pre-Eclampsia 48 0.020
714
ECT026 Ectopic Pregnancy 48 0.020
715
c MCP038 Mucopolysaccharidosis Iva 48 0.020
716
P FNC004 Fanconi Syndrome 48 0.020
717
SCH012 Schizoaffective Disorder 48 0.020
718
GRW007 Growth Hormone Deficiency 48 0.020
719
c CNG415 Congenital Disorder of Glycosylation, Type Ia 48 0.020
720
DRY001 Dry Eye Syndrome 48 0.020
721
P CHL066 Cholangitis 48 0.020
722
P TRN034 Transverse Myelitis 48 0.020
723
P MWT001 Mowat-Wilson Syndrome 48 0.020
724
HYP006 Hypertensive Heart Disease 48 0.020
725
BCL002 B Cell Deficiency 48 0.020
726
P WLL002 Weill-Marchesani Syndrome 48 0.020
727
TRY002 Troyer Syndrome 48 0.020
728
YLL001 Yellow Nail Syndrome 48 0.020
729
P OPN001 Open-Angle Glaucoma 48 0.020
730
BRN056 Bronchopulmonary Dysplasia 48 0.020
731
P LPM005 Lipomatosis 48 0.020
732
NXS001 Naxos Disease 48 0.020
733
PRP021 Peripheral Nervous System Neoplasm 48 0.020
734
MYL001 Myelitis 48 0.020
735
c BRD012 Bardet-Biedl Syndrome 11 48 0.020
736
P PRN026 Porencephaly 48 0.020
737
P CHR345 Chronic Pain 48 0.020
738
P ENC008 Encephalocele 48 0.020
739
c ANT034 Anterior Uveitis 47 0.020
740
MYL003 Myeloid Sarcoma 47 0.020
741
SCH068 Schwartz-Jampel Syndrome, Type 1 47 0.020
742
PPL046 Popliteal Pterygium Syndrome 1 47 0.020
743
BCT015 Bacteremia 47 0.020
744
CGN006 Cogan Syndrome 47 0.020
745
P SCL009 Sclerosing Cholangitis 47 0.020
746
MCL002 Macular Corneal Dystrophy 47 0.020
747
BRN045 Brunner Syndrome 47 0.020
748
DYS073 Dysphagia 47 0.020
749
CHR001 Churg-Strauss Syndrome 47 0.020
750
P CTN003 Cutaneous Lupus Erythematosus 47 0.020
751
TCK001 Tick-Borne Encephalitis 47 0.020
752
P EST001 Estrogen-Receptor Positive Breast Cancer 47 0.020
753
CHR005 Chorioamnionitis 47 0.020
754
MTN003 Motion Sickness 47 0.020
755
P ATR005 Atrophic Gastritis 47 0.020
756
GYN001 Gynecomastia 47 0.020
757
OLV001 Olivopontocerebellar Atrophy 47 0.020
758
LYM104 Lymphoma, Malt, Somatic 47 0.020
759
P PLM006 Pulmonary Alveolar Proteinosis 46 0.020
760
TRN044 Transposition of the Great Arteries 46 0.020
761
P SCL048 Sclerosteosis 46 0.020
762
SKN023 Skin Tag 46 0.020
763
P PLG001 Pelger-Huet Anomaly 46 0.020
764
PLY012 Polyhydramnios 46 0.020
765
LYM008 Lymphangiosarcoma 46 0.020
766
PRN009 Paranoid Schizophrenia 46 0.020
767
P HMR005 Hemorrhoid 46 0.020
768
c SPR009 Sporadic Breast Cancer 46 0.020
769
c ATM024 Autoimmune Pancreatitis 46 0.020
770
PTY003 Pityriasis Rubra Pilaris 46 0.020
771
PLS025 Plasmablastic Lymphoma 46 0.020
772
P CRT033 Corticobasal Degeneration 46 0.020
773
c MLG069 Malignant Hypertension 46 0.020
774
PPL018 Papillary Adenocarcinoma 46 0.020
775
PRN014 Paronychia 46 0.020
776
SCB001 Scabies 46 0.020
777
P SCL015 Scleritis 46 0.020
778
