Search results for twinning

1155 hits were found for twinning

# Family MCID Name MIFTS Score
1
TWN001 Twin-to-Twin Transfusion Syndrome 46 12.243
2
c RNL090 Renal Tubular Dysgenesis Due to Twin-Twin Transfusion 6 3.628
3
OVR079 Ovarian Response to Fsh Stimulation 21 2.553
4
P PLY018 Polycythemia 56 0.170
5
PLY012 Polyhydramnios 46 0.159
6
CRB009 Cerebritis 39 0.156
7
ANN002 Anencephaly 53 0.145
8
P OBS005 Obesity 91 0.115
9
P HRT032 Heart Disease 75 0.113
10
P CRV039 Cervicitis 45 0.111
11
CHL071 Child Syndrome 59 0.104
12
KDS001 Kid Syndrome 57 0.104
13
OLG003 Oligohydramnios 52 0.104
14
HYD012 Hydrops Fetalis 43 0.102
15
P CRD011 Cardiomyopathy 67 0.100
16
CYT008 Cytomegalovirus Infection 51 0.091
17
DWN001 Down Syndrome 69 0.089
18
CHR005 Chorioamnionitis 47 0.089
19
CNG069 Congenital Cytomegalovirus 33 0.086
20
P THY032 Thyroiditis 53 0.084
21
SRN002 Sirenomelia 33 0.084
22
ISC004 Ischemia 59 0.081
23
ADL002 Adult Syndrome 57 0.081
24
P LKM002 Leukemia 72 0.079
25
P PRS038 Personality Disorder 61 0.073
26
OMP004 Omphalocele 51 0.073
27
BRT030 Birth Defects 44 0.073
28
P HYP086 Hypothyroidism 60 0.070
29
URT039 Urticaria 56 0.070
30
ECT026 Ectopic Pregnancy 48 0.070
31
PNT005 Pentalogy of Cantrell 30 0.070
32
NLL002 Null Syndrome 26 0.070
33
P PLM037 Pulmonary Hypertension 77 0.067
34
P EPL164 Epilepsy 65 0.067
35
P LPS004 Lupus Erythematosus 63 0.067
36
PYL006 Pyloric Stenosis 45 0.067
37
INT060 Intestinal Atresia 41 0.067
38
P MYP004 Myopathy 68 0.064
39
P THR014 Thrombocytopenia 63 0.064
40
P ADL010 Adult Respiratory Distress Syndrome 60 0.064
41
P ESP024 Esophagitis 59 0.064
42
c ACT210 Acute Respiratory Distress Syndrome 56 0.064
43
c PRC016 Pre-Eclampsia 56 0.064
44
CRB037 Cerebral Palsy 54 0.064
45
CND002 Conduct Disorder 53 0.064
46
P ECL001 Eclampsia 51 0.064
47
P TRT010 Teratoma 51 0.064
48
P APL006 Aplasia Cutis Congenita 48 0.064
49
P ENC008 Encephalocele 48 0.064
50
NWB001 Newborn Respiratory Distress Syndrome 46 0.064
51
GDS001 Good Syndrome 46 0.064
52
URT008 Urticaria Pigmentosa 36 0.064
53
ENC005 Encephalomalacia 27 0.064
54
RSP007 Respiratory Distress Syndrome, Infant 25 0.064
55
P TYS001 Tay-Sachs Disease 70 0.061
56
DRM006 Dermatitis 63 0.061
57
P NRC002 Narcolepsy 62 0.061
58
P TXP001 Toxoplasmosis 60 0.061
59
WLL006 Wells Syndrome 58 0.061
60
GST033 Gestational Diabetes 55 0.061
61
PLC005 Placental Insufficiency 53 0.061
62
P GND004 Gonadal Dysgenesis 51 0.061
63
ESP020 Esophageal Atresia 50 0.061
64
PRV004 Periventricular Leukomalacia 48 0.061
65
c PST041 Posterior Urethral Valves 46 0.061
66
THR024 Thrombosis 43 0.061
67
LKM006 Leukomalacia 42 0.061
68
P HYP009 Hypertrophic Pyloric Stenosis 41 0.061
69
GST009 Gastroschisis 40 0.061
70
VCT001 Vacterl Association 40 0.061
71
URT001 Urethritis 40 0.061
72
HYD001 Hydranencephaly 35 0.061
73
PND004 Pandas 29 0.061
74
DPR014 Diprosopus 20 0.061
75
P ART022 Arthritis 72 0.058
76
P LYM026 Lymphoblastic Leukemia 60 0.058
77
c CNG006 Congenital Hypothyroidism 60 0.058
78
c CNG021 Congenital Toxoplasmosis 52 0.058
79
IMP002 Imperforate Anus 52 0.058
80
P DBT005 Diabetes Insipidus 52 0.058
81
RTN023 Retinitis 49 0.058
82
PLC007 Placental Abruption 46 0.058
83
c BPL002 Bipolar I Disorder 46 0.058
84
RFR003 Refractive Error 41 0.058
85
CLC011 Cloacal Exstrophy 35 0.058
86
AMN009 Amniotic Band Syndrome 29 0.058
87
ACR022 Acardia 12 0.058
88
P CRN211 Coronary Artery Disease 73 0.054
89
P SCH015 Schizophrenia 71 0.054
90
ANX002 Anxiety Disorder 66 0.054
91
P MSC005 Muscular Dystrophy 65 0.054
92
P HLP001 Holoprosencephaly 65 0.054
93
ART005 Arteriovenous Malformation 63 0.054
94
ALC007 Alcohol Dependence 62 0.054
95
P DYS154 Dystonia 61 0.054
96
P BCK002 Beckwith-Wiedemann Syndrome 58 0.054
97
ART111 Artery Disease 55 0.054
98
ISC006 Ischemic Heart Disease 53 0.054
99
P OST009 Osteochondritis Dissecans 52 0.054
100
P RNL028 Renal Tubular Dysgenesis 52 0.054
101
PTH002 Pathological Gambling 48 0.054
102
MTS001 Mutism 41 0.054
103
TRN007 Transsexualism 40 0.054
104
JJN004 Jejunal Atresia 29 0.054
105
SCR024 Sacrococcygeal Teratoma 27 0.054
106
P RHM011 Rheumatoid Arthritis 87 0.050
107
c SYS001 Systemic Lupus Erythematosus 86 0.050
108
P NRB001 Neuroblastoma 71 0.050
109
P HPT021 Hepatitis 68 0.050
110
ATT013 Attention Deficit-Hyperactivity Disorder 66 0.050
111
VSC007 Vascular Disease 65 0.050
112
LNG099 Lung Disease 61 0.050
113
PLM033 Pulmonary Embolism 59 0.050
114
P INF032 Infertility 57 0.050
115
ART021 Arteriosclerosis 57 0.050
116
P MYS005 Myositis 56 0.050
117
PST028 Post-Traumatic Stress Disorder 55 0.050
118
ALP008 Alopecia 54 0.050
119
DMN002 Dementia 52 0.050
120
BLM002 Bulimia Nervosa 51 0.050
121
P HYP065 Hyperaldosteronism 50 0.050
122
HLL004 Hellp Syndrome 48 0.050
123
CTN014 Cutaneous Mastocytosis 47 0.050
124
TRN044 Transposition of the Great Arteries 46 0.050
125
PRN019 Perinatal Necrotizing Enterocolitis 45 0.050
126
SPS057 Spasticity 42 0.050
127
DDN006 Duodenitis 40 0.050
128
PLY024 Polymicrogyria 36 0.050
129
ANS004 Anisometropia 30 0.050
130
PRT086 Partial Hydatidiform Mole 27 0.050
131
P BRS047 Breast Cancer 100 0.045
132
P MYC007 Myocardial Infarction 77 0.045
133
NRL016 Neural Tube Defects 76 0.045
134
INS024 Insulin-Like Growth Factor I 75 0.045
135
PTZ001 Peutz-Jeghers Syndrome 70 0.045
136
P PNM007 Pneumonia 66 0.045
137
P ATS007 Autism Spectrum Disorder 65 0.045
138
ATH003 Atherosclerosis 65 0.045
139
P CRN015 Cornelia De Lange Syndrome 64 0.045
140
PRT036 Peritonitis 60 0.045
141
P BPL003 Bipolar Disorder 60 0.045
142
P MYP006 Myopia 59 0.045
143
VRL011 Viral Infectious Disease 59 0.045
144
P ALC004 Alcohol Abuse 57 0.045
145
ANR040 Aneurysm 57 0.045
146
P HYP055 Hypoplastic Left Heart Syndrome 56 0.045
147
EPD016 Epidermolysis Bullosa 55 0.045
148
P PRC031 Preeclampsia/eclampsia 1 55 0.045
149
P HYP076 Hyperthyroidism 53 0.045
150
P ICH004 Ichthyosis 53 0.045
