Search results for "twinning"

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

1056 hits were found for 'twinning'

# Family MCID Name MIFTS Score
1
P TWN001 Twin-to-Twin Transfusion Syndrome 55 11.299
2
c TWN006 Twin Twin Transfusion Syndrome 30 8.384
3
c RNL090 Renal Tubular Dysgenesis Due to Twin-Twin Transfusion 6 5.077
4
PLY012 Polyhydramnios 54 0.162
5
ANN002 Anencephaly 59 0.151
6
c PLY018 Polycythemia 59 0.148
7
CRB009 Cerebritis 39 0.146
8
P CRV039 Cervicitis 58 0.115
9
HYD012 Hydrops Fetalis 62 0.111
10
OLG003 Oligohydramnios 60 0.109
11
P OBS005 Obesity 91 0.098
12
P HYP075 Hypertension 87 0.095
13
P RTN012 Retinopathy of Prematurity 57 0.091
14
ACR022 Acardia 15 0.091
15
P CNG401 Congenital Heart Disease 69 0.085
16
c THY032 Thyroiditis 66 0.085
17
DWN001 Down Syndrome 62 0.083
18
CHR005 Chorioamnionitis 50 0.083
19
CYT008 Cytomegalovirus Infection 44 0.083
20
P MGR002 Migraine 70 0.080
21
NCT002 Nicotine Dependence 49 0.080
22
CNG069 Congenital Cytomegalovirus 36 0.080
23
SRN002 Sirenomelia 23 0.080
24
c INT060 Intestinal Atresia 49 0.077
25
URT039 Urticaria 64 0.074
26
P LKM002 Leukemia 77 0.071
27
c DBT009 Diabetes Mellitus 74 0.071
28
c HYP086 Hypothyroidism 69 0.071
29
PYL006 Pyloric Stenosis 50 0.071
30
RNL002 Renal Agenesis 70 0.067
31
ISC004 Ischemia 63 0.067
32
P ENC008 Encephalocele 54 0.067
33
P OMP004 Omphalocele 52 0.067
34
URT008 Urticaria Pigmentosa 47 0.067
35
ENC005 Encephalomalacia 34 0.067
36
AMN009 Amniotic Band Syndrome 27 0.067
37
c TXP001 Toxoplasmosis 66 0.064
38
P INS005 Insulin Resistance 65 0.064
39
c THN001 Thanatophoric Dysplasia 62 0.064
40
VCT001 Vacterl Association 62 0.064
41
P PRS038 Personality Disorder 59 0.064
42
PST041 Posterior Urethral Valves 56 0.064
43
URT001 Urethritis 55 0.064
44
P GND004 Gonadal Dysgenesis 51 0.064
45
HYP009 Hypertrophic Pyloric Stenosis 50 0.064
46
ECT026 Ectopic Pregnancy 46 0.064
47
c LPS004 Lupus Erythematosus 77 0.060
48
P RBN001 Rubinstein-Taybi Syndrome 76 0.060
49
c PLM037 Pulmonary Hypertension 73 0.060
50
DRM006 Dermatitis 66 0.060
51
CRB037 Cerebral Palsy 65 0.060
52
GLD001 Goldenhar Syndrome 62 0.060
53
c TRT010 Teratoma 59 0.060
54
c HYP065 Hyperaldosteronism 58 0.060
55
P CNG021 Congenital Toxoplasmosis 57 0.060
56
RTN023 Retinitis 54 0.060
57
MNT147 Mental Retardation 52 0.060
58
P APL006 Aplasia Cutis Congenita 50 0.060
59
IMP002 Imperforate Anus 48 0.060
60
PLC005 Placental Insufficiency 44 0.060
61
c BPL002 Bipolar I Disorder 39 0.060
62
HYD001 Hydranencephaly 39 0.060
63
P MLT020 Multiple Sclerosis 85 0.056
64
P ART022 Arthritis 75 0.056
65
P MST009 Mastocytosis 75 0.056
66
P BCK002 Beckwith-Wiedemann Syndrome 68 0.056
67
SPN038 Spina Bifida 68 0.056
68
GST009 Gastroschisis 66 0.056
69
P PRM019 Premature Ovarian Failure 66 0.056
70
c CNG006 Congenital Hypothyroidism 64 0.056
71
P ESP024 Esophagitis 64 0.056
72
c HYP055 Hypoplastic Left Heart Syndrome 63 0.056
73
c MSC005 Muscular Dystrophy 62 0.056
74
P MYP004 Myopathy 62 0.056
75
c DYS154 Dystonia 61 0.056
76
CND002 Conduct Disorder 59 0.056
77
P RNL028 Renal Tubular Dysgenesis 59 0.056
78
P DBT005 Diabetes Insipidus 58 0.056
79
KLN001 Klinefelter's Syndrome 56 0.056
80
END072 Endotheliitis 51 0.056
81
TRN007 Transsexualism 50 0.056
82
PRV004 Periventricular Leukomalacia 46 0.056
83
PNT005 Pentalogy of Cantrell 36 0.056
84
LKM006 Leukomalacia 33 0.056
85
P NRF002 Neurofibromatosis 94 0.052
86
P OST009 Osteochondritis Dissecans 67 0.052
87
P ANR007 Anorexia Nervosa 66 0.052
88
PLM033 Pulmonary Embolism 66 0.052
89
P WLM002 Wilms Tumor 66 0.052
90
ART005 Arteriovenous Malformation 63 0.052
91
GST033 Gestational Diabetes 63 0.052
92
P ACT101 Acute Lymphoblastic Leukemia 63 0.052
93
PTH002 Pathological Gambling 60 0.052
94
ALC007 Alcohol Dependence 59 0.052
95
BLM002 Bulimia Nervosa 59 0.052
96
SMT015 Smith Magenis Syndrome 57 0.052
97
ESP020 Esophageal Atresia 57 0.052
98
c LYM026 Lymphoblastic Leukemia 57 0.052
99
CTN014 Cutaneous Mastocytosis 53 0.052
100
THR013 Thoracic Outlet Syndrome 52 0.052
101
TRN044 Transposition of the Great Arteries 49 0.052
102
RFR003 Refractive Error 48 0.052
103
SCR024 Sacrococcygeal Teratoma 47 0.052
104
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 42 0.052
105
PRT086 Partial Hydatidiform Mole 39 0.052
106
SYN053 Syndromic Diarrhea 34 0.052
107
PLY024 Polymicrogyria 34 0.052
108
CLC011 Cloacal Exstrophy 34 0.052
109
JJN004 Jejunal Atresia 26 0.052
110
P RHM011 Rheumatoid Arthritis 94 0.048
111
P SYS001 Systemic Lupus Erythematosus 88 0.048
112
P ATX002 Ataxia Telangiectasia 87 0.048
113
P SCH015 Schizophrenia 82 0.048
114
AND002 Androgen Insensitivity Syndrome 80 0.048
115
P PRC016 Pre-Eclampsia 78 0.048
116
ATT002 Attention Deficit Hyperactivity Disorder 75 0.048
117
P NRB001 Neuroblastoma 70 0.048
118
P ANG001 Angelman Syndrome 70 0.048
119
P MYS005 Myositis 70 0.048
120
NRL016 Neural Tube Defects 68 0.048
121
c AXN002 Axenfeld-Rieger Syndrome 67 0.048
122
DMN002 Dementia 67 0.048
123
P DRM007 Dermatitis Herpetiformis 65 0.048
124
c ECL001 Eclampsia 64 0.048
125
ART019 Aortic Valve Stenosis 64 0.048
126
c HLP001 Holoprosencephaly 64 0.048
127
c NTR004 Neutropenia 64 0.048
128
ACN002 Acanthosis Nigricans 63 0.048
129
VNS009 Venous Thrombosis 60 0.048
130
EPD016 Epidermolysis Bullosa 58 0.048
131
ALP008 Alopecia 57 0.048
132
MGR001 Migraine Without Aura 55 0.048
133
HLL004 Hellp Syndrome 54 0.048
134
c CRN015 Cornelia De Lange Syndrome 53 0.048
135
P ALC004 Alcohol Abuse 52 0.048
136
