Search results for "twinning"

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

1030 hits were found for 'twinning'

# Family MCID Name MIFTS Score
1
P TWN001 Twin-to-Twin Transfusion Syndrome 54 10.306
2
c TWN006 Twin Twin Transfusion Syndrome 30 7.405
3
c RNL090 Renal Tubular Dysgenesis Due to Twin-Twin Transfusion 6 5.074
4
PLY012 Polyhydramnios 54 0.165
5
ANN002 Anencephaly 58 0.151
6
CRB009 Cerebritis 39 0.148
7
c PLY018 Polycythemia 61 0.143
8
HYD012 Hydrops Fetalis 61 0.112
9
OLG003 Oligohydramnios 59 0.112
10
P CRV039 Cervicitis 57 0.108
11
P OBS005 Obesity 89 0.099
12
P HYP075 Hypertension 85 0.096
13
ACR022 Acardia 14 0.091
14
DWN001 Down Syndrome 61 0.083
15
P RTN012 Retinopathy of Prematurity 56 0.083
16
CHR005 Chorioamnionitis 50 0.083
17
CYT008 Cytomegalovirus Infection 43 0.083
18
P MGR002 Migraine 69 0.081
19
c THY032 Thyroiditis 66 0.081
20
CNG069 Congenital Cytomegalovirus 36 0.081
21
SRN002 Sirenomelia 23 0.081
22
P CNG401 Congenital Heart Disease 58 0.078
23
c INT060 Intestinal Atresia 49 0.078
24
NCT002 Nicotine Dependence 48 0.078
25
c DBT009 Diabetes Mellitus 78 0.075
26
P LKM002 Leukemia 77 0.071
27
URT039 Urticaria 61 0.071
28
c HYP086 Hypothyroidism 69 0.068
29
ISC004 Ischemia 63 0.068
30
P OMP004 Omphalocele 52 0.068
31
P ENC008 Encephalocele 52 0.068
32
ECT026 Ectopic Pregnancy 45 0.068
33
ENC017 Encephaloceles 42 0.068
34
AMN009 Amniotic Band Syndrome 37 0.068
35
ENC005 Encephalomalacia 34 0.068
36
RNL002 Renal Agenesis 70 0.065
37
c TXP001 Toxoplasmosis 65 0.065
38
P PRS038 Personality Disorder 58 0.065
39
URT001 Urethritis 54 0.065
40
PST087 Posterior Urethral Valve 52 0.065
41
P GND004 Gonadal Dysgenesis 52 0.065
42
PST041 Posterior Urethral Valves 48 0.065
43
URT008 Urticaria Pigmentosa 47 0.065
44
P RBN001 Rubinstein-Taybi Syndrome 75 0.061
45
DRM006 Dermatitis 69 0.061
46
P INS005 Insulin Resistance 66 0.061
47
CRB037 Cerebral Palsy 65 0.061
48
c THN001 Thanatophoric Dysplasia 61 0.061
49
VCT001 Vacterl Association 61 0.061
50
c HYP065 Hyperaldosteronism 57 0.061
51
P CNG021 Congenital Toxoplasmosis 57 0.061
52
c TRT010 Teratoma 55 0.061
53
RTN023 Retinitis 53 0.061
54
MNT147 Mental Retardation 51 0.061
55
PYL006 Pyloric Stenosis 50 0.061
56
IMP002 Imperforate Anus 48 0.061
57
P APL006 Aplasia Cutis Congenita 40 0.061
58
c BPL002 Bipolar I Disorder 38 0.061
59
HYD001 Hydranencephaly 38 0.061
60
P ART022 Arthritis 75 0.057
61
c LPS004 Lupus Erythematosus 72 0.057
62
c MST009 Mastocytosis 71 0.057
63
P MLT020 Multiple Sclerosis 69 0.057
64
SPN038 Spina Bifida 67 0.057
65
P OST009 Osteochondritis Dissecans 67 0.057
66
GST009 Gastroschisis 66 0.057
67
P ESP024 Esophagitis 63 0.057
68
c MSC005 Muscular Dystrophy 62 0.057
69
P HYP055 Hypoplastic Left Heart Syndrome 62 0.057
70
c MYP004 Myopathy 62 0.057
71
GLD001 Goldenhar Syndrome 61 0.057
72
c DYS154 Dystonia 59 0.057
73
P RNL028 Renal Tubular Dysgenesis 58 0.057
74
P DBT005 Diabetes Insipidus 57 0.057
75
ESP020 Esophageal Atresia 57 0.057
76
KLN001 Klinefelter's Syndrome 52 0.057
77
END072 Endotheliitis 50 0.057
78
TRN007 Transsexualism 49 0.057
79
PRV004 Periventricular Leukomalacia 46 0.057
80
PNT005 Pentalogy of Cantrell 34 0.057
81
LKM006 Leukomalacia 33 0.057
82
P NRF002 Neurofibromatosis 93 0.053
83
c CNG006 Congenital Hypothyroidism 69 0.053
84
P BCK002 Beckwith-Wiedemann Syndrome 67 0.053
85
DMN002 Dementia 66 0.053
86
P ANR007 Anorexia Nervosa 66 0.053
87
P PRM019 Premature Ovarian Failure 66 0.053
88
PLM033 Pulmonary Embolism 64 0.053
89
ART005 Arteriovenous Malformation 62 0.053
90
CTN014 Cutaneous Mastocytosis 61 0.053
91
PTH002 Pathological Gambling 60 0.053
92
CND002 Conduct Disorder 59 0.053
93
BLM002 Bulimia Nervosa 58 0.053
94
ALC007 Alcohol Dependence 58 0.053
95
SMT015 Smith Magenis Syndrome 56 0.053
96
c LYM026 Lymphoblastic Leukemia 54 0.053
97
THR013 Thoracic Outlet Syndrome 52 0.053
98
c WLM002 Wilms Tumor 51 0.053
99
HYP009 Hypertrophic Pyloric Stenosis 49 0.053
100
TRN044 Transposition of the Great Arteries 49 0.053
101
RFR003 Refractive Error 48 0.053
102
SCR024 Sacrococcygeal Teratoma 46 0.053
103
PLC005 Placental Insufficiency 43 0.053
104
PRT086 Partial Hydatidiform Mole 40 0.053
105
PLY024 Polymicrogyria 39 0.053
106
CLC011 Cloacal Exstrophy 35 0.053
107
SYN053 Syndromic Diarrhea 32 0.053
108
JJN004 Jejunal Atresia 26 0.053
109
P RHM011 Rheumatoid Arthritis 93 0.048
110
P ATX002 Ataxia Telangiectasia 86 0.048
111
P SYS001 Systemic Lupus Erythematosus 85 0.048
112
P SCH015 Schizophrenia 82 0.048
113
AND002 Androgen Insensitivity Syndrome 80 0.048
114
PRC016 Pre-Eclampsia 74 0.048
115
P ANG001 Angelman Syndrome 70 0.048
116
ACN002 Acanthosis Nigricans 69 0.048
117
c AXN002 Axenfeld-Rieger Syndrome 66 0.048
118
ECL001 Eclampsia 64 0.048
119
c NTR004 Neutropenia 64 0.048
120
P HLP001 Holoprosencephaly 64 0.048
121
ART019 Aortic Valve Stenosis 64 0.048
122
P DRM007 Dermatitis Herpetiformis 64 0.048
123
GST033 Gestational Diabetes 62 0.048
124
ALP008 Alopecia 56 0.048
125
MGR001 Migraine Without Aura 55 0.048
126
ATT002 Attention Deficit Hyperactivity Disorder 54 0.048
127
HLL004 Hellp Syndrome 54 0.048
128
c CRN015 Cornelia De Lange Syndrome 52 0.048
129
PSD009 Pseudohermaphroditism 50 0.048
130
PLC007 Placental Abruption 50 0.048
131
MTS001 Mutism 48 0.048
132
CHN005 Choanal Atresia 47 0.048
133
BRX001 Bruxism 46 0.048
134
