929 hits were found for 'WAS'

# Family MCID Name MIFTS Score
1
P WSK001 Wiskott-Aldrich Syndrome 87 23.411
2
WSR001 Was-Related Disorders 28 13.923
3
XLN068 X-Linked Thrombocytopenia 48 5.413
4
c THR014 Thrombocytopenia 67 4.894
5
THR065 Thrombocytopenia, X-Linked, Intermittent 9 4.842
6
c NTR004 Neutropenia 65 3.446
7
INT051 Intussusception 59 3.436
8
P SVR003 Severe Congenital Neutropenia 59 3.436
9
c PNC044 Pancreatitis 67 2.500
10
ULC004 Ulcerative Colitis 72 2.473
11
NRN002 Neuronitis 64 2.473
12
P PNC035 Pancreatic Cancer 95 2.450
13
BRK003 Burkitt's Lymphoma 78 2.437
14
P AGM001 Agammaglobulinemia 61 2.437
15
P INF037 Inflammatory Bowel Disease 50 2.437
16
PRT014 Protein S Deficiency 66 2.421
17
SHG001 Shigellosis 63 2.421
18
TNS005 Tonsillitis 62 2.421
19
VCC001 Vaccinia 48 2.421
20
END072 Endotheliitis 47 2.421
21
PRM097 Primary Immunodeficiency Disease 40 2.421
22
HMT018 Hematopoietic Stem Cell Transplantation 29 2.421
23
SVR014 Severe Congenital Neutropenia X-Linked 22 2.421
24
TBR010 Tuberculosis 84 1.762
25
PRP030 Purpura 67 1.762
26
P GT001 Gout 66 1.762
27
c MYL007 Myeloma 59 1.748
28
c THR005 Thrombotic Thrombocytopenic Purpura 57 1.748
29
CRB009 Cerebritis 56 1.748
30
P MLT019 Multiple Myeloma 89 1.733
31
c DRR001 Diarrhea 54 1.733
32
HV1006 Hiv-1 42 1.712
33
P HYP163 Hyperlipidemia Type 3 27 0.223
34
c HPT021 Hepatitis 75 0.100
35
P LKM002 Leukemia 79 0.090
36
CYT018 Cytochrome P450 2d6 Variant 13 0.086
37
P ADN016 Adenocarcinoma 60 0.083
38
P HYP075 Hypertension 86 0.079
39
P ESP024 Esophagitis 60 0.079
40
P BRS047 Breast Cancer 105 0.070
41
P ART022 Arthritis 75 0.070
42
c NPH019 Nephronophthisis 1 20 0.070
43
ESP021 Esophageal Cancer 81 0.066
44
c ACT073 Acute Leukemia 62 0.066
45
c HPT003 Hepatitis a 60 0.066
46
P OPT015 Optic Atrophy Type 1 55 0.066
47
P AST005 Asthma 88 0.061
48
P LNG032 Lung Cancer 74 0.061
49
P CLR023 Colorectal Cancer 73 0.061
50
PRS047 Prostatitis 62 0.061
51
SML019 Smallpox 43 0.061
52
c LBR005 Leber Congenital Amaurosis 10 19 0.061
53
CRV058 Cervicofacial Lymphatic Malformation 11 0.061
54
P PNM007 Pneumonia 79 0.056
55
P SCH015 Schizophrenia 77 0.056
56
LYM017 Lyme Disease 67 0.056
57
ADN018 Adenoma 67 0.056
58
P HPT001 Hepatitis C 66 0.056
59
P CRV039 Cervicitis 52 0.056
60
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 38 0.056
61
P ATX002 Ataxia Telangiectasia 93 0.050
62
HPT023 Hepatocellular Carcinoma 89 0.050
63
P SYS001 Systemic Lupus Erythematosus 87 0.050
64
P DLT002 Dilated Cardiomyopathy 82 0.050
65
ACR007 Acromegaly 80 0.050
66
c DBT009 Diabetes Mellitus 80 0.050
67
c LPS004 Lupus Erythematosus 73 0.050
68
c MYL006 Myeloid Leukemia 72 0.050
69
P INF038 Influenza 69 0.050
70
P HMN010 Hemangioma 68 0.050
71
MYS005 Myositis 67 0.050
72
c HPT016 Hepatitis B 65 0.050
73
P MLN008 Melanoma 65 0.050
74
SRC014 Sarcoma 63 0.050
75
P LRY019 Laryngitis 62 0.050
76
P MMP001 Mumps 59 0.050
77
CRT002 Cartilage-Hair Hypoplasia 56 0.050
78
CHN016 Cohen Syndrome 53 0.050
79
c SCK002 Sick Sinus Syndrome 52 0.050
80
NPH021 Nephropathic Cystinosis 45 0.050
81
WST005 West Nile Virus 35 0.050
82
KRN005 Kuru Encephalopathy 23 0.050
83
VRL002 Variola Minor 22 0.050
84
THY020 Thyroid Hyalinizing Trabecular Adenoma 17 0.050
85
VRL003 Variola Major 17 0.050
86
P ALZ001 Alzheimer's Disease 103 0.043
87
P ACT019 Acute Myeloid Leukemia 94 0.043
88
P OBS005 Obesity 93 0.043
89
P RHM011 Rheumatoid Arthritis 91 0.043
90
P MYC007 Myocardial Infarction 88 0.043
91
P RTN024 Retinoblastoma 86 0.043
92
P MLT020 Multiple Sclerosis 82 0.043
93
P OST018 Osteosarcoma 81 0.043
94
P PHC003 Pheochromocytoma 81 0.043
95
CNG034 Congestive Heart Failure 81 0.043
96
P HMP004 Hemophilia B 80 0.043
97
PRT036 Peritonitis 78 0.043
98
DCH001 Duchenne Muscular Dystrophy 78 0.043
99
OLV001 Olivopontocerebellar Atrophy 77 0.043
100
P FRN006 Frontotemporal Dementia 72 0.043
101
VSC007 Vascular Disease 72 0.043
102
P PRM005 Primary Hyperparathyroidism 72 0.043
103
c MNN013 Meningitis 71 0.043
104
c HYD006 Hydrocephalus 70 0.043
105
c CHR071 Charcot-Marie-Tooth Disease 69 0.043
106
ADL030 Adult-Onset Still's Disease 68 0.043
107
P CLN016 Colon Cancer 67 0.043
108
DMN002 Dementia 66 0.043
109
ISC004 Ischemia 64 0.043
110
P FML020 Familial Combined Hyperlipidemia 63 0.043
111
c HYP069 Hyperparathyroidism 63 0.043
112
P CRV035 Cervical Cancer 62 0.043
113
PHR003 Pharyngitis 62 0.043
114
c MCL015 Mucolipidosis Ii 62 0.043
115
NRP001 Neuropathy 61 0.043
116
SQM006 Squamous Cell Carcinoma 61 0.043
117
PSR002 Psoriasis 60 0.043
118
ENC006 Encephalomyelitis 55 0.043
119
CVR006 Cavernous Hemangioma 54 0.043
120
VGN023 Vaginitis 54 0.043
121
GST045 Gastroenteritis 53 0.043
122
c CNG018 Congenital Heart Block 52 0.043
123
IMP005 Impotence 52 0.043
124
LNG029 Lung Adenocarcinoma 49 0.043
125
RLP002 Relapsing-Remitting Multiple Sclerosis 49 0.043
126
P MCL046 Mucolipidosis Iii Alpha/beta 43 0.043
127
MNK002 Monkeypox 40 0.043
128
NNT008 Neonatal Abstinence Syndrome 39 0.043
129