HRT031 Hartnup Disorder 46 0.020
779
GDS001 Good Syndrome 46 0.020
780
P HRP009 Herpes Simplex Encephalitis 46 0.020
781
P CRN012 Craniometaphyseal Dysplasia 46 0.020
782
ORL005 Oral Candidiasis 46 0.020
783
c MNN044 Mannosidosis, Beta 46 0.020
784
PTT009 Pituitary Gland Disease 46 0.020
785
c OPT053 Optic Atrophy 1 46 0.020
786
PRS039 Prostate Adenocarcinoma 45 0.020
787
JLL001 Jalili Syndrome 45 0.020
788
CRB085 Cerebral Hemorrhage 45 0.020
789
MXD023 Mixed Cell Type Cancer 45 0.020
790
P PRM108 Primary Progressive Multiple Sclerosis 45 0.020
791
CRY004 Cryoglobulinemia 45 0.020
792
AZS001 Azoospermia 45 0.020
793
ALB002 Albinism 45 0.020
794
RSS025 Ras-Associated Autoimmune Leukoproliferative Disorder 45 0.020
795
LYM012 Lymphoplasmacytic Lymphoma 45 0.020
796
BLL003 Bell's Palsy 45 0.020
797
RFT001 Rift Valley Fever 45 0.020
798
SPL018 Splenomegaly 45 0.020
799
MST016 Mesothelioma, Somatic 45 0.020
800
MCR037 Macroglossia 45 0.020
801
VTM002 Vitamin B12 Deficiency 45 0.020
802
DST006 Diastolic Heart Failure 45 0.020
803
STS002 Situs Inversus 45 0.020
804
FLT006 Floating-Harbor Syndrome 44 0.020
805
c SPN305 Spinocerebellar Ataxia 11 44 0.020
806
RTC005 Reticulosarcoma 44 0.020
807
OVR012 Ovarian Serous Cystadenocarcinoma 44 0.020
808
HST006 Histidinemia 44 0.020
809
DBW001 Dubowitz Syndrome 44 0.020
810
CYS008 Cystic Echinococcosis 44 0.020
811
TTR011 Tetraploidy 44 0.020
812
RNS001 Raine Syndrome 44 0.020
813
c ACT078 Acute Porphyria 44 0.020
814
RSD004 Rosai-Dorfman Disease 44 0.020
815
SPL004 Splenic Marginal Zone Lymphoma 44 0.020
816
SNS023 Sensory System Cancer 44 0.020
817
HMP009 Haemophilus Influenzae 44 0.020
818
MTR003 Mitral Valve Stenosis 44 0.020
819
BCT004 Bacteriuria 44 0.020
820
P SLL003 Salla Disease 44 0.020
821
NNS002 Nonspecific Interstitial Pneumonia 44 0.020
822
DNT016 Dentatorubro-Pallidoluysian Atrophy 44 0.020
823
ANX004 Anoxia 44 0.020
824
BRT030 Birth Defects 44 0.020
825
MLT152 Multiple Self-Healing Squamous Epithelioma 44 0.020
826
SKN027 Skin Conditions 44 0.020
827
CTY001 Cat Eye Syndrome 43 0.020
828
HYD012 Hydrops Fetalis 43 0.020
829
P VGN017 Vaginal Cancer 43 0.020
830
SYS003 Systolic Heart Failure 43 0.020
831
MCR165 Microphthalmia with Limb Anomalies 43 0.020
832
CLN044 Colon Adenoma 43 0.020
833
SPN035 Spindle Cell Sarcoma 43 0.020
834
P PRM018 Primary Hypertrophic Osteoarthropathy 43 0.020
835
c CNG124 Congenital Rubella 43 0.020
836
c SPL024 Split-Hand/foot Malformation 3 43 0.020
837
OPP004 Oppositional Defiant Disorder 43 0.020
838
GND001 Gonadoblastoma 43 0.020
839
P PRL003 Proliferative Glomerulonephritis 43 0.020
840
FCL022 Focal Dystonia 43 0.020
841
NDL021 Nodular Lymphocyte Predominant Hodgkin Lymphoma 43 0.020
