Search results for "twinning"

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

958 hits were found for 'twinning'

# Family MCID Name MIFTS Score
1
TWN001 Twin-to-Twin Transfusion Syndrome 48 13.479
2
c RNL090 Renal Tubular Dysgenesis Due to Twin-Twin Transfusion 7 5.071
3
OVR079 Ovarian Response to Fsh Stimulation 7 2.526
4
PLY012 Polyhydramnios 46 0.166
5
P PLY018 Polycythemia 58 0.160
6
ANN002 Anencephaly 57 0.151
7
CRB009 Cerebritis 33 0.147
8
P CRV039 Cervicitis 49 0.114
9
HYD012 Hydrops Fetalis 53 0.110
10
OLG003 Oligohydramnios 51 0.110
11
P OBS005 Obesity 94 0.101
12
P THY032 Thyroiditis 56 0.088
13
DWN001 Down Syndrome 51 0.085
14
MGR002 Migraine 64 0.082
15
P CNG401 Congenital Heart Disease 62 0.082
16
CHR005 Chorioamnionitis 42 0.082
17
CNG069 Congenital Cytomegalovirus 42 0.082
18
CYT008 Cytomegalovirus Infection 39 0.082
19
SRN002 Sirenomelia 29 0.079
20
P LKM002 Leukemia 66 0.076
21
URT039 Urticaria 55 0.076
22
P HYP086 Hypothyroidism 59 0.073
23
P INT060 Intestinal Atresia 42 0.073
24
PYL006 Pyloric Stenosis 41 0.073
25
ECT026 Ectopic Pregnancy 39 0.073
26
P ENC008 Encephalocele 49 0.069
27
OMP004 Omphalocele 43 0.069
28
URT008 Urticaria Pigmentosa 38 0.069
29
ENC005 Encephalomalacia 27 0.069
30
P NRC002 Narcolepsy 67 0.066
31
P TXP001 Toxoplasmosis 56 0.066
32
PST041 Posterior Urethral Valves 50 0.066
33
P PRS038 Personality Disorder 50 0.066
34
URT001 Urethritis 48 0.066
35
P GND004 Gonadal Dysgenesis 43 0.066
36
P HYP009 Hypertrophic Pyloric Stenosis 43 0.066
37
P PLM037 Pulmonary Hypertension 85 0.062
38
P RBN001 Rubinstein-Taybi Syndrome 67 0.062
39
P LPS004 Lupus Erythematosus 67 0.062
40
DRM006 Dermatitis 58 0.062
41
GST009 Gastroschisis 55 0.062
42
CRB037 Cerebral Palsy 55 0.062
43
VCT001 Vacterl Association 55 0.062
44
P ESP024 Esophagitis 54 0.062
45
ISC004 Ischemia 53 0.062
46
P TRT010 Teratoma 50 0.062
47
c CNG021 Congenital Toxoplasmosis 50 0.062
48
KLN001 Klinefelter's Syndrome 47 0.062
49
IMP002 Imperforate Anus 44 0.062
50
RTN023 Retinitis 44 0.062
51
P APL006 Aplasia Cutis Congenita 42 0.062
52
HYD001 Hydranencephaly 33 0.062
53
c BPL002 Bipolar I Disorder 33 0.062
54
AMN009 Amniotic Band Syndrome 27 0.062
55
ACR022 Acardia 12 0.062
56
P ART022 Arthritis 65 0.058
57
P PRM019 Premature Ovarian Failure 63 0.058
58
P BCK002 Beckwith-Wiedemann Syndrome 61 0.058
59
P MST009 Mastocytosis 61 0.058
60
c CNG006 Congenital Hypothyroidism 61 0.058
61
ALC007 Alcohol Dependence 60 0.058
62
P OST009 Osteochondritis Dissecans 59 0.058
63
P LYM026 Lymphoblastic Leukemia 55 0.058
64
P DYS154 Dystonia 55 0.058
65
P MSC005 Muscular Dystrophy 54 0.058
66
P MYP004 Myopathy 53 0.058
67
P DBT005 Diabetes Insipidus 53 0.058
68
CND002 Conduct Disorder 50 0.058
69
PTH002 Pathological Gambling 50 0.058
70
ESP020 Esophageal Atresia 46 0.058
71
TRN007 Transsexualism 42 0.058
72
PRV004 Periventricular Leukomalacia 39 0.058
73
PNT005 Pentalogy of Cantrell 30 0.058
74
LKM006 Leukomalacia 27 0.058
75
P NRF002 Neurofibromatosis 69 0.054
76
P HLP001 Holoprosencephaly 65 0.054
77
P WLM002 Wilms Tumor 70 0.054
78
ATT013 Attention Deficit-Hyperactivity Disorder 63 0.054
79
ANR007 Anorexia Nervosa 62 0.054
80
DMN002 Dementia 58 0.054
81
PLM033 Pulmonary Embolism 56 0.054
82
P ECL001 Eclampsia 53 0.054
83
ART005 Arteriovenous Malformation 53 0.054
84
CTN014 Cutaneous Mastocytosis 53 0.054
85
BLM002 Bulimia Nervosa 49 0.054
86
P MNT147 Mental Retardation 46 0.054
87
TRN044 Transposition of the Great Arteries 41 0.054
88
RFR003 Refractive Error 40 0.054
89
SCR024 Sacrococcygeal Teratoma 40 0.054
90
PLC005 Placental Insufficiency 37 0.054
91
PRT086 Partial Hydatidiform Mole 34 0.054
92
P PLY024 Polymicrogyria 31 0.054
93
CLC011 Cloacal Exstrophy 29 0.054
94
JJN004 Jejunal Atresia 22 0.054
95
P RHM011 Rheumatoid Arthritis 94 0.049
96
c SYS001 Systemic Lupus Erythematosus 91 0.049
97
P SCH015 Schizophrenia 79 0.049
98
NRL016 Neural Tube Defects 78 0.049
99
PTZ001 Peutz-Jeghers Syndrome 68 0.049
100
P NRB001 Neuroblastoma 68 0.049
101
P MYS005 Myositis 63 0.049
102
P HYP055 Hypoplastic Left Heart Syndrome 61 0.049
103
P CRN015 Cornelia De Lange Syndrome 57 0.049
104
INS024 Insulin-Like Growth Factor I 58 0.049
105
P DRM007 Dermatitis Herpetiformis 56 0.049
106
P RNL028 Renal Tubular Dysgenesis 52 0.049
107
ALP008 Alopecia 51 0.049
108
EPD016 Epidermolysis Bullosa 49 0.049
109
ECT006 Ectodermal Dysplasia 48 0.049
110
HLL004 Hellp Syndrome 46 0.049
111
END072 Endotheliitis 44 0.049
112
P ALC004 Alcohol Abuse 48 0.049
113
PSD009 Pseudohermaphroditism 41 0.049
114
P MYP006 Myopia 41 0.049
115
PLC007 Placental Abruption 40 0.049
116
MTS001 Mutism 40 0.049
117
CHN005 Choanal Atresia 39 0.049
118
LMB062 Limb Ischemia 38 0.049
119
ANR040 Aneurysm 35 0.049
120
AST006 Astigmatism 35 0.049
121
EST005 Esotropia 34 0.049
122
PHC006 Phacomatosis Pigmentovascularis 28 0.049
123
EPG004 Epignathus 19 0.049
124
CYS001 Cystic Fibrosis 92 0.044
125
