Search results for "twinning"

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

1233 hits were found for 'twinning'

# Family MCID Name MIFTS Score
1
TWN001 Twin-to-Twin Transfusion Syndrome 46 12.717
2
c RNL090 Renal Tubular Dysgenesis Due to Twin-Twin Transfusion 6 3.798
3
P PLY018 Polycythemia 57 0.154
4
PLY012 Polyhydramnios 47 0.151
5
CRB009 Cerebritis 38 0.147
6
ANN002 Anencephaly 52 0.138
7
PLC008 Placenta Disease 36 0.120
8
P HRT032 Heart Disease 76 0.119
9
P CRV039 Cervicitis 44 0.102
10
P OBS005 Obesity 93 0.098
11
OLG003 Oligohydramnios 52 0.098
12
HYD012 Hydrops Fetalis 44 0.096
13
P CRD011 Cardiomyopathy 67 0.090
14
CHL071 Child Syndrome 58 0.088
15
KDS001 Kid Syndrome 53 0.088
16
CYT008 Cytomegalovirus Infection 51 0.086
17
DWN001 Down Syndrome 65 0.082
18
CHR005 Chorioamnionitis 48 0.082
19
CCN007 Cocoon Syndrome 35 0.082
20
CNG069 Congenital Cytomegalovirus 34 0.082
21
P THY032 Thyroiditis 54 0.079
22
SRN002 Sirenomelia 25 0.079
23
P LKM002 Leukemia 70 0.075
24
DFC004 Deficiency Anemia 65 0.072
25
TNP003 Tn Polyagglutination Syndrome, Somatic 44 0.072
26
P PLM037 Pulmonary Hypertension 79 0.069
27
P HYP086 Hypothyroidism 65 0.069
28
ISC004 Ischemia 59 0.069
29
P PRS038 Personality Disorder 61 0.067
30
URT039 Urticaria 59 0.067
31
OMP004 Omphalocele 50 0.067
32
ECT026 Ectopic Pregnancy 47 0.067
33
NNT011 Neonatal Anemia 34 0.067
34
PYL006 Pyloric Stenosis 46 0.064
35
INT060 Intestinal Atresia 40 0.064
36
P EPL164 Epilepsy 66 0.061
37
P THR014 Thrombocytopenia 64 0.061
38
P LPS004 Lupus Erythematosus 63 0.061
39
CRB037 Cerebral Palsy 54 0.061
40
P ECL001 Eclampsia 54 0.061
41
P TRT010 Teratoma 52 0.061
42
P APL006 Aplasia Cutis Congenita 48 0.061
43
P ENC008 Encephalocele 47 0.061
44
PRT082 Preterm Premature Rupture of the Membranes 47 0.061
45
BRT030 Birth Defects 43 0.061
46
URT008 Urticaria Pigmentosa 38 0.061
47
ENC005 Encephalomalacia 28 0.061
48
P TYS001 Tay-Sachs Disease 71 0.058
49
P MYP004 Myopathy 67 0.058
50
P NRC002 Narcolepsy 62 0.058
51
DRM006 Dermatitis 61 0.058
52
P TXP001 Toxoplasmosis 60 0.058
53
WLL006 Wells Syndrome 56 0.058
54
GST033 Gestational Diabetes 56 0.058
55
P GND004 Gonadal Dysgenesis 53 0.058
56
PLC005 Placental Insufficiency 50 0.058
57
PRV004 Periventricular Leukomalacia 48 0.058
58
c PST041 Posterior Urethral Valves 46 0.058
59
GDS001 Good Syndrome 45 0.058
60
GST009 Gastroschisis 43 0.058
61
LKM006 Leukomalacia 42 0.058
62
P HYP009 Hypertrophic Pyloric Stenosis 41 0.058
63
URT001 Urethritis 40 0.058
64
P UTR038 Uterine Disease 40 0.058
65
HYD001 Hydranencephaly 34 0.058
66
PNT005 Pentalogy of Cantrell 21 0.058
67
DPR014 Diprosopus 17 0.058
68
P ART022 Arthritis 75 0.055
69
P RBN001 Rubinstein-Taybi Syndrome 65 0.055
70
P ESP024 Esophagitis 62 0.055
71
P LYM026 Lymphoblastic Leukemia 60 0.055
72
P ADL010 Adult Respiratory Distress Syndrome 60 0.055
73
