Search results for "twinning"

The MalaCard for "twinning" has been retired.
Searching MalaCards for entries containing "twinning"

1277 hits were found for 'twinning'

# Family MCID Name MIFTS Score
1
TWN001 Twin-to-Twin Transfusion Syndrome 42 13.012
2
c RNL090 Renal Tubular Dysgenesis Due to Twin-Twin Transfusion 7 3.812
3
PLY012 Polyhydramnios 39 0.148
4
P PLY018 Polycythemia 53 0.140
5
ANN002 Anencephaly 38 0.134
6
CRB009 Cerebritis 37 0.127
7
PLC008 Placenta Disease 33 0.117
8
P CNG401 Congenital Heart Disease 68 0.107
9
P CRV039 Cervicitis 42 0.102
10
P OBS005 Obesity 89 0.100
11
OLG003 Oligohydramnios 42 0.098
12
HYD012 Hydrops Fetalis 50 0.096
13
P CRD011 Cardiomyopathy 53 0.090
14
CHL071 Child Syndrome 51 0.088
15
KDS001 Kid Syndrome 44 0.088
16
CYT008 Cytomegalovirus Infection 47 0.081
17
CNG069 Congenital Cytomegalovirus 28 0.079
18
P THY032 Thyroiditis 48 0.077
19
CHR005 Chorioamnionitis 40 0.077
20
DWN001 Down Syndrome 62 0.074
21
SRN002 Sirenomelia 29 0.074
22
P LKM002 Leukemia 61 0.072
23
DFC004 Deficiency Anemia 52 0.072
24
ISC004 Ischemia 47 0.072
25
P PLM037 Pulmonary Hypertension 78 0.069
26
P HYP086 Hypothyroidism 52 0.067
27
URT039 Urticaria 50 0.067
28
NNT011 Neonatal Anemia 25 0.067
29
P PRS038 Personality Disorder 47 0.064
30
ECT026 Ectopic Pregnancy 38 0.064
31
PYL006 Pyloric Stenosis 37 0.064
32
INT060 Intestinal Atresia 33 0.064
33
P THR014 Thrombocytopenia 50 0.061
34
P ENC008 Encephalocele 46 0.061
35
OMP004 Omphalocele 46 0.061
36
URT008 Urticaria Pigmentosa 32 0.061
37
ENC005 Encephalomalacia 29 0.061
38
P TYS001 Tay-Sachs Disease 70 0.058
39
P NRC002 Narcolepsy 66 0.058
40
P LPS004 Lupus Erythematosus 61 0.058
41
c PRC016 Pre-Eclampsia 51 0.058
42
VCT001 Vacterl Association 51 0.058
43
P MYP004 Myopathy 50 0.058
44
P APL006 Aplasia Cutis Congenita 49 0.058
45
WLL006 Wells Syndrome 48 0.058
46
CND002 Conduct Disorder 45 0.058
47
P UTR038 Uterine Disease 44 0.058
48
c PST041 Posterior Urethral Valves 43 0.058
49
GST009 Gastroschisis 43 0.058
50
PRV004 Periventricular Leukomalacia 42 0.058
51
P GND004 Gonadal Dysgenesis 41 0.058
52
P TRT010 Teratoma 40 0.058
53
URT001 Urethritis 40 0.058
54
P HYP009 Hypertrophic Pyloric Stenosis 39 0.058
55
GDS001 Good Syndrome 37 0.058
56
LKM006 Leukomalacia 33 0.058
57
P RBN001 Rubinstein-Taybi Syndrome 66 0.054
58
PRP027 Peripheral Vascular Disease 62 0.054
59
P ART022 Arthritis 61 0.054
60
P LYM026 Lymphoblastic Leukemia 57 0.054
61
KLN001 Klinefelter's Syndrome 57 0.054
62
P ADL010 Adult Respiratory Distress Syndrome 55 0.054
63
P TXP001 Toxoplasmosis 54 0.054
64
DRM006 Dermatitis 54 0.054
65
c ACT210 Acute Respiratory Distress Syndrome 52 0.054
66
P ESP024 Esophagitis 51 0.054
67
P ECL001 Eclampsia 47 0.054
68
GST033 Gestational Diabetes 45 0.054
69
PLC005 Placental Insufficiency 43 0.054
70
RTN023 Retinitis 43 0.054
71
c BPL002 Bipolar I Disorder 40 0.054
72
NWB001 Newborn Respiratory Distress Syndrome 40 0.054
73
PRT082 Preterm Premature Rupture of the Membranes 39 0.054
74
RFR003 Refractive Error 37 0.054
75
HYD001 Hydranencephaly 33 0.054
76
PNT005 Pentalogy of Cantrell 30 0.054
77
AMN009 Amniotic Band Syndrome 25 0.054
78
P RSP007 Respiratory Distress Syndrome, Infant 20 0.054
79
ACR022 Acardia 12 0.054
80
c ADL080 Adult Acute Respiratory Distress Syndrome 11 0.054
81
c HYP595 Hypertension, Essential 68 0.051
82
P CRN211 Coronary Artery Disease 68 0.051
83
P PRM019 Premature Ovarian Failure 66 0.051
84
P NRF002 Neurofibromatosis 66 0.051
85
ALC007 Alcohol Dependence 59 0.051
86
P BCK002 Beckwith-Wiedemann Syndrome 58 0.051
87
c CNG006 Congenital Hypothyroidism 57 0.051
88
ISC006 Ischemic Heart Disease 56 0.051
89
CRB037 Cerebral Palsy 54 0.051
90
P DYS154 Dystonia 53 0.051
91
P MSC005 Muscular Dystrophy 52 0.051
92
P OST009 Osteochondritis Dissecans 51 0.051
93
ART111 Artery Disease 48 0.051
94
P MST009 Mastocytosis 48 0.051
95
ESP020 Esophageal Atresia 46 0.051
96
P DBT005 Diabetes Insipidus 46 0.051
97
IMP002 Imperforate Anus 45 0.051
98
c CNG021 Congenital Toxoplasmosis 43 0.051
99
PTH002 Pathological Gambling 42 0.051
100
TRN007 Transsexualism 35 0.051
101
VND001 Vein Disease 34 0.051
102
c SYS001 Systemic Lupus Erythematosus 90 0.047
103
P RHM011 Rheumatoid Arthritis 88 0.047
104
HV1006 Hiv-1 77 0.047
105
P NRB001 Neuroblastoma 73 0.047
106
ANR002 Aniridia 72 0.047
107
ATT013 Attention Deficit-Hyperactivity Disorder 66 0.047
108
P HLP001 Holoprosencephaly 62 0.047
109
IMG001 Image Syndrome 56 0.047
110
ART005 Arteriovenous Malformation 56 0.047
111
ACQ007 Acquired Immunodeficiency Syndrome 55 0.047
112
SMT008 Smith-Magenis Syndrome 54 0.047
113
P MYS005 Myositis 54 0.047
114
DMN002 Dementia 53 0.047
115
PLM033 Pulmonary Embolism 53 0.047
116
ART021 Arteriosclerosis 51 0.047
117
CTN014 Cutaneous Mastocytosis 45 0.047
118
BLM002 Bulimia Nervosa 44 0.047
119
ADL002 Adult Syndrome 43 0.047
120
PLC007 Placental Abruption 40 0.047
121
TRN044 Transposition of the Great Arteries 39 0.047
122
MTS001 Mutism 34 0.047
123
P PLY024 Polymicrogyria 33 0.047
124
PRN019 Perinatal Necrotizing Enterocolitis 30 0.047
125
CLC011 Cloacal Exstrophy 29 0.047
126
SCR024 Sacrococcygeal Teratoma 28 0.047
127
PRT086 Partial Hydatidiform Mole 25 0.047
128
JJN004 Jejunal Atresia 21 0.047
129
BWM001 Bowman's Membrane Folds or Rupture 7 0.047
130
P SCH015 Schizophrenia 79 0.043
131
P MYC007 Myocardial Infarction 76 0.043
132
NRL016 Neural Tube Defects 74 0.043
133
P SCL016 Scleroderma 69 0.043
134
PTZ001 Peutz-Jeghers Syndrome 67 0.043
135
