Search results for twinning

1295 hits were found for twinning

# Family MCID Name MIFTS Score
1
TWN001 Twin-to-Twin Transfusion Syndrome 48 12.729
2
c RNL090 Renal Tubular Dysgenesis Due to Twin-Twin Transfusion 6 3.803
3
P PLY018 Polycythemia 58 0.151
4
PLY012 Polyhydramnios 47 0.148
5
CRB009 Cerebritis 39 0.145
6
ANN002 Anencephaly 54 0.135
7
PLC008 Placenta Disease 33 0.124
8
P HRT032 Heart Disease 75 0.117
9
P CRV039 Cervicitis 45 0.100
10
P OBS005 Obesity 92 0.096
11
OLG003 Oligohydramnios 53 0.096
12
HYD012 Hydrops Fetalis 43 0.095
13
P CRD011 Cardiomyopathy 68 0.091
14
CHL071 Child Syndrome 58 0.089
15
KDS001 Kid Syndrome 53 0.089
16
CCN007 Cocoon Syndrome 45 0.087
17
CYT008 Cytomegalovirus Infection 52 0.085
18
DWN001 Down Syndrome 66 0.080
19
CHR005 Chorioamnionitis 48 0.080
20
CNG069 Congenital Cytomegalovirus 36 0.080
21
DFC004 Deficiency Anemia 64 0.078
22
P THY032 Thyroiditis 54 0.078
23
SRN002 Sirenomelia 29 0.078
24
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.076
25
P LKM002 Leukemia 71 0.073
26
NNT011 Neonatal Anemia 33 0.071
27
P PLM037 Pulmonary Hypertension 79 0.068
28
P HYP086 Hypothyroidism 64 0.068
29
ISC004 Ischemia 61 0.068
30
P PRS038 Personality Disorder 62 0.065
31
URT039 Urticaria 57 0.065
32
OMP004 Omphalocele 50 0.065
33
ECT026 Ectopic Pregnancy 48 0.065
34
PRT082 Preterm Premature Rupture of the Membranes 46 0.065
35
WLL006 Wells Syndrome 59 0.063
36
PLC005 Placental Insufficiency 50 0.063
37
PYL006 Pyloric Stenosis 46 0.063
38
GDS001 Good Syndrome 44 0.063
39
INT060 Intestinal Atresia 42 0.063
40
P UTR038 Uterine Disease 37 0.063
41
CRB037 Cerebral Palsy 66 0.060
42
P EPL164 Epilepsy 66 0.060
43
P LPS004 Lupus Erythematosus 64 0.060
44
P THR014 Thrombocytopenia 64 0.060
45
c PRC016 Pre-Eclampsia 56 0.060
46
P ECL001 Eclampsia 54 0.060
47
P APL006 Aplasia Cutis Congenita 52 0.060
48
P TRT010 Teratoma 52 0.060
49
P ENC008 Encephalocele 48 0.060
50
BRT030 Birth Defects 43 0.060
51
URT008 Urticaria Pigmentosa 37 0.060
52
ENC005 Encephalomalacia 27 0.060
53
P TYS001 Tay-Sachs Disease 71 0.057
54
P MYP004 Myopathy 67 0.057
55
DRM006 Dermatitis 66 0.057
56
P NRC002 Narcolepsy 62 0.057
57
P TXP001 Toxoplasmosis 61 0.057
58
THR024 Thrombosis 57 0.057
59
GST033 Gestational Diabetes 57 0.057
60
P GND004 Gonadal Dysgenesis 51 0.057
61
PRV004 Periventricular Leukomalacia 48 0.057
62
c PST041 Posterior Urethral Valves 47 0.057
63
GST009 Gastroschisis 47 0.057
64
LKM006 Leukomalacia 43 0.057
65
P HYP009 Hypertrophic Pyloric Stenosis 42 0.057
66
URT001 Urethritis 41 0.057
67
HYD001 Hydranencephaly 35 0.057
68
PNT005 Pentalogy of Cantrell 26 0.057
69
DPR014 Diprosopus 18 0.057
70
P ART022 Arthritis 75 0.053
71
P RBN001 Rubinstein-Taybi Syndrome 64 0.053
72
P LYM026 Lymphoblastic Leukemia 62 0.053
73
P ESP024 Esophagitis 61 0.053
74
P ADL010 Adult Respiratory Distress Syndrome 61 0.053
75
c CNG006 Congenital Hypothyroidism 60 0.053
76
c ACT210 Acute Respiratory Distress Syndrome 57 0.053
77
CND002 Conduct Disorder 54 0.053
78
P DBT005 Diabetes Insipidus 53 0.053
79
ADL002 Adult Syndrome 52 0.053
80
IMP002 Imperforate Anus 52 0.053
81
RTN023 Retinitis 50 0.053
82
KLN001 Klinefelter's Syndrome 50 0.053
83
c CNG021 Congenital Toxoplasmosis 48 0.053
84
c BPL002 Bipolar I Disorder 47 0.053
85
NWB001 Newborn Respiratory Distress Syndrome 45 0.053
86
RFR003 Refractive Error 43 0.053
87
CHR322 Choreoathetosis, Hypothyroidism, and Neonatal Respiratory Distress 40 0.053
88
AMN009 Amniotic Band Syndrome 26 0.053
89
RSP007 Respiratory Distress Syndrome, Infant 22 0.053
90
c ADL080 Adult Acute Respiratory Distress Syndrome 19 0.053
91
ACR022 Acardia 12 0.053
92
P SCH015 Schizophrenia 77 0.050
93
P CRN211 Coronary Artery Disease 74 0.050
94
P NRF002 Neurofibromatosis 71 0.050
95
ISC006 Ischemic Heart Disease 68 0.050
96
ANX002 Anxiety Disorder 67 0.050
97
ART005 Arteriovenous Malformation 66 0.050
98
P MSC005 Muscular Dystrophy 65 0.050
99
P DYS154 Dystonia 65 0.050
100
P PRM019 Premature Ovarian Failure 64 0.050
101
P HLP001 Holoprosencephaly 63 0.050
102
ALC007 Alcohol Dependence 63 0.050
103
P MST009 Mastocytosis 56 0.050
104
PTH002 Pathological Gambling 51 0.050
105
ESP020 Esophageal Atresia 50 0.050
106
P OST009 Osteochondritis Dissecans 49 0.050
107
MTS001 Mutism 43 0.050
108
TRN007 Transsexualism 41 0.050
109
SCR024 Sacrococcygeal Teratoma 27 0.050
110
P RHM011 Rheumatoid Arthritis 89 0.046
111
c SYS001 Systemic Lupus Erythematosus 86 0.046
112
P NRB001 Neuroblastoma 70 0.046
113
ATT013 Attention Deficit-Hyperactivity Disorder 69 0.046
114
PRP027 Peripheral Vascular Disease 68 0.046
115
DMN002 Dementia 65 0.046
116
PLM033 Pulmonary Embolism 60 0.046
117
P INF032 Infertility 59 0.046
118
PST028 Post-Traumatic Stress Disorder 57 0.046
119
ALP008 Alopecia 57 0.046
120
P MYS005 Myositis 57 0.046
121
P BCK002 Beckwith-Wiedemann Syndrome 56 0.046
122
BLM002 Bulimia Nervosa 52 0.046
123
BRN071 Brain Injury 52 0.046
124
P HYP065 Hyperaldosteronism 50 0.046
125
HLL004 Hellp Syndrome 50 0.046
126
CTN014 Cutaneous Mastocytosis 49 0.046
127
TRN044 Transposition of the Great Arteries 48 0.046
128
PLC007 Placental Abruption 47 0.046
129
ACR041 Acromelic Frontonasal Dysostosis 45 0.046
130
BWN001 Bowen-Conradi Syndrome 44 0.046
131
SPS057 Spasticity 42 0.046
132
PRN019 Perinatal Necrotizing Enterocolitis 42 0.046
133
ATN011 Autoinflammation with Infantile Enterocolitis 39 0.046
134
ALR002 Al-Raqad Syndrome 36 0.046
135
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.046
136
PLY024 Polymicrogyria 35 0.046
137
CLC011 Cloacal Exstrophy 32 0.046
138
ANS004 Anisometropia 29 0.046
139
JJN004 Jejunal Atresia 29 0.046
140
PRT086 Partial Hydatidiform Mole 26 0.046
141
P MYC007 Myocardial Infarction 79 0.042
142
NRL016 Neural Tube Defects 76 0.042
143
INS024 Insulin-Like Growth Factor I 75 0.042
144
PTZ001 Peutz-Jeghers Syndrome 71 0.042
145
P HPT021 Hepatitis 69 0.042
146
P PNM007 Pneumonia 68 0.042
147
ATH003 Atherosclerosis 65 0.042