c HMP014 Hemophagocytic Lymphohistiocytosis, Familial, 4 35 0.043
130
OCH001 Ochronosis 34 0.043
131
TXC020 Toxic Oil Syndrome 32 0.043
132
MTG001 Metagonimiasis 22 0.043
133
HRD009 Hereditary Wilms' Tumor 21 0.043
134
SPN151 Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy 19 0.043
135
RMB001 Rombo Syndrome 18 0.043
136
LNR007 Linear and Whorled Nevoid Hypermelanosis 17 0.043
137
DTH005 Diethylstilbestrol Syndrome 16 0.043
138
PRD013 Periodic Fever, Familial, Autosomal Dominant 15 0.043
139
AML003 Amelia Cleft Lip Palate Hydrocephalus Iris Coloboma 1 0.043
140
P TYP009 Type 2 Diabetes Mellitus 93 0.035
141
CDS001 Cadasil 92 0.035
142
P PRK002 Parkinson's Disease 92 0.035
143
P PRS040 Prostate Cancer 91 0.035
144
HDG007 Hodgkin's Lymphoma 91 0.035
145
P SMT004 Smith-Lemli-Opitz Syndrome 84 0.035
146
P GST019 Gastrointestinal Stromal Tumor 83 0.035
147
P CSH001 Cushing's Syndrome 83 0.035
148
P OVR042 Ovarian Cancer 79 0.035
149
CRB011 Cerebrotendinous Xanthomatosis 77 0.035
150
SKN016 Skin Disease 75 0.035
151
P MYL005 Myelofibrosis 75 0.035
152
STR067 Stroke, Ischemic 74 0.035
153
P PRM006 Primary Biliary Cirrhosis 74 0.035
154
DBT011 Diabetic Retinopathy 73 0.035
155
P MLR004 Malaria 73 0.035
156
CRN211 Coronary Artery Disease 72 0.035
157
HYP004 Hypercalcemia 69 0.035
158
P GST044 Gastritis 68 0.035
159
c HYP086 Hypothyroidism 68 0.035
160
P PLY011 Polycystic Ovary Syndrome 68 0.035
161
VSC011 Vasculitis 67 0.035
162
c THY032 Thyroiditis 67 0.035
163
MSL001 Measles 66 0.035
164
DSS009 Disseminated Intravascular Coagulation 66 0.035
165
P GLM007 Glomerulonephritis 66 0.035
166
HYP056 Hypoglycemia 66 0.035
167
P AMY004 Amyloidosis 65 0.035
168
P BCK002 Beckwith-Wiedemann Syndrome 65 0.035
169
MXD005 Mixed Connective Tissue Disease 65 0.035
170
RHM001 Rheumatic Fever 65 0.035
171
SLY001 Sly Syndrome 65 0.035
172
CRM001 Crimean-Congo Hemorrhagic Fever 64 0.035
173
P PRS038 Personality Disorder 64 0.035
174
c PRP029 Porphyria 64 0.035
175
PRT037 Pertussis 64 0.035
176
P TRN001 Transthyretin Amyloidosis 64 0.035
177
BTN003 Biotinidase Deficiency 64 0.035
178
c EPD003 Epidermolysis Bullosa Simplex 63 0.035
179
P QFV001 Q Fever 62 0.035
180
URT001 Urethritis 62 0.035
181
ANG020 Angiosarcoma 61 0.035
182
c HYP076 Hyperthyroidism 61 0.035
183
ACT049 Acute Disseminated Encephalomyelitis 60 0.035
184
P HMR003 Hemorrhagic Disease 59 0.035
185
MCK005 Mckusick-Kaufman Syndrome 59 0.035
186
EPD016 Epidermolysis Bullosa 59 0.035
187
ACR008 Acrocallosal Syndrome 59 0.035
188
HLC001 Holocarboxylase Synthetase Deficiency 59 0.035
189
P CLF002 Cleft Palate 59 0.035
190
INT075 Intracranial Hypertension 59 0.035
191
CHR074 Choriocarcinoma 59 0.035
192
P SYN007 Synovitis 59 0.035
193
P RBL001 Rubella 59 0.035
194
PRV004 Periventricular Leukomalacia 58 0.035
195
P GLC007 Glaucoma 58 0.035
196
P MYP004 Myopathy 58 0.035
197
VSC002 Vascular Dementia 57 0.035
198
CRN017 Coronary Thrombosis 57 0.035
199
PRC013 Pericarditis 57 0.035
200
PRG009 Progressive Multifocal Leukoencephalopathy 57 0.035
201
P SPH001 Sapho Syndrome 56 0.035
202
PRT029 Parathyroid Adenoma 56 0.035
203
END031 Endometrial Stromal Sarcoma 56 0.035
204
ACN011 Acne 56 0.035
205
PLG002 Plague 56 0.035
206
HYP068 Hyperostosis 56 0.035
207
TTH006 Tooth Disease 55 0.035
208
P ANG015 Angioedema 54 0.035
209
NCR004 Nocardiosis 54 0.035
210
PRC012 Pericardial Effusion 54 0.035
211
CHC001 Chickenpox 54 0.035
212
MMB001 Membranoproliferative Glomerulonephritis 53 0.035
213
VLV010 Vulvovaginitis 53 0.035
214
P HRD057 Hereditary Pancreatitis 53 0.035
215
FLT006 Floating-Harbor Syndrome 52 0.035
216
CYS014 Cystadenocarcinoma 52 0.035
217
CRT013 Carotid Stenosis 51 0.035
218
OBS001 Obstructive Jaundice 51 0.035
219
c SPN049 Spinocerebellar Ataxia 51 0.035
220
PLM010 Pulmonary Edema 50 0.035
221
PHC013 Phaeochromocytoma 49 0.035
222
FCL012 Facial Paralysis 49 0.035
223
c KRN004 Kernicterus 47 0.035
224
BTN002 Boutonneuse Fever 47 0.035
225
BRS064 Bursitis 45 0.035
226
ASP007 Aspiration Pneumonia 45 0.035
227
EPM005 Epimerase Deficiency Galactosemia 45 0.035
228
P CNG052 Congenital Amegakaryocytic Thrombocytopenia 45 0.035
229
c FTL001 Fetal Alcohol Syndrome 44 0.035
230
BRL002 Buruli Ulcer Disease 43 0.035
231
c CTR098 Cataract 1, Multiple Types 43 0.035
232
CHL039 Choledocholithiasis 43 0.035
233
P MBS002 Moebius Syndrome 42 0.035
234
WGN003 Wagner Syndrome 42 0.035
235
TMR004 Tumor Necrosis Factor Receptor-Associated Periodic Syndrome 42 0.035
236
MMR004 Memory Impairment 41 0.035
237
INP001 Inappropriate Adh Syndrome 41 0.035
238
BTN004 Biotin Deficiency 41 0.035
239
MTR010 Mature Teratoma 40 0.035
240
c PTR004 Pterygium 40 0.035
241
SCR011 Scrapie 39 0.035
242
DNN002 Donnai-Barrow Syndrome 39 0.035
243
KYS001 Kyasanur Forest Disease 38 0.035
244
WNC001 Winchester Syndrome 37 0.035
245
LMB024 Limbic Encephalitis 37 0.035
246
ELP001 Elephantiasis 36 0.035
247
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 35 0.035
248
LKM006 Leukomalacia 35 0.035