INS024 Insulin-Like Growth Factor I 64 0.043
136
P HYP055 Hypoplastic Left Heart Syndrome 58 0.043
137
P HPT021 Hepatitis 58 0.043
138
P CRN015 Cornelia De Lange Syndrome 58 0.043
139
ANX002 Anxiety Disorder 57 0.043
140
P PNM007 Pneumonia 56 0.043
141
P DRM007 Dermatitis Herpetiformis 51 0.043
142
P SHR029 Short Syndrome 49 0.043
143
EPD016 Epidermolysis Bullosa 49 0.043
144
P HYP076 Hyperthyroidism 48 0.043
145
P ALC004 Alcohol Abuse 47 0.043
146
P PRC031 Preeclampsia/eclampsia 1 47 0.043
147
ALP008 Alopecia 47 0.043
148
P RNL028 Renal Tubular Dysgenesis 47 0.043
149
P MYP006 Myopia 46 0.043
150
GMM002 Gamma Chain Deficiency 44 0.043
151
ECT006 Ectodermal Dysplasia 44 0.043
152
ANR040 Aneurysm 43 0.043
153
c SVR005 Severe Pre-Eclampsia 43 0.043
154
BRN071 Brain Injury 42 0.043
155
HLL004 Hellp Syndrome 42 0.043
156
CRK001 Cork-Handlers' Disease 40 0.043
157
BRX001 Bruxism 39 0.043
158
END072 Endotheliitis 39 0.043
159
PSD009 Pseudohermaphroditism 39 0.043
160
LMB062 Limb Ischemia 38 0.043
161
EST005 Esotropia 38 0.043
162
AST006 Astigmatism 34 0.043
163
SXL003 Sexual Disorder 30 0.043
164
PHC006 Phacomatosis Pigmentovascularis 30 0.043
165
EPG004 Epignathus 20 0.043
166
c CRN173 Coronary Heart Disease 8 9 0.043
167
GNT013 Genetic Brain Disorders 3 0.043
168
P BRS047 Breast Cancer 100 0.038
169
CYS001 Cystic Fibrosis 90 0.038
170
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 84 0.038
171
P AST005 Asthma 77 0.038
172
CNG034 Congestive Heart Failure 65 0.038
173
P PSR002 Psoriasis 64 0.038
174
TBR010 Tuberculosis 64 0.038
175
c NRF018 Neurofibromatosis, Type 1 63 0.038
176
P BPL003 Bipolar Disorder 63 0.038
177
P ATS007 Autism Spectrum Disorder 60 0.038
178
PRT036 Peritonitis 58 0.038
179
RBR001 Roberts Syndrome 54 0.038
180
EYD002 Eye Disease 54 0.038
181
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 52 0.038
182
P GRV001 Graves' Disease 51 0.038
183
P PLY006 Polydactyly 49 0.038
184
BRN004 Brain Edema 47 0.038
185
THR013 Thoracic Outlet Syndrome 47 0.038
186
PRN038 Prune Belly Syndrome 47 0.038
187
GTR002 Goiter 47 0.038
188
ACR012 Aicardi Syndrome 46 0.038
189
P HYP065 Hyperaldosteronism 45 0.038
190
ART031 Aortic Coarctation 44 0.038
191
CHN005 Choanal Atresia 44 0.038
192
END020 Endocardial Fibroelastosis 43 0.038
193
IPX001 Ipex Syndrome 43 0.038
194
P ATX004 Ataxia 43 0.038
195
DYS018 Dysostosis 43 0.038
196
P TRC086 Trichohepatoenteric Syndrome 1 42 0.038
197
P MGR003 Migraine with Aura 41 0.038
198
P NNT009 Neonatal Diabetes Mellitus 41 0.038
199
MCR103 Microtia 40 0.038
200
DDN006 Duodenitis 40 0.038
201
GYN001 Gynecomastia 39 0.038
202
P ICH004 Ichthyosis 38 0.038
203
RNL015 Renal Hypertension 38 0.038
204
BRN080 Brain Ischemia 37 0.038
205
CRV043 Cervical Dystonia 37 0.038
206
RSP006 Respiratory System Disease 36 0.038
207
GND002 Gender Identity Disorder 36 0.038
208
VSC047 Vascular Malformation 35 0.038
209
P ART084 Arteriovenous Fistula 34 0.038
210
HMN014 Human Immunodeficiency Virus Infectious Disease 33 0.038
211
RNL097 Renal Artery Disease 32 0.038
212
SPS057 Spasticity 30 0.038
213
SLP010 Slipped Capital Femoral Epiphysis 30 0.038
214
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 28 0.038
215
ANS004 Anisometropia 25 0.038
216
CLN022 Colonic Atresia 23 0.038
217
BRW006 Brown Syndrome 20 0.038
218
PHC005 Phacomatosis Pigmentokeratotica 12 0.038
219
c CRN178 Coronary Heart Disease 6 10 0.038
220
JMC001 Jamaican Vomiting Sickness 8 0.038
221
FTL016 Fetal Edema 6 0.038
222
CRN073 Coronary Arteries Congenital Malformation 1 0.038
223
CRH001 Crohn's Disease 80 0.033
224
P ATX030 Ataxia-Telangiectasia 76 0.033
225
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 75 0.033
226
P OST005 Osteogenesis Imperfecta 70 0.033
227
P CLC005 Celiac Disease 69 0.033
228
STR067 Stroke, Ischemic 68 0.033
229
INC002 Inclusion Body Myositis 67 0.033
230
P ALG002 Alagille Syndrome 66 0.033
231
P ANG001 Angelman Syndrome 66 0.033
232
AND015 Androgen Insensitivity 65 0.033
233
P INF038 Influenza 64 0.033
234
LNG024 Langerhans-Cell Histiocytosis 63 0.033
235
KWS002 Kawasaki Disease 62 0.033
236
SKN016 Skin Disease 61 0.033
237
P AGM001 Agammaglobulinemia 59 0.033
238
P TRN020 Turner Syndrome 59 0.033
239
WLL001 Williams-Beuren Syndrome 59 0.033
240
P PLY011 Polycystic Ovary Syndrome 58 0.033
241
P CNG015 Congenital Diaphragmatic Hernia 58 0.033
242
OVR029 Ovarian Hyperstimulation Syndrome 57 0.033
243
BRN024 Bronchitis 56 0.033
244
P THL005 Thalassemia 56 0.033
245
CLB001 Coloboma 55 0.033
246
VSC007 Vascular Disease 55 0.033
247
c MCL062 Mucolipidosis Ii Alpha/beta 55 0.033
248
VND002 Van Der Woude Syndrome 54 0.033
249
CDL003 Caudal Regression Syndrome 54 0.033
250
MLN008 Melanoma 54 0.033
251
ACN002 Acanthosis Nigricans 53 0.033
252
P INF032 Infertility 52 0.033
253
P NPH012 Nephrotic Syndrome 52 0.033
254
P ANR007 Anorexia Nervosa 52 0.033
255
P HMP007 Hemophilia 51 0.033
256
TST014 Testicular Cancer 51 0.033
257
P CTS001 Cutis Laxa 51 0.033
258
P MNN013 Meningitis 51 0.033
259
P HST010 Histiocytosis 51 0.033
260
P FTL001 Fetal Alcohol Syndrome 50 0.033
261
ATH003 Atherosclerosis 50 0.033
262
P HYP040 Hypospadias 50 0.033
263
P NTR004 Neutropenia 50 0.033
264
P VNT002 Ventricular Septal Defect 50 0.033
265
CHN016 Cohen Syndrome 49 0.033
266
CNN005 Connective Tissue Disease 49 0.033
267
P INT001 Intrahepatic Cholestasis 49 0.033
268
P FNG005 Feingold Syndrome 48 0.033
269
P NPH009 Nephrolithiasis 48 0.033
270
TTH002 Tooth Agenesis 48 0.033
271
P CTR002 Cataract 48 0.033
272
P RHN004 Rhinitis 47 0.033
273
