Search results for twinning

1373 hits were found for twinning

# Family MCID Name MIFTS Score
1
TWN001 Twin-to-Twin Transfusion Syndrome 50 11.857
2
TWN007 Twinning, Dizygotic 21 4.114
3
TWN012 Twinning Due to Superfetation 5 4.094
4
c RNL090 Renal Tubular Dysgenesis Due to Twin-Twin Transfusion 6 3.359
5
TWN013 Twinning, Monozygotic 4 3.351
6
PLC008 Placenta Disease 61 0.174
7
P PLY018 Polycythemia 58 0.156
8
PLY012 Polyhydramnios 47 0.152
9
AGN016 Aging 64 0.147
10
DPR016 Depression 72 0.145
11
CRB009 Cerebritis 41 0.145
12
ANN002 Anencephaly 56 0.132
13
P HRT032 Heart Disease 74 0.107
14
P CRV039 Cervicitis 49 0.107
15
ANX010 Anxiety 72 0.102
16
OLG003 Oligohydramnios 53 0.097
17
HYD012 Hydrops Fetalis 51 0.093
18
HYD059 Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect 37 0.093
19
P SCH015 Schizophrenia 69 0.092
20
CHR005 Chorioamnionitis 51 0.090
21
PND004 Pandas 42 0.090
22
FTL016 Fetal Edema 25 0.090
23
c EXD008 Exudative Vitreoretinopathy 1 69 0.088
24
ENT011 Enterocolitis 54 0.088
25
NWB001 Newborn Respiratory Distress Syndrome 52 0.084
26
RSP007 Respiratory Distress Syndrome, Infant 34 0.084
27
DWN001 Down Syndrome 69 0.081
28
P ADL010 Adult Respiratory Distress Syndrome 66 0.081
29
c ACT210 Acute Respiratory Distress Syndrome 61 0.081
30
CYT008 Cytomegalovirus Infection 56 0.081
31
P DBT009 Diabetes Mellitus 64 0.079
32
PRN019 Perinatal Necrotizing Enterocolitis 56 0.079
33
P THY032 Thyroiditis 55 0.079
34
PRT082 Preterm Premature Rupture of the Membranes 52 0.079
35
P LKM002 Leukemia 72 0.077
36
P EPL164 Epilepsy 69 0.077
37
P PRS038 Personality Disorder 64 0.077
38
P ECL001 Eclampsia 57 0.077
39
CNG069 Congenital Cytomegalovirus 38 0.077
40
P ATS364 Autism 70 0.075
41
ISC004 Ischemia 65 0.075
42
c PRC016 Pre-Eclampsia 59 0.075
43
NNT011 Neonatal Anemia 35 0.075
44
NRL016 Neural Tube Defects 78 0.072
45
SRN002 Sirenomelia 34 0.072
46
P ART022 Arthritis 76 0.070
47
P LPS004 Lupus Erythematosus 68 0.070
48
P HYP086 Hypothyroidism 64 0.070
49
TBC004 Tobacco Addiction 60 0.070
50
P SMK004 Smoking As a Quantitative Trait Locus 3 36 0.070
51
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.067
52
URT039 Urticaria 60 0.067
53
PLC005 Placental Insufficiency 58 0.067
54
TYP041 Type I 56 0.067
55
P OMP004 Omphalocele 51 0.067
56
PRV004 Periventricular Leukomalacia 50 0.067
57
LKM006 Leukomalacia 41 0.067
58
P RHM011 Rheumatoid Arthritis 80 0.065
59
c LKM062 Leukemia, Acute Lymphoblastic 69 0.065
60
P LYM026 Lymphoblastic Leukemia 64 0.065
61
ECT026 Ectopic Pregnancy 51 0.065
62
PNT005 Pentalogy of Cantrell 33 0.065
63
P MLT020 Multiple Sclerosis 78 0.062
64
P PLM037 Pulmonary Hypertension 75 0.062
65
CRB037 Cerebral Palsy 71 0.062
66
c CRN300 Coronary Heart Disease 1 64 0.062
67
P THR014 Thrombocytopenia 64 0.062
68
P ESP024 Esophagitis 63 0.062
69
BRN056 Bronchopulmonary Dysplasia 60 0.062
70
P HMP007 Hemophilia 60 0.062
71
P TRT010 Teratoma 52 0.062
72
P APL006 Aplasia Cutis Congenita 50 0.062
73
PYL006 Pyloric Stenosis 46 0.062
74
INT060 Intestinal Atresia 43 0.062
75
URT008 Urticaria Pigmentosa 40 0.062
76
c APL023 Aplasia Cutis Congenita, Nonsyndromic 34 0.062
77
MCL067 Maculopapular Cutaneous Mastocytosis 30 0.062
78
P MYP004 Myopathy 68 0.059
79
DRM006 Dermatitis 66 0.059
80
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.059
81
P NRC002 Narcolepsy 63 0.059
82
THR024 Thrombosis 61 0.059
83
GST033 Gestational Diabetes 60 0.059
84
HMF006 Hemifacial Microsomia 58 0.059
85
P RNL100 Renal Hypodysplasia/aplasia 1 57 0.059
86
RTN018 Retinal Disease 56 0.059
87
GST009 Gastroschisis 54 0.059
88
ESP020 Esophageal Atresia 53 0.059
89
RTN023 Retinitis 50 0.059
90
PLC007 Placental Abruption 50 0.059
91
P ENC008 Encephalocele 46 0.059
92
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 42 0.059
93
NNT019 Neonatal Hypothyroidism 39 0.059
94
ENC005 Encephalomalacia 36 0.059
95
AMN009 Amniotic Band Syndrome 32 0.059
96
P ALZ034 Alzheimer Disease 87 0.056
97
P TYS001 Tay-Sachs Disease 71 0.056
98
P PNM007 Pneumonia 69 0.056
99
DMN002 Dementia 68 0.056
100
P THN009 Thanatophoric Dysplasia, Type I 67 0.056
101
P MSC005 Muscular Dystrophy 66 0.056
102
P TXP001 Toxoplasmosis 64 0.056
103
HYP730 Hypogonadotropic Hypogonadism 56 0.056
104
HYD046 Hydatidiform Mole, Recurrent, 1 52 0.056
105
P GND004 Gonadal Dysgenesis 50 0.056
106
c PST041 Posterior Urethral Valves 49 0.056
107
P HYP009 Hypertrophic Pyloric Stenosis 45 0.056
108
VTR016 Vater/vacterl Association 45 0.056
109
GST010 Gestational Trophoblastic Neoplasm 44 0.056
110
URT001 Urethritis 43 0.056
111
VCT001 Vacterl Association 39 0.056
112
HYD001 Hydranencephaly 35 0.056
113
c SYS001 Systemic Lupus Erythematosus 86 0.053
114
ISC006 Ischemic Heart Disease 72 0.053
115
c PRM196 Premature Ovarian Failure 1 71 0.053
116
P CRN018 Coronary Artery Anomaly 68 0.053
117
LNG099 Lung Disease 67 0.053
118
ALC007 Alcohol Dependence 65 0.053
119
CHR593 Chromosome 16p13.3 Deletion Syndrome, Proximal 64 0.053
120
c ATS007 Autism Spectrum Disorder 61 0.053
121
c CNG006 Congenital Hypothyroidism 60 0.053
122
ANR040 Aneurysm 60 0.053
123
P INF032 Infertility 59 0.053
124
P BCK002 Beckwith-Wiedemann Syndrome 57 0.053
125
P OST009 Osteochondritis Dissecans 57 0.053
126
c CNG021 Congenital Toxoplasmosis 57 0.053
127
P DBT005 Diabetes Insipidus 54 0.053
128
ANS023 Anus, Imperforate 54 0.053
129
c BPL002 Bipolar I Disorder 49 0.053
130
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 45 0.053
131
RFR003 Refractive Error 44 0.053
132
MTS001 Mutism 42 0.053
133
BRS090 Breast Reconstruction 41 0.053
134
CLC011 Cloacal Exstrophy 39 0.053
135
HMF010 Hemifacial Microsomia with Radial Defects 31 0.053
136
ELC001 Elective Mutism 22 0.053
137
DPR014 Diprosopus 22 0.053
138
ACR022 Acardia 12 0.053
139
P BRS047 Breast Cancer 100 0.049
140
P HPT021 Hepatitis 76 0.049
141
P HLP001 Holoprosencephaly 66 0.049
142
ART140 Arteries, Anomalies of 65 0.049
143
P DYS154 Dystonia 64 0.049
144
ART005 Arteriovenous Malformation 63 0.049
145
P PLY011 Polycystic Ovary Syndrome 63 0.049
146
