Search results for "WAS"

874 hits were found for 'WAS'

# Family MCID Name MIFTS Score
1
P WSK001 Wiskott-Aldrich Syndrome 69 23.245
2
WSR001 Was-Related Disorders 4 15.233
3
THR042 Thrombocytopenia, X-Linked 32 12.271
4
P THR014 Thrombocytopenia 56 5.288
5
NTR036 Neutropenia, Severe Congenital, X-Linked 23 5.262
6
P NTR004 Neutropenia 56 4.278
7
P THR005 Thrombotic Thrombocytopenic Purpura 53 3.050
8
c SVR003 Severe Congenital Neutropenia 44 3.025
9
INT051 Intussusception 53 3.009
10
PRM097 Primary Immunodeficiency Disease 36 3.009
11
c HRD112 Hereditary Thrombocytopenia with Normal Platelets 12 2.256
12
c HYP163 Hyperlipidemia Type 3 23 0.216
13
P HPT021 Hepatitis 55 0.102
14
P LKM002 Leukemia 66 0.099
15
P ADN016 Adenocarcinoma 49 0.085
16
P ESP024 Esophagitis 54 0.078
17
P ART022 Arthritis 65 0.074
18
P BRS047 Breast Cancer 90 0.070
19
P PNC044 Pancreatitis 59 0.070
20
P CLR023 Colorectal Cancer 96 0.065
21
PRS047 Prostatitis 51 0.065
22
P LNG032 Lung Cancer 94 0.060
23
P AST005 Asthma 84 0.060
24
ESP021 Esophageal Cancer 67 0.060
25
P PNM007 Pneumonia 64 0.060
26
SML019 Smallpox 36 0.060
27
HPT023 Hepatocellular Carcinoma 95 0.055
28
c SYS001 Systemic Lupus Erythematosus 91 0.055
29
P SCH015 Schizophrenia 79 0.055
30
P LPS004 Lupus Erythematosus 67 0.055
31
SRC014 Sarcoma 61 0.055
32
P INF038 Influenza 67 0.055
33
ADN018 Adenoma 55 0.055
34
CLT003 Colitis 54 0.055
35
P CRV039 Cervicitis 49 0.055
36
END072 Endotheliitis 44 0.055
37
WST005 West Nile Virus 40 0.055
38
NRN002 Neuronitis 36 0.055
39
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 30 0.055
40
P OBS005 Obesity 94 0.049
41
P RHM011 Rheumatoid Arthritis 94 0.049
42
ACR007 Acromegaly 69 0.049
43
P MYL006 Myeloid Leukemia 64 0.049
44
P MYS005 Myositis 63 0.049
45
PRT036 Peritonitis 61 0.049
46
P HMN010 Hemangioma 60 0.049
47
c HPT001 Hepatitis C 57 0.049
48
ULC004 Ulcerative Colitis 63 0.049
49
P LRY019 Laryngitis 56 0.049
50
MLN008 Melanoma 55 0.049
51
P SCK002 Sick Sinus Syndrome 50 0.049
52
HDC001 Headache 50 0.049
53
CRT002 Cartilage-Hair Hypoplasia 45 0.049
54
KR002 Kuru 42 0.049
55
CHN016 Cohen Syndrome 40 0.049
56
HMP009 Haemophilus Influenzae 36 0.049
57
VRL002 Variola Minor 20 0.049
58
VRL003 Variola Major 15 0.049
59
P PRS040 Prostate Cancer 84 0.043
60
P MYC007 Myocardial Infarction 81 0.043
61
P PHC003 Pheochromocytoma 79 0.043
62
HV1006 Hiv-1 83 0.043
63
P RTN024 Retinoblastoma 75 0.043
64
P DRV001 Dravet Syndrome 64 0.043
65
c HPT016 Hepatitis B 60 0.043
66
P CHR071 Charcot-Marie-Tooth Disease 60 0.043
67
P GLM007 Glomerulonephritis 59 0.043
68
ACN011 Acne 58 0.043
69
DMN002 Dementia 58 0.043
70
P MNN013 Meningitis 58 0.043
71
P HYP069 Hyperparathyroidism 57 0.043
72
PHR003 Pharyngitis 56 0.043
73
P HYD006 Hydrocephalus 56 0.043
74
P GT001 Gout 56 0.043
75
P PSR002 Psoriasis 54 0.043
76
PRP030 Purpura 54 0.043
77
PRT037 Pertussis 54 0.043
78
ADL030 Adult-Onset Still's Disease 54 0.043
79
ISC004 Ischemia 53 0.043
80
P NRP001 Neuropathy 52 0.043
81
MBS002 Moebius Syndrome 51 0.043
82
VGN023 Vaginitis 51 0.043
83
SYN007 Synovitis 51 0.043
84
c SVR001 Severe Acute Respiratory Syndrome 50 0.043
85
P ATX004 Ataxia 50 0.043
86
P TRT010 Teratoma 50 0.043
87
CVR006 Cavernous Hemangioma 50 0.043
88
c SPN294 Spinocerebellar Ataxia 1 47 0.043
89
IMP005 Impotence 45 0.043
90
GST045 Gastroenteritis 45 0.043
91
MYC021 Mycobacterium Xenopi 45 0.043
92
HYP068 Hyperostosis 43 0.043
93
AML029 Ameloblastoma 42 0.043
94
P CNG018 Congenital Heart Block 42 0.043
95
ASP007 Aspiration Pneumonia 41 0.043
96
RLP002 Relapsing-Remitting Multiple Sclerosis 39 0.043
97
c MCL062 Mucolipidosis Ii Alpha/beta 39 0.043
98
HMT018 Hematopoietic Stem Cell Transplantation 36 0.043
99
MNK002 Monkeypox 35 0.043
100
NNT008 Neonatal Abstinence Syndrome 35 0.043
101
OCH001 Ochronosis 32 0.043
102
c MCL046 Mucolipidosis Iii Alpha/beta 31 0.043
103
SPR006 Sparganosis 29 0.043
104
SPN151 Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy 23 0.043
105
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 23 0.043
106
RMB001 Rombo Syndrome 19 0.043
107
LNR007 Linear and Whorled Nevoid Hypermelanosis 16 0.043
108
MTG001 Metagonimiasis 15 0.043
109
RJS001 Ruijs-Aalfs Syndrome 9 0.043
110
P PNC035 Pancreatic Cancer 82 0.035
111
P DLT002 Dilated Cardiomyopathy 77 0.035
112
P CSH001 Cushing's Syndrome 76 0.035
113
MLR004 Malaria 81 0.035
114
GST019 Gastrointestinal Stromal Tumor 74 0.035
115
SMT004 Smith-Lemli-Opitz Syndrome 74 0.035
116
CDS001 Cadasil 73 0.035
117
TBR010 Tuberculosis 73 0.035
118
P CRN211 Coronary Artery Disease 73 0.035
119
DCH001 Duchenne Muscular Dystrophy 78 0.035