842
WRN003 Wernicke Encephalopathy 43 0.020
843
P ART121 Arthrogryposis Multiplex Congenita, Distal, Type 1 43 0.020
844
c XNT010 Xanthinuria, Type I 43 0.020
845
P OVR106 Ovarian Clear Cell Carcinoma 43 0.020
846
c PRM023 Pre-Malignant Neoplasm 43 0.020
847
ANG011 Angiodysplasia 43 0.020
848
GNT031 Genitopatellar Syndrome 43 0.020
849
LFT009 Left Ventricular Outflow Tract Obstruction 42 0.020
850
c NTR038 Neutropenia, Severe Congenital 3, Autosomal Recessive 42 0.020
851
HND002 Hand, Foot and Mouth Disease 42 0.020
852
BNC003 Bone Cancer 42 0.020
853
BRN015 Bronchiolo-Alveolar Adenocarcinoma 42 0.020
854
HYP085 Hypothalamic Disease 42 0.020
855
P CLB002 Clubfoot 42 0.020
856
GND002 Gender Identity Disorder 42 0.020
857
CHR276 Chronic Active Epstein-Barr Virus Infection 42 0.020
858
NTV001 Native American Myopathy 42 0.020
859
ACT087 Acth Deficiency 42 0.020
860
SMN007 Seminoma 42 0.020
861
P PRG017 Paraganglioma and Gastric Stromal Sarcoma 42 0.020
862
ANC002 Anca-Associated Vasculitis 42 0.020
863
STT002 Status Asthmaticus 42 0.020
864
DCB001 Decubitus Ulcer 42 0.020
865
PLR006 Pleural Cancer 42 0.020
866
MRP001 Morphine Dependence 42 0.020
867
CRY014 Cryptococcal Meningitis 42 0.020
868
MDL009 Medullary Sponge Kidney 42 0.020
869
NM001 Noma 42 0.020
870
c ICH049 Ichthyosis, Congenital, Autosomal Recessive 2 42 0.020
871
P EPT012 Epithelioid Sarcoma 42 0.020
872
MTR010 Mature Teratoma 42 0.020
873
GST052 Gestational Choriocarcinoma 41 0.020
874
c EST002 Estrogen-Receptor Negative Breast Cancer 41 0.020
875
TTZ003 Tietz Albinism-Deafness Syndrome 41 0.020
876
CLS010 Cluster Headache 41 0.020
877
EVN001 Evans' Syndrome 41 0.020
878
BCK006 Back Pain 41 0.020
879
LSS003 Lassa Fever 41 0.020
880
EPD047 Epidermolysis Bullosa Simplex, Koebner Type 41 0.020
881
GST030 Gastrinoma 41 0.020
882
SMD002 Smed Strudwick Type 41 0.020
883
MYC013 Mycobacterium Abscessus 41 0.020
884
PLS016 Plasma Cell Leukemia 41 0.020
885
FBR054 Fibroma 41 0.020
886
IMM011 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 41 0.020
887
URT004 Urethral Syndrome 41 0.020
888
MLT075 Multifocal Motor Neuropathy 41 0.020
889
EXS001 Exostosis 41 0.020
890
MTS001 Mutism 41 0.020
891
CTS005 Catastrophic Antiphospholipid Syndrome 41 0.020
892
EXS017 Exstrophy of Bladder 41 0.020
893
CRY001 Cryptogenic Organizing Pneumonia 41 0.020
894
EMN001 Emanuel Syndrome 41 0.020
895
TLR001 Tularemia 41 0.020
896
SPR008 Supratentorial Primitive Neuroectodermal Tumor 41 0.020
897
GLM008 Glomus Tumor 41 0.020
898
MCL003 Macular Holes 41 0.020
899
DDN006 Duodenitis 40 0.020
900
P XLN110 X-Linked Charcot-Marie-Tooth Disease 40 0.020
901
NLX004 Neu-Laxova Syndrome 1 40 0.020