c CNG006 Congenital Hypothyroidism 59 0.055
74
c ACT210 Acute Respiratory Distress Syndrome 57 0.055
75
CND002 Conduct Disorder 56 0.055
76
KLN001 Klinefelter's Syndrome 55 0.055
77
ADL002 Adult Syndrome 53 0.055
78
P DBT005 Diabetes Insipidus 53 0.055
79
IMP002 Imperforate Anus 52 0.055
80
RTN023 Retinitis 49 0.055
81
NWB001 Newborn Respiratory Distress Syndrome 47 0.055
82
c BPL002 Bipolar I Disorder 47 0.055
83
c CNG021 Congenital Toxoplasmosis 46 0.055
84
RFR003 Refractive Error 42 0.055
85
CHR322 Choreoathetosis, Hypothyroidism, and Neonatal Respiratory Distress 41 0.055
86
RSP007 Respiratory Distress Syndrome, Infant 26 0.055
87
AMN009 Amniotic Band Syndrome 25 0.055
88
c ADL080 Adult Acute Respiratory Distress Syndrome 23 0.055
89
ACR022 Acardia 12 0.055
90
P SCH015 Schizophrenia 76 0.051
91
P CRN211 Coronary Artery Disease 75 0.051
92
ANX002 Anxiety Disorder 69 0.051
93
PRP027 Peripheral Vascular Disease 69 0.051
94
ISC006 Ischemic Heart Disease 68 0.051
95
ALC007 Alcohol Dependence 65 0.051
96
ART005 Arteriovenous Malformation 65 0.051
97
P MSC005 Muscular Dystrophy 64 0.051
98
P PRM019 Premature Ovarian Failure 64 0.051
99
P DYS154 Dystonia 64 0.051
100
P HLP001 Holoprosencephaly 62 0.051
101
P MST009 Mastocytosis 54 0.051
102
PTH002 Pathological Gambling 51 0.051
103
P OST009 Osteochondritis Dissecans 50 0.051
104
ESP020 Esophageal Atresia 49 0.051
105
TRN007 Transsexualism 41 0.051
106
MTS001 Mutism 40 0.051
107
SCR024 Sacrococcygeal Teratoma 26 0.051
108
P RHM011 Rheumatoid Arthritis 88 0.047
109
c SYS001 Systemic Lupus Erythematosus 87 0.047
110
P NRB001 Neuroblastoma 69 0.047
111
ATT013 Attention Deficit-Hyperactivity Disorder 68 0.047
112
DMN002 Dementia 64 0.047
113
PLM033 Pulmonary Embolism 59 0.047
114
PST028 Post-Traumatic Stress Disorder 57 0.047
115
P BCK002 Beckwith-Wiedemann Syndrome 56 0.047
116
P MYS005 Myositis 56 0.047
117
ALP008 Alopecia 55 0.047
118
BLM002 Bulimia Nervosa 54 0.047
119
BRN071 Brain Injury 52 0.047
120
P HYP065 Hyperaldosteronism 51 0.047
121
HLL004 Hellp Syndrome 49 0.047
122
CTN014 Cutaneous Mastocytosis 48 0.047
123
PLC007 Placental Abruption 47 0.047
124
TRN044 Transposition of the Great Arteries 47 0.047
125
ACR041 Acromelic Frontonasal Dysostosis 46 0.047
126
BWN001 Bowen-Conradi Syndrome 45 0.047
127
PRN019 Perinatal Necrotizing Enterocolitis 44 0.047
128
SPS057 Spasticity 42 0.047
129
ATN011 Autoinflammation with Infantile Enterocolitis 41 0.047
130
PLY024 Polymicrogyria 36 0.047
131
ALR002 Al-Raqad Syndrome 36 0.047
132
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.047
133
ANS004 Anisometropia 29 0.047
134
JJN004 Jejunal Atresia 28 0.047
135
PRT086 Partial Hydatidiform Mole 25 0.047
136
HV1006 Hiv-1 82 0.043
137
P MYC007 Myocardial Infarction 79 0.043
138
NRL016 Neural Tube Defects 76 0.043
139
INS024 Insulin-Like Growth Factor I 74 0.043
140