PLM033 Pulmonary Embolism 62 0.049
147
ANR007 Anorexia Nervosa 62 0.049
148
HYP266 Hypoxia 61 0.049
149
c WLM018 Wilms Tumor 5 60 0.049
150
CLF001 Cleft Lip 54 0.049
151
CND002 Conduct Disorder 54 0.049
152
BRN071 Brain Injury 53 0.049
153
HLL004 Hellp Syndrome 52 0.049
154
PTH002 Pathological Gambling 52 0.049
155
P RNL028 Renal Tubular Dysgenesis 48 0.049
156
TRN007 Transsexualism 43 0.049
157
TRN044 Transposition of the Great Arteries 40 0.049
158
c WLM011 Wilms Tumor 6 38 0.049
159
JJN004 Jejunal Atresia 32 0.049
160
SCR024 Sacrococcygeal Teratoma 31 0.049
161
TRN069 Transsexuality 23 0.049
162
CYS001 Cystic Fibrosis 84 0.046
163
AST005 Asthma 82 0.046
164
P NRB001 Neuroblastoma 72 0.046
165
P TRN020 Turner Syndrome 68 0.046
166
VSC007 Vascular Disease 68 0.046
167
PRT036 Peritonitis 66 0.046
168
P MYS005 Myositis 63 0.046
169
P ALC004 Alcohol Abuse 63 0.046
170
P ENC018 Encephalopathy 62 0.046
171
P ART021 Arteriosclerosis 60 0.046
172
P BPL003 Bipolar Disorder 59 0.046
173
PST028 Post-Traumatic Stress Disorder 58 0.046
174
P ALP008 Alopecia 58 0.046
175
BLM002 Bulimia Nervosa 58 0.046
176
ECT006 Ectodermal Dysplasia 57 0.046
177
EPD016 Epidermolysis Bullosa 56 0.046
178
CTN014 Cutaneous Mastocytosis 49 0.046
179
DDN006 Duodenitis 48 0.046
180
c PRC031 Preeclampsia/eclampsia 1 39 0.046
181
PLY024 Polymicrogyria 36 0.046
182
ANS004 Anisometropia 32 0.046
183
PRT086 Partial Hydatidiform Mole 27 0.046
184
BDY007 Body Mass Index Quantitative Trait Locus 1 26 0.046
185
INS024 Insulin-Like Growth Factor I 82 0.042
186
P MYC007 Myocardial Infarction 79 0.042
187
P LYM118 Lymphoma 70 0.042
188
PTZ001 Peutz-Jeghers Syndrome 70 0.042
189
P PSR002 Psoriasis 65 0.042
190
P MJR001 Major Depressive Disorder 65 0.042
191
ATM095 Autoimmune Disease 64 0.042
192
P CRN015 Cornelia De Lange Syndrome 64 0.042
193
WLL001 Williams-Beuren Syndrome 63 0.042
194
P HYP055 Hypoplastic Left Heart Syndrome 62 0.042
195
P NTR004 Neutropenia 60 0.042
196
CHL068 Cholestasis 60 0.042
197
P INT001 Intrahepatic Cholestasis 60 0.042
198
VNW001 Von Willebrand's Disease 60 0.042
199
c ATR087 Atrial Standstill 1 59 0.042
200
VGN023 Vaginitis 58 0.042
201
P PLY006 Polydactyly 57 0.042
202
P MYP006 Myopia 56 0.042
203
P DRM007 Dermatitis Herpetiformis 56 0.042
204
P HYP076 Hyperthyroidism 56 0.042
205
P ICH004 Ichthyosis 54 0.042
206
CLF004 Cleft Lip/palate 53 0.042
207
P FBR031 Febrile Seizures 53 0.042
208
LMB062 Limb Ischemia 51 0.042
209
BRX001 Bruxism 50 0.042
210
ANX004 Anoxia 49 0.042
211
AST006 Astigmatism 49 0.042
212
MGR001 Migraine Without Aura 46 0.042
213
GND002 Gender Identity Disorder 45 0.042
214
END072 Endotheliitis 45 0.042
215
CHN065 Choanal Atresia, Posterior 44 0.042
216
NRL018 Neural Tube Defects, Folate-Sensitive 44 0.042
217
PSD009 Pseudohermaphroditism 44 0.042
218
EST005 Esotropia 44 0.042
219
c HYP543 Hypoplastic Left Heart Syndrome 1 42 0.042
220
SPS057 Spasticity 41 0.042
221
CRV025 Cervical Incompetence 37 0.042
222
c DRM040 Dermatitis Herpetiformis, Familial 36 0.042
223
EPG004 Epignathus 18 0.042
224
PHK006 Phakomatosis Pigmentokeratotica 15 0.042
225
PHC005 Phacomatosis Pigmentokeratotica 14 0.042
226
CRH001 Crohn's Disease 78 0.037
227
NRF026 Neurofibromatosis, Type Iv, of Riccardi 73 0.037
228
KWS002 Kawasaki Disease 70 0.037
229
MSC157 Muscular Dystrophy, Duchenne Type 68 0.037
230
P DRM053 Dermatitis, Atopic 67 0.037
231
c THR092 Thrombophilia Due to Thrombin Defect 67 0.037
232
c NRF024 Neurofibromatosis, Type I 66 0.037
233
OVR029 Ovarian Hyperstimulation Syndrome 64 0.037
234
LNG108 Langerhans Cell Histiocytosis 63 0.037
235
ACQ007 Acquired Immunodeficiency Syndrome 63 0.037
236
THR100 Thrombocytopenic Purpura, Autoimmune 62 0.037
237
RCK004 Rickets 62 0.037
238
HYP056 Hypoglycemia 62 0.037
239
P GRV001 Graves' Disease 61 0.037
240
FTT001 Fatty Liver Disease 60 0.037
241
P HST010 Histiocytosis 59 0.037
242
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 59 0.037
243
P FTL001 Fetal Alcohol Syndrome 59 0.037
244
P DRR001 Diarrhea 56 0.037
245
P SLV001 Silver-Russell Syndrome 56 0.037
246
PNM008 Pneumothorax 56 0.037
247
URN010 Urinary Tract Obstruction 56 0.037
248
GNR004 Generalized Anxiety Disorder 53 0.037
249
P MGR003 Migraine with Aura 53 0.037
250
SMT008 Smith-Magenis Syndrome 53 0.037
251
TST014 Testicular Cancer 53 0.037
252
GTR002 Goiter 52 0.037
253
PRN038 Prune Belly Syndrome 52 0.037
254
ANT011 Antisocial Personality Disorder 50 0.037
255
SYN005 Synostosis 49 0.037
256
P PRN026 Porencephaly 49 0.037
257
PPL021 Papilledema 49 0.037
258
ACR012 Aicardi Syndrome 48 0.037
259
ART031 Aortic Coarctation 47 0.037
260
TRC040 Tracheoesophageal Fistula 47 0.037
261
GYN001 Gynecomastia 46 0.037
262
DYS018 Dysostosis 46 0.037
263
P HRT035 Heart Block, Congenital 46 0.037
264
P ART084 Arteriovenous Fistula 45 0.037
265
END020 Endocardial Fibroelastosis 45 0.037
266
PLC001 Placenta Accreta 45 0.037
267
PNM010 Pneumothorax, Primary Spontaneous 42 0.037
268
CRV043 Cervical Dystonia 41 0.037
269
NRN002 Neuronitis 41 0.037
270
DDN011 Duodenal Atresia 40 0.037
271
ANR018 Anorchia 40 0.037
272
MCR103 Microtia 40 0.037
273
P NNT042 Neonatal Lupus Erythematosus 37 0.037
274
SLP010 Slipped Capital Femoral Epiphysis 37 0.037
275
PHC006 Phacomatosis Pigmentovascularis 31 0.037
276
CLN022 Colonic Atresia 26 0.037
277
ACT170 Acute Ackee Fruit Intoxication 12 0.037
278
JMC001 Jamaican Vomiting Sickness 11 0.037
279
P DLT002 Dilated Cardiomyopathy 76 0.032
280
P PRK057 Parkinson Disease, Late-Onset 76 0.032
281
P OST002 Osteoporosis 76 0.032
282
P INF038 Influenza 76 0.032
283
ALP046 Alport Syndrome, X-Linked 75 0.032
284
P MDL005 Medulloblastoma 75 0.032
285
P LVR013 Liver Disease 75 0.032
286
c ART101 Aortic Valve Disease 2 73 0.032
287
P ALG028 Alagille Syndrome 1 73 0.032
288
P MYS003 Myasthenia Gravis 72 0.032
289
P CLC063 Celiac Disease 1 71 0.032
290
PSY004 Psychotic Disorder 71 0.032
291
CRZ001 Crouzon Syndrome 70 0.032
292
P RTN024 Retinoblastoma 70 0.032
293
P MNN013 Meningitis 70 0.032
294