LMB062 Limb Ischemia 44 0.048
135
AST006 Astigmatism 42 0.048
136
c MYP006 Myopia 40 0.048
137
EST005 Esotropia 40 0.048
138
SPS057 Spasticity 37 0.048
139
PHC006 Phacomatosis Pigmentovascularis 30 0.048
140
P BRS047 Breast Cancer 100 0.043
141
P ALZ001 Alzheimer's Disease 97 0.043
142
CYS001 Cystic Fibrosis 96 0.043
143
P MYC007 Myocardial Infarction 92 0.043
144
TBR010 Tuberculosis 83 0.043
145
P PRM021 Primary Pulmonary Hypertension 82 0.043
146
P NRL016 Neural Tube Defects 77 0.043
147
PTZ001 Peutz-Jeghers Syndrome 76 0.043
148
P BPL003 Bipolar Disorder 75 0.043
149
ANK002 Ankylosing Spondylitis 74 0.043
150
PRT036 Peritonitis 71 0.043
151
P NRB001 Neuroblastoma 70 0.043
152
MYS005 Myositis 66 0.043
153
P FNC001 Fanconi's Anemia 65 0.043
154
c HPT021 Hepatitis 64 0.043
155
P GRV001 Graves' Disease 64 0.043
156
PSR002 Psoriasis 63 0.043
157
c HYP076 Hyperthyroidism 62 0.043
158
DFC004 Deficiency Anemia 62 0.043
159
ART031 Aortic Coarctation 62 0.043
160
P GTR002 Goiter 62 0.043
161
P GLC007 Glaucoma 60 0.043
162
P ATS007 Autism Spectrum Disorder 59 0.043
163
MYC002 Mycobacterium Avium Complex Disease 58 0.043
164
c ATX004 Ataxia 58 0.043
165
ANR004 Anuria 57 0.043
166
EPD016 Epidermolysis Bullosa 56 0.043
167
DDN006 Duodenitis 56 0.043
168
MCR103 Microtia 55 0.043
169
P CRV043 Cervical Dystonia 55 0.043
170
ART001 Arterial Tortuosity Syndrome 54 0.043
171
END020 Endocardial Fibroelastosis 53 0.043
172
AND003 Andersen-Tawil Syndrome 53 0.043
173
P ALC004 Alcohol Abuse 51 0.043
174
GND002 Gender Identity Disorder 51 0.043
175
ACR012 Aicardi Syndrome 50 0.043
176
ECT006 Ectodermal Dysplasia 49 0.043
177
PRN038 Prune Belly Syndrome 49 0.043
178
PRG060 Pregnancy Loss 47 0.043
179
P MGR003 Migraine with Aura 46 0.043
180
DYS018 Dysostosis 45 0.043
181
c ART084 Arteriovenous Fistula 45 0.043
182
ANR040 Aneurysm 44 0.043
183
P ATX010 Ataxia Neuropathy Spectrum 41 0.043
184
PLM074 Pulmonary Function 34 0.043
185
CDL002 Caudal Duplication 31 0.043
186
CLN022 Colonic Atresia 28 0.043
187
TFT003 Tufting Enteropathy 28 0.043
188
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.043
189
ANS004 Anisometropia 27 0.043
190
IRN002 Iron Metabolism Disease 26 0.043
191
P HYP078 Hypertrophy of Breast 25 0.043
192
SLP010 Slipped Capital Femoral Epiphysis 24 0.043
193
EPG004 Epignathus 23 0.043
194
IMG001 Image Syndrome 23 0.043
195
ART007 Aorta Atresia 22 0.043
196
c BNG076 Benign Exophthalmos Syndrome 22 0.043
197
AND005 Androgen Insensitivity Syndrome, Mild 21 0.043
198
PHC005 Phacomatosis Pigmentokeratotica 14 0.043
199
JMC001 Jamaican Vomiting Sickness 11 0.043
200
MCC001 Mccune Albright Syndrome 76 0.037
201
P CLC005 Celiac Disease 74 0.037
202
c NNN003 Noonan Syndrome 73 0.037
203
KWS002 Kawasaki Disease 73 0.037
204
c THL005 Thalassemia 72 0.037
205
BRN024 Bronchitis 69 0.037
206
ATH003 Atherosclerosis 68 0.037
207
ANX002 Anxiety Disorder 68 0.037
208
c HMP007 Hemophilia 67 0.037
209
c NPH012 Nephrotic Syndrome 66 0.037
210
OVR029 Ovarian Hyperstimulation Syndrome 66 0.037
211
P TRN020 Turner Syndrome 66 0.037
212
ANR002 Aniridia 65 0.037
213
c SCL016 Scleroderma 64 0.037
214
CLB001 Coloboma 64 0.037
215
P MLN008 Melanoma 63 0.037
216
P HST010 Histiocytosis 62 0.037
217
VGN023 Vaginitis 62 0.037
218
CDL003 Caudal Regression Syndrome 62 0.037
219
ARC007 Arachnoid Cysts 61 0.037
220
DGN001 Degenerative Disc Disease 61 0.037
221
c AGM001 Agammaglobulinemia 60 0.037
222
CLF001 Cleft Lip 59 0.037
223
c CNG015 Congenital Diaphragmatic Hernia 58 0.037
224
P ADN016 Adenocarcinoma 58 0.037
225
URN010 Urinary Tract Obstruction 57 0.037
226
P NPH009 Nephrolithiasis 57 0.037
227
P DND001 Dandy-Walker Syndrome 57 0.037
228
c CTR002 Cataract 57 0.037
229
LNG024 Langerhans-Cell Histiocytosis 56 0.037
230
P PLY006 Polydactyly 56 0.037
231
PPL021 Papilledema 56 0.037
232
c CTS001 Cutis Laxa 55 0.037
233
P HYP040 Hypospadias 55 0.037
234
c VNT002 Ventricular Septal Defect 54 0.037
235
c SYN005 Synostosis 54 0.037
236
VND002 Van Der Woude Syndrome 54 0.037
237
P JVN003 Juvenile Xanthogranuloma 53 0.037
238
BLN003 Blindness 52 0.037
239
c NNT009 Neonatal Diabetes Mellitus 52 0.037
240
c SPN183 Spontaneous Pneumothorax 52 0.037
241
c HMP006 Hemiplegic Migraine 51 0.037
242
ARR001 Arrhythmogenic Right Ventricular Dysplasia 50 0.037
243
P MJR001 Major Depressive Disorder 50 0.037
244
CHN016 Cohen Syndrome 50 0.037
245
PNM008 Pneumothorax 49 0.037
246
c CNG018 Congenital Heart Block 49 0.037
247
MCN017 Meconium Ileus 49 0.037
248
TRC040 Tracheoesophageal Fistula 48 0.037
249
SBS004 Substance Dependence 48 0.037
250
PRP016 Paraplegia 47 0.037
251
SVR005 Severe Pre-Eclampsia 47 0.037
252
GYN001 Gynecomastia 46 0.037
253
ARC002 Arachnoiditis 45 0.037
254
c FTL001 Fetal Alcohol Syndrome 45 0.037
255
ILS001 Ileus 44 0.037
256
TYP015 Type 2b Von Willebrand Disease 40 0.037
257
CNN001 Cannabis Dependence 38 0.037
258
TTH002 Tooth Agenesis 37 0.037
259
CNN002 Cannabis Abuse 37 0.037
260
OCC011 Occipital Encephalocele 29 0.037
261
CYT004 Cytomegalic Inclusion Disease 26 0.037
262
BRW006 Brown Syndrome 22 0.037
263
FRM001 Freemartinism 15 0.037
264
GST058 Gestational Diabetes Insipidus 13 0.037
265
P AMY001 Amyotrophic Lateral Sclerosis 98 0.030
266
P PRK002 Parkinson's Disease 92 0.030
267
P AST005 Asthma 88 0.030
268
P TYS001 Tay-Sachs Disease 82 0.030
269
VNH001 Von Hippel-Lindau Disease 80 0.030