PSD009 Pseudohermaphroditism 51 0.048
137
PLC007 Placental Abruption 51 0.048
138
ECT006 Ectodermal Dysplasia 49 0.048
139
MTS001 Mutism 49 0.048
140
BRX001 Bruxism 46 0.048
141
LMB062 Limb Ischemia 46 0.048
142
ANR040 Aneurysm 46 0.048
143
EST005 Esotropia 43 0.048
144
AST006 Astigmatism 42 0.048
145
c MYP006 Myopia 41 0.048
146
SPS057 Spasticity 38 0.048
147
PHC006 Phacomatosis Pigmentovascularis 30 0.048
148
P ALZ001 Alzheimer's Disease 100 0.043
149
CYS001 Cystic Fibrosis 97 0.043
150
P MYC007 Myocardial Infarction 93 0.043
151
TBR010 Tuberculosis 87 0.043
152
P BRS047 Breast Cancer 86 0.043
153
PTZ001 Peutz-Jeghers Syndrome 78 0.043
154
P BPL003 Bipolar Disorder 77 0.043
155
ANK002 Ankylosing Spondylitis 77 0.043
156
P PRM021 Primary Pulmonary Hypertension 77 0.043
157
PRT036 Peritonitis 72 0.043
158
P FNC001 Fanconi's Anemia 67 0.043
159
c SCL016 Scleroderma 65 0.043
160
c HPT021 Hepatitis 64 0.043
161
c HYP076 Hyperthyroidism 64 0.043
162
PSR002 Psoriasis 63 0.043
163
DFC004 Deficiency Anemia 63 0.043
164
ANR002 Aniridia 62 0.043
165
P GTR002 Goiter 62 0.043
166
ART031 Aortic Coarctation 62 0.043
167
P ATS007 Autism Spectrum Disorder 59 0.043
168
MYC002 Mycobacterium Avium Complex Disease 59 0.043
169
ANR004 Anuria 59 0.043
170
c ATX004 Ataxia 59 0.043
171
DDN006 Duodenitis 56 0.043
172
MCR103 Microtia 56 0.043
173
P CRV043 Cervical Dystonia 55 0.043
174
ART001 Arterial Tortuosity Syndrome 55 0.043
175
AND003 Andersen-Tawil Syndrome 54 0.043
176
END020 Endocardial Fibroelastosis 54 0.043
177
GND002 Gender Identity Disorder 51 0.043
178
ACR012 Aicardi Syndrome 51 0.043
179
P GRV001 Graves' Disease 51 0.043
180
P MJR001 Major Depressive Disorder 50 0.043
181
PRN038 Prune Belly Syndrome 49 0.043
182
CHN005 Choanal Atresia 48 0.043
183
P MGR003 Migraine with Aura 48 0.043
184
PRG060 Pregnancy Loss 48 0.043
185
P ART084 Arteriovenous Fistula 47 0.043
186
DYS018 Dysostosis 46 0.043
187
ARS002 Arsacs 44 0.043
188
P ATX010 Ataxia Neuropathy Spectrum 43 0.043
189
IMG001 Image Syndrome 37 0.043
190
PLM074 Pulmonary Function 34 0.043
191
CDL002 Caudal Duplication 31 0.043
192
TFT003 Tufting Enteropathy 28 0.043
193
CLN022 Colonic Atresia 28 0.043
194
ANS004 Anisometropia 28 0.043
195
IRN002 Iron Metabolism Disease 28 0.043
196
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.043
197
SLP010 Slipped Capital Femoral Epiphysis 25 0.043
198
EPG004 Epignathus 23 0.043
199
ART007 Aorta Atresia 23 0.043
200
c BNG076 Benign Exophthalmos Syndrome 22 0.043
201
AND005 Androgen Insensitivity Syndrome, Mild 21 0.043
202
PHC005 Phacomatosis Pigmentokeratotica 16 0.043
203
JMC001 Jamaican Vomiting Sickness 11 0.043
204
VNH001 Von Hippel-Lindau Disease 81 0.037
205
c NNN003 Noonan Syndrome 80 0.037
206
MCC001 Mccune Albright Syndrome 76 0.037
207
KWS002 Kawasaki Disease 76 0.037
208
c OST005 Osteogenesis Imperfecta 74 0.037
209
P CLC005 Celiac Disease 73 0.037
210
c THL005 Thalassemia 72 0.037
211
c THR014 Thrombocytopenia 71 0.037
212
ATH003 Atherosclerosis 69 0.037
213
ANX002 Anxiety Disorder 69 0.037
214
CLB001 Coloboma 68 0.037
215
c NPH012 Nephrotic Syndrome 67 0.037
216
BRN024 Bronchitis 67 0.037
217
P TRN020 Turner Syndrome 67 0.037
218
OVR029 Ovarian Hyperstimulation Syndrome 67 0.037
219
P MLN008 Melanoma 65 0.037
220
c HMP007 Hemophilia 65 0.037
221
P HST010 Histiocytosis 64 0.037
222
VGN023 Vaginitis 63 0.037
223
ARC007 Arachnoid Cysts 62 0.037
224
DGN001 Degenerative Disc Disease 61 0.037
225
CDL003 Caudal Regression Syndrome 61 0.037
226
CLF001 Cleft Lip 60 0.037
227
EYD002 Eye Disease 59 0.037
228
P ADN016 Adenocarcinoma 59 0.037
229
c CNG015 Congenital Diaphragmatic Hernia 59 0.037
230
P NPH009 Nephrolithiasis 58 0.037
231
URN010 Urinary Tract Obstruction 58 0.037
232
P DND001 Dandy-Walker Syndrome 58 0.037
233
c CTR002 Cataract 57 0.037
234
LNG024 Langerhans-Cell Histiocytosis 57 0.037
235
P PLY006 Polydactyly 57 0.037
236
P HYP040 Hypospadias 55 0.037
237
VND002 Van Der Woude Syndrome 55 0.037
238
c SYN005 Synostosis 54 0.037
239
P VNT002 Ventricular Septal Defect 54 0.037
240
PPL021 Papilledema 54 0.037
241
P JVN003 Juvenile Xanthogranuloma 53 0.037
242
c NNT009 Neonatal Diabetes Mellitus 53 0.037
243
BLN003 Blindness 53 0.037
244
c SPN183 Spontaneous Pneumothorax 52 0.037
245
TRP014 Triploidy 52 0.037
246
c HMP006 Hemiplegic Migraine 51 0.037
247
CHN016 Cohen Syndrome 50 0.037
248
MCN017 Meconium Ileus 50 0.037
249
PNM008 Pneumothorax 50 0.037
250
c SVR005 Severe Pre-Eclampsia 49 0.037
251
c CTS001 Cutis Laxa 49 0.037
252
SBS004 Substance Dependence 48 0.037
253
c CNG018 Congenital Heart Block 48 0.037
254
PRP016 Paraplegia 48 0.037
255
GYN001 Gynecomastia 46 0.037
256
c FTL001 Fetal Alcohol Syndrome 45 0.037
257
ILS001 Ileus 45 0.037
258
ARC002 Arachnoiditis 44 0.037
259
TTH002 Tooth Agenesis 43 0.037
260
P MNN007 Meningocele 41 0.037
261
TYP015 Type 2b Von Willebrand Disease 40 0.037
262
CNN001 Cannabis Dependence 39 0.037
263
CNN002 Cannabis Abuse 37 0.037
264
CYT004 Cytomegalic Inclusion Disease 30 0.037
265
OCC011 Occipital Encephalocele 29 0.037
266
BRW006 Brown Syndrome 22 0.037
267
GST058 Gestational Diabetes Insipidus 14 0.037
268
FRM001 Freemartinism 14 0.037
269
P PRK002 Parkinson's Disease 93 0.030
270
P LVR011 Liver Cancer 91 0.030
271
P AST005 Asthma 89 0.030
272
INC002 Inclusion Body Myositis 86 0.030
273
P TYS001 Tay-Sachs Disease 83 0.030
274
P MDL005 Medulloblastoma 80 0.030
275
ACH004 Achondroplasia 78 0.030
276
ADR007 Adrenoleukodystrophy 78 0.030
277
P HMP004 Hemophilia B 78 0.030