P MYC007 Myocardial Infarction 81 0.044
126
P BRS047 Breast Cancer 90 0.044
127
TBR010 Tuberculosis 73 0.044
128
P SCL016 Scleroderma 76 0.044
129
P BPL003 Bipolar Disorder 65 0.044
130
ANR002 Aniridia 61 0.044
131
PRT036 Peritonitis 61 0.044
132
c PRC016 Pre-Eclampsia 58 0.044
133
P HPT021 Hepatitis 55 0.044
134
P HYP076 Hyperthyroidism 54 0.044
135
GRV001 Graves' Disease 54 0.044
136
P PSR002 Psoriasis 54 0.044
137
GTR002 Goiter 53 0.044
138
P ATS007 Autism Spectrum Disorder 56 0.044
139
P ATX004 Ataxia 50 0.044
140
P HYP065 Hyperaldosteronism 49 0.044
141
END020 Endocardial Fibroelastosis 49 0.044
142
P PLY006 Polydactyly 48 0.044
143
DDN006 Duodenitis 48 0.044
144
ACR012 Aicardi Syndrome 46 0.044
145
P CRV043 Cervical Dystonia 45 0.044
146
THR013 Thoracic Outlet Syndrome 45 0.044
147
GND002 Gender Identity Disorder 43 0.044
148
MGR003 Migraine with Aura 41 0.044
149
P ART084 Arteriovenous Fistula 40 0.044
150
BRX001 Bruxism 39 0.044
151
P TRC086 Trichohepatoenteric Syndrome 1 39 0.044
152
DYS018 Dysostosis 38 0.044
153
GYN001 Gynecomastia 37 0.044
154
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 38 0.044
155
SPS057 Spasticity 32 0.044
156
PLM074 Pulmonary Function 30 0.044
157
SLP010 Slipped Capital Femoral Epiphysis 23 0.044
158
ANS004 Anisometropia 22 0.044
159
CLN022 Colonic Atresia 22 0.044
160
JMC001 Jamaican Vomiting Sickness 14 0.044
161
PHC005 Phacomatosis Pigmentokeratotica 11 0.044
162
P AST005 Asthma 84 0.038
163
P OST005 Osteogenesis Imperfecta 77 0.038
164
P ATX030 Ataxia-Telangiectasia 76 0.038
165
HV1006 Hiv-1 83 0.038
166
P CLC005 Celiac Disease 69 0.038
167
AND015 Androgen Insensitivity 69 0.038
168
P ANG001 Angelman Syndrome 66 0.038
169
KWS002 Kawasaki Disease 66 0.038
170
P PNM007 Pneumonia 64 0.038
171
c NRF018 Neurofibromatosis, Type 1 65 0.038
172
P THL005 Thalassemia 64 0.038
173
BRN024 Bronchitis 62 0.038
174
OVR029 Ovarian Hyperstimulation Syndrome 60 0.038
175
ANX002 Anxiety Disorder 60 0.038
176
P NPH012 Nephrotic Syndrome 60 0.038
177
P HMP007 Hemophilia 59 0.038
178
P TRN020 Turner Syndrome 58 0.038
179
P NTR004 Neutropenia 56 0.038
180
ATH003 Atherosclerosis 56 0.038
181
P CNG015 Congenital Diaphragmatic Hernia 56 0.038
182
P THR014 Thrombocytopenia 56 0.038
183
MLN008 Melanoma 55 0.038
184
ACN002 Acanthosis Nigricans 55 0.038
185
P HST010 Histiocytosis 55 0.038
186
P FTL001 Fetal Alcohol Syndrome 54 0.038
187
P HYP040 Hypospadias 54 0.038
188
CLB001 Coloboma 54 0.038
189
EYD002 Eye Disease 54 0.038
190
P AGM001 Agammaglobulinemia 59 0.038
191
P NPH009 Nephrolithiasis 51 0.038
192
CLF001 Cleft Lip 51 0.038
193
LNG024 Langerhans-Cell Histiocytosis 51 0.038
194
VGN023 Vaginitis 51 0.038
195
P HMP006 Hemiplegic Migraine 50 0.038
196
DGN001 Degenerative Disc Disease 50 0.038
197
P CTS001 Cutis Laxa 50 0.038
198
TTH002 Tooth Agenesis 49 0.038
199
ARC007 Arachnoid Cysts 49 0.038
200
P ADN016 Adenocarcinoma 49 0.038
201
VND002 Van Der Woude Syndrome 48 0.038
202
P DND001 Dandy-Walker Syndrome 48 0.038
203
P VNT002 Ventricular Septal Defect 47 0.038
204
P BLN003 Blindness 47 0.038
205
GRW007 Growth Hormone Deficiency 46 0.038
206
PPL021 Papilledema 46 0.038
207
URN010 Urinary Tract Obstruction 45 0.038
208
TRP014 Triploidy 45 0.038
209
P SPN183 Spontaneous Pneumothorax 45 0.038
210
MCN017 Meconium Ileus 44 0.038
211
TRC040 Tracheoesophageal Fistula 44 0.038
212
P NNT009 Neonatal Diabetes Mellitus 44 0.038
213
MCR103 Microtia 44 0.038
214
SYN005 Synostosis 43 0.038
215
PNM008 Pneumothorax 43 0.038
216
P CNG018 Congenital Heart Block 42 0.038
217
CHN016 Cohen Syndrome 40 0.038
218
SBS004 Substance Dependence 40 0.038
219
c SVR005 Severe Pre-Eclampsia 40 0.038
220
PRP016 Paraplegia 40 0.038
221
TYP015 Type 2b Von Willebrand Disease 39 0.038
222
ARC002 Arachnoiditis 39 0.038
223
ILS001 Ileus 38 0.038
224
CNN001 Cannabis Dependence 33 0.038
225
CNN002 Cannabis Abuse 29 0.038
226
CYT004 Cytomegalic Inclusion Disease 28 0.038
227
OCC011 Occipital Encephalocele 25 0.038
228
GST058 Gestational Diabetes Insipidus 11 0.038
229
FRM001 Freemartinism 10 0.038
230
ADR007 Adrenoleukodystrophy 76 0.031
231
P PFF001 Pfeiffer Syndrome 74 0.031
232
P TYS001 Tay-Sachs Disease 73 0.031
233
c HMP004 Hemophilia B 72 0.031
234
P MDL005 Medulloblastoma 71 0.031
235
P OST002 Osteoporosis 71 0.031
236
INC002 Inclusion Body Myositis 71 0.031
237
DCH001 Duchenne Muscular Dystrophy 78 0.031
238
ACH004 Achondroplasia 68 0.031
239
SVR004 Severe Combined Immunodeficiency 68 0.031
240
TTR001 Tetralogy of Fallot 67 0.031
241
VNW001 Von Willebrand's Disease 67 0.031
242
CRH001 Crohn's Disease 71 0.031
243
P HYP035 Hypophosphatasia 64 0.031
244
BLM001 Bloom Syndrome 64 0.031
245
P PNC025 Panic Disorder 64 0.031
246
P MYS003 Myasthenia Gravis 64 0.031
247
PCK002 Pick Disease 64 0.031
248
P NMN002 Niemann-Pick Disease 63 0.031
249
ART016 Aortic Aneurysm 62 0.031
250
P SDD001 Sudden Infant Death Syndrome 62 0.031
251
c HYP595 Hypertension, Essential 66 0.031