249
AMN003 Amnestic Disorder 35 0.035
250
SYN036 Syncope 35 0.035
251
MYP071 Myopathy Due to Myoadenylate Deaminase Deficiency 35 0.035
252
CTS011 Cutis Marmorata Telangiectatica Congenita 35 0.035
253
AKN002 Akinetic Mutism 34 0.035
254
BDY001 Body Dysmorphic Disorder 30 0.035
255
P SPN205 Spinal Muscular Atrophy, X-Linked 2, Infantile 29 0.035
256
c LBR004 Leber Congenital Amaurosis 1 29 0.035
257
c CTR096 Cataract 6, Multiple Types 29 0.035
258
P FNC027 Fanconi Anemia, Complementation Group a 28 0.035
259
MNT006 Manitoba Oculotrichoanal Syndrome 27 0.035
260
SPR066 Superficial Siderosis 26 0.035
261
FCT008 Factitious Disorder 25 0.035
262
CRN046 Corneal Fleck Dystrophy 22 0.035
263
c CTR132 Cataract 3, Multiple Types 21 0.035
264
MMS001 Momo Syndrome 21 0.035
265
TST025 Testicular Microlithiasis 20 0.035
266
PRD003 Periodontosis 20 0.035
267
OPH001 Ophthalmomyiasis 20 0.035
268
SNL010 Senile Systemic Amyloidosis 19 0.035
269
UNC001 Uncombable Hair Syndrome 18 0.035
270
MLT011 Multiple Mucosal Neuroma 14 0.035
271
SHR004 Sharp Syndrome 12 0.035
272
MYC021 Mycobacterium Xenopi 12 0.035
273
MLT076 Multiple System Atrophy with Orthostatic Hypotension 10 0.035
274
UND003 Undifferentiated Connective Tissue Syndrome 10 0.035
275
c CTR102 Cataract 2, Multiple Types 9 0.035
276
CNT057 Central Centrifugal Cicatricial Alopecia 8 0.035
277
KRK002 Karak Syndrome 6 0.035
278
HND010 Handigodu Disease 6 0.035
279
YSH001 Yusho Disease 5 0.035
280
LYM053 Lymphomatous Thyroiditis 4 0.035
281
ABS002 Absence of Gluteal Muscle 3 0.035
282
BTH003 Bothriocephalosis 3 0.035
283
P AMY001 Amyotrophic Lateral Sclerosis 100 0.025
284
P FML011 Familial Adenomatous Polyposis 93 0.025
285
VNH001 Von Hippel-Lindau Disease 89 0.025
286
AND002 Androgen Insensitivity Syndrome 88 0.025
287
P FML021 Familial Hypercholesterolemia 87 0.025
288
P NMN002 Niemann-Pick Disease 87 0.025
289
P HRD008 Hereditary Hemorrhagic Telangiectasia 86 0.025
290
ADR007 Adrenoleukodystrophy 86 0.025
291
ACH004 Achondroplasia 83 0.025
292
CRH001 Crohn's Disease 83 0.025
293
P APL001 Aplastic Anemia 83 0.025
294
AGR001 Age Related Macular Degeneration 83 0.025
295
BLM001 Bloom Syndrome 82 0.025
296
P PRM021 Primary Pulmonary Hypertension 82 0.025
297
P PRP003 Porphyria Cutanea Tarda 81 0.025
298
P HMC003 Hemochromatosis 80 0.025
299
c MCP002 Mucopolysaccharidosis I 80 0.025
300
LSC001 Lesch-Nyhan Syndrome 79 0.025
301
P ACT074 Acute Lymphocytic Leukemia 77 0.025
302
P OST002 Osteoporosis 77 0.025
303
RNL002 Renal Agenesis 77 0.025
304
BRN024 Bronchitis 76 0.025
305
LVR012 Liver Cirrhosis 75 0.025
306
WRN001 Werner Syndrome 75 0.025
307
P WGN002 Wegener's Granulomatosis 75 0.025
308
ADD001 Addison's Disease 75 0.025
309
PRP027 Peripheral Vascular Disease 75 0.025
310
P ALP006 Alpha Thalassemia 75 0.025
311
P LYM007 Lymphangioleiomyomatosis 74 0.025
312
c CHR065 Chronic Myeloid Leukemia 74 0.025
313
P PRD006 Prader-Willi Syndrome 74 0.025
314
P OST012 Osteoarthritis 73 0.025
315
CHL065 Cholangiocarcinoma 73 0.025
316
SCH014 Schistosomiasis 72 0.025
317
PRN023 Prion Disease 71 0.025
318
ANR002 Aniridia 71 0.025
319
MYC006 Mycosis Fungoides 71 0.025
320
P MGR002 Migraine 71 0.025
321
P LYN001 Lynch Syndrome 70 0.025
322
CNT009 Central Core Myopathy 70 0.025
323
P DRM010 Dermatomyositis 70 0.025
324
WRM001 Wermer Syndrome 70 0.025
325
SPN038 Spina Bifida 70 0.025
326
P LVR013 Liver Disease 70 0.025
327
P ANG001 Angelman Syndrome 70 0.025
328
P RSP003 Respiratory Failure 70 0.025
329
P PRT010 Parathyroid Carcinoma 69 0.025
330
P END044 Endometriosis 69 0.025
331
P FML032 Familial Hypertrophic Cardiomyopathy 69 0.025
332
HLY001 Hailey-Hailey Disease 68 0.025
333
CCC001 Coccidioidomycosis 68 0.025
334
ART019 Aortic Valve Stenosis 68 0.025
335
c HMP007 Hemophilia 68 0.025
336
P MCP004 Mucopolysaccharidosis Iv 68 0.025
337
PLY017 Polyarteritis Nodosa 68 0.025
338
c THL005 Thalassemia 68 0.025
339
P ATP001 Atopic Dermatitis 68 0.025
340
DRM006 Dermatitis 68 0.025
341
P FCS002 Fucosidosis 67 0.025
342
P DRV001 Dravet Syndrome 67 0.025
343
P UVT001 Uveitis 67 0.025
344
KLP002 Klippel-Trenaunay Syndrome 67 0.025
345
P NRL016 Neural Tube Defects 67 0.025
346
P RCK004 Rickets 67 0.025
347
P DGR001 Digeorge Syndrome 67 0.025
348
c CRN037 Craniosynostosis 67 0.025
349
PSD012 Pseudoachondroplasia 67 0.025
350
P THY023 Thymoma 66 0.025
351
P THR015 Thrombophilia 66 0.025
352
DFC004 Deficiency Anemia 66 0.025
353
c NRN021 Neuronal Ceroid Lipofuscinosis 66 0.025
354
P ART023 Arthropathy 66 0.025
355
P HMP002 Hemophagocytic Lymphohistiocytosis 66 0.025
356
MLG056 Malignant Hyperthermia 65 0.025
357
CHR103 Charge Syndrome 65 0.025
358
HST011 Histoplasmosis 65 0.025
359
CHR066 Chronic Fatigue Syndrome 65 0.025
360
P CMP010 Complex Regional Pain Syndrome 65 0.025
361
MLD001 Melioidosis 65 0.025
362
P GRF002 Graft Versus Host Disease 65 0.025
363
ALK013 Alkaptonuria 65 0.025
364
MDD011 Mood Disorder 64 0.025
365
c SML001 Small Cell Carcinoma 64 0.025
366
