Search results for was

1544 hits were found for was

# Family MCID Name MIFTS Score
1
P WSK001 Wiskott-Aldrich Syndrome 77 20.992
2
c THR071 Thrombocytopenia 1 51 6.500
3
NTR036 Neutropenia, Severe Congenital, X-Linked 23 6.123
4
P THR014 Thrombocytopenia 64 5.301
5
P NTR004 Neutropenia 60 4.855
6
c SVR003 Severe Congenital Neutropenia 58 3.961
7
IMM167 Immune Deficiency Disease 59 3.442
8
P AGM019 Agammaglobulinemia, X-Linked 68 3.433
9
WSR001 Was-Related Disorders 2 2.939
10
BRL010 Buruli Ulcer 50 2.817
11
c SPN327 Spinocerebellar Ataxia, Autosomal Recessive 1 60 2.795
12
c NRD016 Neurodegeneration with Brain Iron Accumulation 6 36 2.795
13
DDN009 Duodenal Obstruction 33 2.795
14
P XLN007 X-Linked Disease 30 2.795
15
TXC008 Toxic Optic Neuropathy 24 2.795
16
P HMR003 Hemorrhagic Disease 60 2.057
17
BLD053 Blood Platelet Disease 55 1.992
18
BRR014 Barrett Esophagus 63 0.130
19
P ADN016 Adenocarcinoma 70 0.096
20
P BRS047 Breast Cancer 100 0.092
21
P LKM002 Leukemia 72 0.092
22
GST053 Gastric Cancer 77 0.090
23
P LYM118 Lymphoma 70 0.086
24
P LNG032 Lung Cancer 98 0.079
25
P CLR023 Colorectal Cancer 97 0.077
26
P HPT021 Hepatitis 76 0.075
27
PLM129 Pulmonary Disease, Chronic Obstructive 72 0.075
28
P ESP024 Esophagitis 63 0.075
29
P PRS040 Prostate Cancer 90 0.073
30
P PNC044 Pancreatitis 64 0.068
31
RNL114 Renal Cell Carcinoma, Nonpapillary 59 0.065
32
P HPT023 Hepatocellular Carcinoma 94 0.059
33
ESP021 Esophageal Cancer 77 0.059
34
P ART022 Arthritis 76 0.059
35
AGN016 Aging 64 0.059
36
LYM027 Lymphopenia 55 0.056
37
P LPS004 Lupus Erythematosus 68 0.053
38
P MYL006 Myeloid Leukemia 68 0.053
39
ADN018 Adenoma 63 0.053
40
PRS047 Prostatitis 60 0.053
41
SQM006 Squamous Cell Carcinoma 59 0.053
42
P BLD051 Blood Coagulation Disease 50 0.053
43
P CRV039 Cervicitis 49 0.053
44
LKC003 Leukocyte Disease 46 0.053
45
c INH004 Inherited Blood Coagulation Disease 41 0.053
46
c SYS001 Systemic Lupus Erythematosus 86 0.050
47
P OVR042 Ovarian Cancer 81 0.050
48
P PNC035 Pancreatic Cancer 79 0.050
49
LYM133 Lymphoma, Hodgkin, Classic 71 0.050
50
c SML038 Small Cell Cancer of the Lung 68 0.050
51
ANG054 Angina Pectoris 66 0.050
52
PRT036 Peritonitis 66 0.050
53
P BCL006 B-Cell Lymphomas 65 0.050
54
P DBT009 Diabetes Mellitus 64 0.050
55
PHR003 Pharyngitis 59 0.050
56
P THY032 Thyroiditis 55 0.050
57
END072 Endotheliitis 45 0.050
58
P ALZ034 Alzheimer Disease 87 0.046
59
AST005 Asthma 82 0.046
60
c HYP595 Hypertension, Essential 76 0.046
61
c LKM071 Leukemia, Chronic Lymphocytic 75 0.046
62
P PNM007 Pneumonia 69 0.046
63
ACR007 Acromegaly 69 0.046
64
P SCH015 Schizophrenia 69 0.046
65
SRC014 Sarcoma 68 0.046
66
P KDN017 Kidney Cancer 58 0.046
67
HMT018 Hematopoietic Stem Cell Transplantation 57 0.046
68
P GLM045 Glioma 54 0.046
69
P MLT020 Multiple Sclerosis 78 0.042
70
P INF038 Influenza 76 0.042
71
P HRT032 Heart Disease 74 0.042
72
GST019 Gastrointestinal Stromal Tumor 73 0.042
73
DPR016 Depression 72 0.042
74
P MNN013 Meningitis 70 0.042
75
P CRV035 Cervical Cancer 69 0.042
76
DMN002 Dementia 68 0.042
77
THY028 Thyroid Cancer 66 0.042
78
BRN024 Bronchitis 66 0.042
79
ATM095 Autoimmune Disease 64 0.042
80
ACQ007 Acquired Immunodeficiency Syndrome 63 0.042
81
CLT003 Colitis 62 0.042
82
P CTR002 Cataract 60 0.042
83
HDC001 Headache 59 0.042
84
GT001 Gout 57 0.042
85
SML019 Smallpox 57 0.042
86
RTN018 Retinal Disease 56 0.042
87
SPS003 Spastic Diplegia 54 0.042
88
MCR359 Macrothrombocytopenia and Granulocyte Inclusions with or Without Nephritis or Sensorineural Hearing Loss 41 0.042
89
NRN002 Neuronitis 41 0.042
90
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 40 0.042
91
KR002 Kuru 38 0.042
92
ELC001 Elective Mutism 22 0.042
93
c MCL042 Macular Degeneration, Age-Related, 1 84 0.037
94
MYL069 Myeloma, Multiple 83 0.037
95
P RHM011 Rheumatoid Arthritis 80 0.037
96
P MYC007 Myocardial Infarction 79 0.037
97
P LNG064 Lung Cancer Susceptibility 3 76 0.037
98
ULC004 Ulcerative Colitis 72 0.037
99
CNG034 Congestive Heart Failure 72 0.037
100
P GRF003 Graft-Versus-Host Disease 71 0.037
101
c HPT001 Hepatitis C 71 0.037
102
P RTN024 Retinoblastoma 70 0.037
103
P BLD134 Bladder Cancer 69 0.037
104
PRT037 Pertussis 68 0.037
105
P DRM053 Dermatitis, Atopic 67 0.037
106
OTT002 Otitis Media 66 0.037
107
P SLP006 Sleep Apnea 66 0.037
108
CRT072 Creutzfeldt-Jakob Disease 65 0.037
109
P LYM026 Lymphoblastic Leukemia 64 0.037
110
GST045 Gastroenteritis 64 0.037
111
P MYS005 Myositis 63 0.037
112
P NRP001 Neuropathy 63 0.037
113
P ENC018 Encephalopathy 62 0.037
114
MLN008 Melanoma 62 0.037
115
HYP056 Hypoglycemia 62 0.037
116
THR024 Thrombosis 61 0.037
117
PRP030 Purpura 61 0.037
118
ANR040 Aneurysm 60 0.037
119
P HMN010 Hemangioma 60 0.037
120
MCS002 Mucositis 60 0.037
121
TNS005 Tonsillitis 60 0.037
122
P WRD001 Waardenburg's Syndrome 58 0.037
123
P LRY019 Laryngitis 56 0.037
124
PRC013 Pericarditis 55 0.037
125
P SCK002 Sick Sinus Syndrome 53 0.037
126
c WRD030 Waardenburg Syndrome, Type 1 51 0.037
127
c WRD033 Waardenburg Syndrome, Type 2e 51 0.037
128
RTN023 Retinitis 50 0.037
129
CHN016 Cohen Syndrome 47 0.037
130
MRG013 Mirage Syndrome 43 0.037
131
c WRD032 Waardenburg Syndrome, Type 2a 39 0.037
132
TXC020 Toxic Oil Syndrome 36 0.037
133
c WRD031 Waardenburg Syndrome, Type 3 34 0.037
134
DTH005 Diethylstilbestrol Syndrome 28 0.037
135
c WRD029 Waardenburg Syndrome, Type 2b 22 0.037
136
c CHN017 Chondrodysplasia Punctata 1, X-Linked 14 0.037
137
YSH001 Yusho Disease 11 0.037
138
c LKM061 Leukemia, Acute Myeloid 80 0.032
139
P DLT002 Dilated Cardiomyopathy 76 0.032
140
P PHC003 Pheochromocytoma 73 0.032
141
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.032
142
c LKM063 Leukemia, Chronic Myeloid 70 0.032
143
HMN044 Human Immunodeficiency Virus Type 1 70 0.032
144
P EPL164 Epilepsy 69 0.032
145
c LKM062 Leukemia, Acute Lymphoblastic 69 0.032
146
P ATR011 Atrial Fibrillation 68 0.032
147
SMT004 Smith-Lemli-Opitz Syndrome 68 0.032
148
P CRN018 Coronary Artery Anomaly 68 0.032
149
LYM017 Lyme Disease 68 0.032
150
APN008 Apnea, Obstructive Sleep 67 0.032
151
c EPL184 Epileptic Encephalopathy, Early Infantile, 6 67 0.032
152
c HPT016 Hepatitis B 67 0.032