PTZ001 Peutz-Jeghers Syndrome 70 0.043
141
P HPT021 Hepatitis 70 0.043
142
P PNM007 Pneumonia 66 0.043
143
ATH003 Atherosclerosis 62 0.043
144
PRT036 Peritonitis 62 0.043
145
P BPL003 Bipolar Disorder 62 0.043
146
P INF032 Infertility 61 0.043
147
P HYP055 Hypoplastic Left Heart Syndrome 60 0.043
148
P ALC004 Alcohol Abuse 60 0.043
149
P MYP006 Myopia 59 0.043
150
ART021 Arteriosclerosis 59 0.043
151
P PRC031 Preeclampsia/eclampsia 1 57 0.043
152
EPD016 Epidermolysis Bullosa 57 0.043
153
ANR040 Aneurysm 57 0.043
154
ART111 Artery Disease 57 0.043
155
P HYP076 Hyperthyroidism 56 0.043
156
URN010 Urinary Tract Obstruction 56 0.043
157
ALL026 Allergic Hypersensitivity Disease 53 0.043
158
P RNL028 Renal Tubular Dysgenesis 52 0.043
159
VND001 Vein Disease 52 0.043
160
BRX001 Bruxism 51 0.043
161
LMB062 Limb Ischemia 48 0.043
162
c SVR005 Severe Pre-Eclampsia 48 0.043
163
ACD009 Acid-Labile Subunit, Deficiency of 48 0.043
164
ECT006 Ectodermal Dysplasia 47 0.043
165
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 47 0.043
166
P DRM007 Dermatitis Herpetiformis 46 0.043
167
AST006 Astigmatism 44 0.043
168
GND002 Gender Identity Disorder 44 0.043
169
END072 Endotheliitis 42 0.043
170
EST005 Esotropia 41 0.043
171
PSD009 Pseudohermaphroditism 40 0.043
172
P CRN178 Coronary Heart Disease 6 24 0.043
173
c CRN173 Coronary Heart Disease 8 20 0.043
174
EPG004 Epignathus 17 0.043
175
P BRS047 Breast Cancer 100 0.039
176
CYS001 Cystic Fibrosis 86 0.039
177
P AST005 Asthma 82 0.039
178
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.039
179
CRZ001 Crouzon Syndrome 70 0.039
180
TBR010 Tuberculosis 69 0.039
181
c NRF018 Neurofibromatosis, Type 1 68 0.039
182
P ATS007 Autism Spectrum Disorder 64 0.039
183
P PSR002 Psoriasis 63 0.039
184
RSP006 Respiratory System Disease 62 0.039
185
LNG099 Lung Disease 62 0.039
186
PRM097 Primary Immunodeficiency Disease 61 0.039
187
P GRV001 Graves' Disease 61 0.039
188
P NPH009 Nephrolithiasis 60 0.039
189
ANR002 Aniridia 60 0.039
190
P SHR029 Short Syndrome 60 0.039
191
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.039
192
c LCL006 Localized Scleroderma 59 0.039
193
RBR001 Roberts Syndrome 59 0.039
194
P UVT001 Uveitis 59 0.039
195
P THR003 Thoracic Aortic Aneurysm 57 0.039
196
P PLY006 Polydactyly 55 0.039
197
GTR002 Goiter 54 0.039
198
P ATX004 Ataxia 53 0.039
199
P NNT009 Neonatal Diabetes Mellitus 52 0.039
200
P MGR003 Migraine with Aura 51 0.039
201
BRN004 Brain Edema 51 0.039
202
SMT008 Smith-Magenis Syndrome 51 0.039
203
HMN014 Human Immunodeficiency Virus Infectious Disease 49 0.039
204
GYN001 Gynecomastia 49 0.039
205
SYN005 Synostosis 45 0.039
206
VSC047 Vascular Malformation 45 0.039
207
ACR012 Aicardi Syndrome 45 0.039
208
PRN038 Prune Belly Syndrome 45 0.039
209
TCL003 T Cell Deficiency 45 0.039
210
END020 Endocardial Fibroelastosis 44 0.039
211