151
P ATX004 Ataxia 52 0.045
152
ECT006 Ectodermal Dysplasia 52 0.045
153
P DRM007 Dermatitis Herpetiformis 52 0.045
154
BRX001 Bruxism 48 0.045
155
BRN056 Bronchopulmonary Dysplasia 48 0.045
156
LMB062 Limb Ischemia 47 0.045
157
AST006 Astigmatism 43 0.045
158
P HYP729 Hypersensitivity Reaction Disease 43 0.045
159
EST005 Esotropia 42 0.045
160
GND002 Gender Identity Disorder 42 0.045
161
END072 Endotheliitis 41 0.045
162
PSD009 Pseudohermaphroditism 39 0.045
163
PHC006 Phacomatosis Pigmentovascularis 27 0.045
164
c ADL080 Adult Acute Respiratory Distress Syndrome 22 0.045
165
EPG004 Epignathus 16 0.045
166
PHC005 Phacomatosis Pigmentokeratotica 12 0.045
167
CYS001 Cystic Fibrosis 86 0.041
168
P AST005 Asthma 81 0.041
169
HV1006 Hiv-1 80 0.041
170
P NRF018 Neurofibromatosis, Type 1 78 0.041
171
TBR010 Tuberculosis 69 0.041
172
KWS002 Kawasaki Disease 67 0.041
173
P ANR002 Aniridia 66 0.041
174
P PSR002 Psoriasis 64 0.041
175
RBR001 Roberts Syndrome 61 0.041
176
P SHR029 Short Syndrome 61 0.041
177
OVR029 Ovarian Hyperstimulation Syndrome 61 0.041
178
c LCL006 Localized Scleroderma 60 0.041
179
ACQ007 Acquired Immunodeficiency Syndrome 60 0.041
180
P INT063 Intellectual Disability 58 0.041
181
EYD002 Eye Disease 57 0.041
182
P GRV001 Graves' Disease 57 0.041
183
P SLV001 Silver-Russell Syndrome 56 0.041
184
SMT008 Smith-Magenis Syndrome 55 0.041
185
P PLY006 Polydactyly 54 0.041
186
IMM136 Immune System Disease 53 0.041
187
GTR002 Goiter 52 0.041
188
BRN071 Brain Injury 50 0.041
189
P MGR003 Migraine with Aura 49 0.041
190
P PLN008 Peeling Skin Syndrome 49 0.041
191
ACR012 Aicardi Syndrome 49 0.041
192
VND001 Vein Disease 49 0.041
193
PRN038 Prune Belly Syndrome 48 0.041
194
P PRN026 Porencephaly 48 0.041
195
PPL021 Papilledema 47 0.041
196
ANT011 Antisocial Personality Disorder 47 0.041
197
GYN001 Gynecomastia 47 0.041
198
TRC040 Tracheoesophageal Fistula 46 0.041
199
SYN005 Synostosis 45 0.041
200
HMN014 Human Immunodeficiency Virus Infectious Disease 45 0.041
201
END020 Endocardial Fibroelastosis 45 0.041
202
HTR003 Heterotaxy 44 0.041
203
VSC047 Vascular Malformation 43 0.041
204
CRV043 Cervical Dystonia 43 0.041
205
P ART084 Arteriovenous Fistula 43 0.041
206
DYS018 Dysostosis 42 0.041
207
VGN023 Vaginitis 41 0.041
208
MCR103 Microtia 39 0.041
209
DDN011 Duodenal Atresia 37 0.041
210
P NNT042 Neonatal Lupus Erythematosus 34 0.041
211
SLP010 Slipped Capital Femoral Epiphysis 33 0.041
212
PLC008 Placenta Disease 32 0.041
213
CLN022 Colonic Atresia 25 0.041
214
JMC001 Jamaican Vomiting Sickness 10 0.041
215
c DLT002 Dilated Cardiomyopathy 74 0.035
216
P MDL005 Medulloblastoma 73 0.035
217
CRH001 Crohn's Disease 73 0.035
218
P LVR013 Liver Disease 72 0.035
219
P INF038 Influenza 71 0.035
220
MLN008 Melanoma 70 0.035
221
P ADN016 Adenocarcinoma 69 0.035
222
P CLC005 Celiac Disease 69 0.035
223
P LYM118 Lymphoma 69 0.035
224
P OST005 Osteogenesis Imperfecta 68 0.035
225
PCK002 Pick Disease 68 0.035
226
P MYS003 Myasthenia Gravis 67 0.035
227
ACH004 Achondroplasia 66 0.035
228
P MNN013 Meningitis 65 0.035
229
P TRN020 Turner Syndrome 65 0.035
230
P CRN037 Craniosynostosis 65 0.035
231
P AGM001 Agammaglobulinemia 64 0.035
232
INC002 Inclusion Body Myositis 63 0.035
233
P PLY011 Polycystic Ovary Syndrome 63 0.035
234
P CNJ013 Conjunctivitis 63 0.035
235
BRN024 Bronchitis 62 0.035
236
P INF037 Inflammatory Bowel Disease 62 0.035
237
WLL001 Williams-Beuren Syndrome 62 0.035
238
P THL005 Thalassemia 61 0.035
239
P CTS001 Cutis Laxa 60 0.035
240
DFC004 Deficiency Anemia 60 0.035
241
P ATP001 Atopic Dermatitis 60 0.035
242
RSP006 Respiratory System Disease 60 0.035
243
P CNG015 Congenital Diaphragmatic Hernia 60 0.035
244
P ANR007 Anorexia Nervosa 60 0.035
245
P DRR001 Diarrhea 59 0.035
246
P NPH012 Nephrotic Syndrome 59 0.035
247
P RHN004 Rhinitis 59 0.035
248
P VNT002 Ventricular Septal Defect 58 0.035
249
P HYP040 Hypospadias 58 0.035
250
CHL068 Cholestasis 58 0.035
251
P NTR004 Neutropenia 58 0.035
252
EXF001 Exfoliation Syndrome 57 0.035
253
GST045 Gastroenteritis 57 0.035
254
P CTR002 Cataract 57 0.035
255
P RCK004 Rickets 57 0.035
256
P MSC007 Muscle Hypertrophy 56 0.035
257
P INT001 Intrahepatic Cholestasis 56 0.035
258
P NPH009 Nephrolithiasis 55 0.035
259
P HMP007 Hemophilia 55 0.035
260
HYP266 Hypoxia 55 0.035
261
CHN016 Cohen Syndrome 54 0.035
262
P HST010 Histiocytosis 54 0.035
263
CLB001 Coloboma 54 0.035
264
P FTL001 Fetal Alcohol Syndrome 53 0.035
265
PNM008 Pneumothorax 53 0.035
266
URN010 Urinary Tract Obstruction 53 0.035
267
TTH002 Tooth Agenesis 52 0.035
268
P ENC018 Encephalopathy 52 0.035
269
TST014 Testicular Cancer 52 0.035
270
P NNT009 Neonatal Diabetes Mellitus 51 0.035
271
IRN001 Iron Deficiency Anemia 51 0.035
272
CDL003 Caudal Regression Syndrome 50 0.035
273
VND002 Van Der Woude Syndrome 50 0.035
274
DGN001 Degenerative Disc Disease 50 0.035
275
P FBR031 Febrile Seizures 49 0.035
276
MCN017 Meconium Ileus 49 0.035
277
GNR004 Generalized Anxiety Disorder 49 0.035
278
SBS004 Substance Dependence 49 0.035
279
CLF001 Cleft Lip 49 0.035
280
PRP016 Paraplegia 48 0.035
281
c SVR005 Severe Pre-Eclampsia 48 0.035
282
GRW007 Growth Hormone Deficiency 48 0.035
283
P MYT002 Myotonic Dystrophy 48 0.035
284
PRT082 Preterm Premature Rupture of the Membranes 47 0.035
285
HYP043 Hyperandrogenism 46 0.035
286
SCL003 Social Phobia 46 0.035
287
RSP019 Respiratory Distress Syndrome in Premature Infants 45 0.035
288
P HMP006 Hemiplegic Migraine 44 0.035
289
GLC008 Glucose Metabolism Disease 44 0.035
290
DND001 Dandy-Walker Syndrome 44 0.035
291
c JVN003 Juvenile Xanthogranuloma 44 0.035
292
RPR002 Reproductive System Disease 43 0.035
293
TCL003 T Cell Deficiency 43 0.035
294
TBR006 Tuberculoid Leprosy 43 0.035
295
TRP014 Triploidy 41 0.035
296
ARC002 Arachnoiditis 41 0.035
297
CNV002 Conversion Disorder 40 0.035
298
CNN002 Cannabis Abuse 40 0.035