270
HPT023 Hepatocellular Carcinoma 79 0.030
271
P MYS003 Myasthenia Gravis 78 0.030
272
P MNN012 Meningioma 78 0.030
273
ADR007 Adrenoleukodystrophy 77 0.030
274
P MDL005 Medulloblastoma 77 0.030
275
P HMP004 Hemophilia B 77 0.030
276
CRZ001 Crouzon Syndrome 77 0.030
277
P PNM007 Pneumonia 76 0.030
278
P HYP035 Hypophosphatasia 75 0.030
279
P OST002 Osteoporosis 75 0.030
280
TTR001 Tetralogy of Fallot 74 0.030
281
BLM001 Bloom Syndrome 74 0.030
282
CRH001 Crohn's Disease 74 0.030
283
DCH001 Duchenne Muscular Dystrophy 74 0.030
284
c OST005 Osteogenesis Imperfecta 72 0.030
285
PRG004 Progeria 72 0.030
286
HYP458 Hyper Ige Syndrome 71 0.030
287
P SDD001 Sudden Infant Death Syndrome 71 0.030
288
SPS077 Sepsis 70 0.030
289
c THR014 Thrombocytopenia 70 0.030
290
VSC007 Vascular Disease 70 0.030
291
P HMN010 Hemangioma 70 0.030
292
c CRN037 Craniosynostosis 70 0.030
293
NPH007 Nephrogenic Diabetes Insipidus 70 0.030
294
P END044 Endometriosis 69 0.030
295
VNW001 Von Willebrand's Disease 69 0.030
296
P GLM007 Glomerulonephritis 68 0.030
297
DNY001 Denys-Drash Syndrome 68 0.030
298
c MNN013 Meningitis 68 0.030
299
GSG001 Gas Gangrene 67 0.030
300
P PLY011 Polycystic Ovary Syndrome 66 0.030
301
P HRP006 Herpes Simplex 66 0.030
302
P ATM003 Autoimmune Thyroiditis 65 0.030
303
c UVT001 Uveitis 65 0.030
304
c MYT002 Myotonic Dystrophy 65 0.030
305
P RHN004 Rhinitis 65 0.030
306
PRP030 Purpura 64 0.030
307
P RCK004 Rickets 64 0.030
308
P SLV001 Silver-Russell Syndrome 64 0.030
309
P ATP001 Atopic Dermatitis 64 0.030
310
HMH002 Hemihypertrophy 64 0.030
311
ADN018 Adenoma 64 0.030
312
LPM004 Lipoma 64 0.030
313
P CNG042 Congenital Central Hypoventilation Syndrome 64 0.030
314
CHR066 Chronic Fatigue Syndrome 64 0.030
315
P PNC025 Panic Disorder 63 0.030
316
HYP056 Hypoglycemia 63 0.030
317
c KDN018 Kidney Disease 62 0.030
318
P RBL001 Rubella 62 0.030
319
MYL020 Myelomeningocele 61 0.030
320
GNR017 Generalized Pustular Psoriasis 61 0.030
321
P SCH018 Schizencephaly 61 0.030
322
NRP001 Neuropathy 61 0.030
323
P EXD001 Exudative Vitreoretinopathy 61 0.030
324
ACQ007 Acquired Immunodeficiency Syndrome 61 0.030
325
SCL003 Social Phobia 60 0.030
326
ELL001 Ellis-Van Creveld Syndrome 60 0.030
327
P HYP080 Hypogonadism 59 0.030
328
ANT011 Antisocial Personality Disorder 59 0.030
329
c GLY013 Glycogen Storage Disease 59 0.030
330
SCB001 Scabies 59 0.030
331
P ALP006 Alpha Thalassemia 58 0.030
332
HDC001 Headache 58 0.030
333
GNR004 Generalized Anxiety Disorder 58 0.030
334
c CNG124 Congenital Rubella 57 0.030
335
c TRC011 Treacher Collins Syndrome 57 0.030
336
P PRT008 Proteus Syndrome 57 0.030
337
c FML023 Familial Hemiplegic Migraine 57 0.030
338
CHR001 Churg-Strauss Syndrome 57 0.030
339
ANK001 Ankylosis 57 0.030
340
KRT006 Keratoconjunctivitis 56 0.030
341
P HYP014 Hyperuricemia 56 0.030
342
c PRM011 Primary Ciliary Dyskinesia 56 0.030
343
P KLL001 Kallmann Syndrome 55 0.030
344
P FTL009 Fetal Akinesia Deformation Sequence 55 0.030
345
c KBK001 Kabuki Syndrome 55 0.030
346
ANR018 Anorchia 55 0.030
347
RTN017 Retinal Detachment 55 0.030
348
c BRG001 Brugada Syndrome 55 0.030
349
SCH012 Schizoaffective Disorder 54 0.030
350
WLL001 Williams-Beuren Syndrome 54 0.030
351
c SPN016 Spondylocostal Dysostosis 53 0.030
352
P KLP003 Klippel-Feil Syndrome 53 0.030
353
STS002 Situs Inversus 53 0.030
354
c ACR001 Aicardi-Goutieres Syndrome 53 0.030
355
SPR004 Supravalvular Aortic Stenosis 53 0.030
356
TRP014 Triploidy 52 0.030
357
HMP005 Hemiplegia 52 0.030
358
CLR003 Clear Cell Adenocarcinoma 52 0.030
359
P LDD002 Liddle Syndrome 52 0.030
360
c CNT048 Central Hypoventilation Syndrome 52 0.030
361
c MYL014 Myeloproliferative Disorder 52 0.030
362
GRW007 Growth Hormone Deficiency 52 0.030
363
FRZ001 Frozen Shoulder 51 0.030
364
P STR020 Strabismus 51 0.030
365
IMP004 Impetigo 51 0.030
366
c FBR031 Febrile Seizures 51 0.030
367
HMG005 Hemoglobinopathy 51 0.030
368
SBC001 Subacute Sclerosing Panencephalitis 51 0.030
369
HTR003 Heterotaxy 51 0.030
370
c DRR001 Diarrhea 51 0.030
371
APP001 Apparent Mineralocorticoid Excess Syndrome 51 0.030
372
MLK003 Melkersson-Rosenthal Syndrome 50 0.030
373
c NPH005 Nephronophthisis 50 0.030
374
c VSC005 Vesicoureteral Reflux 50 0.030
375
CLS010 Cluster Headache 50 0.030
376
c EPS003 Episodic Ataxia 49 0.030
377
TLN003 Telangiectasis 49 0.030
378
HRM002 Hermaphroditism 49 0.030
379
CNV002 Conversion Disorder 49 0.030
380
DRG003 Drug Dependence 49 0.030
381
P BCL006 B-Cell Lymphomas 49 0.030
382
PRS062 Persistent Hyperplastic Primary Vitreous 48 0.030
383
PLC001 Placenta Accreta 48 0.030
384
RFL001 Reflex Sympathetic Dystrophy 48 0.030
385
P HML001 Hemolytic-Uremic Syndrome 48 0.030
386
c PRN026 Porencephaly 47 0.030
387
CNN003 Conn's Syndrome 47 0.030
388
c RNL078 Renal Dysplasia 47 0.030
389
KLN002 Kleine-Levin Syndrome 47 0.030
390
MYS001 Myositis Ossificans 47 0.030
391
BRD004 Borderline Personality Disorder 47 0.030
392
PTY003 Pityriasis Rubra Pilaris 46 0.030
393
DDN011 Duodenal Atresia 46 0.030
394
EVN001 Evans' Syndrome 46 0.030
395
c TRN032 Transient Neonatal Diabetes Mellitus 46 0.030
396
P INF037 Inflammatory Bowel Disease 45 0.030
397
KRT012 Keratoderma 45 0.030
398
P EPS020 Episodic Ataxia Type 1 45 0.030
399
c SBC007 Subacute Thyroiditis 45 0.030
400
MYC033 Myoclonus 45 0.030
401
APR001 Apraxia 44 0.030
402