RSP019 Respiratory Distress Syndrome in Premature Infants 44 0.039
212
DYS018 Dysostosis 44 0.039
213
HYD057 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 44 0.039
214
P ART084 Arteriovenous Fistula 44 0.039
215
DDN006 Duodenitis 44 0.039
216
CRV043 Cervical Dystonia 44 0.039
217
HTR003 Heterotaxy 42 0.039
218
CPL007 Capillary Malformation-Arteriovenous Malformation 41 0.039
219
BRN080 Brain Ischemia 41 0.039
220
NTR005 Nutritional Deficiency Disease 39 0.039
221
MCR103 Microtia 37 0.039
222
SLP010 Slipped Capital Femoral Epiphysis 35 0.039
223
CRB031 Cerebral Arterial Disease 31 0.039
224
BRW006 Brown Syndrome 26 0.039
225
PHC006 Phacomatosis Pigmentovascularis 24 0.039
226
CLN022 Colonic Atresia 24 0.039
227
CD4004 Cd4 Deficiency 17 0.039
228
FTL016 Fetal Edema 17 0.039
229
CRN073 Coronary Arteries Congenital Malformation 13 0.039
230
PHC005 Phacomatosis Pigmentokeratotica 12 0.039
231
JMC001 Jamaican Vomiting Sickness 9 0.039
232
P MDL005 Medulloblastoma 77 0.033
233
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 76 0.033
234
CRH001 Crohn's Disease 76 0.033
235
P INF038 Influenza 74 0.033
236
P ALG002 Alagille Syndrome 72 0.033
237
KWS002 Kawasaki Disease 70 0.033
238
P LYM118 Lymphoma 70 0.033
239
P ADN016 Adenocarcinoma 69 0.033
240
SKN016 Skin Disease 68 0.033
241
P OST005 Osteogenesis Imperfecta 67 0.033
242
PCK002 Pick Disease 67 0.033
243
P CLC005 Celiac Disease 67 0.033
244
VSC007 Vascular Disease 67 0.033
245
P PLY011 Polycystic Ovary Syndrome 66 0.033
246
P MYS003 Myasthenia Gravis 65 0.033
247
P MNN013 Meningitis 65 0.033
248
P CRN037 Craniosynostosis 65 0.033
249
P TRN020 Turner Syndrome 64 0.033
250
P AGM001 Agammaglobulinemia 64 0.033
251
ATP002 Atopy 63 0.033
252
BRN024 Bronchitis 63 0.033
253
P ANR007 Anorexia Nervosa 63 0.033
254
EYD002 Eye Disease 63 0.033
255
INC002 Inclusion Body Myositis 63 0.033
256
P ATP001 Atopic Dermatitis 62 0.033
257
P THL005 Thalassemia 61 0.033
258
WLL001 Williams-Beuren Syndrome 61 0.033
259
P RHN004 Rhinitis 61 0.033
260
OVR029 Ovarian Hyperstimulation Syndrome 60 0.033
261
GST045 Gastroenteritis 60 0.033
262
P RCK004 Rickets 59 0.033
263
P VNT002 Ventricular Septal Defect 59 0.033
264
P CTS001 Cutis Laxa 59 0.033
265
P ENC018 Encephalopathy 59 0.033
266
P NTR004 Neutropenia 59 0.033
267
P CNG015 Congenital Diaphragmatic Hernia 58 0.033
268
CHL068 Cholestasis 58 0.033
269
P CTR002 Cataract 57 0.033
270
P INT001 Intrahepatic Cholestasis 57 0.033
271
P HYP040 Hypospadias 57 0.033
272
P HMP007 Hemophilia 56 0.033
273
HYP266 Hypoxia 55 0.033
274
CHN016 Cohen Syndrome 55 0.033
275
P HST010 Histiocytosis 55 0.033
276
TTH002 Tooth Agenesis 55 0.033
277
P SLV001 Silver-Russell Syndrome 54 0.033
278
MCN017 Meconium Ileus 54 0.033
279
DGN001 Degenerative Disc Disease 53 0.033
280
P FTL001 Fetal Alcohol Syndrome 53 0.033
281
TST014 Testicular Cancer 52 0.033