278
P MYS003 Myasthenia Gravis 78 0.030
279
P MNN012 Meningioma 78 0.030
280
P PNM007 Pneumonia 78 0.030
281
CRZ001 Crouzon Syndrome 78 0.030
282
CRH001 Crohn's Disease 76 0.030
283
P OST002 Osteoporosis 76 0.030
284
TTR001 Tetralogy of Fallot 75 0.030
285
DCH001 Duchenne Muscular Dystrophy 75 0.030
286
P ALP006 Alpha Thalassemia 75 0.030
287
P NRC002 Narcolepsy 75 0.030
288
21H001 21-Hydroxylase Deficiency 74 0.030
289
BLM001 Bloom Syndrome 74 0.030
290
SVR004 Severe Combined Immunodeficiency 74 0.030
291
PRG004 Progeria 73 0.030
292
HYP458 Hyper Ige Syndrome 72 0.030
293
VNW001 Von Willebrand's Disease 72 0.030
294
ACQ007 Acquired Immunodeficiency Syndrome 71 0.030
295
P SDD001 Sudden Infant Death Syndrome 71 0.030
296
P HYP035 Hypophosphatasia 71 0.030
297
ART016 Aortic Aneurysm 71 0.030
298
P HMN010 Hemangioma 71 0.030
299
c CRN037 Craniosynostosis 70 0.030
300
VSC007 Vascular Disease 70 0.030
301
NPH007 Nephrogenic Diabetes Insipidus 70 0.030
302
SPS077 Sepsis 70 0.030
303
P END044 Endometriosis 70 0.030
304
P PNC025 Panic Disorder 69 0.030
305
P GLM007 Glomerulonephritis 69 0.030
306
DNY001 Denys-Drash Syndrome 69 0.030
307
P RCK004 Rickets 68 0.030
308
P PLY011 Polycystic Ovary Syndrome 68 0.030
309
c MNN013 Meningitis 68 0.030
310
GSG001 Gas Gangrene 68 0.030
311
P HRP006 Herpes Simplex 68 0.030
312
P ATP001 Atopic Dermatitis 67 0.030
313
P HYP056 Hypoglycemia 67 0.030
314
c AMY001 Amyotrophic Lateral Sclerosis 67 0.030
315
P HRD011 Hereditary Spherocytosis 67 0.030
316
P ATM003 Autoimmune Thyroiditis 67 0.030
317
PRP030 Purpura 66 0.030
318
CHR066 Chronic Fatigue Syndrome 66 0.030
319
c UVT001 Uveitis 66 0.030
320
ADN018 Adenoma 66 0.030
321
P RHN004 Rhinitis 65 0.030
322
P SLV001 Silver-Russell Syndrome 65 0.030
323
P CNG042 Congenital Central Hypoventilation Syndrome 65 0.030
324
LPM004 Lipoma 65 0.030
325
HMH002 Hemihypertrophy 64 0.030
326
HYP013 Hypohidrotic Ectodermal Dysplasia 63 0.030
327
GNR017 Generalized Pustular Psoriasis 63 0.030
328
c INT070 Intestinal Obstruction 63 0.030
329
P RBL001 Rubella 63 0.030
330
c KDN018 Kidney Disease 63 0.030
331
SCL003 Social Phobia 63 0.030
332
MYL020 Myelomeningocele 62 0.030
333
c MYT002 Myotonic Dystrophy 62 0.030
334
TST014 Testicular Cancer 62 0.030
335
NRP001 Neuropathy 62 0.030
336
P SCH018 Schizencephaly 61 0.030
337
SCB001 Scabies 61 0.030
338
P PRT008 Proteus Syndrome 61 0.030
339
c AGM001 Agammaglobulinemia 61 0.030
340
ELL001 Ellis-Van Creveld Syndrome 61 0.030
341
c AMY077 Amyotrophic Lateral Sclerosis Type 18 60 0.030
342
P HYP080 Hypogonadism 60 0.030
343
c GLY013 Glycogen Storage Disease 60 0.030
344
P PRM011 Primary Ciliary Dyskinesia 59 0.030
345
c FML023 Familial Hemiplegic Migraine 59 0.030
346
c LCL006 Localized Scleroderma 59 0.030
347
ANT011 Antisocial Personality Disorder 59 0.030
348
c BRG001 Brugada Syndrome 59 0.030
349
c TRC011 Treacher Collins Syndrome 58 0.030
350
HDC001 Headache 58 0.030
351
P EXD001 Exudative Vitreoretinopathy 58 0.030
352
GNR004 Generalized Anxiety Disorder 58 0.030
353
c CNG124 Congenital Rubella 58 0.030
354
CHR001 Churg-Strauss Syndrome 58 0.030
355
c THR003 Thoracic Aortic Aneurysm 57 0.030
356
ANK001 Ankylosis 57 0.030
357
P BCL006 B-Cell Lymphomas 57 0.030
358
KRT006 Keratoconjunctivitis 57 0.030
359
P KLL001 Kallmann Syndrome 57 0.030
360
c KBK001 Kabuki Syndrome 57 0.030
361
P PRV002 Periventricular Nodular Heterotopia 57 0.030
362
P AMY074 Amyotrophic Lateral Sclerosis Type 14 56 0.030
363
c OCL002 Oculocutaneous Albinism 56 0.030
364
P FTL009 Fetal Akinesia Deformation Sequence 56 0.030
365
RTN017 Retinal Detachment 56 0.030
366
P HYP014 Hyperuricemia 56 0.030
367
ANR018 Anorchia 55 0.030
368
c PFF001 Pfeiffer Syndrome 55 0.030
369
P SPN016 Spondylocostal Dysostosis 55 0.030
370
P KLP003 Klippel-Feil Syndrome 55 0.030
371
c ACR001 Aicardi-Goutieres Syndrome 54 0.030
372
SPR004 Supravalvular Aortic Stenosis 54 0.030
373
SCH012 Schizoaffective Disorder 54 0.030
374
P LDD002 Liddle Syndrome 54 0.030
375
WLL001 Williams-Beuren Syndrome 54 0.030
376
STS002 Situs Inversus 53 0.030
377
HMP005 Hemiplegia 53 0.030
378
CLR003 Clear Cell Adenocarcinoma 53 0.030
379
c CNT048 Central Hypoventilation Syndrome 53 0.030
380
c FBR031 Febrile Seizures 53 0.030
381
RFL001 Reflex Sympathetic Dystrophy 52 0.030
382
GRW007 Growth Hormone Deficiency 52 0.030
383
FRZ001 Frozen Shoulder 52 0.030
384
P NPH005 Nephronophthisis 52 0.030
385
SBC001 Subacute Sclerosing Panencephalitis 52 0.030
386
P STR020 Strabismus 52 0.030
387
c DRR001 Diarrhea 52 0.030
388
HMG005 Hemoglobinopathy 51 0.030
389
APP001 Apparent Mineralocorticoid Excess Syndrome 51 0.030
390
c VSC005 Vesicoureteral Reflux 51 0.030
391
RHB017 Rhabdoid Tumor 51 0.030
392
MLK003 Melkersson-Rosenthal Syndrome 51 0.030
393
c EPS003 Episodic Ataxia 51 0.030
394
CLS010 Cluster Headache 50 0.030
395
DRG003 Drug Dependence 49 0.030
396
TLN003 Telangiectasis 49 0.030
397
IMP004 Impetigo 49 0.030
398
HRM002 Hermaphroditism 49 0.030
399
ALB002 Albinism 49 0.030
400
CNV002 Conversion Disorder 49 0.030
401
PLC001 Placenta Accreta 49 0.030
402
TRC040 Tracheoesophageal Fistula 49 0.030
403
P HML001 Hemolytic-Uremic Syndrome 48 0.030
404
PRT082 Preterm Premature Rupture of the Membranes 48 0.030
405
HTR003 Heterotaxy 48 0.030
406
c PRN026 Porencephaly 48 0.030
407
CNN003 Conn's Syndrome 48 0.030
408
c RNL078 Renal Dysplasia 48 0.030
409
MYS001 Myositis Ossificans 47 0.030
410
KLN002 Kleine-Levin Syndrome 47 0.030
411
BRD004 Borderline Personality Disorder 47 0.030