DGN001 Degenerative Disc Disease 47 0.033
274
c MLG069 Malignant Hypertension 46 0.033
275
P SLP006 Sleep Apnea 46 0.033
276
CLF001 Cleft Lip 45 0.033
277
GST045 Gastroenteritis 45 0.033
278
CHL068 Cholestasis 45 0.033
279
MCN017 Meconium Ileus 45 0.033
280
VGN023 Vaginitis 44 0.033
281
ARC002 Arachnoiditis 43 0.033
282
BRN056 Bronchopulmonary Dysplasia 43 0.033
283
GRN039 Greenberg Skeletal Dysplasia 43 0.033
284
HYP266 Hypoxia 42 0.033
285
RNL078 Renal Dysplasia 42 0.033
286
URN010 Urinary Tract Obstruction 42 0.033
287
P ENC018 Encephalopathy 42 0.033
288
SYN005 Synostosis 41 0.033
289
PNM008 Pneumothorax 41 0.033
290
NTR005 Nutritional Deficiency Disease 41 0.033
291
PRP016 Paraplegia 41 0.033
292
P CNG018 Congenital Heart Block 41 0.033
293
TRP014 Triploidy 40 0.033
294
c JVN003 Juvenile Xanthogranuloma 40 0.033
295
TRC040 Tracheoesophageal Fistula 40 0.033
296
ARC007 Arachnoid Cysts 39 0.033
297
P DND001 Dandy-Walker Syndrome 39 0.033
298
P HMP006 Hemiplegic Migraine 39 0.033
299
GRW007 Growth Hormone Deficiency 38 0.033
300
P HYP071 Hypersensitivity Reaction Type Ii Disease 38 0.033
301
PPL021 Papilledema 38 0.033
302
SBS004 Substance Dependence 38 0.033
303
CNV002 Conversion Disorder 37 0.033
304
P MNN007 Meningocele 36 0.033
305
PRS030 Persistent Fetal Circulation Syndrome 36 0.033
306
P PLN008 Peeling Skin Syndrome 36 0.033
307
TCL003 T Cell Deficiency 35 0.033
308
NSY001 N Syndrome 34 0.033
309
TYP015 Type 2b Von Willebrand Disease 33 0.033
310
c MTR002 Mitral Valve Insufficiency 32 0.033
311
SPS004 Spastic Quadriplegia 32 0.033
312
CNN001 Cannabis Dependence 31 0.033
313
CNN002 Cannabis Abuse 31 0.033
314
P HYP120 Hypoaldosteronism 31 0.033
315
FXF001 Fox Fordyce Disease 28 0.033
316
CYT004 Cytomegalic Inclusion Disease 27 0.033
317
OCC011 Occipital Encephalocele 26 0.033
318
c INF131 Infant Acute Respiratory Distress Syndrome 25 0.033
319
FRM001 Freemartinism 24 0.033
320
ATM012 Autoimmune Disease of Blood 24 0.033
321
MLR007 Male Reproductive System Disease 23 0.033
322
c ANR038 Anorexia Nervosa 1 19 0.033
323
CRB031 Cerebral Arterial Disease 19 0.033
324
SPS090 Sepsis in Premature Infants 16 0.033
325
GST058 Gestational Diabetes Insipidus 12 0.033
326
CD4004 Cd4 Deficiency 4 0.033
327
P HYP607 Hypercholesterolemia, Familial 79 0.027
328
DCH001 Duchenne Muscular Dystrophy 78 0.027
329
ADR007 Adrenoleukodystrophy 76 0.027
330
ULC004 Ulcerative Colitis 75 0.027
331
P OST002 Osteoporosis 75 0.027
332
P PFF001 Pfeiffer Syndrome 71 0.027
333
P MDL005 Medulloblastoma 69 0.027
334
MYL009 Myelodysplastic Syndrome 69 0.027
335
TTR001 Tetralogy of Fallot 68 0.027
336
CRZ001 Crouzon Syndrome 67 0.027
337
c SPN225 Spondyloarthropathy 1 66 0.027
338
P TBR001 Tuberous Sclerosis 65 0.027
339
c HMP004 Hemophilia B 65 0.027
340
ACH004 Achondroplasia 65 0.027
341
SVR004 Severe Combined Immunodeficiency 65 0.027
342
VNW001 Von Willebrand's Disease 63 0.027
343
NRR002 Norrie Disease 63 0.027
344
BLM001 Bloom Syndrome 63 0.027
345
ATS001 Autistic Disorder 62 0.027
346
PCK002 Pick Disease 61 0.027
347
ALL003 Allergic Rhinitis 61 0.027
348
P END044 Endometriosis 61 0.027
349
P HRP006 Herpes Simplex 60 0.027
350
THY028 Thyroid Cancer 60 0.027
351
P AXN010 Axenfeld-Rieger Syndrome, Type 3 60 0.027
352
THR006 Thromboangiitis Obliterans 60 0.027
353
PRG004 Progeria 60 0.027
354
P MYS003 Myasthenia Gravis 59 0.027
355
P LVR013 Liver Disease 59 0.027
356
BRN028 Brain Cancer 59 0.027
357
P SDD001 Sudden Infant Death Syndrome 59 0.027
358
P NMN002 Niemann-Pick Disease 59 0.027
359
ART001 Arterial Tortuosity Syndrome 59 0.027
360
P SLV001 Silver-Russell Syndrome 58 0.027
361
P AND016 Andersen Syndrome 58 0.027
362
CRB039 Cerebrovascular Disease 58 0.027
363
P KLL001 Kallmann Syndrome 58 0.027
364
P PNC025 Panic Disorder 58 0.027
365
P HYP035 Hypophosphatasia 58 0.027
366
P DRM010 Dermatomyositis 57 0.027
367
P ATP001 Atopic Dermatitis 57 0.027
368
c ATM003 Autoimmune Thyroiditis 57 0.027
369
DNY001 Denys-Drash Syndrome 57 0.027
370
P KDN018 Kidney Disease 57 0.027
371
ELL001 Ellis-Van Creveld Syndrome 57 0.027
372
P CRN037 Craniosynostosis 57 0.027
373
P BCL006 B-Cell Lymphomas 57 0.027
374
P ADN016 Adenocarcinoma 56 0.027
375
P HYP061 Hypertrophic Cardiomyopathy 56 0.027
376
P RCK004 Rickets 55 0.027
377
ART016 Aortic Aneurysm 55 0.027
378
P ATR011 Atrial Fibrillation 55 0.027
379
TTN003 Tetanus 55 0.027
380
CHR066 Chronic Fatigue Syndrome 55 0.027
381
P HMN010 Hemangioma 54 0.027
382
P PRM011 Primary Ciliary Dyskinesia 54 0.027
383
P RHB017 Rhabdoid Tumor 54 0.027
384
ADN018 Adenoma 54 0.027
385
P SCH018 Schizencephaly 54 0.027
386
P ACR001 Aicardi-Goutieres Syndrome 53 0.027
387
PST028 Post-Traumatic Stress Disorder 53 0.027
388
CHR001 Churg-Strauss Syndrome 53 0.027
389
P NPH005 Nephronophthisis 53 0.027
390
P HRD011 Hereditary Spherocytosis 52 0.027
391
c LCL006 Localized Scleroderma 52 0.027
392
P BRG001 Brugada Syndrome 52 0.027
393
c MTB001 Metabolic Syndrome X 52 0.027
394
P FTL009 Fetal Akinesia Deformation Sequence 51 0.027
395
c ACT075 Acute Myocardial Infarction 50 0.027
396
VHW001 Vohwinkel Syndrome 50 0.027
397
c EXD008 Exudative Vitreoretinopathy 1 50 0.027
398
P RBL001 Rubella 50 0.027
399
P CNJ013 Conjunctivitis 50 0.027
400
PRN023 Prion Disease 50 0.027
401
PTY003 Pityriasis Rubra Pilaris 50 0.027
402
KBG001 Kbg Syndrome 50 0.027
403
HYP056 Hypoglycemia 49 0.027
404
P GLY013 Glycogen Storage Disease 49 0.027
405
P UVT001 Uveitis 49 0.027
406
P GLM007 Glomerulonephritis 49 0.027
407
LPM004 Lipoma 48 0.027
408