282
PNM008 Pneumothorax 52 0.033
283
GNR004 Generalized Anxiety Disorder 51 0.033
284
P HYP071 Hypersensitivity Reaction Type Ii Disease 51 0.033
285
VND002 Van Der Woude Syndrome 51 0.033
286
CDL003 Caudal Regression Syndrome 51 0.033
287
P DRR001 Diarrhea 51 0.033
288
SBS004 Substance Dependence 50 0.033
289
CLF001 Cleft Lip 49 0.033
290
PRP016 Paraplegia 49 0.033
291
BRN056 Bronchopulmonary Dysplasia 49 0.033
292
GRW007 Growth Hormone Deficiency 48 0.033
293
PPL021 Papilledema 48 0.033
294
SCL003 Social Phobia 48 0.033
295
P MYT002 Myotonic Dystrophy 47 0.033
296
SXL003 Sexual Disorder 47 0.033
297
GLC008 Glucose Metabolism Disease 47 0.033
298
ANT011 Antisocial Personality Disorder 47 0.033
299
P PLN008 Peeling Skin Syndrome 47 0.033
300
ALN001 Aland Island Eye Disease 45 0.033
301
RNL078 Renal Dysplasia 45 0.033
302
P HMP006 Hemiplegic Migraine 44 0.033
303
DND001 Dandy-Walker Syndrome 44 0.033
304
TBR006 Tuberculoid Leprosy 44 0.033
305
CNV002 Conversion Disorder 42 0.033
306
VGN023 Vaginitis 42 0.033
307
c BLD124 Bleeding Disorder, Platelet-Type, 11 42 0.033
308
NRN002 Neuronitis 42 0.033
309
CNN002 Cannabis Abuse 41 0.033
310
TRC040 Tracheoesophageal Fistula 41 0.033
311
c JVN003 Juvenile Xanthogranuloma 40 0.033
312
TRP014 Triploidy 40 0.033
313
NSY001 N Syndrome 39 0.033
314
ARC007 Arachnoid Cysts 38 0.033
315
ARC002 Arachnoiditis 38 0.033
316
ATM012 Autoimmune Disease of Blood 37 0.033
317
CNN001 Cannabis Dependence 37 0.033
318
P MNN007 Meningocele 36 0.033
319
P NNT042 Neonatal Lupus Erythematosus 35 0.033
320
CRV069 Cervix Disease 34 0.033
321
IMM068 Immunodeficiency 8 32 0.033
322
TYP015 Type 2b Von Willebrand Disease 30 0.033
323
CYT004 Cytomegalic Inclusion Disease 30 0.033
324
c ANR038 Anorexia Nervosa 1 29 0.033
325
OCC011 Occipital Encephalocele 23 0.033
326
SPS090 Sepsis in Premature Infants 23 0.033
327
FRM001 Freemartinism 22 0.033
328
GST058 Gestational Diabetes Insipidus 11 0.033
329
DCH001 Duchenne Muscular Dystrophy 80 0.027
330
P RTT002 Rett Syndrome 78 0.027
331
P HYP607 Hypercholesterolemia, Familial 77 0.027
332
ULC004 Ulcerative Colitis 75 0.027
333
P PFF001 Pfeiffer Syndrome 73 0.027
334
P LVR013 Liver Disease 72 0.027
335
P HMC003 Hemochromatosis 72 0.027
336
ADR007 Adrenoleukodystrophy 71 0.027
337
CNG034 Congestive Heart Failure 71 0.027
338
TTR001 Tetralogy of Fallot 71 0.027
339
BRN028 Brain Cancer 70 0.027
340
c HYP595 Hypertension, Essential 69 0.027
341
SVR004 Severe Combined Immunodeficiency 68 0.027
342
THY028 Thyroid Cancer 68 0.027
343
ART016 Aortic Aneurysm 67 0.027
344
P MYL006 Myeloid Leukemia 67 0.027
345
ACH004 Achondroplasia 66 0.027
346
P CNJ013 Conjunctivitis 65 0.027
347
P HRP006 Herpes Simplex 65 0.027
348
P ATR011 Atrial Fibrillation 64 0.027
349
P OST002 Osteoporosis 64 0.027
350
P BCL006 B-Cell Lymphomas 64 0.027
351
ALL003 Allergic Rhinitis 64 0.027
