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

1098 hits were found for 'twinning'

# ++ Fam MCID Name MIFTS Score
1
P TWN001 Twin-to-Twin Transfusion Syndrome 39 9.508
2
c TWN006 Twin Twin Transfusion Syndrome 51 7.679
3
RNL090 Renal Tubular Dysgenesis Due to Twin-Twin Transfusion 1 5.068
4
NSY001 N Syndrome 57 0.274
5
RNL028 Renal Tubular Dysgenesis 49 0.180
6
PLY012 Polyhydramnios 49 0.175
7
END072 Endotheliitis 51 0.169
8
ART109 Arterial Thoracic Outlet Syndrome 17 0.164
9
ANN002 Anencephaly 53 0.146
10
WDM003 Wiedemann Opitz Syndrome 9 0.144
11
HYD012 Hydrops Fetalis 61 0.143
12
PLY018 Polycythemia 55 0.135
13
GNR028 Generalized Essential Telangiectasia 16 0.135
14
ACR022 Acardia 15 0.121
15
FTL044 Fetal Cytomegalovirus Syndrome 22 0.114
16
c RNG028 Ring Chromosome Y 17 0.114
17
IDP042 Idiopathic Recurrent Stupor 15 0.110
18
CYT008 Cytomegalovirus Infection 50 0.108
19
OLG003 Oligohydramnios 45 0.108
20
HYP179 Hypertrichosis Congenital Generalized X-Linked 18 0.106
21
DWN001 Down Syndrome 58 0.102
22
ART031 Aortic Coarctation 56 0.102
23
ANK002 Ankylosing Spondylitis 75 0.093
24
CNG069 Congenital Cytomegalovirus 33 0.093
25
HNM001 Hinman's Syndrome 28 0.093
26
P OBS005 Obesity 79 0.088
27
P HYP075 Hypertension 76 0.088
28
THR013 Thoracic Outlet Syndrome 53 0.088
29
NDP002 Ndp-Related Retinopathy of Prematurity 7 0.088
30
FCT013 Factor V Leiden Thrombophilia 31 0.083
31
NCT002 Nicotine Dependence 49 0.081
32
CHR101 Char Syndrome 42 0.081
33
P MGR002 Migraine 61 0.078
34
c PRG060 Pregnancy Loss 48 0.078
35
MLR006 Male Reproductive Organ Cancer 21 0.078
36
SRN002 Sirenomelia 21 0.078
37
WDM004 Wiedemann-Steiner Syndrome 20 0.078
38
URT039 Urticaria 61 0.075
39
c INT060 Intestinal Atresia 42 0.075
40
P BPL003 Bipolar Disorder 76 0.072
41
c DBT009 Diabetes Mellitus 68 0.072
42
P HMP004 Hemophilia B 66 0.072
43
PRC016 Pre-Eclampsia 64 0.072
44
P BCK002 Beckwith-Wiedemann Syndrome 62 0.072
45
ALC007 Alcohol Dependence 59 0.072
46
HYP571 Hypotonia-Speech Impairment-Severe Cognitive Delay Syndrome 11 0.072
47
LKM002 Leukemia 70 0.069
48
c LCL006 Localized Scleroderma 64 0.069
49
P SHR029 Short Syndrome 55 0.069
50
CHR005 Chorioamnionitis 52 0.069
51
c HYP086 Hypothyroidism 59 0.066
52
CRB037 Cerebral Palsy 58 0.066
53
ISC004 Ischemia 57 0.066
54
P OMP004 Omphalocele 53 0.066
55
ECT026 Ectopic Pregnancy 50 0.066
56
c ENC008 Encephalocele 47 0.066
57
URT008 Urticaria Pigmentosa 40 0.066
58
ENC005 Encephalomalacia 30 0.066
59
ABL001 Ablepharon Macrostomia Syndrome 27 0.066
60
TFT003 Tufting Enteropathy 26 0.066
61
SPS044 Spastic Paraplegia Epilepsy Mental Retardation 11 0.066
62
ATX002 Ataxia Telangiectasia 81 0.062
63
RNL002 Renal Agenesis 68 0.062
64
P ANR007 Anorexia Nervosa 64 0.062
65
P INS005 Insulin Resistance 62 0.062
66
c TXP001 Toxoplasmosis 59 0.062
67
P PRS038 Personality Disorder 56 0.062
68
VNS009 Venous Thrombosis 56 0.062
69
PST087 Posterior Urethral Valve 47 0.062
70
P GND004 Gonadal Dysgenesis 47 0.062
71
PYL006 Pyloric Stenosis 44 0.062
72
PST042 Posterior Valve Urethra 14 0.062
73
CNG034 Congestive Heart Failure 74 0.059
74
P RBN001 Rubinstein-Taybi Syndrome 68 0.059
75
KLN001 Klinefelter's Syndrome 66 0.059
76
ACT073 Acute Leukemia 62 0.059
77
ART005 Arteriovenous Malformation 62 0.059
78
DRM006 Dermatitis 60 0.059
79
P VCT001 Vacterl Association 59 0.059
80
SCN006 Secondary Syphilis 53 0.059
81
c THN001 Thanatophoric Dysplasia 53 0.059
82
c TRT010 Teratoma 53 0.059
83
P CNG021 Congenital Toxoplasmosis 48 0.059
84
IMP002 Imperforate Anus 47 0.059
85
CRB009 Cerebritis 46 0.059
86
PST041 Posterior Urethral Valves 42 0.059
87
APL006 Aplasia Cutis Congenita 41 0.059
88
P HYD001 Hydranencephaly 34 0.059
89
c HYP543 Hypoplastic Left Heart Syndrome 1 26 0.059
90
LKM059 Leukemia, Megakaryoblastic, with or Without Down Syndrome, Somatic 24 0.059
91
PRT015 Partial Third-Nerve Palsy 19 0.059
92
SPS082 Spastic Paraplegia - Epilepsy - Intellectual Deficit 12 0.059
93
P ART022 Arthritis 75 0.055
94
P MLT020 Multiple Sclerosis 75 0.055
95
BRN024 Bronchitis 71 0.055
96
P CNG006 Congenital Hypothyroidism 69 0.055
97
c MST009 Mastocytosis 67 0.055
98
ADN018 Adenoma 67 0.055
99
c LPS004 Lupus Erythematosus 65 0.055
100
P PRM019 Premature Ovarian Failure 64 0.055
101
SPN038 Spina Bifida 63 0.055
102
P OST009 Osteochondritis Dissecans 60 0.055
103
GST009 Gastroschisis 58 0.055
104
GLD001 Goldenhar Syndrome 57 0.055
105
P DBT005 Diabetes Insipidus 56 0.055
106
P HYP055 Hypoplastic Left Heart Syndrome 55 0.055
107
ESP020 Esophageal Atresia 54 0.055
108
c MSC005 Muscular Dystrophy 54 0.055
109
PRV004 Periventricular Leukomalacia 54 0.055
110
c MYP004 Myopathy 52 0.055
111
c MNT147 Mental Retardation 51 0.055
112
PLM070 Pulmonic Stenosis 48 0.055
113
HYP009 Hypertrophic Pyloric Stenosis 47 0.055
114
TRN007 Transsexualism 47 0.055
115
LKM006 Leukomalacia 45 0.055
116
CNN001 Cannabis Dependence 37 0.055
117
P JJN004 Jejunal Atresia 22 0.055
118
P NRF002 Neurofibromatosis 86 0.051
119
PRT036 Peritonitis 67 0.051
120
ACQ007 Acquired Immunodeficiency Syndrome 62 0.051
121
P DMN002 Dementia 61 0.051
122
PLM033 Pulmonary Embolism 60 0.051
123
BLM002 Bulimia Nervosa 58 0.051
124
SMT015 Smith Magenis Syndrome 58 0.051
125
CND002 Conduct Disorder 56 0.051
126
P PRT008 Proteus Syndrome 55 0.051
127
PTH002 Pathological Gambling 55 0.051
128
THY089 Thymic Epithelial Neoplasm 53 0.051
129
LFT009 Left Ventricular Outflow Tract Obstruction 52 0.051
130
NRF007 Neurofibroma 51 0.051
131
c HYP065 Hyperaldosteronism 50 0.051
132
c WLM002 Wilms Tumor 50 0.051
133
EVN001 Evans' Syndrome 50 0.051
134
LYM026 Lymphoblastic Leukemia 49 0.051
135
P CTN014 Cutaneous Mastocytosis 49 0.051
136
RFR003 Refractive Error 48 0.051
137