120
CNG034 Congestive Heart Failure 69 0.035
121
c FNC027 Fanconi Anemia, Complementation Group a 68 0.035
122
P MYL005 Myelofibrosis 68 0.035
123
CRB011 Cerebrotendinous Xanthomatosis 66 0.035
124
CRH001 Crohn's Disease 71 0.035
125
SKN016 Skin Disease 64 0.035
126
c MCP003 Mucopolysaccharidosis Vii 64 0.035
127
CCC001 Coccidioidomycosis 63 0.035
128
P RSP003 Respiratory Failure 62 0.035
129
P HYP117 Hypertriglyceridemia 61 0.035
130
ANR002 Aniridia 61 0.035
131
P HYP086 Hypothyroidism 59 0.035
132
P PLY011 Polycystic Ovary Syndrome 59 0.035
133
c PRM005 Primary Hyperparathyroidism 58 0.035
134
MSL001 Measles 58 0.035
135
P HYP004 Hypercalcemia 57 0.035
136
ACT049 Acute Disseminated Encephalomyelitis 57 0.035
137
P PRP029 Porphyria 57 0.035
138
P UVT001 Uveitis 57 0.035
139
ALK013 Alkaptonuria 57 0.035
140
VSC011 Vasculitis 57 0.035
141
P GST044 Gastritis 56 0.035
142
P PRM006 Primary Biliary Cirrhosis 56 0.035
143
P THY032 Thyroiditis 56 0.035
144
LYM017 Lyme Disease 56 0.035
145
BTN003 Biotinidase Deficiency 56 0.035
146
MXD005 Mixed Connective Tissue Disease 56 0.035
147
P LYM026 Lymphoblastic Leukemia 55 0.035
148
RHM001 Rheumatic Fever 55 0.035
149
ART111 Artery Disease 55 0.035
150
P FTL001 Fetal Alcohol Syndrome 54 0.035
151
P MYL007 Myeloma 53 0.035
152
P RBL001 Rubella 53 0.035
153
HYP056 Hypoglycemia 53 0.035
154
P EPD003 Epidermolysis Bullosa Simplex 53 0.035
155
c PNC108 Pancreatitis, Hereditary 54 0.035
156
P MYP004 Myopathy 53 0.035
157
DSS009 Disseminated Intravascular Coagulation 52 0.035
158
SPH001 Sapho Syndrome 52 0.035
159
c HPT073 Hepatitis C Virus 51 0.035
160
P ANG015 Angioedema 51 0.035
161
P RBN002 Robinow Syndrome 51 0.035
162
CHR074 Choriocarcinoma 50 0.035
163
P MST018 Mesothelioma 51 0.035
164
CRN017 Coronary Thrombosis 50 0.035
165
P SLP006 Sleep Apnea 50 0.035
166
P PRS038 Personality Disorder 50 0.035
167
EPD016 Epidermolysis Bullosa 49 0.035
168
ANG020 Angiosarcoma 49 0.035
169
PRC012 Pericardial Effusion 49 0.035
170
P QFV001 Q Fever 49 0.035
171
FLT006 Floating-Harbor Syndrome 49 0.035
172
P SNS014 Sinusitis 56 0.035
173
VSC002 Vascular Dementia 48 0.035
174
URT001 Urethritis 48 0.035
175
NCR004 Nocardiosis 47 0.035
176
PLG002 Plague 47 0.035
177
FSH001 Fish-Eye Disease 47 0.035
178
P BLN003 Blindness 47 0.035
179
P BCL006 B-Cell Lymphomas 47 0.035
180
DPH001 Diphtheria 47 0.035
181
TTH006 Tooth Disease 46 0.035
182
P PRT029 Parathyroid Adenoma 46 0.035
183
END031 Endometrial Stromal Sarcoma 46 0.035
184
P KRN004 Kernicterus 46 0.035
185
PRC013 Pericarditis 45 0.035
186
BRL010 Buruli Ulcer 46 0.035
187
PRG009 Progressive Multifocal Leukoencephalopathy 45 0.035
188
RTN023 Retinitis 44 0.035
189
BRS064 Bursitis 44 0.035
190
AVN001 Avian Influenza 43 0.035
191
INT075 Intracranial Hypertension 43 0.035
192
OBS001 Obstructive Jaundice 42 0.035
193
P CST002 Castleman's Disease 42 0.035
194
LMB024 Limbic Encephalitis 42 0.035
195
MMB001 Membranoproliferative Glomerulonephritis 42 0.035
196
HDN002 Head Injury 41 0.035
197
PLM010 Pulmonary Edema 41 0.035
198
CHY006 Chylous Ascites 40 0.035
199
P CLR108 Colorectal Adenoma 49 0.035
200
P HYP614 Hyperlipidemia, Familial Combined 41 0.035
201
CRT013 Carotid Stenosis 39 0.035
202
PRV004 Periventricular Leukomalacia 39 0.035
203
CHL039 Choledocholithiasis 39 0.035
204
CTS011 Cutis Marmorata Telangiectatica Congenita 39 0.035
205
VLV010 Vulvovaginitis 38 0.035
206
MTB004 Metabolic Acidosis 38 0.035
207
P CLR017 Clear Cell Sarcoma 37 0.035
208
SCR011 Scrapie 37 0.035
209
KSH001 Keshan Disease 36 0.035
210
DNN002 Donnai-Barrow Syndrome 36 0.035
211
ANR040 Aneurysm 35 0.035
212
FCL012 Facial Paralysis 35 0.035
213
OST097 Osteoporotic Fracture 34 0.035
214
ELP001 Elephantiasis 34 0.035
215
SPR066 Superficial Siderosis 33 0.035
216
WNC001 Winchester Syndrome 34 0.035
217
CRB009 Cerebritis 33 0.035
218
TST025 Testicular Microlithiasis 31 0.035
219
AKN002 Akinetic Mutism 31 0.035
220
P DYS005 Dyslexia 30 0.035
221
c LBR004 Leber Congenital Amaurosis 1 29 0.035
222
SPN205 Spinal Muscular Atrophy, X-Linked 2, Infantile 28 0.035
223
GLC011 Galactose Epimerase Deficiency 28 0.035
224
c THR103 Thrombocytopenia, Congenital Amegakaryocytic 28 0.035
225
BDY001 Body Dysmorphic Disorder 26 0.035
226
MNT006 Manitoba Oculotrichoanal Syndrome 25 0.035
227
HYP548 Hypogonadotropic Hypogonadism 2 with or Without Anosmia 24 0.035
228
EPD046 Epididymitis 24 0.035
229
NRC003 Narcissistic Personality Disorder 23 0.035
230
UNC001 Uncombable Hair Syndrome 23 0.035
231
c CTR102 Cataract 2, Multiple Types 22 0.035
232
MMS001 Momo Syndrome 22 0.035
233
OPH001 Ophthalmomyiasis 20 0.035