P FCS001 Facioscapulohumeral Muscular Dystrophy 44 0.030
403
TRN012 Transient Global Amnesia 43 0.030
404
NRN002 Neuronitis 43 0.030
405
DXT001 Dextrocardia 43 0.030
406
c LFT003 Left Ventricular Noncompaction 43 0.030
407
NNT019 Neonatal Hypothyroidism 42 0.030
408
LMB052 Lumbar Disc Herniation 42 0.030
409
PHC013 Phaeochromocytoma 42 0.030
410
IRT001 Iritis 42 0.030
411
FRY002 Fryns Syndrome 42 0.030
412
P PRV002 Periventricular Nodular Heterotopia 42 0.030
413
CRN088 Craniorachischisis 40 0.030
414
P MNN007 Meningocele 40 0.030
415
SPL040 Split Hand 40 0.030
416
NNT012 Neonatal Jaundice 39 0.030
417
TRC010 Trichotillomania 39 0.030
418
MSC006 Muscle Glycogenosis 39 0.030
419
KBG001 Kbg Syndrome 38 0.030
420
BLP004 Blepharophimosis 37 0.030
421
EMN001 Emanuel Syndrome 36 0.030
422
RTR008 Root Resorption 36 0.030
423
PRN019 Perinatal Necrotizing Enterocolitis 35 0.030
424
ADS002 Adie Syndrome 35 0.030
425
P MLT015 Multiple Intestinal Atresia 34 0.030
426
TRD003 Taurodontism 34 0.030
427
CRV025 Cervical Incompetence 34 0.030
428
ABL001 Ablepharon Macrostomia Syndrome 34 0.030
429
LKM059 Leukemia, Megakaryoblastic, with or Without Down Syndrome, Somatic 34 0.030
430
GLC004 Galactokinase Deficiency 31 0.030
431
P INF069 Infantile Neuroaxonal Dystrophy 1 31 0.030
432
CHL109 Childhood Apraxia of Speech 31 0.030
433
PNS012 Paine Syndrome 30 0.030
434
BLN010 Balanitis 29 0.030
435
MYF001 Myofibroma 29 0.030
436
HYP362 Hyperopia 28 0.030
437
c HYP543 Hypoplastic Left Heart Syndrome 1 28 0.030
438
P SCH009 Scheuermann's Disease 28 0.030
439
RGH009 Right Atrial Isomerism 28 0.030
440
HNM002 Hinman Syndrome 27 0.030
441
PSL001 Pasli Disease 27 0.030
442
NRC003 Narcissistic Personality Disorder 27 0.030
443
FXF001 Fox Fordyce Disease 26 0.030
444
NNT018 Neonatal Herpes 26 0.030
445
PRS030 Persistent Fetal Circulation Syndrome 25 0.030
446
MTG002 Mutagen Sensitivity 24 0.030
447
PL2001 Pla2g6-Associated Neurodegeneration 24 0.030
448
BLN002 Balanitis Xerotica Obliterans 23 0.030
449
FXC001 Foix Chavany Marie Syndrome 23 0.030
450
IMP001 Impetigo Herpetiformis 23 0.030
451
CLC002 Calcaneonavicular Coalition 20 0.030
452
ART109 Arterial Thoracic Outlet Syndrome 18 0.030
453
WLS002 Wilson-Mikity Syndrome 17 0.030
454
TWN005 Twenty-Nail Dystrophy 17 0.030
455
OMP002 Omphalocele Exstrophy Imperforate Anus 16 0.030
456
CYS021 Cystic Adenomatoid Malformation of Lung 16 0.030
457
LMB009 Lambdoid Synostosis 14 0.030
458
TRG006 Trigger Thumb 13 0.030
459
HLC002 Holoacardius Amorphus 13 0.030
460
FBL005 Fibular Aplasia 12 0.030
461
SYM006 Symmetrical Thalamic Calcifications 11 0.030
462
TRG003 Trigeminal Nerve Disease 11 0.030
463
P TYP008 Type 1 Diabetes Mellitus 93 0.022
464
P ACT019 Acute Myeloid Leukemia 92 0.022
465
MTC003 Metachromatic Leukodystrophy 86 0.022
466
P TBR001 Tuberous Sclerosis 85 0.022
467
CDS001 Cadasil 84 0.022
468
INF030 Infectious Mononucleosis 84 0.022
469
CRN211 Coronary Artery Disease 84 0.022
470
P MLT019 Multiple Myeloma 82 0.022
471
P SMT004 Smith-Lemli-Opitz Syndrome 82 0.022
472
P RTT002 Rett Syndrome 82 0.022
473
FBR012 Fabry Disease 81 0.022
474
P RTN024 Retinoblastoma 81 0.022
475
P NMN002 Niemann-Pick Disease 81 0.022
476
P RTN008 Retinitis Pigmentosa 80 0.022
477
SVR004 Severe Combined Immunodeficiency 80 0.022
478
P ALG002 Alagille Syndrome 80 0.022
479
OLV001 Olivopontocerebellar Atrophy 79 0.022
480
P HMC003 Hemochromatosis 78 0.022
481
P WSK001 Wiskott-Aldrich Syndrome 78 0.022
482
P CLN016 Colon Cancer 78 0.022
483
ACH004 Achondroplasia 78 0.022
484
CLD001 Cleidocranial Dysplasia 77 0.022
485
INC002 Inclusion Body Myositis 77 0.022
486
P LPR003 Leprosy 77 0.022
487
P GCH001 Gaucher's Disease 77 0.022
488
P OST012 Osteoarthritis 75 0.022
489
P ALX003 Alexander Disease 73 0.022
490
21H001 21-Hydroxylase Deficiency 73 0.022
491
P CLR023 Colorectal Cancer 73 0.022
492
P FRG001 Fragile X Syndrome 73 0.022
493
HST011 Histoplasmosis 73 0.022
494
c ESS002 Essential Hypertension 72 0.022
495
c MYL006 Myeloid Leukemia 72 0.022
496
ASP006 Aspergillosis 72 0.022
497
P PRM006 Primary Biliary Cirrhosis 72 0.022
498
P MYL005 Myelofibrosis 72 0.022
499
P NRC002 Narcolepsy 71 0.022
500
BLS001 Blau Syndrome 71 0.022
501
ATS001 Autistic Disorder 71 0.022
502
P PND002 Pendred Syndrome 70 0.022
503
P CHR071 Charcot-Marie-Tooth Disease 70 0.022
504
P EPD002 Epidermolytic Hyperkeratosis 70 0.022
505
ART016 Aortic Aneurysm 70 0.022
506
P PRP001 Propionic Acidemia 70 0.022
507
MLT021 Multiple System Atrophy 70 0.022
508
TNG002 Tangier Disease 70 0.022
509
c XRD001 Xeroderma Pigmentosum 70 0.022
510
c PNC044 Pancreatitis 69 0.022
511
P JVN004 Juvenile Myelomonocytic Leukemia 69 0.022
512
P LVR013 Liver Disease 69 0.022
513
P RTH001 Rothmund-Thomson Syndrome 68 0.022
514
c SRC013 Sarcoidosis 68 0.022
515
P ADD001 Addison's Disease 68 0.022
516
SCR008 Scrub Typhus 68 0.022
517
P DRM010 Dermatomyositis 68 0.022
518
P INF038 Influenza 68 0.022
519
KLP002 Klippel-Trenaunay Syndrome 67 0.022
520
ALP001 Alopecia Universalis 67 0.022
521
DSM004 Desmoid Tumor 67 0.022
522
PSD007 Pseudomyxoma Peritonei 67 0.022
523
CHR452 Chorea-Acanthocytosis 67 0.022
524
P AMY004 Amyloidosis 67 0.022
525
P DGR001 Digeorge Syndrome 67 0.022
526
ALL008 Allergic Bronchopulmonary Aspergillosis 66 0.022
527
P SYS004 Systemic Mastocytosis 66 0.022
528
P BLD042 Bladder Carcinoma 66 0.022
529