P PLY024 Polymicrogyria 45 0.051
138
PLC005 Placental Insufficiency 42 0.051
139
SCR024 Sacrococcygeal Teratoma 42 0.051
140
P CRV039 Cervicitis 41 0.051
141
ENT001 Enterocele 39 0.051
142
AMN009 Amniotic Band Syndrome 34 0.051
143
PRT086 Partial Hydatidiform Mole 32 0.051
144
GRD005 Geroderma Osteodysplasticum 31 0.051
145
CLC011 Cloacal Exstrophy 30 0.051
146
c ERL004 Early Yaws 29 0.051
147
P BRS047 Breast Cancer 85 0.047
148
P SYS001 Systemic Lupus Erythematosus 83 0.047
149
P RHM011 Rheumatoid Arthritis 83 0.047
150
ATT002 Attention Deficit Hyperactivity Disorder 72 0.047
151
ACN002 Acanthosis Nigricans 70 0.047
152
P SCH015 Schizophrenia 69 0.047
153
P ANG001 Angelman Syndrome 67 0.047
154
ART019 Aortic Valve Stenosis 64 0.047
155
ECL001 Eclampsia 62 0.047
156
P HLP001 Holoprosencephaly 61 0.047
157
MYS005 Myositis 61 0.047
158
c THY032 Thyroiditis 61 0.047
159
P NRB001 Neuroblastoma 60 0.047
160
GST033 Gestational Diabetes 59 0.047
161
c NTR004 Neutropenia 59 0.047
162
ALP008 Alopecia 59 0.047
163
P DRM007 Dermatitis Herpetiformis 57 0.047
164
HLL004 Hellp Syndrome 54 0.047
165
PLC007 Placental Abruption 51 0.047
166
PSD009 Pseudohermaphroditism 49 0.047
167
P ECT006 Ectodermal Dysplasia 46 0.047
168
MTS001 Mutism 45 0.047
169
P CHN005 Choanal Atresia 43 0.047
170
BRX001 Bruxism 39 0.047
171
AST006 Astigmatism 38 0.047
172
c MYP006 Myopia 36 0.047
173
EST005 Esotropia 33 0.047
174
MCR029 Micro Syndrome 31 0.047
175
PHC006 Phacomatosis Pigmentovascularis 24 0.047
176
CYS001 Cystic Fibrosis 91 0.042
177
P MYC007 Myocardial Infarction 82 0.042
178
TBR010 Tuberculosis 82 0.042
179
P PRM021 Primary Pulmonary Hypertension 74 0.042
180
PTZ001 Peutz-Jeghers Syndrome 73 0.042
181
HPT023 Hepatocellular Carcinoma 69 0.042
182
RLP001 Relapsing Polychondritis 66 0.042
183
WST001 West Syndrome 64 0.042
184
P GRV001 Graves' Disease 63 0.042
185
P ATS007 Autism Spectrum Disorder 59 0.042
186
P CRN157 Coronary Heart Disease 59 0.042
187
P MJR001 Major Depressive Disorder 58 0.042
188
c ATX004 Ataxia 56 0.042
189
MYC002 Mycobacterium Avium Complex Disease 56 0.042
190
P GTR002 Goiter 55 0.042
191
P ALC004 Alcohol Abuse 55 0.042
192
KDS001 Kid Syndrome 55 0.042
193
c HYP076 Hyperthyroidism 55 0.042
194
ANR004 Anuria 53 0.042
195
c EPD016 Epidermolysis Bullosa 53 0.042
196
PSR002 Psoriasis 51 0.042
197
c CNG018 Congenital Heart Block 50 0.042
198
TXC012 Toxic Epidermal Necrolysis 49 0.042
199
P GLC007 Glaucoma 49 0.042
200
P THR090 Thrombocythemia 1 48 0.042
201
ACR012 Aicardi Syndrome 47 0.042
202
END020 Endocardial Fibroelastosis 46 0.042
203
c RSM001 Rasmussen Encephalitis 46 0.042
204
c ACR001 Aicardi-Goutieres Syndrome 46 0.042
205
APP001 Apparent Mineralocorticoid Excess Syndrome 45 0.042
206
DYS018 Dysostosis 45 0.042
207
PRN038 Prune Belly Syndrome 44 0.042
208
P CRV043 Cervical Dystonia 44 0.042
209
GND002 Gender Identity Disorder 43 0.042
210
MLK003 Melkersson-Rosenthal Syndrome 43 0.042
211
c MCR103 Microtia 40 0.042
212
RTN012 Retinopathy of Prematurity 40 0.042
213
ATX019 Ataxia with Vitamin E Deficiency 40 0.042
214
PLM074 Pulmonary Function 38 0.042
215
MSS002 Mass Syndrome 37 0.042
216
HYD028 Hydrops, Ectopic Calcification, Moth-Eaten Skeletal Dysplasia 37 0.042
217
TRN044 Transposition of the Great Arteries 36 0.042
218
ARC004 Arc Syndrome 34 0.042
219
ADS002 Adie Syndrome 32 0.042
220
PRS030 Persistent Fetal Circulation Syndrome 29 0.042
221
CDL002 Caudal Duplication 27 0.042
222
c HMP017 Hemophilia a, Congenital 26 0.042
223
NNS006 Non-Suppurative Otitis Media 24 0.042
224
CLN022 Colonic Atresia 24 0.042
225
ANS004 Anisometropia 24 0.042
226
P DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 23 0.042
227
SLP010 Slipped Capital Femoral Epiphysis 21 0.042
228
P HYP078 Hypertrophy of Breast 20 0.042
229
EPG004 Epignathus 20 0.042
230
PTZ002 Peutz–jeghers Syndrome 17 0.042
231
PL2001 Pla2g6-Associated Neurodegeneration 14 0.042
232
CMV001 Cmv Antenatal Infection 13 0.042
233
FTL016 Fetal Edema 13 0.042
234
PHC005 Phacomatosis Pigmentokeratotica 12 0.042
235
CYS021 Cystic Adenomatoid Malformation of Lung 11 0.042
236
JMC001 Jamaican Vomiting Sickness 10 0.042
237
AND002 Androgen Insensitivity Syndrome 75 0.036
238
c NNN003 Noonan Syndrome 73 0.036
239
ANX002 Anxiety Disorder 73 0.036
240
MCC001 Mccune Albright Syndrome 71 0.036
241
P TRN020 Turner Syndrome 71 0.036
242
P CLC005 Celiac Disease 71 0.036
243
ATH003 Atherosclerosis 69 0.036
244
KWS002 Kawasaki Disease 69 0.036
245
NRL016 Neural Tube Defects 69 0.036
246
VSC007 Vascular Disease 69 0.036
247
THL005 Thalassemia 69 0.036
248
P CNG026 Congenital Heart Defect 65 0.036
249
c HMP007 Hemophilia 64 0.036
250
LNG024 Langerhans-Cell Histiocytosis 63 0.036
251
OVR029 Ovarian Hyperstimulation Syndrome 61 0.036
252
P HST010 Histiocytosis 61 0.036
253
BRN029 Brain Disease 60 0.036
254
P ADN016 Adenocarcinoma 60 0.036
255
P CLF002 Cleft Palate 60 0.036
256
ANR002 Aniridia 59 0.036
257
DSS009 Disseminated Intravascular Coagulation 59 0.036
258
P CTS001 Cutis Laxa 59 0.036
259
P AGM001 Agammaglobulinemia 58 0.036
260
c NPH012 Nephrotic Syndrome 57 0.036
261
P HYP013 Hypohidrotic Ectodermal Dysplasia 57 0.036
262
P NPH009 Nephrolithiasis 57 0.036
263
c AXN002 Axenfeld-Rieger Syndrome 57 0.036
264
P HYP040 Hypospadias 56 0.036
265
CLB001 Coloboma 56 0.036
266
P MLN008 Melanoma 56 0.036
267
GYN001 Gynecomastia 56 0.036
268
c EMR001 Emery-Dreifuss Muscular Dystrophy 56 0.036
269
P PLY006 Polydactyly 55 0.036
270
CDL003 Caudal Regression Syndrome 55 0.036
271
c VNT002 Ventricular Septal Defect 54 0.036
272
DGN001 Degenerative Disc Disease 54 0.036
273
c SCL016 Scleroderma 53 0.036
274
CNN003 Conn's Syndrome 52 0.036
275
P CNG015 Congenital Diaphragmatic Hernia 52 0.036