148
PRT036 Peritonitis 63 0.042
149
P CRN015 Cornelia De Lange Syndrome 62 0.042
150
P BPL003 Bipolar Disorder 62 0.042
151
P HYP055 Hypoplastic Left Heart Syndrome 61 0.042
152
P ALC004 Alcohol Abuse 59 0.042
153
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 57 0.042
154
ANR040 Aneurysm 57 0.042
155
EPD016 Epidermolysis Bullosa 57 0.042
156
P MYP006 Myopia 56 0.042
157
P HYP076 Hyperthyroidism 55 0.042
158
P ATX004 Ataxia 53 0.042
159
ALL026 Allergic Hypersensitivity Disease 52 0.042
160
ECT006 Ectodermal Dysplasia 52 0.042
161
P DRM007 Dermatitis Herpetiformis 51 0.042
162
P PRC031 Preeclampsia/eclampsia 1 51 0.042
163
P RNL028 Renal Tubular Dysgenesis 51 0.042
164
BRX001 Bruxism 49 0.042
165
c SVR005 Severe Pre-Eclampsia 49 0.042
166
LMB062 Limb Ischemia 48 0.042
167
AST006 Astigmatism 45 0.042
168
ACD009 Acid-Labile Subunit, Deficiency of 45 0.042
169
RSP019 Respiratory Distress Syndrome in Premature Infants 43 0.042
170
GND002 Gender Identity Disorder 42 0.042
171
END072 Endotheliitis 42 0.042
172
EST005 Esotropia 41 0.042
173
PSD009 Pseudohermaphroditism 40 0.042
174
CRV069 Cervix Disease 32 0.042
175
PHC006 Phacomatosis Pigmentovascularis 25 0.042
176
P CRN178 Coronary Heart Disease 6 21 0.042
177
c CRN173 Coronary Heart Disease 8 18 0.042
178
EPG004 Epignathus 17 0.042
179
P BRS047 Breast Cancer 100 0.038
180
CYS001 Cystic Fibrosis 83 0.038
181
P AST005 Asthma 82 0.038
182
HV1006 Hiv-1 80 0.038
183
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.038
184
KWS002 Kawasaki Disease 70 0.038
185
TBR010 Tuberculosis 70 0.038
186
c NRF018 Neurofibromatosis, Type 1 67 0.038
187
P ATS007 Autism Spectrum Disorder 65 0.038
188
P ANR002 Aniridia 64 0.038
189
LNG099 Lung Disease 64 0.038
190
P PSR002 Psoriasis 61 0.038
191
OVR029 Ovarian Hyperstimulation Syndrome 61 0.038
192
P NPH009 Nephrolithiasis 60 0.038
193
ACQ007 Acquired Immunodeficiency Syndrome 60 0.038
194
PRM097 Primary Immunodeficiency Disease 60 0.038
195
RBR001 Roberts Syndrome 60 0.038
196
P GRV001 Graves' Disease 59 0.038
197
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.038
198
P SHR029 Short Syndrome 58 0.038
199
ART021 Arteriosclerosis 58 0.038
200
P PLY006 Polydactyly 56 0.038
201
GTR002 Goiter 52 0.038
202
P NNT009 Neonatal Diabetes Mellitus 52 0.038
203
BRN004 Brain Edema 52 0.038
204
P ICH004 Ichthyosis 52 0.038
205
P MGR003 Migraine with Aura 52 0.038
206
SMT008 Smith-Magenis Syndrome 52 0.038
207
HMN014 Human Immunodeficiency Virus Infectious Disease 50 0.038
208
THR013 Thoracic Outlet Syndrome 50 0.038
209
P PRN026 Porencephaly 48 0.038
210
FML039 Female Reproductive System Disease 48 0.038
211
GYN001 Gynecomastia 48 0.038
212
VND001 Vein Disease 47 0.038
213
SYN005 Synostosis 46 0.038
214
ACR012 Aicardi Syndrome 46 0.038
215
TCL003 T Cell Deficiency 45 0.038
216
VSC047 Vascular Malformation 45 0.038
217
PRN038 Prune Belly Syndrome 45 0.038
218
END020 Endocardial Fibroelastosis 44 0.038
219
HTR003 Heterotaxy 44 0.038
220
CRV043 Cervical Dystonia 44 0.038
221
DYS018 Dysostosis 44 0.038
222
P ART084 Arteriovenous Fistula 44 0.038
223
DDN006 Duodenitis 42 0.038
224
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.038
225
BRN080 Brain Ischemia 41 0.038
226
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.038
227
MCR103 Microtia 37 0.038
228
NTR005 Nutritional Deficiency Disease 36 0.038
229
SLP010 Slipped Capital Femoral Epiphysis 34 0.038
230
BRW006 Brown Syndrome 29 0.038
231
CRB031 Cerebral Arterial Disease 27 0.038
232
CLN022 Colonic Atresia 24 0.038
233
FTL016 Fetal Edema 15 0.038
234
CD4004 Cd4 Deficiency 14 0.038
235
PHC005 Phacomatosis Pigmentokeratotica 12 0.038
236
CRN073 Coronary Arteries Congenital Malformation 10 0.038
237
JMC001 Jamaican Vomiting Sickness 9 0.038
238
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 78 0.033
239
P MDL005 Medulloblastoma 77 0.033
240
CRH001 Crohn's Disease 75 0.033
241
P ALG002 Alagille Syndrome 72 0.033
242
P INF038 Influenza 72 0.033
243
P ADN016 Adenocarcinoma 69 0.033
244
P LYM118 Lymphoma 69 0.033
245
P OST005 Osteogenesis Imperfecta 69 0.033
246
PCK002 Pick Disease 68 0.033
247
P CLC005 Celiac Disease 68 0.033
248
VSC007 Vascular Disease 67 0.033
249
P MNN013 Meningitis 67 0.033
250
P MYS003 Myasthenia Gravis 67 0.033
251
SKN016 Skin Disease 66 0.033
252
INC002 Inclusion Body Myositis 66 0.033
253
ATP002 Atopy 66 0.033
254
P CRN037 Craniosynostosis 66 0.033
255
P TRN020 Turner Syndrome 65 0.033
256
P PLY011 Polycystic Ovary Syndrome 65 0.033
257
P AGM001 Agammaglobulinemia 64 0.033
258
P THL005 Thalassemia 64 0.033
259
BRN024 Bronchitis 64 0.033
260
P INF037 Inflammatory Bowel Disease 63 0.033
261
MLN008 Melanoma 62 0.033
262
P ATP001 Atopic Dermatitis 62 0.033
263
P RCK004 Rickets 61 0.033
264
P ANR007 Anorexia Nervosa 61 0.033
265
EYD002 Eye Disease 61 0.033
266
P CNG015 Congenital Diaphragmatic Hernia 60 0.033
267
WLL001 Williams-Beuren Syndrome 60 0.033
268
P DRR001 Diarrhea 60 0.033
269
P RHN004 Rhinitis 60 0.033
270
P VNT002 Ventricular Septal Defect 60 0.033
271
GST045 Gastroenteritis 59 0.033
272
P ENC018 Encephalopathy 59 0.033
273
P NTR004 Neutropenia 59 0.033
274
P INT001 Intrahepatic Cholestasis 59 0.033
275
CHL068 Cholestasis 59 0.033
276
P NPH012 Nephrotic Syndrome 59 0.033
277
P CTS001 Cutis Laxa 58 0.033
278
RSP006 Respiratory System Disease 58 0.033
279
P CTR002 Cataract 58 0.033
280
P HST010 Histiocytosis 58 0.033
281
P HMP007 Hemophilia 57 0.033
282
BLS001 Blau Syndrome 57 0.033
283
P HYP040 Hypospadias 57 0.033
284
SFT003 Soft Tissue Sarcoma 57 0.033
285
HYP266 Hypoxia 56 0.033
286
PRS047 Prostatitis 56 0.033
287
ART111 Artery Disease 55 0.033
288
ASP002 Aspartylglucosaminuria 55 0.033
289
URN010 Urinary Tract Obstruction 55 0.033
290
P SLV001 Silver-Russell Syndrome 54 0.033
291
TTH002 Tooth Agenesis 54 0.033
292
CHN016 Cohen Syndrome 54 0.033
293
MCN017 Meconium Ileus 54 0.033
294
TST014 Testicular Cancer 53 0.033
295
PNM008 Pneumothorax 53 0.033