HMN044 Human Immunodeficiency Virus Type 1 70 0.032
295
P ADN016 Adenocarcinoma 70 0.032
296
P AGM001 Agammaglobulinemia 69 0.032
297
BRT054 Brittle Bone Disorder 69 0.032
298
P KDN018 Kidney Disease 68 0.032
299
P CRN037 Craniosynostosis 67 0.032
300
ACH004 Achondroplasia 66 0.032
301
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.032
302
BRN024 Bronchitis 66 0.032
303
P ANR048 Aniridia 1 65 0.032
304
MCC012 Mccune-Albright Syndrome 64 0.032
305
GST045 Gastroenteritis 64 0.032
306
P THL005 Thalassemia 64 0.032
307
c SCL052 Scleroderma, Familial Progressive 64 0.032
308
INC002 Inclusion Body Myositis 63 0.032
309
VRL011 Viral Infectious Disease 63 0.032
310
P CNJ013 Conjunctivitis 63 0.032
311
P NRP001 Neuropathy 63 0.032
312
c DPH024 Diaphragmatic Hernia, Congenital 63 0.032
313
P CTS001 Cutis Laxa 62 0.032
314
MLN008 Melanoma 62 0.032
315
P RHN004 Rhinitis 61 0.032
316
PRP030 Purpura 61 0.032
317
DFC004 Deficiency Anemia 61 0.032
318
P NMN002 Niemann-Pick Disease 60 0.032
319
P CTR002 Cataract 60 0.032
320
P NPH012 Nephrotic Syndrome 59 0.032
321
P HYP040 Hypospadias 59 0.032
322
P VNT002 Ventricular Septal Defect 58 0.032
323
HMT018 Hematopoietic Stem Cell Transplantation 57 0.032
324
c VSC019 Vesicoureteral Reflux 1 57 0.032
325
PRR016 Pierre Robin Syndrome 56 0.032
326
NPH009 Nephrolithiasis 55 0.032
327
IRN002 Iron Metabolism Disease 55 0.032
328
IRN001 Iron Deficiency Anemia 55 0.032
329
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 55 0.032
330
VND007 Van Der Woude Syndrome 1 55 0.032
331
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.032
332
PRP016 Paraplegia 53 0.032
333
P INF037 Inflammatory Bowel Disease 53 0.032
334
c SVR005 Severe Pre-Eclampsia 53 0.032
335
MYL020 Myelomeningocele 53 0.032
336
DGN001 Degenerative Disc Disease 53 0.032
337
TTH002 Tooth Agenesis 53 0.032
338
GRW007 Growth Hormone Deficiency 51 0.032
339
MCN017 Meconium Ileus 51 0.032
340
P END046 Endometritis 50 0.032
341
SBS004 Substance Dependence 50 0.032
342
P MYT002 Myotonic Dystrophy 50 0.032
343
STS002 Situs Inversus 50 0.032
344
HYP043 Hyperandrogenism 50 0.032
345
SCL003 Social Phobia 48 0.032
346
P NNT009 Neonatal Diabetes Mellitus 48 0.032
347
P HMP006 Hemiplegic Migraine 48 0.032
348
c JVN003 Juvenile Xanthogranuloma 48 0.032
349
CHN016 Cohen Syndrome 47 0.032
350
EXS017 Exstrophy of Bladder 46 0.032
351
P CHR342 Chiari Malformation 45 0.032
352
ARC002 Arachnoiditis 45 0.032
353
HTR003 Heterotaxy 44 0.032
354
PHC013 Phaeochromocytoma 43 0.032
355
PNN005 Panencephalitis, Subacute Sclerosing 43 0.032
356
TRP014 Triploidy 42 0.032
357
SCR020 Sacral Defect with Anterior Meningocele 42 0.032
358
AVD001 Avoidant Personality Disorder 42 0.032
359
CNN001 Cannabis Dependence 41 0.032
360
P MNN007 Meningocele 41 0.032
361
DND001 Dandy-Walker Syndrome 40 0.032
362
P CHR084 Chromosomal Disease 40 0.032
363
CNN002 Cannabis Abuse 40 0.032
364
RNL025 Renal Hypoplasia 39 0.032
365
P DYS005 Dyslexia 39 0.032
366
ARC007 Arachnoid Cysts 39 0.032
367
PLY161 Polymicrogyria, Bilateral Perisylvian, X-Linked 34 0.032
368
CYT004 Cytomegalic Inclusion Disease 34 0.032
369
OSC001 Oeis Complex 31 0.032
370
c MYS011 Myasthenia Gravis Congenital 30 0.032
371
URN022 Urinary Tract Infections, Recurrent 29 0.032
372
OCC011 Occipital Encephalocele 28 0.032
373
BRW006 Brown Syndrome 27 0.032
374
KLB005 Kleeblattschaedel 27 0.032
375
MYT026 Myotonia Atrophica 27 0.032
376
OLG021 Oligomeganephronia 27 0.032
377
FRM001 Freemartinism 23 0.032
378
GST058 Gestational Diabetes Insipidus 12 0.032
379
FTZ005 Fitzsimmons-Guilbert Syndrome 11 0.032
380
P CLR023 Colorectal Cancer 97 0.026
381
c MCL042 Macular Degeneration, Age-Related, 1 84 0.026
382
P RTT002 Rett Syndrome 82 0.026
383
P FNC027 Fanconi Anemia, Complementation Group a 78 0.026
384
GST053 Gastric Cancer 77 0.026
385
P NNN008 Noonan Syndrome 1 77 0.026
386
PFF001 Pfeiffer Syndrome 73 0.026
387
P NRV007 Nervous System Disease 73 0.026
388
ULC004 Ulcerative Colitis 72 0.026
389
CNG034 Congestive Heart Failure 72 0.026
390
ADR007 Adrenoleukodystrophy 71 0.026
391
c MLT156 Multiple Endocrine Neoplasia, Type I 71 0.026
392
c JVN010 Juvenile Rheumatoid Arthritis 69 0.026
393
P HRP006 Herpes Simplex 69 0.026
394
ART016 Aortic Aneurysm 69 0.026
395
SVR004 Severe Combined Immunodeficiency 69 0.026
396
P TTR001 Tetralogy of Fallot 69 0.026
397
P FRG001 Fragile X Syndrome 69 0.026
398
P ATR011 Atrial Fibrillation 68 0.026
399
P TBR001 Tuberous Sclerosis 68 0.026
400
c NMN015 Niemann-Pick Disease, Type C1 68 0.026
401
P MYL006 Myeloid Leukemia 68 0.026
402
P AGM019 Agammaglobulinemia, X-Linked 68 0.026
403
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 67 0.026
404
CRB039 Cerebrovascular Disease 67 0.026
405
c HMP004 Hemophilia B 67 0.026
406
P FCS012 Facioscapulohumeral Muscular Dystrophy 1 66 0.026
407
P ART067 Aortic Aneurysm, Familial Thoracic 1 66 0.026
408
OBS002 Obsessive-Compulsive Disorder 66 0.026
409
CHR066 Chronic Fatigue Syndrome 66 0.026
410
P PRT008 Proteus Syndrome 66 0.026
411
P SLP006 Sleep Apnea 66 0.026
412
END057 Endometrial Cancer 65 0.026
413
P BCL006 B-Cell Lymphomas 65 0.026
414
GST050 Gastrointestinal System Disease 64 0.026
415
CMB081 Combined Immunodeficiency, X-Linked 64 0.026
416
P END044 Endometriosis 64 0.026
417
P HYP061 Hypertrophic Cardiomyopathy 64 0.026
418
c LCL006 Localized Scleroderma 64 0.026
419
CNN005 Connective Tissue Disease 64 0.026
420
CNT097 Central Hypoventilation Syndrome, Congenital 64 0.026
421
GST092 Gastroesophageal Reflux 64 0.026
422
TTN003 Tetanus 64 0.026
423
P DRM010 Dermatomyositis 64 0.026
424
P ALP009 Alopecia Areata 63 0.026
425
HYP066 Hyperglycemia 63 0.026
426
P KBK002 Kabuki Syndrome 1 63 0.026
427
P KLL001 Kallmann Syndrome 63 0.026
428
ADN018 Adenoma 63 0.026
429
RSP006 Respiratory System Disease 63 0.026
430
PRP001 Propionic Acidemia 62 0.026
431
P PRP029 Porphyria 62 0.026
432
RHB001 Rhabdoid Cancer 62 0.026
433
CLT003 Colitis 62 0.026
434
IRR002 Irritable Bowel Syndrome 62 0.026
435
P RBL001 Rubella 62 0.026
436
c PNS012 Paine Syndrome 62 0.026