234
c CTR096 Cataract 6, Multiple Types 20 0.035
235
PRD003 Periodontosis 18 0.035
236
CGN001 Cogan-Reese Syndrome 18 0.035
237
c CTR098 Cataract 1, Multiple Types 15 0.035
238
c CTR132 Cataract 3, Multiple Types 13 0.035
239
MNS002 Mini Stroke 13 0.035
240
SHR004 Sharp Syndrome 13 0.035
241
NDD001 Nodding Syndrome 10 0.035
242
MLT076 Multiple System Atrophy with Orthostatic Hypotension 10 0.035
243
CNT057 Central Centrifugal Cicatricial Alopecia 10 0.035
244
YSH001 Yusho Disease 10 0.035
245
ERB002 Erb's Palsy 8 0.035
246
HND010 Handigodu Disease 8 0.035
247
ABS002 Absence of Gluteal Muscle 5 0.035
248
KRK002 Karak Syndrome 5 0.035
249
ADN069 Adenosine Monophosphate Deaminase Deficiency Erythrocyte Type 4 0.035
250
P ALZ034 Alzheimer Disease 100 0.025
251
P LFR001 Li-Fraumeni Syndrome 81 0.025
252
P PLM037 Pulmonary Hypertension 85 0.025
253
HDG012 Hodgkin Lymphoma 79 0.025
254
ADR007 Adrenoleukodystrophy 76 0.025
255
P APL001 Aplastic Anemia 76 0.025
256
FBR012 Fabry Disease 76 0.025
257
c MLT019 Multiple Myeloma 75 0.025
258
P HRD008 Hereditary Hemorrhagic Telangiectasia 75 0.025
259
P HMC003 Hemochromatosis 75 0.025
260
P RNL014 Renal Cell Carcinoma 83 0.025
261
P PFF001 Pfeiffer Syndrome 74 0.025
262
c AMY091 Amyotrophic Lateral Sclerosis 1 82 0.025
263
P CHR090 Chronic Lymphocytic Leukemia 74 0.025
264
P ALG002 Alagille Syndrome 73 0.025
265
c HMP004 Hemophilia B 72 0.025
266
P OST002 Osteoporosis 71 0.025
267
END057 Endometrial Cancer 71 0.025
268
P SCL016 Scleroderma 76 0.025
269
OBS002 Obsessive-Compulsive Disorder 69 0.025
270
PRP003 Porphyria Cutanea Tarda 69 0.025
271
LSC001 Lesch-Nyhan Syndrome 69 0.025
272
AND015 Androgen Insensitivity 69 0.025
273
P LYN001 Lynch Syndrome 66 0.025
274
P ANG001 Angelman Syndrome 66 0.025
275
LVR012 Liver Cirrhosis 66 0.025
276
P LYM007 Lymphangioleiomyomatosis 65 0.025
277
ADD001 Addison's Disease 65 0.025
278
CYS008 Cystic Echinococcosis 64 0.025
279
MGR002 Migraine 64 0.025
280
P CRT072 Creutzfeldt-Jakob Disease 64 0.025
281
HST011 Histoplasmosis 64 0.025
282
P THL005 Thalassemia 64 0.025
283
BLM001 Bloom Syndrome 64 0.025
284
P PRD006 Prader-Willi Syndrome 64 0.025
285
ALL003 Allergic Rhinitis 63 0.025
286
c PRK057 Parkinson Disease, Late-Onset 63 0.025
287
P AMY004 Amyloidosis 63 0.025
288
MLG056 Malignant Hyperthermia 62 0.025
289
P DRM010 Dermatomyositis 62 0.025
290
BRN024 Bronchitis 62 0.025
291
P LNG028 Long Qt Syndrome 62 0.025
292
MYC006 Mycosis Fungoides 62 0.025
293
P LVR013 Liver Disease 62 0.025
294
P BCK002 Beckwith-Wiedemann Syndrome 61 0.025
295
CNT098 Central Core Disease 62 0.025
296
P ATR011 Atrial Fibrillation 62 0.025
297
P MCH002 Machado-Joseph Disease 61 0.025
298
P HYP055 Hypoplastic Left Heart Syndrome 61 0.025
299
P HRM001 Hermansky-Pudlak Syndrome 60 0.025
300
SCH014 Schistosomiasis 60 0.025
301
P DYS007 Dyskeratosis Congenita 60 0.025
302
PSD012 Pseudoachondroplasia 60 0.025
303
PLY017 Polyarteritis Nodosa 60 0.025
304
BLL006 Bullous Pemphigoid 60 0.025
305
P CRN037 Craniosynostosis 60 0.025
306
P FCS002 Fucosidosis 59 0.025
307
CHL065 Cholangiocarcinoma 59 0.025
308
P OST009 Osteochondritis Dissecans 59 0.025
309
HLY001 Hailey-Hailey Disease 59 0.025
310
DRM014 Dermatofibrosarcoma Protuberans 59 0.025
311
SCR008 Scrub Typhus 59 0.025
312
PSD007 Pseudomyxoma Peritonei 59 0.025
313
P GLB002 Glioblastoma 59 0.025
314
PRP027 Peripheral Vascular Disease 60 0.025
315
VSC007 Vascular Disease 59 0.025
316
STR008 Strongyloidiasis 58 0.025
317
P RCK004 Rickets 58 0.025
318
DRM006 Dermatitis 58 0.025
319
P HRP006 Herpes Simplex 63 0.025
320
P THY023 Thymoma 57 0.025
321
P THR015 Thrombophilia 57 0.025
322
GNT003 Genital Herpes 57 0.025
323
c SML001 Small Cell Carcinoma 57 0.025
324
CYS010 Cystinosis 57 0.025
325
ANN002 Anencephaly 57 0.025
326
CNR002 Cone-Rod Dystrophy 56 0.025
327
P TXP001 Toxoplasmosis 56 0.025
328
P ATP001 Atopic Dermatitis 56 0.025
329
TRG002 Trigeminal Neuralgia 56 0.025
330
ALV010 Alveolar Soft-Part Sarcoma 57 0.025
331
P ENC004 Encephalitis 56 0.025
332
P LPS002 Liposarcoma 56 0.025
333
CHL014 Cholera 56 0.025
334
DNG003 Dengue Disease 64 0.025
335
PPL022 Papilloma 55 0.025
336
P ANT006 Antiphospholipid Syndrome 55 0.025
337
FLT001 Felty's Syndrome 55 0.025
338
CHR066 Chronic Fatigue Syndrome 55 0.025
339
c ACT027 Acute Pancreatitis 55 0.025
340
VCT001 Vacterl Association 55 0.025
341
P NRN021 Neuronal Ceroid Lipofuscinosis 55 0.025
342
P DYS154 Dystonia 55 0.025
343
ACR008 Acrocallosal Syndrome 55 0.025
344
MLT022 Malt Lymphoma 54 0.025
345
PRT011 Protein C Deficiency 54 0.025
346
P HYP076 Hyperthyroidism 54 0.025