P PRD008 Periodontitis 66 0.022
530
P CRN008 Carney Complex 66 0.022
531
VSC011 Vasculitis 66 0.022
532
P GT001 Gout 65 0.022
533
c JVN010 Juvenile Rheumatoid Arthritis 65 0.022
534
HYP004 Hypercalcemia 65 0.022
535
VRG001 Variegate Porphyria 65 0.022
536
ANT006 Antiphospholipid Syndrome 65 0.022
537
STT001 Status Epilepticus 65 0.022
538
c ENC004 Encephalitis 65 0.022
539
CMP005 Campomelic Dysplasia 65 0.022
540
P BRN019 Bernard-Soulier Syndrome 64 0.022
541
c LNG028 Long Qt Syndrome 64 0.022
542
GST034 Gastroesophageal Reflux Disease 64 0.022
543
P ALP009 Alopecia Areata 64 0.022
544
MLG056 Malignant Hyperthermia 64 0.022
545
CST001 Costello Syndrome 64 0.022
546
P SHR002 Short Stature 64 0.022
547
P HRD057 Hereditary Pancreatitis 64 0.022
548
CRB039 Cerebrovascular Disease 64 0.022
549
THR079 Thromboembolism 64 0.022
550
ALL003 Allergic Rhinitis 64 0.022
551
P OLG002 Oligodendroglioma 64 0.022
552
c CHR129 Charcot-Marie-Tooth Disease Type 1a 64 0.022
553
FLT001 Felty's Syndrome 63 0.022
554
ULC004 Ulcerative Colitis 63 0.022
555
ARS001 Aarskog-Scott Syndrome 63 0.022
556
PRL009 Prolactinoma 63 0.022
557
P HMP002 Hemophagocytic Lymphohistiocytosis 63 0.022
558
c MCP010 Mucopolysaccharidosis 63 0.022
559
P CNJ013 Conjunctivitis 63 0.022
560
FCT003 Factor X Deficiency 63 0.022
561
CRY002 Cryptorchidism 63 0.022
562
c MLG069 Malignant Hypertension 63 0.022
563
MXD005 Mixed Connective Tissue Disease 63 0.022
564
P VTL001 Vitelliform Macular Dystrophy 63 0.022
565
c HYP061 Hypertrophic Cardiomyopathy 63 0.022
566
MNK003 Muenke Syndrome 63 0.022
567
STF001 Stiff-Person Syndrome 63 0.022
568
PTT006 Pituitary Adenoma 63 0.022
569
EPD006 Epidermolysis Bullosa Acquisita 63 0.022
570
P VLC001 Velocardiofacial Syndrome 63 0.022
571
LYM009 Lymphocytic Choriomeningitis 63 0.022
572
CYS005 Cysticercosis 63 0.022
573
P STM004 Stomach Cancer 63 0.022
574
CMM004 Common Variable Immunodeficiency 63 0.022
575
c CCK001 Cockayne Syndrome 63 0.022
576
LRN003 Learning Disability 62 0.022
577
RHM001 Rheumatic Fever 62 0.022
578
P KRT004 Keratitis 62 0.022
579
DSS009 Disseminated Intravascular Coagulation 62 0.022
580
BLR001 Biliary Atresia 62 0.022
581
c TMP001 Temporal Lobe Epilepsy 62 0.022
582
HYP013 Hypohidrotic Ectodermal Dysplasia 62 0.022
583
P FML001 Familial Atrial Fibrillation 62 0.022
584
P HRD011 Hereditary Spherocytosis 62 0.022
585
P ESN007 Eosinophilia 61 0.022
586
c PRP029 Porphyria 61 0.022
587
LWY001 Lewy Body Dementia 61 0.022
588
KRN002 Kearns-Sayre Syndrome 61 0.022
589
PRT037 Pertussis 61 0.022
590
HV1006 Hiv-1 61 0.022
591
P CND004 Candidiasis 61 0.022
592
c PLY014 Polycystic Kidney Disease 61 0.022
593
c HRD010 Hereditary Spastic Paraplegia 61 0.022
594
c MYL007 Myeloma 61 0.022
595
BCK001 Becker Muscular Dystrophy 61 0.022
596
c HYP050 Hyperinsulinemic Hypoglycemia 60 0.022
597
BLL003 Bell's Palsy 60 0.022
598
P DDN001 Duodenal Ulcer 60 0.022
599
PLM001 Pulmonary Tuberculosis 60 0.022
600
PMP001 Pemphigus 60 0.022
601
PSY004 Psychotic Disorder 60 0.022
602
P PLY019 Polyneuropathy 60 0.022
603
VGT001 Vogt-Koyanagi-Harada Disease 60 0.022
604
EYD002 Eye Disease 60 0.022
605
P FRS003 Fraser Syndrome 60 0.022
606
RBR001 Roberts Syndrome 60 0.022
607
ART111 Artery Disease 60 0.022
608
ALP004 Alport Syndrome 60 0.022
609
CHL068 Cholestasis 60 0.022
610
PRS047 Prostatitis 60 0.022
611
P SYR001 Syringomyelia 60 0.022
612
c GNG009 Gangliosidosis 60 0.022
613
P JNC001 Junctional Epidermolysis Bullosa 59 0.022
614
WGR001 Wagr Syndrome 59 0.022
615
P ATY010 Atypical Hemolytic-Uremic Syndrome 59 0.022
616
SPN020 Spondylosis 59 0.022
617
CHR074 Choriocarcinoma 59 0.022
618
c MLT074 Multiple Endocrine Neoplasia 59 0.022
619
MGC001 Megacolon 59 0.022
620
FBR032 Fibromuscular Dysplasia 59 0.022
621
P CNG046 Congenital Fiber-Type Disproportion 59 0.022
622
c DMN001 Diamond-Blackfan Anemia 59 0.022
623
P IDP010 Idiopathic Generalized Epilepsy 59 0.022
624
VSC002 Vascular Dementia 59 0.022
625
P HLL001 Hallermann-Streiff Syndrome 59 0.022
626
c LCL006 Localized Scleroderma 59 0.022
627
P PRM030 Permanent Neonatal Diabetes Mellitus 59 0.022
628
OST014 Osteopoikilosis 58 0.022
629
CVR006 Cavernous Hemangioma 58 0.022
630
TST014 Testicular Cancer 58 0.022
631
c TYR004 Tyrosinemia 58 0.022
632
P ALT001 Alternating Hemiplegia of Childhood 58 0.022
633
ACR003 Acrodermatitis Enteropathica 58 0.022
634
c THR005 Thrombotic Thrombocytopenic Purpura 58 0.022
635
CHR063 Chronic Mucocutaneous Candidiasis 58 0.022
636
PLC003 Placental Site Trophoblastic Tumor 58 0.022
637
c OCL002 Oculocutaneous Albinism 58 0.022
638
NPH021 Nephropathic Cystinosis 58 0.022
639
FMR011 Fumarate Hydratase Deficiency 58 0.022
640
P FND001 Fundus Albipunctatus 58 0.022
641
OST017 Osteomyelitis 58 0.022
642
FLL008 Folliculitis 58 0.022
643
P PPL020 Papillary Thyroid Carcinoma 58 0.022
644
CNN005 Connective Tissue Disease 58 0.022
645
PRC012 Pericardial Effusion 58 0.022
646
NTH001 Netherton Syndrome 58 0.022
647
GLC003 Glucose Intolerance 58 0.022
648
AMN001 Amenorrhea 57 0.022
649
P SYP003 Syphilis 57 0.022
650
c JBR001 Joubert Syndrome 57 0.022
651
P EPD009 Epidermolysis Bullosa Dystrophica 57 0.022
652
LST001 Listeriosis 57 0.022
653
PRT039 Proteinuria 57 0.022
654
PRN023 Prion Disease 57 0.022
655
MRG003 Marginal Zone B-Cell Lymphoma 57 0.022
656
P MYC008 Myocarditis 57 0.022
657
HYP266 Hypoxia 57 0.022