PPL022 Papilloma 64 0.025
367
GLB015 Glioblastoma Multiforme 64 0.025
368
INS001 Insulinoma 64 0.025
369
c ENC004 Encephalitis 64 0.025
370
MTR014 Motor Neuron Disease 63 0.025
371
TTN003 Tetanus 63 0.025
372
P ESS001 Essential Tremor 63 0.025
373
ACQ007 Acquired Immunodeficiency Syndrome 63 0.025
374
TRG002 Trigeminal Neuralgia 63 0.025
375
P CND004 Candidiasis 63 0.025
376
P DFF005 Diffuse Large B-Cell Lymphoma 63 0.025
377
VCT001 Vacterl Association 63 0.025
378
P HRP006 Herpes Simplex 63 0.025
379
P GRV001 Graves' Disease 63 0.025
380
ECH003 Echinococcosis 63 0.025
381
P MCH002 Machado-Joseph Disease 63 0.025
382
PLM001 Pulmonary Tuberculosis 63 0.025
383
GLC003 Glucose Intolerance 63 0.025
384
THR004 Thrombocytosis 63 0.025
385
c CHR090 Chronic Lymphocytic Leukemia 63 0.025
386
PMP001 Pemphigus 63 0.025
387
P RTN012 Retinopathy of Prematurity 62 0.025
388
FLT001 Felty's Syndrome 62 0.025
389
RCT015 Reactive Arthritis 62 0.025
390
DDN006 Duodenitis 62 0.025
391
PSD007 Pseudomyxoma Peritonei 62 0.025
392
P OST009 Osteochondritis Dissecans 62 0.025
393
ALS001 Alstrom Syndrome 62 0.025
394
DWN001 Down Syndrome 62 0.025
395
c TXP001 Toxoplasmosis 62 0.025
396
CHL067 Cholecystitis 62 0.025
397
c MSC005 Muscular Dystrophy 62 0.025
398
BRN029 Brain Disease 62 0.025
399
P WVR001 Weaver Syndrome 62 0.025
400
P OCL017 Oculocutaneous Albinism Type 1 62 0.025
401
RTN023 Retinitis 61 0.025
402
P MLS001 Melas Syndrome 61 0.025
403
P GTR002 Goiter 61 0.025
404
P INT068 Intestinal Disease 61 0.025
405
P ACT009 Acute Monocytic Leukemia 61 0.025
406
P ANP001 Anaplastic Large Cell Lymphoma 61 0.025
407
c ACT075 Acute Myocardial Infarction 61 0.025
408
HYP014 Hyperuricemia 61 0.025
409
CRY004 Cryoglobulinemia 61 0.025
410
STR008 Strongyloidiasis 61 0.025
411
BRN002 Bronchiolitis 61 0.025
412
CHL014 Cholera 61 0.025
413
DNT005 Dentatorubral-Pallidoluysian Atrophy 61 0.025
414
THY019 Thyroid Hormone Resistance Syndrome 61 0.025
415
P LPS002 Liposarcoma 61 0.025
416
P MMB002 Membranous Glomerulonephritis 60 0.025
417
P VLC001 Velocardiofacial Syndrome 60 0.025
418
CLR003 Clear Cell Adenocarcinoma 60 0.025
419
RTN017 Retinal Detachment 60 0.025
420
c OCL002 Oculocutaneous Albinism 60 0.025
421
PLM034 Pulmonary Emphysema 60 0.025
422
EYD002 Eye Disease 60 0.025
423
PRT011 Protein C Deficiency 60 0.025
424
c MLG069 Malignant Hypertension 60 0.025
425
MYX005 Myxoid Liposarcoma 59 0.025
426
P RNL014 Renal Cell Carcinoma 59 0.025
427
CHR001 Churg-Strauss Syndrome 59 0.025
428
SCR008 Scrub Typhus 59 0.025
429
MCL002 Macular Corneal Dystrophy 59 0.025
430
ALV005 Alveolar Soft Part Sarcoma 59 0.025
431
OST017 Osteomyelitis 59 0.025
432
CMM005 Common Cold 59 0.025
433
c MNC007 Monocytic Leukemia 59 0.025
434
PRN009 Paranoid Schizophrenia 59 0.025
435
CLF001 Cleft Lip 59 0.025
436
DPH001 Diphtheria 59 0.025
437
c FML035 Familial Hyperlipidemia 59 0.025
438
ARR001 Arrhythmogenic Right Ventricular Dysplasia 59 0.025
439
c SCL016 Scleroderma 59 0.025
440
PLY023 Polycystic Liver Disease 59 0.025
441
MYM001 Myoma 59 0.025
442
P MJR001 Major Depressive Disorder 58 0.025
443
P HMN013 Hemangiopericytoma 58 0.025
444
P HYP083 Hypopituitarism 58 0.025
445
LYM021 Lymphadenitis 58 0.025
446
LYM027 Lymphopenia 58 0.025
447
P ESN001 Eosinophilic Esophagitis 58 0.025
448
TYP011 Typhus 58 0.025
449
NRL004 Neuroleptic Malignant Syndrome 58 0.025
450
APP008 Appendicitis 57 0.025
451
CYS008 Cystic Echinococcosis 57 0.025
452
P DBT005 Diabetes Insipidus 57 0.025
453
STT002 Status Asthmaticus 57 0.025
454
P ATS007 Autism Spectrum Disorder 57 0.025
455
ANR008 Aneurysm Disease 57 0.025
456
NRN001 Neuroendocrine Carcinoma 57 0.025
457
P PSR001 Psoriatic Arthritis 57 0.025
458
c HRM001 Hermansky-Pudlak Syndrome 57 0.025
459
SRS001 Serous Cystadenocarcinoma 57 0.025
460
P SCL015 Scleritis 57 0.025
461
MTN003 Motion Sickness 57 0.025
462
SCH012 Schizoaffective Disorder 57 0.025
463
RSC001 Rosacea 57 0.025
464
DRG003 Drug Dependence 57 0.025
465
P LYM026 Lymphoblastic Leukemia 56 0.025
466
P PLM006 Pulmonary Alveolar Proteinosis 56 0.025
467
P MYC008 Myocarditis 56 0.025
468
P PRT008 Proteus Syndrome 56 0.025
469
BLL003 Bell's Palsy 56 0.025
470
HYP006 Hypertensive Heart Disease 56 0.025
471
LYM009 Lymphocytic Choriomeningitis 56 0.025
472
MDS022 Mediastinitis 56 0.025
473
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 56 0.025
474
P SYP003 Syphilis 56 0.025
475
MMM001 Mammary Paget's Disease 56 0.025
476
c OPN001 Open-Angle Glaucoma 56 0.025
477
RBS001 Rabies 56 0.025
478
GLM008 Glomus Tumor 56 0.025
479
P INF032 Infertility 56 0.025
480
P HYP055 Hypoplastic Left Heart Syndrome 56 0.025
481
CLL003 Cellulitis 56 0.025
482
BRS051 Breast Disease 56 0.025
483
P ALT001 Alternating Hemiplegia of Childhood 55 0.025
484
ORL005 Oral Candidiasis 55 0.025
485
NNS002 Nonspecific Interstitial Pneumonia 55 0.025
486
AVN001 Avian Influenza 55 0.025
487
VRY001 Very Long-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 55 0.025
488