252
PRG004 Progeria 61 0.031
253
P ATR011 Atrial Fibrillation 62 0.031
254
DNY001 Denys-Drash Syndrome 61 0.031
255
P HMN010 Hemangioma 60 0.031
256
P KLL001 Kallmann Syndrome 60 0.031
257
P PLY011 Polycystic Ovary Syndrome 59 0.031
258
P HYP061 Hypertrophic Cardiomyopathy 59 0.031
259
P GLM007 Glomerulonephritis 59 0.031
260
P END044 Endometriosis 59 0.031
261
VSC007 Vascular Disease 59 0.031
262
P RCK004 Rickets 58 0.031
263
P MNN013 Meningitis 58 0.031
264
WLL001 Williams-Beuren Syndrome 58 0.031
265
c ATM003 Autoimmune Thyroiditis 58 0.031
266
P HRP006 Herpes Simplex 63 0.031
267
P MYT002 Myotonic Dystrophy 57 0.031
268
P SLV001 Silver-Russell Syndrome 57 0.031
269
P KDN018 Kidney Disease 57 0.031
270
P UVT001 Uveitis 57 0.031
271
CDL003 Caudal Regression Syndrome 57 0.031
272
P ATP001 Atopic Dermatitis 56 0.031
273
P HRD011 Hereditary Spherocytosis 56 0.031
274
LPM004 Lipoma 56 0.031
275
P BRG001 Brugada Syndrome 56 0.031
276
ADN018 Adenoma 55 0.031
277
P SCH018 Schizencephaly 55 0.031
278
SMT008 Smith-Magenis Syndrome 56 0.031
279
CHR066 Chronic Fatigue Syndrome 55 0.031
280
P RHB017 Rhabdoid Tumor 54 0.031
281
P RHN004 Rhinitis 54 0.031
282
PRP030 Purpura 54 0.031
283
DFC004 Deficiency Anemia 54 0.031
284
P KLP003 Klippel-Feil Syndrome 54 0.031
285
P NPH005 Nephronophthisis 54 0.031
286
P ACR001 Aicardi-Goutieres Syndrome 54 0.031
287
MYL020 Myelomeningocele 54 0.031
288
P RBL001 Rubella 53 0.031
289
HYP056 Hypoglycemia 53 0.031
290
ELL001 Ellis-Van Creveld Syndrome 53 0.031
291
P AND016 Andersen Syndrome 54 0.031
292
P INT070 Intestinal Obstruction 53 0.031
293
TST014 Testicular Cancer 53 0.031
294
P NRP001 Neuropathy 52 0.031
295
ART031 Aortic Coarctation 52 0.031
296
MYC002 Mycobacterium Avium Complex Disease 51 0.031
297
P HYP080 Hypogonadism 51 0.031
298
P GLY013 Glycogen Storage Disease 51 0.031
299
c LCL006 Localized Scleroderma 51 0.031
300
P PRM011 Primary Ciliary Dyskinesia 51 0.031
301
c CNG124 Congenital Rubella 51 0.031
302
SCB001 Scabies 50 0.031
303
P THR003 Thoracic Aortic Aneurysm 50 0.031
304
P CTR002 Cataract 50 0.031
305
HDC001 Headache 50 0.031
306
P OCL002 Oculocutaneous Albinism 50 0.031
307
P MYC008 Myocarditis 50 0.031
308
ANT011 Antisocial Personality Disorder 50 0.031
309
P AXN010 Axenfeld-Rieger Syndrome, Type 3 50 0.031
310
CHR001 Churg-Strauss Syndrome 49 0.031
311
GNR004 Generalized Anxiety Disorder 49 0.031
312
ANR004 Anuria 48 0.031
313
ANR018 Anorchia 48 0.031
314
P FTL009 Fetal Akinesia Deformation Sequence 48 0.031
315
ART001 Arterial Tortuosity Syndrome 48 0.031
316
KRT006 Keratoconjunctivitis 48 0.031
317
c FML023 Familial Hemiplegic Migraine 48 0.031
318
c SPN225 Spondyloarthropathy 1 48 0.031
319
SCL003 Social Phobia 48 0.031
320
ANK001 Ankylosis 48 0.031
321
P PRN026 Porencephaly 48 0.031
322
RTN017 Retinal Detachment 48 0.031
323
HTR003 Heterotaxy 48 0.031
324
PRT082 Preterm Premature Rupture of the Membranes 47 0.031
325
SBC001 Subacute Sclerosing Panencephalitis 47 0.031
326
P HYP014 Hyperuricemia 47 0.031
327
HYP458 Hyper Ige Syndrome 47 0.031
328
P FBR031 Febrile Seizures 47 0.031
329
P BCL006 B-Cell Lymphomas 47 0.031
330
P LFT003 Left Ventricular Noncompaction 46 0.031
331
STS002 Situs Inversus 46 0.031
332
RNL078 Renal Dysplasia 46 0.031
333
c JVN003 Juvenile Xanthogranuloma 46 0.031
334
P VSC005 Vesicoureteral Reflux 46 0.031
335
ACQ007 Acquired Immunodeficiency Syndrome 46 0.031
336
P EPS003 Episodic Ataxia 45 0.031
337
P KRT007 Keratoconus 45 0.031
338
FRZ001 Frozen Shoulder 45 0.031
339
CLR003 Clear Cell Adenocarcinoma 44 0.031
340
HMG005 Hemoglobinopathy 44 0.031
341
HMP005 Hemiplegia 44 0.031
342
P STR020 Strabismus 44 0.031
343
P DRR001 Diarrhea 44 0.031
344
ALB002 Albinism 43 0.031
345
CLS010 Cluster Headache 43 0.031
346
RFL001 Reflex Sympathetic Dystrophy 43 0.031
347
P HML001 Hemolytic-Uremic Syndrome 43 0.031
348
IMP004 Impetigo 43 0.031
349
CNV002 Conversion Disorder 42 0.031
350
LCH009 Lichen Sclerosus 42 0.031
351
P SPN016 Spondylocostal Dysostosis 42 0.031
352
DRG003 Drug Dependence 41 0.031
353
TLN003 Telangiectasis 41 0.031
354
P PRV002 Periventricular Nodular Heterotopia 41 0.031
355
PTY003 Pityriasis Rubra Pilaris 41 0.031
356
PLC001 Placenta Accreta 41 0.031
357
KLN002 Kleine-Levin Syndrome 40 0.031
358
NNT012 Neonatal Jaundice 40 0.031
359
CNN003 Conn's Syndrome 40 0.031
360
MTG002 Mutagen Sensitivity 40 0.031
361
HRM002 Hermaphroditism 40 0.031
362
IMG001 Image Syndrome 39 0.031
363
BRD004 Borderline Personality Disorder 39 0.031
364
MYS001 Myositis Ossificans 39 0.031
365
KRT012 Keratoderma 39 0.031
366
P INF037 Inflammatory Bowel Disease 39 0.031
367
P PRS062 Persistent Hyperplastic Primary Vitreous 39 0.031
368
DDN011 Duodenal Atresia 38 0.031
369
CRN025 Corneal Dystrophy 38 0.031
370
c SBC007 Subacute Thyroiditis 38 0.031
371
APR001 Apraxia 38 0.031
372
DXT001 Dextrocardia 37 0.031
373
P CHR342 Chiari Malformation 37 0.031
374