437
P GLY013 Glycogen Storage Disease 61 0.026
438
P TRC072 Treacher Collins Syndrome 1 61 0.026
439
ETN001 Eating Disorder 61 0.026
440
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 61 0.026
441
P GLM007 Glomerulonephritis 61 0.026
442
BLM001 Bloom Syndrome 60 0.026
443
P UVT001 Uveitis 60 0.026
444
SDD001 Sudden Infant Death Syndrome 60 0.026
445
P BRG001 Brugada Syndrome 60 0.026
446
P HMN010 Hemangioma 60 0.026
447
P PLY014 Polycystic Kidney Disease 60 0.026
448
ELL001 Ellis-Van Creveld Syndrome 60 0.026
449
PRS047 Prostatitis 60 0.026
450
NRM005 Neuromuscular Disease 60 0.026
451
c ALP101 Alpha-Thalassemia 59 0.026
452
SCH078 Schimmelpenning-Feuerstein-Mims Syndrome 59 0.026
453
WLF001 Wolff-Parkinson-White Syndrome 59 0.026
454
HDC001 Headache 59 0.026
455
P UTR058 Uterine Anomalies 59 0.026
456
RTN017 Retinal Detachment 58 0.026
457
P OCL002 Oculocutaneous Albinism 58 0.026
458
c ORF040 Orofaciodigital Syndrome Viii 58 0.026
459
P MSC007 Muscle Hypertrophy 58 0.026
460
P MYC008 Myocarditis 58 0.026
461
P HYP035 Hypophosphatasia 58 0.026
462
VSC002 Vascular Dementia 58 0.026
463
P INT030 Intracranial Aneurysm 57 0.026
464
P MCR010 Microcephaly 57 0.026
465
RSC001 Rosacea 57 0.026
466
BLR001 Biliary Atresia 57 0.026
467
P MMB011 Membranous Nephropathy 57 0.026
468
c EPS042 Episodic Ataxia, Type 1 57 0.026
469
P NPH005 Nephronophthisis 56 0.026
470
CLR003 Clear Cell Adenocarcinoma 56 0.026
471
P EPS003 Episodic Ataxia 56 0.026
472
HYP060 Hyperinsulinism 56 0.026
473
AND002 Androgen Insensitivity Syndrome 56 0.026
474
STR020 Strabismus 56 0.026
475
CHL028 Childhood Type Dermatomyositis 56 0.026
476
P INT070 Intestinal Obstruction 56 0.026
477
P PYL005 Pyelonephritis 56 0.026
478
ASP002 Aspartylglucosaminuria 56 0.026
479
MST005 Mastitis 55 0.026
480
KRT006 Keratoconjunctivitis 55 0.026
481
P HYP014 Hyperuricemia 55 0.026
482
BNF002 Bone Fracture 55 0.026
483
P MLT074 Multiple Endocrine Neoplasia 55 0.026
484
P PMP005 Pemphigus Vulgaris 55 0.026
485
P SCL018 Scoliosis 55 0.026
486
P PNC025 Panic Disorder 55 0.026
487
HMP005 Hemiplegia 55 0.026
488
P HRD011 Hereditary Spherocytosis 55 0.026
489
ANK001 Ankylosis 55 0.026
490
AMN001 Amenorrhea 55 0.026
491
P ATS308 Autosomal Dominant Cerebellar Ataxia 54 0.026
492
LST001 Listeriosis 54 0.026
493
P PMP001 Pemphigus 54 0.026
494
SCH012 Schizoaffective Disorder 54 0.026
495
DNY001 Denys-Drash Syndrome 53 0.026
496
FTL009 Fetal Akinesia Deformation Sequence 53 0.026
497
SPR004 Supravalvular Aortic Stenosis 53 0.026
498
TTH006 Tooth Disease 53 0.026
499
P PRM011 Primary Ciliary Dyskinesia 53 0.026
500
HPT082 Hepatic Adenomas, Familial 53 0.026
501
APR001 Apraxia 53 0.026
502
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 53 0.026
503
HMG005 Hemoglobinopathy 53 0.026
504
P LFT003 Left Ventricular Noncompaction 52 0.026
505
INT075 Intracranial Hypertension 52 0.026
506
DSS008 Disease of Mental Health 52 0.026
507
P MSC033 Muscle Disorders 52 0.026
508
DXT001 Dextrocardia 52 0.026
509
ACR056 Acrodermatitis Enteropathica, Zinc-Deficiency Type 52 0.026
510
KBG001 Kbg Syndrome 52 0.026
511
P SCH018 Schizencephaly 52 0.026
512
CHR001 Churg-Strauss Syndrome 51 0.026
513
TLN003 Telangiectasis 51 0.026
514
HYP080 Hypogonadism 51 0.026
515
PNC001 Pancytopenia 51 0.026
516
P HYP760 Hypothyroidism, Congenital, Nongoitrous, 2 51 0.026
517
c FML023 Familial Hemiplegic Migraine 51 0.026
518
RFL001 Reflex Sympathetic Dystrophy 51 0.026
519
P NNL004 Nonalcoholic Fatty Liver Disease 51 0.026
520
DRG003 Drug Dependence 51 0.026
521
NNT012 Neonatal Jaundice 51 0.026
522
SCB001 Scabies 50 0.026
523
P HML001 Hemolytic-Uremic Syndrome 50 0.026
524
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 50 0.026
525
P PSD015 Pseudohypoparathyroidism 50 0.026
526
HYP077 Hypertrichosis 50 0.026
527
THR013 Thoracic Outlet Syndrome 50 0.026
528
P PTY003 Pityriasis Rubra Pilaris 50 0.026
529
ANR004 Anuria 50 0.026
530
P OVR046 Ovarian Cyst 50 0.026
531
BRD004 Borderline Personality Disorder 49 0.026
532
P FBR025 Fibrochondrogenesis 49 0.026
533
P MRC003 Mercury Poisoning 49 0.026
534
P EPT020 Epithelioid Hemangioendothelioma 49 0.026
535
BLL003 Bell's Palsy 49 0.026
536
HYP458 Hyper Ige Syndrome 49 0.026
537
ANH002 Anhidrosis 48 0.026
538
MTB004 Metabolic Acidosis 48 0.026
539
KLN009 Kleine-Levin Hibernation Syndrome 48 0.026
540
c NRP037 Neuropathy, Hereditary Sensory and Autonomic, Type V 48 0.026
541
FRZ001 Frozen Shoulder 48 0.026
542
P KRT007 Keratoconus 48 0.026
543
RGH009 Right Atrial Isomerism 47 0.026
544
P CMP008 Compartment Syndrome 47 0.026
545
CMP034 Complete Androgen Insensitivity Syndrome 47 0.026
546
P LYD001 Leydig Cell Tumor 47 0.026
547
c DBT064 Diabetes Mellitus, Transient Neonatal, 1 47 0.026
548
VSC006 Vascular Cancer 47 0.026
549
c CNG124 Congenital Rubella 47 0.026
550
RNL078 Renal Dysplasia 46 0.026
551
P KLP003 Klippel-Feil Syndrome 46 0.026
552
P CLS010 Cluster Headache 46 0.026
553
TRC010 Trichotillomania 46 0.026
554
ALB002 Albinism 46 0.026
555
BLD063 Bile Duct Cysts 46 0.026
556
PYG006 Pyogenic Granuloma 45 0.026
557
IMP004 Impetigo 45 0.026
558
OCL033 Oculocerebral Syndrome with Hypopigmentation 45 0.026
559
RTR008 Root Resorption 44 0.026
560
BCK006 Back Pain 44 0.026
561
LCH009 Lichen Sclerosus 44 0.026
562
MCS006 Macs Syndrome 44 0.026
563
MCR225 Macrophage Activation Syndrome 44 0.026
564
c PSR021 Psoriasis 14, Pustular 44 0.026
565
c SPN297 Spondylocostal Dysostosis 3, Autosomal Recessive 43 0.026
566
P PRV002 Periventricular Nodular Heterotopia 43 0.026
567
CNV002 Conversion Disorder 42 0.026
568
P VTL001 Vitelliform Macular Dystrophy 42 0.026
569
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 42 0.026
570
LPD014 Lipodermatosclerosis 42 0.026
571
FRY002 Fryns Syndrome 42 0.026
572
c SBC007 Subacute Thyroiditis 42 0.026
573
MYC033 Myoclonus 41 0.026
574
GLC004 Galactokinase Deficiency 41 0.026
575
MTG002 Mutagen Sensitivity 41 0.026
576
P PRS062 Persistent Hyperplastic Primary Vitreous 40 0.026
577
P PST059 Pustular Psoriasis 40 0.026
578