299
NRN002 Neuronitis 39 0.035
300
RNL025 Renal Hypoplasia 39 0.035
301
ARC007 Arachnoid Cysts 38 0.035
302
CNN001 Cannabis Dependence 37 0.035
303
ATM012 Autoimmune Disease of Blood 37 0.035
304
P CHR084 Chromosomal Disease 37 0.035
305
P UTR038 Uterine Disease 36 0.035
306
CRV025 Cervical Incompetence 36 0.035
307
P MNN007 Meningocele 35 0.035
308
BRW006 Brown Syndrome 31 0.035
309
CYT004 Cytomegalic Inclusion Disease 30 0.035
310
TYP015 Type 2b Von Willebrand Disease 30 0.035
311
OSC001 Oeis Complex 29 0.035
312
c ANR038 Anorexia Nervosa 1 27 0.035
313
OCC011 Occipital Encephalocele 23 0.035
314
FRM001 Freemartinism 21 0.035
315
CD4004 Cd4 Deficiency 17 0.035
316
GST058 Gestational Diabetes Insipidus 14 0.035
317
FTZ005 Fitzsimmons-Guilbert Syndrome 11 0.035
318
P RTT002 Rett Syndrome 82 0.029
319
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.029
320
DCH001 Duchenne Muscular Dystrophy 79 0.029
321
P HMC003 Hemochromatosis 72 0.029
322
ADR007 Adrenoleukodystrophy 72 0.029
323
ULC004 Ulcerative Colitis 72 0.029
324
P PFF001 Pfeiffer Syndrome 71 0.029
325
CNG034 Congestive Heart Failure 70 0.029
326
CRZ001 Crouzon Syndrome 70 0.029
327
TTR001 Tetralogy of Fallot 69 0.029
328
SVR004 Severe Combined Immunodeficiency 69 0.029
329
P TBR001 Tuberous Sclerosis 67 0.029
330
PSY004 Psychotic Disorder 67 0.029
331
ART016 Aortic Aneurysm 67 0.029
332
P NMN002 Niemann-Pick Disease 66 0.029
333
P ATR011 Atrial Fibrillation 65 0.029
334
P KDN018 Kidney Disease 65 0.029
335
P BCL006 B-Cell Lymphomas 64 0.029
336
P MYL006 Myeloid Leukemia 64 0.029
337
ALL003 Allergic Rhinitis 63 0.029
338
P OST002 Osteoporosis 63 0.029
339
CRB039 Cerebrovascular Disease 63 0.029
340
ATS001 Autistic Disorder 63 0.029
341
P KLL001 Kallmann Syndrome 62 0.029
342
c HMP004 Hemophilia B 62 0.029
343
P HRP006 Herpes Simplex 62 0.029
344
CRY002 Cryptorchidism 61 0.029
345
CHR066 Chronic Fatigue Syndrome 61 0.029
346
BLM001 Bloom Syndrome 61 0.029
347
ATP002 Atopy 61 0.029
348
CNN005 Connective Tissue Disease 61 0.029
349
HYP056 Hypoglycemia 60 0.029
350
P ALP009 Alopecia Areata 60 0.029
351
P SDD001 Sudden Infant Death Syndrome 60 0.029
352
VNW001 Von Willebrand's Disease 60 0.029
353
TTN003 Tetanus 60 0.029
354
P DRM010 Dermatomyositis 59 0.029
355
P GLY013 Glycogen Storage Disease 59 0.029
356
ELL001 Ellis-Van Creveld Syndrome 59 0.029
357
P HMN010 Hemangioma 59 0.029
358
P PRP029 Porphyria 59 0.029
359
P BRG001 Brugada Syndrome 59 0.029
360
FTT001 Fatty Liver Disease 59 0.029
361
P PNC025 Panic Disorder 58 0.029
362
LYS001 Loeys-Dietz Syndrome 58 0.029
363
P TMT001 Timothy Syndrome 58 0.029
364
ADN018 Adenoma 58 0.029
365
CLT003 Colitis 58 0.029
366
PRP030 Purpura 57 0.029
367
P HYP060 Hyperinsulinism 57 0.029
368
P HYP035 Hypophosphatasia 57 0.029
369
P UVT001 Uveitis 57 0.029
370
P NRP001 Neuropathy 57 0.029
371
P SCL018 Scoliosis 56 0.029
372
ASP002 Aspartylglucosaminuria 56 0.029
373
LTT002 Letterer-Siwe Disease 56 0.029
374
P PRM011 Primary Ciliary Dyskinesia 56 0.029
375
NRM005 Neuromuscular Disease 55 0.029
376
STF002 Stiff Skin Syndrome 55 0.029
377
P INT070 Intestinal Obstruction 55 0.029
378
P GLM007 Glomerulonephritis 55 0.029
379
P OCL002 Oculocutaneous Albinism 55 0.029
380
PLN006 Poland Syndrome 54 0.029
381
P NPH005 Nephronophthisis 54 0.029
382
RTN017 Retinal Detachment 54 0.029
383
DNY001 Denys-Drash Syndrome 54 0.029
384
P EPS003 Episodic Ataxia 54 0.029
385
GST050 Gastrointestinal System Disease 53 0.029
386
P HRD011 Hereditary Spherocytosis 53 0.029
387
P MYC008 Myocarditis 53 0.029
388
PRP019 Peripheral Nervous System Disease 53 0.029
389
CLR003 Clear Cell Adenocarcinoma 53 0.029
390
P RBL001 Rubella 53 0.029
391
HDC001 Headache 53 0.029
392
P END044 Endometriosis 53 0.029
393
P FTL009 Fetal Akinesia Deformation Sequence 53 0.029
394
PYR010 Peyronie's Disease 52 0.029
395
P SCH018 Schizencephaly 52 0.029
396
KLD001 Keloids 52 0.029
397
P STR020 Strabismus 52 0.029
398
HYP080 Hypogonadism 52 0.029
399
KRT006 Keratoconjunctivitis 52 0.029
400
ART002 Arts Syndrome 52 0.029
401
P VSC005 Vesicoureteral Reflux 52 0.029
402
ALL026 Allergic Hypersensitivity Disease 52 0.029
403
P MSC033 Muscle Disorders 52 0.029
404
P LFT003 Left Ventricular Noncompaction 52 0.029
405
P PMP005 Pemphigus Vulgaris 51 0.029
406
RTN018 Retinal Disease 51 0.029
407
HMG005 Hemoglobinopathy 51 0.029
408
ANK001 Ankylosis 51 0.029
409
MYC002 Mycobacterium Avium Complex Disease 51 0.029
410
c FML023 Familial Hemiplegic Migraine 50 0.029
411
ACR003 Acrodermatitis Enteropathica 50 0.029
412
NPH018 Nephrogenic Systemic Fibrosis 50 0.029
413
MST005 Mastitis 50 0.029
414
P OVR046 Ovarian Cyst 50 0.029
415
TLN003 Telangiectasis 50 0.029
416
MSC006 Muscle Glycogenosis 50 0.029
417
HMP005 Hemiplegia 50 0.029
418
P HYP014 Hyperuricemia 50 0.029
419
RNL078 Renal Dysplasia 50 0.029
420
MYL020 Myelomeningocele 50 0.029
421
P FBR025 Fibrochondrogenesis 50 0.029
422
PNC001 Pancytopenia 49 0.029
423
KBG001 Kbg Syndrome 49 0.029
424
PMP001 Pemphigus 49 0.029
425
AMN001 Amenorrhea 49 0.029
426
NSD001 Nose Disease 49 0.029
427
P HML001 Hemolytic-Uremic Syndrome 49 0.029
428
APR001 Apraxia 49 0.029
429
THR013 Thoracic Outlet Syndrome 49 0.029
430
DRG003 Drug Dependence 48 0.029
431
SCH012 Schizoaffective Disorder 48 0.029
432
RGH009 Right Atrial Isomerism 48 0.029
433
P KRT007 Keratoconus 48 0.029
434
NNT012 Neonatal Jaundice 47 0.029
435
RFL001 Reflex Sympathetic Dystrophy 47 0.029
436
CHR001 Churg-Strauss Syndrome 47 0.029
437
P RNL015 Renal Hypertension 47 0.029
438
PTY003 Pityriasis Rubra Pilaris 46 0.029
439
P MRC003 Mercury Poisoning 46 0.029
440
SCB001 Scabies 46 0.029
441
RNL077 Renal Fibrosis 46 0.029
442
BRD004 Borderline Personality Disorder 45 0.029
443
ALB002 Albinism 45 0.029
444
HYP458 Hyper Ige Syndrome 45 0.029
445
STS002 Situs Inversus 45 0.029
446
ANR004 Anuria 44 0.029
447
HYP457 Hypertrophic Scars 44 0.029