347
GRV001 Graves' Disease 54 0.025
348
BLL003 Bell's Palsy 54 0.025
349
P ALT001 Alternating Hemiplegia of Childhood 54 0.025
350
CMM005 Common Cold 54 0.025
351
P CND004 Candidiasis 54 0.025
352
CHR103 Charge Syndrome 54 0.025
353
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.025
354
DFC004 Deficiency Anemia 54 0.025
355
P MSC005 Muscular Dystrophy 54 0.025
356
TTN003 Tetanus 54 0.025
357
LYM009 Lymphocytic Choriomeningitis 54 0.025
358
c MLG069 Malignant Hypertension 54 0.025
359
P ART023 Arthropathy 54 0.025
360
PLY023 Polycystic Liver Disease 54 0.025
361
JCB001 Jacobsen Syndrome 53 0.025
362
P ANP001 Anaplastic Large Cell Lymphoma 53 0.025
363
HYD012 Hydrops Fetalis 53 0.025
364
MLD001 Melioidosis 62 0.025
365
RSD004 Rosai-Dorfman Disease 53 0.025
366
P CFF001 Coffin-Siris Syndrome 53 0.025
367
P SPN049 Spinocerebellar Ataxia 53 0.025
368
GTR002 Goiter 53 0.025
369
c PRM126 Primary Peritoneal Carcinoma 53 0.025
370
MTR014 Motor Neuron Disease 53 0.025
371
CHL067 Cholecystitis 53 0.025
372
P DBT005 Diabetes Insipidus 53 0.025
373
P HMR012 Hemorrhagic Fever 52 0.025
374
TTR011 Tetraploidy 52 0.025
375
P DYS026 Dysfibrinogenemia 52 0.025
376
LCH002 Lichen Planus 52 0.025
377
NPH018 Nephrogenic Systemic Fibrosis 52 0.025
378
NRL004 Neuroleptic Malignant Syndrome 52 0.025
379
P AGM001 Agammaglobulinemia 59 0.025
380
HLC001 Holocarboxylase Synthetase Deficiency 52 0.025
381
PLM001 Pulmonary Tuberculosis 60 0.025
382
STT002 Status Asthmaticus 52 0.025
383
BRN002 Bronchiolitis 52 0.025
384
P OPN001 Open-Angle Glaucoma 51 0.025
385
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 59 0.025
386
TST021 Testicular Germ Cell Tumor 51 0.025
387
c ACT075 Acute Myocardial Infarction 57 0.025
388
PLY041 Polymyositis 51 0.025
389
P HMN013 Hemangiopericytoma 51 0.025
390
P ATS007 Autism Spectrum Disorder 56 0.025
391
OLG003 Oligohydramnios 51 0.025
392
CHC001 Chickenpox 51 0.025
393
P CRT033 Corticobasal Degeneration 51 0.025
394
P STC001 Stickler Syndrome 51 0.025
395
PMP001 Pemphigus 51 0.025
396
ECH003 Echinococcosis 51 0.025
397
P MMP001 Mumps 51 0.025
398
CTS003 Coats Disease 51 0.025
399
GLB015 Glioblastoma Multiforme 51 0.025
400
c HPT003 Hepatitis a 51 0.025
401
SCB001 Scabies 50 0.025
402
P SCL015 Scleritis 50 0.025
403
P CTR002 Cataract 50 0.025
404
GLC003 Glucose Intolerance 50 0.025
405
BCT004 Bacteriuria 50 0.025
406
P PSR001 Psoriatic Arthritis 50 0.025
407
GNR005 Gonorrhea 50 0.025
408
GLM008 Glomus Tumor 51 0.025
409
DFF005 Diffuse Large B-Cell Lymphoma 50 0.025
410
P OCL002 Oculocutaneous Albinism 50 0.025
411
EPT020 Epithelioid Hemangioendothelioma 50 0.025
412
CLL021 Collagenous Colitis 50 0.025
413
P MYC008 Myocarditis 50 0.025
414
CRD002 Cri-Du-Chat Syndrome 50 0.025
415
THR004 Thrombocytosis 50 0.025
416
c ACT009 Acute Monocytic Leukemia 50 0.025
417
OST017 Osteomyelitis 50 0.025
418
c MLG002 Malignant Peritoneal Mesothelioma 50 0.025
419
RCT015 Reactive Arthritis 50 0.025
420
P MLS001 Melas Syndrome 50 0.025
421
CLL003 Cellulitis 50 0.025
422
FLR002 Filariasis 50 0.025
423
RBS001 Rabies 50 0.025
424
c USH006 Usher Syndrome, Type 1b 49 0.025
425
ORL005 Oral Candidiasis 49 0.025
426
INS001 Insulinoma 49 0.025
427
P CRN012 Craniometaphyseal Dysplasia 49 0.025
428
MMM001 Mammary Paget's Disease 49 0.025
429
NNS002 Nonspecific Interstitial Pneumonia 49 0.025
430
P WVR001 Weaver Syndrome 49 0.025
431
ALV006 Alveolar Capillary Dysplasia 49 0.025
432
BRN056 Bronchopulmonary Dysplasia 49 0.025
433
P BRC006 Brachydactyly 49 0.025
434
P SHR029 Short Syndrome 49 0.025
435
c MCP037 Mucopolysaccharidosis is 50 0.025
436
PRN023 Prion Disease 49 0.025
437
CHR001 Churg-Strauss Syndrome 49 0.025
438
P MNC007 Monocytic Leukemia 49 0.025
439
P DGR001 Digeorge Syndrome 49 0.025
440
c ACT078 Acute Porphyria 49 0.025
441
P ENC008 Encephalocele 49 0.025
442
CRY004 Cryoglobulinemia 49 0.025
443
P PLY006 Polydactyly 48 0.025
444
MCR004 Macroglobulinemia 48 0.025
445
OBS061 Obstructive Sleep Apnea 48 0.025
446
MYL003 Myeloid Sarcoma 48 0.025
447
c CHR285 Chronic Myelomonocytic Leukemia 48 0.025
448
P PRN026 Porencephaly 48 0.025
449
RTN017 Retinal Detachment 48 0.025
450
BLS002 Blastomycosis 48 0.025
451
c ACT134 Acute Liver Failure 48 0.025
452
MDL009 Medullary Sponge Kidney 48 0.025
453
MDD011 Mood Disorder 48 0.025
454
ANG011 Angiodysplasia 48 0.025
455
DDN006 Duodenitis 48 0.025
456
PLM034 Pulmonary Emphysema 53 0.025
457
TYP011 Typhus 47 0.025
458
P VNT002 Ventricular Septal Defect 47 0.025
459
SBC001 Subacute Sclerosing Panencephalitis 47 0.025
460
P PMP005 Pemphigus Vulgaris 47 0.025
461
P HYP014 Hyperuricemia 47 0.025