153
SKN016 Skin Disease 66 0.032
154
P FCS012 Facioscapulohumeral Muscular Dystrophy 1 66 0.032
155
END057 Endometrial Cancer 65 0.032
156
P PSR002 Psoriasis 65 0.032
157
ART140 Arteries, Anomalies of 65 0.032
158
ISC004 Ischemia 65 0.032
159
P CHR071 Charcot-Marie-Tooth Disease 65 0.032
160
VSC011 Vasculitis 65 0.032
161
P HYP086 Hypothyroidism 64 0.032
162
c CHR417 Chronic Graft Versus Host Disease 64 0.032
163
P INT068 Intestinal Disease 64 0.032
164
MSL001 Measles 64 0.032
165
P PLY011 Polycystic Ovary Syndrome 63 0.032
166
P THR005 Thrombotic Thrombocytopenic Purpura 63 0.032
167
THR100 Thrombocytopenic Purpura, Autoimmune 62 0.032
168
c OVR114 Ovarian Cancer 1 62 0.032
169
P SNS014 Sinusitis 62 0.032
170
P GLM007 Glomerulonephritis 61 0.032
171
SYN007 Synovitis 60 0.032
172
CLR108 Colorectal Adenoma 60 0.032
173
P GST049 Gastrointestinal System Cancer 59 0.032
174
c ATR087 Atrial Standstill 1 59 0.032
175
P ANP001 Anaplastic Large Cell Lymphoma 59 0.032
176
VGN023 Vaginitis 58 0.032
177
P HYP069 Hyperparathyroidism 58 0.032
178
CRT002 Cartilage-Hair Hypoplasia 58 0.032
179
P TWN003 Townes-Brocks Syndrome 58 0.032
180
c SPN294 Spinocerebellar Ataxia 1 58 0.032
181
P INT030 Intracranial Aneurysm 57 0.032
182
RLP002 Relapsing-Remitting Multiple Sclerosis 57 0.032
183
c ACT135 Acute Graft Versus Host Disease 56 0.032
184
P DRR001 Diarrhea 56 0.032
185
P HYP614 Hyperlipidemia, Familial Combined 56 0.032
186
P HYP076 Hyperthyroidism 56 0.032
187
c INS002 in Situ Carcinoma 56 0.032
188
URN009 Urinary System Disease 55 0.032
189
DCT002 Ductal Carcinoma in Situ 55 0.032
190
IMP005 Impotence 55 0.032
191
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 55 0.032
192
P RTN016 Retinal Degeneration 54 0.032
193
CLN019 Colonic Disease 54 0.032
194
HYP068 Hyperostosis 53 0.032
195
KNS001 Kniest Dysplasia 53 0.032
196
CLN015 Colon Adenocarcinoma 53 0.032
197
P OBS001 Obstructive Jaundice 52 0.032
198
P TRT010 Teratoma 52 0.032
199
c AMG001 Amegakaryocytic Thrombocytopenia, Congenital 52 0.032
200
MBS002 Moebius Syndrome 51 0.032
201
AML029 Ameloblastoma 50 0.032
202
RPP001 Rapp-Hodgkin Syndrome 50 0.032
203
PRN023 Prion Disease 50 0.032
204
ACT049 Acute Disseminated Encephalomyelitis 50 0.032
205
MMM001 Mammary Paget's Disease 50 0.032
206
CVR006 Cavernous Hemangioma 49 0.032
207
CHC001 Chickenpox 49 0.032
208
P KRN004 Kernicterus 48 0.032
209
CRB045 Cerebellar Hypoplasia 48 0.032
210
ASP007 Aspiration Pneumonia 47 0.032
211
CHR074 Choriocarcinoma 47 0.032
212
CRD002 Cri-Du-Chat Syndrome 47 0.032
213
c MCR256 Microphthalmia, Syndromic 9 46 0.032
214
P HRT035 Heart Block, Congenital 46 0.032
215
VRL003 Variola Major 45 0.032
216
OCL033 Oculocerebral Syndrome with Hypopigmentation 45 0.032
217
WLS003 Wilson-Turner X-Linked Mental Retardation Syndrome 44 0.032
218
c ACR116 Aicardi-Goutieres Syndrome 1 43 0.032
219
DNN002 Donnai-Barrow Syndrome 43 0.032
220
JLL001 Jalili Syndrome 41 0.032
221
FXF002 Fox-Fordyce Disease 40 0.032
222
MNK002 Monkeypox 40 0.032
223
RCT017 Rectal Disease 39 0.032
224
NNT008 Neonatal Abstinence Syndrome 38 0.032
225
FRN039 Frank-Ter Haar Syndrome 38 0.032
226
MLN003 Melancholia 38 0.032
227
WNC001 Winchester Syndrome 37 0.032
228
OCH001 Ochronosis 36 0.032
229
OGD001 Ogden Syndrome 35 0.032
230
SPR006 Sparganosis 34 0.032
231
c HRD146 Hereditary Methemoglobinemia 31 0.032
232
OTD001 Otodental Dysplasia 31 0.032
233
MTG001 Metagonimiasis 30 0.032
234
HSD004 Hsd10 Mitochondrial Disease 30 0.032
235
c ALB020 Albinism, Oculocutaneous, Type Iii 29 0.032
236
ASH001 Asherman's Syndrome 29 0.032
237
SPN151 Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy 28 0.032
238
LGH003 Leigh Syndrome, French Canadian Type 28 0.032
239
VRL002 Variola Minor 28 0.032
240
MYC021 Mycobacterium Xenopi 27 0.032
241
RJS001 Ruijs-Aalfs Syndrome 22 0.032
242
RMB001 Rombo Syndrome 20 0.032
243
SPN356 Spinocerebellar Degeneration with Macular Corneal Dystrophy, Congenital Cataracts, and Myopia 19 0.032
244
HML018 Homologous Wasting Disease 18 0.032
245
ATS012 Autosomal Dominant Partial Epilepsy with Auditory Features 16 0.032
246
BLD153 Blood Group--Swann System 12 0.032
247
BRM001 Barmah Forest Virus Disease 12 0.032
248
YTB001 Yt Blood Group Antigen 7 0.032
249
MLR004 Malaria 83 0.026
250
OST012 Osteoarthritis 82 0.026
251
P HYP607 Hypercholesterolemia, Familial 79 0.026
252
CRH001 Crohn's Disease 78 0.026
253
P OST002 Osteoporosis 76 0.026
254
P NRV007 Nervous System Disease 73 0.026
255
ACR006 Aceruloplasminemia 73 0.026
256
ANX010 Anxiety 72 0.026
257
c HPT073 Hepatitis C Virus 72 0.026
258
PLM001 Pulmonary Tuberculosis 71 0.026
259
CNN003 Conn's Syndrome 71 0.026
260
P ATS364 Autism 70 0.026
261
P RSP003 Respiratory Failure 70 0.026
262
P MYL005 Myelofibrosis 70 0.026
263
c EXD008 Exudative Vitreoretinopathy 1 69 0.026
264
P HYD006 Hydrocephalus 69 0.026
265
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 69 0.026
266
P MYP004 Myopathy 68 0.026
267
MSC157 Muscular Dystrophy, Duchenne Type 68 0.026
268
SCH036 Scheie Syndrome 68 0.026
269
ALL003 Allergic Rhinitis 67 0.026
270
P ART023 Arthropathy 67 0.026
271
c HMP004 Hemophilia B 67 0.026
272
c PLM164 Pulmonary Hypertension, Primary, 1 66 0.026
273
OBS002 Obsessive-Compulsive Disorder 66 0.026
274
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 66 0.026
275
BSL036 Basal Cell Nevus Syndrome 65 0.026
276
P LNG028 Long Qt Syndrome 65 0.026
277
INS001 Insulinoma 65 0.026
278
MXD005 Mixed Connective Tissue Disease 65 0.026
279
DRM014 Dermatofibrosarcoma Protuberans 64 0.026
280
P HYP061 Hypertrophic Cardiomyopathy 64 0.026
281
TTN003 Tetanus 64 0.026
282
P DRM010 Dermatomyositis 64 0.026
283
P PRS038 Personality Disorder 64 0.026
284
CRB011 Cerebrotendinous Xanthomatosis 63 0.026
285
VRL011 Viral Infectious Disease 63 0.026
286
BLL006 Bullous Pemphigoid 63 0.026
287
MYL031 Myeloproliferative Neoplasm 63 0.026
288
CLF027 Cleft Palate, Isolated 63 0.026
289
HYP066 Hyperglycemia 63 0.026
290
HMT002 Hematologic Cancer 63 0.026
291
c MCP049 Mucopolysaccharidosis, Type Vii 63 0.026
292
P PRP029 Porphyria 62 0.026
293
BLD034 Bile Duct Carcinoma 62 0.026
294