352
CHR066 Chronic Fatigue Syndrome 64 0.027
353
P NMN002 Niemann-Pick Disease 63 0.027
354
c HMP004 Hemophilia B 62 0.027
355
FBR011 Fibrodysplasia Ossificans Progressiva 62 0.027
356
FCT003 Factor X Deficiency 62 0.027
357
BLM001 Bloom Syndrome 62 0.027
358
P SDD001 Sudden Infant Death Syndrome 61 0.027
359
TTN003 Tetanus 61 0.027
360
HYP056 Hypoglycemia 61 0.027
361
P ALP009 Alopecia Areata 61 0.027
362
VNW001 Von Willebrand's Disease 61 0.027
363
CNN005 Connective Tissue Disease 61 0.027
364
P HMN010 Hemangioma 60 0.027
365
P ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 60 0.027
366
c MCL062 Mucolipidosis Ii Alpha/beta 60 0.027
367
P NRP001 Neuropathy 60 0.027
368
c EXD008 Exudative Vitreoretinopathy 1 60 0.027
369
P KLL001 Kallmann Syndrome 60 0.027
370
P PNC025 Panic Disorder 60 0.027
371
ATS001 Autistic Disorder 59 0.027
372
P BRG001 Brugada Syndrome 59 0.027
373
CLT003 Colitis 59 0.027
374
P HYP060 Hyperinsulinism 59 0.027
375
PRP030 Purpura 59 0.027
376
ADN018 Adenoma 59 0.027
377
P GLY013 Glycogen Storage Disease 59 0.027
378
P PRM011 Primary Ciliary Dyskinesia 58 0.027
379
P DRM010 Dermatomyositis 58 0.027
380
LPM004 Lipoma 58 0.027
381
RTN017 Retinal Detachment 57 0.027
382
ELL001 Ellis-Van Creveld Syndrome 57 0.027
383
EXF001 Exfoliation Syndrome 57 0.027
384
NRM005 Neuromuscular Disease 57 0.027
385
P MCR129 Microvascular Complications of Diabetes 1 57 0.027
386
P EPS003 Episodic Ataxia 56 0.027
387
P GLM007 Glomerulonephritis 56 0.027
388
P RBL001 Rubella 56 0.027
389
P SCL018 Scoliosis 56 0.027
390
P INT070 Intestinal Obstruction 56 0.027
391
RTN018 Retinal Disease 56 0.027
392
P TMT001 Timothy Syndrome 56 0.027
393
P NPH005 Nephronophthisis 55 0.027
394
c FML023 Familial Hemiplegic Migraine 55 0.027
395
P MLT074 Multiple Endocrine Neoplasia 55 0.027
396
GST050 Gastrointestinal System Disease 54 0.027
397
HYP080 Hypogonadism 54 0.027
398
P PRP019 Peripheral Nervous System Disease 54 0.027
399
CLR003 Clear Cell Adenocarcinoma 54 0.027
400
P VSC005 Vesicoureteral Reflux 54 0.027
401
HDC001 Headache 54 0.027
402
HMP005 Hemiplegia 54 0.027
403
LTT002 Letterer-Siwe Disease 54 0.027
404
P MYC008 Myocarditis 54 0.027
405
P HRD011 Hereditary Spherocytosis 53 0.027
406
P END044 Endometriosis 53 0.027
407
P STR020 Strabismus 53 0.027
408
ART002 Arts Syndrome 53 0.027
409
STF002 Stiff Skin Syndrome 53 0.027
410
C3D001 C3 Deficiency 53 0.027
411
PYR010 Peyronie's Disease 53 0.027
412
DNY001 Denys-Drash Syndrome 53 0.027
413
DRG003 Drug Dependence 53 0.027
414
INT007 Intermediate Coronary Syndrome 52 0.027
415
ANK001 Ankylosis 52 0.027
416
TLN003 Telangiectasis 52 0.027
417
P MSC033 Muscle Disorders 52 0.027
418
KRT006 Keratoconjunctivitis 52 0.027
419
P FBR031 Febrile Seizures 52 0.027
420
P PNC001 Pancytopenia 52 0.027
421
LYS001 Loeys-Dietz Syndrome 52 0.027
422
MST005 Mastitis 52 0.027