448
P KLP003 Klippel-Feil Syndrome 44 0.029
449
FRZ001 Frozen Shoulder 44 0.029
450
HPT074 Hepatic Adenoma, Somatic 44 0.029
451
ANX004 Anoxia 44 0.029
452
P CMP008 Compartment Syndrome 44 0.029
453
CRB090 Cerebral Hypoxia 44 0.029
454
LCH009 Lichen Sclerosus 44 0.029
455
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 43 0.029
456
c PLN018 Peeling Skin Syndrome 2 43 0.029
457
c CNG124 Congenital Rubella 43 0.029
458
DXT001 Dextrocardia 43 0.029
459
URT031 Ureteral Disease 43 0.029
460
P BLD051 Blood Coagulation Disease 43 0.029
461
SPS007 Spastic Cerebral Palsy 43 0.029
462
BLL004 Bullous Keratopathy 43 0.029
463
PHY002 Physical Disorder 43 0.029
464
ART031 Aortic Coarctation 43 0.029
465
IMP004 Impetigo 42 0.029
466
ANH002 Anhidrosis 42 0.029
467
PLC001 Placenta Accreta 42 0.029
468
CRN025 Corneal Dystrophy 41 0.029
469
CLS010 Cluster Headache 41 0.029
470
MYC033 Myoclonus 41 0.029
471
PHC013 Phaeochromocytoma 41 0.029
472
RTR008 Root Resorption 41 0.029
473
HMH002 Hemihypertrophy 40 0.029
474
HMT018 Hematopoietic Stem Cell Transplantation 40 0.029
475
TRC010 Trichotillomania 40 0.029
476
FRY002 Fryns Syndrome 40 0.029
477
c SBC007 Subacute Thyroiditis 39 0.029
478
MYF001 Myofibroma 39 0.029
479
VTR016 Vater/vacterl Association 39 0.029
480
AVD001 Avoidant Personality Disorder 39 0.029
481
BFD003 Bifid Uvula 39 0.029
482
TRN012 Transient Global Amnesia 39 0.029
483
LYS017 Loeys-Dietz Syndrome 4 38 0.029
484
HYP391 Hyperammonemia 38 0.029
485
P CHR342 Chiari Malformation 38 0.029
486
P PRS062 Persistent Hyperplastic Primary Vitreous 38 0.029
487
P NRX001 Neuroaxonal Dystrophy 38 0.029
488
HRM002 Hermaphroditism 38 0.029
489
P VTL001 Vitelliform Macular Dystrophy 38 0.029
490
MSC004 Muscle Tissue Disease 37 0.029
491
FXF002 Fox-Fordyce Disease 37 0.029
492
ANR018 Anorchia 37 0.029
493
SPL040 Split Hand 36 0.029
494
FNS001 Funisitis 36 0.029
495
P PST059 Pustular Psoriasis 36 0.029
496
c BLD124 Bleeding Disorder, Platelet-Type, 11 36 0.029
497
BLP004 Blepharophimosis 36 0.029
498
MTG002 Mutagen Sensitivity 36 0.029
499
HYP041 Hypochondrogenesis 35 0.029
500
PNL013 Penile Disease 35 0.029
501
BLN002 Balanitis Xerotica Obliterans 35 0.029
502
ACR005 Acrodermatitis 35 0.029
503
CRN088 Craniorachischisis 35 0.029
504
NNT011 Neonatal Anemia 35 0.029
505
GNT005 Giant Hemangioma 34 0.029
506
CND006 Candida Glabrata 34 0.029
507
IRT001 Iritis 34 0.029
508
IMM068 Immunodeficiency 8 34 0.029
509
P GRM010 Germ Cells Tumors 34 0.029
510
CRV069 Cervix Disease 33 0.029
511
IMM082 Immunodeficiency 18 33 0.029
512
ATN011 Autoinflammation with Infantile Enterocolitis 33 0.029
513
HRS011 Horseshoe Kidney 33 0.029
514
BLN010 Balanitis 33 0.029
515
NNT019 Neonatal Hypothyroidism 33 0.029
516
c PLN024 Peeling Skin Syndrome 4 32 0.029
517
c PLN021 Peeling Skin Syndrome 3 32 0.029
518
RTC010 Reticuloendotheliosis 32 0.029
519
PDT040 Pediatric Hypertension 31 0.029
520
MYS001 Myositis Ossificans 30 0.029
521
ALR002 Al-Raqad Syndrome 29 0.029
522
IMM076 Immunodeficiency 24 29 0.029
523
TRD003 Taurodontism 29 0.029
524
IVC001 Ivic Syndrome 29 0.029
525
SVN002 Sveinsson Chorioretinal Atrophy 28 0.029
526
NRC003 Narcissistic Personality Disorder 28 0.029
527
MLT003 Multilocular Clear Cell Renal Cell Carcinoma 28 0.029
528
P ATX010 Ataxia Neuropathy Spectrum 27 0.029
529
HMN031 Human Venous Malformation 27 0.029
530
ENT007 Enteropathica 27 0.029
531
HNM002 Hinman Syndrome 27 0.029
532
HRT037 Heart and Brain Malformation Syndrome 26 0.029
533
IMP001 Impetigo Herpetiformis 25 0.029
534
RHH001 Rohhad 24 0.029
535
NNT018 Neonatal Herpes 24 0.029
536
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 23 0.029
537
CDL005 Caudal Duplication Anomaly 23 0.029
538
CLC002 Calcaneonavicular Coalition 22 0.029
539
VSC009 Vascular Skin Disease 20 0.029
540
HYD059 Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect 20 0.029
541
TRG006 Trigger Thumb 18 0.029
542
TGF006 Tgfb2-Related Loeys-Dietz Syndrome 17 0.029
543
LMB009 Lambdoid Synostosis 16 0.029
544
AND005 Androgen Insensitivity Syndrome, Mild 16 0.029
545
ECT085 Ectopia Cordis 15 0.029
546
CLP002 Colpocephaly 15 0.029
547
FTL016 Fetal Edema 15 0.029
548
SYM006 Symmetrical Thalamic Calcifications 14 0.029
549
LNR009 Linear Atrophoderma of Moulin 14 0.029
550
WLS002 Wilson-Mikity Syndrome 14 0.029
551
FBL005 Fibular Aplasia 10 0.029
552
P CLR023 Colorectal Cancer 95 0.020
553
P MLT019 Multiple Myeloma 82 0.020
554
P RTN008 Retinitis Pigmentosa 80 0.020
555
P DBT085 Diabetes Mellitus, Insulin-Dependent 79 0.020
556
P OST012 Osteoarthritis 79 0.020
557
P ATX030 Ataxia-Telangiectasia 78 0.020
558
P ALZ034 Alzheimer Disease 76 0.020
559
P RTN024 Retinoblastoma 75 0.020
560
END057 Endometrial Cancer 74 0.020
561
P WSK001 Wiskott-Aldrich Syndrome 74 0.020
562
HDG012 Hodgkin Lymphoma 73 0.020
563
P STM004 Stomach Cancer 72 0.020
564
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.020
565
FBR012 Fabry Disease 71 0.020
566
BCK001 Becker Muscular Dystrophy 71 0.020
567
c HPT073 Hepatitis C Virus 70 0.020
568
P NRV007 Nervous System Disease 70 0.020
569
P ESS003 Essential Thrombocythemia 70 0.020
570
P MTC003 Metachromatic Leukodystrophy 70 0.020
571
KRT004 Keratitis 70 0.020
572
P ALP004 Alport Syndrome 70 0.020
573
MLT021 Multiple System Atrophy 70 0.020
574
P DMN001 Diamond-Blackfan Anemia 70 0.020
575
c JVN004 Juvenile Myelomonocytic Leukemia 69 0.020
576
SMT004 Smith-Lemli-Opitz Syndrome 69 0.020
577
CMM004 Common Variable Immunodeficiency 68 0.020
578
THY028 Thyroid Cancer 68 0.020
579
APR006 Apert Syndrome 68 0.020
580
TST021 Testicular Germ Cell Tumor 67 0.020
581
KPS004 Kaposi Sarcoma 67 0.020
582
P FRG001 Fragile X Syndrome 67 0.020
583
P CHR071 Charcot-Marie-Tooth Disease 67 0.020
584
CST001 Costello Syndrome 67 0.020
585
c HRD010 Hereditary Spastic Paraplegia 66 0.020
586
P NSP012 Nasopharyngeal Carcinoma 66 0.020