276
URN010 Urinary Tract Obstruction 52 0.036
277
DND001 Dandy-Walker Syndrome 52 0.036
278
c SYN005 Synostosis 51 0.036
279
c NNT009 Neonatal Diabetes Mellitus 51 0.036
280
LPM004 Lipoma 51 0.036
281
TCL004 T-Cell Leukemia 50 0.036
282
SBS004 Substance Dependence 49 0.036
283
EPD037 Epidermal Nevus 49 0.036
284
c CTR002 Cataract 48 0.036
285
PNM008 Pneumothorax 48 0.036
286
ILS001 Ileus 47 0.036
287
TRP014 Triploidy 46 0.036
288
P JVN003 Juvenile Xanthogranuloma 46 0.036
289
CHN016 Cohen Syndrome 44 0.036
290
c FTL001 Fetal Alcohol Syndrome 44 0.036
291
PPL021 Papilledema 44 0.036
292
c HMP006 Hemiplegic Migraine 44 0.036
293
TRC040 Tracheoesophageal Fistula 44 0.036
294
c SPN183 Spontaneous Pneumothorax 44 0.036
295
PRP016 Paraplegia 42 0.036
296
NNT019 Neonatal Hypothyroidism 41 0.036
297
MCN017 Meconium Ileus 41 0.036
298
TTH002 Tooth Agenesis 38 0.036
299
MYF001 Myofibroma 37 0.036
300
FTL005 Fetal Adenoma 37 0.036
301
ESP029 Esophageal Atresia/tracheoesophageal Fistula 35 0.036
302
CNN002 Cannabis Abuse 33 0.036
303
BRW006 Brown Syndrome 28 0.036
304
P MLT015 Multiple Intestinal Atresia 27 0.036
305
CYT004 Cytomegalic Inclusion Disease 24 0.036
306
OCC011 Occipital Encephalocele 23 0.036
307
MCC005 Mccune–albright Syndrome 20 0.036
308
FRM001 Freemartinism 18 0.036
309
GST058 Gestational Diabetes Insipidus 12 0.036
310
P AMY001 Amyotrophic Lateral Sclerosis 87 0.029
311
P AST005 Asthma 86 0.029
312
BLM001 Bloom Syndrome 74 0.029
313
P OST002 Osteoporosis 73 0.029
314
P MYS003 Myasthenia Gravis 71 0.029
315
ADR007 Adrenoleukodystrophy 70 0.029
316
DCH001 Duchenne Muscular Dystrophy 70 0.029
317
P OST005 Osteogenesis Imperfecta 69 0.029
318
ALP006 Alpha Thalassemia 68 0.029
319
PRG004 Progeria 68 0.029
320
P PNM007 Pneumonia 67 0.029
321
SPS077 Sepsis 67 0.029
322
P MNN012 Meningioma 67 0.029
323
CRZ001 Crouzon Syndrome 67 0.029
324
c THR014 Thrombocytopenia 66 0.029
325
HYP035 Hypophosphatasia 66 0.029
326
INC002 Inclusion Body Myositis 66 0.029
327
FNC001 Fanconi's Anemia 66 0.029
328
P MDL005 Medulloblastoma 66 0.029
329
P UVT001 Uveitis 66 0.029
330
P PLY011 Polycystic Ovary Syndrome 66 0.029
331
P ATM003 Autoimmune Thyroiditis 66 0.029
332
HYP056 Hypoglycemia 66 0.029
333
DFC004 Deficiency Anemia 65 0.029
334
P RCK004 Rickets 65 0.029
335
P SDD001 Sudden Infant Death Syndrome 65 0.029
336
NPH007 Nephrogenic Diabetes Insipidus 65 0.029
337
P ATP001 Atopic Dermatitis 64 0.029
338
CHR066 Chronic Fatigue Syndrome 63 0.029
339
P PNC025 Panic Disorder 62 0.029
340
c CRN037 Craniosynostosis 62 0.029
341
c MNN013 Meningitis 62 0.029
342
HMN010 Hemangioma 62 0.029
343
VLV011 Vulvovaginal Candidiasis 61 0.029
344
P END044 Endometriosis 61 0.029
345
PRP030 Purpura 60 0.029
346
P GLM007 Glomerulonephritis 60 0.029
347
PPL002 Papillary Carcinoma 60 0.029
348
P DGR001 Digeorge Syndrome 60 0.029
349
P SLV001 Silver-Russell Syndrome 59 0.029
350
ACT020 Acute T Cell Leukemia 59 0.029
351
P RHN004 Rhinitis 59 0.029
352
P KLL001 Kallmann Syndrome 58 0.029
353
HDC001 Headache 58 0.029
354
CLR003 Clear Cell Adenocarcinoma 58 0.029
355
HYP014 Hyperuricemia 58 0.029
356
DNY001 Denys-Drash Syndrome 58 0.029
357
HMH002 Hemihypertrophy 57 0.029
358
P HRP006 Herpes Simplex 57 0.029
359
CHR001 Churg-Strauss Syndrome 56 0.029
360
STS002 Situs Inversus 56 0.029
361
c BRG001 Brugada Syndrome 55 0.029
362
c RBL001 Rubella 55 0.029
363
c CNG042 Congenital Central Hypoventilation Syndrome 55 0.029
364
ANT011 Antisocial Personality Disorder 55 0.029
365
c SBC007 Subacute Thyroiditis 55 0.029
366
HYP080 Hypogonadism 54 0.029
367
SCH012 Schizoaffective Disorder 54 0.029
368
c MYL014 Myeloproliferative Disorder 54 0.029
369
NRP001 Neuropathy 54 0.029
370
c PRM011 Primary Ciliary Dyskinesia 54 0.029
371
SCL003 Social Phobia 54 0.029
372
RTN017 Retinal Detachment 53 0.029
373
c MLG069 Malignant Hypertension 53 0.029
374
GNR004 Generalized Anxiety Disorder 53 0.029
375
P STR020 Strabismus 53 0.029
376
SPR004 Supravalvular Aortic Stenosis 53 0.029
377
GSG001 Gas Gangrene 53 0.029
378
LDD002 Liddle Syndrome 52 0.029
379
GRW007 Growth Hormone Deficiency 52 0.029
380
EDW001 Edwards Syndrome 52 0.029
381
c KDN018 Kidney Disease 52 0.029
382
ARC007 Arachnoid Cysts 52 0.029
383
APR001 Apraxia 52 0.029
384
KRT006 Keratoconjunctivitis 52 0.029
385
ART001 Arterial Tortuosity Syndrome 52 0.029
386
HML001 Hemolytic-Uremic Syndrome 52 0.029
387
BRD004 Borderline Personality Disorder 52 0.029
388
P EXD001 Exudative Vitreoretinopathy 52 0.029
389
GNR017 Generalized Pustular Psoriasis 51 0.029
390
MYL020 Myelomeningocele 51 0.029
391
P CNG124 Congenital Rubella 51 0.029
392
c TRC011 Treacher Collins Syndrome 51 0.029
393
CLS010 Cluster Headache 51 0.029
394
ANK001 Ankylosis 51 0.029
395
SBC001 Subacute Sclerosing Panencephalitis 50 0.029
396
WLL003 Williams Syndrome 50 0.029
397
DRG003 Drug Dependence 50 0.029
398
c EPS003 Episodic Ataxia 50 0.029
399
ADL002 Adult Syndrome 50 0.029
400
RYS001 Reye Syndrome 50 0.029
401
RTN018 Retinal Disease 49 0.029
402
PPL020 Papillary Thyroid Carcinoma 49 0.029
403
c MYT002 Myotonic Dystrophy 49 0.029
404
c GLY013 Glycogen Storage Disease 49 0.029
405
RHB017 Rhabdoid Tumor 49 0.029
406
c SPN016 Spondylocostal Dysostosis 49 0.029
407
c DRR001 Diarrhea 49 0.029
408
FTL009 Fetal Akinesia Deformation Sequence 49 0.029
409
PHC013 Phaeochromocytoma 48 0.029
410
c FML023 Familial Hemiplegic Migraine 48 0.029
411
c NPH005 Nephronophthisis 48 0.029
412
P KLP003 Klippel-Feil Syndrome 48 0.029
413
c FBR031 Febrile Seizures 48 0.029
414
CNV002 Conversion Disorder 48 0.029
415
c LFT003 Left Ventricular Noncompaction 48 0.029
416
HMG005 Hemoglobinopathy 47 0.029
417
HMP005 Hemiplegia 47 0.029
418
MYC033 Myoclonus 47 0.029
419