462
MTN003 Motion Sickness 47 0.025
463
P PLM006 Pulmonary Alveolar Proteinosis 47 0.025
464
LPM005 Lipomatosis 47 0.025
465
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 47 0.025
466
MLT075 Multifocal Motor Neuropathy 51 0.025
467
KLN001 Klinefelter's Syndrome 47 0.025
468
P HYP027 Hypobetalipoproteinemia 47 0.025
469
ACR005 Acrodermatitis 47 0.025
470
PRP082 Porphyria, Congenital Erythropoietic 48 0.025
471
RDC002 Radiculopathy 47 0.025
472
P HYP083 Hypopituitarism 47 0.025
473
FLL013 Follicular Dendritic Cell Sarcoma 47 0.025
474
MCL002 Macular Corneal Dystrophy 47 0.025
475
DST006 Diastolic Heart Failure 46 0.025
476
P MNT147 Mental Retardation 46 0.025
477
CRM001 Crimean-Congo Hemorrhagic Fever 46 0.025
478
MYM001 Myoma 46 0.025
479
P PRG013 Paraganglioma 46 0.025
480
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 46 0.025
481
NPH051 Nephritis 46 0.025
482
P SLL003 Salla Disease 46 0.025
483
ETH011 Ethylmalonic Encephalopathy 46 0.025
484
MYL001 Myelitis 46 0.025
485
PLS025 Plasmablastic Lymphoma 46 0.025
486
PLY012 Polyhydramnios 46 0.025
487
P INF032 Infertility 46 0.025
488
NWC001 Newcastle Disease 46 0.025
489
P DMN033 Dementia, Frontotemporal 47 0.025
490
ACQ007 Acquired Immunodeficiency Syndrome 46 0.025
491
KRT009 Keratosis 45 0.025
492
TCK001 Tick-Borne Encephalitis 45 0.025
493
TLR001 Tularemia 45 0.025
494
c ANT034 Anterior Uveitis 45 0.025
495
P MWT001 Mowat-Wilson Syndrome 45 0.025
496
ASP001 Asperger Syndrome 45 0.025
497
RPP001 Rapp-Hodgkin Syndrome 45 0.025
498
STN007 Stenotrophomonas Maltophilia 45 0.025
499
PRN009 Paranoid Schizophrenia 45 0.025
500
c HPT007 Hepatitis E 45 0.025
501
BCT015 Bacteremia 45 0.025
502
SPT005 Spotted Fever 45 0.025
503
CTS005 Catastrophic Antiphospholipid Syndrome 45 0.025
504
DYS073 Dysphagia 45 0.025
505
P D2H001 D-2-Hydroxyglutaric Aciduria 45 0.025
506
ADN020 Adenosarcoma 44 0.025
507
ATR057 Atrioventricular Block 44 0.025
508
P FNC004 Fanconi Syndrome 44 0.025
509
CLR003 Clear Cell Adenocarcinoma 44 0.025
510
LGS001 Legius Syndrome 44 0.025
511
DNT011 Dentinogenesis Imperfecta 44 0.025
512
TRN015 Transient Cerebral Ischemia 44 0.025
513
LPS007 Lupus Nephritis 44 0.025
514
MTC027 Mitochondrial Trifunctional Protein Deficiency 44 0.025
515
P DRR001 Diarrhea 44 0.025
516
P ACT135 Acute Graft Versus Host Disease 44 0.025
517
c ATM024 Autoimmune Pancreatitis 44 0.025
518
NSP001 Nasopharynx Carcinoma 44 0.025
519
EGG001 Egg Allergy 43 0.025
520
ALB002 Albinism 43 0.025
521
DBW001 Dubowitz Syndrome 43 0.025
522
RSC001 Rosacea 43 0.025
523
CTY001 Cat Eye Syndrome 43 0.025
524
CYS009 Cystadenoma 43 0.025
525
TRF001 Trifunctional Protein Deficiency 43 0.025
526
CLS010 Cluster Headache 43 0.025
527
EXS001 Exostosis 43 0.025
528
GND002 Gender Identity Disorder 43 0.025
529
P GND004 Gonadal Dysgenesis 43 0.025
530
BLD034 Bile Duct Carcinoma 43 0.025
531
LYM027 Lymphopenia 43 0.025
532
MYC013 Mycobacterium Abscessus 43 0.025
533
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 43 0.025
534
CHL052 Choledochal Cyst 43 0.025
535
ORC001 Orchitis 43 0.025
536
END041 Endometrial Adenocarcinoma 43 0.025
537
MNN014 Mononeuritis 43 0.025
538
OMP004 Omphalocele 43 0.025
539
HYP006 Hypertensive Heart Disease 43 0.025
540
CHR288 Chronic Recurrent Multifocal Osteomyelitis 42 0.025
541
BRN018 Borna Disease 42 0.025
542
FBR047 Fibromyalgia 42 0.025
543
P KBK002 Kabuki Syndrome 1 42 0.025
544
CHR005 Chorioamnionitis 42 0.025
545
c BCT007 Bacterial Meningitis 42 0.025
546
SMN007 Seminoma 42 0.025
547
PLS016 Plasma Cell Leukemia 42 0.025
548
ACT087 Acth Deficiency 42 0.025
549
P LCT001 Lactic Acidosis 42 0.025
550
CWP001 Cowpox 42 0.025
551
P SPN016 Spondylocostal Dysostosis 42 0.025
552
BRN013 Bronchiolitis Obliterans Organizing Pneumonia 41 0.025
553
TRN044 Transposition of the Great Arteries 41 0.025
554
END028 Endemic Goiter 41 0.025
555
DRG003 Drug Dependence 41 0.025
556
ALC010 Alcoholic Cardiomyopathy 41 0.025
557
AZS001 Azoospermia 41 0.025
558
PRN014 Paronychia 41 0.025
559
FCL022 Focal Dystonia 41 0.025
560
PTY003 Pityriasis Rubra Pilaris 41 0.025
561
P TRN034 Transverse Myelitis 41 0.025
562
P HMR005 Hemorrhoid 41 0.025
563
HRT012 Heart Valve Disease 41 0.025
564
BLP005 Blepharitis 40 0.025
565
MDY003 Mody, Type Ii 41 0.025
566
SPL004 Splenic Marginal Zone Lymphoma 40 0.025
567
NDL021 Nodular Lymphocyte Predominant Hodgkin Lymphoma 40 0.025
568
MYX005 Myxoid Liposarcoma 40 0.025
569
SPL018 Splenomegaly 40 0.025
570
c CHR527 Charcot-Marie-Tooth Disease, Type 1b 41 0.025
571
PPL018 Papillary Adenocarcinoma 40 0.025
572
VTM002 Vitamin B12 Deficiency 40 0.025