587
SRC014 Sarcoma 66 0.020
588
ACR007 Acromegaly 66 0.020
589
ALX003 Alexander Disease 65 0.020
590
c HMP029 Hemophilia a 64 0.020
591
P HMP002 Hemophagocytic Lymphohistiocytosis 64 0.020
592
OBS002 Obsessive-Compulsive Disorder 64 0.020
593
P LNG028 Long Qt Syndrome 64 0.020
594
P AMY004 Amyloidosis 64 0.020
595
P VLC001 Velocardiofacial Syndrome 64 0.020
596
P LPR003 Leprosy 63 0.020
597
AND015 Androgen Insensitivity 63 0.020
598
P GCH001 Gaucher's Disease 63 0.020
599
PLM001 Pulmonary Tuberculosis 63 0.020
600
PSR001 Psoriatic Arthritis 63 0.020
601
PRT037 Pertussis 63 0.020
602
MNK001 Menkes Disease 63 0.020
603
CRB011 Cerebrotendinous Xanthomatosis 62 0.020
604
c HPT001 Hepatitis C 62 0.020
605
c HPT016 Hepatitis B 62 0.020
606
P ANG001 Angelman Syndrome 62 0.020
607
TNG002 Tangier Disease 62 0.020
608
MTH009 Mouth Disease 62 0.020
609
P CCK001 Cockayne Syndrome 62 0.020
610
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 62 0.020
611
P ADD001 Addison's Disease 62 0.020
612
GST092 Gastroesophageal Reflux 62 0.020
613
VSC011 Vasculitis 62 0.020
614
P CLD001 Cleidocranial Dysplasia 62 0.020
615
P ART023 Arthropathy 62 0.020
616
P LBR001 Leber Congenital Amaurosis 62 0.020
617
P SYS005 Systemic Scleroderma 61 0.020
618
P ENC004 Encephalitis 61 0.020
619
CHR063 Chronic Mucocutaneous Candidiasis 61 0.020
620
SHW002 Shwachman-Diamond Syndrome 61 0.020
621
P HRM001 Hermansky-Pudlak Syndrome 61 0.020
622
CNC002 Cinca Syndrome 61 0.020
623
c MYT021 Myotonic Dystrophy 1 61 0.020
624
BLS001 Blau Syndrome 61 0.020
625
MXD005 Mixed Connective Tissue Disease 61 0.020
626
P ASP006 Aspergillosis 60 0.020
627
P MYM002 Moyamoya Disease 60 0.020
628
P SLP006 Sleep Apnea 60 0.020
629
P PNC044 Pancreatitis 60 0.020
630
SYS004 Systemic Mastocytosis 60 0.020
631
P WVR001 Weaver Syndrome 60 0.020
632
c CNT035 Central Nervous System Disease 60 0.020
633
DSM004 Desmoid Tumor 60 0.020
634
MNK003 Muenke Syndrome 60 0.020
635
STR026 Star Syndrome 59 0.020
636
P INT068 Intestinal Disease 59 0.020
637
P NRV006 Nervous System Cancer 59 0.020
638
SCR008 Scrub Typhus 59 0.020
639
FCT003 Factor X Deficiency 59 0.020
640
CNT047 Contact Dermatitis 59 0.020
641
PLM070 Pulmonic Stenosis 59 0.020
642
CRD119 Cardiac Arrest 59 0.020
643
OST017 Osteomyelitis 58 0.020
644
c CHR536 Charcot-Marie-Tooth Disease, Type 1a 58 0.020
645
CHL123 Chlamydia 58 0.020
646
WLM001 Wolman Disease 58 0.020
647
NRF007 Neurofibroma 58 0.020
648
P IDP010 Idiopathic Generalized Epilepsy 58 0.020
649
P MCR010 Microcephaly 58 0.020
650
P PLR004 Pleuropulmonary Blastoma 58 0.020
651
CMP005 Campomelic Dysplasia 58 0.020
652
STT001 Status Epilepticus 58 0.020
653
KRN002 Kearns-Sayre Syndrome 57 0.020
654
P THR005 Thrombotic Thrombocytopenic Purpura 57 0.020
655
P RTH001 Rothmund-Thomson Syndrome 57 0.020
656
MLG056 Malignant Hyperthermia 57 0.020
657
ALP001 Alopecia Universalis 57 0.020
658
RHM027 Rheumatic Disease 57 0.020
659
P RTN025 Retinoschisis 57 0.020
660
LPT001 Leptospirosis 57 0.020
661
STF001 Stiff-Person Syndrome 56 0.020
662
P PND002 Pendred Syndrome 56 0.020
663
CNS004 Constipation 56 0.020
664
PTT006 Pituitary Adenoma 56 0.020
665
P STC001 Stickler Syndrome 56 0.020
666
P CND004 Candidiasis 56 0.020
667
MVL001 Mevalonic Aciduria 56 0.020
668
P LKD001 Leukodystrophy 56 0.020
669
ACN002 Acanthosis Nigricans 56 0.020
670
ETN001 Eating Disorder 56 0.020
671
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 56 0.020
672
P BDD001 Budd-Chiari Syndrome 56 0.020
673
P EPD009 Epidermolysis Bullosa Dystrophica 56 0.020
674
c HRD002 Hereditary Angioedema 56 0.020
675
SFT003 Soft Tissue Sarcoma 56 0.020
676
JNT002 Joint Disorders 55 0.020
677
P GT001 Gout 55 0.020
678
ACS001 Acoustic Neuroma 55 0.020
679
P OLG002 Oligodendroglioma 55 0.020
680
NTH001 Netherton Syndrome 55 0.020
681
VGT001 Vogt-Koyanagi-Harada Disease 55 0.020
682
P EMR001 Emery-Dreifuss Muscular Dystrophy 55 0.020
683
P FND001 Fundus Albipunctatus 55 0.020
684
WLF001 Wolff-Parkinson-White Syndrome 55 0.020
685
BLD034 Bile Duct Carcinoma 55 0.020
686
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.020
687
APH002 Aphasia 55 0.020
688
c TBR024 Tuberous Sclerosis-1 55 0.020
689
P BRC006 Brachydactyly 55 0.020
690
P HLL001 Hallermann-Streiff Syndrome 55 0.020
691
PRS047 Prostatitis 55 0.020
692
P ANT006 Antiphospholipid Syndrome 54 0.020
693
P INT143 Interstitial Cystitis 54 0.020
694
GLC003 Glucose Intolerance 54 0.020
695
P DGR001 Digeorge Syndrome 54 0.020
696
RHM001 Rheumatic Fever 54 0.020
697
P GRS003 Griscelli Syndrome 54 0.020
698
P PLY019 Polyneuropathy 54 0.020
699
P MLT074 Multiple Endocrine Neoplasia 54 0.020
700
P OVR049 Ovarian Disease 54 0.020
701
ARS001 Aarskog-Scott Syndrome 54 0.020
702
SLP005 Sleep Disorder 54 0.020
703
c FML001 Familial Atrial Fibrillation 54 0.020
704
P HYP027 Hypobetalipoproteinemia 54 0.020
705
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.020
706
HMF006 Hemifacial Microsomia 54 0.020
707
c GRS014 Griscelli Syndrome, Type 2 53 0.020
708
c RCS002 Recessive Dystrophic Epidermolysis Bullosa 53 0.020
709
WGR001 Wagr Syndrome 53 0.020
710
P INT030 Intracranial Aneurysm 53 0.020
711
DMY004 Demyelinating Disease 53 0.020
712
CYS010 Cystinosis 53 0.020
713
MGL013 Megalencephaly 53 0.020
714
P EPD002 Epidermolytic Hyperkeratosis 53 0.020
715
P LRS001 Larsen Syndrome 53 0.020
716
OCL020 Ocular Cicatricial Pemphigoid 53 0.020
717
CSY001 C Syndrome 53 0.020
718
RSC001 Rosacea 53 0.020
719
P ALT001 Alternating Hemiplegia of Childhood 53 0.020
720
HYP730 Hypogonadotropic Hypogonadism 52 0.020
721
P ANG015 Angioedema 52 0.020
722
P PLY014 Polycystic Kidney Disease 52 0.020
723
VSC002 Vascular Dementia 52 0.020
724
c PSD066 Pseudohypoparathyroidism, Type Ib 52 0.020
725
P PLY041 Polymyositis 52 0.020
726
BRN002 Bronchiolitis 52 0.020
727
ALP014 Alpha-Thalassemia/mental Retardation Syndrome 52 0.020