AMN001 Amenorrhea 48 0.027
409
P OCL002 Oculocutaneous Albinism 48 0.027
410
P MYT002 Myotonic Dystrophy 48 0.027
411
KRT006 Keratoconjunctivitis 48 0.027
412
P NRP001 Neuropathy 48 0.027
413
P TMT001 Timothy Syndrome 48 0.027
414
HYP080 Hypogonadism 47 0.027
415
CLT003 Colitis 47 0.027
416
P MYC008 Myocarditis 47 0.027
417
PRP030 Purpura 47 0.027
418
P THR003 Thoracic Aortic Aneurysm 47 0.027
419
P KLP003 Klippel-Feil Syndrome 47 0.027
420
BLD044 Bladder Disease 47 0.027
421
c CNG124 Congenital Rubella 47 0.027
422
P STR020 Strabismus 47 0.027
423
SCB001 Scabies 46 0.027
424
OBS061 Obstructive Sleep Apnea 46 0.027
425
STS002 Situs Inversus 46 0.027
426
RTN018 Retinal Disease 46 0.027
427
IMP005 Impotence 46 0.027
428
c ART101 Aortic Valve Disease 2 46 0.027
429
SPN020 Spondylosis 46 0.027
430
c INF069 Infantile Neuroaxonal Dystrophy 1 46 0.027
431
MYC002 Mycobacterium Avium Complex Disease 46 0.027
432
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 46 0.027
433
P MTR012 Mitral Valve Disease 46 0.027
434
P PRT013 Portal Hypertension 45 0.027
435
EXF001 Exfoliation Syndrome 45 0.027
436
NRM005 Neuromuscular Disease 45 0.027
437
c CNT033 Central Nervous System Cancer 45 0.027
438
P DRR001 Diarrhea 45 0.027
439
INT007 Intermediate Coronary Syndrome 45 0.027
440
P INT070 Intestinal Obstruction 45 0.027
441
P HYP014 Hyperuricemia 45 0.027
442
HMH002 Hemihypertrophy 45 0.027
443
PLM010 Pulmonary Edema 45 0.027
444
TRC010 Trichotillomania 44 0.027
445
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 44 0.027
446
P VSC005 Vesicoureteral Reflux 44 0.027
447
RTN017 Retinal Detachment 44 0.027
448
KLN002 Kleine-Levin Syndrome 44 0.027
449
P EPS003 Episodic Ataxia 44 0.027
450
MYL020 Myelomeningocele 44 0.027
451
c FML023 Familial Hemiplegic Migraine 44 0.027
452
P HML001 Hemolytic-Uremic Syndrome 44 0.027
453
CLS010 Cluster Headache 44 0.027
454
PRT058 Pure Autonomic Failure 44 0.027
455
c BRC079 Brachydactyly, Type A2 44 0.027
456
P LFT003 Left Ventricular Noncompaction 44 0.027
457
SBC001 Subacute Sclerosing Panencephalitis 43 0.027
458
P FBR031 Febrile Seizures 43 0.027
459
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 43 0.027
460
ANR004 Anuria 43 0.027
461
P MLT074 Multiple Endocrine Neoplasia 43 0.027
462
HMP005 Hemiplegia 43 0.027
463
P PRV002 Periventricular Nodular Heterotopia 43 0.027
464
ANK001 Ankylosis 43 0.027
465
P RNV001 Renovascular Hypertension 43 0.027
466
P KRT007 Keratoconus 42 0.027
467
P PRN026 Porencephaly 42 0.027
468
HDC001 Headache 42 0.027
469
ANR018 Anorchia 42 0.027
470
PLN006 Poland Syndrome 42 0.027
471
TLN003 Telangiectasis 41 0.027
472
NNT012 Neonatal Jaundice 41 0.027
473
DXT001 Dextrocardia 41 0.027
474
CNN003 Conn's Syndrome 41 0.027
475
DRG003 Drug Dependence 41 0.027
476
P PLM025 Pulmonary Venoocclusive Disease 41 0.027
477
HMG005 Hemoglobinopathy 40 0.027
478
HRT012 Heart Valve Disease 40 0.027
479
APR001 Apraxia 40 0.027
480
PRN037 Prinzmetal's Variant Angina 40 0.027
481
LCH009 Lichen Sclerosus 40 0.027
482
P PRS062 Persistent Hyperplastic Primary Vitreous 40 0.027
483
PRV006 Pervasive Developmental Disorder 40 0.027
484
ANT011 Antisocial Personality Disorder 40 0.027
485
GNR004 Generalized Anxiety Disorder 40 0.027
486
NRN002 Neuronitis 40 0.027
487
ALB002 Albinism 40 0.027
488
HYP043 Hyperandrogenism 40 0.027
489
HPT009 Hepatopulmonary Syndrome 39 0.027
490
BRD004 Borderline Personality Disorder 39 0.027
491
TRN012 Transient Global Amnesia 39 0.027
492
CRP017 Carpal Tunnel Syndrome, Familial 39 0.027
493
HPT014 Hepatorenal Syndrome 39 0.027
494
P MSC033 Muscle Disorders 38 0.027
495
SCL003 Social Phobia 38 0.027
496
CRN025 Corneal Dystrophy 38 0.027
497
ESN011 Eisenmenger Syndrome 38 0.027
498
HTR003 Heterotaxy 38 0.027
499
ISC002 Ischemic Optic Neuropathy 38 0.027
500
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 38 0.027
501
DST006 Diastolic Heart Failure 38 0.027
502
HYP458 Hyper Ige Syndrome 38 0.027
503
c SBC007 Subacute Thyroiditis 38 0.027
504
MYS001 Myositis Ossificans 38 0.027
505
FRZ001 Frozen Shoulder 38 0.027
506
P SPN016 Spondylocostal Dysostosis 38 0.027
507
HRM002 Hermaphroditism 37 0.027
508
MSC006 Muscle Glycogenosis 37 0.027
509
FRY002 Fryns Syndrome 37 0.027
510
SYS003 Systolic Heart Failure 37 0.027
511
P OVR046 Ovarian Cyst 36 0.027
512
P CMP008 Compartment Syndrome 36 0.027
513
RYN001 Raynaud Disease 36 0.027
514
PLC001 Placenta Accreta 36 0.027
515
HRT015 Heritable Pulmonary Arterial Hypertension 36 0.027
516
IRN002 Iron Metabolism Disease 36 0.027
517
RGH009 Right Atrial Isomerism 36 0.027
518
IDP033 Idiopathic Edema 36 0.027
519
c ACT068 Acute Cystitis 36 0.027
520
MYC033 Myoclonus 35 0.027
521
CRN088 Craniorachischisis 35 0.027
522
DDN011 Duodenal Atresia 35 0.027
523
AVD001 Avoidant Personality Disorder 35 0.027
524
RFL001 Reflex Sympathetic Dystrophy 35 0.027
525
P CHR342 Chiari Malformation 35 0.027
526
CHR466 Chronic Thromboembolic Pulmonary Hypertension 35 0.027
527
RTR008 Root Resorption 35 0.027
528
P SCH009 Scheuermann's Disease 35 0.027
529
CRB090 Cerebral Hypoxia 35 0.027
530
c CNT015 Central Sleep Apnea 34 0.027
531
ADS002 Adie Syndrome 34 0.027
532
PRP021 Peripheral Nervous System Neoplasm 34 0.027
533
PHC013 Phaeochromocytoma 34 0.027
534
IMP004 Impetigo 34 0.027
535
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 34 0.027
536
CRV025 Cervical Incompetence 33 0.027
537
PHY002 Physical Disorder 33 0.027
538
BLP004 Blepharophimosis 33 0.027
539
MTG002 Mutagen Sensitivity 33 0.027
540
c CHR546 Chronic Mountain Sickness 32 0.027