P RHN004 Rhinitis 61 0.026
295
c ATS007 Autism Spectrum Disorder 61 0.026
296
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 61 0.026
297
HYP266 Hypoxia 61 0.026
298
c MNN043 Meningioma, Familial 60 0.026
299
P UVT001 Uveitis 60 0.026
300
QFV001 Q Fever 60 0.026
301
P GST044 Gastritis 60 0.026
302
c PNC108 Pancreatitis, Hereditary 59 0.026
303
P ACT074 Acute Lymphocytic Leukemia 59 0.026
304
ING001 Inguinal Hernia 59 0.026
305
CCC001 Coccidioidomycosis 59 0.026
306
P CRD132 Cardiac Conduction Defect 59 0.026
307
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 59 0.026
308
c MST023 Mesothelioma, Malignant 59 0.026
309
LNG039 Lung Squamous Cell Carcinoma 59 0.026
310
c PRM005 Primary Hyperparathyroidism 59 0.026
311
P FTL001 Fetal Alcohol Syndrome 59 0.026
312
NRN004 Neuroendocrine Tumor 58 0.026
313
P VNT002 Ventricular Septal Defect 58 0.026
314
RHM001 Rheumatic Fever 58 0.026
315
LYS001 Loeys-Dietz Syndrome 58 0.026
316
c BCT007 Bacterial Meningitis 58 0.026
317
P SML001 Small Cell Carcinoma 58 0.026
318
P MYC008 Myocarditis 58 0.026
319
VSC002 Vascular Dementia 58 0.026
320
TRP002 Tropical Spastic Paraparesis 57 0.026
321
P BCK002 Beckwith-Wiedemann Syndrome 57 0.026
322
AVN001 Avian Influenza 57 0.026
323
CHL067 Cholecystitis 57 0.026
324
c AMY087 Amyloidosis, Hereditary, Transthyretin-Related 57 0.026
325
WST005 West Nile Virus 57 0.026
326
P MMB011 Membranous Nephropathy 57 0.026
327
GST023 Gastric Ulcer 57 0.026
328
ANG020 Angiosarcoma 56 0.026
329
PLM010 Pulmonary Edema 56 0.026
330
EPD016 Epidermolysis Bullosa 56 0.026
331
TYP041 Type I 56 0.026
332
BRN106 Burns 56 0.026
333
P ACR001 Aicardi-Goutieres Syndrome 56 0.026
334
P CYS018 Cystitis 56 0.026
335
PLG002 Plague 56 0.026
336
BTN003 Biotinidase Deficiency 56 0.026
337
ALK013 Alkaptonuria 56 0.026
338
PRP082 Porphyria, Congenital Erythropoietic 55 0.026
339
ATH013 Atherosclerosis Susceptibility 55 0.026
340
PRG009 Progressive Multifocal Leukoencephalopathy 55 0.026
341
DSS009 Disseminated Intravascular Coagulation 55 0.026
342
VSC044 Visceral Myopathy 55 0.026
343
BLD044 Bladder Disease 55 0.026
344
THR004 Thrombocytosis 54 0.026
345
P INF016 Infantile Epileptic Encephalopathy 54 0.026
346
CYS014 Cystadenocarcinoma 54 0.026
347
c GST103 Gastric Cancer, Hereditary Diffuse 54 0.026
348
P PRT096 Peritoneal Mesothelioma 54 0.026
349
P INF037 Inflammatory Bowel Disease 53 0.026
350
PSD007 Pseudomyxoma Peritonei 53 0.026
351
TTH006 Tooth Disease 53 0.026
352
P PRC012 Pericardial Effusion 53 0.026
353
INT075 Intracranial Hypertension 52 0.026
354
c BNG091 Benign Chronic Pemphigus 52 0.026
355
FRN051 Frontotemporal Lobar Degeneration with Tdp43 Inclusions, Grn-Related 52 0.026
356
c EPL099 Epileptic Encephalopathy, Early Infantile, 15 52 0.026
357
PNC041 Pancreatic Ductal Adenocarcinoma 52 0.026
358
CRT013 Carotid Stenosis 52 0.026
359
END031 Endometrial Stromal Sarcoma 52 0.026
360
c ACT134 Acute Liver Failure 52 0.026
361
P CHR345 Chronic Pain 51 0.026
362
SPH001 Sapho Syndrome 51 0.026
363
P EPD003 Epidermolysis Bullosa Simplex 51 0.026
364
ATR002 Atransferrinemia 51 0.026
365
P SYP003 Syphilis 51 0.026
366
FCL012 Facial Paralysis 51 0.026
367
c CLR017 Clear Cell Sarcoma 50 0.026
368
MMB001 Membranoproliferative Glomerulonephritis 50 0.026
369
c MLG002 Malignant Peritoneal Mesothelioma 50 0.026
370
DNT005 Dentatorubral-Pallidoluysian Atrophy 50 0.026
371
LYM009 Lymphocytic Choriomeningitis 50 0.026
372
PRT029 Parathyroid Adenoma 49 0.026
373
c LBR014 Leber Congenital Amaurosis 4 49 0.026
374
CTS011 Cutis Marmorata Telangiectatica Congenita 49 0.026
375
ADL002 Adult Syndrome 49 0.026
376
RNL011 Renal Osteodystrophy 49 0.026
377
MTB004 Metabolic Acidosis 48 0.026
378
c INH020 Inherited Metabolic Disorder 48 0.026
379
ACR012 Aicardi Syndrome 48 0.026
380
DDN006 Duodenitis 48 0.026
381
HDN002 Head Injury 47 0.026
382
SPN028 Spondyloepimetaphyseal Dysplasia, Strudwick Type 47 0.026
383
MYC005 Myocardial Stunning 47 0.026
384
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 47 0.026
385
c CHR418 Chronic Leukemia 47 0.026
386
CRN017 Coronary Thrombosis 47 0.026
387
P RBN002 Robinow Syndrome 47 0.026
388
CRN024 Corneal Disease 47 0.026
389
P DNT011 Dentinogenesis Imperfecta 46 0.026
390
CHR594 Chromosome 3q29 Deletion Syndrome 46 0.026
391
P MWT001 Mowat-Wilson Syndrome 46 0.026
392
MGS001 Megaesophagus 46 0.026
393
BLD063 Bile Duct Cysts 46 0.026
394
PRD003 Periodontosis 46 0.026
395
GND002 Gender Identity Disorder 45 0.026
396
ANC002 Anca-Associated Vasculitis 45 0.026
397
c PSD106 Pseudo-Torch Syndrome 1 45 0.026
398
GLC011 Galactose Epimerase Deficiency 45 0.026
399
MNN032 Meningococcal Meningitis 44 0.026
400
VLV010 Vulvovaginitis 44 0.026
401
AMN003 Amnestic Disorder 44 0.026
402
NCR004 Nocardiosis 44 0.026
403
RSS025 Ras-Associated Autoimmune Leukoproliferative Disorder 43 0.026
404
URT001 Urethritis 43 0.026
405
CLL002 Collecting Duct Carcinoma 43 0.026
406
PHC013 Phaeochromocytoma 43 0.026
407
PNN005 Panencephalitis, Subacute Sclerosing 43 0.026
408
MRB001 Marburg Hemorrhagic Fever 43 0.026
409
BRS064 Bursitis 43 0.026
410
BDY001 Body Dysmorphic Disorder 42 0.026
411
PRP056 Porphyria, Acute Hepatic 42 0.026
412
PNM010 Pneumothorax, Primary Spontaneous 42 0.026
413
c CNG029 Congenital Mesoblastic Nephroma 42 0.026
414
WDM004 Wiedemann-Steiner Syndrome 42 0.026
415
MYL057 Myelopathy, Htlv-1-Associated 42 0.026
416
BTN002 Boutonneuse Fever 42 0.026
417
MNT317 Mental Retardation, Enteropathy, Deafness, Peripheral Neuropathy, Ichthyosis, and Keratoderma 42 0.026
418
SMT001 Somatization Disorder 41 0.026
419
LMB024 Limbic Encephalitis 41 0.026
420
CRP002 Croup 41 0.026
421
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 41 0.026
422
HMP001 Hemopericardium 41 0.026
423
PTC002 Potocki-Lupski Syndrome 41 0.026
424
UNV001 Unverricht-Lundborg Syndrome 41 0.026
425
CRB009 Cerebritis 41 0.026
426
OST097 Osteoporotic Fracture 41 0.026
427
c SPN290 Spinocerebellar Ataxia 15 40 0.026
428
SPR066 Superficial Siderosis 40 0.026
429
SCR011 Scrapie 40 0.026
430
RHM035 Rheumatic Fever-Related Antigen 39 0.026
431
KYS001 Kyasanur Forest Disease 39 0.026
432
WHP002 Whiplash 39 0.026
