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