728
P PTS002 Ptosis 52 0.020
729
ISL003 Isolated Growth Hormone Deficiency 52 0.020
730
RST001 Restless Legs Syndrome 52 0.020
731
CYS005 Cysticercosis 52 0.020
732
P CYS018 Cystitis 52 0.020
733
P CNT005 Central Nervous System Lymphoma 52 0.020
734
P ALL008 Allergic Bronchopulmonary Aspergillosis 52 0.020
735
P CNT004 Centronuclear Myopathy 52 0.020
736
VRN004 Vernal Keratoconjunctivitis 52 0.020
737
CHL014 Cholera 52 0.020
738
P PYL005 Pyelonephritis 52 0.020
739
MVM001 Movement Disease 52 0.020
740
c PRK031 Parkinson Disease 1 51 0.020
741
c INT064 Intermediate Uveitis 51 0.020
742
SCT005 Scott Syndrome 51 0.020
743
FDL002 Food Allergy 51 0.020
744
MRG003 Marginal Zone B-Cell Lymphoma 51 0.020
745
BLR001 Biliary Atresia 51 0.020
746
MYM001 Myoma 51 0.020
747
TTH006 Tooth Disease 51 0.020
748
P AXN002 Axenfeld-Rieger Syndrome 51 0.020
749
P SJG002 Sjogren-Larsson Syndrome 51 0.020
750
P SYP003 Syphilis 51 0.020
751
BNF002 Bone Fracture 51 0.020
752
QDR001 Quadriplegia 51 0.020
753
HST011 Histoplasmosis 51 0.020
754
BLL001 Baller-Gerold Syndrome 51 0.020
755
ESN005 Eosinophilic Gastroenteritis 51 0.020
756
CLN019 Colonic Disease 51 0.020
757
CRV040 Cervix Carcinoma 51 0.020
758
CRH005 Crohn's Colitis 50 0.020
759
DSS009 Disseminated Intravascular Coagulation 50 0.020
760
LST001 Listeriosis 50 0.020
761
PRV006 Pervasive Developmental Disorder 50 0.020
762
PRC012 Pericardial Effusion 50 0.020
763
PRR016 Pierre Robin Syndrome 50 0.020
764
CHN055 Chanarin-Dorfman Syndrome 50 0.020
765
P MMB011 Membranous Nephropathy 50 0.020
766
NNL002 Nonalcoholic Steatohepatitis 50 0.020
767
NRG002 Neurogenic Bladder 50 0.020
768
P CLL015 Collagen Disease 50 0.020
769
PTS001 Patau Syndrome 50 0.020
770
ALL009 Allergic Conjunctivitis 50 0.020
771
P PRM006 Primary Biliary Cirrhosis 50 0.020
772
TMP001 Temporal Lobe Epilepsy 50 0.020
773
P MSC003 Muscular Atrophy 49 0.020
774
PSD007 Pseudomyxoma Peritonei 49 0.020
775
MSS002 Mass Syndrome 49 0.020
776
THY030 Thyroid Gland Disease 49 0.020
777
P CNG046 Congenital Fiber-Type Disproportion 49 0.020
778
PRT011 Protein C Deficiency 49 0.020
779
ASP001 Asperger Syndrome 49 0.020
780
DBT084 Diabetes Mellitus, Ketosis-Prone 49 0.020
781
MGL001 Megaloblastic Anemia 49 0.020
782
P LSS002 Lissencephaly 48 0.020
783
GNG002 Ganglioneuroma 48 0.020
784
P JNC001 Junctional Epidermolysis Bullosa 48 0.020
785
HYP077 Hypertrichosis 48 0.020
786
RNL007 Renal Tubular Acidosis 48 0.020
787
KRT009 Keratosis 48 0.020
788
INC021 Incontinentia Pigmenti 48 0.020
789
P DDN001 Duodenal Ulcer 48 0.020
790
SPN019 Spondylolisthesis 48 0.020
791
c TRC092 Trichorhinophalangeal Syndrome, Type I 48 0.020
792
C3D001 C3 Deficiency 48 0.020
793
c PRM226 Primary Central Nervous System Lymphoma 48 0.020
794
P LPM005 Lipomatosis 48 0.020
795
PRP021 Peripheral Nervous System Neoplasm 48 0.020
796
HMG002 Hemoglobinuria 48 0.020
797
STM006 Stomach Disease 47 0.020
798
CHL069 Cholesteatoma 47 0.020
799
MTB004 Metabolic Acidosis 47 0.020
800
P KLF001 Kleefstra Syndrome 47 0.020
801
JHN001 Johanson-Blizzard Syndrome 47 0.020
802
GGR001 Geographic Tongue 47 0.020
803
P RBN002 Robinow Syndrome 47 0.020
804
CCT002 Cicatricial Pemphigoid 47 0.020
805
OST011 Osteomalacia 47 0.020
806
CHL004 Cholelithiasis 47 0.020
807
EST007 Estrogen Resistance 47 0.020
808
NPH003 Nephrocalcinosis 47 0.020
809
MTN003 Motion Sickness 47 0.020
810
CCN002 Cocaine Abuse 47 0.020
811
OLV001 Olivopontocerebellar Atrophy 47 0.020
812
P INF049 Infantile Myofibromatosis 47 0.020
813
P SYR001 Syringomyelia 47 0.020
814
c TYR013 Tyrosinemia, Type Ii 47 0.020
815
SPN020 Spondylosis 46 0.020
816
XNT003 Xanthomatosis 46 0.020
817
c ERL020 Early-Onset Schizophrenia 46 0.020
818
LRN003 Learning Disability 46 0.020
819
NRM004 Neuroma 46 0.020
820
LPD011 Lipoid Adrenal Hyperplasia 46 0.020
821
PRN023 Prion Disease 46 0.020
822
P PRD008 Periodontitis 46 0.020
823
HRT007 Heart Cancer 46 0.020
824
c MLG069 Malignant Hypertension 46 0.020
825
PPL018 Papillary Adenocarcinoma 46 0.020
826
PRR002 Pure Red-Cell Aplasia 46 0.020
827
LKC003 Leukocyte Disease 46 0.020
828
P D2H001 D-2-Hydroxyglutaric Aciduria 46 0.020
829
P ICH001 Ichthyosis Vulgaris 46 0.020
830
PLM041 Pulmonary Valve Stenosis 46 0.020
831
MNL001 Monilethrix 46 0.020
832
SLD003 Sialadenitis 46 0.020
833
FBR032 Fibromuscular Dysplasia 46 0.020
834
HMN032 Human Herpesvirus 8 46 0.020
835
KRT010 Kartagener Syndrome 46 0.020
836
FML039 Female Reproductive System Disease 46 0.020
837
P PSD015 Pseudohypoparathyroidism 46 0.020
838
WRN002 Wernicke-Korsakoff Syndrome 46 0.020
839
DNT012 Dental Caries 46 0.020
840
MGC001 Megacolon 46 0.020
841
CRB085 Cerebral Hemorrhage 45 0.020
842
EPD006 Epidermolysis Bullosa Acquisita 45 0.020
843
ALV007 Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins 45 0.020
844
ART004 Aortic Atherosclerosis 45 0.020
845
FLL008 Folliculitis 45 0.020
846
CVR006 Cavernous Hemangioma 45 0.020
847
MNN009 Meningoencephalitis 45 0.020
848
IDP024 Idiopathic Inflammatory Myopathy 45 0.020
849
SDD007 Sudden Cardiac Death 45 0.020
850
ADN027 Adenomyosis 45 0.020
851
CNJ012 Conjunctival Disease 45 0.020
852
BLL003 Bell's Palsy 45 0.020
853
CRD118 Cardiovascular Cancer 45 0.020
854
PLM035 Pulmonary Eosinophilia 45 0.020
855
MCR037 Macroglossia 45 0.020
856
CHR074 Choriocarcinoma 45 0.020
857
c MTR002 Mitral Valve Insufficiency 45 0.020
858
CTS002 Cat-Scratch Disease 45 0.020
859
CMP034 Complete Androgen Insensitivity Syndrome 44 0.020
860
NVS001 Neovascular Glaucoma 44 0.020
861
DSC009 Discoid Lupus Erythematosus 44 0.020
862
DBW001 Dubowitz Syndrome 44 0.020
863
P MLG086 Malignant Hyperthermia Susceptibility 44 0.020
864
P TYR004 Tyrosinemia 44 0.020
865
SYN036 Syncope 44 0.020
866
c ACT076 Acute Myocarditis 44 0.020
867
MLT006 Multidrug-Resistant Tuberculosis 44 0.020
868
BSL008 Basal Ganglia Disease 44 0.020
869