433
TRC077 Trichomegaly 39 0.026
434
ELP001 Elephantiasis 38 0.026
435
ADN067 Adenoid Hypertrophy 38 0.026
436
PLX004 Plexopathy 37 0.026
437
BRS062 Breast Secretory Carcinoma 37 0.026
438
CHL039 Choledocholithiasis 37 0.026
439
EPD046 Epididymitis 36 0.026
440
ASC009 Ascites, Chylous 36 0.026
441
c CTR098 Cataract 1, Multiple Types 35 0.026
442
OMS001 Omsk Hemorrhagic Fever 34 0.026
443
c TRC078 Trichohepatoenteric Syndrome 2 34 0.026
444
PRM056 Primrose Syndrome 34 0.026
445
BLC004 Blackwater Fever 34 0.026
446
PLC009 Placenta Praevia 33 0.026
447
AKN002 Akinetic Mutism 33 0.026
448
c SPN200 Spinocerebellar Ataxia, Autosomal Recessive 2 31 0.026
449
SPN402 Spinal Muscular Atrophy, X-Linked 2 31 0.026
450
MMS001 Momo Syndrome 30 0.026
451
PRX008 Paroxysmal Cold Hemoglobinuria 30 0.026
452
CHL040 Cholangiolocellular Carcinoma 30 0.026
453
c CTR096 Cataract 6, Multiple Types 29 0.026
454
c CTR102 Cataract 2, Multiple Types 28 0.026
455
c CTR132 Cataract 3, Multiple Types 28 0.026
456
c PMP006 Pemphigus Vulgaris, Familial 28 0.026
457
TST025 Testicular Microlithiasis 28 0.026
458
GNT033 Genetic Prion Diseases 28 0.026
459
TRN066 Transmitted_by 27 0.026
460
MNT006 Manitoba Oculotrichoanal Syndrome 26 0.026
461
CRD231 Cardiomyopathy, Infantile Histiocytoid 26 0.026
462
CRT028 Cor Triatriatum 24 0.026
463
CNT057 Central Centrifugal Cicatricial Alopecia 24 0.026
464
MNS002 Mini Stroke 23 0.026
465
OPH001 Ophthalmomyiasis 23 0.026
466
CGN001 Cogan-Reese Syndrome 23 0.026
467
GLT009 Gelatinous Ascites 21 0.026
468
c PYL018 Pyloric Stenosis, Infantile Hypertrophic, 1 21 0.026
469
BNG086 Bangstad Syndrome 21 0.026
470
NDD001 Nodding Syndrome 21 0.026
471
OSL001 Oslam Syndrome 20 0.026
472
c NPH067 Nephronophthisis 12 20 0.026
473
DYS180 Dyschondrosteosis and Nephritis 18 0.026
474
MRZ001 Mirizzi Syndrome 17 0.026
475
KRK002 Karak Syndrome 17 0.026
476
LNR009 Linear Atrophoderma of Moulin 15 0.026
477
BLD151 Blood Group--Wright Antigen 15 0.026
478
GLT037 Gluteal Muscles, Absence of 14 0.026
479
CHR603 Chronic Enteropathy Associated with Slco2a1 Gene 13 0.026
480
MLP003 Male Pseudohermaphroditism Intellectual Disability Syndrome, Verloes Type 12 0.026
481
ERB002 Erb's Palsy 11 0.026
482
HND010 Handigodu Disease 11 0.026
483
CDC001 Cdc73-Related Disorders 5 0.026
484
RTR017 Retrovirus-Associated Myelopathy 4 0.026
485
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.019
486
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.019
487
CYS001 Cystic Fibrosis 84 0.019
488
INS024 Insulin-Like Growth Factor I 82 0.019
489
P RTT002 Rett Syndrome 82 0.019
490
P RTN008 Retinitis Pigmentosa 81 0.019
491
NRL016 Neural Tube Defects 78 0.019
492
P FNC027 Fanconi Anemia, Complementation Group a 78 0.019
493
SQM013 Squamous Cell Carcinoma, Head and Neck 76 0.019
494
P PRK057 Parkinson Disease, Late-Onset 76 0.019
495
P LVR013 Liver Disease 75 0.019
496
c ART101 Aortic Valve Disease 2 73 0.019
497
MNT001 Mantle Cell Lymphoma 73 0.019
498
PFF001 Pfeiffer Syndrome 73 0.019
499
KPS004 Kaposi Sarcoma 73 0.019
500
APL001 Aplastic Anemia 73 0.019
501
P FML018 Familial Mediterranean Fever 73 0.019
502
P ALG028 Alagille Syndrome 1 73 0.019
503
GLB002 Glioblastoma 72 0.019
504
MYC006 Mycosis Fungoides 72 0.019
505
MLD001 Melioidosis 72 0.019
506
P CLC063 Celiac Disease 1 71 0.019
507
ADR007 Adrenoleukodystrophy 71 0.019
508
P MCR115 Microvascular Complications of Diabetes 5 71 0.019
509
WLS001 Wilson Disease 71 0.019
510
P FML011 Familial Adenomatous Polyposis 71 0.019
511
c MLT156 Multiple Endocrine Neoplasia, Type I 71 0.019
512
FBR012 Fabry Disease 71 0.019
513
P LYN001 Lynch Syndrome 71 0.019
514
PRP027 Peripheral Vascular Disease 70 0.019
515
WGN006 Wegener Granulomatosis 70 0.019
516
P LFR001 Li-Fraumeni Syndrome 70 0.019
517
ADR054 Adrenocortical Carcinoma, Hereditary 70 0.019
518
MYL009 Myelodysplastic Syndrome 70 0.019
519
KWS002 Kawasaki Disease 70 0.019
520
PTZ001 Peutz-Jeghers Syndrome 70 0.019
521
BRC012 Brucellosis 70 0.019
522
P SPR120 Supranuclear Palsy, Progressive, 1 70 0.019
523
P HRP006 Herpes Simplex 69 0.019
524
P FLL037 Follicular Lymphoma 69 0.019
525
P AGM001 Agammaglobulinemia 69 0.019
526
LVR012 Liver Cirrhosis 68 0.019
527
P AMY004 Amyloidosis 68 0.019
528
EWN003 Ewing Sarcoma 68 0.019
529
VSC007 Vascular Disease 68 0.019
530
P KDN018 Kidney Disease 68 0.019
531
c DNG003 Dengue Disease 68 0.019
532
P ORT004 Orthostatic Intolerance 68 0.019
533
P DYS007 Dyskeratosis Congenita 67 0.019
534
P CRN037 Craniosynostosis 67 0.019
535
LYM007 Lymphangioleiomyomatosis 67 0.019
536
P HMP002 Hemophagocytic Lymphohistiocytosis 67 0.019
537
LNG099 Lung Disease 67 0.019
538
P PRP003 Porphyria Cutanea Tarda 66 0.019
539
P MSC005 Muscular Dystrophy 66 0.019
540
BRS051 Breast Disease 66 0.019
541
CHR066 Chronic Fatigue Syndrome 66 0.019
542
P PRT008 Proteus Syndrome 66 0.019
543
DRM006 Dermatitis 66 0.019
544
TYP007 Typhoid Fever 66 0.019
545
P THY023 Thymoma 65 0.019
546
P MPL001 Maple Syrup Urine Disease 65 0.019
547
NRF007 Neurofibroma 65 0.019
548
PSR001 Psoriatic Arthritis 65 0.019
549
P ENC004 Encephalitis 65 0.019
550
P HYP098 Hypereosinophilic Syndrome 65 0.019
551
LGN002 Legionellosis 65 0.019
552
ALC007 Alcohol Dependence 65 0.019
553
c CRN300 Coronary Heart Disease 1 64 0.019
554
GST050 Gastrointestinal System Disease 64 0.019
555
PNC033 Pancreas Adenocarcinoma 64 0.019
556
P DYS154 Dystonia 64 0.019
557
P THL005 Thalassemia 64 0.019
558
P TXP001 Toxoplasmosis 64 0.019
559
P END044 Endometriosis 64 0.019
560
ADL030 Adult-Onset Still's Disease 64 0.019
561
CHR593 Chromosome 16p13.3 Deletion Syndrome, Proximal 64 0.019
562
c SCL052 Scleroderma, Familial Progressive 64 0.019
563
SCR008 Scrub Typhus 64 0.019
564
c MCP050 Mucopolysaccharidosis, Type Ii 63 0.019
565
MDD011 Mood Disorder 63 0.019
566
c CNT035 Central Nervous System Disease 63 0.019
567
RCT015 Reactive Arthritis 63 0.019
568
SZR001 Sezary's Disease 63 0.019
569
ABT001 Abetalipoproteinemia 63 0.019
570
OST017 Osteomyelitis 63 0.019
571
P ALC004 Alcohol Abuse 63 0.019
572
P KBK002 Kabuki Syndrome 1 63 0.019
573
MNK001 Menkes Disease 63 0.019
574
MTH009 Mouth Disease 63 0.019
575