412
MTG002 Mutagen Sensitivity 47 0.030
413
LCH009 Lichen Sclerosus 47 0.030
414
DDN011 Duodenal Atresia 47 0.030
415
c TRN032 Transient Neonatal Diabetes Mellitus 46 0.030
416
EVN001 Evans' Syndrome 46 0.030
417
KRT012 Keratoderma 46 0.030
418
c SBC007 Subacute Thyroiditis 46 0.030
419
APR001 Apraxia 46 0.030
420
MYC033 Myoclonus 45 0.030
421
P FCS001 Facioscapulohumeral Muscular Dystrophy 45 0.030
422
P EPS020 Episodic Ataxia Type 1 45 0.030
423
NNT012 Neonatal Jaundice 44 0.030
424
TRN012 Transient Global Amnesia 44 0.030
425
NRN002 Neuronitis 44 0.030
426
DXT001 Dextrocardia 43 0.030
427
c LFT003 Left Ventricular Noncompaction 43 0.030
428
LMB052 Lumbar Disc Herniation 43 0.030
429
PHC013 Phaeochromocytoma 43 0.030
430
IRT001 Iritis 43 0.030
431
FRY002 Fryns Syndrome 42 0.030
432
NNT019 Neonatal Hypothyroidism 42 0.030
433
MSC006 Muscle Glycogenosis 41 0.030
434
SPL040 Split Hand 40 0.030
435
CRN088 Craniorachischisis 40 0.030
436
c INF037 Inflammatory Bowel Disease 40 0.030
437
TRC010 Trichotillomania 40 0.030
438
KBG001 Kbg Syndrome 38 0.030
439
BLP004 Blepharophimosis 38 0.030
440
EMN001 Emanuel Syndrome 37 0.030
441
HNG003 Hangover 36 0.030
442
RTR008 Root Resorption 36 0.030
443
PRN019 Perinatal Necrotizing Enterocolitis 36 0.030
444
ADS002 Adie Syndrome 35 0.030
445
TRD003 Taurodontism 35 0.030
446
CRV025 Cervical Incompetence 34 0.030
447
IMM088 Immunodeficiency 36 34 0.030
448
P MLT015 Multiple Intestinal Atresia 34 0.030
449
ABL001 Ablepharon Macrostomia Syndrome 34 0.030
450
GLC004 Galactokinase Deficiency 33 0.030
451
RGH009 Right Atrial Isomerism 33 0.030
452
PRS062 Persistent Hyperplastic Primary Vitreous 32 0.030
453
P HYP543 Hypoplastic Left Heart Syndrome 1 32 0.030
454
P INF069 Infantile Neuroaxonal Dystrophy 1 31 0.030
455
CHL109 Childhood Apraxia of Speech 31 0.030
456
BLN010 Balanitis 29 0.030
457
MYF001 Myofibroma 29 0.030
458
HYP362 Hyperopia 28 0.030
459
HNM002 Hinman Syndrome 28 0.030
460
NRC003 Narcissistic Personality Disorder 27 0.030
461
FXF001 Fox Fordyce Disease 27 0.030
462
P SCH009 Scheuermann's Disease 27 0.030
463
PRS030 Persistent Fetal Circulation Syndrome 26 0.030
464
HYP179 Hypertrichosis Congenital Generalized X-Linked 26 0.030
465
NNT018 Neonatal Herpes 26 0.030
466
c NNT042 Neonatal Lupus Erythematosus 25 0.030
467
PL2001 Pla2g6-Associated Neurodegeneration 25 0.030
468
BLN002 Balanitis Xerotica Obliterans 24 0.030
469
FXC001 Foix Chavany Marie Syndrome 23 0.030
470
IMP001 Impetigo Herpetiformis 23 0.030
471
CLC002 Calcaneonavicular Coalition 20 0.030
472
ART109 Arterial Thoracic Outlet Syndrome 18 0.030
473
WLS002 Wilson-Mikity Syndrome 17 0.030
474
TWN005 Twenty-Nail Dystrophy 17 0.030
475
OMP002 Omphalocele Exstrophy Imperforate Anus 16 0.030
476
CYS021 Cystic Adenomatoid Malformation of Lung 15 0.030
477
LMB009 Lambdoid Synostosis 14 0.030
478
TRG006 Trigger Thumb 14 0.030
479
FBL005 Fibular Aplasia 13 0.030
480
SYM006 Symmetrical Thalamic Calcifications 11 0.030
481
TRG003 Trigeminal Nerve Disease 11 0.030
482
P TYP008 Type 1 Diabetes Mellitus 96 0.021
483
P ACT019 Acute Myeloid Leukemia 93 0.021
484
P MLT019 Multiple Myeloma 88 0.021
485
P RTN008 Retinitis Pigmentosa 86 0.021
486
FBR012 Fabry Disease 86 0.021
487
P TBR001 Tuberous Sclerosis 86 0.021
488
INF030 Infectious Mononucleosis 84 0.021
489
SMT004 Smith-Lemli-Opitz Syndrome 84 0.021
490
CDS001 Cadasil 84 0.021
491
P GCH001 Gaucher's Disease 84 0.021
492
P HMC003 Hemochromatosis 83 0.021
493
P RTT002 Rett Syndrome 83 0.021
494
MTC003 Metachromatic Leukodystrophy 83 0.021
495
P RTN024 Retinoblastoma 82 0.021
496
P ALG002 Alagille Syndrome 81 0.021
497
P NMN002 Niemann-Pick Disease 80 0.021
498
OLV001 Olivopontocerebellar Atrophy 80 0.021
499
P WSK001 Wiskott-Aldrich Syndrome 79 0.021
500
CLD001 Cleidocranial Dysplasia 79 0.021
501
P LPR003 Leprosy 78 0.021
502
P CLR023 Colorectal Cancer 77 0.021
503
P FRG001 Fragile X Syndrome 76 0.021
504
P ALX003 Alexander Disease 76 0.021
505
P OST012 Osteoarthritis 76 0.021
506
c MYL006 Myeloid Leukemia 75 0.021
507
THY028 Thyroid Cancer 75 0.021
508
P MYL005 Myelofibrosis 75 0.021
509
P SRC013 Sarcoidosis 75 0.021
510
BLS001 Blau Syndrome 73 0.021
511
P PRM006 Primary Biliary Cirrhosis 73 0.021
512
HST011 Histoplasmosis 73 0.021
513
ASP006 Aspergillosis 73 0.021
514
c ESS002 Essential Hypertension 73 0.021
515
WLF001 Wolff-Parkinson-White Syndrome 73 0.021
516
ALL003 Allergic Rhinitis 73 0.021
517
P EPD002 Epidermolytic Hyperkeratosis 72 0.021
518
P ADD001 Addison's Disease 72 0.021
519
P CHR071 Charcot-Marie-Tooth Disease 72 0.021
520
P DRM010 Dermatomyositis 71 0.021
521
ATS001 Autistic Disorder 71 0.021
522
P PRP001 Propionic Acidemia 71 0.021
523
TNG002 Tangier Disease 71 0.021
524
MLT021 Multiple System Atrophy 71 0.021
525
P JVN004 Juvenile Myelomonocytic Leukemia 70 0.021
526
P RTH001 Rothmund-Thomson Syndrome 70 0.021
527
P STM004 Stomach Cancer 69 0.021
528
CRB039 Cerebrovascular Disease 69 0.021
529
c PNC044 Pancreatitis 69 0.021
530
KLP002 Klippel-Trenaunay Syndrome 69 0.021
531
P LVR013 Liver Disease 69 0.021
532
DSM004 Desmoid Tumor 69 0.021
533
PSD007 Pseudomyxoma Peritonei 68 0.021
534
P AMY004 Amyloidosis 68 0.021
535
SCR008 Scrub Typhus 68 0.021
536
P SHR002 Short Stature 68 0.021
537
P INF038 Influenza 68 0.021
538
P BLD042 Bladder Carcinoma 68 0.021
539
CMM004 Common Variable Immunodeficiency 67 0.021
540
ALL008 Allergic Bronchopulmonary Aspergillosis 67 0.021
541
P CRN008 Carney Complex 67 0.021
542