RNL078 Renal Dysplasia 47 0.029
420
ANR018 Anorchia 47 0.029
421
c KBK001 Kabuki Syndrome 47 0.029
422
SCH018 Schizencephaly 47 0.029
423
DNT012 Dental Caries 46 0.029
424
P HTR003 Heterotaxy 46 0.029
425
LMB052 Lumbar Disc Herniation 46 0.029
426
WLL001 Williams-Beuren Syndrome 46 0.029
427
P FCS001 Facioscapulohumeral Muscular Dystrophy 46 0.029
428
TLN003 Telangiectasis 46 0.029
429
c DXT001 Dextrocardia 45 0.029
430
BRS081 Breast Cancer Susceptibility 45 0.029
431
FRZ001 Frozen Shoulder 45 0.029
432
PTS001 Patau Syndrome 45 0.029
433
FRY002 Fryns Syndrome 45 0.029
434
SCB001 Scabies 45 0.029
435
P INF037 Inflammatory Bowel Disease 44 0.029
436
c CNT048 Central Hypoventilation Syndrome 44 0.029
437
KRT012 Keratoderma 44 0.029
438
IRN002 Iron Metabolism Disease 44 0.029
439
RCR001 Recurrent Corneal Erosion 43 0.029
440
HRM002 Hermaphroditism 43 0.029
441
LMB051 Lumbar Disc Disease 43 0.029
442
SVR005 Severe Pre-Eclampsia 43 0.029
443
PLC001 Placenta Accreta 43 0.029
444
NNT012 Neonatal Jaundice 42 0.029
445
MYS001 Myositis Ossificans 42 0.029
446
RFL001 Reflex Sympathetic Dystrophy 42 0.029
447
DDN011 Duodenal Atresia 41 0.029
448
RTR008 Root Resorption 41 0.029
449
c BPL002 Bipolar I Disorder 41 0.029
450
IMP004 Impetigo 41 0.029
451
c BLP004 Blepharophimosis 41 0.029
452
P PRV012 Periventricular Heterotopia 41 0.029
453
PTY003 Pityriasis Rubra Pilaris 41 0.029
454
PRS062 Persistent Hyperplastic Primary Vitreous 41 0.029
455
c OPT004 Optic Atrophy 41 0.029
456
c PRN026 Porencephaly 40 0.029
457
TRN012 Transient Global Amnesia 40 0.029
458
GDS001 Good Syndrome 40 0.029
459
MTG002 Mutagen Sensitivity 40 0.029
460
MSC006 Muscle Glycogenosis 39 0.029
461
AND003 Andersen-Tawil Syndrome 39 0.029
462
IRT001 Iritis 39 0.029
463
KLN002 Kleine-Levin Syndrome 39 0.029
464
BLN010 Balanitis 38 0.029
465
UNL007 Unilateral Renal Agenesis 38 0.029
466
P MNN007 Meningocele 38 0.029
467
P PRV002 Periventricular Nodular Heterotopia 37 0.029
468
PRN019 Perinatal Necrotizing Enterocolitis 36 0.029
469
CRN088 Craniorachischisis 36 0.029
470
TRC062 Tricuspid Atresia 36 0.029
471
c TRN032 Transient Neonatal Diabetes Mellitus 36 0.029
472
c GLC030 Glaucoma, Congenital 35 0.029
473
LTT002 Letterer-Siwe Disease 35 0.029
474
EMN001 Emanuel Syndrome 34 0.029
475
TRC010 Trichotillomania 34 0.029
476
CRV025 Cervical Incompetence 34 0.029
477
P SPL040 Split Hand 33 0.029
478
c GRS003 Griscelli Syndrome 33 0.029
479
c ATX010 Ataxia Neuropathy Spectrum 33 0.029
480
PRX035 Paroxysmal Dyskinesia 32 0.029
481
CRB028 Cerebellar Medulloblastoma 31 0.029
482
HYP362 Hyperopia 31 0.029
483
P SLP004 Salpingo-Oophoritis 30 0.029
484
TRD003 Taurodontism 29 0.029
485
STR026 Star Syndrome 29 0.029
486
GLC004 Galactokinase Deficiency 28 0.029
487
ARM003 Aromatic Amino Acid Decarboxylase Deficiency 27 0.029
488
P SCH009 Scheuermann's Disease 26 0.029
489
ART007 Aorta Atresia 26 0.029
490
NNT018 Neonatal Herpes 24 0.029
491
NRC003 Narcissistic Personality Disorder 24 0.029
492
BLN002 Balanitis Xerotica Obliterans 23 0.029
493
CTN027 Cutaneous Mastocytoma 21 0.029
494
FXC001 Foix Chavany Marie Syndrome 21 0.029
495
IMG001 Image Syndrome 20 0.029
496
CLC002 Calcaneonavicular Coalition 20 0.029
497
AND005 Androgen Insensitivity Syndrome, Mild 19 0.029
498
IMP001 Impetigo Herpetiformis 19 0.029
499
c KRN003 Kernicterus Due to Isoimmunization 18 0.029
500
c BNG076 Benign Exophthalmos Syndrome 17 0.029
501
TWN005 Twenty-Nail Dystrophy 15 0.029
502
CLP002 Colpocephaly 15 0.029
503
c BLT015 Bilateral Choanal Atresia 15 0.029
504
WLS002 Wilson-Mikity Syndrome 15 0.029
505
FBL005 Fibular Aplasia 15 0.029
506
OMP002 Omphalocele Exstrophy Imperforate Anus 14 0.029
507
P ISC010 Isochromosome Yp 14 0.029
508
TRG006 Trigger Thumb 13 0.029
509
LMB009 Lambdoid Synostosis 12 0.029
510
c UNL004 Unilateral Choanal Atresia 11 0.029
511
TRG003 Trigeminal Nerve Disease 10 0.029
512
CCN007 Cocoon Syndrome 9 0.029
513
HLC002 Holoacardius Amorphus 8 0.029
514
SYM006 Symmetrical Thalamic Calcifications 7 0.029
515
ENC009 Encephalocele Anencephaly 4 0.029
516
P ALZ001 Alzheimer's Disease 93 0.021
517
ACT019 Acute Myeloid Leukemia 87 0.021
518
P TBR001 Tuberous Sclerosis 81 0.021
519
CDS001 Cadasil 80 0.021
520
CRH001 Crohn's Disease 78 0.021
521
ACH004 Achondroplasia 77 0.021
522
P WSK001 Wiskott-Aldrich Syndrome 76 0.021
523
P PRS040 Prostate Cancer 76 0.021
524
P RTN008 Retinitis Pigmentosa 76 0.021
525
P MLT019 Multiple Myeloma 76 0.021
526
SVR004 Severe Combined Immunodeficiency 75 0.021
527
P RTT002 Rett Syndrome 75 0.021
528
MTC003 Metachromatic Leukodystrophy 75 0.021
529
FBR012 Fabry Disease 74 0.021
530
P HMC003 Hemochromatosis 73 0.021
531
P GCH001 Gaucher's Disease 73 0.021
532
P OST012 Osteoarthritis 72 0.021
533
P NMN002 Niemann-Pick Disease 72 0.021
534
P SMT004 Smith-Lemli-Opitz Syndrome 72 0.021
535
ATS001 Autistic Disorder 71 0.021
536
ULC004 Ulcerative Colitis 71 0.021
537
CST001 Costello Syndrome 71 0.021
538
BLD042 Bladder Carcinoma 70 0.021
539
OLV001 Olivopontocerebellar Atrophy 70 0.021
540
P MCP002 Mucopolysaccharidosis I 70 0.021
541
P RTN024 Retinoblastoma 70 0.021
542
P PRM006 Primary Biliary Cirrhosis 69 0.021
543
HYP004 Hypercalcemia 69 0.021
544
P ALG002 Alagille Syndrome 68 0.021
545
P CRN008 Carney Complex 68 0.021
546
CRN211 Coronary Artery Disease, 68 0.021
547
ASP006 Aspergillosis 68 0.021
548
CLD001 Cleidocranial Dysplasia 68 0.021
549
P MYL005 Myelofibrosis 67 0.021
550
P NRC002 Narcolepsy 67 0.021
551
P LPR003 Leprosy 67 0.021
552
P CLR023 Colorectal Cancer 66 0.021
553
GT001 Gout 66 0.021
554
CLN016 Colon Cancer 66 0.021
555
P HPT001 Hepatitis C 66 0.021
556
MLG056 Malignant Hyperthermia 66 0.021
557
P AMY004 Amyloidosis 65 0.021
558