902
CNV002 Conversion Disorder 40 0.020
903
TND004 Tendinopathy 40 0.020
904
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 40 0.020
905
ADN010 Adenosquamous Cell Lung Carcinoma 40 0.020
906
CYS009 Cystadenoma 40 0.020
907
C1Q001 C1q Deficiency 40 0.020
908
c LSS005 Lissencephaly 1 40 0.020
909
EGG001 Egg Allergy 40 0.020
910
c CTR130 Cataract 9, Multiple Types 40 0.020
911
c PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 40 0.020
912
WLS004 Wilson-Turner Syndrome 40 0.020
913
P HMN036 Hemangiopericytoma, Malignant 40 0.020
914
BLS002 Blastomycosis 40 0.020
915
RPD002 Rapadilino Syndrome 40 0.020
916
MDY003 Mody, Type Ii 40 0.020
917
c MCL060 Macular Dystrophy, Vitelliform, 3 40 0.020
918
ALP093 Alpha-Thalassemia/mental Retardation Syndrome, Chromosome 16-Related 40 0.020
919
MDS022 Mediastinitis 40 0.020
920
VLV042 Vulvar Vestibulitis Syndrome 40 0.020
921
HRT012 Heart Valve Disease 40 0.020
922
c MSC113 Muscular Dystrophy, Limb-Girdle, Type 2b 40 0.020
923
BLP005 Blepharitis 40 0.020
924
WTH001 Withdrawal Disorder 40 0.020
925
CHR211 Chromosome 18p Deletion Syndrome 40 0.020
926
c PRS116 Prostate Cancer 1 39 0.020
927
WNC001 Winchester Syndrome 39 0.020
928
GLL028 Gillespie Syndrome 39 0.020
929
BLD054 Blood Protein Disease 39 0.020
930
c ICH069 Ichthyosis, Congenital, Autosomal Recessive 4b 39 0.020
931
OCL025 Ocular Toxoplasmosis 39 0.020
932
DYS009 Dysthymic Disorder 39 0.020
933
VTR016 Vater/vacterl Association 39 0.020
934
FLL013 Follicular Dendritic Cell Sarcoma 39 0.020
935
c CTR129 Cataract 31, Multiple Types 39 0.020
936
c INH004 Inherited Blood Coagulation Disease 39 0.020
937
CYC008 Cyclic Vomiting Syndrome 39 0.020
938
MSN002 Mesenteric Lymphadenitis 39 0.020
939
c SKN012 Skin Carcinoma in Situ 39 0.020
940
BRN018 Borna Disease 39 0.020
941
TBR008 Tuberculous Peritonitis 39 0.020
942
c CTR115 Cataract 16, Multiple Types 38 0.020
943
SPN369 Spinal Disease 38 0.020
944
TRN021 Transaldolase Deficiency 38 0.020
945
IGG007 Igg4-Related Disease 38 0.020
946
INF013 Inferior Myocardial Infarction 38 0.020
947
ALC010 Alcoholic Cardiomyopathy 38 0.020
948
CNT025 Central Pontine Myelinolysis 38 0.020
949
c CTR141 Cataract 21, Multiple Types 38 0.020
950
MCN008 Mucinous Cystadenocarcinoma 38 0.020
951
INT221 Intravascular Large B-Cell Lymphoma 38 0.020
952
CHR492 Chromosome 13q14 Deletion Syndrome 38 0.020
953
EPS026 Epispadias 38 0.020
954
LCR004 La Crosse Encephalitis 38 0.020
955
c CTR118 Cataract 14, Multiple Types 38 0.020
956
CLL021 Collagenous Colitis 38 0.020
957
RTR011 Retroperitoneal Fibrosis 38 0.020
958
MYC017 Mycobacterium Kansasii 38 0.020
959
c CHR350 Charcot-Marie-Tooth Disease, Axonal, Type 2k 38 0.020
960