P FML001 Familial Atrial Fibrillation 67 0.021
543
P PND002 Pendred Syndrome 67 0.021
544
ALP001 Alopecia Universalis 67 0.021
545
P DGR001 Digeorge Syndrome 67 0.021
546
CHR452 Chorea-Acanthocytosis 67 0.021
547
P PRD008 Periodontitis 67 0.021
548
MLG056 Malignant Hyperthermia 66 0.021
549
MGL001 Megaloblastic Anemia 66 0.021
550
P GT001 Gout 66 0.021
551
ANT006 Antiphospholipid Syndrome 66 0.021
552
VSC011 Vasculitis 66 0.021
553
VRG001 Variegate Porphyria 66 0.021
554
STT001 Status Epilepticus 66 0.021
555
c JVN010 Juvenile Rheumatoid Arthritis 66 0.021
556
P HRD057 Hereditary Pancreatitis 66 0.021
557
GST034 Gastroesophageal Reflux Disease 66 0.021
558
c JBR001 Joubert Syndrome 66 0.021
559
RHM001 Rheumatic Fever 66 0.021
560
c XRD001 Xeroderma Pigmentosum 66 0.021
561
THR079 Thromboembolism 66 0.021
562
c ENC004 Encephalitis 66 0.021
563
CMP005 Campomelic Dysplasia 65 0.021
564
ULC004 Ulcerative Colitis 65 0.021
565
P BRN019 Bernard-Soulier Syndrome 65 0.021
566
c LNG028 Long Qt Syndrome 65 0.021
567
CST001 Costello Syndrome 65 0.021
568
c HYP061 Hypertrophic Cardiomyopathy 65 0.021
569
P CLN016 Colon Cancer 65 0.021
570
P ALP009 Alopecia Areata 65 0.021
571
HYP004 Hypercalcemia 65 0.021
572
P VTL001 Vitelliform Macular Dystrophy 65 0.021
573
ARS001 Aarskog-Scott Syndrome 64 0.021
574
c MCP010 Mucopolysaccharidosis 64 0.021
575
FLT001 Felty's Syndrome 64 0.021
576
CHL014 Cholera 64 0.021
577
c MLG069 Malignant Hypertension 64 0.021
578
MXD005 Mixed Connective Tissue Disease 64 0.021
579
c CCK001 Cockayne Syndrome 64 0.021
580
c CHR129 Charcot-Marie-Tooth Disease Type 1a 64 0.021
581
HV1006 Hiv-1 64 0.021
582
CLT003 Colitis 64 0.021
583
P VLC001 Velocardiofacial Syndrome 64 0.021
584
STF001 Stiff-Person Syndrome 64 0.021
585
FCT003 Factor X Deficiency 64 0.021
586
BLL003 Bell's Palsy 64 0.021
587
P OLG002 Oligodendroglioma 64 0.021
588
CRN018 Coronary Artery Anomaly 63 0.021
589
EPD006 Epidermolysis Bullosa Acquisita 63 0.021
590
LYM009 Lymphocytic Choriomeningitis 63 0.021
591
MNK003 Muenke Syndrome 63 0.021
592
CRY002 Cryptorchidism 63 0.021
593
CYS005 Cysticercosis 63 0.021
594
LRN003 Learning Disability 63 0.021
595
BLR001 Biliary Atresia 63 0.021
596
PRL009 Prolactinoma 63 0.021
597
c PRP029 Porphyria 63 0.021
598
LWY001 Lewy Body Dementia 63 0.021
599
P ESN007 Eosinophilia 63 0.021
600
KRN002 Kearns-Sayre Syndrome 63 0.021
601
PRT037 Pertussis 62 0.021
602
P KRT004 Keratitis 62 0.021
603
RBR001 Roberts Syndrome 62 0.021
604
P ATY010 Atypical Hemolytic-Uremic Syndrome 62 0.021
605
c DMN001 Diamond-Blackfan Anemia 62 0.021
606
P DDN001 Duodenal Ulcer 62 0.021
607
P CNJ013 Conjunctivitis 62 0.021
608
DSS009 Disseminated Intravascular Coagulation 62 0.021
609
c PLY014 Polycystic Kidney Disease 62 0.021
610
PTT006 Pituitary Adenoma 62 0.021
611
P CND004 Candidiasis 62 0.021
612
P PRM030 Permanent Neonatal Diabetes Mellitus 62 0.021
613
GLC003 Glucose Intolerance 62 0.021
614
ART111 Artery Disease 62 0.021
615
c TYR004 Tyrosinemia 62 0.021
616
CHR074 Choriocarcinoma 61 0.021
617
P FRS003 Fraser Syndrome 61 0.021
618
c MYL007 Myeloma 61 0.021
619
c HYP050 Hyperinsulinemic Hypoglycemia 61 0.021
620
PLM001 Pulmonary Tuberculosis 61 0.021
621
BCK001 Becker Muscular Dystrophy 61 0.021
622
c MLT074 Multiple Endocrine Neoplasia 61 0.021
623
c ANG015 Angioedema 61 0.021
624
VGT001 Vogt-Koyanagi-Harada Disease 61 0.021
625
PSY004 Psychotic Disorder 61 0.021
626
MVL001 Mevalonic Aciduria 61 0.021
627
RST001 Restless Legs Syndrome 61 0.021
628
P PLY019 Polyneuropathy 61 0.021
629
ALP004 Alport Syndrome 61 0.021
630
P CNG046 Congenital Fiber-Type Disproportion 60 0.021
631
c GNG009 Gangliosidosis 60 0.021
632
PRS047 Prostatitis 60 0.021
633
c MPL001 Maple Syrup Urine Disease 60 0.021
634
WGR001 Wagr Syndrome 60 0.021
635
c HMP002 Hemophagocytic Lymphohistiocytosis 60 0.021
636
SPN020 Spondylosis 60 0.021
637
PMP001 Pemphigus 60 0.021
638
FMR011 Fumarate Hydratase Deficiency 60 0.021
639
P IDP010 Idiopathic Generalized Epilepsy 60 0.021
640
MGC001 Megacolon 60 0.021
641
P ALT001 Alternating Hemiplegia of Childhood 60 0.021
642
FBR032 Fibromuscular Dysplasia 60 0.021
643
c SYS004 Systemic Mastocytosis 59 0.021
644
MRG003 Marginal Zone B-Cell Lymphoma 59 0.021
645
CVR006 Cavernous Hemangioma 59 0.021
646
AMN001 Amenorrhea 59 0.021
647
ACR003 Acrodermatitis Enteropathica 59 0.021
648
c THR005 Thrombotic Thrombocytopenic Purpura 59 0.021
649
CHL068 Cholestasis 59 0.021
650
P HLL001 Hallermann-Streiff Syndrome 59 0.021
651
GRW001 Growth Hormone Secreting Pituitary Adenoma 59 0.021
652
CHR063 Chronic Mucocutaneous Candidiasis 59 0.021
653
P PPL020 Papillary Thyroid Carcinoma 59 0.021
654
OST014 Osteopoikilosis 59 0.021
655
P NPH021 Nephropathic Cystinosis 59 0.021
656
PLC003 Placental Site Trophoblastic Tumor 59 0.021
657
P FND001 Fundus Albipunctatus 59 0.021
658
TMP001 Temporal Lobe Epilepsy 59 0.021
659
OST017 Osteomyelitis 59 0.021
660
CNN005 Connective Tissue Disease 58 0.021
661
PRC012 Pericardial Effusion 58 0.021
662
NTH001 Netherton Syndrome 58 0.021
663
P MYC008 Myocarditis 58 0.021
664
P SYP003 Syphilis 58 0.021
665
c HRD010 Hereditary Spastic Paraplegia 58 0.021
666
CCT002 Cicatricial Pemphigoid 58 0.021
667
FLL008 Folliculitis 58 0.021
668
ISC006 Ischemic Heart Disease 58 0.021
669
P CYS010 Cystinosis 58 0.021
670
LST001 Listeriosis 58 0.021
671
P MYM002 Moyamoya Disease 58 0.021
672
c HRD002 Hereditary Angioedema 58 0.021
673
P PRM100 Primary Spontaneous Pneumothorax 58 0.021
674