INF030 Infectious Mononucleosis 65 0.021
559
GST034 Gastroesophageal Reflux Disease 65 0.021
560
c HPT021 Hepatitis 65 0.021
561
P SYS004 Systemic Mastocytosis 65 0.021
562
VSC011 Vasculitis 65 0.021
563
c XRD001 Xeroderma Pigmentosum 65 0.021
564
ANT006 Antiphospholipid Syndrome 64 0.021
565
P SHR002 Short Stature 64 0.021
566
CMM004 Common Variable Immunodeficiency 64 0.021
567
P ALX003 Alexander Disease 64 0.021
568
TNG002 Tangier Disease 64 0.021
569
c ESS002 Essential Hypertension 64 0.021
570
PRL009 Prolactinoma 64 0.021
571
STT001 Status Epilepticus 64 0.021
572
MYL006 Myeloid Leukemia 64 0.021
573
P MLT021 Multiple System Atrophy 64 0.021
574
P INF038 Influenza 63 0.021
575
DSM004 Desmoid Tumor 63 0.021
576
THR079 Thromboembolism 63 0.021
577
P SYS005 Systemic Scleroderma 63 0.021
578
AMN001 Amenorrhea 63 0.021
579
P DDN001 Duodenal Ulcer 63 0.021
580
P RTH001 Rothmund-Thomson Syndrome 63 0.021
581
P LVR013 Liver Disease 62 0.021
582
c HPT016 Hepatitis B 62 0.021
583
c JVN010 Juvenile Rheumatoid Arthritis 62 0.021
584
ALL003 Allergic Rhinitis 62 0.021
585
ISC006 Ischemic Heart Disease 62 0.021
586
P PLY014 Polycystic Kidney Disease 62 0.021
587
PSY004 Psychotic Disorder 62 0.021
588
PLM001 Pulmonary Tuberculosis 62 0.021
589
ART016 Aortic Aneurysm 62 0.021
590
EPD002 Epidermolytic Hyperkeratosis 62 0.021
591
P STM004 Stomach Cancer 62 0.021
592
GLC003 Glucose Intolerance 62 0.021
593
HMP002 Hemophagocytic Lymphohistiocytosis 62 0.021
594
BCK001 Becker Muscular Dystrophy 62 0.021
595
CHR063 Chronic Mucocutaneous Candidiasis 61 0.021
596
DMN001 Diamond-Blackfan Anemia 61 0.021
597
P CHR071 Charcot-Marie-Tooth Disease 61 0.021
598
HYP266 Hypoxia 60 0.021
599
c SPN046 Spinal Muscular Atrophy 60 0.021
600
RHM001 Rheumatic Fever 60 0.021
601
P BLR001 Biliary Atresia 60 0.021
602
PND002 Pendred Syndrome 60 0.021
603
KLP002 Klippel-Trenaunay Syndrome 60 0.021
604
MXD005 Mixed Connective Tissue Disease 60 0.021
605
PMP001 Pemphigus 60 0.021
606
P PRN023 Prion Disease 60 0.021
607
c SRC013 Sarcoidosis 60 0.021
608
PRP001 Propionic Acidemia 60 0.021
609
LWY001 Lewy Body Dementia 60 0.021
610
ALP001 Alopecia Universalis 59 0.021
611
P DRM010 Dermatomyositis 59 0.021
612
P HRD011 Hereditary Spherocytosis 59 0.021
613
c HYP061 Hypertrophic Cardiomyopathy 59 0.021
614
BLS001 Blau Syndrome 59 0.021
615
P ALP009 Alopecia Areata 59 0.021
616
CRY002 Cryptorchidism 59 0.021
617
PRT011 Protein C Deficiency 59 0.021
618
HYP050 Hyperinsulinemic Hypoglycemia 59 0.021
619
CYS005 Cysticercosis 59 0.021
620
c CCK001 Cockayne Syndrome 58 0.021
621
MLT074 Multiple Endocrine Neoplasia 58 0.021
622
c PNC044 Pancreatitis 58 0.021
623
ALL008 Allergic Bronchopulmonary Aspergillosis 58 0.021
624
PSD007 Pseudomyxoma Peritonei 58 0.021
625
P PRD008 Periodontitis 58 0.021
626
CCT002 Cicatricial Pemphigoid 58 0.021
627
GRW001 Growth Hormone Secreting Pituitary Adenoma 58 0.021
628
c HRD002 Hereditary Angioedema 58 0.021
629
P VLC001 Velocardiofacial Syndrome 57 0.021
630
c HPT003 Hepatitis a 57 0.021
631
RNL007 Renal Tubular Acidosis 57 0.021
632
P TMP001 Temporal Lobe Epilepsy 57 0.021
633
P PMP005 Pemphigus Vulgaris 57 0.021
634
MYM001 Myoma 56 0.021
635
c PRP029 Porphyria 56 0.021
636
P BRN019 Bernard-Soulier Syndrome 56 0.021
637
c OCL002 Oculocutaneous Albinism 56 0.021
638
PTT006 Pituitary Adenoma 56 0.021
639
LST001 Listeriosis 56 0.021
640
c ENC004 Encephalitis 56 0.021
641
OST011 Osteomalacia 56 0.021
642
P EPD009 Epidermolysis Bullosa Dystrophica 56 0.021
643
P OLG002 Oligodendroglioma 56 0.021
644
NTH001 Netherton Syndrome 56 0.021
645
P CMP005 Campomelic Dysplasia 56 0.021
646
P RST001 Restless Legs Syndrome 56 0.021
647
KRT004 Keratitis 56 0.021
648
P PSR001 Psoriatic Arthritis 56 0.021
649
ALP004 Alport Syndrome 55 0.021
650
TST014 Testicular Cancer 55 0.021
651
c THR005 Thrombotic Thrombocytopenic Purpura 55 0.021
652
ETN001 Eating Disorder 55 0.021
653
CHL068 Cholestasis 55 0.021
654
c HRM001 Hermansky-Pudlak Syndrome 55 0.021
655
P CNJ013 Conjunctivitis 55 0.021
656
SCR008 Scrub Typhus 55 0.021
657
EPD006 Epidermolysis Bullosa Acquisita 55 0.021
658
c OST026 Osteogenesis Imperfecta Type I 55 0.021
659
VSC002 Vascular Dementia 55 0.021
660
NPH051 Nephritis 55 0.021
661
P CND004 Candidiasis 55 0.021
662
ALL009 Allergic Conjunctivitis 55 0.021
663
STF001 Stiff-Person Syndrome 55 0.021
664
RBR001 Roberts Syndrome 55 0.021
665
P INT030 Intracranial Aneurysm 55 0.021
666
PRX003 Paroxysmal Nocturnal Hemoglobinuria 55 0.021
667
c MCP010 Mucopolysaccharidosis 55 0.021
668
ARS001 Aarskog-Scott Syndrome 55 0.021
669
c SYP003 Syphilis 55 0.021
670
P PNC001 Pancytopenia 55 0.021
671
LRN003 Learning Disability 54 0.021
672
MNK003 Muenke Syndrome 54 0.021
673
HRD010 Hereditary Spastic Paraplegia 54 0.021
674
FLT001 Felty's Syndrome 54 0.021
675
ACS001 Acoustic Neuroma 54 0.021
676
HST011 Histoplasmosis 54 0.021
677
MVL001 Mevalonic Aciduria 54 0.021
678
P PLY019 Polyneuropathy 54 0.021
679
P FML001 Familial Atrial Fibrillation 54 0.021
680
PNH001 Panhypopituitarism 54 0.021
681
c THR003 Thoracic Aortic Aneurysm 54 0.021
682
CCN001 Cocaine Dependence 54 0.021
683
P ESN007 Eosinophilia 54 0.021
684
P IDP010 Idiopathic Generalized Epilepsy 54 0.021
685
FBR032 Fibromuscular Dysplasia 54 0.021
686
TTH006 Tooth Disease 54 0.021
687
c MCR010 Microcephaly 54 0.021
688
PRT037 Pertussis 54 0.021
689
NRG002 Neurogenic Bladder 54 0.021
690
LYM009 Lymphocytic Choriomeningitis 54 0.021
691
P ANG015 Angioedema 54 0.021
692
MGL001 Megaloblastic Anemia 54 0.021
693
PLM034 Pulmonary Emphysema 53 0.021
694
JVN004 Juvenile Myelomonocytic Leukemia 53 0.021
695
HRD057 Hereditary Pancreatitis 53 0.021
696
ATY010 Atypical Hemolytic-Uremic Syndrome 53 0.021
697