HMP009 Haemophilus Influenzae 44 0.020
870
FBR009 Fibrous Dysplasia 44 0.020
871
c SPN100 Spinocerebellar Ataxia 27 44 0.020
872
PRM003 Premature Ejaculation 44 0.020
873
ANV001 Anovulation 44 0.020
874
P AML002 Amelogenesis Imperfecta 44 0.020
875
P PRM001 Primary Cutaneous Amyloidosis 44 0.020
876
NSY001 N Syndrome 44 0.020
877
PLL012 Pollen Allergy 44 0.020
878
P LYD001 Leydig Cell Tumor 44 0.020
879
c HMG001 Hemoglobin C Disease 44 0.020
880
NPH091 Nephrolithiasis, Calcium Oxalate 44 0.020
881
CHR008 Choroiditis 43 0.020
882
TST015 Testicular Disease 43 0.020
883
P PSD003 Pseudohypoaldosteronism 43 0.020
884
PRN011 Pernicious Anemia 43 0.020
885
OPP004 Oppositional Defiant Disorder 43 0.020
886
AGR002 Agoraphobia 43 0.020
887
PRP009 Peripartum Cardiomyopathy 43 0.020
888
GND001 Gonadoblastoma 43 0.020
889
NDL021 Nodular Lymphocyte Predominant Hodgkin Lymphoma 43 0.020
890
FCL041 Focal Myositis 43 0.020
891
CD4003 Cd40 Ligand Deficiency 43 0.020
892
NRW001 Norwegian Scabies 43 0.020
893
PRS012 Pars Planitis 42 0.020
894
HND002 Hand, Foot and Mouth Disease 42 0.020
895
PLC003 Placental Site Trophoblastic Tumor 42 0.020
896
CNG048 Congenital Hepatic Fibrosis 42 0.020
897
c BRC082 Brachydactyly, Type E 42 0.020
898
AND001 Anodontia 42 0.020
899
WDM004 Wiedemann-Steiner Syndrome 42 0.020
900
ANM001 Anemia of Prematurity 42 0.020
901
PLG004 Plagiocephaly 42 0.020
902
SBP004 Subependymoma 42 0.020
903
BLN001 Blount's Disease 42 0.020
904
MST006 Mast Syndrome 42 0.020
905
DRM011 Dermatophytosis 42 0.020
906
HYP101 Hyperinsulinism-Hyperammonemia Syndrome 42 0.020
907
MTR010 Mature Teratoma 42 0.020
908
PRG014 Progesterone Resistance 41 0.020
909
GST052 Gestational Choriocarcinoma 41 0.020
910
MHC001 Mhc Class Ii Deficiency 41 0.020
911
BCK006 Back Pain 41 0.020
912
PRD003 Periodontosis 41 0.020
913
VSC018 Visceral Steatosis 41 0.020
914
DFF003 Diffuse Scleroderma 41 0.020
915
PRM013 Premature Menopause 41 0.020
916
NRN008 Neuronal Intranuclear Inclusion Disease 41 0.020
917
DFF001 Diffuse Cutaneous Mastocytosis 41 0.020
918
P TST026 Testicular Germ Cell Cancer 40 0.020
919
P SML002 Small Cell Sarcoma 40 0.020
920
FMR004 Fumarase Deficiency 40 0.020
921
P ACH011 Achondrogenesis 40 0.020
922
GND003 Gonadal Disease 40 0.020
923
P SDR003 Sideroblastic Anemia 40 0.020
924
SPR007 Superior Mesenteric Artery Syndrome 40 0.020
925
MDY003 Mody, Type Ii 40 0.020
926
CRD144 Cardiovascular Disease Risk Factor ) 40 0.020
927
NSP002 Nasopharyngitis 40 0.020
928
RTT001 Ritter's Disease 40 0.020
929
TLP001 Talipes Equinovarus 40 0.020
930
ADR009 Adrenal Cortex Disease 39 0.020
931
RNL012 Renal Tuberculosis 39 0.020
932
IRN004 Iron-Refractory Iron Deficiency Anemia 39 0.020
933
DLS001 Delusional Disorder 39 0.020
934
PRS030 Persistent Fetal Circulation Syndrome 39 0.020
935
OCL069 Ocular Motor Apraxia 39 0.020
936
SMT001 Somatization Disorder 39 0.020
937
BLD054 Blood Protein Disease 39 0.020
938
c CNG031 Congenital Nervous System Abnormality 39 0.020
939
ARM002 Aromatic L-Amino Acid Decarboxylase Deficiency 39 0.020
940
PNG002 Pain Agnosia 39 0.020
941
CHL052 Choledochal Cyst 39 0.020
942
c PRG001 Progressive Muscular Atrophy 39 0.020
943
P CNG024 Congenital Nystagmus 39 0.020
944
LYM009 Lymphocytic Choriomeningitis 39 0.020
945
IDP070 Idiopathic Scoliosis 39 0.020
946
MNN017 Mononeuropathy 39 0.020
947
HYP068 Hyperostosis 38 0.020
948
ART035 Arterial Calcification of Infancy 38 0.020
949
c CHR091 Chronic Meningitis 38 0.020
950
SPN029 Spondylolysis 38 0.020
951
ASP004 Asphyxia Neonatorum 38 0.020
952
LYM127 Lymphatic Malformations 38 0.020
953
PRS108 Persistent Polyclonal B-Cell Lymphocytosis 38 0.020
954
MNN021 Meningococcemia 38 0.020
955
BDY001 Body Dysmorphic Disorder 38 0.020
956
c DBT082 Diabetes Mellitus, Insulin-Dependent, 12 38 0.020
957
EPS026 Epispadias 38 0.020
958
c CNG029 Congenital Mesoblastic Nephroma 38 0.020
959
CND005 Cone Dystrophy 38 0.020
960
P PRT042 Parietal Foramina 38 0.020
961
P PNT019 Pontocerebellar Hypoplasia 38 0.020
962
ANG016 Angiokeratoma 38 0.020
963
PCH002 Pachygyria 37 0.020
964
SPS004 Spastic Quadriplegia 37 0.020
965
BST007 Best Vitelliform Macular Dystrophy 37 0.020
966
GST007 Gastric Dilatation 37 0.020
967
P CRB059 Cerebellar Degeneration 37 0.020
968
P FML187 Familial Hypertension 37 0.020
969
CNG035 Congenital Bilateral Absence of Vas Deferens 37 0.020
970
DFF021 Diffuse Mesangial Sclerosis 37 0.020
971
BLS003 Blastoma 37 0.020
972
INT011 Interstitial Emphysema 37 0.020
973
OLG001 Oligospermia 37 0.020
974
c ADL027 Adult Dermatomyositis 37 0.020
975
CHR078 Chorioretinitis 37 0.020
976
ALX002 Alexithymia 37 0.020
977
OBS003 Obsessive-Compulsive Personality Disorder 37 0.020
978
CLR033 Color Vision Deficiency 37 0.020
979
C6D001 C6 Deficiency 37 0.020
980
c CNG033 Congenital Syphilis 37 0.020
981
SML028 Semilobar Holoprosencephaly 36 0.020
982
CVR010 Cavernous Malformation 36 0.020
983
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 36 0.020
984
GRN007 Granuloma Annulare 36 0.020
985
P TRC005 Tracheal Stenosis 36 0.020
986
TCL012 T-Cell/histiocyte Rich Large B Cell Lymphoma 36 0.020
987
P HYP120 Hypoaldosteronism 36 0.020
988
P DYS005 Dyslexia 36 0.020
989
PMP002 Pemphigoid Gestationis 36 0.020
990
CMB021 Combined Pituitary Hormone Deficiency 36 0.020
991
PRT019 Protein-Losing Enteropathy 36 0.020
992
IMM065 Immunodeficiency 10 36 0.020
993
RDN001 Reading Disorder 36 0.020
994
MLR007 Male Reproductive System Disease 36 0.020
995
ATM014 Autoimmune Disease of Endocrine System 35 0.020
996
c CHR098 Chronic Pyelonephritis 35 0.020
997
HYP015 Hyperlucent Lung 35 0.020
998
OLM001 Olmsted Syndrome 35 0.020
999
WRT001 Worth's Syndrome 35 0.020
1000
PRM129 Primary Cutaneous Marginal Zone B-Cell Lymphoma 35 0.020
1001
HYP064 Hypogonadotropism 35 0.020
1002
SCH072 Scheuermann Disease 35 0.020
1003
XNT009 Xanthoma Disseminatum 34 0.020
1004