TRN012 Transient Global Amnesia 37 0.031
375
NRN002 Neuronitis 36 0.031
376
c INF069 Infantile Neuroaxonal Dystrophy 1 36 0.031
377
NNT019 Neonatal Hypothyroidism 36 0.031
378
CND006 Candida Glabrata 36 0.031
379
FRY002 Fryns Syndrome 36 0.031
380
TRC010 Trichotillomania 35 0.031
381
IRT001 Iritis 35 0.031
382
CRN088 Craniorachischisis 35 0.031
383
SPL040 Split Hand 35 0.031
384
KBG001 Kbg Syndrome 35 0.031
385
PHC013 Phaeochromocytoma 34 0.031
386
P MNN007 Meningocele 34 0.031
387
MSC006 Muscle Glycogenosis 34 0.031
388
BLP004 Blepharophimosis 33 0.031
389
c ART101 Aortic Valve Disease 2 32 0.031
390
PRN019 Perinatal Necrotizing Enterocolitis 31 0.031
391
PSL001 Pasli Disease 30 0.031
392
ADS002 Adie Syndrome 30 0.031
393
P ATX010 Ataxia Neuropathy Spectrum 29 0.031
394
RTR008 Root Resorption 29 0.031
395
TRD003 Taurodontism 29 0.031
396
CRV025 Cervical Incompetence 28 0.031
397
UND005 Undifferentiated Pleomorphic Sarcoma 28 0.031
398
TFT003 Tufting Enteropathy 26 0.031
399
MYF001 Myofibroma 25 0.031
400
HNM002 Hinman Syndrome 26 0.031
401
BLN010 Balanitis 24 0.031
402
HYP362 Hyperopia 24 0.031
403
P NNT042 Neonatal Lupus Erythematosus 23 0.031
404
LMB009 Lambdoid Synostosis 23 0.031
405
NRC003 Narcissistic Personality Disorder 23 0.031
406
CDL005 Caudal Duplication Anomaly 23 0.031
407
IRN002 Iron Metabolism Disease 22 0.031
408
FXF001 Fox Fordyce Disease 22 0.031
409
FXC001 Foix Chavany Marie Syndrome 22 0.031
410
NNT018 Neonatal Herpes 21 0.031
411
RGH009 Right Atrial Isomerism 20 0.031
412
HYP179 Hypertrichosis Congenital Generalized X-Linked 20 0.031
413
BLN002 Balanitis Xerotica Obliterans 19 0.031
414
BRW006 Brown Syndrome 19 0.031
415
CLC002 Calcaneonavicular Coalition 18 0.031
416
c BNG076 Benign Exophthalmos Syndrome 19 0.031
417
TWN005 Twenty-Nail Dystrophy 17 0.031
418
AND005 Androgen Insensitivity Syndrome, Mild 17 0.031
419
IMP001 Impetigo Herpetiformis 16 0.031
420
ART109 Arterial Thoracic Outlet Syndrome 17 0.031
421
CLP002 Colpocephaly 15 0.031
422
WLS002 Wilson-Mikity Syndrome 14 0.031
423
OMP002 Omphalocele Exstrophy Imperforate Anus 14 0.031
424
TRG006 Trigger Thumb 12 0.031
425
FBL005 Fibular Aplasia 11 0.031
426
SYM006 Symmetrical Thalamic Calcifications 11 0.031
427
TRG003 Trigeminal Nerve Disease 9 0.031
428
P ALZ034 Alzheimer Disease 100 0.022
429
P CLR023 Colorectal Cancer 96 0.022
430
HDG012 Hodgkin Lymphoma 79 0.022
431
P MTC003 Metachromatic Leukodystrophy 76 0.022
432
P DLT002 Dilated Cardiomyopathy 77 0.022
433
FBR012 Fabry Disease 76 0.022
434
c MLT019 Multiple Myeloma 75 0.022
435
P HMC003 Hemochromatosis 75 0.022
436
P RTN024 Retinoblastoma 75 0.022
437
SMT004 Smith-Lemli-Opitz Syndrome 74 0.022
438
P RTT002 Rett Syndrome 73 0.022
439
P ALG002 Alagille Syndrome 73 0.022
440
CDS001 Cadasil 73 0.022
441
P CRN211 Coronary Artery Disease 73 0.022
442
P RTN008 Retinitis Pigmentosa 72 0.022
443
P LPR003 Leprosy 71 0.022
444
P OST012 Osteoarthritis 80 0.022
445
P CLD001 Cleidocranial Dysplasia 70 0.022
446
P GCH001 Gaucher's Disease 70 0.022
447
MLT021 Multiple System Atrophy 70 0.022
448
OBS002 Obsessive-Compulsive Disorder 69 0.022
449
P WSK001 Wiskott-Aldrich Syndrome 69 0.022
450
ACR007 Acromegaly 69 0.022
451
P TBR001 Tuberous Sclerosis 68 0.022
452
P MYL005 Myelofibrosis 68 0.022
453
CRZ001 Crouzon Syndrome 68 0.022
454
CMM004 Common Variable Immunodeficiency 67 0.022
455
P ALX003 Alexander Disease 66 0.022
456
P DMN001 Diamond-Blackfan Anemia 66 0.022
457
P FRG001 Fragile X Syndrome 66 0.022
458
WLF001 Wolff-Parkinson-White Syndrome 65 0.022
459
ADD001 Addison's Disease 65 0.022
460
c HMP029 Hemophilia a 66 0.022
461
APR006 Apert Syndrome 66 0.022
462
P MYL006 Myeloid Leukemia 64 0.022
463
HST011 Histoplasmosis 64 0.022
464
P EPD002 Epidermolytic Hyperkeratosis 64 0.022
465
ALL003 Allergic Rhinitis 63 0.022
466
THY028 Thyroid Cancer 63 0.022
467
CHR063 Chronic Mucocutaneous Candidiasis 63 0.022
468
P AMY004 Amyloidosis 63 0.022
469
ASP006 Aspergillosis 63 0.022
470
TNG002 Tangier Disease 63 0.022
471
P CCK001 Cockayne Syndrome 62 0.022
472
MLG056 Malignant Hyperthermia 62 0.022
473
P DRM010 Dermatomyositis 62 0.022
474
P PND002 Pendred Syndrome 62 0.022
475
P LNG028 Long Qt Syndrome 62 0.022
476
P LVR013 Liver Disease 62 0.022
477
ATS001 Autistic Disorder 61 0.022
478
P VLC001 Velocardiofacial Syndrome 60 0.022
479
P HRM001 Hermansky-Pudlak Syndrome 60 0.022
480
P CHR071 Charcot-Marie-Tooth Disease 60 0.022
481
BLS001 Blau Syndrome 60 0.022
482
P ALP004 Alport Syndrome 60 0.022
483
P BDD001 Budd-Chiari Syndrome 61 0.022
484
c SYS004 Systemic Mastocytosis 60 0.022
485
KRT004 Keratitis 60 0.022
486
P CRN037 Craniosynostosis 60 0.022
487
P PRD008 Periodontitis 59 0.022
488
CST001 Costello Syndrome 59 0.022
489
P PNC044 Pancreatitis 59 0.022
490
GST092 Gastroesophageal Reflux 60 0.022
491
SCR008 Scrub Typhus 59 0.022
492
PSD007 Pseudomyxoma Peritonei 59 0.022
493
CMP005 Campomelic Dysplasia 59 0.022
494