KRN002 Kearns-Sayre Syndrome 53 0.021
698
VRG001 Variegate Porphyria 53 0.021
699
c MYL007 Myeloma 53 0.021
700
P CNT005 Central Nervous System Lymphoma 53 0.021
701
RTN023 Retinitis 53 0.021
702
CHR452 Chorea-Acanthocytosis 53 0.021
703
BNF002 Bone Fracture 53 0.021
704
c CHR345 Chronic Pain 53 0.021
705
CRB039 Cerebrovascular Disease 53 0.021
706
TYP011 Typhus 53 0.021
707
RSC001 Rosacea 53 0.021
708
ACR003 Acrodermatitis Enteropathica 53 0.021
709
OST017 Osteomyelitis 53 0.021
710
SPN020 Spondylosis 53 0.021
711
P LKD001 Leukodystrophy 53 0.021
712
P EPL002 Epilepsy Syndrome 52 0.021
713
P MYM002 Moyamoya Disease 52 0.021
714
RNL015 Renal Hypertension 52 0.021
715
HMG002 Hemoglobinuria 52 0.021
716
HYP043 Hyperandrogenism 52 0.021
717
c HPT007 Hepatitis E 52 0.021
718
VNS003 Venous Insufficiency 52 0.021
719
P SYR001 Syringomyelia 52 0.021
720
c TYR004 Tyrosinemia 52 0.021
721
CHR074 Choriocarcinoma 52 0.021
722
NPH003 Nephrocalcinosis 52 0.021
723
CCN002 Cocaine Abuse 52 0.021
724
CHL069 Cholesteatoma 52 0.021
725
ATP002 Atopy 52 0.021
726
VGT001 Vogt-Koyanagi-Harada Disease 52 0.021
727
PRN011 Pernicious Anemia 52 0.021
728
P JNC001 Junctional Epidermolysis Bullosa 52 0.021
729
CNG048 Congenital Hepatic Fibrosis 52 0.021
730
CNG046 Congenital Fiber-Type Disproportion 52 0.021
731
P CYS010 Cystinosis 51 0.021
732
MLT006 Multidrug-Resistant Tuberculosis 51 0.021
733
P WVR001 Weaver Syndrome 51 0.021
734
ART004 Aortic Atherosclerosis 51 0.021
735
P PRT039 Proteinuria 51 0.021
736
c SPN049 Spinocerebellar Ataxia 51 0.021
737
TCL003 T Cell Deficiency 51 0.021
738
P HYP027 Hypobetalipoproteinemia 51 0.021
739
FBR009 Fibrous Dysplasia 51 0.021
740
c VSC005 Vesicoureteral Reflux 51 0.021
741
P MSC003 Muscular Atrophy 51 0.021
742
c LSS002 Lissencephaly 51 0.021
743
P MYC008 Myocarditis 51 0.021
744
P PYL005 Pyelonephritis 51 0.021
745
CNN005 Connective Tissue Disease 51 0.021
746
LPT001 Leptospirosis 50 0.021
747
P TYR002 Tyrosinemia Type I 50 0.021
748
FMR011 Fumarate Hydratase Deficiency 50 0.021
749
MTN003 Motion Sickness 50 0.021
750
P VTL001 Vitelliform Macular Dystrophy 50 0.021
751
BCL002 B Cell Deficiency 50 0.021
752
ALB002 Albinism 50 0.021
753
WRN002 Wernicke-Korsakoff Syndrome 50 0.021
754
c TRP001 Triple-a Syndrome 50 0.021
755
OST014 Osteopoikilosis 50 0.021
756
MGC001 Megacolon 50 0.021
757
c MCK006 Meckel Syndrome 50 0.021
758
c MCL001 Mucolipidosis 50 0.021
759
WGR001 Wagr Syndrome 50 0.021
760
HYP068 Hyperostosis 50 0.021
761
c INT001 Intrahepatic Cholestasis 50 0.021
762
SJG001 Sjogren's Syndrome 50 0.021
763
P PRM100 Primary Spontaneous Pneumothorax 49 0.021
764
CNT047 Contact Dermatitis 49 0.021
765
TLP001 Talipes Equinovarus 49 0.021
766
BLD034 Bile Duct Carcinoma 49 0.021
767
PLC003 Placental Site Trophoblastic Tumor 49 0.021
768
SYN036 Syncope 49 0.021
769
c JBR001 Joubert Syndrome 49 0.021
770
P HRD021 Hereditary Sensory Neuropathy 49 0.021
771
APH002 Aphasia 49 0.021
772
PRM013 Premature Menopause 49 0.021
773
NPH011 Nephroblastoma 49 0.021
774
LYM022 Lymphangioma 49 0.021
775
MYX004 Myxedema 49 0.021
776
MCR037 Macroglossia 49 0.021
777
PRM052 Primary Progressive Aphasia 48 0.021
778
c MYP011 Myopathy Congenital 48 0.021
779
BRS051 Breast Disease 48 0.021
780
P PRM030 Permanent Neonatal Diabetes Mellitus 48 0.021
781
ASP001 Asperger Syndrome 48 0.021
782
PRM003 Premature Ejaculation 48 0.021
783
NRM004 Neuroma 48 0.021
784
P HLL001 Hallermann-Streiff Syndrome 48 0.021
785
P RCS002 Recessive Dystrophic Epidermolysis Bullosa 48 0.021
786
c OST019 Osteosclerosis 48 0.021
787
c BRC006 Brachydactyly 48 0.021
788
MTB004 Metabolic Acidosis 48 0.021
789
ISL003 Isolated Growth Hormone Deficiency 47 0.021
790
CVR006 Cavernous Hemangioma 47 0.021
791
NPH021 Nephropathic Cystinosis 47 0.021
792
FND001 Fundus Albipunctatus 47 0.021
793
P AML002 Amelogenesis Imperfecta 47 0.021
794
LCH009 Lichen Sclerosus 47 0.021
795
LDP002 Lead Poisoning 47 0.021
796
P CRB126 Cerebral Cavernous Malformation 47 0.021
797
CRN030 Coronary Stenosis 47 0.021
798
P SJG002 Sjogren-Larsson Syndrome 47 0.021
799
P RBN002 Robinow Syndrome 47 0.021
800
PRC012 Pericardial Effusion 47 0.021
801
EBS001 Ebstein Anomaly 47 0.021
802
OVR006 Ovarian Endometriosis 47 0.021
803
P CYS018 Cystitis 47 0.021
804
c PSD003 Pseudohypoaldosteronism 46 0.021
805
P KRT007 Keratoconus 46 0.021
806
CMB021 Combined Pituitary Hormone Deficiency 46 0.021
807
VRN004 Vernal Keratoconjunctivitis 46 0.021
808
CHN015 Chondrodysplasia 46 0.021
809
P CHR104 Chorea 46 0.021
810
P LYD001 Leydig Cell Tumor 46 0.021
811
GST045 Gastroenteritis 46 0.021
812
P FRS003 Fraser Syndrome 46 0.021
813
PRT019 Protein-Losing Enteropathy 46 0.021
814
c GNG009 Gangliosidosis 46 0.021
815
NRX001 Neuroaxonal Dystrophy 46 0.021
816
BCK006 Back Pain 46 0.021
817
SPN019 Spondylolisthesis 45 0.021
818
P HYP192 Hypocalcemia, Autosomal Dominant 45 0.021
819
WLM001 Wolman Disease 45 0.021
820
BLL001 Baller-Gerold Syndrome 45 0.021
821
ACR005 Acrodermatitis 45 0.021
822
LPM005 Lipomatosis 45 0.021
823
c FML024 Familial Melanoma 45 0.021
824
P CMP008 Compartment Syndrome 45 0.021
825
P GRM009 Germ Cell Tumors 45 0.021
826
AGR002 Agoraphobia 45 0.021
827
c ERL020 Early-Onset Schizophrenia 44 0.021
828
GRN007 Granuloma Annulare 44 0.021
829
P OVR046 Ovarian Cyst 44 0.021
830
NRN008 Neuronal Intranuclear Inclusion Disease 44 0.021
831
NDL021 Nodular Lymphocyte Predominant Hodgkin Lymphoma 44 0.021
832
DSC009 Discoid Lupus Erythematosus 44 0.021
833
PPL018 Papillary Adenocarcinoma 44 0.021
834
MCL007 Macular Dystrophy 44 0.021
835
FCL041 Focal Myositis 44 0.021
836
OCL020 Ocular Cicatricial Pemphigoid 44 0.021
837
AND001 Anodontia 44 0.021
838
SDR003 Sideroblastic Anemia 44 0.021
839