296
P FTL001 Fetal Alcohol Syndrome 53 0.033
297
DGN001 Degenerative Disc Disease 52 0.033
298
CRH005 Crohn's Colitis 52 0.033
299
IRN001 Iron Deficiency Anemia 52 0.033
300
GNR004 Generalized Anxiety Disorder 51 0.033
301
VND002 Van Der Woude Syndrome 50 0.033
302
GRW007 Growth Hormone Deficiency 50 0.033
303
CDL003 Caudal Regression Syndrome 50 0.033
304
P DDN001 Duodenal Ulcer 50 0.033
305
CLF001 Cleft Lip 50 0.033
306
PRP016 Paraplegia 49 0.033
307
P INT063 Intellectual Disability 49 0.033
308
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.033
309
P MYT002 Myotonic Dystrophy 48 0.033
310
BRN056 Bronchopulmonary Dysplasia 48 0.033
311
SBS004 Substance Dependence 47 0.033
312
ANT011 Antisocial Personality Disorder 47 0.033
313
PPL021 Papilledema 47 0.033
314
SCL003 Social Phobia 46 0.033
315
RNL078 Renal Dysplasia 45 0.033
316
P PLN008 Peeling Skin Syndrome 45 0.033
317
ALN001 Aland Island Eye Disease 45 0.033
318
TRC040 Tracheoesophageal Fistula 45 0.033
319
P HMP006 Hemiplegic Migraine 45 0.033
320
DND001 Dandy-Walker Syndrome 44 0.033
321
c JVN003 Juvenile Xanthogranuloma 44 0.033
322
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 43 0.033
323
GLC008 Glucose Metabolism Disease 42 0.033
324
VGN023 Vaginitis 42 0.033
325
SXL003 Sexual Disorder 42 0.033
326
RNL025 Renal Hypoplasia 42 0.033
327
ANM001 Anemia of Prematurity 41 0.033
328
ARC002 Arachnoiditis 41 0.033
329
CNV002 Conversion Disorder 41 0.033
330
NRN002 Neuronitis 41 0.033
331
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.033
332
CNN002 Cannabis Abuse 40 0.033
333
TRP014 Triploidy 40 0.033
334
ARC007 Arachnoid Cysts 39 0.033
335
P OCY001 Oocyte Maturation Defect 38 0.033
336
CNN001 Cannabis Dependence 38 0.033
337
CRV025 Cervical Incompetence 36 0.033
338
NSY001 N Syndrome 36 0.033
339
P MNN007 Meningocele 36 0.033
340
ATM012 Autoimmune Disease of Blood 35 0.033
341
P NNT042 Neonatal Lupus Erythematosus 34 0.033
342
CYT004 Cytomegalic Inclusion Disease 31 0.033
343
TYP015 Type 2b Von Willebrand Disease 30 0.033
344
IMM068 Immunodeficiency 8 30 0.033
345
c ANR038 Anorexia Nervosa 1 26 0.033
346
OCC011 Occipital Encephalocele 24 0.033
347
FRM001 Freemartinism 22 0.033
348
SPS090 Sepsis in Premature Infants 21 0.033
349
GST058 Gestational Diabetes Insipidus 11 0.033
350
P HNT016 Huntington Disease 80 0.027
351
DCH001 Duchenne Muscular Dystrophy 79 0.027
352
P RTT002 Rett Syndrome 77 0.027
353
c DLT002 Dilated Cardiomyopathy 76 0.027
354
P HYP607 Hypercholesterolemia, Familial 76 0.027
355
ULC004 Ulcerative Colitis 76 0.027
356
P LVR013 Liver Disease 75 0.027
357
P PFF001 Pfeiffer Syndrome 73 0.027
358
CNG034 Congestive Heart Failure 72 0.027
359
P HMC003 Hemochromatosis 72 0.027
360
ADR007 Adrenoleukodystrophy 72 0.027
361
TTR001 Tetralogy of Fallot 71 0.027
362
BRN028 Brain Cancer 70 0.027
363
CRZ001 Crouzon Syndrome 70 0.027
364
THY028 Thyroid Cancer 69 0.027
365
SVR004 Severe Combined Immunodeficiency 69 0.027
366
c HYP595 Hypertension, Essential 69 0.027
367
ART016 Aortic Aneurysm 69 0.027
368
P TBR001 Tuberous Sclerosis 67 0.027
369
P END044 Endometriosis 66 0.027
370
P ATR011 Atrial Fibrillation 66 0.027
371
P KDN018 Kidney Disease 66 0.027
372
ACH004 Achondroplasia 66 0.027
373
P MYL006 Myeloid Leukemia 66 0.027
374
P BCL006 B-Cell Lymphomas 65 0.027
375
P NMN002 Niemann-Pick Disease 65 0.027
376
P HRP006 Herpes Simplex 65 0.027
377
P CNJ013 Conjunctivitis 64 0.027
378
CHR066 Chronic Fatigue Syndrome 64 0.027
379
P OST002 Osteoporosis 64 0.027
380
ATS001 Autistic Disorder 63 0.027
381
CRB039 Cerebrovascular Disease 63 0.027
382
ALL003 Allergic Rhinitis 63 0.027
383
P FML161 Familial Mediterranean Fever, Ar 63 0.027
384
BLM001 Bloom Syndrome 63 0.027
385
c HMP004 Hemophilia B 62 0.027
386
CNN005 Connective Tissue Disease 62 0.027
387
APH001 Aphthous Stomatitis 62 0.027
388
P DRM010 Dermatomyositis 62 0.027
389
P ALP009 Alopecia Areata 62 0.027
390
FCT003 Factor X Deficiency 61 0.027
391
HYP056 Hypoglycemia 61 0.027
392
P KLL001 Kallmann Syndrome 61 0.027
393
VNW001 Von Willebrand's Disease 61 0.027
394
P SDD001 Sudden Infant Death Syndrome 61 0.027
395
TTN003 Tetanus 61 0.027
396
c LCL006 Localized Scleroderma 61 0.027
397
CLT003 Colitis 60 0.027
398
QFV001 Q Fever 60 0.027
399
LPM004 Lipoma 60 0.027
400
P GLY013 Glycogen Storage Disease 60 0.027
401
P PNC025 Panic Disorder 60 0.027
402
P BRG001 Brugada Syndrome 59 0.027
403
P HMN010 Hemangioma 59 0.027
404
P NRP001 Neuropathy 59 0.027
405
P GLM007 Glomerulonephritis 59 0.027
406
ADL030 Adult-Onset Still's Disease 59 0.027
407
c EXD008 Exudative Vitreoretinopathy 1 59 0.027
408
PRP030 Purpura 58 0.027
409
P HYP060 Hyperinsulinism 58 0.027
410
ADN018 Adenoma 58 0.027
411
P UVT001 Uveitis 58 0.027
412
PPT005 Peptic Ulcer Disease 58 0.027
413
ELL001 Ellis-Van Creveld Syndrome 58 0.027
414
P THR003 Thoracic Aortic Aneurysm 57 0.027
415
CRT002 Cartilage-Hair Hypoplasia 57 0.027
416
P RBL001 Rubella 57 0.027
417
P PRM011 Primary Ciliary Dyskinesia 57 0.027
418
P EPS003 Episodic Ataxia 57 0.027
419
EXF001 Exfoliation Syndrome 57 0.027
420
P HYP035 Hypophosphatasia 57 0.027
421
P INT070 Intestinal Obstruction 57 0.027
422
RTN017 Retinal Detachment 56 0.027
423
NRM005 Neuromuscular Disease 56 0.027
424
P MLT074 Multiple Endocrine Neoplasia 56 0.027
425
CLR003 Clear Cell Adenocarcinoma 56 0.027
426
GST023 Gastric Ulcer 56 0.027
427
LTT002 Letterer-Siwe Disease 56 0.027
428
GST050 Gastrointestinal System Disease 56 0.027
429
PRP019 Peripheral Nervous System Disease 55 0.027
430
P SCL018 Scoliosis 55 0.027
431
P TMT001 Timothy Syndrome 55 0.027
432
P CDS001 Cadasil 55 0.027
433
MLN007 Male Infertility 55 0.027
434
P NPH005 Nephronophthisis 55 0.027
435
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.027
436
P HRD011 Hereditary Spherocytosis 54 0.027
437
HDC001 Headache 54 0.027
438
P MYC008 Myocarditis 54 0.027
439
c VRL007 Viral Encephalitis 54 0.027
440