541
VSC004 Vasculogenic Impotence 32 0.027
542
DVL002 Developmental Disabilities 32 0.027
543
CRN019 Coronary Artery Vasospasm 32 0.027
544
IRT001 Iritis 31 0.027
545
P ATX010 Ataxia Neuropathy Spectrum 31 0.027
546
PRP019 Peripheral Nervous System Disease 31 0.027
547
UND005 Undifferentiated Pleomorphic Sarcoma 31 0.027
548
CND006 Candida Glabrata 30 0.027
549
HPT074 Hepatic Adenoma, Somatic 30 0.027
550
P PST059 Pustular Psoriasis 30 0.027
551
c CHR096 Chronic Pulmonary Heart Disease 30 0.027
552
BLN002 Balanitis Xerotica Obliterans 30 0.027
553
NNT019 Neonatal Hypothyroidism 30 0.027
554
BLL012 Bullous Impetigo 30 0.027
555
SPL040 Split Hand 30 0.027
556
ART110 Arteritic Anterior Ischemic Optic Neuropathy 30 0.027
557
NSD001 Nose Disease 28 0.027
558
LKC003 Leukocyte Disease 28 0.027
559
P NNT042 Neonatal Lupus Erythematosus 28 0.027
560
MYF001 Myofibroma 28 0.027
561
TRD003 Taurodontism 28 0.027
562
TFT003 Tufting Enteropathy 27 0.027
563
BLN010 Balanitis 27 0.027
564
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 27 0.027
565
HNM002 Hinman Syndrome 27 0.027
566
IMP001 Impetigo Herpetiformis 27 0.027
567
c ATM017 Autoimmune Disease of the Nervous System 26 0.027
568
RPR002 Reproductive System Disease 26 0.027
569
P SCN008 Secondary Parkinson Disease 26 0.027
570
FCL044 Fecal Incontinence 25 0.027
571
NRC003 Narcissistic Personality Disorder 25 0.027
572
c PLN018 Peeling Skin Syndrome 2 25 0.027
573
CDL005 Caudal Duplication Anomaly 25 0.027
574
PNL013 Penile Disease 24 0.027
575
ALR002 Al-Raqad Syndrome 23 0.027
576
CLC002 Calcaneonavicular Coalition 23 0.027
577
MSC004 Muscle Tissue Disease 23 0.027
578
FXC001 Foix Chavany Marie Syndrome 22 0.027
579
PSY003 Psychosexual Disorder 22 0.027
580
c MLG003 Malignant Renovascular Hypertension 22 0.027
581
c ATM007 Autoimmune Disease of Central Nervous System 22 0.027
582
NNT018 Neonatal Herpes 21 0.027
583
PDT040 Pediatric Hypertension 21 0.027
584
IMM082 Immunodeficiency 18 21 0.027
585
HYP179 Hypertrichosis Congenital Generalized X-Linked 21 0.027
586
c BNG076 Benign Exophthalmos Syndrome 21 0.027
587
CHM005 Chemical Colitis 20 0.027
588
HMN031 Human Venous Malformation 20 0.027
589
RNL008 Renal Artery Atheroma 19 0.027
590
IMM068 Immunodeficiency 8 19 0.027
591
ART109 Arterial Thoracic Outlet Syndrome 19 0.027
592
AND005 Androgen Insensitivity Syndrome, Mild 19 0.027
593
NNT021 Neonatal Meningitis 18 0.027
594
TRG003 Trigeminal Nerve Disease 18 0.027
595
IDP075 Idiopathic and/or Familial Pulmonary Arterial Hypertension 16 0.027
596
c PLN021 Peeling Skin Syndrome 3 16 0.027
597
P LMB009 Lambdoid Synostosis 16 0.027
598
CLP002 Colpocephaly 15 0.027
599
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 15 0.027
600
TRG006 Trigger Thumb 14 0.027
601
RHH001 Rohhad 14 0.027
602
WLS002 Wilson-Mikity Syndrome 14 0.027
603
IMM076 Immunodeficiency 24 14 0.027
604
SYM006 Symmetrical Thalamic Calcifications 13 0.027
605
FBL005 Fibular Aplasia 11 0.027
606
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 11 0.027
607
P CRN214 Coronary Heart Disease 5 10 0.027
608
VSC009 Vascular Skin Disease 9 0.027
609
NNT002 Neonatal Urinary Tract Infectious Disease 7 0.027
610
P ALZ034 Alzheimer Disease 98 0.019
611
P CLR023 Colorectal Cancer 95 0.019
612
P PRS040 Prostate Cancer 90 0.019
613
P DBT085 Diabetes Mellitus, Insulin-Dependent 82 0.019
614
P RTT002 Rett Syndrome 79 0.019
615
P OST012 Osteoarthritis 79 0.019
616
c MLT019 Multiple Myeloma 77 0.019
617
GLC006 Galactosemia 76 0.019
618
P RTN008 Retinitis Pigmentosa 75 0.019
619
HDG012 Hodgkin Lymphoma 75 0.019
620
FBR012 Fabry Disease 75 0.019
621
P HMC003 Hemochromatosis 75 0.019
622
P RTN024 Retinoblastoma 74 0.019
623
c DLT002 Dilated Cardiomyopathy 73 0.019
624
c PRK057 Parkinson Disease, Late-Onset 73 0.019
625
P MTC003 Metachromatic Leukodystrophy 72 0.019
626
CDS001 Cadasil 70 0.019
627
P OVR042 Ovarian Cancer 69 0.019
628
P WSK001 Wiskott-Aldrich Syndrome 68 0.019
629
SMT004 Smith-Lemli-Opitz Syndrome 67 0.019
630
P FML161 Familial Mediterranean Fever, Ar 67 0.019
631
BCK001 Becker Muscular Dystrophy 66 0.019
632
P FRG001 Fragile X Syndrome 66 0.019
633
P DMN001 Diamond-Blackfan Anemia 66 0.019
634
P CLD001 Cleidocranial Dysplasia 66 0.019
635
P ALP004 Alport Syndrome 66 0.019
636
MNK001 Menkes Disease 65 0.019
637
KPS004 Kaposi Sarcoma 65 0.019
638
c HMP029 Hemophilia a 64 0.019
639
c HPT001 Hepatitis C 64 0.019
640
c HRD010 Hereditary Spastic Paraplegia 64 0.019
641
CMM004 Common Variable Immunodeficiency 64 0.019
642
P EPD002 Epidermolytic Hyperkeratosis 64 0.019
643
P GCH001 Gaucher's Disease 64 0.019
644
CST001 Costello Syndrome 64 0.019
645
P MYL005 Myelofibrosis 64 0.019
646
c JVN010 Juvenile Rheumatoid Arthritis 64 0.019
647
P STM004 Stomach Cancer 63 0.019
648
P LPR003 Leprosy 63 0.019
649
P KRT004 Keratitis 63 0.019
650
MLT021 Multiple System Atrophy 63 0.019
651
P PND002 Pendred Syndrome 63 0.019
652
CMP005 Campomelic Dysplasia 63 0.019
653
APR006 Apert Syndrome 63 0.019
654
c MLT136 Multiple Endocrine Neoplasia 1 62 0.019
655
c SYS005 Systemic Scleroderma 62 0.019
656
P HRM001 Hermansky-Pudlak Syndrome 62 0.019
657
OBS002 Obsessive-Compulsive Disorder 62 0.019
658
P VLC001 Velocardiofacial Syndrome 61 0.019
659
c MLT024 Multiple Endocrine Neoplasia Iia 61 0.019
660
P ALX003 Alexander Disease 61 0.019
661
ACR007 Acromegaly 61 0.019
662
P ADD001 Addison's Disease 60 0.019
663
P AMY004 Amyloidosis 60 0.019
664
WLF001 Wolff-Parkinson-White Syndrome 60 0.019
665
c HPT073 Hepatitis C Virus 60 0.019