CRN025 Corneal Dystrophy 40 0.026
579
FXF002 Fox-Fordyce Disease 40 0.026
580
NRX001 Neuroaxonal Dystrophy 40 0.026
581
c NLD009 Nail Disorder, Nonsyndromic Congenital, 1 40 0.026
582
TRN012 Transient Global Amnesia 40 0.026
583
INS023 Insensitivity to Pain, Congenital, with Anhidrosis 40 0.026
584
FNS001 Funisitis 39 0.026
585
ALG001 Algoneurodystrophy 39 0.026
586
MYF001 Myofibroma 39 0.026
587
HRM002 Hermaphroditism 39 0.026
588
INT011 Interstitial Emphysema 39 0.026
589
LTT002 Letterer-Siwe Disease 39 0.026
590
MYS001 Myositis Ossificans 39 0.026
591
MSC004 Muscle Tissue Disease 39 0.026
592
PRT019 Protein-Losing Enteropathy 39 0.026
593
NNT008 Neonatal Abstinence Syndrome 38 0.026
594
HTR014 Heterotaxy, Visceral, 1, X-Linked 38 0.026
595
TLP001 Talipes Equinovarus 38 0.026
596
c BLD124 Bleeding Disorder, Platelet-Type, 11 37 0.026
597
CRN088 Craniorachischisis 37 0.026
598
CND006 Candida Glabrata 37 0.026
599
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 37 0.026
600
BLN002 Balanitis Xerotica Obliterans 37 0.026
601
HMC038 Hemochromatosis, Neonatal 37 0.026
602
IRT001 Iritis 36 0.026
603
P GRM010 Germ Cells Tumors 36 0.026
604
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 36 0.026
605
CNC014 Cancer-Associated Retinopathy 36 0.026
606
BLN010 Balanitis 35 0.026
607
MLD002 Mild Pre-Eclampsia 35 0.026
608
CRV069 Cervix Disease 35 0.026
609
HRS011 Horseshoe Kidney 34 0.026
610
ACR005 Acrodermatitis 34 0.026
611
BLP004 Blepharophimosis 34 0.026
612
ATM052 Autoimmune Disease 1 34 0.026
613
TRD003 Taurodontism 33 0.026
614
FMR011 Fumarate Hydratase Deficiency 32 0.026
615
ALR002 Al-Raqad Syndrome 31 0.026
616
RTC010 Reticuloendotheliosis 31 0.026
617
ATN011 Autoinflammation with Infantile Enterocolitis 31 0.026
618
CLB019 Clubfoot, Congenital, with or Without Deficiency of Long Bones and/or Mirror-Image Polydactyly 30 0.026
619
GLM001 Glomeruloid Hemangioma 29 0.026
620
IMP001 Impetigo Herpetiformis 29 0.026
621
NRC003 Narcissistic Personality Disorder 29 0.026
622
ENT007 Enteropathica 29 0.026
623
SVN002 Sveinsson Chorioretinal Atrophy 29 0.026
624
IVC001 Ivic Syndrome 28 0.026
625
c PMP006 Pemphigus Vulgaris, Familial 28 0.026
626
RHH001 Rohhad 27 0.026
627
NNT018 Neonatal Herpes 27 0.026
628
SYN086 Synostoses, Tarsal, Carpal, and Digital 26 0.026
629
TRG006 Trigger Thumb 26 0.026
630
CHR190 Chromosome 12p Duplication 26 0.026
631
ALL012 Allergic Angiitis 25 0.026
632
CDL005 Caudal Duplication Anomaly 25 0.026
633
LKP001 Leukoplakia of Penis 23 0.026
634
BLD165 Blood Group, Colton System 23 0.026
635
BLD163 Blood Group, Dombrock System 22 0.026
636
c ICH014 Ichthyosis Lamellar 1 21 0.026
637
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.026
638
LMB009 Lambdoid Synostosis 19 0.026
639
c PSD047 Pseudo-Turner Syndrome 18 0.026
640
SYM006 Symmetrical Thalamic Calcifications 17 0.026
641
BLD137 Blood Group--Ahonen 17 0.026
642
OMP007 Omphalocele, Exstrophy of the Cloaca, Imperforate Anus, and Spinal Defects Complex 17 0.026
643
ECT085 Ectopia Cordis 17 0.026
644
CLP002 Colpocephaly 17 0.026
645
WLS002 Wilson-Mikity Syndrome 16 0.026
646
AND005 Androgen Insensitivity Syndrome, Mild 16 0.026
647
P CNG515 Congenital Zika Syndrome 16 0.026
648
LNR009 Linear Atrophoderma of Moulin 15 0.026
649
NNT054 Neonatal Alloimmune Neutropenia 15 0.026
650
PST092 Posttransplant Acute Limbic Encephalitis 11 0.026
651
P LNG032 Lung Cancer 98 0.019
652
MYL069 Myeloma, Multiple 83 0.019
653
OST012 Osteoarthritis 82 0.019
654
P OVR042 Ovarian Cancer 81 0.019
655
P RTN008 Retinitis Pigmentosa 81 0.019
656
c LKM061 Leukemia, Acute Myeloid 80 0.019
657
P ATX030 Ataxia-Telangiectasia 79 0.019
658
P HYP607 Hypercholesterolemia, Familial 79 0.019
659
P WSK001 Wiskott-Aldrich Syndrome 77 0.019
660
c HYP595 Hypertension, Essential 76 0.019
661
MLT157 Multiple System Atrophy 1 73 0.019
662
KPS004 Kaposi Sarcoma 73 0.019
663
c HPT073 Hepatitis C Virus 72 0.019
664
P GRF003 Graft-Versus-Host Disease 71 0.019
665
P MTC003 Metachromatic Leukodystrophy 71 0.019
666
LYM133 Lymphoma, Hodgkin, Classic 71 0.019
667
PLM001 Pulmonary Tuberculosis 71 0.019
668
c SPN225 Spondyloarthropathy 1 71 0.019
669
c HPT001 Hepatitis C 71 0.019
670
FBR012 Fabry Disease 71 0.019
671
CMM004 Common Variable Immunodeficiency 70 0.019
672
P RSP003 Respiratory Failure 70 0.019
673
P MYL005 Myelofibrosis 70 0.019
674
P ESS003 Essential Thrombocythemia 70 0.019
675
ACR007 Acromegaly 69 0.019
676
P CRV035 Cervical Cancer 69 0.019
677
P DMN001 Diamond-Blackfan Anemia 69 0.019
678
SKN019 Skin Melanoma 69 0.019
679
P NRF023 Neurofibromatosis, Type Ii 68 0.019
680
P AMY004 Amyloidosis 68 0.019
681
SMT004 Smith-Lemli-Opitz Syndrome 68 0.019
682
PRT037 Pertussis 68 0.019
683
SRC014 Sarcoma 68 0.019
684
P XRD010 Xeroderma Pigmentosum, Variant Type 68 0.019
685
c MYT021 Myotonic Dystrophy 1 68 0.019
686
APR006 Apert Syndrome 68 0.019
687
c HMP029 Hemophilia a 68 0.019
688
APN008 Apnea, Obstructive Sleep 67 0.019
689
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.019
690
ALL003 Allergic Rhinitis 67 0.019
691
P ART023 Arthropathy 67 0.019
692
P NSP012 Nasopharyngeal Carcinoma 67 0.019
693
c HRD010 Hereditary Spastic Paraplegia 67 0.019
694
c HPT016 Hepatitis B 67 0.019
695
P HMP002 Hemophagocytic Lymphohistiocytosis 67 0.019
696
P JBR020 Joubert Syndrome 1 67 0.019
697
P SYS005 Systemic Scleroderma 66 0.019
698
NVS017 Nevus, Epidermal 66 0.019
699
THY028 Thyroid Cancer 66 0.019
700
DMN031 Dementia, Lewy Body 66 0.019
701
CST001 Costello Syndrome 66 0.019
702
P PRD008 Periodontitis 66 0.019
703
SYS004 Systemic Mastocytosis 65 0.019
704
P DBT085 Diabetes Mellitus, Insulin-Dependent 65 0.019
705
P MPL001 Maple Syrup Urine Disease 65 0.019
706
P ASP006 Aspergillosis 65 0.019
707
CHR063 Chronic Mucocutaneous Candidiasis 65 0.019
708
NRF007 Neurofibroma 65 0.019
709
PSR001 Psoriatic Arthritis 65 0.019
710
P LNG028 Long Qt Syndrome 65 0.019
711
P ENC004 Encephalitis 65 0.019
712
P CHR071 Charcot-Marie-Tooth Disease 65 0.019
713
MXD005 Mixed Connective Tissue Disease 65 0.019