c JVN010 Juvenile Rheumatoid Arthritis 59 0.022
495
P STM004 Stomach Cancer 59 0.022
496
P INF038 Influenza 67 0.022
497
CRB039 Cerebrovascular Disease 59 0.022
498
FCT003 Factor X Deficiency 58 0.022
499
P RTH001 Rothmund-Thomson Syndrome 58 0.022
500
OLV001 Olivopontocerebellar Atrophy 58 0.022
501
c FML001 Familial Atrial Fibrillation 58 0.022
502
P HYP004 Hypercalcemia 57 0.022
503
ALL008 Allergic Bronchopulmonary Aspergillosis 57 0.022
504
ALP001 Alopecia Universalis 57 0.022
505
P PRP029 Porphyria 57 0.022
506
WGR001 Wagr Syndrome 57 0.022
507
CYS010 Cystinosis 57 0.022
508
VSC011 Vasculitis 57 0.022
509
CRY002 Cryptorchidism 57 0.022
510
MNK003 Muenke Syndrome 56 0.022
511
P PRM006 Primary Biliary Cirrhosis 56 0.022
512
GLC085 Glucose-6-Phosphate Dehydrogenase Deficiency 57 0.022
513
P GT001 Gout 56 0.022
514
ARS001 Aarskog-Scott Syndrome 56 0.022
515
ULC004 Ulcerative Colitis 63 0.022
516
MGL001 Megaloblastic Anemia 56 0.022
517
P ENC004 Encephalitis 56 0.022
518
STT001 Status Epilepticus 56 0.022
519
CHL014 Cholera 56 0.022
520
P ALP009 Alopecia Areata 56 0.022
521
P MCP010 Mucopolysaccharidosis 56 0.022
522
MXD005 Mixed Connective Tissue Disease 56 0.022
523
P ANT006 Antiphospholipid Syndrome 55 0.022
524
FLT001 Felty's Syndrome 55 0.022
525
EPD006 Epidermolysis Bullosa Acquisita 55 0.022
526
P OLG002 Oligodendroglioma 55 0.022
527
P INT001 Intrahepatic Cholestasis 55 0.022
528
CCT002 Cicatricial Pemphigoid 55 0.022
529
ATP002 Atopy 55 0.022
530
RHM001 Rheumatic Fever 55 0.022
531
ART111 Artery Disease 55 0.022
532
PRT011 Protein C Deficiency 54 0.022
533
BLL003 Bell's Palsy 54 0.022
534
CYS005 Cysticercosis 54 0.022
535
P ALT001 Alternating Hemiplegia of Childhood 54 0.022
536
CLT003 Colitis 54 0.022
537
P ESN007 Eosinophilia 54 0.022
538
P CND004 Candidiasis 54 0.022
539
c HRD010 Hereditary Spastic Paraplegia 62 0.022
540
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.022
541
PRT037 Pertussis 54 0.022
542
LYM009 Lymphocytic Choriomeningitis 54 0.022
543
CNC002 Cinca Syndrome 55 0.022
544
c MLG069 Malignant Hypertension 54 0.022
545
BCK001 Becker Muscular Dystrophy 61 0.022
546
WLM001 Wolman Disease 53 0.022
547
P MYL007 Myeloma 53 0.022
548
P MLT074 Multiple Endocrine Neoplasia 53 0.022
549
FBR032 Fibromuscular Dysplasia 53 0.022
550
P PLY014 Polycystic Kidney Disease 53 0.022
551
RBR001 Roberts Syndrome 53 0.022
552
LRN003 Learning Disability 53 0.022
553
P HYP050 Hyperinsulinemic Hypoglycemia 53 0.022
554
VGT001 Vogt-Koyanagi-Harada Disease 53 0.022
555
PSY004 Psychotic Disorder 53 0.022
556
P CNJ013 Conjunctivitis 53 0.022
557
P TYR004 Tyrosinemia 53 0.022
558
P SPN049 Spinocerebellar Ataxia 53 0.022
559
P DDN001 Duodenal Ulcer 53 0.022
560
P FRS003 Fraser Syndrome 53 0.022
561
P THR005 Thrombotic Thrombocytopenic Purpura 53 0.022
562
DSS009 Disseminated Intravascular Coagulation 52 0.022
563
STF001 Stiff-Person Syndrome 52 0.022
564
KRN002 Kearns-Sayre Syndrome 52 0.022
565
PTT006 Pituitary Adenoma 52 0.022
566
c PSD066 Pseudohypoparathyroidism, Type Ib 53 0.022
567
ACR003 Acrodermatitis Enteropathica 52 0.022
568
P GNG009 Gangliosidosis 52 0.022
569
P HLL001 Hallermann-Streiff Syndrome 52 0.022
570
P FND001 Fundus Albipunctatus 52 0.022
571
P PLY019 Polyneuropathy 52 0.022
572
PLM001 Pulmonary Tuberculosis 60 0.022
573
ISC006 Ischemic Heart Disease 51 0.022
574
P ANG015 Angioedema 51 0.022
575
CNG048 Congenital Hepatic Fibrosis 51 0.022
576
SPN020 Spondylosis 51 0.022
577
P JNC001 Junctional Epidermolysis Bullosa 51 0.022
578
P STC001 Stickler Syndrome 51 0.022
579
PMP001 Pemphigus 51 0.022
580
P RBN002 Robinow Syndrome 51 0.022
581
PLC003 Placental Site Trophoblastic Tumor 51 0.022
582
MRG003 Marginal Zone B-Cell Lymphoma 51 0.022
583
MGC001 Megacolon 51 0.022
584
PRS047 Prostatitis 51 0.022
585
BLR001 Biliary Atresia 51 0.022
586
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 51 0.022
587
MVL001 Mevalonic Aciduria 51 0.022
588
P EMR001 Emery-Dreifuss Muscular Dystrophy 51 0.022
589
CHR074 Choriocarcinoma 50 0.022
590
PRL009 Prolactinoma 50 0.022
591
c HRD117 Hereditary Breast Cancer 51 0.022
592
P PRM001 Primary Cutaneous Amyloidosis 50 0.022
593
GLC003 Glucose Intolerance 50 0.022
594
P PSR001 Psoriatic Arthritis 50 0.022
595
CHL068 Cholestasis 50 0.022
596
CNN005 Connective Tissue Disease 50 0.022
597
RST001 Restless Legs Syndrome 50 0.022
598
CVR006 Cavernous Hemangioma 50 0.022
599
TMP001 Temporal Lobe Epilepsy 50 0.022
600
OST017 Osteomyelitis 50 0.022
601
NTH001 Netherton Syndrome 49 0.022
602
P SYR001 Syringomyelia 49 0.022
603
P WVR001 Weaver Syndrome 49 0.022
604
HYP266 Hypoxia 49 0.022
605
ETN001 Eating Disorder 49 0.022
606
BRN056 Bronchopulmonary Dysplasia 49 0.022
607
P BRC006 Brachydactyly 49 0.022
608
CHN055 Chanarin-Dorfman Syndrome 50 0.022
609
PRC012 Pericardial Effusion 49 0.022
610
P EPD009 Epidermolysis Bullosa Dystrophica 49 0.022
611
LST001 Listeriosis 49 0.022
612