PRT039 Proteinuria 58 0.021
675
HYP266 Hypoxia 58 0.021
676
P PSR001 Psoriatic Arthritis 58 0.021
677
PRN023 Prion Disease 58 0.021
678
P HRD021 Hereditary Sensory Neuropathy 57 0.021
679
WLM001 Wolman Disease 57 0.021
680
c LSS002 Lissencephaly 57 0.021
681
ETN001 Eating Disorder 57 0.021
682
c BRC006 Brachydactyly 57 0.021
683
P WVR001 Weaver Syndrome 57 0.021
684
RNL007 Renal Tubular Acidosis 57 0.021
685
CNG048 Congenital Hepatic Fibrosis 57 0.021
686
LDP002 Lead Poisoning 57 0.021
687
P INT030 Intracranial Aneurysm 56 0.021
688
PRT011 Protein C Deficiency 56 0.021
689
P CMP008 Compartment Syndrome 56 0.021
690
TTH006 Tooth Disease 56 0.021
691
P SYR001 Syringomyelia 56 0.021
692
P CNG052 Congenital Amegakaryocytic Thrombocytopenia 56 0.021
693
c SPN049 Spinocerebellar Ataxia 56 0.021
694
LPM005 Lipomatosis 56 0.021
695
PRR002 Pure Red-Cell Aplasia 56 0.021
696
MYM001 Myoma 56 0.021
697
TLP001 Talipes Equinovarus 56 0.021
698
EPD037 Epidermal Nevus 56 0.021
699
TYP011 Typhus 56 0.021
700
WRN002 Wernicke-Korsakoff Syndrome 56 0.021
701
P ESN001 Eosinophilic Esophagitis 55 0.021
702
c MCK006 Meckel Syndrome 55 0.021
703
ACR005 Acrodermatitis 55 0.021
704
PSD002 Pseudotumor Cerebri 55 0.021
705
P RCS002 Recessive Dystrophic Epidermolysis Bullosa 55 0.021
706
P PMP005 Pemphigus Vulgaris 55 0.021
707
c HRM001 Hermansky-Pudlak Syndrome 55 0.021
708
P INF032 Infertility 55 0.021
709
MTN003 Motion Sickness 55 0.021
710
PRM003 Premature Ejaculation 55 0.021
711
CNT047 Contact Dermatitis 55 0.021
712
ASP001 Asperger Syndrome 55 0.021
713
NPH011 Nephroblastoma 55 0.021
714
P PYL005 Pyelonephritis 55 0.021
715
P STC005 Stickler Syndrome Type 1 55 0.021
716
P INT064 Intermediate Uveitis 55 0.021
717
MLT006 Multidrug-Resistant Tuberculosis 55 0.021
718
CHL069 Cholesteatoma 55 0.021
719
PRM013 Premature Menopause 55 0.021
720
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 54 0.021
721
CHR008 Choroiditis 54 0.021
722
LPT001 Leptospirosis 54 0.021
723
NPH051 Nephritis 54 0.021
724
P SJG002 Sjogren-Larsson Syndrome 54 0.021
725
P RBN002 Robinow Syndrome 54 0.021
726
P MSC003 Muscular Atrophy 54 0.021
727
MYX004 Myxedema 54 0.021
728
GST045 Gastroenteritis 54 0.021
729
P JNC001 Junctional Epidermolysis Bullosa 54 0.021
730
PRN011 Pernicious Anemia 53 0.021
731
c INT001 Intrahepatic Cholestasis 53 0.021
732
P KRT007 Keratoconus 53 0.021
733
c MCL001 Mucolipidosis 53 0.021
734
BLL001 Baller-Gerold Syndrome 53 0.021
735
JHN001 Johanson-Blizzard Syndrome 53 0.021
736
BRS081 Breast Cancer Susceptibility 53 0.021
737
P ALP014 Alpha-Thalassemia/mental Retardation Syndrome 53 0.021
738
NRG002 Neurogenic Bladder 53 0.021
739
PRV006 Pervasive Developmental Disorder 53 0.021
740
P CNT005 Central Nervous System Lymphoma 53 0.021
741
c INT099 Intrahepatic Cholestasis of Pregnancy 53 0.021
742
OST011 Osteomalacia 53 0.021
743
MMB002 Membranous Glomerulonephritis 53 0.021
744
GRN007 Granuloma Annulare 53 0.021
745
ATP002 Atopy 53 0.021
746
c TYR003 Tyrosinemia Type Ii 53 0.021
747
RSC001 Rosacea 52 0.021
748
ISL003 Isolated Growth Hormone Deficiency 52 0.021
749
CNG064 Congenital Chloride Diarrhea 52 0.021
750
ACS001 Acoustic Neuroma 52 0.021
751
NRN008 Neuronal Intranuclear Inclusion Disease 52 0.021
752
P PRM052 Primary Progressive Aphasia 52 0.021
753
ESN005 Eosinophilic Gastroenteritis 52 0.021
754
HMG002 Hemoglobinuria 52 0.021
755
OST019 Osteosclerosis 52 0.021
756
c FML024 Familial Melanoma 52 0.021
757
P CYS018 Cystitis 51 0.021
758
ALX002 Alexithymia 51 0.021
759
AGR002 Agoraphobia 51 0.021
760
SPN019 Spondylolisthesis 51 0.021
761
PRT019 Protein-Losing Enteropathy 51 0.021
762
FBR009 Fibrous Dysplasia 51 0.021
763
LKD001 Leukodystrophy 51 0.021
764
P LYD001 Leydig Cell Tumor 51 0.021
765
XLN068 X-Linked Thrombocytopenia 51 0.021
766
c PRM001 Primary Cutaneous Amyloidosis 51 0.021
767
c CRB126 Cerebral Cavernous Malformation 51 0.021
768
c STC001 Stickler Syndrome 51 0.021
769
c EPD009 Epidermolysis Bullosa Dystrophica 51 0.021
770
P HYP027 Hypobetalipoproteinemia 51 0.021
771
HYP043 Hyperandrogenism 51 0.021
772
CCN002 Cocaine Abuse 51 0.021
773
c EMR001 Emery-Dreifuss Muscular Dystrophy 51 0.021
774
OCL020 Ocular Cicatricial Pemphigoid 51 0.021
775
HYP068 Hyperostosis 50 0.021
776
ACT099 Acute Fatty Liver of Pregnancy 50 0.021
777
ASP002 Aspartylglucosaminuria 50 0.021
778
GRM009 Germ Cell Tumors 50 0.021
779
FCL041 Focal Myositis 50 0.021
780
c MSB002 Mesoblastic Nephroma 50 0.021
781
DBW001 Dubowitz Syndrome 50 0.021
782
SCT005 Scott Syndrome 50 0.021
783
CTS002 Cat-Scratch Disease 50 0.021
784
c OPT004 Optic Atrophy 50 0.021
785
DNT012 Dental Caries 49 0.021
786
c PSD003 Pseudohypoaldosteronism 49 0.021
787
NRX001 Neuroaxonal Dystrophy 49 0.021
788
NPH003 Nephrocalcinosis 49 0.021
789
MST005 Mastitis 49 0.021
790
DFF021 Diffuse Mesangial Sclerosis 49 0.021
791
ACN014 Acanthocytosis 49 0.021
792
DSC009 Discoid Lupus Erythematosus 49 0.021
793
P PNC001 Pancytopenia 48 0.021
794
NSP002 Nasopharyngitis 48 0.021
795
P GRS008 Griscelli Syndrome Type 2 48 0.021
796
MNN021 Meningococcemia 48 0.021
797
NNT016 Neonatal Hemochromatosis 48 0.021
798
BLD034 Bile Duct Carcinoma 48 0.021
799
LPD011 Lipoid Adrenal Hyperplasia 48 0.021
800
P CNG029 Congenital Mesoblastic Nephroma 48 0.021
801
KWS001 Kwashiorkor 48 0.021
802
PPL018 Papillary Adenocarcinoma 48 0.021
803
c CHR098 Chronic Pyelonephritis 48 0.021
804
VRN004 Vernal Keratoconjunctivitis 47 0.021
805
P OVR046 Ovarian Cyst 47 0.021
806
PLM070 Pulmonic Stenosis 47 0.021