OST003 Osteonecrosis 63 0.019
576
CHL065 Cholangiocarcinoma 63 0.019
577
PLM033 Pulmonary Embolism 62 0.019
578
RBS001 Rabies 62 0.019
579
RCK004 Rickets 62 0.019
580
ATY005 Atypical Teratoid Rhabdoid Tumor 62 0.019
581
DPH001 Diphtheria 62 0.019
582
c ADL017 Adult T-Cell Leukemia 62 0.019
583
P MCH002 Machado-Joseph Disease 62 0.019
584
c MCP024 Mucopolysaccharidosis Type Vi 62 0.019
585
P HML002 Hemolytic Anemia 62 0.019
586
P BRD002 Bardet-Biedl Syndrome 62 0.019
587
CRD119 Cardiac Arrest 62 0.019
588
INT066 Interstitial Lung Disease 62 0.019
589
P HRM001 Hermansky-Pudlak Syndrome 62 0.019
590
P HYP055 Hypoplastic Left Heart Syndrome 62 0.019
591
LSC001 Lesch-Nyhan Syndrome 62 0.019
592
P RBL001 Rubella 62 0.019
593
SCH014 Schistosomiasis 62 0.019
594
P NRN021 Neuronal Ceroid Lipofuscinosis 61 0.019
595
TRN018 Transitional Cell Carcinoma 61 0.019
596
MTR014 Motor Neuron Disease 61 0.019
597
P TST021 Testicular Germ Cell Tumor 61 0.019
598
P MMP001 Mumps 61 0.019
599
FCT007 Factor Vii Deficiency 61 0.019
600
P HRD008 Hereditary Hemorrhagic Telangiectasia 61 0.019
601
P GRV001 Graves' Disease 61 0.019
602
INT002 Intermittent Claudication 61 0.019
603
LYM021 Lymphadenitis 61 0.019
604
WVR001 Weaver Syndrome 61 0.019
605
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 61 0.019
606
SPP011 Suppression of Tumorigenicity 12 61 0.019
607
CMM005 Common Cold 61 0.019
608
c HPT003 Hepatitis a 61 0.019
609
P ANG001 Angelman Syndrome 61 0.019
610
DRR014 Darier-White Disease 61 0.019
611
DFC004 Deficiency Anemia 61 0.019
612
THY025 Thymus Cancer 60 0.019
613
BLM001 Bloom Syndrome 60 0.019
614
BRN056 Bronchopulmonary Dysplasia 60 0.019
615
FTT001 Fatty Liver Disease 60 0.019
616
GST033 Gestational Diabetes 60 0.019
617
CHL068 Cholestasis 60 0.019
618
P HMP007 Hemophilia 60 0.019
619
c ACT027 Acute Pancreatitis 60 0.019
620
BLD131 Bladder Urothelial Carcinoma 60 0.019
621
VGT001 Vogt-Koyanagi-Harada Disease 60 0.019
622
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 60 0.019
623
P FCS002 Fucosidosis 60 0.019
624
END041 Endometrial Adenocarcinoma 60 0.019
625
c PRM126 Primary Peritoneal Carcinoma 60 0.019
626
KLP010 Klippel-Trenaunay-Weber Syndrome 60 0.019
627
P CND004 Candidiasis 60 0.019
628
GLB015 Glioblastoma Multiforme 60 0.019
629
CHR103 Charge Syndrome 60 0.019
630
P MLG056 Malignant Hyperthermia 59 0.019
631
BLS001 Blau Syndrome 59 0.019
632
P INF032 Infertility 59 0.019
633
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 0.019
634
c ALP101 Alpha-Thalassemia 59 0.019
635
INC021 Incontinentia Pigmenti 59 0.019
636
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 59 0.019
637
BRN002 Bronchiolitis 59 0.019
638
P LPS002 Liposarcoma 59 0.019
639
JNT002 Joint Disorders 59 0.019
640
P NPH012 Nephrotic Syndrome 59 0.019
641
ACT119 Acute Promyelocytic Leukemia 59 0.019
642
SLP005 Sleep Disorder 59 0.019
643
c PRC016 Pre-Eclampsia 59 0.019
644
HRY003 Hairy Cell Leukemia 59 0.019
645
P ANT006 Antiphospholipid Syndrome 59 0.019
646
c NMN013 Niemann-Pick Disease, Type a 59 0.019
647
c ANM038 Anemia, Autoimmune Hemolytic 59 0.019
648
RTN017 Retinal Detachment 58 0.019
649
CRM001 Crimean-Congo Hemorrhagic Fever 58 0.019
650
P PLM034 Pulmonary Emphysema 58 0.019
651
P BRS044 Breast Adenocarcinoma 58 0.019
652
LPD008 Lipid Metabolism Disorder 58 0.019
653
P OCL002 Oculocutaneous Albinism 58 0.019
654
c MSC113 Muscular Dystrophy, Limb-Girdle, Type 2b 58 0.019
655
P HYP083 Hypopituitarism 58 0.019
656
P MSC007 Muscle Hypertrophy 58 0.019
657
MYX005 Myxoid Liposarcoma 58 0.019
658
PRT118 Protoporphyria, Erythropoietic 58 0.019
659
c ACT075 Acute Myocardial Infarction 58 0.019
660
PPL022 Papilloma 58 0.019
661
P ESP035 Esophagitis, Eosinophilic, 1 58 0.019
662
CMP005 Campomelic Dysplasia 57 0.019
663
FBR047 Fibromyalgia 57 0.019
664
NRT004 Neuritis 57 0.019
665
DMY004 Demyelinating Disease 57 0.019
666
ANT009 Antithrombin Iii Deficiency 57 0.019
667
P OST009 Osteochondritis Dissecans 57 0.019
668
FLR002 Filariasis 57 0.019
669
P MNC007 Monocytic Leukemia 57 0.019
670
P HMR012 Hemorrhagic Fever 57 0.019
671
P THR015 Thrombophilia 57 0.019
672
P LCH002 Lichen Planus 57 0.019
673
P PLY006 Polydactyly 57 0.019
674
P MCR010 Microcephaly 57 0.019
675
OPT006 Optic Nerve Disease 57 0.019
676
RSC001 Rosacea 57 0.019
677
P SBS003 Substance Abuse 57 0.019
678
c VSC019 Vesicoureteral Reflux 1 57 0.019
679
WST001 West Syndrome 57 0.019
680
ACR008 Acrocallosal Syndrome 57 0.019
681
c GLC092 Glaucoma, Primary Open Angle 57 0.019
682
P ECL001 Eclampsia 57 0.019
683
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 57 0.019
684
c CNG021 Congenital Toxoplasmosis 57 0.019
685
CRV038 Cervical Squamous Cell Carcinoma 57 0.019
686
ANN002 Anencephaly 56 0.019
687
CLR003 Clear Cell Adenocarcinoma 56 0.019
688
GLC003 Glucose Intolerance 56 0.019
689
P HYP097 Hyperekplexia 56 0.019
690
P PLY041 Polymyositis 56 0.019
691
PRN019 Perinatal Necrotizing Enterocolitis 56 0.019
692
DFF005 Diffuse Large B-Cell Lymphoma 56 0.019
693
PTT009 Pituitary Gland Disease 56 0.019
694
P STC001 Stickler Syndrome 56 0.019
695
HRD029 Hereditary Leiomyomatosis and Renal Cell Cancer 56 0.019
696
BRS099 Breast Ductal Carcinoma 56 0.019
697
CHL014 Cholera 56 0.019
698
CNT105 Central Core Disease of Muscle 56 0.019
699
P PRG013 Paraganglioma 56 0.019
700
CYT008 Cytomegalovirus Infection 56 0.019
701
AND002 Androgen Insensitivity Syndrome 56 0.019
702
ECH003 Echinococcosis 56 0.019
703
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 56 0.019
704
PRR016 Pierre Robin Syndrome 56 0.019
705
TRN015 Transient Cerebral Ischemia 56 0.019
706
ASP002 Aspartylglucosaminuria 56 0.019
707
P HYP014 Hyperuricemia 55 0.019
708
PRM236 Primary Biliary Cholangitis 55 0.019
709
ORL004 Oral Submucous Fibrosis 55 0.019
710
SPT005 Spotted Fever 55 0.019
711
P MLT074 Multiple Endocrine Neoplasia 55 0.019
712
ALV005 Alveolar Soft Part Sarcoma 55 0.019
713
P PMP005 Pemphigus Vulgaris 55 0.019
714
c BRS049 Breast Carcinoma in Situ 55 0.019
715
MYM001 Myoma 55 0.019
716
P DNG005 Dengue Virus 55 0.019
717
c LKM070 Leukemia, Acute Monocytic 55 0.019
718
LPD016 Lipoid Proteinosis of Urbach and Wiethe 55 0.019