AMN001 Amenorrhea 49 0.022
613
PRN023 Prion Disease 49 0.022
614
P CNG046 Congenital Fiber-Type Disproportion 49 0.022
615
P DGR001 Digeorge Syndrome 49 0.022
616
P MCR010 Microcephaly 49 0.022
617
FLL008 Folliculitis 49 0.022
618
RNL007 Renal Tubular Acidosis 48 0.022
619
TLP001 Talipes Equinovarus 48 0.022
620
ANH002 Anhidrosis 48 0.022
621
P SYP003 Syphilis 48 0.022
622
VSC002 Vascular Dementia 48 0.022
623
CMP034 Complete Androgen Insensitivity Syndrome 48 0.022
624
P INT030 Intracranial Aneurysm 48 0.022
625
JHN001 Johanson-Blizzard Syndrome 48 0.022
626
P PSD015 Pseudohypoparathyroidism 47 0.022
627
P LSS002 Lissencephaly 47 0.022
628
TYP011 Typhus 47 0.022
629
c RCS002 Recessive Dystrophic Epidermolysis Bullosa 47 0.022
630
P CMP008 Compartment Syndrome 47 0.022
631
P PMP005 Pemphigus Vulgaris 47 0.022
632
PSD002 Pseudotumor Cerebri 47 0.022
633
MTN003 Motion Sickness 47 0.022
634
P SJG002 Sjogren-Larsson Syndrome 47 0.022
635
LPM005 Lipomatosis 47 0.022
636
BLL001 Baller-Gerold Syndrome 47 0.022
637
FBR009 Fibrous Dysplasia 47 0.022
638
P HYP027 Hypobetalipoproteinemia 47 0.022
639
ACR005 Acrodermatitis 47 0.022
640
PRM013 Premature Menopause 47 0.022
641
PRT019 Protein-Losing Enteropathy 47 0.022
642
c MYT021 Myotonic Dystrophy 1 47 0.022
643
P INF049 Infantile Myofibromatosis 46 0.022
644
CNT047 Contact Dermatitis 46 0.022
645
TTH006 Tooth Disease 46 0.022
646
PRN011 Pernicious Anemia 46 0.022
647
MYM001 Myoma 46 0.022
648
WRN002 Wernicke-Korsakoff Syndrome 46 0.022
649
c INT064 Intermediate Uveitis 46 0.022
650
PRM003 Premature Ejaculation 46 0.022
651
NPH051 Nephritis 46 0.022
652
MLT006 Multidrug-Resistant Tuberculosis 46 0.022
653
PRR002 Pure Red-Cell Aplasia 46 0.022
654
P INF032 Infertility 46 0.022
655
P HRD021 Hereditary Sensory Neuropathy 46 0.022
656
LPT001 Leptospirosis 46 0.022
657
CHR008 Choroiditis 45 0.022
658
P MCL001 Mucolipidosis 45 0.022
659
c GRS014 Griscelli Syndrome, Type 2 46 0.022
660
P LKD001 Leukodystrophy 45 0.022
661
P GRS003 Griscelli Syndrome 45 0.022
662
SPN019 Spondylolisthesis 45 0.022
663
P AML002 Amelogenesis Imperfecta 45 0.022
664
CHL069 Cholesteatoma 45 0.022
665
c TYR013 Tyrosinemia, Type Ii 46 0.022
666
P CNT005 Central Nervous System Lymphoma 45 0.022
667
ASP001 Asperger Syndrome 45 0.022
668
SCT005 Scott Syndrome 45 0.022
669
GST045 Gastroenteritis 45 0.022
670
MYX004 Myxedema 45 0.022
671
OST011 Osteomalacia 45 0.022
672
P D2H001 D-2-Hydroxyglutaric Aciduria 45 0.022
673
ISL003 Isolated Growth Hormone Deficiency 45 0.022
674
DSC009 Discoid Lupus Erythematosus 44 0.022
675
P MSC003 Muscular Atrophy 44 0.022
676
ESN005 Eosinophilic Gastroenteritis 44 0.022
677
OCL020 Ocular Cicatricial Pemphigoid 44 0.022
678
ASP002 Aspartylglucosaminuria 44 0.022
679
PRV006 Pervasive Developmental Disorder 44 0.022
680
GRN007 Granuloma Annulare 44 0.022
681
P EPL002 Epilepsy Syndrome 44 0.022
682
NRG002 Neurogenic Bladder 44 0.022
683
P SCL018 Scoliosis 45 0.022
684
NRN008 Neuronal Intranuclear Inclusion Disease 44 0.022
685
P ACH011 Achondrogenesis 44 0.022
686
PRT039 Proteinuria 43 0.022
687
HMG002 Hemoglobinuria 43 0.022
688
FCL041 Focal Myositis 43 0.022
689
NSP012 Nasopharyngeal Carcinoma 44 0.022
690
DBW001 Dubowitz Syndrome 43 0.022
691
P MLG086 Malignant Hyperthermia Susceptibility 43 0.022
692
RSC001 Rosacea 43 0.022
693
ACS001 Acoustic Neuroma 43 0.022
694
P PYL005 Pyelonephritis 43 0.022
695
PLM070 Pulmonic Stenosis 43 0.022
696
CND005 Cone Dystrophy 43 0.022
697
ART035 Arterial Calcification of Infancy 43 0.022
698
P CYS018 Cystitis 43 0.022
699
P NRX001 Neuroaxonal Dystrophy 43 0.022
700
ALX002 Alexithymia 43 0.022
701
BLD034 Bile Duct Carcinoma 43 0.022
702
MST005 Mastitis 43 0.022
703
CHL052 Choledochal Cyst 43 0.022
704
MTH009 Mouth Disease 43 0.022
705
HYP068 Hyperostosis 43 0.022
706
P VTL001 Vitelliform Macular Dystrophy 42 0.022
707
c CHR536 Charcot-Marie-Tooth Disease, Type 1a 43 0.022
708
P PSD003 Pseudohypoaldosteronism 42 0.022
709
CCN002 Cocaine Abuse 42 0.022
710
CTS002 Cat-Scratch Disease 42 0.022
711
P MSB002 Mesoblastic Nephroma 42 0.022
712
AGR002 Agoraphobia 42 0.022
713
DNT012 Dental Caries 42 0.022
714
P LYD001 Leydig Cell Tumor 42 0.022
715
DFF021 Diffuse Mesangial Sclerosis 42 0.022
716
P HYP120 Hypoaldosteronism 42 0.022
717
c BRC082 Brachydactyly, Type E 42 0.022
718
P CNG390 Congenital Pulmonary Airway Malformation 41 0.022
719
ALP014 Alpha-Thalassemia/mental Retardation Syndrome 41 0.022
720
LPD011 Lipoid Adrenal Hyperplasia 41 0.022
721
NPH003 Nephrocalcinosis 41 0.022
722
MNN021 Meningococcemia 41 0.022
723
GRM004 Germinoma 41 0.022
724
P PNC001 Pancytopenia 41 0.022
725
VRN004 Vernal Keratoconjunctivitis 41 0.022
726
c CNG029 Congenital Mesoblastic Nephroma 41 0.022
727
NNT016 Neonatal Hemochromatosis 41 0.022
728
KWS001 Kwashiorkor 41 0.022
729
HYP043 Hyperandrogenism 40 0.022
730
P FNG005 Feingold Syndrome 40 0.022
731
CHR078 Chorioretinitis 40 0.022
732