666
PLM001 Pulmonary Tuberculosis 60 0.019
667
P PLY014 Polycystic Kidney Disease 60 0.019
668
TNG002 Tangier Disease 60 0.019
669
c HPT016 Hepatitis B 59 0.019
670
P HMP002 Hemophagocytic Lymphohistiocytosis 59 0.019
671
CYS010 Cystinosis 59 0.019
672
P MYL006 Myeloid Leukemia 59 0.019
673
P CHR071 Charcot-Marie-Tooth Disease 59 0.019
674
GST092 Gastroesophageal Reflux 58 0.019
675
INC021 Incontinentia Pigmenti 58 0.019
676
FCT003 Factor X Deficiency 58 0.019
677
c MYT021 Myotonic Dystrophy 1 58 0.019
678
BLS001 Blau Syndrome 57 0.019
679
P CCK001 Cockayne Syndrome 57 0.019
680
P RTH001 Rothmund-Thomson Syndrome 57 0.019
681
P PSR001 Psoriatic Arthritis 57 0.019
682
SRC014 Sarcoma 57 0.019
683
MLG056 Malignant Hyperthermia 56 0.019
684
P LBR001 Leber Congenital Amaurosis 56 0.019
685
P ASP006 Aspergillosis 56 0.019
686
P BDD001 Budd-Chiari Syndrome 56 0.019
687
c SYS004 Systemic Mastocytosis 56 0.019
688
c CHR536 Charcot-Marie-Tooth Disease, Type 1a 56 0.019
689
P PRM006 Primary Biliary Cirrhosis 56 0.019
690
P EMR001 Emery-Dreifuss Muscular Dystrophy 56 0.019
691
ARS001 Aarskog-Scott Syndrome 55 0.019
692
P ANT006 Antiphospholipid Syndrome 55 0.019
693
PRT037 Pertussis 55 0.019
694
LPT001 Leptospirosis 55 0.019
695
P MYM002 Moyamoya Disease 55 0.019
696
PSY004 Psychotic Disorder 55 0.019
697
WGR001 Wagr Syndrome 55 0.019
698
P SPN049 Spinocerebellar Ataxia 54 0.019
699
WST001 West Syndrome 54 0.019
700
MVL001 Mevalonic Aciduria 54 0.019
701
ALP001 Alopecia Universalis 54 0.019
702
P FND001 Fundus Albipunctatus 54 0.019
703
P MYL007 Myeloma 54 0.019
704
c HRD002 Hereditary Angioedema 54 0.019
705
WLM001 Wolman Disease 54 0.019
706
MNK003 Muenke Syndrome 54 0.019
707
P PRP029 Porphyria 54 0.019
708
P EPL002 Epilepsy Syndrome 54 0.019
709
BLL001 Baller-Gerold Syndrome 54 0.019
710
P EPD009 Epidermolysis Bullosa Dystrophica 53 0.019
711
RHM001 Rheumatic Fever 53 0.019
712
CNT047 Contact Dermatitis 53 0.019
713
P HLL001 Hallermann-Streiff Syndrome 53 0.019
714
c FML001 Familial Atrial Fibrillation 53 0.019
715
P FRS003 Fraser Syndrome 53 0.019
716
CNC002 Cinca Syndrome 53 0.019
717
P MCP010 Mucopolysaccharidosis 53 0.019
718
MXD005 Mixed Connective Tissue Disease 53 0.019
719
P LNG028 Long Qt Syndrome 53 0.019
720
KRN002 Kearns-Sayre Syndrome 53 0.019
721
P SJG002 Sjogren-Larsson Syndrome 53 0.019
722
ASP002 Aspartylglucosaminuria 53 0.019
723
P STC001 Stickler Syndrome 52 0.019
724
P PRD008 Periodontitis 52 0.019
725
ETN001 Eating Disorder 52 0.019
726
P ALP009 Alopecia Areata 52 0.019
727
CHR063 Chronic Mucocutaneous Candidiasis 52 0.019
728
CRY002 Cryptorchidism 52 0.019
729
P HYP004 Hypercalcemia 52 0.019
730
P ALT001 Alternating Hemiplegia of Childhood 52 0.019
731
MDD011 Mood Disorder 52 0.019
732
c CNT035 Central Nervous System Disease 52 0.019
733
P IDP010 Idiopathic Generalized Epilepsy 51 0.019
734
STT001 Status Epilepticus 51 0.019
735
ACR003 Acrodermatitis Enteropathica 51 0.019
736
CHN055 Chanarin-Dorfman Syndrome 51 0.019
737
P DGR001 Digeorge Syndrome 51 0.019
738
NTH001 Netherton Syndrome 51 0.019
739
P GT001 Gout 51 0.019
740
VLV011 Vulvovaginal Candidiasis 51 0.019
741
LST001 Listeriosis 51 0.019
742
P WVR001 Weaver Syndrome 51 0.019
743
P PNC044 Pancreatitis 51 0.019
744
HST011 Histoplasmosis 51 0.019
745
OLV001 Olivopontocerebellar Atrophy 51 0.019
746
P CND004 Candidiasis 50 0.019
747
ATP002 Atopy 50 0.019
748
VSC011 Vasculitis 50 0.019
749
RSC001 Rosacea 50 0.019
750
CHL014 Cholera 50 0.019
751
DSM004 Desmoid Tumor 50 0.019
752
P NSP012 Nasopharyngeal Carcinoma 50 0.019
753
ALV007 Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins 50 0.019
754
PRS047 Prostatitis 50 0.019
755
MLN007 Male Infertility 50 0.019
756
VRL011 Viral Infectious Disease 50 0.019
757
P ART023 Arthropathy 50 0.019
758
MYM001 Myoma 49 0.019
759
JHN001 Johanson-Blizzard Syndrome 49 0.019
760
P MCR010 Microcephaly 49 0.019
761
PRL009 Prolactinoma 49 0.019
762
P NRV007 Nervous System Disease 49 0.019
763
GLC003 Glucose Intolerance 49 0.019
764
FTT001 Fatty Liver Disease 49 0.019
765
CNG048 Congenital Hepatic Fibrosis 49 0.019
766
CYS005 Cysticercosis 49 0.019
767
c TYR013 Tyrosinemia, Type Ii 49 0.019
768
EDW001 Edwards Syndrome 49 0.019
769
P ESN007 Eosinophilia 48 0.019
770
VGT001 Vogt-Koyanagi-Harada Disease 48 0.019
771
P CNG046 Congenital Fiber-Type Disproportion 48 0.019
772
P SZR006 Seizure Disorder 48 0.019
773
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 48 0.019
774
c INF071 Inflammatory Bowel Disease 1 48 0.019
775
DSS009 Disseminated Intravascular Coagulation 48 0.019
776
P ENC004 Encephalitis 48 0.019
777
c GRS014 Griscelli Syndrome, Type 2 48 0.019
778
SFT003 Soft Tissue Sarcoma 48 0.019
779
OST017 Osteomyelitis 48 0.019
780
P OLG002 Oligodendroglioma 48 0.019
781
P THR005 Thrombotic Thrombocytopenic Purpura 48 0.019
782
BRN002 Bronchiolitis 48 0.019
783
P BRC006 Brachydactyly 48 0.019
784
P HYP050 Hyperinsulinemic Hypoglycemia 48 0.019
785
c MLG077 Malignant Peripheral Nerve Sheath Tumor 48 0.019
786
TMP001 Temporal Lobe Epilepsy 48 0.019
787
c PSD066 Pseudohypoparathyroidism, Type Ib 47 0.019
788
MGL001 Megaloblastic Anemia 47 0.019
789
THR100 Thrombocytopenic Purpura, Autoimmune 47 0.019
790
SPT004 Septic Arthritis 47 0.019
791
ALL008 Allergic Bronchopulmonary Aspergillosis 47 0.019
792
P HYP027 Hypobetalipoproteinemia 47 0.019
793
FDL002 Food Allergy 47 0.019
794
P JNC001 Junctional Epidermolysis Bullosa 47 0.019
795
NRG002 Neurogenic Bladder 47 0.019
796
SLP005 Sleep Disorder 47 0.019