P MCR129 Microvascular Complications of Diabetes 1 54 0.027
441
CHK001 Chikungunya 54 0.027
442
PLN006 Poland Syndrome 54 0.027
443
P OCL002 Oculocutaneous Albinism 54 0.027
444
P LRY019 Laryngitis 54 0.027
445
P BRN009 Burning Mouth Syndrome 54 0.027
446
C3D001 C3 Deficiency 53 0.027
447
GST027 Gastric Lymphoma 53 0.027
448
SLC006 Silicosis 53 0.027
449
HYP080 Hypogonadism 53 0.027
450
P FBR031 Febrile Seizures 53 0.027
451
P VSC005 Vesicoureteral Reflux 53 0.027
452
RTN018 Retinal Disease 53 0.027
453
PRV006 Pervasive Developmental Disorder 53 0.027
454
TLN003 Telangiectasis 52 0.027
455
DNY001 Denys-Drash Syndrome 52 0.027
456
KRT006 Keratoconjunctivitis 52 0.027
457
BRN106 Burns 52 0.027
458
PRG009 Progressive Multifocal Leukoencephalopathy 52 0.027
459
P SCH018 Schizencephaly 52 0.027
460
P PNC001 Pancytopenia 52 0.027
461
PMS001 Poems Syndrome 52 0.027
462
HMG005 Hemoglobinopathy 52 0.027
463
BCT002 Bacterial Vaginosis 52 0.027
464
P MSC033 Muscle Disorders 52 0.027
465
MYC002 Mycobacterium Avium Complex Disease 52 0.027
466
PRC013 Pericarditis 51 0.027
467
BLD044 Bladder Disease 51 0.027
468
ART002 Arts Syndrome 51 0.027
469
P OVR046 Ovarian Cyst 51 0.027
470
ANK001 Ankylosis 51 0.027
471
P STR020 Strabismus 51 0.027
472
ASP003 Aseptic Meningitis 51 0.027
473
P HML001 Hemolytic-Uremic Syndrome 51 0.027
474
PNN001 Panniculitis 51 0.027
475
P PMP005 Pemphigus Vulgaris 51 0.027
476
P PNM006 Pneumoconiosis 51 0.027
477
MYL020 Myelomeningocele 51 0.027
478
c FML023 Familial Hemiplegic Migraine 51 0.027
479
APR001 Apraxia 51 0.027
480
HMP005 Hemiplegia 51 0.027
481
MST005 Mastitis 51 0.027
482
P HYP014 Hyperuricemia 50 0.027
483
P LFT003 Left Ventricular Noncompaction 50 0.027
484
INT007 Intermediate Coronary Syndrome 50 0.027
485
AMN001 Amenorrhea 50 0.027
486
FML038 Female Reproductive Organ Cancer 50 0.027
487
PMP001 Pemphigus 50 0.027
488
NNT012 Neonatal Jaundice 50 0.027
489
c ACT068 Acute Cystitis 50 0.027
490
P FTL009 Fetal Akinesia Deformation Sequence 50 0.027
491
DRG003 Drug Dependence 50 0.027
492
HPT074 Hepatic Adenoma, Somatic 50 0.027
493
CSY001 C Syndrome 50 0.027
494
MSC006 Muscle Glycogenosis 49 0.027
495
ACR003 Acrodermatitis Enteropathica 49 0.027
496
CHR001 Churg-Strauss Syndrome 49 0.027
497
P KRT007 Keratoconus 48 0.027
498
KBG001 Kbg Syndrome 48 0.027
499
RTN003 Retinal Ischemia 48 0.027
500
NSD001 Nose Disease 48 0.027
501
P CMP008 Compartment Syndrome 48 0.027
502
RFL001 Reflex Sympathetic Dystrophy 48 0.027
503
P RNL015 Renal Hypertension 48 0.027
504
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 47 0.027
505
HYP043 Hyperandrogenism 47 0.027
506
BRD004 Borderline Personality Disorder 47 0.027
507
PLP001 Pulpitis 47 0.027
508
SCB001 Scabies 47 0.027
509
CRB085 Cerebral Hemorrhage 46 0.027
510
PRP021 Peripheral Nervous System Neoplasm 46 0.027
511
CNT046 Central Nervous System Vasculitis 46 0.027
512
ADR038 Adermatoglyphia 46 0.027
513
P KLP003 Klippel-Feil Syndrome 46 0.027
514
VTR016 Vater/vacterl Association 46 0.027
515
INC022 Inclusion-Cell Disease 46 0.027
516
PTY003 Pityriasis Rubra Pilaris 46 0.027
517
ALB002 Albinism 46 0.027
518
STS002 Situs Inversus 46 0.027
519
c MLG081 Malignant Teratoma 46 0.027
520
ANR004 Anuria 45 0.027
521
CRB090 Cerebral Hypoxia 45 0.027
522
P MRC003 Mercury Poisoning 45 0.027
523
c RTN160 Retinitis Pigmentosa 60 45 0.027
524
FRZ001 Frozen Shoulder 45 0.027
525
OVR012 Ovarian Serous Cystadenocarcinoma 44 0.027
526
PRG004 Progeria 44 0.027
527
PLC001 Placenta Accreta 44 0.027
528
RGH009 Right Atrial Isomerism 44 0.027
529
SPS007 Spastic Cerebral Palsy 44 0.027
530
IRR003 Irritant Dermatitis 44 0.027
531
CLS010 Cluster Headache 44 0.027
532
c CNG124 Congenital Rubella 44 0.027
533
DNG001 Dengue Shock Syndrome 43 0.027
534
PHY002 Physical Disorder 43 0.027
535
DXT001 Dextrocardia 43 0.027
536
RNL097 Renal Artery Disease 43 0.027
537
OLG020 Oligoarticular Juvenile Idiopathic Arthritis 43 0.027
538
ART031 Aortic Coarctation 43 0.027
539
MLR006 Male Reproductive Organ Cancer 43 0.027
540
LKC003 Leukocyte Disease 43 0.027
541
IMP004 Impetigo 42 0.027
542
CRN025 Corneal Dystrophy 42 0.027
543
BLD130 Bladder Exstrophy 42 0.027
544
HYP458 Hyper Ige Syndrome 42 0.027
545
CRD003 Cardiac Sarcoidosis 42 0.027
546
P BLD051 Blood Coagulation Disease 42 0.027
547
MYC033 Myoclonus 42 0.027
548
RTR008 Root Resorption 42 0.027
549
OBS015 Obesity, Hyperphagia, and Developmental Delay 41 0.027
550
PHC013 Phaeochromocytoma 41 0.027
551
HMH002 Hemihypertrophy 41 0.027
552
LCH009 Lichen Sclerosus 41 0.027
553
RPR002 Reproductive System Disease 41 0.027
554
STP004 Staphylococcal Toxic Shock Syndrome 41 0.027
555
HMT018 Hematopoietic Stem Cell Transplantation 41 0.027
556
ALK016 Alk-Negative Anaplastic Large Cell Lymphoma 41 0.027
557
AVD001 Avoidant Personality Disorder 40 0.027
558
c PLN018 Peeling Skin Syndrome 2 40 0.027
559
c SBC007 Subacute Thyroiditis 40 0.027
560
TRC010 Trichotillomania 40 0.027
561
VLV042 Vulvar Vestibulitis Syndrome 40 0.027
562
TRN012 Transient Global Amnesia 39 0.027
563
HYP391 Hyperammonemia 38 0.027
564
P PRS062 Persistent Hyperplastic Primary Vitreous 38 0.027
565
HRM002 Hermaphroditism 38 0.027
566
BLP004 Blepharophimosis 38 0.027
567
P NRX001 Neuroaxonal Dystrophy 38 0.027
568
P CHR342 Chiari Malformation 38 0.027
569
MYS001 Myositis Ossificans 37 0.027
570
DDN011 Duodenal Atresia 37 0.027
571
MYF001 Myofibroma 37 0.027
572
FRY002 Fryns Syndrome 37 0.027
573
FNS001 Funisitis 37 0.027
574
P PST059 Pustular Psoriasis 36 0.027
575
MTG002 Mutagen Sensitivity 36 0.027
576
ETH004 Euthyroid Sick Syndrome 36 0.027
577
FXF002 Fox-Fordyce Disease 36 0.027
578
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 36 0.027
579
ANR018 Anorchia 36 0.027
580
BLN002 Balanitis Xerotica Obliterans 36 0.027
581
SPL040 Split Hand 36 0.027
582
IMM065 Immunodeficiency 10 36 0.027
583
OST008 Osteosclerotic Myeloma 36 0.027
584
ACR005 Acrodermatitis 36 0.027
585
ACT060 Acute Vascular Insufficiency of Intestine 35 0.027