c CND005 Cone Dystrophy 43 0.021
840
GRM004 Germinoma 43 0.021
841
ATR057 Atrioventricular Block 43 0.021
842
c INT064 Intermediate Uveitis 43 0.021
843
ASP002 Aspartylglucosaminuria 43 0.021
844
PLM035 Pulmonary Eosinophilia 43 0.021
845
ACN014 Acanthocytosis 43 0.021
846
PRV006 Pervasive Developmental Disorder 43 0.021
847
ALX002 Alexithymia 43 0.021
848
KWS001 Kwashiorkor 43 0.021
849
FLL008 Folliculitis 43 0.021
850
c STC001 Stickler Syndrome 43 0.021
851
PSD002 Pseudotumor Cerebri 43 0.021
852
c PRM001 Primary Cutaneous Amyloidosis 42 0.021
853
MNN021 Meningococcemia 42 0.021
854
ALP014 Alpha-Thalassemia/mental Retardation Syndrome 42 0.021
855
c MSB002 Mesoblastic Nephroma 42 0.021
856
ESN005 Eosinophilic Gastroenteritis 42 0.021
857
HYP120 Hypoaldosteronism 42 0.021
858
SCT005 Scott Syndrome 42 0.021
859
INT063 Intellectual Disability 42 0.021
860
WRT003 Warthin Tumor 42 0.021
861
QDR001 Quadriplegia 42 0.021
862
DBW001 Dubowitz Syndrome 42 0.021
863
RNL029 Renal Coloboma Syndrome 42 0.021
864
CRD053 Cardiovascular Disease Risk Factor 42 0.021
865
MGL013 Megalencephaly 41 0.021
866
c MLG086 Malignant Hyperthermia Susceptibility 41 0.021
867
SPN050 Spinocerebellar Degeneration 41 0.021
868
NNT016 Neonatal Hemochromatosis 41 0.021
869
SPS007 Spastic Cerebral Palsy 41 0.021
870
OCL001 Ocular Albinism 41 0.021
871
CHR078 Chorioretinitis 41 0.021
872
GND001 Gonadoblastoma 41 0.021
873
c TRC005 Tracheal Stenosis 40 0.021
874
CLS008 Clostridium Difficile 40 0.021
875
DFF021 Diffuse Mesangial Sclerosis 40 0.021
876
FND002 Fundus Dystrophy 40 0.021
877
RTT001 Ritter's Disease 40 0.021
878
FTL007 Fetal Hydantoin Syndrome 40 0.021
879
CD4002 Cd40 Deficiency 40 0.021
880
c SNR001 Senior-Loken Syndrome 40 0.021
881
PLG004 Plagiocephaly 40 0.021
882
P CNG024 Congenital Nystagmus 40 0.021
883
P PRR010 Pierre Robin Sequence 39 0.021
884
CND006 Candida Glabrata 39 0.021
885
HRS011 Horseshoe Kidney 39 0.021
886
OLG001 Oligospermia 39 0.021
887
c NRX003 Neuroaxonal Dystrophy, Infantile 39 0.021
888
P SLL003 Salla Disease 39 0.021
889
P MTR002 Mitral Valve Insufficiency 39 0.021
890
SCH008 Schmid Metaphyseal Chondrodysplasia 39 0.021
891
PRS012 Pars Planitis 39 0.021
892
CNG064 Congenital Chloride Diarrhea 38 0.021
893
ENT007 Enteropathica 38 0.021
894
NVS001 Neovascular Glaucoma 38 0.021
895
DLS001 Delusional Disorder 38 0.021
896
c CHR455 Chiari Malformations 38 0.021
897
c CNG029 Congenital Mesoblastic Nephroma 38 0.021
898
EPS026 Epispadias 38 0.021
899
SPC005 Speech Disorder 38 0.021
900
c CHR098 Chronic Pyelonephritis 37 0.021
901
c CTR120 Cataract, Congenital 37 0.021
902
VCL001 Vacuolar Myopathy 37 0.021
903
MRC003 Mercury Poisoning 37 0.021
904
CMP034 Complete Androgen Insensitivity Syndrome 37 0.021
905
NCR002 Necrobiosis Lipoidica 37 0.021
906
CVR010 Cavernous Malformation 37 0.021
907
P CTN015 Cutaneous T Cell Lymphoma 37 0.021
908
P PCH002 Pachygyria 37 0.021
909
DRM011 Dermatophytosis 37 0.021
910
LND001 Landau-Kleffner Syndrome 37 0.021
911
c CRB059 Cerebellar Degeneration 36 0.021
912
P FNG005 Feingold Syndrome 36 0.021
913
MGC004 Megacystis Microcolon Intestinal Hypoperistalsis Syndrome 36 0.021
914
SPS004 Spastic Quadriplegia 36 0.021
915
c PTR004 Pterygium 36 0.021
916
P DYS005 Dyslexia 36 0.021
917
c NRC009 Narcolepsy 1 36 0.021
918
CD4003 Cd40 Ligand Deficiency 35 0.021
919
GST064 Gastric Outlet Obstruction 35 0.021
920
c TRS004 Torsion Dystonia 35 0.021
921
c ACH011 Achondrogenesis 35 0.021
922
IPX001 Ipex Syndrome 35 0.021
923
SPR007 Superior Mesenteric Artery Syndrome 35 0.021
924
RNL022 Renal Vascular Disease 35 0.021
925
MNN017 Mononeuropathy 35 0.021
926
P SPR035 Superior Vena Cava Syndrome 34 0.021
927
TBR006 Tuberculoid Leprosy 34 0.021
928
CNG105 Congenital Lobar Emphysema 34 0.021
929
c PRG001 Progressive Muscular Atrophy 34 0.021
930
c CNG033 Congenital Syphilis 34 0.021
931
P FBR025 Fibrochondrogenesis 34 0.021
932
URT004 Urethral Syndrome 34 0.021
933
P END046 Endometritis 34 0.021
934
LNG030 Lung Adenoma 33 0.021
935
SML028 Semilobar Holoprosencephaly 33 0.021
936
P PTT002 Potter's Syndrome 33 0.021
937
RNL012 Renal Tuberculosis 33 0.021
938
GST007 Gastric Dilatation 33 0.021
939
RNL025 Renal Hypoplasia 32 0.021
940
ATR003 Atrophic Rhinitis 32 0.021
941
ANN005 Annular Pancreas 32 0.021
942
IRR003 Irritant Dermatitis 32 0.021
943
c SPL039 Split Foot 32 0.021
944
SPR034 Superior Limbic Keratoconjunctivitis 32 0.021
945
c INF049 Infantile Myofibromatosis 32 0.021
946
c ACQ027 Acquired Cutis Laxa 32 0.021
947
AMY005 Amyloid Neuropathy 32 0.021
948
PNT019 Pontocerebellar Hypoplasia 32 0.021
949
c PPL025 Popliteal Pterygium Syndrome 31 0.021
950
OBS019 Obesity, Variation in 31 0.021
951
SCH011 Schizotypal Personality Disorder 31 0.021
952
ANG004 Angioid Streaks 31 0.021
953
FCL003 Facial Hemiatrophy 31 0.021
954
LYM097 Lymphatic Malformation 31 0.021
955
NRT001 Neurotic Disorder 31 0.021
956
ENM001 Enamel Caries 31 0.021
957
SMT001 Somatization Disorder 31 0.021
958
NRG004 Neurogenic Diabetes Insipidus 31 0.021
959
RTN006 Retinal Drusen 30 0.021
960
OHT001 Ohtahara Syndrome 30 0.021
961
LYM095 Lymphangiomatosis 30 0.021
962
DFF001 Diffuse Cutaneous Mastocytosis 30 0.021
963
c TRN047 Transient Congenital Hypothyroidism 30 0.021
964
OLM001 Olmsted Syndrome 30 0.021
965
THL009 Thiolase Deficiency 30 0.021
966
SPN029 Spondylolysis 29 0.021
967
INF133 Inferior Vena Cava Interruption 29 0.021
968
NMN003 Niemann–pick Disease 29 0.021
969
BDY001 Body Dysmorphic Disorder 29 0.021
970
SYS006 Say Syndrome 29 0.021
971
GST052 Gestational Choriocarcinoma 29 0.021
972
MST006 Mast Syndrome 29 0.021
973
EXS013 Exstrophy-Epispadias Complex 29 0.021
974
c CNG115 Congenital Myotonic Dystrophy 29 0.021
975