714
VSC011 Vasculitis 65 0.019
715
c WLM013 Wilms Tumor 1 64 0.019
716
P INT068 Intestinal Disease 64 0.019
717
P PNC044 Pancreatitis 64 0.019
718
TNG002 Tangier Disease 64 0.019
719
P LBR001 Leber Congenital Amaurosis 64 0.019
720
LPT001 Leptospirosis 64 0.019
721
SCR008 Scrub Typhus 64 0.019
722
CHL123 Chlamydia 64 0.019
723
CRB011 Cerebrotendinous Xanthomatosis 63 0.019
724
GLL008 Gilles De La Tourette Syndrome 63 0.019
725
P CCK001 Cockayne Syndrome 63 0.019
726
CLF027 Cleft Palate, Isolated 63 0.019
727
VLC001 Velocardiofacial Syndrome 63 0.019
728
ABT001 Abetalipoproteinemia 63 0.019
729
OST017 Osteomyelitis 63 0.019
730
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 63 0.019
731
MGK001 Megakaryocytic Leukemia 63 0.019
732
CNT047 Contact Dermatitis 63 0.019
733
MNK001 Menkes Disease 63 0.019
734
MTH009 Mouth Disease 63 0.019
735
P THR005 Thrombotic Thrombocytopenic Purpura 63 0.019
736
c TBR025 Tuberous Sclerosis 1 62 0.019
737
DSM004 Desmoid Tumor 62 0.019
738
c ADL017 Adult T-Cell Leukemia 62 0.019
739
P INT143 Interstitial Cystitis 62 0.019
740
CNC002 Cinca Syndrome 62 0.019
741
P CLD001 Cleidocranial Dysplasia 62 0.019
742
P GCH001 Gaucher's Disease 62 0.019
743
BLD034 Bile Duct Carcinoma 62 0.019
744
CRD119 Cardiac Arrest 62 0.019
745
P HYP802 Hypocalcemia, Autosomal Dominant 1 62 0.019
746
P HRM001 Hermansky-Pudlak Syndrome 62 0.019
747
RHM027 Rheumatic Disease 62 0.019
748
P SHW006 Shwachman-Diamond Syndrome 1 62 0.019
749
PTR032 Peters-Plus Syndrome 62 0.019
750
P CRN038 Carney Complex Variant 61 0.019
751
P OST001 Osteopetrosis 61 0.019
752
P EXN002 Exanthem 61 0.019
753
P TST021 Testicular Germ Cell Tumor 61 0.019
754
P HRD008 Hereditary Hemorrhagic Telangiectasia 61 0.019
755
WVR001 Weaver Syndrome 61 0.019
756
ALP103 Alpha-1-Antitrypsin Deficiency 61 0.019
757
PRP083 Porphyria, Acute Intermittent 61 0.019
758
CNT061 Conotruncal Heart Malformations 61 0.019
759
P ANG001 Angelman Syndrome 61 0.019
760
DRR014 Darier-White Disease 61 0.019
761
NRV006 Nervous System Cancer 60 0.019
762
ACS001 Acoustic Neuroma 60 0.019
763
LYS012 Lysosomal Acid Lipase Deficiency 60 0.019
764
VGT001 Vogt-Koyanagi-Harada Disease 60 0.019
765
DBT083 Diabetes Mellitus, Permanent Neonatal 60 0.019
766
NTH001 Netherton Syndrome 60 0.019
767
MVM001 Movement Disease 60 0.019
768
STF001 Stiff-Person Syndrome 60 0.019
769
c ATS347 Autosomal Dominant Polycystic Kidney Disease 60 0.019
770
PLM070 Pulmonic Stenosis 60 0.019
771
KLP010 Klippel-Trenaunay-Weber Syndrome 60 0.019
772
P CND004 Candidiasis 60 0.019
773
KRN002 Kearns-Sayre Syndrome 60 0.019
774
PRP019 Peripheral Nervous System Disease 60 0.019
775
MSC152 Muscular Dystrophy, Becker Type 60 0.019
776
STT001 Status Epilepticus 60 0.019
777
ACN002 Acanthosis Nigricans 60 0.019
778
P MLG056 Malignant Hyperthermia 59 0.019
779
c PNC108 Pancreatitis, Hereditary 59 0.019
780
BLS001 Blau Syndrome 59 0.019
781
P PLR004 Pleuropulmonary Blastoma 59 0.019
782
INC021 Incontinentia Pigmenti 59 0.019
783
P OLG002 Oligodendroglioma 59 0.019
784
PRD013 Periodic Fever, Familial, Autosomal Dominant 59 0.019
785
c ALZ049 Alzheimer Disease 2 59 0.019
786
P CRD132 Cardiac Conduction Defect 59 0.019
787
BRN002 Bronchiolitis 59 0.019
788
JNT002 Joint Disorders 59 0.019
789
MNK003 Muenke Syndrome 59 0.019
790
c 3MT016 3-Methylglutaconic Aciduria, Type Iii 59 0.019
791
SLP005 Sleep Disorder 59 0.019
792
P OVR049 Ovarian Disease 59 0.019
793
P ANT006 Antiphospholipid Syndrome 59 0.019
794
P BRN019 Bernard-Soulier Syndrome 59 0.019
795
P MLN066 Melanoma, Cutaneous Malignant 1 59 0.019
796
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 59 0.019
797
SFT003 Soft Tissue Sarcoma 58 0.019
798
RHM001 Rheumatic Fever 58 0.019
799
APH002 Aphasia 58 0.019
800
P EPD009 Epidermolysis Bullosa Dystrophica 58 0.019
801
BDD001 Budd-Chiari Syndrome 58 0.019
802
P ESP035 Esophagitis, Eosinophilic, 1 58 0.019
803
P HLL001 Hallermann-Streiff Syndrome 58 0.019
804
CMP005 Campomelic Dysplasia 57 0.019
805
NRT004 Neuritis 57 0.019
806
DMY004 Demyelinating Disease 57 0.019
807
P PLY019 Polyneuropathy 57 0.019
808
P EPL140 Epilepsy, Idiopathic Generalized 57 0.019
809
P CRB048 Cerebral Cavernous Malformations 57 0.019
810
c GNG001 Gangliosidosis Gm1 57 0.019
811
GT001 Gout 57 0.019
812
c RCS002 Recessive Dystrophic Epidermolysis Bullosa 57 0.019
813
P SBS003 Substance Abuse 57 0.019
814
P LKD001 Leukodystrophy 57 0.019
815
OCL020 Ocular Cicatricial Pemphigoid 57 0.019
816
P ALL008 Allergic Bronchopulmonary Aspergillosis 57 0.019
817
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 57 0.019
818
ALX003 Alexander Disease 57 0.019
819
P ANG015 Angioedema 57 0.019
820
FCT003 Factor X Deficiency 57 0.019
821
PTT046 Pituitary Hormone Deficiency, Combined, 2 56 0.019
822
P HML033 Hemolytic Uremic Syndrome, Atypical 1 56 0.019
823
c ACT135 Acute Graft Versus Host Disease 56 0.019
824
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.019
825
GLC003 Glucose Intolerance 56 0.019
826
CNS004 Constipation 56 0.019
827
CYS005 Cysticercosis 56 0.019
828
P GRS003 Griscelli Syndrome 56 0.019
829
P PLY041 Polymyositis 56 0.019
830
P RTH001 Rothmund-Thomson Syndrome 56 0.019
831
ILT001 Ileitis 56 0.019
832
P STC001 Stickler Syndrome 56 0.019
833
IMM136 Immune System Disease 56 0.019
834
c PSD108 Pseudohypoparathyroidism, Type Ia 56 0.019
835
P CNT005 Central Nervous System Lymphoma 56 0.019
836
CHL014 Cholera 56 0.019
837
P STS008 Sotos Syndrome 1 56 0.019
838
P SPN301 Spinocerebellar Ataxia 2 56 0.019
839
ADN027 Adenomyosis 56 0.019
840
c HRD002 Hereditary Angioedema 56 0.019
841
P CYS018 Cystitis 56 0.019
842
MRG003 Marginal Zone B-Cell Lymphoma 56 0.019
843
BRN022 Bronchiectasis 55 0.019
844
P PTN014 Patent Ductus Arteriosus 1 55 0.019
845
PRM236 Primary Biliary Cholangitis 55 0.019
846
DGR001 Digeorge Syndrome 55 0.019
847
DSS009 Disseminated Intravascular Coagulation 55 0.019
848
PND002 Pendred Syndrome 55 0.019
849
VRN004 Vernal Keratoconjunctivitis 55 0.019
850
MYM001 Myoma 55 0.019
851