ACT119 Acute Promyelocytic Leukemia 55 0.025
489
PLM020 Pleomorphic Xanthoastrocytoma 55 0.025
490
SPT005 Spotted Fever 55 0.025
491
MCR004 Macroglobulinemia 55 0.025
492
P MTR005 Mitral Valve Prolapse 55 0.025
493
BCT004 Bacteriuria 55 0.025
494
TCK001 Tick-Borne Encephalitis 55 0.025
495
P PLY006 Polydactyly 54 0.025
496
c BCT007 Bacterial Meningitis 54 0.025
497
EXS001 Exostosis 54 0.025
498
NWC001 Newcastle Disease 54 0.025
499
P JRV001 Jervell-Lange Nielsen Syndrome 54 0.025
500
EGG001 Egg Allergy 54 0.025
501
c DNT011 Dentinogenesis Imperfecta 54 0.025
502
CLL002 Collecting Duct Carcinoma 54 0.025
503
MYL003 Myeloid Sarcoma 54 0.025
504
MLB002 Male Breast Cancer 54 0.025
505
SBC001 Subacute Sclerosing Panencephalitis 53 0.025
506
c VNT002 Ventricular Septal Defect 53 0.025
507
P BTM001 Beta-Mannosidosis 53 0.025
508
c CTR002 Cataract 53 0.025
509
P LFR002 Lafora Disease 53 0.025
510
GNR005 Gonorrhea 53 0.025
511
END041 Endometrial Adenocarcinoma 53 0.025
512
P MGR003 Migraine with Aura 53 0.025
513
CNR004 Cone-Rod Dystrophy 2 53 0.025
514
SSN001 Seasonal Affective Disorder 53 0.025
515
P FNC004 Fanconi Syndrome 53 0.025
516
P CYS010 Cystinosis 53 0.025
517
CWP001 Cowpox 53 0.025
518
DRM004 Dermatofibrosarcoma 53 0.025
519
MRG003 Marginal Zone B-Cell Lymphoma 53 0.025
520
PRP023 Peripheral Neuropathy 53 0.025
521
SPL004 Splenic Marginal Zone Lymphoma 53 0.025
522
NSP001 Nasopharynx Carcinoma 53 0.025
523
ADL002 Adult Syndrome 52 0.025
524
P GND004 Gonadal Dysgenesis 52 0.025
525
MGR001 Migraine Without Aura 52 0.025
526
DST006 Diastolic Heart Failure 52 0.025
527
MNR002 Meniere's Disease 52 0.025
528
MYL001 Myelitis 52 0.025
529
CHL061 Childhood Leukemia 52 0.025
530
P CLR017 Clear Cell Sarcoma 52 0.025
531
LPM005 Lipomatosis 52 0.025
532
P INT063 Intellectual Disability 51 0.025
533
SYS003 Systolic Heart Failure 51 0.025
534
c PRM010 Primary Open Angle Glaucoma 51 0.025
535
EST003 Eastern Equine Encephalitis 51 0.025
536
c SPN016 Spondylocostal Dysostosis 51 0.025
537
FLL013 Follicular Dendritic Cell Sarcoma 51 0.025
538
THY022 Thymic Carcinoma 51 0.025
539
SCB001 Scabies 51 0.025
540
VTM002 Vitamin B12 Deficiency 51 0.025
541
CYS009 Cystadenoma 51 0.025
542
BLS002 Blastomycosis 51 0.025
543
BRN018 Borna Disease 51 0.025
544
DBW001 Dubowitz Syndrome 51 0.025
545
PPL018 Papillary Adenocarcinoma 51 0.025
546
ALB002 Albinism 50 0.025
547
DBT006 Diabetic Macular Edema 50 0.025
548
P ATR005 Atrophic Gastritis 50 0.025
549
ANG011 Angiodysplasia 50 0.025
550
OLG003 Oligohydramnios 50 0.025
551
ALV006 Alveolar Capillary Dysplasia 50 0.025
552
RFT001 Rift Valley Fever 50 0.025
553
PYR014 Pyridoxine-Dependent Epilepsy 50 0.025
554
LGS001 Legius Syndrome 50 0.025
555
c HPT007 Hepatitis E 50 0.025
556
ADN020 Adenosarcoma 49 0.025
557
c PRG013 Paraganglioma 49 0.025
558
ORC001 Orchitis 49 0.025
559
P SHR029 Short Syndrome 49 0.025
560
PLY012 Polyhydramnios 49 0.025
561
P ACH020 Achromatopsia 2 49 0.025
562
MTB004 Metabolic Acidosis 49 0.025
563
PRS039 Prostate Adenocarcinoma 48 0.025
564
GND002 Gender Identity Disorder 48 0.025
565
JCB001 Jacobsen Syndrome 48 0.025
566
c ACT078 Acute Porphyria 48 0.025
567
TND004 Tendinopathy 48 0.025
568
P CYS017 Cystic Teratoma 48 0.025
569
P MWT001 Mowat-Wilson Syndrome 48 0.025
570
ALC010 Alcoholic Cardiomyopathy 48 0.025
571
RDC002 Radiculopathy 48 0.025
572
c KBK001 Kabuki Syndrome 48 0.025
573
CHK001 Chikungunya 48 0.025
574
c BRC006 Brachydactyly 48 0.025
575
GST040 Gastric Adenocarcinoma 48 0.025
576
SMN007 Seminoma 48 0.025
577
MNN014 Mononeuritis 48 0.025
578
CRN012 Craniometaphyseal Dysplasia 47 0.025
579
OST097 Osteoporotic Fracture 47 0.025
580
PTY003 Pityriasis Rubra Pilaris 47 0.025
581
P PRM126 Primary Peritoneal Carcinoma 47 0.025
582
ASC002 Ascariasis 47 0.025
583
END028 Endemic Goiter 47 0.025
584
BRN056 Bronchopulmonary Dysplasia 47 0.025
585
CTY001 Cat Eye Syndrome 47 0.025
586
ANR018 Anorchia 47 0.025
587
EPD029 Epidermolysis Bullosa Simplex, Generalized 47 0.025
588
P PRM100 Primary Spontaneous Pneumothorax 46 0.025
589
HRT012 Heart Valve Disease 46 0.025
590
CHL052 Choledochal Cyst 46 0.025
591
CRD002 Cri-Du-Chat Syndrome 46 0.025
592
P BRS044 Breast Adenocarcinoma 46 0.025
593
DNR002 Duane-Radial Ray Syndrome 46 0.025
594
MCN008 Mucinous Cystadenocarcinoma 46 0.025
595
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 46 0.025
596
OVR012 Ovarian Serous Cystadenocarcinoma 46 0.025
597
P FNN001 Finnish Type Amyloidosis 46 0.025
598
MTS001 Mutism 46 0.025
599
c CHR285 Chronic Myelomonocytic Leukemia 46 0.025
600
ACR005 Acrodermatitis 45 0.025
601
ANS003 Anisakiasis 45 0.025
602
LPD006 Lipoid Proteinosis 45 0.025
603
P ICH047 Ichthyosis, Congenital, Autosomal Recessive 1 45 0.025
604
LNG039 Lung Squamous Cell Carcinoma 45 0.025
605
LSS003 Lassa Fever 45 0.025
606
LYM020 Lymph Node Cancer 45 0.025
607
FRN002 Frontal Lobe Epilepsy 44 0.025
608
P LSS005 Lissencephaly 1 44 0.025
609
c STC001 Stickler Syndrome 44 0.025
610
NPH018 Nephrogenic Systemic Fibrosis 44 0.025