586
FCL044 Fecal Incontinence 35 0.027
587
IRT001 Iritis 34 0.027
588
CRN088 Craniorachischisis 34 0.027
589
MLR007 Male Reproductive System Disease 34 0.027
590
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 34 0.027
591
CND006 Candida Glabrata 34 0.027
592
NNT019 Neonatal Hypothyroidism 34 0.027
593
KSH004 Kashin-Beck Disease 33 0.027
594
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 33 0.027
595
HRS011 Horseshoe Kidney 33 0.027
596
c DGT005 Digital Arthropathy-Brachydactyly, Familial 33 0.027
597
P CHR084 Chromosomal Disease 32 0.027
598
DNT014 Dental Pulp Disease 31 0.027
599
IMM082 Immunodeficiency 18 31 0.027
600
ENT007 Enteropathica 31 0.027
601
TRG003 Trigeminal Nerve Disease 30 0.027
602
P ATX010 Ataxia Neuropathy Spectrum 30 0.027
603
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 30 0.027
604
PDT040 Pediatric Hypertension 30 0.027
605
BLN010 Balanitis 29 0.027
606
c PLN021 Peeling Skin Syndrome 3 29 0.027
607
RNL008 Renal Artery Atheroma 29 0.027
608
PHY001 Physiological Polycythemia 28 0.027
609
TRD003 Taurodontism 28 0.027
610
NRC003 Narcissistic Personality Disorder 28 0.027
611
NNT021 Neonatal Meningitis 28 0.027
612
IMP001 Impetigo Herpetiformis 28 0.027
613
RTC010 Reticuloendotheliosis 28 0.027
614
IMM076 Immunodeficiency 24 27 0.027
615
SVN001 Sveinsson Choreoretinal Atrophy 26 0.027
616
LKM059 Leukemia, Megakaryoblastic, with or Without Down Syndrome, Somatic 26 0.027
617
NNT018 Neonatal Herpes 26 0.027
618
OSC001 Oeis Complex 26 0.027
619
HYP711 Hypotonia, Ataxia, and Delayed Development Syndrome 26 0.027
620
HMN031 Human Venous Malformation 25 0.027
621
HNM002 Hinman Syndrome 25 0.027
622
c ATM007 Autoimmune Disease of Central Nervous System 25 0.027
623
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.027
624
RHH001 Rohhad 24 0.027
625
CDL005 Caudal Duplication Anomaly 23 0.027
626
c CRN214 Coronary Heart Disease 5 22 0.027
627
CLC002 Calcaneonavicular Coalition 21 0.027
628
VSC009 Vascular Skin Disease 19 0.027
629
TRG006 Trigger Thumb 18 0.027
630
HYD057 Hydrops Fetalis, Non-Immune, and/or Atrial Septal Defect 17 0.027
631
AND005 Androgen Insensitivity Syndrome, Mild 16 0.027
632
LMB009 Lambdoid Synostosis 16 0.027
633
CLP002 Colpocephaly 15 0.027
634
ECT085 Ectopia Cordis 15 0.027
635
c BNG076 Benign Exophthalmos Syndrome 15 0.027
636
LNR009 Linear Atrophoderma of Moulin 14 0.027
637
WLS002 Wilson-Mikity Syndrome 14 0.027
638
NNT002 Neonatal Urinary Tract Infectious Disease 11 0.027
639
SYM006 Symmetrical Thalamic Calcifications 11 0.027
640
FBL005 Fibular Aplasia 10 0.027
641
P CLR023 Colorectal Cancer 97 0.019
642
P ALZ034 Alzheimer Disease 92 0.019
643
P PRS040 Prostate Cancer 90 0.019
644
P OST012 Osteoarthritis 83 0.019
645
P MLT019 Multiple Myeloma 83 0.019
646
P RTN008 Retinitis Pigmentosa 80 0.019
647
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.019
648
P ATX030 Ataxia-Telangiectasia 77 0.019
649
HDG012 Hodgkin Lymphoma 77 0.019
650
P OVR042 Ovarian Cancer 76 0.019
651
END057 Endometrial Cancer 75 0.019
652
STR067 Stroke, Ischemic 75 0.019
653
P RTN024 Retinoblastoma 74 0.019
654
P WSK001 Wiskott-Aldrich Syndrome 73 0.019
655
c HPT073 Hepatitis C Virus 73 0.019
656
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.019
657
P NRV007 Nervous System Disease 71 0.019
658
KRT004 Keratitis 71 0.019
659
MLT021 Multiple System Atrophy 70 0.019
660
P PRK057 Parkinson Disease, Late-Onset 70 0.019
661
P ESS003 Essential Thrombocythemia 70 0.019
662
P MTC003 Metachromatic Leukodystrophy 70 0.019
663
BCK001 Becker Muscular Dystrophy 69 0.019
664
TST021 Testicular Germ Cell Tumor 69 0.019
665
c MLT136 Multiple Endocrine Neoplasia 1 69 0.019
666
P DMN001 Diamond-Blackfan Anemia 69 0.019
667
FBR012 Fabry Disease 69 0.019
668
P ALP004 Alport Syndrome 69 0.019
669
P FRG001 Fragile X Syndrome 69 0.019
670
P LPR003 Leprosy 69 0.019
671
c HPT001 Hepatitis C 68 0.019
672
CMM004 Common Variable Immunodeficiency 68 0.019
673
CST001 Costello Syndrome 68 0.019
674
PSY004 Psychotic Disorder 67 0.019
675
PLM001 Pulmonary Tuberculosis 67 0.019
676
KPS004 Kaposi Sarcoma 67 0.019
677
P MYL005 Myelofibrosis 67 0.019
678
c HRD010 Hereditary Spastic Paraplegia 67 0.019
679
APR006 Apert Syndrome 67 0.019
680
P CHR071 Charcot-Marie-Tooth Disease 67 0.019
681
P NSP012 Nasopharyngeal Carcinoma 66 0.019
682
SMT004 Smith-Lemli-Opitz Syndrome 66 0.019
683
OBS061 Obstructive Sleep Apnea 66 0.019
684
OBS002 Obsessive-Compulsive Disorder 66 0.019
685
ACR007 Acromegaly 66 0.019
686
SRC014 Sarcoma 66 0.019
687
CRV047 Cervical Cancer, Somatic 65 0.019
688
PTR006 Peters Anomaly 65 0.019
689
P AMY004 Amyloidosis 65 0.019
690
c HPT016 Hepatitis B 64 0.019
691
P ART023 Arthropathy 64 0.019
692
AND015 Androgen Insensitivity 64 0.019
693
PRT037 Pertussis 64 0.019
694
c MLT024 Multiple Endocrine Neoplasia Iia 64 0.019
695
P LNG028 Long Qt Syndrome 64 0.019
696
PSR001 Psoriatic Arthritis 64 0.019
697
P HMP002 Hemophagocytic Lymphohistiocytosis 64 0.019
698
c HMP029 Hemophilia a 63 0.019
699
P PRD008 Periodontitis 63 0.019
700
P ALX003 Alexander Disease 63 0.019
701
c MYT021 Myotonic Dystrophy 1 63 0.019
702
P ENC004 Encephalitis 63 0.019
703
CHR063 Chronic Mucocutaneous Candidiasis 63 0.019
704
c TBR024 Tuberous Sclerosis-1 63 0.019
705
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 62 0.019
706
P ADD001 Addison's Disease 62 0.019
707
LPT001 Leptospirosis 62 0.019
708
MXD005 Mixed Connective Tissue Disease 62 0.019
709
VSC011 Vasculitis 62 0.019
710
P VLC001 Velocardiofacial Syndrome 62 0.019
711
GST092 Gastroesophageal Reflux 62 0.019
712
P GCH001 Gaucher's Disease 62 0.019
713
P CLD001 Cleidocranial Dysplasia 62 0.019
714
TNG002 Tangier Disease 62 0.019
715
CNT047 Contact Dermatitis 61 0.019
716
P SLP006 Sleep Apnea 61 0.019
717
OST017 Osteomyelitis 61 0.019
718
P ASP006 Aspergillosis 61 0.019
719
P ANG001 Angelman Syndrome 61 0.019
720
P IDP010 Idiopathic Generalized Epilepsy 61 0.019