573
SCL025 Scleromyxedema 40 0.025
574
EPD047 Epidermolysis Bullosa Simplex, Koebner Type 41 0.025
575
MMB002 Membranous Glomerulonephritis 40 0.025
576
MTS001 Mutism 40 0.025
577
P HMR003 Hemorrhagic Disease 39 0.025
578
ASC002 Ascariasis 39 0.025
579
FRN002 Frontal Lobe Epilepsy 39 0.025
580
STC004 Stachybotrys Chartarum 39 0.025
581
c CNG415 Congenital Disorder of Glycosylation, Type Ia 40 0.025
582
P PRM018 Primary Hypertrophic Osteoarthropathy 39 0.025
583
LYM021 Lymphadenitis 39 0.025
584
MDS022 Mediastinitis 39 0.025
585
MYS001 Myositis Ossificans 39 0.025
586
ECT026 Ectopic Pregnancy 39 0.025
587
TBR008 Tuberculous Peritonitis 39 0.025
588
P BRS044 Breast Adenocarcinoma 39 0.025
589
P ATR005 Atrophic Gastritis 39 0.025
590
RTR011 Retroperitoneal Fibrosis 39 0.025
591
FBR054 Fibroma 39 0.025
592
P INF037 Inflammatory Bowel Disease 39 0.025
593
P PRL003 Proliferative Glomerulonephritis 39 0.025
594
ZYG002 Zygomycosis 39 0.025
595
TXC020 Toxic Oil Syndrome 39 0.025
596
P WGN003 Wagner Syndrome 39 0.025
597
RNP001 Renpenning Syndrome 38 0.025
598
MCR037 Macroglossia 38 0.025
599
VNW005 Von Willebrand Disease, Type 1 39 0.025
600
P LTT001 Lattice Corneal Dystrophy 38 0.025
601
ANS003 Anisakiasis 38 0.025
602
VLC002 Vlcad Deficiency 39 0.025
603
HST006 Histidinemia 38 0.025
604
P CYS017 Cystic Teratoma 38 0.025
605
BRB001 Beriberi 38 0.025
606
c LSS005 Lissencephaly 1 37 0.025
607
CHR276 Chronic Active Epstein-Barr Virus Infection 37 0.025
608
GND001 Gonadoblastoma 37 0.025
609
c ACT004 Acute Diarrhea 37 0.025
610
P FRN036 Frontonasal Dysplasia 1 37 0.025
611
CLL002 Collecting Duct Carcinoma 37 0.025
612
EPS026 Epispadias 37 0.025
613
CRP018 Cor Pulmonale 37 0.025
614
RBF001 Riboflavin Deficiency 37 0.025
615
PST086 Posterior Cortical Atrophy 37 0.025
616
MYC019 Mycobacterium Marinum 37 0.025
617
MCK002 Meckel's Diverticulum 36 0.025
618
PPL046 Popliteal Pterygium Syndrome 1 36 0.025
619
c ICH049 Ichthyosis, Congenital, Autosomal Recessive 2 36 0.025
620
NCR002 Necrobiosis Lipoidica 36 0.025
621
OBS004 Obstructive Hydrocephalus 36 0.025
622
CND006 Candida Glabrata 36 0.025
623
JLL001 Jalili Syndrome 37 0.025
624
c XNT010 Xanthinuria, Type I 37 0.025
625
WHP002 Whiplash 36 0.025
626
PMP002 Pemphigoid Gestationis 36 0.025
627
BTN004 Biotin Deficiency 35 0.025
628
MYC017 Mycobacterium Kansasii 35 0.025
629
LPB001 Lipoblastoma 35 0.025
630
P VGN017 Vaginal Cancer 35 0.025
631
EMN001 Emanuel Syndrome 36 0.025
632
PYR011 Pyropoikilocytosis 35 0.025
633
IRT001 Iritis 35 0.025
634
c ALB009 Albinism, Oculocutaneous, Type Ia 36 0.025
635
BLR015 Blue Rubber Bleb Nevus Syndrome 35 0.025
636
CRB085 Cerebral Hemorrhage 35 0.025
637
c MCP038 Mucopolysaccharidosis Iva 35 0.025
638
PHC013 Phaeochromocytoma 34 0.025
639
MTR010 Mature Teratoma 34 0.025
640
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 35 0.025
641
OCL025 Ocular Toxoplasmosis 34 0.025
642
GST052 Gestational Choriocarcinoma 34 0.025
643
URT004 Urethral Syndrome 34 0.025
644
INT079 Intrahepatic Cholangiocarcinoma 34 0.025
645
SPR035 Superior Vena Cava Syndrome 34 0.025
646
ATY013 Atypical Rett Syndrome 34 0.025
647
ACL001 Acalculous Cholecystitis 34 0.025
648
INF013 Inferior Myocardial Infarction 33 0.025
649
TRN021 Transaldolase Deficiency 33 0.025
650
IRD001 Iridocyclitis 33 0.025
651
DNR002 Duane-Radial Ray Syndrome 34 0.025
652
PRD019 Periodic Fever, Familial 33 0.025
653
FNT004 Fainting 33 0.025
654
MNN002 Mononeuritis Multiplex 33 0.025
655
MGS001 Megaesophagus 33 0.025
656
CRB151 Cerebral Creatine Deficiency Syndrome 1 34 0.025
657
ANG037 Angiomatosis 33 0.025
658
SMD002 Smed Strudwick Type 33 0.025
659
TND004 Tendinopathy 32 0.025
660
BRN055 Bronchogenic Cyst 32 0.025
661
CRP002 Croup 32 0.025
662
MTR003 Mitral Valve Stenosis 32 0.025
663
HRP002 Herpes Gestationis 32 0.025
664
c NMN013 Niemann-Pick Disease, Type a 33 0.025
665
P PRT096 Peritoneal Mesothelioma 32 0.025
666
MNN032 Meningococcal Meningitis 32 0.025
667
FRS004 Free Sialic Acid Storage Disorders 32 0.025
668
GLD002 Goldberg-Shprintzen Megacolon Syndrome 32 0.025
669
HNS001 Hansen's Disease 31 0.025
670
INT020 Intravenous Leiomyomatosis 31 0.025
671
c ICH041 Ichthyosis, Autosomal Recessive 4b 31 0.025
672
PRR016 Pierre Robin Syndrome 32 0.025
673
c ATM040 Autoimmune Lymphoproliferative Syndrome Type Iv 31 0.025
674
c EHL027 Ehlers-Danlos Syndrome, Type Viic 32 0.025
675
SYS003 Systolic Heart Failure 31 0.025
676
P GLM006 Glomangioma 31 0.025
677
ANX004 Anoxia 31 0.025
678
MLK004 Malakoplakia 31 0.025
679
TTZ003 Tietz Albinism-Deafness Syndrome 31 0.025
680
GLL028 Gillespie Syndrome 30 0.025