611
HST006 Histidinemia 44 0.025
612
CRY001 Cryptogenic Organizing Pneumonia 44 0.025
613
P AZS001 Azoospermia 44 0.025
614
TLR001 Tularemia 44 0.025
615
EPT020 Epithelioid Hemangioendothelioma 44 0.025
616
BRB001 Beriberi 43 0.025
617
c ORF002 Orofacial Cleft 43 0.025
618
P D2H001 D-2-Hydroxyglutaric Aciduria 43 0.025
619
c ICH049 Ichthyosis, Congenital, Autosomal Recessive 2 43 0.025
620
AND003 Andersen-Tawil Syndrome 43 0.025
621
INT079 Intrahepatic Cholangiocarcinoma 43 0.025
622
SPN050 Spinocerebellar Degeneration 43 0.025
623
c USH006 Usher Syndrome, Type 1b 43 0.025
624
ETH011 Ethylmalonic Encephalopathy 43 0.025
625
EPD037 Epidermal Nevus 43 0.025
626
TBR008 Tuberculous Peritonitis 43 0.025
627
MYS001 Myositis Ossificans 43 0.025
628
BRN038 Bronchial Disease 42 0.025
629
GLD002 Goldberg-Shprintzen Megacolon Syndrome 42 0.025
630
P PRM052 Primary Progressive Aphasia 42 0.025
631
BRN013 Bronchiolitis Obliterans Organizing Pneumonia 42 0.025
632
P CTR103 Cataract 4, Multiple Types 42 0.025
633
c CNG224 Congenital Disorder of Glycosylation Type 1a 42 0.025
634
FRM007 Freeman Sheldon Syndrome 42 0.025
635
BLP005 Blepharitis 42 0.025
636
PSD010 Pseudogout 42 0.025
637
PLN006 Poland Syndrome 42 0.025
638
ANT024 Anthrax Disease 41 0.025
639
GND001 Gonadoblastoma 41 0.025
640
DNR001 Duane Retraction Syndrome 41 0.025
641
c CHR130 Charcot-Marie-Tooth Disease Type 1b 41 0.025
642
NCR007 Necrotizing Fasciitis 41 0.025
643
P RBN002 Robinow Syndrome 41 0.025
644
BSL033 Basal Ganglia Cancification, Idiopathic, 1 41 0.025
645
MDL009 Medullary Sponge Kidney 41 0.025
646
c WLM002 Wilms Tumor 41 0.025
647
EPC002 Epicondylitis 41 0.025
648
OBS004 Obstructive Hydrocephalus 41 0.025
649
P DYS026 Dysfibrinogenemia 41 0.025
650
RMS001 Rem Sleep Behavior Disorder 40 0.025
651
P VGN017 Vaginal Cancer 40 0.025
652
TYP013 Type 1 Von Willebrand Disease 40 0.025
653
P HMR005 Hemorrhoid 39 0.025
654
DCB001 Decubitus Ulcer 39 0.025
655
NCR002 Necrobiosis Lipoidica 39 0.025
656
SPN028 Spondyloepimetaphyseal Dysplasia, Strudwick Type 39 0.025
657
ACT099 Acute Fatty Liver of Pregnancy 39 0.025
658
BLK001 Balkan Nephropathy 39 0.025
659
LNG030 Lung Adenoma 39 0.025
660
P XNT005 Xanthinuria Type 1 39 0.025
661
PRN014 Paronychia 39 0.025
662
MTR003 Mitral Valve Stenosis 39 0.025
663
PNC041 Pancreatic Ductal Adenocarcinoma 38 0.025
664
GST052 Gestational Choriocarcinoma 38 0.025
665
URT004 Urethral Syndrome 38 0.025
666
HRP002 Herpes Gestationis 38 0.025
667
INF013 Inferior Myocardial Infarction 38 0.025
668
P SLL003 Salla Disease 38 0.025
669
FGS001 Fg Syndrome 38 0.025
670
PRM018 Primary Hypertrophic Osteoarthropathy 38 0.025
671
ACL001 Acalculous Cholecystitis 37 0.025
672
MGS001 Megaesophagus 37 0.025
673
EMN001 Emanuel Syndrome 36 0.025
674
P GLM006 Glomangioma 36 0.025
675
HDN002 Head Injury 36 0.025
676
c LTT001 Lattice Corneal Dystrophy 36 0.025
677
TNC003 Tinea Corporis 36 0.025
678
c 3Q2003 3q29 Microdeletion Syndrome 36 0.025
679
P DYS005 Dyslexia 36 0.025
680
P XLN007 X-Linked Disease 36 0.025
681
MCK002 Meckel's Diverticulum 36 0.025
682
OVR059 Ovary Adenocarcinoma 36 0.025
683
c ACT004 Acute Diarrhea 35 0.025
684
CTS005 Catastrophic Antiphospholipid Syndrome 35 0.025
685
TBS001 Tabes Dorsalis 35 0.025
686
RTR001 Retrograde Amnesia 35 0.025
687
P OPT051 Opitz Gbbb Syndrome, Type I 35 0.025
688
STN007 Stenotrophomonas Maltophilia 35 0.025
689
MNT147 Mental Retardation 35 0.025
690
DFN222 Deafness-Dystonia-Optic Neuronopathy Syndrome 35 0.025
691
THM001 Thomsen Disease 35 0.025
692
DSQ001 Desquamative Interstitial Pneumonia 35 0.025
693
CRP002 Croup 34 0.025
694
RPP001 Rapp-Hodgkin Syndrome 34 0.025
695
MLT075 Multifocal Motor Neuropathy 34 0.025
696
MNT061 Mental Retardation-Hypotonic Facies Syndrome, X-Linked 34 0.025
697
RHB022 Rhabdoid Tumors, Somatic 34 0.025
698
INT020 Intravenous Leiomyomatosis 34 0.025
699
c OCL035 Oculocutaneous Albinism Type 1b 34 0.025
700
MYC013 Mycobacterium Abscessus 33 0.025
701
UNV001 Unverricht-Lundborg Syndrome 33 0.025
702
MNT003 Mental Retardation in Cri-Du-Chat Syndrome 33 0.025
703
SPR009 Sporadic Breast Cancer 33 0.025
704
MNN002 Mononeuritis Multiplex 33 0.025
705
TNC001 Tinea Cruris 33 0.025
706
RSD004 Rosai-Dorfman Disease 33 0.025
707
SLL001 Sialolithiasis 33 0.025
708
STC004 Stachybotrys Chartarum 32 0.025
709
c OST039 Osteogenesis Imperfecta Type 5 32 0.025
710
HYP034 Hypertensive Encephalopathy 32 0.025
711
c PRN026 Porencephaly 32 0.025
712
TYL002 Tylosis with Esophageal Cancer 32 0.025
713
P CHR288 Chronic Recurrent Multifocal Osteomyelitis 31 0.025
714
HRP001 Herpangina 31 0.025
715
CTN013 Cutaneous Anthrax 31 0.025
716
EHL012 Ehlers-Danlos Syndrome Dermatosparaxis Type 31 0.025
717
VGN019 Vaginal Discharge 31 0.025
718
TTZ002 Tietz Syndrome 31 0.025
719
c ICH041 Ichthyosis, Autosomal Recessive 4b 31 0.025
720
P CMM008 Communicating Hydrocephalus 31 0.025
721
P CNG119 Congenital Porphyria 31 0.025
722
P SVR013 Severe Congenital Neutropenia Autosomal Recessive 3 31 0.025