DRM011 Dermatophytosis 40 0.022
733
NDL021 Nodular Lymphocyte Predominant Hodgkin Lymphoma 40 0.022
734
NSP002 Nasopharyngitis 40 0.022
735
c ACT076 Acute Myocarditis 40 0.022
736
CNG064 Congenital Chloride Diarrhea 40 0.022
737
P EPL003 Epulis 40 0.022
738
OHT001 Ohtahara Syndrome 40 0.022
739
PPL018 Papillary Adenocarcinoma 40 0.022
740
c CHR098 Chronic Pyelonephritis 40 0.022
741
PRS012 Pars Planitis 40 0.022
742
P CNG024 Congenital Nystagmus 40 0.022
743
MMB002 Membranous Glomerulonephritis 40 0.022
744
HYP064 Hypogonadotropism 39 0.022
745
LND001 Landau-Kleffner Syndrome 39 0.022
746
NRM004 Neuroma 39 0.022
747
PLG004 Plagiocephaly 39 0.022
748
MNN017 Mononeuropathy 39 0.022
749
HND002 Hand, Foot and Mouth Disease 39 0.022
750
P MRC003 Mercury Poisoning 39 0.022
751
MNN009 Meningoencephalitis 39 0.022
752
MYC033 Myoclonus 39 0.022
753
P OVR046 Ovarian Cyst 39 0.022
754
DLS001 Delusional Disorder 39 0.022
755
HRS011 Horseshoe Kidney 38 0.022
756
UNL007 Unilateral Renal Agenesis 38 0.022
757
P PTS002 Ptosis 39 0.022
758
MCR037 Macroglossia 38 0.022
759
P FBR025 Fibrochondrogenesis 38 0.022
760
MTB004 Metabolic Acidosis 38 0.022
761
P PNT019 Pontocerebellar Hypoplasia 38 0.022
762
P LTT001 Lattice Corneal Dystrophy 38 0.022
763
ART004 Aortic Atherosclerosis 38 0.022
764
PLM035 Pulmonary Eosinophilia 38 0.022
765
C3D001 C3 Deficiency 38 0.022
766
P SDR003 Sideroblastic Anemia 38 0.022
767
SPS007 Spastic Cerebral Palsy 38 0.022
768
P TRC005 Tracheal Stenosis 37 0.022
769
c ACQ027 Acquired Cutis Laxa 37 0.022
770
GND001 Gonadoblastoma 37 0.022
771
OPP004 Oppositional Defiant Disorder 37 0.022
772
TBL013 Tubulointerstitial Nephritis and Uveitis 37 0.022
773
EPS026 Epispadias 37 0.022
774
SYN036 Syncope 37 0.022
775
OLM001 Olmsted Syndrome 37 0.022
776
P TRS004 Torsion Dystonia 37 0.022
777
CHN015 Chondrodysplasia 37 0.022
778
NVS001 Neovascular Glaucoma 37 0.022
779
PCH002 Pachygyria 36 0.022
780
RNL025 Renal Hypoplasia 36 0.022
781
NCR002 Necrobiosis Lipoidica 36 0.022
782
OLG001 Oligospermia 36 0.022
783
HMT018 Hematopoietic Stem Cell Transplantation 36 0.022
784
HMP009 Haemophilus Influenzae 36 0.022
785
BTN004 Biotin Deficiency 35 0.022
786
c CNG004 Congenital Epulis 35 0.022
787
CNG035 Congenital Bilateral Absence of Vas Deferens 36 0.022
788
APH002 Aphasia 35 0.022
789
CMB021 Combined Pituitary Hormone Deficiency 35 0.022
790
ANN005 Annular Pancreas 35 0.022
791
TRN060 Truncus Arteriosus 36 0.022
792
ALB014 Alobar Holoprosencephaly 35 0.022
793
CD4003 Cd40 Ligand Deficiency 35 0.022
794
CRD053 Cardiovascular Disease Risk Factor 34 0.022
795
FMR004 Fumarase Deficiency 35 0.022
796
c CNG033 Congenital Syphilis 34 0.022
797
PLN006 Poland Syndrome 35 0.022
798
SPR034 Superior Limbic Keratoconjunctivitis 34 0.022
799
CRB028 Cerebellar Medulloblastoma 34 0.022
800
GST052 Gestational Choriocarcinoma 34 0.022
801
P END046 Endometritis 34 0.022
802
TRN030 Transient Erythroblastopenia of Childhood 34 0.022
803
SPR035 Superior Vena Cava Syndrome 34 0.022
804
FMR011 Fumarate Hydratase Deficiency 34 0.022
805
SPL039 Split Foot 33 0.022
806
c TRC092 Trichorhinophalangeal Syndrome, Type I 34 0.022
807
CNG105 Congenital Lobar Emphysema 34 0.022
808
GST064 Gastric Outlet Obstruction 33 0.022
809
SML028 Semilobar Holoprosencephaly 33 0.022
810
BCK006 Back Pain 33 0.022
811
c RNG018 Ring Chromosome 22 33 0.022
812
ENT007 Enteropathica 32 0.022
813
TBR006 Tuberculoid Leprosy 32 0.022
814
VCL001 Vacuolar Myopathy 32 0.022
815
AND001 Anodontia 32 0.022
816
LWT001 Low Tension Glaucoma 32 0.022
817
LYM095 Lymphangiomatosis 32 0.022
818
P PLN008 Peeling Skin Syndrome 32 0.022
819
IPX001 Ipex Syndrome 32 0.022
820
c PRG001 Progressive Muscular Atrophy 31 0.022
821
SCH011 Schizotypal Personality Disorder 31 0.022
822
PTC005 Pituicytoma 31 0.022
823
MHC001 Mhc Class Ii Deficiency 31 0.022
824
c JVN041 Juvenile Nephronophthisis 31 0.022
825
P DYS005 Dyslexia 30 0.022
826
P MLD013 Mild Hemophilia a 30 0.022
827
PRS108 Persistent Polyclonal B-Cell Lymphocytosis 30 0.022
828
HYP461 Hypocomplementemic Urticarial Vasculitis Syndrome 30 0.022
829
NRW001 Norwegian Scabies 30 0.022
830
NNM005 Non-Immune Hydrops Fetalis 30 0.022
831
RNL012 Renal Tuberculosis 30 0.022
832
BLN001 Blount's Disease 31 0.022
833
CVR010 Cavernous Malformation 29 0.022
834
IMM039 Immune Hydrops Fetalis 29 0.022
835
DFF001 Diffuse Cutaneous Mastocytosis 29 0.022
836
ARM002 Aromatic L-Amino Acid Decarboxylase Deficiency 30 0.022
837
c INF131 Infant Acute Respiratory Distress Syndrome 29 0.022
838
SHK001 Shaken Baby Syndrome 29 0.022
839
P CRB059 Cerebellar Degeneration 29 0.022
840
SPR012 Separation Anxiety Disorder 28 0.022
841
PRM129 Primary Cutaneous Marginal Zone B-Cell Lymphoma 28 0.022
842
SPR007 Superior Mesenteric Artery Syndrome 28 0.022
843
DYS012 Dyshidrosis 28 0.022
844
PLM064 Pulmonary Sequestration 28 0.022
845
THL009 Thiolase Deficiency 28 0.022
846
SBP004 Subependymoma 28 0.022