CRD003 Cardiac Sarcoidosis 38 0.020
961
P CYS017 Cystic Teratoma 38 0.020
962
PRT035 Peritoneum Cancer 37 0.020
963
c ALB009 Albinism, Oculocutaneous, Type Ia 37 0.020
964
P PRG002 Progesterone-Receptor Positive Breast Cancer 37 0.020
965
ADN020 Adenosarcoma 37 0.020
966
ASC002 Ascariasis 37 0.020
967
c ACT004 Acute Diarrhea 37 0.020
968
P CHR102 Charcot-Marie-Tooth Neuropathy 37 0.020
969
RTR001 Retrograde Amnesia 37 0.020
970
EPC002 Epicondylitis 37 0.020
971
c OPT050 Opitz Gbbb Syndrome, Type Ii 37 0.020
972
c PRD030 Periodontitis 1, Juvenile 37 0.020
973
SLL001 Sialolithiasis 37 0.020
974
INV004 Invasive Bladder Transitional Cell Carcinoma 37 0.020
975
FMR003 Femoral Neuropathy 37 0.020
976
CPP003 Cap Polyposis 37 0.020
977
CRP002 Croup 37 0.020
978
FCL010 Focal Epithelial Hyperplasia 37 0.020
979
BLR027 Blue Rubber Bleb Nevus 37 0.020
980
P ENC011 Encephalomyopathy 37 0.020
981
PYR011 Pyropoikilocytosis 37 0.020
982
PDT025 Pediatric Multiple Sclerosis 37 0.020
983
c PRG003 Progesterone-Receptor Negative Breast Cancer 36 0.020
984
BRB001 Beriberi 36 0.020
985
c ACT059 Acute Maxillary Sinusitis 36 0.020
986
P DYS005 Dyslexia 36 0.020
987
PMP002 Pemphigoid Gestationis 36 0.020
988
c SPN297 Spondylocostal Dysostosis 3, Autosomal Recessive 36 0.020
989
P MXL015 Maxillary Sinusitis 36 0.020
990
IDM001 Ideomotor Apraxia 36 0.020
991
ACL001 Acalculous Cholecystitis 35 0.020
992
ADN067 Adenoid Hypertrophy 35 0.020
993
GRV012 Grover's Disease 35 0.020
994
c RTN054 Retinitis Pigmentosa 25 35 0.020
995
ACR005 Acrodermatitis 35 0.020
996
NTR006 Neutrophil Immunodeficiency Syndrome 35 0.020
997
MCK002 Meckel's Diverticulum 35 0.020
998
c OST147 Osteoarthritis 1 35 0.020
999
LYM042 Lymphocytic Colitis 35 0.020
1000
GST020 Gastric Antral Vascular Ectasia 35 0.020
1001
PGT003 Paget Disease, Extramammary 35 0.020
1002
P GLM006 Glomangioma 35 0.020
1003
c CTR125 Cataract 7 35 0.020
1004
P SRT002 Sertoli Cell Tumor 35 0.020
1005
HRP002 Herpes Gestationis 35 0.020
1006
CHR079 Choroid Disease 35 0.020
1007
END028 Endemic Goiter 35 0.020
1008
HYP548 Hypogonadotropic Hypogonadism 2 with or Without Anosmia 35 0.020
1009
P PHS005 Peho Syndrome 35 0.020
1010
TNC003 Tinea Corporis 34 0.020
1011
ECT004 Ecthyma 34 0.020
1012
c CTR095 Cataract 8, Multiple Types 34 0.020
1013
BRS057 Breast Mucinous Carcinoma 34 0.020
1014
c EHL027 Ehlers-Danlos Syndrome, Type Viic 34 0.020
1015
c SBC035 Subacute Cutaneous Lupus Erythematosus 34 0.020
1016
LPB001 Lipoblastoma 34 0.020
1017
KKC001 Kikuchi Disease 34 0.020
1018
c MCP036 Mucopolysaccharidosis Ih/s 34 0.020
1019
INT304 Interstitial Pneumonitis, Desquamative, Familial 34 0.020
1020
IMM068 Immunodeficiency 8 34 0.020
1021