807
c EPL003 Epulis 47 0.021
808
c MLG086 Malignant Hyperthermia Susceptibility 47 0.021
809
PTY003 Pityriasis Rubra Pilaris 47 0.021
810
ART035 Arterial Calcification of Infancy 47 0.021
811
P CNG390 Congenital Pulmonary Airway Malformation 47 0.021
812
c AML002 Amelogenesis Imperfecta 47 0.021
813
PRS012 Pars Planitis 47 0.021
814
HYP120 Hypoaldosteronism 47 0.021
815
DRM011 Dermatophytosis 47 0.021
816
MCR037 Macroglossia 47 0.021
817
DLS001 Delusional Disorder 46 0.021
818
HYP064 Hypogonadotropism 46 0.021
819
NRM004 Neuroma 46 0.021
820
SHR003 Short-Chain Acyl-Coa Dehydrogenase Deficiency 46 0.021
821
MNN017 Mononeuropathy 46 0.021
822
PNH001 Panhypopituitarism 46 0.021
823
NDL021 Nodular Lymphocyte Predominant Hodgkin Lymphoma 46 0.021
824
CMP034 Complete Androgen Insensitivity Syndrome 46 0.021
825
CRN025 Corneal Dystrophy 46 0.021
826
EPL002 Epilepsy Syndrome 46 0.021
827
PLG004 Plagiocephaly 46 0.021
828
PLM035 Pulmonary Eosinophilia 46 0.021
829
ART004 Aortic Atherosclerosis 46 0.021
830
P FNG005 Feingold Syndrome 45 0.021
831
MTB004 Metabolic Acidosis 45 0.021
832
MGL013 Megalencephaly 45 0.021
833
GRM004 Germinoma 45 0.021
834
SPS007 Spastic Cerebral Palsy 45 0.021
835
c BRC013 Brachydactyly Type E 45 0.021
836
HRS011 Horseshoe Kidney 45 0.021
837
c TRC005 Tracheal Stenosis 45 0.021
838
c LTT001 Lattice Corneal Dystrophy 45 0.021
839
UNL007 Unilateral Renal Agenesis 45 0.021
840
MRC003 Mercury Poisoning 45 0.021
841
OPP004 Oppositional Defiant Disorder 45 0.021
842
FTL007 Fetal Hydantoin Syndrome 45 0.021
843
CHR078 Chorioretinitis 44 0.021
844
SYN036 Syncope 44 0.021
845
c SNR001 Senior-Loken Syndrome 44 0.021
846
CHN015 Chondrodysplasia 44 0.021
847
c APH002 Aphasia 44 0.021
848
P SDR003 Sideroblastic Anemia 44 0.021
849
NVS001 Neovascular Glaucoma 44 0.021
850
QDR001 Quadriplegia 44 0.021
851
c CHR342 Chiari Malformation 44 0.021
852
NCR002 Necrobiosis Lipoidica 44 0.021
853
c INF049 Infantile Myofibromatosis 44 0.021
854
PRR010 Pierre Robin Sequence 44 0.021
855
RNL029 Renal Coloboma Syndrome 43 0.021
856
P D2H001 D-2-Hydroxyglutaric Aciduria 43 0.021
857
P GM1001 Gm1 Gangliosidosis Type 1 43 0.021
858
c PTR004 Pterygium 43 0.021
859
CND006 Candida Glabrata 43 0.021
860
CNG024 Congenital Nystagmus 43 0.021
861
OLG001 Oligospermia 43 0.021
862
TBL013 Tubulointerstitial Nephritis and Uveitis 43 0.021
863
c ACH011 Achondrogenesis 43 0.021
864
GND001 Gonadoblastoma 43 0.021
865
PCH002 Pachygyria 42 0.021
866
c CHR104 Chorea 42 0.021
867
EPS026 Epispadias 42 0.021
868
MGC004 Megacystis Microcolon Intestinal Hypoperistalsis Syndrome 42 0.021
869
P CNG004 Congenital Epulis 42 0.021
870
P FBR025 Fibrochondrogenesis 42 0.021
871
BTN004 Biotin Deficiency 42 0.021
872
LWT001 Low Tension Glaucoma 41 0.021
873
c PNT019 Pontocerebellar Hypoplasia 41 0.021
874
CND005 Cone Dystrophy 41 0.021
875
CD4003 Cd40 Ligand Deficiency 41 0.021
876
c TRS004 Torsion Dystonia 41 0.021
877
ANN005 Annular Pancreas 41 0.021
878
CRB028 Cerebellar Medulloblastoma 41 0.021
879
HMT018 Hematopoietic Stem Cell Transplantation 41 0.021
880
c TRC004 Trichorhinophalangeal Syndrome Type I 41 0.021
881
HMP009 Haemophilus Influenzae 41 0.021
882
c ACQ027 Acquired Cutis Laxa 41 0.021
883
c GRS003 Griscelli Syndrome 41 0.021
884
P END046 Endometritis 41 0.021
885
PLN006 Poland Syndrome 41 0.021
886
c CNG033 Congenital Syphilis 41 0.021
887
CRD053 Cardiovascular Disease Risk Factor 41 0.021
888
OHT001 Ohtahara Syndrome 40 0.021
889
GST052 Gestational Choriocarcinoma 40 0.021
890
MCL007 Macular Dystrophy 40 0.021
891
NRG004 Neurogenic Diabetes Insipidus 40 0.021
892
SCH008 Schmid Metaphyseal Chondrodysplasia 40 0.021
893
SPR035 Superior Vena Cava Syndrome 40 0.021
894
TRN030 Transient Erythroblastopenia of Childhood 40 0.021
895
ENT007 Enteropathica 40 0.021
896
SML028 Semilobar Holoprosencephaly 39 0.021
897
TBR006 Tuberculoid Leprosy 39 0.021
898
CNG105 Congenital Lobar Emphysema 39 0.021
899
GST064 Gastric Outlet Obstruction 39 0.021
900
AND001 Anodontia 39 0.021
901
SPR034 Superior Limbic Keratoconjunctivitis 39 0.021
902
c NRC009 Narcolepsy 1 39 0.021
903
c PRG001 Progressive Muscular Atrophy 39 0.021
904
BCK006 Back Pain 39 0.021
905
c RNG018 Ring Chromosome 22 39 0.021
906
CMB021 Combined Pituitary Hormone Deficiency 38 0.021
907
MHC001 Mhc Class Ii Deficiency 38 0.021
908
NNM005 Non-Immune Hydrops Fetalis 38 0.021
909
SCH011 Schizotypal Personality Disorder 38 0.021
910
RNL025 Renal Hypoplasia 38 0.021
911
VCL001 Vacuolar Myopathy 38 0.021
912
SPL039 Split Foot 38 0.021
913
LYM095 Lymphangiomatosis 38 0.021
914
IPX001 Ipex Syndrome 37 0.021
915
BLN001 Blount's Disease 37 0.021
916
RTN006 Retinal Drusen 36 0.021
917
CVR010 Cavernous Malformation 36 0.021
918
RNL012 Renal Tuberculosis 36 0.021
919
c PPL025 Popliteal Pterygium Syndrome 36 0.021
920
PRS054 Persistent Truncus Arteriosus 36 0.021
921
C3D001 C3 Deficiency 36 0.021
922
PTC005 Pituicytoma 36 0.021
923
SPS004 Spastic Quadriplegia 35 0.021
924
P DYS005 Dyslexia 35 0.021
925
P MLD013 Mild Hemophilia a 35 0.021
926
NRW001 Norwegian Scabies 35 0.021
927
P AND009 Androgenetic Alopecia 35 0.021
928
c CRB059 Cerebellar Degeneration 35 0.021
929
DYS012 Dyshidrosis 34 0.021
930
IMM039 Immune Hydrops Fetalis 34 0.021
931
SPR007 Superior Mesenteric Artery Syndrome 34 0.021
932
SHK001 Shaken Baby Syndrome 34 0.021
933
c JVN041 Juvenile Nephronophthisis 34 0.021
934
EXS013 Exstrophy-Epispadias Complex 34 0.021
935
BDY001 Body Dysmorphic Disorder 34 0.021