721
P CCK001 Cockayne Syndrome 61 0.019
722
CRB011 Cerebrotendinous Xanthomatosis 61 0.019
723
CRD119 Cardiac Arrest 61 0.019
724
P LBR001 Leber Congenital Amaurosis 61 0.019
725
SHW002 Shwachman-Diamond Syndrome 61 0.019
726
MTH009 Mouth Disease 61 0.019
727
KRN002 Kearns-Sayre Syndrome 61 0.019
728
P MYM002 Moyamoya Disease 61 0.019
729
P PNC044 Pancreatitis 61 0.019
730
P SYS005 Systemic Scleroderma 61 0.019
731
CRY002 Cryptorchidism 60 0.019
732
MNK001 Menkes Disease 60 0.019
733
P MCP010 Mucopolysaccharidosis 60 0.019
734
P INT068 Intestinal Disease 60 0.019
735
MNK003 Muenke Syndrome 60 0.019
736
c SYS004 Systemic Mastocytosis 60 0.019
737
P NRV006 Nervous System Cancer 60 0.019
738
CHL123 Chlamydia 60 0.019
739
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.019
740
SPT004 Septic Arthritis 60 0.019
741
OCL009 Ocular Cancer 59 0.019
742
P HRM001 Hermansky-Pudlak Syndrome 59 0.019
743
FTT001 Fatty Liver Disease 59 0.019
744
STT001 Status Epilepticus 59 0.019
745
INC021 Incontinentia Pigmenti 59 0.019
746
PLM070 Pulmonic Stenosis 59 0.019
747
P LKD001 Leukodystrophy 59 0.019
748
P PRP029 Porphyria 59 0.019
749
LPD008 Lipid Metabolism Disorder 58 0.019
750
c FML001 Familial Atrial Fibrillation 58 0.019
751
P GT001 Gout 58 0.019
752
P RTN025 Retinoschisis 58 0.019
753
ETN001 Eating Disorder 58 0.019
754
P MCR010 Microcephaly 58 0.019
755
RHM027 Rheumatic Disease 58 0.019
756
MLG056 Malignant Hyperthermia 58 0.019
757
ALP001 Alopecia Universalis 58 0.019
758
P MSC007 Muscle Hypertrophy 58 0.019
759
c CHR536 Charcot-Marie-Tooth Disease, Type 1a 58 0.019
760
ACS001 Acoustic Neuroma 58 0.019
761
P CND004 Candidiasis 57 0.019
762
WLM001 Wolman Disease 57 0.019
763
c CWD006 Cowden Syndrome 1 57 0.019
764
CNS004 Constipation 57 0.019
765
ADM013 Adamantinoma of Long Bones 57 0.019
766
WST001 West Syndrome 57 0.019
767
ACN002 Acanthosis Nigricans 57 0.019
768
P INT143 Interstitial Cystitis 57 0.019
769
STR026 Star Syndrome 57 0.019
770
PLY023 Polycystic Liver Disease 56 0.019
771
P SZR006 Seizure Disorder 56 0.019
772
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 56 0.019
773
PTT006 Pituitary Adenoma 56 0.019
774
P FRS003 Fraser Syndrome 56 0.019
775
BRN002 Bronchiolitis 56 0.019
776
P OLG002 Oligodendroglioma 56 0.019
777
P PLY019 Polyneuropathy 56 0.019
778
P BDD001 Budd-Chiari Syndrome 56 0.019
779
WLF001 Wolff-Parkinson-White Syndrome 56 0.019
780
DSM004 Desmoid Tumor 56 0.019
781
MVL001 Mevalonic Aciduria 56 0.019
782
P WVR001 Weaver Syndrome 56 0.019
783
STF001 Stiff-Person Syndrome 56 0.019
784
P ANT006 Antiphospholipid Syndrome 56 0.019
785
P OVR049 Ovarian Disease 56 0.019
786
BLD034 Bile Duct Carcinoma 56 0.019
787
P HYP050 Hyperinsulinemic Hypoglycemia 56 0.019
788
CMP005 Campomelic Dysplasia 55 0.019
789
VRL011 Viral Infectious Disease 55 0.019
790
c HRD002 Hereditary Angioedema 55 0.019
791
JNT002 Joint Disorders 55 0.019
792
P PND002 Pendred Syndrome 55 0.019
793
GLC003 Glucose Intolerance 55 0.019
794
LPD011 Lipoid Adrenal Hyperplasia 55 0.019
795
P RTH001 Rothmund-Thomson Syndrome 55 0.019
796
P STC001 Stickler Syndrome 55 0.019
797
P EMR001 Emery-Dreifuss Muscular Dystrophy 55 0.019
798
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.019
799
P FND001 Fundus Albipunctatus 55 0.019
800
SCR008 Scrub Typhus 55 0.019
801
CNC002 Cinca Syndrome 55 0.019
802
P EPD009 Epidermolysis Bullosa Dystrophica 54 0.019
803
VGT001 Vogt-Koyanagi-Harada Disease 54 0.019
804
c PND001 Pain Disorder 54 0.019
805
P MMB011 Membranous Nephropathy 54 0.019
806
APH002 Aphasia 54 0.019
807
VSC002 Vascular Dementia 54 0.019
808
RHM001 Rheumatic Fever 54 0.019
809
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 54 0.019
810
NTH001 Netherton Syndrome 54 0.019
811
P BRC006 Brachydactyly 54 0.019
812
P INT030 Intracranial Aneurysm 54 0.019
813
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.019
814
CYS005 Cysticercosis 54 0.019
815
RST001 Restless Legs Syndrome 54 0.019
816
CRV040 Cervix Carcinoma 53 0.019
817
DMY004 Demyelinating Disease 53 0.019
818
P HYP027 Hypobetalipoproteinemia 53 0.019
819
FDL002 Food Allergy 53 0.019
820
WGR001 Wagr Syndrome 53 0.019
821
SLP005 Sleep Disorder 53 0.019
822
LST001 Listeriosis 53 0.019
823
P PLY014 Polycystic Kidney Disease 53 0.019
824
OLV001 Olivopontocerebellar Atrophy 53 0.019
825
SCT005 Scott Syndrome 53 0.019
826
P SYP003 Syphilis 53 0.019
827
P CNT005 Central Nervous System Lymphoma 53 0.019
828
NRF007 Neurofibroma 53 0.019
829
P DGR001 Digeorge Syndrome 53 0.019
830
P HLL001 Hallermann-Streiff Syndrome 53 0.019
831
CHL014 Cholera 53 0.019
832
CYS010 Cystinosis 53 0.019
833
P CYS018 Cystitis 52 0.019
834
RSC001 Rosacea 52 0.019
835
P PLY041 Polymyositis 52 0.019
836
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.019
837
TTH006 Tooth Disease 52 0.019
838
ISL003 Isolated Growth Hormone Deficiency 52 0.019
839
TRM010 Traumatic Brain Injury 52 0.019
840
QDR001 Quadriplegia 52 0.019
841
P ANG015 Angioedema 52 0.019
842
P PYL005 Pyelonephritis 52 0.019
843
OCL020 Ocular Cicatricial Pemphigoid 52 0.019
844
ARS001 Aarskog-Scott Syndrome 52 0.019
845
MRG003 Marginal Zone B-Cell Lymphoma 52 0.019
846
PRT011 Protein C Deficiency 52 0.019
847
HST011 Histoplasmosis 52 0.019
848
MGL013 Megalencephaly 52 0.019
849
PRS042 Prostate Disease 52 0.019
850
MYM001 Myoma 52 0.019
851
BLR001 Biliary Atresia 52 0.019
852
c INT064 Intermediate Uveitis 52 0.019
853
c PRK031 Parkinson Disease 1 51 0.019
854
P PRM006 Primary Biliary Cirrhosis 51 0.019
855
P ALL008 Allergic Bronchopulmonary Aspergillosis 51 0.019
856
c INF071 Inflammatory Bowel Disease 1 51 0.019
857
P PTS002 Ptosis 51 0.019
858
ALP014 Alpha-Thalassemia/mental Retardation Syndrome 51 0.019
859
VSC006 Vascular Cancer 51 0.019
860
BLL001 Baller-Gerold Syndrome 51 0.019
861
P GRS003 Griscelli Syndrome 51 0.019
862
P LRS001 Larsen Syndrome 51 0.019
863
IMM136 Immune System Disease 51 0.019
864