723
BRK004 Barakat Syndrome 30 0.025
724
PLC009 Placenta Praevia 30 0.025
725
BRS061 Breast Sarcoma 30 0.025
726
NRC001 Neurocirculatory Asthenia 30 0.025
727
INF045 Infantile Convulsions and Paroxysmal Choreoathetosis, Familial 30 0.025
728
VLV032 Vulva Cancer 30 0.025
729
CHR028 Chronic Wasting Disease 29 0.025
730
CRN061 Corneal Dystrophy Avellino Type 29 0.025
731
PMP002 Pemphigoid Gestationis 29 0.025
732
c DMN027 Dominant Optic Atrophy 29 0.025
733
PYR011 Pyropoikilocytosis 29 0.025
734
SBD001 Subdural Empyema 29 0.025
735
ANH001 Ainhum 29 0.025
736
c LSS006 Lissencephaly 2 29 0.025
737
END014 Endemic Typhus 29 0.025
738
DYS036 Dysequilibrium Syndrome 28 0.025
739
INT003 Intracranial Hypotension 28 0.025
740
CHR084 Chromosomal Disease 28 0.025
741
SPL007 Splenic Abscess 28 0.025
742
KKC001 Kikuchi Disease 28 0.025
743
PST086 Posterior Cortical Atrophy 28 0.025
744
TTZ001 Tietze's Syndrome 28 0.025
745
END060 Endolymphatic Hydrops 27 0.025
746
SPP009 Sepiapterin Reductase Deficiency 27 0.025
747
CNZ006 Coenzyme Q10 Deficiency, Primary, 1 27 0.025
748
CWC001 Cowchock Syndrome 27 0.025
749
OCL025 Ocular Toxoplasmosis 27 0.025
750
TRN021 Transaldolase Deficiency 27 0.025
751
CGN002 Cogan's Syndrome 27 0.025
752
c LMB018 Limb-Girdle Muscular Dystrophy, Type 1a 27 0.025
753
P SKN012 Skin Carcinoma in Situ 27 0.025
754
OVR047 Ovarian Cystadenocarcinoma 27 0.025
755
INT011 Interstitial Emphysema 26 0.025
756
FMR003 Femoral Neuropathy 26 0.025
757
PRS051 Parastremmatic Dwarfism 26 0.025
758
c ORF007 Orofaciodigital Syndrome 2 26 0.025
759
BRN005 Brain Glioblastoma Multiforme 26 0.025
760
PNM003 Pneumatosis Cystoides Intestinalis 26 0.025
761
P DNT025 Dentinogenesis Imperfecta 1 26 0.025
762
MDL006 Madelung Disease 26 0.025
763
CND006 Candida Glabrata 26 0.025
764
JPN001 Japanese Spotted Fever 26 0.025
765
TRL003 Toriello Carey Syndrome 25 0.025
766
CNR008 Cone-Rod Dystrophy Amelogenesis Imperfecta 25 0.025
767
ANS006 Anosognosia 25 0.025
768
NRC003 Narcissistic Personality Disorder 25 0.025
769
c CTR124 Cataract 10, Multiple Types 25 0.025
770
HST001 Histrionic Personality Disorder 25 0.025
771
DYS009 Dysthymic Disorder 25 0.025
772
c CHR057 Chronic Laryngitis 25 0.025
773
c SPN073 Spinocerebellar Ataxia Type 12 25 0.025
774
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 25 0.025
775
SML008 Small Intestine Lymphoma 25 0.025
776
DND007 Dandy-Walker Like Malformation with Atrioventricular Septal Defect 25 0.025
777
IDM001 Ideomotor Apraxia 25 0.025
778
TRT003 Tertiary Syphilis 25 0.025
779
CNG049 Congenital Stromal Corneal Dystrophy 24 0.025
780
c PPL025 Popliteal Pterygium Syndrome 24 0.025
781
MYC018 Mycobacterium Malmoense 24 0.025
782
c TRP015 Triphalangeal Thumb 24 0.025
783
c ACT072 Acute Laryngitis 24 0.025
784
MSN002 Mesenteric Lymphadenitis 24 0.025
785
BLN002 Balanitis Xerotica Obliterans 23 0.025
786
PGM003 Pigmentation Disease 23 0.025
787
P CTR101 Cataract 39, Multiple Types, Autosomal Dominant 23 0.025
788
YNG002 Young Syndrome 23 0.025
789
LJH001 Lujo Hemorrhagic Fever 23 0.025
790
EXS013 Exstrophy-Epispadias Complex 23 0.025
791
OMS001 Omsk Hemorrhagic Fever 23 0.025
792
CLC010 Calcifying Epithelial Odontogenic Tumor 23 0.025
793
MLK004 Malakoplakia 23 0.025
794
c FRN036 Frontonasal Dysplasia 1 22 0.025
795
PLR006 Pleural Cancer 22 0.025
796
RCT017 Rectal Disease 22 0.025
797
PLY031 Polydactyly Myopia Syndrome 22 0.025
798
ATM021 Autoimmune Inner Ear Disease 22 0.025
799
c ELL007 Elliptocytosis-1 21 0.025
800
STY001 Satoyoshi Syndrome 21 0.025
801
HRT003 Heart Lymphoma 21 0.025
802
ANN010 Anonychia-Onychodystrophy with Hypoplasia or Absence of Distal Phalanges 21 0.025
803
ADT001 Auditory Agnosia 21 0.025
804
INN003 Iniencephaly 21 0.025
805
HRD052 Hereditary Mucoepithelial Dysplasia 21 0.025
806
c ACT059 Acute Maxillary Sinusitis 21 0.025
807
c TTR013 Tetrasomy X 20 0.025
808
BNT002 Bantu Siderosis 20 0.025
809
CNG219 Congenital Aural Atresia 20 0.025
810
NRM009 Normokalemic Periodic Paralysis 20 0.025
811
c AMY008 Amyotrophic Lateral Sclerosis Type 2 20 0.025
812
c HYP440 Hyperphosphatasia with Mental Retardation Syndrome 20 0.025
813
c PST061 Posterior Polymorphous Corneal Dystrophy 19 0.025
814
EPS001 Epstein-Barr Virus Hepatitis 19 0.025
815
FMR012 Femur-Fibula-Ulna Complex 19 0.025
816
c NTR033 Neutropenia, Severe Congenital 1, Autosomal Dominant 19 0.025
817
LKC003 Leukocyte Disease 19 0.025
818
GTP001 Gait Apraxia 19 0.025
819
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 19 0.025
820
PRG072 Progressive Myoclonic Epilepsy 3 with or Without Intracellular Inclusions 19 0.025
821
FML211 Familial Papillary or Follicular Thyroid Carcinoma 19 0.025
822
LRP001 Leri Pleonosteosis 19 0.025
823
PNT006 Pentosuria 19 0.025
824
HYP160 Hyperkeratosis Lenticularis Perstans 19 0.025
825
PRS002 Prostate Lymphoma 19 0.025
826
URC001 Urachus Cancer 18 0.025
827
SHR027 Short Stature Wormian Bones Dextrocardia 18 0.025
828