847
SPN029 Spondylolysis 27 0.022
848
SPN221 Spina Bifida Occulta 27 0.022
849
LMB014 Limb-Body Wall Complex 28 0.022
850
LTM002 Luteoma 27 0.022
851
CNG133 Congenital Varicella Syndrome 27 0.022
852
BDY001 Body Dysmorphic Disorder 26 0.022
853
c PRM032 Primary Congenital Glaucoma 26 0.022
854
WRT003 Warthin Tumor 26 0.022
855
c MTR002 Mitral Valve Insufficiency 25 0.022
856
NRG004 Neurogenic Diabetes Insipidus 25 0.022
857
FCL003 Facial Hemiatrophy 25 0.022
858
P SCH009 Scheuermann's Disease 26 0.022
859
DVL001 Developmental Coordination Disorder 25 0.022
860
P PTT002 Potter's Syndrome 24 0.022
861
c HMG001 Hemoglobin C Disease 24 0.022
862
PHT008 Photosensitive Epilepsy 24 0.022
863
CRN051 Craniofacial Microsomia 24 0.022
864
RTT001 Ritter's Disease 25 0.022
865
NNT021 Neonatal Meningitis 24 0.022
866
PLM058 Pulmonary Atresia with Intact Ventricular Septum 24 0.022
867
XNT009 Xanthoma Disseminatum 24 0.022
868
15Q002 15q24 Microdeletion Syndrome 24 0.022
869
c HYP163 Hyperlipidemia Type 3 23 0.022
870
P SPR036 Supernumerary Nipples 23 0.022
871
CRL004 Caroli Disease 24 0.022
872
SYS006 Say Syndrome 24 0.022
873
EXS013 Exstrophy-Epispadias Complex 23 0.022
874
DPR001 Diaper Rash 23 0.022
875
ANG004 Angioid Streaks 23 0.022
876
GST007 Gastric Dilatation 23 0.022
877
AMY005 Amyloid Neuropathy 23 0.022
878
RTN006 Retinal Drusen 23 0.022
879
TRC035 Tracheal Agenesis 23 0.022
880
GGR001 Geographic Tongue 23 0.022
881
BLD052 Blood Group Incompatibility 22 0.022
882
MCR039 Macrophagic Myofasciitis 23 0.022
883
PNS015 Penoscrotal Transposition 23 0.022
884
ATR003 Atrophic Rhinitis 23 0.022
885
SMT001 Somatization Disorder 23 0.022
886
LCH003 Lichen Nitidus 22 0.022
887
3HY001 3-Hydroxyisobutyric Aciduria 22 0.022
888
MSC016 Mosaic Trisomy 14 22 0.022
889
DDN009 Duodenal Obstruction 22 0.022
890
C6D001 C6 Deficiency 21 0.022
891
SLT009 Solitary Bone Cyst 22 0.022
892
ACC003 Accommodative Esotropia 20 0.022
893
ART034 Aortopulmonary Window 21 0.022
894
AVD001 Avoidant Personality Disorder 20 0.022
895
P HYD015 Hydroa Vacciniforme 21 0.022
896
FTS001 Fetishism 20 0.022
897
PLN001 Plantar Wart 21 0.022
898
TLH001 Tel Hashomer Camptodactyly Syndrome 20 0.022
899
TCL012 T-Cell/histiocyte Rich Large B Cell Lymphoma 20 0.022
900
ARM003 Aromatic Amino Acid Decarboxylase Deficiency 19 0.022
901
CLC003 Cloacogenic Carcinoma 19 0.022
902
SPS087 Spasmus Nutans 20 0.022
903
SYN041 Synesthesia 20 0.022
904
PTN004 Patent Ductus Venosus 19 0.022
905
c CNG370 Congenital Tracheal Stenosis 19 0.022
906
INT011 Interstitial Emphysema 19 0.022
907
LPM007 Lipomyelomeningocele 19 0.022
908
PNL023 Penile Agenesis 19 0.022
909
SCH025 Schisis Association 18 0.022
910
MYL044 Myelocystocele 18 0.022
911
FTZ005 Fitzsimmons-Guilbert Syndrome 18 0.022
912
CLR033 Color Vision Deficiency 18 0.022
913
PRD003 Periodontosis 18 0.022
914
SCR022 Sacral Meningocele Conotruncal Heart Defects 17 0.022
915
LBY003 Labyrinthine Disease 17 0.022
916
P NNT006 Neonatal Myasthenia Gravis 16 0.022
917
MSL004 Mesial Temporal Lobe Epilepsy with Hippocampal Sclerosis 16 0.022
918
BRN097 Brainstem Auditory Evoked Responses 17 0.022
919
HCS001 Hec Syndrome 17 0.022
920
RTN127 Retinal Cavernous Hemangioma 16 0.022
921
DCR002 Dacryocystocele 16 0.022
922
LBN004 Liebenberg Syndrome 16 0.022
923
c CNG129 Congenital Torticollis 16 0.022
924
MRG006 Morgagni-Stewart-Morel Syndrome 16 0.022
925
CNG125 Congenital Short Femur 16 0.022
926
HYP015 Hyperlucent Lung 16 0.022
927
CNG329 Congenital Onychodysplasia 16 0.022
928
RTN019 Retinal Telangiectasia 15 0.022
929
ELC001 Elective Mutism 15 0.022
930
c MLG039 Malignant Essential Hypertension 14 0.022
931
PRR001 Periarthritis 15 0.022
932
AQG002 Aquagenic Urticaria 15 0.022
933
MTR027 Mitral Atresia 15 0.022
934
c PTR018 Paternal Uniparental Disomy of Chromosome 6 14 0.022
935
c NRC009 Narcolepsy 1 14 0.022
936
JVN026 Jeavons Syndrome 14 0.022
937
HYP018 Hyperglobulinemic Purpura 13 0.022
938
HYD031 Hydroxyprolinemia 14 0.022
939
TBR007 Tuberculum Sellae Meningioma 14 0.022
940
OLG008 Oligomeganephronic Renal Hypoplasia 13 0.022
941
FBL006 Fibular Aplasia Ectrodactyly 12 0.022
942
RHH001 Rohhad 12 0.022
943
VLF002 Velo-Facial-Skeletal Syndrome 11 0.022
944
c RNG014 Ring Chromosome 19 11 0.022
945
LCH012 Lichstenstein Syndrome 11 0.022
946
KCH001 Kocher-Debre-Semelaigne Syndrome 11 0.022
947
c CNG406 Congenital Pulmonary Airway Malformation Type 0 10 0.022
948
HMF003 Hemifacial Myohyperplasia 9 0.022
949
FNG010 Fingerprint Body Myopathy 9 0.022
950
FSD001 Fused Mandibular Incisors 9 0.022
951
DDY001 Didymosis Aplasticosebacea 9 0.022
952
MCH006 Mechanical Strabismus 8 0.022
953
CRB080 Cor Biloculare 8 0.022
954
HLC002 Holoacardius Amorphus 8 0.022
955
CHR458 Chromosome 9 Inversion 7 0.022
956
P AGR014 Age-Related Hearing Impairment 2 7 0.022
957
2MT002 2-Methylacetoacetyl Coa Thiolase Deficiency 7 0.022
958
c AGR013 Age-Related Hearing Impairment 1 6 0.022