SHK001 Shaken Baby Syndrome 29 0.021
976
DYS012 Dyshidrosis 28 0.021
977
LTM002 Luteoma 28 0.021
978
NRW001 Norwegian Scabies 28 0.021
979
PTC005 Pituicytoma 28 0.021
980
SX2002 Sox2 Anophthalmia Syndrome 28 0.021
981
DVL001 Developmental Coordination Disorder 27 0.021
982
HYP461 Hypocomplementemic Urticarial Vasculitis Syndrome 27 0.021
983
SPR012 Separation Anxiety Disorder 27 0.021
984
LMB014 Limb-Body Wall Complex 27 0.021
985
PRS054 Persistent Truncus Arteriosus 27 0.021
986
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 26 0.021
987
IMM039 Immune Hydrops Fetalis 26 0.021
988
NNT021 Neonatal Meningitis 26 0.021
989
DBT042 Diabetes, Permanent Neonatal 26 0.021
990
HMP008 Hemophagocytic Lymphohistiocytosis, Familial 26 0.021
991
LCH003 Lichen Nitidus 26 0.021
992
c CNT058 Central Nervous System Lymphoma, Primary 26 0.021
993
SPN221 Spina Bifida Occulta 25 0.021
994
P PLM064 Pulmonary Sequestration 25 0.021
995
c FML034 Familial Dystonia 25 0.021
996
c ENL009 Enlarged Parietal Foramina 25 0.021
997
CLR033 Color Vision Deficiency 25 0.021
998
RDT006 Radiation Induced Meningioma 25 0.021
999
HMG004 Hemoglobin D Disease 24 0.021
1000
ACT118 Acute Non Lymphoblastic Leukemia 24 0.021
1001
c BRC038 Brachydactyly Type B 24 0.021
1002
INT011 Interstitial Emphysema 24 0.021
1003
CRN051 Craniofacial Microsomia 24 0.021
1004
SBP004 Subependymoma 24 0.021
1005
c SPN081 Spondylocostal Dysostosis, Autosomal Recessive 23 0.021
1006
ALZ008 Alzheimer Disease Risk Factor 23 0.021
1007
XNT009 Xanthoma Disseminatum 23 0.021
1008
PHT008 Photosensitive Epilepsy 23 0.021
1009
3HY001 3-Hydroxyisobutyric Aciduria 23 0.021
1010
c PRM032 Primary Congenital Glaucoma 23 0.021
1011
RNL094 Renal Dysplasia, Cystic 22 0.021
1012
CLC003 Cloacogenic Carcinoma 22 0.021
1013
P HYP163 Hyperlipidemia Type 3 22 0.021
1014
P CNG369 Congenital Tracheal Stenosis 22 0.021
1015
DDN009 Duodenal Obstruction 22 0.021
1016
PNT005 Pentalogy of Cantrell 22 0.021
1017
P TRC035 Tracheal Agenesis 22 0.021
1018
PLN001 Plantar Wart 21 0.021
1019
RTN019 Retinal Telangiectasia 21 0.021
1020
ACC003 Accommodative Esotropia 21 0.021
1021
AVD001 Avoidant Personality Disorder 21 0.021
1022
MCR039 Macrophagic Myofasciitis 21 0.021
1023
ART034 Aortopulmonary Window 21 0.021
1024
VSL002 Visual Epilepsy 21 0.021
1025
IVC001 Ivic Syndrome 20 0.021
1026
BLD052 Blood Group Incompatibility 20 0.021
1027
BMR002 Beemer-Langer Syndrome 20 0.021
1028
PRR001 Periarthritis 20 0.021
1029
PRT056 Protein R Deficiency 20 0.021
1030
PNS015 Penoscrotal Transposition 19 0.021
1031
c BRC050 Brachydactyly Type D 19 0.021
1032
SLT009 Solitary Bone Cyst 19 0.021
1033
CHL109 Childhood Apraxia of Speech 19 0.021
1034
c SPR036 Supernumerary Nipples 19 0.021
1035
P HYD015 Hydroa Vacciniforme 18 0.021
1036
PLM108 Pulmonary Interstitial Glycogenosis 18 0.021
1037
PRD003 Periodontosis 18 0.021
1038
BRN097 Brainstem Auditory Evoked Responses 18 0.021
1039
P JVN020 Juvenile-Onset Dystonia 18 0.021
1040
FTS001 Fetishism 17 0.021
1041
DCR002 Dacryocystocele 17 0.021
1042
MTR027 Mitral Atresia 17 0.021
1043
LBY003 Labyrinthine Disease 17 0.021
1044
c MLG039 Malignant Essential Hypertension 17 0.021
1045
HYP015 Hyperlucent Lung 16 0.021
1046
c CNG129 Congenital Torticollis 16 0.021
1047
CMB002 Combat Disorder 16 0.021
1048
HYP018 Hyperglobulinemic Purpura 15 0.021
1049
HCS001 Hec Syndrome 15 0.021
1050
DDL001 Didelphys Uterus 15 0.021
1051
MRG006 Morgagni-Stewart-Morel Syndrome 15 0.021
1052
PTN004 Patent Ductus Venosus 15 0.021
1053
CNG329 Congenital Onychodysplasia 15 0.021
1054
CVR008 Cavernous Lymphangioma 15 0.021
1055
c HYD032 Hydatidiform Mole, Recurrent 15 0.021
1056
c DMN011 Dominant Dystrophic Epidermolysis Bullosa 15 0.021
1057
CNT091 Cant� Syndrome 15 0.021
1058
SCH025 Schisis Association 14 0.021
1059
c NNT006 Neonatal Myasthenia Gravis 14 0.021
1060
ELC001 Elective Mutism 14 0.021
1061
FBL006 Fibular Aplasia Ectrodactyly 14 0.021
1062
AQG002 Aquagenic Urticaria 13 0.021
1063
TBR007 Tuberculum Sellae Meningioma 13 0.021
1064
MYL044 Myelocystocele 13 0.021
1065
SPS087 Spasmus Nutans 13 0.021
1066
MCR033 Macrocephaly-Capillary Malformation 13 0.021
1067
ATS090 Autosomal Dominant Neovascular Inflammatory Vitreoretinopathy 13 0.021
1068
CD4004 Cd4 Deficiency 12 0.021
1069
HMF003 Hemifacial Myohyperplasia 12 0.021
1070
SDR005 Sideroblastic Anemia Acquired 11 0.021
1071
RTN127 Retinal Cavernous Hemangioma 11 0.021
1072
ANT002 Anti-Basement Membrane Glomerulonephritis 11 0.021
1073
VLK001 Volkmann Contracture 11 0.021
1074
JVN026 Jeavons Syndrome 10 0.021
1075
P HYP067 Hyperimmunoglobulin Syndrome 10 0.021
1076
RHH001 Rohhad 10 0.021
1077
HYD031 Hydroxyprolinemia 10 0.021
1078
PLM065 Pulmonary Supravalvular Stenosis 10 0.021
1079
KZL001 Kozlowski Brown Hardwick Syndrome 10 0.021
1080
c FML153 Familial Wilms Tumor 9 0.021
1081
OLG008 Oligomeganephronic Renal Hypoplasia 9 0.021
1082
FTZ003 Fitzsimmons Syndrome 9 0.021
1083
FSD001 Fused Mandibular Incisors 9 0.021
1084
MCH006 Mechanical Strabismus 9 0.021
1085
CNG125 Congenital Short Femur 9 0.021
1086
VTR013 Vitreoretinopathy, Neovascular Inflammatory 9 0.021
1087
VLF002 Velo-Facial-Skeletal Syndrome 8 0.021
1088
KCH001 Kocher-Debre-Semelaigne Syndrome 8 0.021
1089
LCH012 Lichstenstein Syndrome 7 0.021
1090
FNG010 Fingerprint Body Myopathy 7 0.021
1091
FML158 Familial Hemangioma 6 0.021
1092
DDY001 Didymosis Aplasticosebacea 6 0.021
1093
c SPL043 Split Hand, Bilateral 6 0.021
1094
OBS014 Obsessive-Compulsive Disorder, Protection Against 5 0.021
1095
P SPL045 Split Foot, Bilateral 5 0.021
1096
FTZ005 Fitzsimmons-Guilbert Syndrome 4 0.021
1097
CNG104 Congenital Ichthyosis, Microcephalus, Quadriplegia 2 0.021
1098
c SPL042 Split Hand, Unilateral 2 0.021