797
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 47 0.019
798
LRN003 Learning Disability 47 0.019
799
TTH006 Tooth Disease 47 0.019
800
P CYS018 Cystitis 47 0.019
801
ACS001 Acoustic Neuroma 47 0.019
802
FLT001 Felty's Syndrome 47 0.019
803
P D2H001 D-2-Hydroxyglutaric Aciduria 47 0.019
804
VSC002 Vascular Dementia 47 0.019
805
P TYR004 Tyrosinemia 47 0.019
806
ALL009 Allergic Conjunctivitis 46 0.019
807
CCT002 Cicatricial Pemphigoid 46 0.019
808
SCR008 Scrub Typhus 46 0.019
809
DBW001 Dubowitz Syndrome 46 0.019
810
PSD007 Pseudomyxoma Peritonei 46 0.019
811
P SPR013 Spiradenoma 46 0.019
812
RST001 Restless Legs Syndrome 46 0.019
813
RNL007 Renal Tubular Acidosis 46 0.019
814
PRD019 Periodic Fever, Familial 46 0.019
815
P ANG015 Angioedema 46 0.019
816
P PLY019 Polyneuropathy 46 0.019
817
ALP014 Alpha-Thalassemia/mental Retardation Syndrome 46 0.019
818
GLC085 Glucose-6-Phosphate Dehydrogenase Deficiency 46 0.019
819
STF001 Stiff-Person Syndrome 46 0.019
820
P MCL001 Mucolipidosis 46 0.019
821
PRT011 Protein C Deficiency 46 0.019
822
P DDN001 Duodenal Ulcer 46 0.019
823
BLL003 Bell's Palsy 46 0.019
824
LYM009 Lymphocytic Choriomeningitis 46 0.019
825
MTN003 Motion Sickness 45 0.019
826
LPD008 Lipid Metabolism Disorder 45 0.019
827
EPD006 Epidermolysis Bullosa Acquisita 45 0.019
828
TYP011 Typhus 45 0.019
829
P LSS002 Lissencephaly 45 0.019
830
PLC003 Placental Site Trophoblastic Tumor 45 0.019
831
P RBN002 Robinow Syndrome 45 0.019
832
P PLY041 Polymyositis 45 0.019
833
HMT018 Hematopoietic Stem Cell Transplantation 45 0.019
834
NRF007 Neurofibroma 45 0.019
835
BLD034 Bile Duct Carcinoma 45 0.019
836
PMP001 Pemphigus 45 0.019
837
CMP034 Complete Androgen Insensitivity Syndrome 45 0.019
838
PTT006 Pituitary Adenoma 45 0.019
839
P LKD001 Leukodystrophy 45 0.019
840
MGC001 Megacolon 45 0.019
841
HYP068 Hyperostosis 45 0.019
842
P AML002 Amelogenesis Imperfecta 45 0.019
843
CRD119 Cardiac Arrest 45 0.019
844
PLS009 Plasma Cell Neoplasm 45 0.019
845
CLR003 Clear Cell Adenocarcinoma 45 0.019
846
P MSC003 Muscular Atrophy 45 0.019
847
BLR001 Biliary Atresia 44 0.019
848
P CNT005 Central Nervous System Lymphoma 44 0.019
849
P INT068 Intestinal Disease 44 0.019
850
P HYP060 Hyperinsulinism 44 0.019
851
P GRS003 Griscelli Syndrome 44 0.019
852
c BRC082 Brachydactyly, Type E 44 0.019
853
CTS002 Cat-Scratch Disease 44 0.019
854
MTH009 Mouth Disease 44 0.019
855
P OVR049 Ovarian Disease 44 0.019
856
ART002 Arts Syndrome 44 0.019
857
PRN011 Pernicious Anemia 44 0.019
858
CLS007 Classic Kaposi Sarcoma 44 0.019
859
CNG035 Congenital Bilateral Absence of Vas Deferens 44 0.019
860
P NRV006 Nervous System Cancer 44 0.019
861
MGL013 Megalencephaly 44 0.019
862
P SYP003 Syphilis 44 0.019
863
P SCL018 Scoliosis 44 0.019
864
MST005 Mastitis 44 0.019
865
CSY001 C Syndrome 44 0.019
866
MCR037 Macroglossia 44 0.019
867
c HYP163 Hyperlipidemia Type 3 44 0.019
868
c TRC092 Trichorhinophalangeal Syndrome, Type I 43 0.019
869
NNL002 Nonalcoholic Steatohepatitis 43 0.019
870
SCT005 Scott Syndrome 43 0.019
871
ASP001 Asperger Syndrome 43 0.019
872
P PMP005 Pemphigus Vulgaris 43 0.019
873
TBR006 Tuberculoid Leprosy 43 0.019
874
AND001 Anodontia 43 0.019
875
CHR074 Choriocarcinoma 43 0.019
876
c PND001 Pain Disorder 43 0.019
877
PRM013 Premature Menopause 43 0.019
878
P GNG009 Gangliosidosis 43 0.019
879
MST017 Mast Cell Disease 43 0.019
880
DMY004 Demyelinating Disease 43 0.019
881
CVR006 Cavernous Hemangioma 43 0.019
882
GST050 Gastrointestinal System Disease 43 0.019
883
CHL069 Cholesteatoma 43 0.019
884
c TBR024 Tuberous Sclerosis-1 43 0.019
885
PRR002 Pure Red-Cell Aplasia 43 0.019
886
P FBR025 Fibrochondrogenesis 43 0.019
887
OST011 Osteomalacia 42 0.019
888
PSD002 Pseudotumor Cerebri 42 0.019
889
PLM070 Pulmonic Stenosis 42 0.019
890
P PYL005 Pyelonephritis 42 0.019
891
FBR032 Fibromuscular Dysplasia 42 0.019
892
P PTS002 Ptosis 42 0.019
893
P PSD015 Pseudohypoparathyroidism 42 0.019
894
NRM004 Neuroma 42 0.019
895
P ACH011 Achondrogenesis 42 0.019
896
PPL018 Papillary Adenocarcinoma 42 0.019
897
P LPD011 Lipoid Adrenal Hyperplasia 42 0.019
898
C3D001 C3 Deficiency 42 0.019
899
FBR009 Fibrous Dysplasia 42 0.019
900
MRG003 Marginal Zone B-Cell Lymphoma 41 0.019
901
P INT030 Intracranial Aneurysm 41 0.019
902
PRS042 Prostate Disease 41 0.019
903
CHR078 Chorioretinitis 41 0.019
904
PRC012 Pericardial Effusion 41 0.019
905
P PNC001 Pancytopenia 41 0.019
906
STR026 Star Syndrome 41 0.019
907
BLN001 Blount's Disease 41 0.019
908
DSC009 Discoid Lupus Erythematosus 41 0.019
909
CLN019 Colonic Disease 41 0.019
910
APH002 Aphasia 40 0.019
911
AGR002 Agoraphobia 40 0.019
912
c RCS002 Recessive Dystrophic Epidermolysis Bullosa 40 0.019
913
VRN004 Vernal Keratoconjunctivitis 40 0.019
914
MMB002 Membranous Glomerulonephritis 40 0.019
915
P PSD003 Pseudohypoaldosteronism 40 0.019
916
SPN019 Spondylolisthesis 40 0.019
917
VSC006 Vascular Cancer 40 0.019
918
TRN060 Truncus Arteriosus 40 0.019
919
HYP077 Hypertrichosis 40 0.019
920
P MLG086 Malignant Hyperthermia Susceptibility 40 0.019
921
FLL008 Folliculitis 40 0.019
922
P PRM001 Primary Cutaneous Amyloidosis 40 0.019
923
P PRP023 Peripheral Neuropathy 40 0.019
924
EPS026 Epispadias 40 0.019
925
PRT019 Protein-Losing Enteropathy 40 0.019
926
MNN009 Meningoencephalitis 40 0.019
927
P END046 Endometritis 40 0.019
928
DFF001 Diffuse Cutaneous Mastocytosis 40 0.019
929
ASP004 Asphyxia Neonatorum 40 0.019
930
DFF021 Diffuse Mesangial Sclerosis 40 0.019
931
P INF049 Infantile Myofibromatosis 40 0.019