PRN010 Paranoid Personality Disorder 18 0.025
829
OVR027 Ovarian Squamous Cell Carcinoma 18 0.025
830
NTV001 Native American Myopathy 18 0.025
831
KHL001 Kohler's Disease 18 0.025
832
ATY013 Atypical Rett Syndrome 18 0.025
833
PLM015 Pulmonary Systemic Sclerosis 18 0.025
834
FRS004 Free Sialic Acid Storage Disorders 17 0.025
835
SML010 Simultanagnosia 17 0.025
836
CTR010 Cataract Congenital Volkmann Type 17 0.025
837
NRS005 Neurosarcoidosis 17 0.025
838
OSL001 Oslam Syndrome 17 0.025
839
ARR026 Arrhythmogenic Right Ventricular Dysplasia 1 17 0.025
840
c CRD093 Cardiomyopathy, Dilated, 1a 17 0.025
841
RBN004 Robin Sequence and Oligodactyly 16 0.025
842
c PRK057 Parkinson Disease, Late-Onset 16 0.025
843
HYP145 Hyperbetaalaninemia 16 0.025
844
c CHR247 Chromosome 4p Deletion 16 0.025
845
ISS001 Isosporiasis 15 0.025
846
AMR001 American Histoplasmosis 15 0.025
847
NVS007 Nevus of Ota 15 0.025
848
CHR158 Charles Bonnet Syndrome 15 0.025
849
NNN015 Noonan-Like/multiple Giant Cell Lesion Syndrome 15 0.025
850
RHM006 Rheumatic Aortic Valve Stenosis 15 0.025
851
CRN126 Corneal Dystrophy, Lisch Epithelial 15 0.025
852
TRN028 Transient Acantholytic Dermatosis 14 0.025
853
PRM040 Primary Basilar Impression 14 0.025
854
AKN001 Akinetopsia 14 0.025
855
SCH004 Schizoid Personality Disorder 14 0.025
856
c DST049 Distal Spinal Muscular Atrophy Type 3 14 0.025
857
c RNP003 Renpenning Syndrome 1 14 0.025
858
HYP548 Hypogonadotropic Hypogonadism 2 with or Without Anosmia 14 0.025
859
SCL022 Scleredema 14 0.025
860
ORP002 Oropouche Fever 14 0.025
861
PSD027 Pseudoaminopterin Syndrome 13 0.025
862
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 13 0.025
863
P ENC021 Encephalopathy, Neonatal Severe 13 0.025
864
SBP006 Subepithelial Mucinous Corneal Dystrophy 13 0.025
865
c RNG013 Ring Chromosome 18 13 0.025
866
HRL002 Harlequin Syndrome 13 0.025
867
c PRD030 Periodontitis 1, Juvenile 13 0.025
868
ALK001 Alkhurma Hemorrhagic Fever 12 0.025
869
ORF018 Orofacial Cleft11 12 0.025
870
RGN005 Regional Odontodysplasia 12 0.025
871
ACC005 Accessory Pancreas 12 0.025
872
ERY040 Erythema Palmaris Hereditarium 12 0.025
873
c ICH040 Ichthyosis, Congenital, Autosomal Recessive 4a 12 0.025
874
c MNT171 Mental Retardation, Autosomal Dominant 17 12 0.025
875
APP004 Appendix Mucinous Cystadenocarcinoma 11 0.025
876
c CTR118 Cataract 14, Multiple Types 11 0.025
877
PSD078 Pseudofolliculitis Barbae 11 0.025
878
P HYD015 Hydroa Vacciniforme 11 0.025
879
c ICH042 Ichthyosis, Congenital, Autosomal Recessive 6 11 0.025
880
INF048 Infantile Histiocytoid Cardiomyopathy 11 0.025
881
TRS006 Triose Phosphate-Isomerase Deficiency 11 0.025
882
c ICH050 Ichthyosis, Congenital, Autosomal Recessive 5 10 0.025
883
DYS135 Dysphagia Lusoria 10 0.025
884
PRM056 Primrose Syndrome 10 0.025
885
ACC001 Accessory Nerve Disease 10 0.025
886
SPN187 Spinocerebellar Atrophy 10 0.025
887
c ICH038 Ichthyosis, Congenital, Autosomal Recessive 3 10 0.025
888
CNT067 Central Cord Syndrome 9 0.025
889
GST005 Gastric Hemangioma 9 0.025
890
c CTR122 Cataract 5, Multiple Types 9 0.025
891
c CTR130 Cataract 9, Multiple Types 9 0.025
892
BLN017 Balint Syndrome 9 0.025
893
DPH012 Diphallia 9 0.025
894
PRV008 Parvovirus Antenatal Infection 9 0.025
895
c CTS012 Cutis Verticis Gyrata 9 0.025
896
BNG042 Benign Multicystic Peritoneal Mesothelioma 9 0.025
897
ELC001 Elective Mutism 8 0.025
898
CTR043 Cataract, Pulverulent or Cerulean, with or Without Microcornea 8 0.025
899
c ICH039 Ichthyosis, Congenital, Autosomal Recessive 10 8 0.025
900
c ICH048 Ichthyosis, Congenital, Autosomal Recessive 9 8 0.025
901
MNM003 Minimally Differentiated Acute Myeloblastic Leukemia 8 0.025
902
URC004 Urachal Cancer 8 0.025
903
BRN045 Brunner Syndrome 8 0.025
904
c CTR104 Cataract 18, Autosomal Recessive 7 0.025
905
c CTR113 Cataract 11, Multiple Types 7 0.025
906
c CTR115 Cataract 16, Multiple Types 7 0.025
907
c CTR129 Cataract 31, Multiple Types 7 0.025
908
c CTR133 Cataract 22, Autosomal Recessive 7 0.025
909
HYP512 Hyperproinsulinemia, Familial 7 0.025
910
c ICH044 Ichthyosis, Congenital, Autosomal Recessive 8 7 0.025
911
KYR001 Kyrle Disease 7 0.025
912
JMP002 Jumping Frenchmen of Maine 7 0.025
913
c CTR131 Cataract 17, Multiple Types 6 0.025
914
OBS014 Obsessive-Compulsive Disorder, Protection Against 6 0.025
915
c PRX050 Peroxisome Biogenesis Disorder 9b 6 0.025
916
PST044 Postorgasmic Illness Syndrome 6 0.025
917
UHL001 Uhl Anomaly 6 0.025
918
HYD031 Hydroxyprolinemia 6 0.025
919
MLP004 Malpuech Facial Clefting Syndrome 6 0.025
920
CNG067 Congenital Cystic Eye 5 0.025
921
CRT056 Carotidynia 5 0.025
922
c ICH045 Ichthyosis, Congenital, Autosomal Recessive 7 5 0.025
923
MRG007 Morgellons 5 0.025
924
PHS019 Phosphohydroxylysinuria 5 0.025
925
c PRX053 Peroxisome Biogenesis Disorder 14b 5 0.025
926
SPN092 Spinal Shock 5 0.025
927
PRS107 Persistent Sexual Arousal Syndrome 4 0.025
928
MCK010 Mickleson Syndrome 2 0.025
929
MTR033 Motor Sensory Neuropathy Type 1 Aplasia Cutis Congenita 2 0.025