PRP032 Porphyria Variegata 55 0.019
852
c CLR131 Ciliary Dyskinesia, Primary, 1 55 0.019
853
ISL003 Isolated Growth Hormone Deficiency 55 0.019
854
ESN005 Eosinophilic Gastroenteritis 55 0.019
855
P SNR003 Senior-Loken Syndrome 1 55 0.019
856
c INT064 Intermediate Uveitis 55 0.019
857
RBR001 Roberts Syndrome 55 0.019
858
SPN019 Spondylolisthesis 55 0.019
859
PRV006 Pervasive Developmental Disorder 55 0.019
860
VSC044 Visceral Myopathy 55 0.019
861
SPN051 Spondylitis 55 0.019
862
EPD002 Epidermolytic Hyperkeratosis 55 0.019
863
TRM010 Traumatic Brain Injury 55 0.019
864
P MGL013 Megalencephaly 54 0.019
865
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 54 0.019
866
CCT002 Cicatricial Pemphigoid 54 0.019
867
HST011 Histoplasmosis 54 0.019
868
CYS010 Cystinosis 54 0.019
869
P TRC086 Trichohepatoenteric Syndrome 1 54 0.019
870
MVL001 Mevalonic Aciduria 54 0.019
871
P MSC003 Muscular Atrophy 54 0.019
872
c MLG074 Malignant Mesenchymoma 54 0.019
873
P HYP818 Hypobetalipoproteinemia, Familial, 1 54 0.019
874
P HYP050 Hyperinsulinemic Hypoglycemia 54 0.019
875
CLN019 Colonic Disease 54 0.019
876
ARS001 Aarskog-Scott Syndrome 54 0.019
877
SCK005 Sickle Cell Disease 54 0.019
878
P INF016 Infantile Epileptic Encephalopathy 54 0.019
879
c FML001 Familial Atrial Fibrillation 54 0.019
880
MTN003 Motion Sickness 54 0.019
881
PPL025 Popliteal Pterygium Syndrome 54 0.019
882
P PRM006 Primary Biliary Cirrhosis 53 0.019
883
c INF071 Inflammatory Bowel Disease 1 53 0.019
884
PSD007 Pseudomyxoma Peritonei 53 0.019
885
HYP068 Hyperostosis 53 0.019
886
CRV040 Cervix Carcinoma 53 0.019
887
P PRC012 Pericardial Effusion 53 0.019
888
NRG002 Neurogenic Bladder 53 0.019
889
PRP021 Peripheral Nervous System Neoplasm 53 0.019
890
P PTS002 Ptosis 53 0.019
891
P AXN002 Axenfeld-Rieger Syndrome 53 0.019
892
FND001 Fundus Albipunctatus 53 0.019
893
c ACH041 Achondrogenesis, Type Ii 53 0.019
894
XNT003 Xanthomatosis 53 0.019
895
WLM014 Wilms Tumor, Aniridia, Genitourinary Anomalies, and Mental Retardation Syndrome 53 0.019
896
PRP009 Peripartum Cardiomyopathy 53 0.019
897
SNS003 Sensory Peripheral Neuropathy 53 0.019
898
OVR063 Overnutrition 53 0.019
899
KRT009 Keratosis 53 0.019
900
P CNT004 Centronuclear Myopathy 53 0.019
901
c PSD066 Pseudohypoparathyroidism, Type Ib 53 0.019
902
P EMR001 Emery-Dreifuss Muscular Dystrophy 52 0.019
903
RST001 Restless Legs Syndrome 52 0.019
904
TMP001 Temporal Lobe Epilepsy 52 0.019
905
P CLL015 Collagen Disease 52 0.019
906
c GLC097 Glaucoma 3, Primary Congenital, a 52 0.019
907
FBR032 Fibromuscular Dysplasia 52 0.019
908
P DDN001 Duodenal Ulcer 52 0.019
909
c ACT020 Acute T Cell Leukemia 52 0.019
910
FRN051 Frontotemporal Lobar Degeneration with Tdp43 Inclusions, Grn-Related 52 0.019
911
P PTT006 Pituitary Adenoma 52 0.019
912
P CTN003 Cutaneous Lupus Erythematosus 52 0.019
913
OST011 Osteomalacia 52 0.019
914
c AMG001 Amegakaryocytic Thrombocytopenia, Congenital 52 0.019
915
WRN002 Wernicke-Korsakoff Syndrome 52 0.019
916
GLC008 Glucose Metabolism Disease 52 0.019
917
QDR001 Quadriplegia 52 0.019
918
HMG002 Hemoglobinuria 52 0.019
919
GGR001 Geographic Tongue 52 0.019
920
P RNL007 Renal Tubular Acidosis 52 0.019
921
NRM004 Neuroma 51 0.019
922
SPN020 Spondylosis 51 0.019
923
BCL010 B-Cell Expansion with Nfkb and T-Cell Anergy 51 0.019
924
HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 51 0.019
925
P SJG002 Sjogren-Larsson Syndrome 51 0.019
926
GNG002 Ganglioneuroma 51 0.019
927
c ERL020 Early-Onset Schizophrenia 51 0.019
928
MCL006 Macular Retinal Edema 51 0.019
929
c FRS014 Fraser Syndrome 1 51 0.019
930
P MGL001 Megaloblastic Anemia 51 0.019
931
c THR071 Thrombocytopenia 1 51 0.019
932
PRR002 Pure Red-Cell Aplasia 51 0.019
933
c PRM226 Primary Central Nervous System Lymphoma 51 0.019
934
P MYM013 Moyamoya Disease 1 51 0.019
935
THY030 Thyroid Gland Disease 51 0.019
936
CHN055 Chanarin-Dorfman Syndrome 51 0.019
937
NPH091 Nephrolithiasis, Calcium Oxalate 51 0.019
938
P SYP003 Syphilis 51 0.019
939
FCL012 Facial Paralysis 51 0.019
940
DNT012 Dental Caries 51 0.019
941
P ASP001 Asperger Syndrome 51 0.019
942
P LCT001 Lactic Acidosis 50 0.019
943
PTS001 Patau Syndrome 50 0.019
944
P BRC006 Brachydactyly 50 0.019
945
CHL004 Cholelithiasis 50 0.019
946
PRN023 Prion Disease 50 0.019
947
BLL001 Baller-Gerold Syndrome 50 0.019
948
P LPM005 Lipomatosis 50 0.019
949
INT303 Intracranial Hypertension, Idiopathic 50 0.019
950
CTS002 Cat-Scratch Disease 50 0.019
951
NSD001 Nose Disease 50 0.019
952
LRN003 Learning Disability 50 0.019
953
P TCL004 T-Cell Leukemia 50 0.019
954
P EXD001 Exudative Vitreoretinopathy 50 0.019
955
P SYR001 Syringomyelia 50 0.019
956
P OLV001 Olivopontocerebellar Atrophy 50 0.019
957
PRN011 Pernicious Anemia 50 0.019
958
FLL008 Folliculitis 50 0.019
959
NDL021 Nodular Lymphocyte Predominant Hodgkin Lymphoma 50 0.019
960
PPL048 Papillorenal Syndrome 50 0.019
961
PLN006 Poland Syndrome 50 0.019
962
LYM009 Lymphocytic Choriomeningitis 50 0.019
963
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.019
964
INT051 Intussusception 49 0.019
965
MGC001 Megacolon 49 0.019
966
HMN032 Human Herpesvirus 8 49 0.019
967
CCN002 Cocaine Abuse 49 0.019
968
LNT004 Lentigines 49 0.019
969
SLD003 Sialadenitis 49 0.019
970
HND002 Hand, Foot and Mouth Disease 49 0.019
971
DRR008 Diarrhea 1, Secretory Chloride, Congenital 49 0.019
972
IDP024 Idiopathic Inflammatory Myopathy 49 0.019
973
c LBR014 Leber Congenital Amaurosis 4 49 0.019
974
HMF009 Hemifacial Hyperplasia 49 0.019
975
EPD006 Epidermolysis Bullosa Acquisita 49 0.019
976
MNN009 Meningoencephalitis 49 0.019
977
HMP009 Haemophilus Influenzae 49 0.019
978
P INF049 Infantile Myofibromatosis 49 0.019
979
c GRS014 Griscelli Syndrome, Type 2 49 0.019
980
PRT011 Protein C Deficiency 49 0.019
981
FND002 Fundus Dystrophy 49 0.019
982
CVR006 Cavernous Hemangioma 49 0.019
983
HYD038 Hydrops Fetalis, Nonimmune 49 0.019
984
PPL018 Papillary Adenocarcinoma 49 0.019
985
P HRD021 Hereditary Sensory Neuropathy 48 0.019
986
HYP085 Hypothalamic Disease 48 0.019
987