P GRM010 Germ Cells Tumors 34 0.020
1022
EPL131 Epilepsy, Pyridoxine-Dependent 34 0.020
1023
INT003 Intracranial Hypotension 33 0.020
1024
THR099 Third-Degree Atrioventricular Block 33 0.020
1025
P FRN036 Frontonasal Dysplasia 1 33 0.020
1026
KFM001 Kaufman Oculocerebrofacial Syndrome 33 0.020
1027
OBS004 Obstructive Hydrocephalus 33 0.020
1028
BTN004 Biotin Deficiency 33 0.020
1029
LTH002 Lathosterolosis 33 0.020
1030
c CLR087 Colorectal Cancer 12 33 0.020
1031
c ICH051 Ichthyosis, Congenital, Autosomal Recessive 11 33 0.020
1032
FNT004 Fainting 33 0.020
1033
MGS001 Megaesophagus 33 0.020
1034
c CTR122 Cataract 5, Multiple Types 32 0.020
1035
P ENC021 Encephalopathy, Neonatal Severe 32 0.020
1036
BLK001 Balkan Nephropathy 32 0.020
1037
CHR028 Chronic Wasting Disease 32 0.020
1038
MND020 Mandibulofacial Dysostosis, Guion-Almeida Type 32 0.020
1039
PLX004 Plexopathy 32 0.020
1040
c OPT051 Opitz Gbbb Syndrome, Type I 32 0.020
1041
c CTR113 Cataract 11, Multiple Types 32 0.020
1042
MLD002 Mild Pre-Eclampsia 32 0.020
1043
HMR023 Hemorrhagic Cystitis 32 0.020
1044
c ALB010 Albinism, Oculocutaneous, Type Ib 32 0.020
1045
GLD002 Goldberg-Shprintzen Megacolon Syndrome 32 0.020
1046
ANG037 Angiomatosis 32 0.020
1047
ACT012 Acute Hemorrhagic Conjunctivitis 32 0.020
1048
ZYG002 Zygomycosis 32 0.020
1049
P LTT001 Lattice Corneal Dystrophy 32 0.020
1050
GLT031 Glut1 Deficiency Syndrome 1, Infantile Onset, Severe 32 0.020
1051
ORC001 Orchitis 32 0.020
1052
PNN005 Panencephalitis, Subacute Sclerosing 32 0.020
1053
VGN019 Vaginal Discharge 32 0.020
1054
SCL025 Scleromyxedema 32 0.020
1055
NCR002 Necrobiosis Lipoidica 32 0.020
1056
c PRK082 Porokeratosis 1, Multiple Types 32 0.020
1057
P CMM008 Communicating Hydrocephalus 32 0.020
1058
MYC014 Mycobacterium Chelonae 32 0.020
1059
CRN237 Corneal Dystrophy, Avellino Type 32 0.020
1060
CYL001 Cayler Cardiofacial Syndrome 32 0.020
1061
LVD002 Livedoid Vasculopathy 32 0.020
1062
P KNB001 Knobloch Syndrome 31 0.020
1063
c CTR124 Cataract 10, Multiple Types 31 0.020
1064
MLK004 Malakoplakia 31 0.020
1065
c BRS049 Breast Carcinoma in Situ 31 0.020
1066
NVS007 Nevus of Ota 31 0.020
1067
RTN002 Retinal Perforation 31 0.020
1068
IRN008 Iron Overload in Africa 31 0.020
1069
CHL012 Childhood Disintegrative Disease 31 0.020
1070
LNZ003 Lenz-Majewski Hyperostotic Dwarfism 31 0.020
1071
c DRR007 Diarrhea 7 30 0.020
1072
INT020 Intravenous Leiomyomatosis 30 0.020
1073
ANS003 Anisakiasis 30 0.020
1074
MXL016 Maxillonasal Dysplasia, Binder Type 30 0.020
1075
CYT004 Cytomegalic Inclusion Disease 30 0.020
1076
PST086 Posterior Cortical Atrophy 30 0.020
1077
PSY003 Psychosexual Disorder 30 0.020
1078
c WGN005 Wagner Syndrome 1 30 0.020
