Search results for "WAS"

978 hits were found for 'WAS'

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