658
MGL001 Megaloblastic Anemia 57 0.022
659
GRW001 Growth Hormone Secreting Pituitary Adenoma 57 0.022
660
P RNL007 Renal Tubular Acidosis 57 0.022
661
P INT030 Intracranial Aneurysm 57 0.022
662
c THR003 Thoracic Aortic Aneurysm 57 0.022
663
c ANG015 Angioedema 57 0.022
664
ETN001 Eating Disorder 57 0.022
665
LDP002 Lead Poisoning 56 0.022
666
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 56 0.022
667
P MYM002 Moyamoya Disease 56 0.022
668
c HRD002 Hereditary Angioedema 56 0.022
669
P WVR001 Weaver Syndrome 56 0.022
670
c LSS002 Lissencephaly 56 0.022
671
P CMP008 Compartment Syndrome 56 0.022
672
CNG048 Congenital Hepatic Fibrosis 56 0.022
673
c SPN049 Spinocerebellar Ataxia 56 0.022
674
P HRD021 Hereditary Sensory Neuropathy 56 0.022
675
P PRM052 Primary Progressive Aphasia 55 0.022
676
WLM001 Wolman Disease 55 0.022
677
P PRM100 Primary Spontaneous Pneumothorax 55 0.022
678
TLP001 Talipes Equinovarus 55 0.022
679
TYP011 Typhus 55 0.022
680
MVL001 Mevalonic Aciduria 55 0.022
681
PRT011 Protein C Deficiency 55 0.022
682
TTH006 Tooth Disease 55 0.022
683
P PMP005 Pemphigus Vulgaris 55 0.022
684
P PSR001 Psoriatic Arthritis 55 0.022
685
ACR005 Acrodermatitis 55 0.022
686
VNS009 Venous Thrombosis 55 0.022
687
PSD002 Pseudotumor Cerebri 55 0.022
688
CCT002 Cicatricial Pemphigoid 55 0.022
689
CHR008 Choroiditis 55 0.022
690
c BRC006 Brachydactyly 55 0.022
691
RST001 Restless Legs Syndrome 55 0.022
692
LPM005 Lipomatosis 54 0.022
693
PRM003 Premature Ejaculation 54 0.022
694
MTN003 Motion Sickness 54 0.022
695
NPH051 Nephritis 54 0.022
696
NPH011 Nephroblastoma 54 0.022
697
CHL069 Cholesteatoma 54 0.022
698
MLT006 Multidrug-Resistant Tuberculosis 54 0.022
699
PRM013 Premature Menopause 54 0.022
700
P INT064 Intermediate Uveitis 54 0.022
701
WRN002 Wernicke-Korsakoff Syndrome 54 0.022
702
P PYL005 Pyelonephritis 54 0.022
703
EPD037 Epidermal Nevus 54 0.022
704
BRS081 Breast Cancer Susceptibility 54 0.022
705
ASP001 Asperger Syndrome 53 0.022
706
c HRM001 Hermansky-Pudlak Syndrome 53 0.022
707
LPT001 Leptospirosis 53 0.022
708
MYX004 Myxedema 53 0.022
709
P MSC003 Muscular Atrophy 53 0.022
710
CNT047 Contact Dermatitis 53 0.022
711
P SJG002 Sjogren-Larsson Syndrome 53 0.022
712
P ALP014 Alpha-Thalassemia/mental Retardation Syndrome 53 0.022
713
GST045 Gastroenteritis 53 0.022
714
P RBN002 Robinow Syndrome 53 0.022
715
PRN011 Pernicious Anemia 53 0.022
716
c INT001 Intrahepatic Cholestasis 52 0.022
717
PRV006 Pervasive Developmental Disorder 52 0.022
718
P CNT005 Central Nervous System Lymphoma 52 0.022
719
HMG002 Hemoglobinuria 52 0.022
720
CNG064 Congenital Chloride Diarrhea 52 0.022
721
LKD001 Leukodystrophy 52 0.022
722
XLN068 X-Linked Thrombocytopenia 52 0.022
723
MYM001 Myoma 52 0.022
724
OST011 Osteomalacia 52 0.022
725
ATP002 Atopy 52 0.022
726
GRN007 Granuloma Annulare 52 0.022
727
BLL001 Baller-Gerold Syndrome 52 0.022
728
P CYS010 Cystinosis 52 0.022
729
c MCL001 Mucolipidosis 52 0.022
730
ESN005 Eosinophilic Gastroenteritis 52 0.022
731
NRN008 Neuronal Intranuclear Inclusion Disease 52 0.022
732
MMB002 Membranous Glomerulonephritis 51 0.022
733
c TYR003 Tyrosinemia Type Ii 51 0.022
734
c ERL020 Early-Onset Schizophrenia 51 0.022
735
ACS001 Acoustic Neuroma 51 0.022
736
c KRT007 Keratoconus 51 0.022
737
OST019 Osteosclerosis 51 0.022
738
c FML024 Familial Melanoma 51 0.022
739
ISL003 Isolated Growth Hormone Deficiency 51 0.022
740
NRG002 Neurogenic Bladder 51 0.022
741
c MCK006 Meckel Syndrome 51 0.022
742
P CYS018 Cystitis 51 0.022
743
ALX002 Alexithymia 51 0.022
744
P LYD001 Leydig Cell Tumor 50 0.022
745
PRT019 Protein-Losing Enteropathy 50 0.022
746
RSC001 Rosacea 50 0.022
747
RHB017 Rhabdoid Tumor 50 0.022
748
CCN002 Cocaine Abuse 50 0.022
749
c OPT004 Optic Atrophy 50 0.022
750
FBR009 Fibrous Dysplasia 50 0.022
751
c STC001 Stickler Syndrome 50 0.022
752
c CRB126 Cerebral Cavernous Malformation 50 0.022
753
P INT063 Intellectual Disability 50 0.022
754
c PRM001 Primary Cutaneous Amyloidosis 50 0.022
755
SCT005 Scott Syndrome 50 0.022
756
SPN019 Spondylolisthesis 50 0.022
757
HYP068 Hyperostosis 50 0.022
758
FCL041 Focal Myositis 50 0.022
759
c MSB002 Mesoblastic Nephroma 50 0.022
760
OCL020 Ocular Cicatricial Pemphigoid 49 0.022
761
ASP002 Aspartylglucosaminuria 49 0.022
762
CTS002 Cat-Scratch Disease 49 0.022
763
c EMR001 Emery-Dreifuss Muscular Dystrophy 49 0.022
764
P HYP027 Hypobetalipoproteinemia 49 0.022
765
DBW001 Dubowitz Syndrome 49 0.022
766
AGR002 Agoraphobia 49 0.022
767
c INT099 Intrahepatic Cholestasis of Pregnancy 49 0.022
768
HYP043 Hyperandrogenism 49 0.022
769
c PSD003 Pseudohypoaldosteronism 49 0.022
770
DSC009 Discoid Lupus Erythematosus 49 0.022
771
NRX001 Neuroaxonal Dystrophy 49 0.022
772
ALB002 Albinism 49 0.022
773
P GRM009 Germ Cell Tumors 49 0.022
774
DFF021 Diffuse Mesangial Sclerosis 48 0.022
775
DNT012 Dental Caries 48 0.022
776
ACN014 Acanthocytosis 48 0.022
777
c CNG029 Congenital Mesoblastic Nephroma 48 0.022
778
NPH003 Nephrocalcinosis 48 0.022
779
P BLD034 Bile Duct Carcinoma 48 0.022
780
MNN021 Meningococcemia 48 0.022
781
P PNC001 Pancytopenia 48 0.022
782
NSP002 Nasopharyngitis 48 0.022
783
P GRS008 Griscelli Syndrome Type 2 47 0.022
784
c CHR098 Chronic Pyelonephritis 47 0.022
785
PPL018 Papillary Adenocarcinoma 47 0.022
786
NNT016 Neonatal Hemochromatosis 47 0.022
787