681
LNG039 Lung Squamous Cell Carcinoma 30 0.025
682
CGN006 Cogan Syndrome 31 0.025
683
EPC002 Epicondylitis 30 0.025
684
c OST124 Osteogenesis Imperfecta, Type V 31 0.025
685
TBS001 Tabes Dorsalis 30 0.025
686
c PNM010 Pneumothorax, Primary Spontaneous 31 0.025
687
NRS005 Neurosarcoidosis 30 0.025
688
PNC041 Pancreatic Ductal Adenocarcinoma 38 0.025
689
RTR001 Retrograde Amnesia 29 0.025
690
c MCP036 Mucopolysaccharidosis Ih/s 29 0.025
691
DCB001 Decubitus Ulcer 29 0.025
692
PRS064 Persistent Vegetative State 29 0.025
693
c MNN044 Mannosidosis, Beta 30 0.025
694
ATM021 Autoimmune Inner Ear Disease 29 0.025
695
TNC003 Tinea Corporis 29 0.025
696
HYP034 Hypertensive Encephalopathy 29 0.025
697
CYC008 Cyclic Vomiting Syndrome 28 0.025
698
P HYP440 Hyperphosphatasia with Mental Retardation Syndrome 28 0.025
699
CTN013 Cutaneous Anthrax 28 0.025
700
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 27 0.025
701
ADG002 Audiogenic Seizures 27 0.025
702
c LSS006 Lissencephaly 2 27 0.025
703
c CTR130 Cataract 9, Multiple Types 27 0.025
704
c NTR038 Neutropenia, Severe Congenital 3, Autosomal Recessive 28 0.025
705
PRS051 Parastremmatic Dwarfism 27 0.025
706
VBR003 Vibrio Vulnificus Infection 27 0.025
707
P CRN231 Corneal Dystrophy, Posterior Polymorphous, 1 27 0.025
708
c ALB010 Albinism, Oculocutaneous, Type Ib 28 0.025
709
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 28 0.025
710
CYT004 Cytomegalic Inclusion Disease 28 0.025
711
TNC001 Tinea Cruris 26 0.025
712
RTS001 Ritscher-Schinzel Syndrome 27 0.025
713
BLK001 Balkan Nephropathy 26 0.025
714
MTH047 Methanol Poisoning 26 0.025
715
CRT028 Cor Triatriatum 27 0.025
716
P DNT033 Dentinogenesis Imperfecta, Shields Type Ii 27 0.025
717
c MSC115 Muscular Dystrophy, Limb-Girdle, Type 1a 27 0.025
718
c CRN240 Craniometaphyseal Dysplasia, Autosomal Recessive 27 0.025
719
INN003 Iniencephaly 27 0.025
720
PDT027 Pediatric Ulcerative Colitis 25 0.025
721
SPR009 Sporadic Breast Cancer 25 0.025
722
CHR028 Chronic Wasting Disease 25 0.025
723
P CMM008 Communicating Hydrocephalus 25 0.025
724
ANH001 Ainhum 26 0.025
725
ARB001 Ariboflavinosis 25 0.025
726
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 26 0.025
727
CRN237 Corneal Dystrophy, Avellino Type 26 0.025
728
TRL003 Toriello Carey Syndrome 26 0.025
729
SPL007 Splenic Abscess 25 0.025
730
NRM009 Normokalemic Periodic Paralysis 24 0.025
731
PRM056 Primrose Syndrome 24 0.025
732
P CTS012 Cutis Verticis Gyrata 25 0.025
733
PLC009 Placenta Praevia 24 0.025
734
IDM001 Ideomotor Apraxia 24 0.025
735
STY001 Satoyoshi Syndrome 24 0.025
736
FMR008 Femur Fibula Ulna Syndrome 24 0.025
737
c ORF007 Orofaciodigital Syndrome 2 24 0.025
738
KKC001 Kikuchi Disease 24 0.025
739
c CRD093 Cardiomyopathy, Dilated, 1a 23 0.025
740
MYC014 Mycobacterium Chelonae 23 0.025
741
INT003 Intracranial Hypotension 23 0.025
742
CWC001 Cowchock Syndrome 24 0.025
743
JPN001 Japanese Spotted Fever 23 0.025
744
HRP001 Herpangina 23 0.025
745
SCL022 Scleredema 24 0.025
746
TTR013 Tetrasomy X 23 0.025
747
c HYP438 Hyperaldosteronism, Familial, Type Iii 22 0.025
748
NTV001 Native American Myopathy 22 0.025
749
c ACH034 Achromatopsia-2 23 0.025
750
SLL001 Sialolithiasis 23 0.025
751
VGN019 Vaginal Discharge 22 0.025
752
3Q2001 3q29 Deletion Syndrome 23 0.025
753
PLR006 Pleural Cancer 22 0.025
754
PNT006 Pentosuria 22 0.025
755
OVR098 Ovarian Fibroma 22 0.025
756
CPP003 Cap Polyposis 22 0.025
757
PLY031 Polydactyly Myopia Syndrome 23 0.025
758
SBD001 Subdural Empyema 23 0.025
759
ADT001 Auditory Agnosia 22 0.025
760
TRN028 Transient Acantholytic Dermatosis 21 0.025
761
PLN007 Plantar Fasciitis 21 0.025
762
P ENC021 Encephalopathy, Neonatal Severe 21 0.025
763
LCH008 Lichen Planus Pigmentosus 21 0.025
764
DYS009 Dysthymic Disorder 21 0.025
765
OTD001 Otodental Dysplasia 22 0.025
766
ADN067 Adenoid Hypertrophy 22 0.025
767
CHR158 Charles Bonnet Syndrome 21 0.025
768
c CTR095 Cataract 8, Multiple Types 22 0.025
769
HYP145 Hyperbetaalaninemia 22 0.025
770
c RNG013 Ring Chromosome 18 21 0.025
771
NVS007 Nevus of Ota 21 0.025
772
c CTR113 Cataract 11, Multiple Types 20 0.025
773
P HYD015 Hydroa Vacciniforme 21 0.025
774
DPR002 Depersonalization Disorder 20 0.025
775
c PRD030 Periodontitis 1, Juvenile 20 0.025
776
c ICH047 Ichthyosis, Congenital, Autosomal Recessive 1 20 0.025
777
SPR063 Superior Canal Dehiscence Syndrome 21 0.025
778
HRL002 Harlequin Syndrome 21 0.025
779
PNM003 Pneumatosis Cystoides Intestinalis 21 0.025
780
c NTR033 Neutropenia, Severe Congenital 1, Autosomal Dominant 19 0.025
781
OPT054 Opitz-Kaveggia Syndrome 20 0.025
782