719
NPH018 Nephrogenic Systemic Fibrosis 55 0.019
720
CHL061 Childhood Leukemia 55 0.019
721
P CNG001 Congenital Myasthenic Syndrome 55 0.019
722
HPT022 Hepatoblastoma 55 0.019
723
AMN001 Amenorrhea 55 0.019
724
IGG001 Iga Glomerulonephritis 55 0.019
725
c CWD006 Cowden Syndrome 1 55 0.019
726
P MGL013 Megalencephaly 54 0.019
727
P ATS308 Autosomal Dominant Cerebellar Ataxia 54 0.019
728
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 54 0.019
729
HST011 Histoplasmosis 54 0.019
730
CYS010 Cystinosis 54 0.019
731
P MSC003 Muscular Atrophy 54 0.019
732
STR008 Strongyloidiasis 54 0.019
733
P HYP818 Hypobetalipoproteinemia, Familial, 1 54 0.019
734
MTC027 Mitochondrial Trifunctional Protein Deficiency 54 0.019
735
TCK001 Tick-Borne Encephalitis 54 0.019
736
CHR288 Chronic Recurrent Multifocal Osteomyelitis 54 0.019
737
P CRY007 Cryoglobulinemia, Familial Mixed 54 0.019
738
APP015 Apparent Mineralocorticoid Excess 54 0.019
739
P MTC133 Mitochondrial Myopathy 54 0.019
740
CLF001 Cleft Lip 54 0.019
741
P PMP001 Pemphigus 54 0.019
742
P DBT005 Diabetes Insipidus 54 0.019
743
ALS001 Alstrom Syndrome 54 0.019
744
SRS001 Serous Cystadenocarcinoma 54 0.019
745
SCH012 Schizoaffective Disorder 54 0.019
746
MTN003 Motion Sickness 54 0.019
747
PPL025 Popliteal Pterygium Syndrome 54 0.019
748
P ATR010 Atrial Heart Septal Defect 54 0.019
749
ENT011 Enterocolitis 54 0.019
750
RDC002 Radiculopathy 53 0.019
751
P PRM006 Primary Biliary Cirrhosis 53 0.019
752
CTS003 Coats Disease 53 0.019
753
P JRV004 Jervell and Lange-Nielsen Syndrome 1 53 0.019
754
MCR004 Macroglobulinemia 53 0.019
755
P SCL009 Sclerosing Cholangitis 53 0.019
756
PLY131 Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes 53 0.019
757
c HPT007 Hepatitis E 53 0.019
758
c SVR005 Severe Pre-Eclampsia 53 0.019
759
OPT009 Optic Neuritis 53 0.019
760
c ICH047 Ichthyosis, Congenital, Autosomal Recessive 1 53 0.019
761
OLG003 Oligohydramnios 53 0.019
762
P HMN036 Hemangiopericytoma, Malignant 53 0.019
763
FML037 Female Breast Cancer 53 0.019
764
CLL003 Cellulitis 53 0.019
765
P PTS002 Ptosis 53 0.019
766
P BRN009 Burning Mouth Syndrome 53 0.019
767
PLS025 Plasmablastic Lymphoma 53 0.019
768
PLY023 Polycystic Liver Disease 53 0.019
769
HPT082 Hepatic Adenomas, Familial 53 0.019
770
KRT009 Keratosis 53 0.019
771
HYD046 Hydatidiform Mole, Recurrent, 1 52 0.019
772
GTR002 Goiter 52 0.019
773
TMP001 Temporal Lobe Epilepsy 52 0.019
774
P FNC004 Fanconi Syndrome 52 0.019
775
RSD004 Rosai-Dorfman Disease 52 0.019
776
P TRN034 Transverse Myelitis 52 0.019
777
c CNG415 Congenital Disorder of Glycosylation, Type Ia 52 0.019
778
MCN001 Mucinous Adenocarcinoma 52 0.019
779
YLL001 Yellow Nail Syndrome 52 0.019
780
HLL004 Hellp Syndrome 52 0.019
781
INT079 Intrahepatic Cholangiocarcinoma 52 0.019
782
PHL006 Phelan-Mcdermid Syndrome 52 0.019
783
P GLM040 Glioma Susceptibility 1 52 0.019
784
SCH068 Schwartz-Jampel Syndrome, Type 1 52 0.019
785
LPR001 Lepromatous Leprosy 52 0.019
786
P CTN003 Cutaneous Lupus Erythematosus 52 0.019
787
ATR057 Atrioventricular Block 52 0.019
788
CRT033 Corticobasal Degeneration 52 0.019
789
P CHL066 Cholangitis 52 0.019
790
c OPT053 Optic Atrophy 1 52 0.019
791
CGN006 Cogan Syndrome 52 0.019
792
DRY001 Dry Eye Syndrome 51 0.019
793
CHR005 Chorioamnionitis 51 0.019
794
CHR001 Churg-Strauss Syndrome 51 0.019
795
P SHR029 Short Syndrome 51 0.019
796
GRW007 Growth Hormone Deficiency 51 0.019
797
MYL001 Myelitis 51 0.019
798
PRN014 Paronychia 51 0.019
799
TRS021 Triosephosphate Isomerase Deficiency 51 0.019
800
c SPS222 Spastic Paraplegia 20, Autosomal Recessive 51 0.019
801
MYL003 Myeloid Sarcoma 51 0.019
802
HYD012 Hydrops Fetalis 51 0.019
803
P OMP004 Omphalocele 51 0.019
804
46X052 46,xx Sex Reversal 1 51 0.019
805
P EST001 Estrogen-Receptor Positive Breast Cancer 51 0.019
806
SPL004 Splenic Marginal Zone Lymphoma 51 0.019
807
ACH005 Achalasia 51 0.019
808
c CRD183 Ceroid Lipofuscinosis, Neuronal, 2 51 0.019
809
P MYM013 Moyamoya Disease 1 51 0.019
810
ECT026 Ectopic Pregnancy 51 0.019
811
P OPN001 Open-Angle Glaucoma 51 0.019
812
P PLY017 Polyarteritis Nodosa 51 0.019
813
LYM008 Lymphangiosarcoma 51 0.019
814
DRG003 Drug Dependence 51 0.019
815
P HMR005 Hemorrhoid 51 0.019
816
P LCT001 Lactic Acidosis 50 0.019
817
SCB001 Scabies 50 0.019
818
c THY112 Thyroid Hormone Resistance, Generalized, Autosomal Dominant 50 0.019
819
P BRC006 Brachydactyly 50 0.019
820
PSD012 Pseudoachondroplasia 50 0.019
821
PRR007 Perry Syndrome 50 0.019
822
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 50 0.019
823
P LPM005 Lipomatosis 50 0.019
824
INT303 Intracranial Hypertension, Idiopathic 50 0.019
825
URC002 Urea Cycle Disorder 50 0.019
826
P GND004 Gonadal Dysgenesis 50 0.019
827
CRB151 Cerebral Creatine Deficiency Syndrome 1 50 0.019
828
P TCL004 T-Cell Leukemia 50 0.019
829
EPD001 Epidermodysplasia Verruciformis 50 0.019
830
SCN001 Secondary Hyperparathyroidism of Renal Origin 50 0.019
831
STS002 Situs Inversus 50 0.019
832
P OLV001 Olivopontocerebellar Atrophy 50 0.019
833
ORL005 Oral Candidiasis 50 0.019
834
c ATM024 Autoimmune Pancreatitis 50 0.019
835
c ANT034 Anterior Uveitis 50 0.019
836
LYM012 Lymphoplasmacytic Lymphoma 50 0.019
837
LGS001 Legius Syndrome 50 0.019
838
P SCL015 Scleritis 50 0.019
839
NDL021 Nodular Lymphocyte Predominant Hodgkin Lymphoma 50 0.019
840
HYP006 Hypertensive Heart Disease 50 0.019
841
P PTY003 Pityriasis Rubra Pilaris 50 0.019
842
PLN006 Poland Syndrome 50 0.019
843
JCB001 Jacobsen Syndrome 50 0.019
844
c PRD039 Periodontitis, Aggressive, 1 50 0.019
845
INT051 Intussusception 49 0.019
846
CYC008 Cyclic Vomiting Syndrome 49 0.019
847
c PRM108 Primary Progressive Multiple Sclerosis 49 0.019
848
TTR011 Tetraploidy 49 0.019
849
MLT075 Multifocal Motor Neuropathy 49 0.019
850
RTC005 Reticulosarcoma 49 0.019
851
NM001 Noma 49 0.019
852
ORT008 Orotic Aciduria 49 0.019
853
P PLM006 Pulmonary Alveolar Proteinosis 49 0.019
854
HND002 Hand, Foot and Mouth Disease 49 0.019
855
P PRN026 Porencephaly 49 0.019
856
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 49 0.019
857
ANX004 Anoxia 49 0.019
858
KLD001 Keloids 49 0.019
859