PRT082 Preterm Premature Rupture of the Membranes 47 0.022
788
P OVR046 Ovarian Cyst 47 0.022
789
c MLG086 Malignant Hyperthermia Susceptibility 47 0.022
790
NRM004 Neuroma 47 0.022
791
VRN004 Vernal Keratoconjunctivitis 47 0.022
792
PRS012 Pars Planitis 46 0.022
793
HYP120 Hypoaldosteronism 46 0.022
794
LCH009 Lichen Sclerosus 46 0.022
795
DRM011 Dermatophytosis 46 0.022
796
NDL021 Nodular Lymphocyte Predominant Hodgkin Lymphoma 46 0.022
797
MCR037 Macroglossia 46 0.022
798
c AML002 Amelogenesis Imperfecta 46 0.022
799
PLM070 Pulmonic Stenosis 46 0.022
800
KWS001 Kwashiorkor 46 0.022
801
MNN017 Mononeuropathy 45 0.022
802
PNH001 Panhypopituitarism 45 0.022
803
EPL002 Epilepsy Syndrome 45 0.022
804
PLG004 Plagiocephaly 45 0.022
805
PLM035 Pulmonary Eosinophilia 45 0.022
806
SHR003 Short-Chain Acyl-Coa Dehydrogenase Deficiency 45 0.022
807
ART004 Aortic Atherosclerosis 45 0.022
808
c BRC013 Brachydactyly Type E 45 0.022
809
DLS001 Delusional Disorder 45 0.022
810
MGL013 Megalencephaly 45 0.022
811
CMP034 Complete Androgen Insensitivity Syndrome 45 0.022
812
SPS007 Spastic Cerebral Palsy 45 0.022
813
P FNG005 Feingold Syndrome 45 0.022
814
UNL007 Unilateral Renal Agenesis 44 0.022
815
FTL007 Fetal Hydantoin Syndrome 44 0.022
816
HRS011 Horseshoe Kidney 44 0.022
817
ART035 Arterial Calcification of Infancy 44 0.022
818
c TRC005 Tracheal Stenosis 44 0.022
819
c APH002 Aphasia 44 0.022
820
P STC005 Stickler Syndrome Type 1 44 0.022
821
MRC003 Mercury Poisoning 44 0.022
822
CHR078 Chorioretinitis 44 0.022
823
SYN036 Syncope 44 0.022
824
P SDR003 Sideroblastic Anemia 44 0.022
825
RNL029 Renal Coloboma Syndrome 43 0.022
826
QDR001 Quadriplegia 43 0.022
827
c SNR001 Senior-Loken Syndrome 43 0.022
828
c INF049 Infantile Myofibromatosis 43 0.022
829
NVS001 Neovascular Glaucoma 43 0.022
830
LND001 Landau-Kleffner Syndrome 43 0.022
831
PRR010 Pierre Robin Sequence 43 0.022
832
NCR002 Necrobiosis Lipoidica 43 0.022
833
c PTR004 Pterygium 43 0.022
834
c CND005 Cone Dystrophy 43 0.022
835
CNG024 Congenital Nystagmus 43 0.022
836
MTB004 Metabolic Acidosis 43 0.022
837
CND006 Candida Glabrata 43 0.022
838
CHN015 Chondrodysplasia 43 0.022
839
OLG001 Oligospermia 43 0.022
840
P D2H001 D-2-Hydroxyglutaric Aciduria 43 0.022
841
OPP004 Oppositional Defiant Disorder 43 0.022
842
EPS026 Epispadias 42 0.022
843
GND001 Gonadoblastoma 42 0.022
844
PCH002 Pachygyria 42 0.022
845
c CHR104 Chorea 42 0.022
846
TBL013 Tubulointerstitial Nephritis and Uveitis 42 0.022
847
c ACQ027 Acquired Cutis Laxa 42 0.022
848
P FBR025 Fibrochondrogenesis 42 0.022
849
c ACH011 Achondrogenesis 42 0.022
850
MGC004 Megacystis Microcolon Intestinal Hypoperistalsis Syndrome 42 0.022
851
P SPR035 Superior Vena Cava Syndrome 42 0.022
852
OVR006 Ovarian Endometriosis 41 0.022
853
c CHR342 Chiari Malformation 41 0.022
854
LWT001 Low Tension Glaucoma 41 0.022
855
MCL007 Macular Dystrophy 41 0.022
856
c TRS004 Torsion Dystonia 41 0.022
857
ANN005 Annular Pancreas 41 0.022
858
HMT018 Hematopoietic Stem Cell Transplantation 40 0.022
859
c TRC004 Trichorhinophalangeal Syndrome Type I 40 0.022
860
GST052 Gestational Choriocarcinoma 40 0.022
861
CRD053 Cardiovascular Disease Risk Factor 40 0.022
862
c CNG033 Congenital Syphilis 40 0.022
863
c PNT019 Pontocerebellar Hypoplasia 40 0.022
864
OHT001 Ohtahara Syndrome 40 0.022
865
CD4003 Cd40 Ligand Deficiency 40 0.022
866
P END046 Endometritis 40 0.022
867
SHR044 Short Rib-Polydactyly Syndrome 40 0.022
868
SCH008 Schmid Metaphyseal Chondrodysplasia 39 0.022
869
HYP064 Hypogonadotropism 39 0.022
870
c TRN047 Transient Congenital Hypothyroidism 39 0.022
871
CRB028 Cerebellar Medulloblastoma 39 0.022
872
SPR034 Superior Limbic Keratoconjunctivitis 39 0.022
873
ENT007 Enteropathica 39 0.022
874
TRN030 Transient Erythroblastopenia of Childhood 39 0.022
875
NRG004 Neurogenic Diabetes Insipidus 39 0.022
876
AND001 Anodontia 39 0.022
877
GRM004 Germinoma 39 0.022
878
TBR006 Tuberculoid Leprosy 39 0.022
879
c NRC009 Narcolepsy 1 39 0.022
880
GST064 Gastric Outlet Obstruction 39 0.022
881
SML028 Semilobar Holoprosencephaly 39 0.022
882
c GRS003 Griscelli Syndrome 39 0.022
883
c PRG001 Progressive Muscular Atrophy 38 0.022
884
c RNG018 Ring Chromosome 22 38 0.022
885
BCK006 Back Pain 38 0.022
886
MHC001 Mhc Class Ii Deficiency 38 0.022
887
RNL025 Renal Hypoplasia 38 0.022
888
SPL039 Split Foot 38 0.022
889
LYM097 Lymphatic Malformation 38 0.022
890
SCH011 Schizotypal Personality Disorder 38 0.022
891
VCL001 Vacuolar Myopathy 38 0.022
892
NNM005 Non-Immune Hydrops Fetalis 37 0.022
893
OLM001 Olmsted Syndrome 37 0.022
894
LYM095 Lymphangiomatosis 37 0.022
895
IPX001 Ipex Syndrome 37 0.022
896
BLN001 Blount's Disease 36 0.022
897
CMB021 Combined Pituitary Hormone Deficiency 36 0.022
898
c CNG115 Congenital Myotonic Dystrophy 36 0.022
899
PTC005 Pituicytoma 36 0.022
900
RTN006 Retinal Drusen 36 0.022
901
C3D001 C3 Deficiency 36 0.022
902
PRS054 Persistent Truncus Arteriosus 36 0.022
903
RNL012 Renal Tuberculosis 36 0.022
904
CVR010 Cavernous Malformation 36 0.022
905
P DYS005 Dyslexia 35 0.022
906
c PPL025 Popliteal Pterygium Syndrome 35 0.022
907
SPS004 Spastic Quadriplegia 35 0.022
908
P MLD013 Mild Hemophilia a 35 0.022
909
DYS012 Dyshidrosis 34 0.022
910
IMM039 Immune Hydrops Fetalis 34 0.022
911
SHK001 Shaken Baby Syndrome 34 0.022
912
DFF001 Diffuse Cutaneous Mastocytosis 34 0.022
913