BLN002 Balanitis Xerotica Obliterans 19 0.025
783
FMR003 Femoral Neuropathy 20 0.025
784
ACK001 Ackerman Syndrome 19 0.025
785
PSD078 Pseudofolliculitis Barbae 19 0.025
786
THR099 Third-Degree Atrioventricular Block 18 0.025
787
c ICH042 Ichthyosis, Congenital, Autosomal Recessive 6 18 0.025
788
c ICH040 Ichthyosis, Congenital, Autosomal Recessive 4a 18 0.025
789
TBR003 Tuberculous Epididymitis 19 0.025
790
DMN026 Dementia Pugilistica 18 0.025
791
P ACT059 Acute Maxillary Sinusitis 19 0.025
792
RHB022 Rhabdoid Tumors, Somatic 18 0.025
793
BLC015 Balo Concentric Sclerosis 18 0.025
794
NNN015 Noonan-Like/multiple Giant Cell Lesion Syndrome 18 0.025
795
c ICH050 Ichthyosis, Congenital, Autosomal Recessive 5 17 0.025
796
c ICH051 Ichthyosis, Congenital, Autosomal Recessive 11 17 0.025
797
ARR026 Arrhythmogenic Right Ventricular Dysplasia 1 17 0.025
798
MSN002 Mesenteric Lymphadenitis 18 0.025
799
c ACT072 Acute Laryngitis 18 0.025
800
MNG007 Manganese Poisoning 18 0.025
801
RDT005 Radiation Induced Cancer 18 0.025
802
INF048 Infantile Histiocytoid Cardiomyopathy 18 0.025
803
YNG002 Young Syndrome 17 0.025
804
c PRX050 Peroxisome Biogenesis Disorder 9b 17 0.025
805
c CHR057 Chronic Laryngitis 17 0.025
806
HMC012 Hemicrania Continua 17 0.025
807
MRZ001 Mirizzi Syndrome 16 0.025
808
c CTR133 Cataract 22, Autosomal Recessive 16 0.025
809
c SCK009 Seckel Syndrome 1 17 0.025
810
PRN010 Paranoid Personality Disorder 16 0.025
811
c OPT050 Opitz Gbbb Syndrome, Type Ii 17 0.025
812
c CTR104 Cataract 18, Autosomal Recessive 16 0.025
813
c OPT051 Opitz Gbbb Syndrome, Type I 16 0.025
814
DYS135 Dysphagia Lusoria 16 0.025
815
LRP001 Leri Pleonosteosis 16 0.025
816
THN005 Thunderclap Headache 16 0.025
817
c BSL038 Basal Ganglia Calcification, Idiopathic, 1 16 0.025
818
SHR027 Short Stature Wormian Bones Dextrocardia 16 0.025
819
c CTR118 Cataract 14, Multiple Types 15 0.025
820
c WGN005 Wagner Syndrome 1 16 0.025
821
P ELL007 Elliptocytosis-1 15 0.025
822
UHL001 Uhl Anomaly 16 0.025
823
c ICH038 Ichthyosis, Congenital, Autosomal Recessive 3 15 0.025
824
c ICH039 Ichthyosis, Congenital, Autosomal Recessive 10 15 0.025
825
c PRX053 Peroxisome Biogenesis Disorder 14b 15 0.025
826
OSL001 Oslam Syndrome 15 0.025
827
ELC001 Elective Mutism 15 0.025
828
EPL143 Epilepsy, Progressive Myoclonic 3, with or Without Intracellular Inclusions 15 0.025
829
c CTR131 Cataract 17, Multiple Types 14 0.025
830
ACC005 Accessory Pancreas 15 0.025
831
c CTR115 Cataract 16, Multiple Types 14 0.025
832
c ICH048 Ichthyosis, Congenital, Autosomal Recessive 9 14 0.025
833
DPH012 Diphallia 15 0.025
834
c CTR122 Cataract 5, Multiple Types 14 0.025
835
c CTR125 Cataract 7 15 0.025
836
c CTR129 Cataract 31, Multiple Types 14 0.025
837
ACH028 Acheiria 14 0.025
838
c CTR124 Cataract 10, Multiple Types 13 0.025
839
SCH004 Schizoid Personality Disorder 13 0.025
840
OVR027 Ovarian Squamous Cell Carcinoma 14 0.025
841
BRN045 Brunner Syndrome 13 0.025
842
c CTR123 Cataract 24, Anterior Polar 14 0.025
843
HYD031 Hydroxyprolinemia 14 0.025
844
CNZ006 Coenzyme Q10 Deficiency, Primary, 1 13 0.025
845
SPN092 Spinal Shock 13 0.025
846
c ICH044 Ichthyosis, Congenital, Autosomal Recessive 8 13 0.025
847
c CTR141 Cataract 21, Multiple Types 13 0.025
848
ORP002 Oropouche Fever 13 0.025
849
c ORF027 Orofacial Cleft 11 13 0.025
850
CNG408 Congenital Deafness with Vitiligo and Achalasia 13 0.025
851
c CTR110 Cataract 26, Multiple Types 13 0.025
852
c ANT041 Antiphospholipid Syndrome, Familial 13 0.025
853
PRS119 Persistent Genital Arousal Disorder 12 0.025
854
c MNT187 Mental Retardation, X-Linked 49 12 0.025
855
BNG042 Benign Multicystic Peritoneal Mesothelioma 12 0.025
856
URC004 Urachal Cancer 11 0.025
857
CRT056 Carotidynia 12 0.025
858
TRG006 Trigger Thumb 12 0.025
859
MRG007 Morgellons 12 0.025
860
KYR001 Kyrle Disease 12 0.025
861
ANG024 Angiofollicular Lymph Hyperplasia 12 0.025
862
c ICH045 Ichthyosis, Congenital, Autosomal Recessive 7 11 0.025
863
ARL004 Aural Atresia, Congenital 11 0.025
864
JMP002 Jumping Frenchmen of Maine 10 0.025
865
c MNT171 Mental Retardation, Autosomal Dominant 17 9 0.025
866
SBP006 Subepithelial Mucinous Corneal Dystrophy 10 0.025
867
MLP004 Malpuech Facial Clefting Syndrome 9 0.025
868
PHS019 Phosphohydroxylysinuria 8 0.025
869
ACC001 Accessory Nerve Disease 9 0.025
870
PST096 Post Orgasmic Illness Syndrome 9 0.025
871
c HYP512 Hyperproinsulinemia, Familial 7 0.025
872
MNM003 Minimally Differentiated Acute Myeloblastic Leukemia 7 0.025
873
MDP001 Midphalangeal Hair 4 0.025
874
MTR033 Motor Sensory Neuropathy Type 1 Aplasia Cutis Congenita 3 0.025