423
GNG012 Gingival Overgrowth 52 0.027
424
NSD001 Nose Disease 52 0.027
425
IRN001 Iron Deficiency Anemia 51 0.027
426
NNT012 Neonatal Jaundice 51 0.027
427
P KRT007 Keratoconus 51 0.027
428
AMN001 Amenorrhea 51 0.027
429
NPH018 Nephrogenic Systemic Fibrosis 51 0.027
430
HPT074 Hepatic Adenoma, Somatic 51 0.027
431
BLD044 Bladder Disease 51 0.027
432
KLD001 Keloids 51 0.027
433
P OCL002 Oculocutaneous Albinism 51 0.027
434
P SCH018 Schizencephaly 51 0.027
435
P OVR046 Ovarian Cyst 50 0.027
436
c ACT068 Acute Cystitis 50 0.027
437
HMG005 Hemoglobinopathy 50 0.027
438
MYL020 Myelomeningocele 50 0.027
439
P HYP014 Hyperuricemia 50 0.027
440
VTR013 Vitreoretinopathy, Neovascular Inflammatory 50 0.027
441
PRP021 Peripheral Nervous System Neoplasm 50 0.027
442
CDS001 Cadasil 50 0.027
443
P HML001 Hemolytic-Uremic Syndrome 50 0.027
444
PRV006 Pervasive Developmental Disorder 50 0.027
445
MSC006 Muscle Glycogenosis 49 0.027
446
CSY001 C Syndrome 49 0.027
447
PMP001 Pemphigus 49 0.027
448
CHR001 Churg-Strauss Syndrome 49 0.027
449
P FTL009 Fetal Akinesia Deformation Sequence 49 0.027
450
THR013 Thoracic Outlet Syndrome 49 0.027
451
KBG001 Kbg Syndrome 49 0.027
452
P LFT003 Left Ventricular Noncompaction 49 0.027
453
FML039 Female Reproductive System Disease 48 0.027
454
APR001 Apraxia 48 0.027
455
P CMP008 Compartment Syndrome 48 0.027
456
ADR038 Adermatoglyphia 48 0.027
457
RFL001 Reflex Sympathetic Dystrophy 48 0.027
458
CRB090 Cerebral Hypoxia 48 0.027
459
HYP043 Hyperandrogenism 48 0.027
460
PLN006 Poland Syndrome 48 0.027
461
P RNL015 Renal Hypertension 47 0.027
462
URT031 Ureteral Disease 47 0.027
463
RNL077 Renal Fibrosis 47 0.027
464
P PRN026 Porencephaly 47 0.027
465
LKC003 Leukocyte Disease 47 0.027
466
PTY003 Pityriasis Rubra Pilaris 46 0.027
467
BRD004 Borderline Personality Disorder 46 0.027
468
RPR002 Reproductive System Disease 46 0.027
469
OBS015 Obesity, Hyperphagia, and Developmental Delay 46 0.027
470
ANR004 Anuria 46 0.027
471
VTR016 Vater/vacterl Association 46 0.027
472
P KLP003 Klippel-Feil Syndrome 46 0.027
473
SCB001 Scabies 45 0.027
474
P THR027 Thoracic Aortic Aneurysms and Aortic Dissections 45 0.027
475
CLS010 Cluster Headache 45 0.027
476
HYP457 Hypertrophic Scars 45 0.027
477
RNL097 Renal Artery Disease 45 0.027
478
SPS007 Spastic Cerebral Palsy 45 0.027
479
NNS002 Nonspecific Interstitial Pneumonia 44 0.027
480
PHY002 Physical Disorder 44 0.027
481
FRZ001 Frozen Shoulder 44 0.027
482
BLL004 Bullous Keratopathy 44 0.027
483
DXT001 Dextrocardia 44 0.027
484
ALB002 Albinism 43 0.027
485
P PMP005 Pemphigus Vulgaris 43 0.027
486
PLC001 Placenta Accreta 43 0.027
487
ART031 Aortic Coarctation 42 0.027
488
NPH010 Nephrosclerosis 42 0.027
489
LCH009 Lichen Sclerosus 42 0.027
490
c INF069 Infantile Neuroaxonal Dystrophy 1 42 0.027
491
IMP004 Impetigo 42 0.027
492
RTR008 Root Resorption 41 0.027