HYP193 Hypocomplementemic Urticarial Vasculitis 34 0.020
1005
P HRT017 Heart Tumor 34 0.020
1006
OST014 Osteopoikilosis 34 0.020
1007
IMM066 Immunodeficiency 9 34 0.020
1008
ALB014 Alobar Holoprosencephaly 34 0.020
1009
FMR011 Fumarate Hydratase Deficiency 34 0.020
1010
MYX004 Myxedema 34 0.020
1011
FTL007 Fetal Hydantoin Syndrome 34 0.020
1012
NNT008 Neonatal Abstinence Syndrome 34 0.020
1013
LND001 Landau-Kleffner Syndrome 34 0.020
1014
SPN221 Spina Bifida Occulta 34 0.020
1015
TRN030 Transient Erythroblastopenia of Childhood 34 0.020
1016
KWS001 Kwashiorkor 34 0.020
1017
PHT008 Photosensitive Epilepsy 34 0.020
1018
SPR012 Separation Anxiety Disorder 34 0.020
1019
SYS006 Say Syndrome 33 0.020
1020
SPL039 Split Foot 33 0.020
1021
BTN004 Biotin Deficiency 33 0.020
1022
P CRB154 Cerebrocostomandibular Syndrome 33 0.020
1023
CNG064 Congenital Chloride Diarrhea 33 0.020
1024
IMM039 Immune Hydrops Fetalis 33 0.020
1025
WRT003 Warthin Tumor 33 0.020
1026
c CNG004 Congenital Epulis 33 0.020
1027
SCH011 Schizotypal Personality Disorder 32 0.020
1028
DVL001 Developmental Coordination Disorder 32 0.020
1029
c PRM032 Primary Congenital Glaucoma 32 0.020
1030
ADL086 Adolescent Idiopathic Scoliosis 32 0.020
1031
GRN016 Grant Syndrome 32 0.020
1032
CLC003 Cloacogenic Carcinoma 32 0.020
1033
CHR010 Chorioangioma 32 0.020
1034
CRL004 Caroli Disease 32 0.020
1035
P LTT001 Lattice Corneal Dystrophy 32 0.020
1036
NCR002 Necrobiosis Lipoidica 32 0.020
1037
CHD004 Chudley-Mccullough Syndrome 32 0.020
1038
P END046 Endometritis 32 0.020
1039
LYM095 Lymphangiomatosis 32 0.020
1040
c ALZ046 Alzheimer's Disease 5 31 0.020
1041
P EPL003 Epulis 31 0.020
1042
CYT002 Cytokine Deficiency 31 0.020
1043
DDN009 Duodenal Obstruction 31 0.020
1044
c NRC009 Narcolepsy 1 31 0.020
1045
P PTT002 Potter's Syndrome 31 0.020
1046
SPR034 Superior Limbic Keratoconjunctivitis 30 0.020
1047
ATR003 Atrophic Rhinitis 30 0.020
1048
STR096 Striate Palmoplantar Keratoderma 30 0.020
1049
LCH003 Lichen Nitidus 30 0.020
1050
FNC005 Functional Colonic Disease 30 0.020
1051
DYS001 Dyskinetic Cerebral Palsy 30 0.020
1052
LTM002 Luteoma 29 0.020
1053
SPR035 Superior Vena Cava Syndrome 29 0.020
1054
P MLD013 Mild Hemophilia a 29 0.020
1055
FCL003 Facial Hemiatrophy 29 0.020
1056
RTN006 Retinal Drusen 29 0.020
1057
c MLG039 Malignant Essential Hypertension 29 0.020
1058
DFC001 Defective Apolipoprotein B-100 29 0.020
1059
CNG133 Congenital Varicella Syndrome 28 0.020
1060
RTN019 Retinal Telangiectasia 28 0.020
1061
CRB028 Cerebellar Medulloblastoma 28 0.020
1062
PLN001 Plantar Wart 28 0.020
1063
SWY001 Swayback 27 0.020
1064
CHL109 Childhood Apraxia of Speech 27 0.020
1065
ATM052 Autoimmune Disease 1 27 0.020
1066
NNT021 Neonatal Meningitis 27 0.020
1067
P SPC019 Specific Language Impairment 27 0.020
1068
AMY005 Amyloid Neuropathy 26 0.020
1069
P PLM064 Pulmonary Sequestration 26 0.020
1070
c ACQ027 Acquired Cutis Laxa 26 0.020
1071
RGH006 Right Aortic Arch 26 0.020
1072
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 26 0.020
1073
PTC005 Pituicytoma 26 0.020
1074
PLM058 Pulmonary Atresia with Intact Ventricular Septum 26 0.020
1075
ANG004 Angioid Streaks 26 0.020
1076
TBL008 Tibial Hemimelia 25 0.020
1077
SLT009 Solitary Bone Cyst 25 0.020
1078
BLD052 Blood Group Incompatibility 25 0.020
1079
P TRS029 Trisomy 1q 25 0.020
1080
LBN004 Liebenberg Syndrome 25 0.020
1081
c MNS008 Monosomy 21 25 0.020
1082
FTS001 Fetishism 25 0.020
1083
c PLY105 Polycystic Ovary Syndrome 1 25 0.020
1084
CRN051 Craniofacial Microsomia 25 0.020
1085
PLS031 Plastic Bronchitis 25 0.020
1086
MSC016 Mosaic Trisomy 14 25 0.020
1087
ACC003 Accommodative Esotropia 24 0.020
1088
PRR001 Periarthritis 24 0.020
1089
KRT014 Keratosis Follicularis Spinulosa Decalvans 24 0.020
1090
TBR007 Tuberculum Sellae Meningioma 24 0.020
1091
P NNT006 Neonatal Myasthenia Gravis 24 0.020
1092
TTR014 Tetrasomy 18p 24 0.020
1093
PNL023 Penile Agenesis 23 0.020
1094
c SYS053 Systemic Lupus Erythematosus 5 23 0.020
1095
FXC001 Foix Chavany Marie Syndrome 22 0.020
1096
P ART034 Aortopulmonary Window 22 0.020
1097
P CRN178 Coronary Heart Disease 6 22 0.020
1098
BRN097 Brainstem Auditory Evoked Responses 22 0.020
1099
MCR039 Macrophagic Myofasciitis 22 0.020
1100
MYL044 Myelocystocele 22 0.020
1101
MCH006 Mechanical Strabismus 22 0.020
1102
P TTH021 Tethered Cord Syndrome 22 0.020
1103
PTN004 Patent Ductus Venosus 22 0.020
1104
SCH025 Schisis Association 22 0.020
1105
c PTR018 Paternal Uniparental Disomy of Chromosome 6 21 0.020
1106
c CRN174 Coronary Heart Disease 2 21 0.020
1107
PNS015 Penoscrotal Transposition 21 0.020
1108
P TRC031 Trichorhinophalangeal Syndrome 21 0.020
1109
HYP018 Hyperglobulinemic Purpura 21 0.020
1110
PRR031 Pruritic Urticarial Papules and Plaques of Pregnancy 21 0.020
1111
DCR002 Dacryocystocele 21 0.020
1112
LPM007 Lipomyelomeningocele 21 0.020
1113
LMB014 Limb-Body Wall Complex 20 0.020
1114
c RNG018 Ring Chromosome 22 20 0.020
1115
P HYD015 Hydroa Vacciniforme 20 0.020
1116
c CNG129 Congenital Torticollis 20 0.020
1117
SPS087 Spasmus Nutans 19 0.020
1118
SHK001 Shaken Baby Syndrome 19 0.020
1119
c CNG370 Congenital Tracheal Stenosis 19 0.020
1120
OCL044 Oculo-Auriculo-Vertebral Spectrum 18 0.020
1121
MSL004 Mesial Temporal Lobe Epilepsy with Hippocampal Sclerosis 18 0.020
1122
LCH010 Lichtenstein Syndrome 18 0.020
1123
P HML046 Heimler Syndrome 2 18 0.020
1124
SYN041 Synesthesia 18 0.020
1125
AQG002 Aquagenic Urticaria 18 0.020
1126
MTR027 Mitral Atresia 17 0.020
1127
ELC001 Elective Mutism 16 0.020
1128
CMP052 Complication in Hemodialysis 15 0.020
1129
DDL001 Didelphys Uterus 15 0.020
1130
c RNG014 Ring Chromosome 19 14 0.020
1131
HYD031 Hydroxyprolinemia 14 0.020
1132
VGN024 Vagina, Absence of 14 0.020
1133
JVN026 Jeavons Syndrome 14 0.020
1134
OLG008 Oligomeganephronic Renal Hypoplasia 14 0.020
1135
PLM108 Pulmonary Interstitial Glycogenosis</