936
DFF001 Diffuse Cutaneous Mastocytosis 34 0.021
937
HYP461 Hypocomplementemic Urticarial Vasculitis Syndrome 33 0.021
938
PRM129 Primary Cutaneous Marginal Zone B-Cell Lymphoma 33 0.021
939
c ENL009 Enlarged Parietal Foramina 33 0.021
940
c ACH010 Achondrogenesis Type Ii 33 0.021
941
SPN029 Spondylolysis 33 0.021
942
THL009 Thiolase Deficiency 33 0.021
943
FCL003 Facial Hemiatrophy 32 0.021
944
PHT008 Photosensitive Epilepsy 32 0.021
945
SPR012 Separation Anxiety Disorder 32 0.021
946
LTM002 Luteoma 32 0.021
947
c MNS008 Monosomy 21 32 0.021
948
SBP004 Subependymoma 32 0.021
949
ARM003 Aromatic Amino Acid Decarboxylase Deficiency 32 0.021
950
PRS108 Persistent Polyclonal B-Cell Lymphocytosis 32 0.021
951
SPN221 Spina Bifida Occulta 31 0.021
952
WRT003 Warthin Tumor 31 0.021
953
c MTR002 Mitral Valve Insufficiency 31 0.021
954
CRL004 Caroli Disease 30 0.021
955
c PRM032 Primary Congenital Glaucoma 30 0.021
956
LMB014 Limb-Body Wall Complex 30 0.021
957
P BRS089 Breast and Colorectal Cancer 30 0.021
958
P PTT002 Potter's Syndrome 30 0.021
959
DVL001 Developmental Coordination Disorder 30 0.021
960
P PLM064 Pulmonary Sequestration 29 0.021
961
CRN051 Craniofacial Microsomia 29 0.021
962
c HMG001 Hemoglobin C Disease 29 0.021
963
PLM058 Pulmonary Atresia with Intact Ventricular Septum 29 0.021
964
RTT001 Ritter's Disease 29 0.021
965
ANG004 Angioid Streaks 29 0.021
966
ATR003 Atrophic Rhinitis 29 0.021
967
NNT021 Neonatal Meningitis 28 0.021
968
OCL044 Oculo-Auriculo-Vertebral Spectrum 28 0.021
969
GST007 Gastric Dilatation 28 0.021
970
SYS006 Say Syndrome 28 0.021
971
SMT001 Somatization Disorder 28 0.021
972
IVC001 Ivic Syndrome 28 0.021
973
BLD052 Blood Group Incompatibility 28 0.021
974
P HYP163 Hyperlipidemia Type 3 28 0.021
975
GGR001 Geographic Tongue 27 0.021
976
LCH003 Lichen Nitidus 27 0.021
977
AMY005 Amyloid Neuropathy 27 0.021
978
OLM001 Olmsted Syndrome 27 0.021
979
DDN009 Duodenal Obstruction 27 0.021
980
ACC003 Accommodative Esotropia 27 0.021
981
XNT009 Xanthoma Disseminatum 26 0.021
982
TRC035 Tracheal Agenesis 26 0.021
983
FTS001 Fetishism 26 0.021
984
MCR039 Macrophagic Myofasciitis 25 0.021
985
3HY001 3-Hydroxyisobutyric Aciduria 25 0.021
986
RGH006 Right Aortic Arch 25 0.021
987
c JVN020 Juvenile-Onset Dystonia 25 0.021
988
PNS015 Penoscrotal Transposition 25 0.021
989
PLN001 Plantar Wart 25 0.021
990
P CNG370 Congenital Tracheal Stenosis 25 0.021
991
CLC003 Cloacogenic Carcinoma 25 0.021
992
ART034 Aortopulmonary Window 24 0.021
993
c MSC016 Mosaic Trisomy 14 24 0.021
994
AVD001 Avoidant Personality Disorder 24 0.021
995
LBN004 Liebenberg Syndrome 24 0.021
996
PNL023 Penile Agenesis 23 0.021
997
SLT009 Solitary Bone Cyst 23 0.021
998
P HYD015 Hydroa Vacciniforme 23 0.021
999
INT011 Interstitial Emphysema 23 0.021
1000
TLH001 Tel Hashomer Camptodactyly Syndrome 23 0.021
1001
TCL012 T-Cell/histiocyte Rich Large B Cell Lymphoma 22 0.021
1002
MRG006 Morgagni-Stewart-Morel Syndrome 22 0.021
1003
PRD003 Periodontosis 22 0.021
1004
CNG133 Congenital Varicella Syndrome 21 0.021
1005
LPM007 Lipomyelomeningocele 21 0.021
1006
SPS087 Spasmus Nutans 21 0.021
1007
c NNT006 Neonatal Myasthenia Gravis 20 0.021
1008
MYL044 Myelocystocele 20 0.021
1009
CLR033 Color Vision Deficiency 20 0.021
1010
DCR002 Dacryocystocele 20 0.021
1011
PRR001 Periarthritis 20 0.021
1012
BRN097 Brainstem Auditory Evoked Responses 20 0.021
1013
RTN019 Retinal Telangiectasia 20 0.021
1014
HCS001 Hec Syndrome 20 0.021
1015
SCH025 Schisis Association 19 0.021
1016
CNG329 Congenital Onychodysplasia 19 0.021
1017
HYP015 Hyperlucent Lung 19 0.021
1018
MSL004 Mesial Temporal Lobe Epilepsy with Hippocampal Sclerosis 19 0.021
1019
LBY003 Labyrinthine Disease 19 0.021
1020
c MLG039 Malignant Essential Hypertension 19 0.021
1021
PTN004 Patent Ductus Venosus 18 0.021
1022
RDT006 Radiation Induced Meningioma 18 0.021
1023
c CNG129 Congenital Torticollis 18 0.021
1024
CLP002 Colpocephaly 18 0.021
1025
HYP018 Hyperglobulinemic Purpura 18 0.021
1026
MTR027 Mitral Atresia 17 0.021
1027
TBR007 Tuberculum Sellae Meningioma 17 0.021
1028
c PTR018 Paternal Uniparental Disomy of Chromosome 6 17 0.021
1029
RTN127 Retinal Cavernous Hemangioma 17 0.021
1030
ELC001 Elective Mutism 16 0.021
1031
JVN026 Jeavons Syndrome 16 0.021
1032
PLM108 Pulmonary Interstitial Glycogenosis 16 0.021
1033
C6D001 C6 Deficiency 16 0.021
1034
MCR033 Macrocephaly-Capillary Malformation 15 0.021
1035
FBL006 Fibular Aplasia Ectrodactyly 15 0.021
1036
AQG002 Aquagenic Urticaria 15 0.021
1037
OLG008 Oligomeganephronic Renal Hypoplasia 13 0.021
1038
VLF002 Velo-Facial-Skeletal Syndrome 13 0.021
1039
KZL001 Kozlowski Brown Hardwick Syndrome 13 0.021
1040
HMF003 Hemifacial Myohyperplasia 13 0.021
1041
LCH012 Lichstenstein Syndrome 13 0.021
1042
RHH001 Rohhad 13 0.021
1043
KCH001 Kocher-Debre-Semelaigne Syndrome 12 0.021
1044
FSD001 Fused Mandibular Incisors 12 0.021
1045
HYD031 Hydroxyprolinemia 12 0.021
1046
c RNG014 Ring Chromosome 19 12 0.021
1047
MCH006 Mechanical Strabismus 11 0.021
1048
FNG010 Fingerprint Body Myopathy 11 0.021
1049
c CNG406 Congenital Pulmonary Airway Malformation Type 0 10 0.021
1050
CNG125 Congenital Short Femur 10 0.021
1051
CRB080 Cor Biloculare 10 0.021
1052
DDY001 Didymosis Aplasticosebacea 10 0.021
1053
FTZ005 Fitzsimmons-Guilbert Syndrome 8 0.021
1054
2MT002 2-Methylacetoacetyl Coa Thiolase Deficiency 8 0.021
1055
OBS014 Obsessive-Compulsive Disorder, Protection Against 6 0.021
1056
HLC002 Holoacardius Amorphus 5 0.021