P WLL002 Weill-Marchesani Syndrome 49 0.019
860
HMP009 Haemophilus Influenzae 49 0.019
861
PRT011 Protein C Deficiency 49 0.019
862
NLX004 Neu-Laxova Syndrome 1 49 0.019
863
BLL003 Bell's Palsy 49 0.019
864
P BRN120 Bronchus Cancer 49 0.019
865
PPL018 Papillary Adenocarcinoma 49 0.019
866
CRY004 Cryoglobulinemia 49 0.019
867
P ATR005 Atrophic Gastritis 48 0.019
868
OVR012 Ovarian Serous Cystadenocarcinoma 48 0.019
869
PRN009 Paranoid Schizophrenia 48 0.019
870
YNS002 Yunis-Varon Syndrome 48 0.019
871
JCK001 Jackson-Weiss Syndrome 48 0.019
872
HYP085 Hypothalamic Disease 48 0.019
873
SRS007 Sorsby Fundus Dystrophy 48 0.019
874
P ALT001 Alternating Hemiplegia of Childhood 48 0.019
875
GLC009 Glucosephosphate Dehydrogenase Deficiency 48 0.019
876
c MLG069 Malignant Hypertension 48 0.019
877
NWC001 Newcastle Disease 48 0.019
878
PRS129 Prostatic Hyperplasia, Benign 48 0.019
879
c THR045 Thrombotic Thrombocytopenic Purpura, Congenital 48 0.019
880
IDP035 Idiopathic Achalasia 48 0.019
881
SKN027 Skin Conditions 48 0.019
882
c OST124 Osteogenesis Imperfecta, Type V 47 0.019
883
GLD006 Goldberg-Shprintzen Syndrome 47 0.019
884
BCT004 Bacteriuria 47 0.019
885
P PLG001 Pelger-Huet Anomaly 47 0.019
886
ART031 Aortic Coarctation 47 0.019
887
P EPT012 Epithelioid Sarcoma 47 0.019
888
HRT031 Hartnup Disorder 47 0.019
889
CWP001 Cowpox 47 0.019
890
P MNN019 Mannosidosis, Beta a, Lysosomal 47 0.019
891
NXS001 Naxos Disease 47 0.019
892
P VGN017 Vaginal Cancer 47 0.019
893
c ACT078 Acute Porphyria 47 0.019
894
PLM041 Pulmonary Valve Stenosis 47 0.019
895
ESN020 Eosinophilic Granulomatosis with Polyangiitis 47 0.019
896
PLY012 Polyhydramnios 47 0.019
897
FCL022 Focal Dystonia 47 0.019
898
OPP004 Oppositional Defiant Disorder 47 0.019
899
ANG011 Angiodysplasia 47 0.019
900
CRB085 Cerebral Hemorrhage 47 0.019
901
c CNG124 Congenital Rubella 47 0.019
902
PRT014 Protein S Deficiency 47 0.019
903
P CRN052 Craniometaphyseal Dysplasia, Autosomal Dominant 47 0.019
904
c OPT051 Opitz Gbbb Syndrome, Type I 47 0.019
905
VTM002 Vitamin B12 Deficiency 47 0.019
906
SPN035 Spindle Cell Sarcoma 47 0.019
907
ADN010 Adenosquamous Cell Lung Carcinoma 46 0.019
908
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 46 0.019
909
GYN001 Gynecomastia 46 0.019
910
TND004 Tendinopathy 46 0.019
911
MGR001 Migraine Without Aura 46 0.019
912
P CLS010 Cluster Headache 46 0.019
913
P NRP053 Neuropathy, Hereditary Sensory and Autonomic, Type Iia 46 0.019
914
c SPR009 Sporadic Breast Cancer 46 0.019
915
ALP093 Alpha-Thalassemia/mental Retardation Syndrome, Chromosome 16-Related 46 0.019
916
DYS073 Dysphagia 46 0.019
917
SMN007 Seminoma 46 0.019
918
CYS008 Cystic Echinococcosis 46 0.019
919
RFT001 Rift Valley Fever 46 0.019
920
MCL075 Macular Dystrophy, Corneal 46 0.019
921
FML026 Familial Lipoprotein Lipase Deficiency 46 0.019
922
ALB002 Albinism 46 0.019
923
P SCL048 Sclerosteosis 46 0.019
924
MLB001 Mulibrey Nanism 46 0.019
925
SYS003 Systolic Heart Failure 46 0.019
926
SPL018 Splenomegaly 46 0.019
927
MCR037 Macroglossia 46 0.019
928
NNS002 Nonspecific Interstitial Pneumonia 46 0.019
929
CLB002 Clubfoot 46 0.019
930
P ENC008 Encephalocele 46 0.019
931
DST006 Diastolic Heart Failure 46 0.019
932
EXS017 Exstrophy of Bladder 46 0.019
933
TBR008 Tuberculous Peritonitis 46 0.019
934
BRN015 Bronchiolo-Alveolar Adenocarcinoma 45 0.019
935
FCT005 Factor Xiii Deficiency 45 0.019
936
WRN003 Wernicke Encephalopathy 45 0.019
937
c BRD012 Bardet-Biedl Syndrome 11 45 0.019
938
MTR010 Mature Teratoma 45 0.019
939
HST006 Histidinemia 45 0.019
940
MDL009 Medullary Sponge Kidney 45 0.019
941
OPT054 Opitz-Kaveggia Syndrome 45 0.019
942
MTR003 Mitral Valve Stenosis 45 0.019
943
c SPL024 Split-Hand/foot Malformation 3 45 0.019
944
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 45 0.019
945
STT002 Status Asthmaticus 45 0.019
946
P LNG035 Lung Large Cell Carcinoma 45 0.019
947
DNB001 Danubian Endemic Familial Nephropathy 45 0.019
948
ENC055 Encephalopathy, Ethylmalonic 45 0.019
949
CRY014 Cryptococcal Meningitis 45 0.019
950
P PRM018 Primary Hypertrophic Osteoarthropathy 45 0.019
951
CNT025 Central Pontine Myelinolysis 45 0.019
952
c ICH069 Ichthyosis, Congenital, Autosomal Recessive 4b 45 0.019
953
ORL015 Oral Squamous Cell Carcinoma 45 0.019
954
AZS001 Azoospermia 45 0.019
955
EXS001 Exostosis 45 0.019
956
GND001 Gonadoblastoma 45 0.019
957
LCR004 La Crosse Encephalitis 45 0.019
958
RNS001 Raine Syndrome 45 0.019
959
MCR165 Microphthalmia with Limb Anomalies 45 0.019
960
DCB001 Decubitus Ulcer 45 0.019
961
MYC013 Mycobacterium Abscessus 45 0.019
962
VTR016 Vater/vacterl Association 45 0.019
963
HRT012 Heart Valve Disease 44 0.019
964
GST010 Gestational Trophoblastic Neoplasm 44 0.019
965
GLM008 Glomus Tumor 44 0.019
966
GST030 Gastrinoma 44 0.019
967
VLV042 Vulvar Vestibulitis Syndrome 44 0.019
968
MCL003 Macular Holes 44 0.019
969
LNR006 Linear Iga Disease 44 0.019
970
FLL013 Follicular Dendritic Cell Sarcoma 44 0.019
971
c 46X001 46 Xy Gonadal Dysgenesis 44 0.019
972
IMM011 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 44 0.019
973
BCK006 Back Pain 44 0.019
974
BRN045 Brunner Syndrome 44 0.019
975
TLR001 Tularemia 44 0.019
976
c ART144 Arthrogryposis, Distal, Type 1a 44 0.019
977
FLT006 Floating-Harbor Syndrome 44 0.019
978
BLS002 Blastomycosis 44 0.019
979
LSS003 Lassa Fever 44 0.019
980
CRY001 Cryptogenic Organizing Pneumonia 44 0.019
981
c RBN009 Robinow Syndrome, Autosomal Recessive 44 0.019
982
PRS042 Prostate Disease 44 0.019
983
P SLL003 Salla Disease 44 0.019
984
c EST002 Estrogen-Receptor Negative Breast Cancer 44 0.019
985
c MCP047 Mucopolysaccharidosis, Type Iva 44 0.019
986
P PRL003 Proliferative Glomerulonephritis 44 0.019
987
SPR008 Supratentorial Primitive Neuroectodermal Tumor 44 0.019
988
P OVR106 Ovarian Clear Cell Carcinoma 44 0.019
989
EPD029 Epidermolysis Bullosa Simplex, Generalized 44 0.019
990
MLT152 Multiple Self-Healing Squamous Epithelioma 43 0.019
991
DNR002 Duane-Radial Ray Syndrome 43 0.019
992
c SPN297 Spondylocostal Dysostosis 3, Autosomal Recessive 43 0.019
993
KRT008 Keratopathy 43 0.019
994
CHR276 Chronic Active Epstein-Barr Virus Infection 43 0.019
995