VRN004 Vernal Keratoconjunctivitis 51 0.019
865
ALL009 Allergic Conjunctivitis 51 0.019
866
DSS009 Disseminated Intravascular Coagulation 51 0.019
867
c PSD066 Pseudohypoparathyroidism, Type Ib 51 0.019
868
CLN019 Colonic Disease 51 0.019
869
c GRS014 Griscelli Syndrome, Type 2 51 0.019
870
PRC012 Pericardial Effusion 51 0.019
871
STM006 Stomach Disease 50 0.019
872
P ALT001 Alternating Hemiplegia of Childhood 50 0.019
873
ASP001 Asperger Syndrome 50 0.019
874
ESN005 Eosinophilic Gastroenteritis 50 0.019
875
c RCS002 Recessive Dystrophic Epidermolysis Bullosa 50 0.019
876
P EPD002 Epidermolytic Hyperkeratosis 50 0.019
877
CCT002 Cicatricial Pemphigoid 50 0.019
878
MST017 Mast Cell Disease 50 0.019
879
BNF002 Bone Fracture 50 0.019
880
P MSC003 Muscular Atrophy 50 0.019
881
FML037 Female Breast Cancer 50 0.019
882
P PRM001 Primary Cutaneous Amyloidosis 50 0.019
883
RNL007 Renal Tubular Acidosis 50 0.019
884
NNL002 Nonalcoholic Steatohepatitis 50 0.019
885
P SJG002 Sjogren-Larsson Syndrome 50 0.019
886
P CLL015 Collagen Disease 50 0.019
887
MGL001 Megaloblastic Anemia 50 0.019
888
NRG002 Neurogenic Bladder 50 0.019
889
P CNG046 Congenital Fiber-Type Disproportion 50 0.019
890
TMP001 Temporal Lobe Epilepsy 50 0.019
891
P JNC001 Junctional Epidermolysis Bullosa 49 0.019
892
MVM001 Movement Disease 49 0.019
893
SPN019 Spondylolisthesis 49 0.019
894
c PRM226 Primary Central Nervous System Lymphoma 49 0.019
895
CHN055 Chanarin-Dorfman Syndrome 49 0.019
896
LRN003 Learning Disability 49 0.019
897
OST011 Osteomalacia 49 0.019
898
CHL069 Cholesteatoma 49 0.019
899
P LSS002 Lissencephaly 49 0.019
900
P RBN002 Robinow Syndrome 49 0.019
901
SLD003 Sialadenitis 49 0.019
902
BCL002 B Cell Deficiency 49 0.019
903
HMG002 Hemoglobinuria 48 0.019
904
MTN003 Motion Sickness 48 0.019
905
PRN023 Prion Disease 48 0.019
906
QBC001 Quebec Platelet Disorder 48 0.019
907
BLL003 Bell's Palsy 48 0.019
908
PLS009 Plasma Cell Neoplasm 48 0.019
909
PSD007 Pseudomyxoma Peritonei 48 0.019
910
MSS002 Mass Syndrome 48 0.019
911
P FBR025 Fibrochondrogenesis 48 0.019
912
MTB004 Metabolic Acidosis 48 0.019
913
NPH003 Nephrocalcinosis 48 0.019
914
CCN002 Cocaine Abuse 48 0.019
915
THY030 Thyroid Gland Disease 48 0.019
916
NRM004 Neuroma 48 0.019
917
SPN020 Spondylosis 48 0.019
918
c HMG001 Hemoglobin C Disease 47 0.019
919
DBT084 Diabetes Mellitus, Ketosis-Prone 47 0.019
920
c ERL020 Early-Onset Schizophrenia 47 0.019
921
MNN009 Meningoencephalitis 47 0.019
922
HND002 Hand, Foot and Mouth Disease 47 0.019
923
PLC003 Placental Site Trophoblastic Tumor 47 0.019
924
SDD007 Sudden Cardiac Death 47 0.019
925
SYN036 Syncope 47 0.019
926
c MLG069 Malignant Hypertension 47 0.019
927
TMR010 Tumor Predisposition Syndrome 47 0.019
928
P SYR001 Syringomyelia 47 0.019
929
LPM005 Lipomatosis 47 0.019
930
PLM041 Pulmonary Valve Stenosis 47 0.019
931
GNG002 Ganglioneuroma 47 0.019
932
BRD001 Brody Myopathy 47 0.019
933
PRR002 Pure Red-Cell Aplasia 47 0.019
934
PPL018 Papillary Adenocarcinoma 46 0.019
935
RSP002 Respiratory Syncytial Virus Infectious Disease 46 0.019
936
DRM011 Dermatophytosis 46 0.019
937
HRT007 Heart Cancer 46 0.019
938
FLL008 Folliculitis 46 0.019
939
MLT006 Multidrug-Resistant Tuberculosis 46 0.019
940
ART004 Aortic Atherosclerosis 46 0.019
941
HMN032 Human Herpesvirus 8 46 0.019
942
BLD053 Blood Platelet Disease 46 0.019
943
GGR001 Geographic Tongue 46 0.019
944
CTS002 Cat-Scratch Disease 46 0.019
945
DNT012 Dental Caries 46 0.019
946
P HRD021 Hereditary Sensory Neuropathy 46 0.019
947
CHR074 Choriocarcinoma 46 0.019
948
CD4003 Cd40 Ligand Deficiency 46 0.019
949
MNL001 Monilethrix 46 0.019
950
c TRC092 Trichorhinophalangeal Syndrome, Type I 46 0.019
951
CVR006 Cavernous Hemangioma 46 0.019
952
P PSD015 Pseudohypoparathyroidism 46 0.019
953
c TYR013 Tyrosinemia, Type Ii 46 0.019
954
EST007 Estrogen Resistance 46 0.019
955
XNT003 Xanthomatosis 46 0.019
956
IDP024 Idiopathic Inflammatory Myopathy 46 0.019
957
JHN001 Johanson-Blizzard Syndrome 46 0.019
958
PLM035 Pulmonary Eosinophilia 46 0.019
959
ADN027 Adenomyosis 46 0.019
960
MGC001 Megacolon 45 0.019
961
EPD006 Epidermolysis Bullosa Acquisita 45 0.019
962
P TYR004 Tyrosinemia 45 0.019
963
P MLG086 Malignant Hyperthermia Susceptibility 45 0.019
964
CRB004 Cerebral Artery Occlusion 45 0.019
965
DSC009 Discoid Lupus Erythematosus 45 0.019
966
IPX001 Ipex Syndrome 45 0.019
967
KRT010 Kartagener Syndrome 45 0.019
968
MCR037 Macroglossia 45 0.019
969
PRM003 Premature Ejaculation 45 0.019
970
HMP009 Haemophilus Influenzae 45 0.019
971
c DBT064 Diabetes Mellitus, Transient Neonatal, 1 45 0.019
972
FBR009 Fibrous Dysplasia 45 0.019
973
P AML002 Amelogenesis Imperfecta 45 0.019
974
NVS001 Neovascular Glaucoma 44 0.019
975
PLL012 Pollen Allergy 44 0.019
976
ANV001 Anovulation 44 0.019
977
NDL021 Nodular Lymphocyte Predominant Hodgkin Lymphoma 44 0.019
978
P LYD001 Leydig Cell Tumor 44 0.019
979
P D2H001 D-2-Hydroxyglutaric Aciduria 44 0.019
980
CHR008 Choroiditis 44 0.019
981
CNJ012 Conjunctival Disease 44 0.019
982
CNG048 Congenital Hepatic Fibrosis 44 0.019
983
BND015 Band-Like Calcification with Simplified Gyration and Polymicrogyria 44 0.019
984
P PSD003 Pseudohypoaldosteronism 44 0.019
985
PRN011 Pernicious Anemia 44 0.019
986
CRD118 Cardiovascular Cancer 44 0.019
987
OCL069 Ocular Motor Apraxia 44 0.019
988
c MTR002 Mitral Valve Insufficiency 44 0.019
989
TST015 Testicular Disease 44 0.019
990
WRN002 Wernicke-Korsakoff Syndrome 44 0.019
991
AGR002 Agoraphobia 44 0.019
992
ALV007 Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins 44 0.019
993
HYP077 Hypertrichosis 44 0.019
994
FBR032 Fibromuscular Dysplasia 43 0.019
995
P INF049 Infantile Myofibromatosis 43 0.019
996
TBR006 Tuberculoid Leprosy 43 0.019
997
CMP034 Complete Androgen Insensitivity Syndrome 43 0.019
998
LYM009 Lymphocytic Choriomeningitis 43 0.019
999
AND001 Anodontia 43 0.019
1000
PLG004 Plagiocephaly 43 0.019
1001
DFF001 Diffuse Cutaneous Mastocytosis 43 0.019