CNJ012 Conjunctival Disease 48 0.019
988
ANV001 Anovulation 48 0.019
989
NPH003 Nephrocalcinosis 48 0.019
990
P ALT001 Alternating Hemiplegia of Childhood 48 0.019
991
CYS036 Cystinosis, Nephropathic 48 0.019
992
FBR009 Fibrous Dysplasia 48 0.019
993
c MLG069 Malignant Hypertension 48 0.019
994
MTY001 Mutyh-Associated Polyposis 48 0.019
995
P TYR004 Tyrosinemia 48 0.019
996
DNN001 Danon Disease 48 0.019
997
P PRM001 Primary Cutaneous Amyloidosis 48 0.019
998
PLM035 Pulmonary Eosinophilia 48 0.019
999
P LSS002 Lissencephaly 48 0.019
1000
ALP097 Alopecia Universalis Congenita 48 0.019
1001
CNG046 Congenital Fiber-Type Disproportion 48 0.019
1002
PRS129 Prostatic Hyperplasia, Benign 48 0.019
1003
NVS001 Neovascular Glaucoma 48 0.019
1004
P ORF001 Orofaciodigital Syndrome 48 0.019
1005
SCT005 Scott Syndrome 48 0.019
1006
PRS012 Pars Planitis 47 0.019
1007
HDN002 Head Injury 47 0.019
1008
P JNC001 Junctional Epidermolysis Bullosa 47 0.019
1009
P GRW001 Growth Hormone Secreting Pituitary Adenoma 47 0.019
1010
MLT006 Multidrug-Resistant Tuberculosis 47 0.019
1011
CHR074 Choriocarcinoma 47 0.019
1012
DSC009 Discoid Lupus Erythematosus 47 0.019
1013
c TRC092 Trichorhinophalangeal Syndrome, Type I 47 0.019
1014
c ACT076 Acute Myocarditis 47 0.019
1015
VLP002 Valproate Embryopathy 47 0.019
1016
ART004 Aortic Atherosclerosis 47 0.019
1017
JHN001 Johanson-Blizzard Syndrome 47 0.019
1018
PLM041 Pulmonary Valve Stenosis 47 0.019
1019
CRD002 Cri-Du-Chat Syndrome 47 0.019
1020
PLM029 Palmoplantar Keratosis 47 0.019
1021
DRM011 Dermatophytosis 47 0.019
1022
P D2H002 D-2-Hydroxyglutaric Aciduria 1 47 0.019
1023
P RBN002 Robinow Syndrome 47 0.019
1024
OPP004 Oppositional Defiant Disorder 47 0.019
1025
SYN036 Syncope 47 0.019
1026
P ALP061 Alopecia, Androgenetic, 1 47 0.019
1027
P PSD003 Pseudohypoaldosteronism 47 0.019
1028
CRB085 Cerebral Hemorrhage 47 0.019
1029
SPS007 Spastic Cerebral Palsy 47 0.019
1030
FBR019 Fibromatosis 47 0.019
1031
c OPT051 Opitz Gbbb Syndrome, Type I 47 0.019
1032
PRM003 Premature Ejaculation 47 0.019
1033
P KLF001 Kleefstra Syndrome 46 0.019
1034
AGR002 Agoraphobia 46 0.019
1035
TRC062 Tricuspid Atresia 46 0.019
1036
MCR011 Microinvasive Gastric Cancer 46 0.019
1037
ENT004 Enthesopathy 46 0.019
1038
c TYR013 Tyrosinemia, Type Ii 46 0.019
1039
CHR008 Choroiditis 46 0.019
1040
ALP093 Alpha-Thalassemia/mental Retardation Syndrome, Chromosome 16-Related 46 0.019
1041
GLT007 Glutathione Synthetase Deficiency 46 0.019
1042
P LRS001 Larsen Syndrome 46 0.019
1043
NSP002 Nasopharyngitis 46 0.019
1044
GND003 Gonadal Disease 46 0.019
1045
NRW001 Norwegian Scabies 46 0.019
1046
MNL001 Monilethrix 46 0.019
1047
c MTR002 Mitral Valve Insufficiency 46 0.019
1048
KRT010 Kartagener Syndrome 46 0.019
1049
P TRT019 Torticollis 46 0.019
1050
PRD003 Periodontosis 46 0.019
1051
MCR037 Macroglossia 46 0.019
1052
AND001 Anodontia 46 0.019
1053
BSL008 Basal Ganglia Disease 46 0.019
1054
P FNG006 Feingold Syndrome 1 45 0.019
1055
MTR010 Mature Teratoma 45 0.019
1056
P ICH001 Ichthyosis Vulgaris 45 0.019
1057
PRM013 Premature Menopause 45 0.019
1058
SBP004 Subependymoma 45 0.019
1059
LYM127 Lymphatic Malformations 45 0.019
1060
P AML002 Amelogenesis Imperfecta 45 0.019
1061
c SPN100 Spinocerebellar Ataxia 27 45 0.019
1062
TBR006 Tuberculoid Leprosy 45 0.019
1063
INT071 Intestinal Perforation 45 0.019
1064
GND001 Gonadoblastoma 45 0.019
1065
BNG009 Benign Epilepsy with Centrotemporal Spikes 45 0.019
1066
PLC003 Placental Site Trophoblastic Tumor 45 0.019
1067
P CHN044 Chondrodysplasia Punctata Syndrome 44 0.019
1068
OCL052 Ocular Dominance 44 0.019
1069
c 46X001 46 Xy Gonadal Dysgenesis 44 0.019
1070
ALV007 Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins 44 0.019
1071
BRN080 Brain Ischemia 44 0.019
1072
NRN008 Neuronal Intranuclear Inclusion Disease 44 0.019
1073
RSP019 Respiratory Distress Syndrome in Premature Infants 44 0.019
1074
CD4003 Cd40 Ligand Deficiency 44 0.019
1075
MYP136 Myopathy, Centronuclear, X-Linked 44 0.019
1076
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 44 0.019
1077
TTH032 Tooth Size 44 0.019
1078
DFF003 Diffuse Scleroderma 44 0.019
1079
DFF001 Diffuse Cutaneous Mastocytosis 44 0.019
1080
P ACH011 Achondrogenesis 44 0.019
1081
SLR001 Sialuria 43 0.019
1082
DBW001 Dubowitz Syndrome 43 0.019
1083
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.019
1084
MYX004 Myxedema 43 0.019
1085
c RNL122 Renal Hypodysplasia/aplasia 3 43 0.019
1086
P SDR003 Sideroblastic Anemia 43 0.019
1087
MNN017 Mononeuropathy 43 0.019
1088
PRS030 Persistent Fetal Circulation Syndrome 43 0.019
1089
ASP030 Aspirin Resistance 43 0.019
1090
END011 Endometriosis of Ovary 43 0.019
1091
ASP004 Asphyxia Neonatorum 43 0.019
1092
c EMR018 Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant 43 0.019
1093
CND005 Cone Dystrophy 43 0.019
1094
c ACR116 Aicardi-Goutieres Syndrome 1 43 0.019
1095
MMM006 Mammographic Density 43 0.019
1096
BDY001 Body Dysmorphic Disorder 42 0.019
1097
PRP056 Porphyria, Acute Hepatic 42 0.019
1098
PNG002 Pain Agnosia 42 0.019
1099
c CNG029 Congenital Mesoblastic Nephroma 42 0.019
1100
WDM004 Wiedemann-Steiner Syndrome 42 0.019
1101
MNN021 Meningococcemia 42 0.019
1102
SPN029 Spondylolysis 42 0.019
1103
ALX002 Alexithymia 42 0.019
1104
PLG004 Plagiocephaly 42 0.019
1105
KWS001 Kwashiorkor 42 0.019
1106
OCL069 Ocular Motor Apraxia 42 0.019
1107
IRN004 Iron-Refractory Iron Deficiency Anemia 42 0.019
1108
EPC002 Epicondylitis 42 0.019
1109
SPR007 Superior Mesenteric Artery Syndrome 42 0.019
1110
SMT001 Somatization Disorder 41 0.019
1111
FCL041 Focal Myositis 41 0.019
1112
P PNT019 Pontocerebellar Hypoplasia 41 0.019
1113
HMP001 Hemopericardium 41 0.019
1114
P TST026 Testicular Germ Cell Cancer 41 0.019
1115
c PRG001 Progressive Muscular Atrophy 41 0.019
1116
DLS001 Delusional Disorder 41 0.019
1117
BST007 Best Vitelliform Macular Dystrophy 41 0.019
1118
IDP070 Idiopathic Scoliosis 41 0.019
1119
P CNG048 Congenital Hepatic Fibrosis 41 0.019
1120
RTT001 Ritter's Disease 41 0.019
1121
CHR078 Chorioretinitis 40 0.019