SPR007 Superior Mesenteric Artery Syndrome 34 0.022
914
EXS013 Exstrophy-Epispadias Complex 33 0.022
915
c GM1001 Gm1 Gangliosidosis Type 1 33 0.022
916
PRM129 Primary Cutaneous Marginal Zone B-Cell Lymphoma 33 0.022
917
c CRB059 Cerebellar Degeneration 33 0.022
918
HYP461 Hypocomplementemic Urticarial Vasculitis Syndrome 33 0.022
919
THL009 Thiolase Deficiency 33 0.022
920
c ACH010 Achondrogenesis Type Ii 33 0.022
921
SPN029 Spondylolysis 32 0.022
922
PHT008 Photosensitive Epilepsy 32 0.022
923
FCL003 Facial Hemiatrophy 32 0.022
924
SBP004 Subependymoma 32 0.022
925
BDY001 Body Dysmorphic Disorder 32 0.022
926
LTM002 Luteoma 32 0.022
927
SPR012 Separation Anxiety Disorder 32 0.022
928
PRS108 Persistent Polyclonal B-Cell Lymphocytosis 32 0.022
929
c ENL009 Enlarged Parietal Foramina 32 0.022
930
c MNS008 Monosomy 21 31 0.022
931
SPN221 Spina Bifida Occulta 31 0.022
932
NRW001 Norwegian Scabies 31 0.022
933
c PRM032 Primary Congenital Glaucoma 31 0.022
934
c MTR002 Mitral Valve Insufficiency 31 0.022
935
WRT003 Warthin Tumor 30 0.022
936
RTT001 Ritter's Disease 30 0.022
937
P PTT002 Potter's Syndrome 30 0.022
938
P BRS089 Breast and Colorectal Cancer 30 0.022
939
DVL001 Developmental Coordination Disorder 29 0.022
940
ATR003 Atrophic Rhinitis 29 0.022
941
c HMG001 Hemoglobin C Disease 29 0.022
942
PLM058 Pulmonary Atresia with Intact Ventricular Septum 29 0.022
943
P PLM064 Pulmonary Sequestration 29 0.022
944
SMT001 Somatization Disorder 29 0.022
945
ANG004 Angioid Streaks 28 0.022
946
NNT021 Neonatal Meningitis 28 0.022
947
LMB014 Limb-Body Wall Complex 28 0.022
948
GST007 Gastric Dilatation 28 0.022
949
SYS006 Say Syndrome 28 0.022
950
DDN009 Duodenal Obstruction 28 0.022
951
IVC001 Ivic Syndrome 28 0.022
952
BLD052 Blood Group Incompatibility 28 0.022
953
P HYP163 Hyperlipidemia Type 3 27 0.022
954
LCH003 Lichen Nitidus 27 0.022
955
AMY005 Amyloid Neuropathy 27 0.022
956
CRN051 Craniofacial Microsomia 27 0.022
957
ARM003 Aromatic Amino Acid Decarboxylase Deficiency 27 0.022
958
XNT009 Xanthoma Disseminatum 27 0.022
959
RGH006 Right Aortic Arch 26 0.022
960
ACC003 Accommodative Esotropia 26 0.022
961
TRC035 Tracheal Agenesis 26 0.022
962
OCL044 Oculo-Auriculo-Vertebral Spectrum 26 0.022
963
MCR039 Macrophagic Myofasciitis 25 0.022
964
c JVN020 Juvenile-Onset Dystonia 25 0.022
965
PNS015 Penoscrotal Transposition 25 0.022
966
P CNG370 Congenital Tracheal Stenosis 25 0.022
967
3HY001 3-Hydroxyisobutyric Aciduria 24 0.022
968
PLN001 Plantar Wart 24 0.022
969
ART034 Aortopulmonary Window 24 0.022
970
CLC003 Cloacogenic Carcinoma 24 0.022
971
INT011 Interstitial Emphysema 24 0.022
972
FTS001 Fetishism 24 0.022
973
SLT009 Solitary Bone Cyst 24 0.022
974
AVD001 Avoidant Personality Disorder 23 0.022
975
c NNT042 Neonatal Lupus Erythematosus 23 0.022
976
TLH001 Tel Hashomer Camptodactyly Syndrome 23 0.022
977
TCL012 T-Cell/histiocyte Rich Large B Cell Lymphoma 23 0.022
978
P HYD015 Hydroa Vacciniforme 23 0.022
979
c SPR036 Supernumerary Nipples 22 0.022
980
PRR001 Periarthritis 22 0.022
981
MRG006 Morgagni-Stewart-Morel Syndrome 21 0.022
982
PRD003 Periodontosis 21 0.022
983
SPS087 Spasmus Nutans 21 0.022
984
MYL044 Myelocystocele 20 0.022
985
c NNT006 Neonatal Myasthenia Gravis 20 0.022
986
LBY003 Labyrinthine Disease 20 0.022
987
DCR002 Dacryocystocele 20 0.022
988
BRN097 Brainstem Auditory Evoked Responses 20 0.022
989
HCS001 Hec Syndrome 19 0.022
990
RTN019 Retinal Telangiectasia 19 0.022
991
SCH025 Schisis Association 19 0.022
992
CNG329 Congenital Onychodysplasia 19 0.022
993
RTN127 Retinal Cavernous Hemangioma 19 0.022
994
HYP015 Hyperlucent Lung 19 0.022
995
CLR033 Color Vision Deficiency 19 0.022
996
MTR027 Mitral Atresia 19 0.022
997
RDT006 Radiation Induced Meningioma 19 0.022
998
c MLG039 Malignant Essential Hypertension 18 0.022
999
MSL004 Mesial Temporal Lobe Epilepsy with Hippocampal Sclerosis 18 0.022
1000
PTN004 Patent Ductus Venosus 18 0.022
1001
c CNG129 Congenital Torticollis 18 0.022
1002
CLP002 Colpocephaly 17 0.022
1003
HYP018 Hyperglobulinemic Purpura 17 0.022
1004
c PTR018 Paternal Uniparental Disomy of Chromosome 6 17 0.022
1005
C6D001 C6 Deficiency 16 0.022
1006
TBR007 Tuberculum Sellae Meningioma 16 0.022
1007
ELC001 Elective Mutism 16 0.022
1008
JVN026 Jeavons Syndrome 15 0.022
1009
PLM108 Pulmonary Interstitial Glycogenosis 15 0.022
1010
FBL006 Fibular Aplasia Ectrodactyly 15 0.022
1011
AQG002 Aquagenic Urticaria 15 0.022
1012
OLG008 Oligomeganephronic Renal Hypoplasia 14 0.022
1013
MCR033 Macrocephaly-Capillary Malformation 14 0.022
1014
VLF002 Velo-Facial-Skeletal Syndrome 13 0.022
1015
KZL001 Kozlowski Brown Hardwick Syndrome 13 0.022
1016
HMF003 Hemifacial Myohyperplasia 13 0.022
1017
LCH012 Lichstenstein Syndrome 12 0.022
1018
FSD001 Fused Mandibular Incisors 12 0.022
1019
HYD031 Hydroxyprolinemia 12 0.022
1020
c RNG014 Ring Chromosome 19 12 0.022
1021
KCH001 Kocher-Debre-Semelaigne Syndrome 12 0.022
1022
RHH001 Rohhad 12 0.022
1023
FNG010 Fingerprint Body Myopathy 11 0.022
1024
MCH006 Mechanical Strabismus 11 0.022
1025
CRB080 Cor Biloculare 10 0.022
1026
CNG125 Congenital Short Femur 10 0.022
1027
DDY001 Didymosis Aplasticosebacea 10 0.022
1028
FTZ005 Fitzsimmons-Guilbert Syndrome 8 0.022
1029
2MT002 2-Methylacetoacetyl Coa Thiolase Deficiency 8 0.022
1030
OBS014 Obsessive-Compulsive Disorder, Protection Against 6 0.022