1002
OPP004 Oppositional Defiant Disorder 43 0.019
1003
c SPN100 Spinocerebellar Ataxia 27 43 0.019
1004
SNS023 Sensory System Cancer 43 0.019
1005
MST006 Mast Syndrome 43 0.019
1006
PRS012 Pars Planitis 43 0.019
1007
BCK006 Back Pain 43 0.019
1008
MTR010 Mature Teratoma 42 0.019
1009
BHR001 Behr Syndrome 42 0.019
1010
c ACT076 Acute Myocarditis 42 0.019
1011
GST052 Gestational Choriocarcinoma 42 0.019
1012
NRW001 Norwegian Scabies 42 0.019
1013
P FNG005 Feingold Syndrome 42 0.019
1014
PRT019 Protein-Losing Enteropathy 42 0.019
1015
FCL041 Focal Myositis 42 0.019
1016
SMT001 Somatization Disorder 42 0.019
1017
SBP004 Subependymoma 42 0.019
1018
PRP009 Peripartum Cardiomyopathy 42 0.019
1019
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.019
1020
c BRC082 Brachydactyly, Type E 42 0.019
1021
PRD011 Proud Syndrome 42 0.019
1022
SPR007 Superior Mesenteric Artery Syndrome 41 0.019
1023
VGN020 Vaginal Disease 41 0.019
1024
CHL052 Choledochal Cyst 41 0.019
1025
PRM013 Premature Menopause 41 0.019
1026
SPC010 Speech and Communication Disorders 41 0.019
1027
c CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 41 0.019
1028
DLS001 Delusional Disorder 41 0.019
1029
GND001 Gonadoblastoma 41 0.019
1030
PRD003 Periodontosis 41 0.019
1031
ANH002 Anhidrosis 41 0.019
1032
DBW001 Dubowitz Syndrome 41 0.019
1033
BLN001 Blount's Disease 41 0.019
1034
IDP070 Idiopathic Scoliosis 41 0.019
1035
P KLF001 Kleefstra Syndrome 41 0.019
1036
P CNG390 Congenital Pulmonary Airway Malformation 41 0.019
1037
DFF003 Diffuse Scleroderma 41 0.019
1038
HYP101 Hyperinsulinism-Hyperammonemia Syndrome 41 0.019
1039
P CNG024 Congenital Nystagmus 40 0.019
1040
P CNN004 Connective Tissue Cancer 40 0.019
1041
NSP002 Nasopharyngitis 40 0.019
1042
CRD144 Cardiovascular Disease Risk Factor ) 40 0.019
1043
ACT084 Acute Stress Disorder 40 0.019
1044
KWS001 Kwashiorkor 40 0.019
1045
P SDR003 Sideroblastic Anemia 40 0.019
1046
BSL008 Basal Ganglia Disease 40 0.019
1047
PDT035 Pediatric Systemic Lupus Erythematosus 40 0.019
1048
ANG016 Angiokeratoma 40 0.019
1049
CRL004 Caroli Disease 40 0.019
1050
MNN017 Mononeuropathy 40 0.019
1051
RNL012 Renal Tuberculosis 40 0.019
1052
EPS026 Epispadias 40 0.019
1053
HYP068 Hyperostosis 40 0.019
1054
RTT001 Ritter's Disease 40 0.019
1055
PRG014 Progesterone Resistance 40 0.019
1056
CHR078 Chorioretinitis 40 0.019
1057
P TST026 Testicular Germ Cell Cancer 39 0.019
1058
LYM127 Lymphatic Malformations 39 0.019
1059
SPN029 Spondylolysis 39 0.019
1060
c PRG001 Progressive Muscular Atrophy 39 0.019
1061
CND005 Cone Dystrophy 39 0.019
1062
GND003 Gonadal Disease 39 0.019
1063
P ACH011 Achondrogenesis 39 0.019
1064
NRN008 Neuronal Intranuclear Inclusion Disease 39 0.019
1065
SPS004 Spastic Quadriplegia 39 0.019
1066
c CNG033 Congenital Syphilis 39 0.019
1067
ADR009 Adrenal Cortex Disease 39 0.019
1068
BDY001 Body Dysmorphic Disorder 39 0.019
1069
MNN021 Meningococcemia 39 0.019
1070
P TRC005 Tracheal Stenosis 39 0.019
1071
c CHR091 Chronic Meningitis 39 0.019
1072
MHC001 Mhc Class Ii Deficiency 39 0.019
1073
PCH002 Pachygyria 39 0.019
1074
WDM004 Wiedemann-Steiner Syndrome 38 0.019
1075
P FML187 Familial Hypertension 38 0.019
1076
IRN004 Iron-Refractory Iron Deficiency Anemia 38 0.019
1077
P VTL001 Vitelliform Macular Dystrophy 38 0.019
1078
GST007 Gastric Dilatation 38 0.019
1079
FMR004 Fumarase Deficiency 38 0.019
1080
P PNT019 Pontocerebellar Hypoplasia 38 0.019
1081
DFF021 Diffuse Mesangial Sclerosis 38 0.019
1082
INT011 Interstitial Emphysema 38 0.019
1083
ARM002 Aromatic L-Amino Acid Decarboxylase Deficiency 38 0.019
1084
TLP001 Talipes Equinovarus 38 0.019
1085
c CNG029 Congenital Mesoblastic Nephroma 37 0.019
1086
BLD054 Blood Protein Disease 37 0.019
1087
PRS030 Persistent Fetal Circulation Syndrome 37 0.019
1088
CVR010 Cavernous Malformation 37 0.019
1089
ALX002 Alexithymia 37 0.019
1090
CHD004 Chudley-Mccullough Syndrome 37 0.019
1091
P DYS005 Dyslexia 37 0.019
1092
PRP080 Peripheral Artery Disease 37 0.019
1093
c CNG031 Congenital Nervous System Abnormality 37 0.019
1094
ART035 Arterial Calcification of Infancy 37 0.019
1095
GRN007 Granuloma Annulare 37 0.019
1096
NNT008 Neonatal Abstinence Syndrome 37 0.019
1097
C6D001 C6 Deficiency 37 0.019
1098
VSC018 Visceral Steatosis 37 0.019
1099
HYP064 Hypogonadotropism 37 0.019
1100
CMB021 Combined Pituitary Hormone Deficiency 37 0.019
1101
SML028 Semilobar Holoprosencephaly 37 0.019
1102
P HYP120 Hypoaldosteronism 36 0.019
1103
CNG035 Congenital Bilateral Absence of Vas Deferens 36 0.019
1104
MDY003 Mody, Type Ii 36 0.019
1105
OLG001 Oligospermia 36 0.019
1106
SCH072 Scheuermann Disease 36 0.019
1107
c CHR098 Chronic Pyelonephritis 36 0.019
1108
OBS003 Obsessive-Compulsive Personality Disorder 36 0.019
1109
c DBT082 Diabetes Mellitus, Insulin-Dependent, 12 36 0.019
1110
HYP015 Hyperlucent Lung 36 0.019
1111
ATM014 Autoimmune Disease of Endocrine System 36 0.019
1112
P CRB154 Cerebrocostomandibular Syndrome 36 0.019
1113
DVL001 Developmental Coordination Disorder 36 0.019
1114
PDT025 Pediatric Multiple Sclerosis 36 0.019
1115
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.019
1116
PRS108 Persistent Polyclonal B-Cell Lymphocytosis 35 0.019
1117
TCL012 T-Cell/histiocyte Rich Large B Cell Lymphoma 35 0.019
1118
PMP002 Pemphigoid Gestationis 35 0.019
1119
ASP004 Asphyxia Neonatorum 35 0.019
1120
PRM129 Primary Cutaneous Marginal Zone B-Cell Lymphoma 35 0.019
1121
NTR006 Neutrophil Immunodeficiency Syndrome 35 0.019
1122
ALB014 Alobar Holoprosencephaly 35 0.019
1123
MYX004 Myxedema 35 0.019
1124
LND001 Landau-Kleffner Syndrome 35 0.019
1125
SPN221 Spina Bifida Occulta 34 0.019
1126
WRT001 Worth's Syndrome 34 0.019
1127
FMR011 Fumarate Hydratase Deficiency 34 0.019
1128
MSC004 Muscle Tissue Disease 34 0.019
1129
TRN030 Transient Erythroblastopenia of Childhood 34 0.019
1130
RDN001 Reading Disorder 34 0.019
1131
INT259 Interleukin 1 Receptor Antagonist Deficiency 34 0.019
1132