932
JNT002 Joint Disorders 39 0.019
933
KRT010 Kartagener Syndrome 39 0.019
934
CD4003 Cd40 Ligand Deficiency 39 0.019
935
BNF002 Bone Fracture 39 0.019
936
OCL020 Ocular Cicatricial Pemphigoid 39 0.019
937
QBC001 Quebec Platelet Disorder 39 0.019
938
HMG002 Hemoglobinuria 39 0.019
939
c CWD006 Cowden Syndrome 1 39 0.019
940
P SYR001 Syringomyelia 39 0.019
941
NPH003 Nephrocalcinosis 39 0.019
942
DNT012 Dental Caries 39 0.019
943
CRD144 Cardiovascular Disease Risk Factor ) 39 0.019
944
ART004 Aortic Atherosclerosis 39 0.019
945
ART035 Arterial Calcification of Infancy 39 0.019
946
MLT006 Multidrug-Resistant Tuberculosis 39 0.019
947
DFF003 Diffuse Scleroderma 39 0.019
948
FMR004 Fumarase Deficiency 39 0.019
949
PRP080 Peripheral Artery Disease 39 0.019
950
LPM005 Lipomatosis 39 0.019
951
QDR001 Quadriplegia 39 0.019
952
CRL004 Caroli Disease 39 0.019
953
GGR001 Geographic Tongue 38 0.019
954
PRP009 Peripartum Cardiomyopathy 38 0.019
955
P PNT019 Pontocerebellar Hypoplasia 38 0.019
956
NRN008 Neuronal Intranuclear Inclusion Disease 38 0.019
957
c INT064 Intermediate Uveitis 38 0.019
958
P VTL001 Vitelliform Macular Dystrophy 38 0.019
959
GNG002 Ganglioneuroma 38 0.019
960
WRN002 Wernicke-Korsakoff Syndrome 38 0.019
961
HND002 Hand, Foot and Mouth Disease 38 0.019
962
NRW001 Norwegian Scabies 38 0.019
963
CCN002 Cocaine Abuse 38 0.019
964
NSP002 Nasopharyngitis 38 0.019
965
P SDR003 Sideroblastic Anemia 38 0.019
966
P LYD001 Leydig Cell Tumor 38 0.019
967
ANH002 Anhidrosis 38 0.019
968
IDP021 Idiopathic Myopathy 38 0.019
969
c CNG004 Congenital Epulis 38 0.019
970
FML027 Female Breast Carcinoma 38 0.019
971
OHT001 Ohtahara Syndrome 38 0.019
972
OLM001 Olmsted Syndrome 38 0.019
973
P TMR010 Tumor Predisposition Syndrome 38 0.019
974
HYP064 Hypogonadotropism 37 0.019
975
PLM035 Pulmonary Eosinophilia 37 0.019
976
P MRC003 Mercury Poisoning 37 0.019
977
NNT016 Neonatal Hemochromatosis 37 0.019
978
P HRD021 Hereditary Sensory Neuropathy 37 0.019
979
P PTT002 Potter's Syndrome 37 0.019
980
FCL041 Focal Myositis 37 0.019
981
DRM011 Dermatophytosis 37 0.019
982
FML038 Female Reproductive Organ Cancer 37 0.019
983
TST015 Testicular Disease 37 0.019
984
MST006 Mast Syndrome 37 0.019
985
PRM003 Premature Ejaculation 37 0.019
986
ANV001 Anovulation 37 0.019
987
CHR564 Chronic Mucocutaneous Candidosis 37 0.019
988
CHR008 Choroiditis 37 0.019
989
P CNG024 Congenital Nystagmus 37 0.019
990
SPR007 Superior Mesenteric Artery Syndrome 37 0.019
991
PCH002 Pachygyria 37 0.019
992
SDD007 Sudden Cardiac Death 36 0.019
993
GND001 Gonadoblastoma 36 0.019
994
CNG105 Congenital Lobar Emphysema 36 0.019
995
MSS002 Mass Syndrome 36 0.019
996
c HMG001 Hemoglobin C Disease 36 0.019
997
CNG064 Congenital Chloride Diarrhea 36 0.019
998
HMP009 Haemophilus Influenzae 36 0.019
999
GST052 Gestational Choriocarcinoma 36 0.019
1000
c ACT076 Acute Myocarditis 36 0.019
1001
MYX004 Myxedema 36 0.019
1002
P INT063 Intellectual Disability 36 0.019
1003
TRN030 Transient Erythroblastopenia of Childhood 36 0.019
1004
GRM004 Germinoma 36 0.019
1005
OBS003 Obsessive-Compulsive Personality Disorder 36 0.019
1006
RNL012 Renal Tuberculosis 36 0.019
1007
SYN036 Syncope 36 0.019
1008
RNL025 Renal Hypoplasia 36 0.019
1009
WDM004 Wiedemann-Steiner Syndrome 36 0.019
1010
P NRL007 Neurologic Diseases 35 0.019
1011
MHC001 Mhc Class Ii Deficiency 35 0.019
1012
c CNG033 Congenital Syphilis 35 0.019
1013
ESN005 Eosinophilic Gastroenteritis 35 0.019
1014
CRH005 Crohn's Colitis 35 0.019
1015
P EPL003 Epulis 35 0.019
1016
PRS012 Pars Planitis 35 0.019
1017
ANN005 Annular Pancreas 35 0.019
1018
c PRK031 Parkinson Disease 1 35 0.019
1019
THY030 Thyroid Gland Disease 35 0.019
1020
GRN007 Granuloma Annulare 35 0.019
1021
NVS001 Neovascular Glaucoma 35 0.019
1022
c CNG029 Congenital Mesoblastic Nephroma 35 0.019
1023
PRD003 Periodontosis 35 0.019
1024
SKN027 Skin Conditions 34 0.019
1025
P LTT001 Lattice Corneal Dystrophy 34 0.019
1026
P NRX001 Neuroaxonal Dystrophy 34 0.019
1027
CND005 Cone Dystrophy 34 0.019
1028
ARM002 Aromatic L-Amino Acid Decarboxylase Deficiency 34 0.019
1029
LCH003 Lichen Nitidus 34 0.019
1030
NDL021 Nodular Lymphocyte Predominant Hodgkin Lymphoma 34 0.019
1031
HRT007 Heart Cancer 34 0.019
1032
TLP001 Talipes Equinovarus 34 0.019
1033
GNT006 Giant Papillary Conjunctivitis 34 0.019
1034
DPR001 Diaper Rash 34 0.019
1035
MTR010 Mature Teratoma 34 0.019
1036
CHL052 Choledochal Cyst 34 0.019
1037
CMB021 Combined Pituitary Hormone Deficiency 34 0.019
1038
c DBT064 Diabetes Mellitus, Transient Neonatal, 1 34 0.019
1039
ACT084 Acute Stress Disorder 34 0.019
1040
PDT035 Pediatric Systemic Lupus Erythematosus 34 0.019
1041
XNT009 Xanthoma Disseminatum 34 0.019
1042
HMN032 Human Herpesvirus 8 34 0.019
1043
DLS001 Delusional Disorder 34 0.019
1044
ACR005 Acrodermatitis 34 0.019
1045
ALB014 Alobar Holoprosencephaly 34 0.019
1046
EST007 Estrogen Resistance 33 0.019
1047
P CRB154 Cerebrocostomandibular Syndrome 33 0.019
1048
CRB004 Cerebral Artery Occlusion 33 0.019
1049
PLG004 Plagiocephaly 33 0.019
1050
RTT001 Ritter's Disease 33 0.019
1051
NNM005 Non-Immune Hydrops Fetalis 33 0.019
1052
ISL003 Isolated Growth Hormone Deficiency 33 0.019
1053
WRT003 Warthin Tumor 33 0.019
1054
FTS001 Fetishism 33 0.019
1055
MLR006 Male Reproductive Organ Cancer 33 0.019
1056
P CNG390 Congenital Pulmonary Airway Malformation 33 0.019
1057
MNN021 Meningococcemia 33 0.019
1058
TBL013 Tubulointerstitial Nephritis and Uveitis 33 0.019
1059
CNJ012 Conjunctival Disease 33 0.019