c LSS005 Lissencephaly 1 43 0.019
996
c ACQ042 Acquired Hemophilia a 43 0.019
997
DBW001 Dubowitz Syndrome 43 0.019
998
c SPN305 Spinocerebellar Ataxia 11 43 0.019
999
CYS009 Cystadenoma 43 0.019
1000
IGG007 Igg4-Related Disease 43 0.019
1001
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 43 0.019
1002
P AMY084 Amyloidosis, Finnish Type 43 0.019
1003
c XNT010 Xanthinuria, Type I 43 0.019
1004
ADN020 Adenosarcoma 43 0.019
1005
CHR211 Chromosome 18p Deletion Syndrome 43 0.019
1006
BLP005 Blepharitis 43 0.019
1007
HPT067 Hepatocellular Adenoma 43 0.019
1008
c PRK082 Porokeratosis 1, Multiple Types 43 0.019
1009
MYC017 Mycobacterium Kansasii 43 0.019
1010
CLL021 Collagenous Colitis 43 0.019
1011
CHL010 Childhood Kidney Cell Carcinoma 43 0.019
1012
MRP001 Morphine Dependence 43 0.019
1013
MTS001 Mutism 42 0.019
1014
CNV002 Conversion Disorder 42 0.019
1015
c HYP543 Hypoplastic Left Heart Syndrome 1 42 0.019
1016
c ICH049 Ichthyosis, Congenital, Autosomal Recessive 2 42 0.019
1017
PLS016 Plasma Cell Leukemia 42 0.019
1018
CLN044 Colon Adenoma 42 0.019
1019
RTR011 Retroperitoneal Fibrosis 42 0.019
1020
c CHR350 Charcot-Marie-Tooth Disease, Axonal, Type 2k 42 0.019
1021
PST011 Pustulosis of Palm and Sole 42 0.019
1022
RMS001 Rem Sleep Behavior Disorder 42 0.019
1023
OCL025 Ocular Toxoplasmosis 42 0.019
1024
TTL012 Total Anomalous Pulmonary Venous Return 1 42 0.019
1025
SPN369 Spinal Disease 42 0.019
1026
EPC002 Epicondylitis 42 0.019
1027
DYS009 Dysthymic Disorder 41 0.019
1028
EST003 Eastern Equine Encephalitis 41 0.019
1029
INT221 Intravascular Large B-Cell Lymphoma 41 0.019
1030
BBN001 Bubonic Plague 41 0.019
1031
EGG001 Egg Allergy 41 0.019
1032
CMM003 Common Wart 41 0.019
1033
MCN008 Mucinous Cystadenocarcinoma 41 0.019
1034
ALC010 Alcoholic Cardiomyopathy 41 0.019
1035
PLR006 Pleural Cancer 41 0.019
1036
BRB001 Beriberi 41 0.019
1037
c LKM056 Leukemia, Chronic Lymphocytic 2 41 0.019
1038
c OPT050 Opitz Gbbb Syndrome, Type Ii 41 0.019
1039
GNT031 Genitopatellar Syndrome 41 0.019
1040
ADN002 Adenoiditis 41 0.019
1041
c CTR130 Cataract 9, Multiple Types 41 0.019
1042
c ALB009 Albinism, Oculocutaneous, Type Ia 41 0.019
1043
PST086 Posterior Cortical Atrophy 41 0.019
1044
CRD003 Cardiac Sarcoidosis 41 0.019
1045
RTR001 Retrograde Amnesia 40 0.019
1046
MDS022 Mediastinitis 40 0.019
1047
TRN044 Transposition of the Great Arteries 40 0.019
1048
ATX029 Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia 40 0.019
1049
SLL001 Sialolithiasis 40 0.019
1050
URT004 Urethral Syndrome 40 0.019
1051
P CRN035 Cranial Nerve Palsy 40 0.019
1052
P CYS017 Cystic Teratoma 40 0.019
1053
c ACT004 Acute Diarrhea 40 0.019
1054
c MGL009 Megalencephalic Leukoencephalopathy with Subcortical Cysts 1 40 0.019
1055
EPS026 Epispadias 40 0.019
1056
c NLD009 Nail Disorder, Nonsyndromic Congenital, 1 40 0.019
1057
P PRG002 Progesterone-Receptor Positive Breast Cancer 40 0.019
1058
HRL004 Hurler-Scheie Syndrome 40 0.019
1059
P ENC011 Encephalomyopathy 40 0.019
1060
NTV001 Native American Myopathy 40 0.019
1061
PRG017 Paraganglioma and Gastric Stromal Sarcoma 40 0.019
1062
PMP002 Pemphigoid Gestationis 40 0.019
1063
P DYS005 Dyslexia 39 0.019
1064
C1Q001 C1q Deficiency 39 0.019
1065
TNC003 Tinea Corporis 39 0.019
1066
MHR001 Mohr-Tranebjaerg Syndrome 39 0.019
1067
P KLN006 Koolen-De Vries Syndrome 39 0.019
1068
MYS001 Myositis Ossificans 39 0.019
1069
RPD002 Rapadilino Syndrome 39 0.019
1070
c FRN036 Frontonasal Dysplasia 1 39 0.019
1071
PDT025 Pediatric Multiple Sclerosis 39 0.019
1072
FMR003 Femoral Neuropathy 39 0.019
1073
GST052 Gestational Choriocarcinoma 39 0.019
1074
STC004 Stachybotrys Chartarum 39 0.019
1075
BLR027 Blue Rubber Bleb Nevus 39 0.019
1076
PRK003 Parkes Weber Syndrome 39 0.019
1077
END028 Endemic Goiter 39 0.019
1078
P UVS001 Uv-Sensitive Syndrome 39 0.019
1079
ACL001 Acalculous Cholecystitis 38 0.019
1080
BRN018 Borna Disease 38 0.019
1081
CHR492 Chromosome 13q14 Deletion Syndrome 38 0.019
1082
PGT003 Paget Disease, Extramammary 38 0.019
1083
MXL016 Maxillonasal Dysplasia, Binder Type 38 0.019
1084
IDM001 Ideomotor Apraxia 38 0.019
1085
LYM042 Lymphocytic Colitis 38 0.019
1086
P MXL015 Maxillary Sinusitis 38 0.019
1087
c MCL060 Macular Dystrophy, Vitelliform, 3 38 0.019
1088
P GLM006 Glomangioma 38 0.019
1089
NCR002 Necrobiosis Lipoidica 38 0.019
1090
CHR079 Choroid Disease 38 0.019
1091
PLM175 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 38 0.019
1092
MSN002 Mesenteric Lymphadenitis 38 0.019
1093
c CTR115 Cataract 16, Multiple Types 38 0.019
1094
c ACT059 Acute Maxillary Sinusitis 38 0.019
1095
OBS004 Obstructive Hydrocephalus 38 0.019
1096
ORC001 Orchitis 37 0.019
1097
FLR001 Filarial Elephantiasis 37 0.019
1098
ECT004 Ecthyma 37 0.019
1099
c PRG003 Progesterone-Receptor Negative Breast Cancer 37 0.019
1100
BTN004 Biotin Deficiency 37 0.019
1101
CHL012 Childhood Disintegrative Disease 37 0.019
1102
GST020 Gastric Antral Vascular Ectasia 37 0.019
1103
LPB001 Lipoblastoma 37 0.019
1104
KKC001 Kikuchi Disease 37 0.019
1105
GLT018 Glut1 Deficiency Syndrome 1 37 0.019
1106
CND006 Candida Glabrata 37 0.019
1107
c RNG008 Ring Chromosome 13 37 0.019
1108
MNT309 Mental Retardation-Hypotonic Facies Syndrome, X-Linked, 1 37 0.019
1109
ATM021 Autoimmune Inner Ear Disease 37 0.019
1110
HYD059 Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect 37 0.019
1111
47X003 47, Xxy 37 0.019
1112
c SBC035 Subacute Cutaneous Lupus Erythematosus 37 0.019
1113
c CTR118 Cataract 14, Multiple Types 37 0.019
1114
LVD002 Livedoid Vasculopathy 37 0.019
1115
EPL131 Epilepsy, Pyridoxine-Dependent 37 0.019
1116
CWC001 Cowchock Syndrome 37 0.019
1117
c PLM150 Pulmonary Alveolar Proteinosis, Acquired 36 0.019
1118
ANS012 Anus Disease 36 0.019
1119
c MJR008 Major Affective Disorder 2 36 0.019
1120
c HYP768 Hyperlipoproteinemia, Type I 36 0.019
1121
HMR023 Hemorrhagic Cystitis 36 0.019
1122
c CNG189 Congenital Disorder of Glycosylation, Type Ib 36 0.019
1123
CYL001 Cayler Cardiofacial Syndrome 36 0.019
1124
EMN001 Emanuel Syndrome 36 0.019
1125
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 36 0.019
1126
c HYP331 Hyperphenylalaninemia, Bh4-Deficient, a 36 0.019