1079
c ICH040 Ichthyosis, Congenital, Autosomal Recessive 4a 30 0.020
1080
MYS001 Myositis Ossificans 30 0.020
1081
BLC015 Balo Concentric Sclerosis 30 0.020
1082
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 30 0.020
1083
PNC048 Pancreatic Lipase Deficiency 30 0.020
1084
HMC001 Homocarnosinosis 30 0.020
1085
c CHR057 Chronic Laryngitis 30 0.020
1086
PTT044 Pituitary Hormone Deficiency, Combined, 4 30 0.020
1087
c ACT072 Acute Laryngitis 30 0.020
1088
MTH047 Methanol Poisoning 30 0.020
1089
STC016 Sticky Platelet Syndrome 30 0.020
1090
MCR183 Microcephaly-Capillary Malformation Syndrome 30 0.020
1091
CTN013 Cutaneous Anthrax 29 0.020
1092
SBD001 Subdural Empyema 29 0.020
1093
SPR035 Superior Vena Cava Syndrome 29 0.020
1094
HNS001 Hansen's Disease 29 0.020
1095
PRS064 Persistent Vegetative State 29 0.020
1096
RHB022 Rhabdoid Tumors, Somatic 29 0.020
1097
OVR098 Ovarian Fibroma 29 0.020
1098
ANH001 Ainhum 29 0.020
1099
SPL007 Splenic Abscess 29 0.020
1100
MCD002 Mcdonough Syndrome 29 0.020
1101
IMM075 Immunodeficiency 22 29 0.020
1102
PRK069 Parkinsonism-Dystonia, Infantile 29 0.020
1103
LGH016 Leigh Syndrome, French-Canadian Type 29 0.020
1104
ASC004 Ascending Colon Cancer 29 0.020
1105
c ICH038 Ichthyosis, Congenital, Autosomal Recessive 3 28 0.020
1106
PNM003 Pneumatosis Cystoides Intestinalis 28 0.020
1107
ATM021 Autoimmune Inner Ear Disease 28 0.020
1108
IMM120 Immunodeficiency 40 28 0.020
1109
STY001 Satoyoshi Syndrome 28 0.020
1110
CHR594 Chromosome 3q29 Deletion Syndrome 28 0.020
1111
CRY032 Carey-Fineman-Ziter Syndrome 28 0.020
1112
BRN055 Bronchogenic Cyst 28 0.020
1113
TBS001 Tabes Dorsalis 28 0.020
1114
PDT027 Pediatric Ulcerative Colitis 28 0.020
1115
c ICH042 Ichthyosis, Congenital, Autosomal Recessive 6 28 0.020
1116
c BRC047 Bruck Syndrome 1 28 0.020
1117
c ICH050 Ichthyosis, Congenital, Autosomal Recessive 5 28 0.020
1118
c CTR167 Cataract 22 28 0.020
1119
SPN251 Spondyloenchondrodysplasia with Immune Dysregulation 28 0.020
1120
SDD002 Sudden Infant Death with Dysgenesis of the Testes Syndrome 28 0.020
1121
c DFN178 Deafness, Autosomal Recessive 59 28 0.020
1122
c HRD015 Hereditary Night Blindness 28 0.020
1123
CLC010 Calcifying Epithelial Odontogenic Tumor 28 0.020
1124
NRC003 Narcissistic Personality Disorder 28 0.020
1125
JPN001 Japanese Spotted Fever 28 0.020
1126
PLN001 Plantar Wart 28 0.020
1127
TNC001 Tinea Cruris 28 0.020
1128
TST033 Testicular Regression Syndrome 27 0.020
1129
OMS001 Omsk Hemorrhagic Fever 27 0.020
1130
MYC019 Mycobacterium Marinum 27 0.020
1131
P BRC003 Brachyolmia 27 0.020
1132
INN003 Iniencephaly 27 0.020
1133
MKL001 Mikulicz Disease 27 0.020
1134
TRT003 Tertiary Syphilis 27 0.020
1135