493
HYP458 Hyper Ige Syndrome 41 0.027
494
CRS001 Crescentic Glomerulonephritis 41 0.027
495
TRC010 Trichotillomania 41 0.027
496
MCL003 Macular Holes 41 0.027
497
CRN025 Corneal Dystrophy 41 0.027
498
MYS001 Myositis Ossificans 41 0.027
499
PHC013 Phaeochromocytoma 41 0.027
500
MYC033 Myoclonus 41 0.027
501
HMT018 Hematopoietic Stem Cell Transplantation 41 0.027
502
c CNG124 Congenital Rubella 40 0.027
503
HYP041 Hypochondrogenesis 40 0.027
504
IMM065 Immunodeficiency 10 40 0.027
505
c SBC007 Subacute Thyroiditis 39 0.027
506
TRN012 Transient Global Amnesia 39 0.027
507
BLP004 Blepharophimosis 39 0.027
508
PNL013 Penile Disease 39 0.027
509
P OCY001 Oocyte Maturation Defect 39 0.027
510
HYP391 Hyperammonemia 39 0.027
511
HMH002 Hemihypertrophy 39 0.027
512
DDN011 Duodenal Atresia 39 0.027
513
BLN002 Balanitis Xerotica Obliterans 39 0.027
514
P NRX001 Neuroaxonal Dystrophy 39 0.027
515
FXF002 Fox-Fordyce Disease 39 0.027
516
HRM002 Hermaphroditism 38 0.027
517
P MRC003 Mercury Poisoning 38 0.027
518
FNS001 Funisitis 38 0.027
519
c CHR054 Chronic Closed-Angle Glaucoma 38 0.027
520
BFD003 Bifid Uvula 38 0.027
521
P CHR342 Chiari Malformation 37 0.027
522
P PRS062 Persistent Hyperplastic Primary Vitreous 37 0.027
523
P CHR084 Chromosomal Disease 37 0.027
524
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.027
525
CRV025 Cervical Incompetence 37 0.027
526
SPL040 Split Hand 37 0.027
527
FRY002 Fryns Syndrome 36 0.027
528
MTG002 Mutagen Sensitivity 36 0.027
529
LYS017 Loeys-Dietz Syndrome 4 36 0.027
530
ANR018 Anorchia 36 0.027
531
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 36 0.027
532
FCL044 Fecal Incontinence 35 0.027
533
IRT001 Iritis 35 0.027
534
c PLN018 Peeling Skin Syndrome 2 35 0.027
535
c DGT005 Digital Arthropathy-Brachydactyly, Familial 35 0.027
536
HRS011 Horseshoe Kidney 35 0.027
537
P PST059 Pustular Psoriasis 35 0.027
538
NNT019 Neonatal Hypothyroidism 35 0.027
539
MYF001 Myofibroma 35 0.027
540
CND006 Candida Glabrata 34 0.027
541
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 34 0.027
542
ADP007 Adie Pupil 34 0.027
543
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 33 0.027
544
CRN088 Craniorachischisis 32 0.027
545
RGH009 Right Atrial Isomerism 32 0.027
546
TRG003 Trigeminal Nerve Disease 31 0.027
547
PDT040 Pediatric Hypertension 31 0.027
548
IMM082 Immunodeficiency 18 31 0.027
549
c PLN021 Peeling Skin Syndrome 3 31 0.027
550
BLN010 Balanitis 30 0.027
551
INT309 Intellectual Developmental Disorder with Persistence of Fetal Hemoglobin 29 0.027
552
AVD001 Avoidant Personality Disorder 29 0.027
553
NRC003 Narcissistic Personality Disorder 28 0.027
554
IMP001 Impetigo Herpetiformis 28 0.027
555
c ATM007 Autoimmune Disease of Central Nervous System 28 0.027
556
IMM076 Immunodeficiency 24 27 0.027
557
MLT003 Multilocular Clear Cell Renal Cell Carcinoma 27 0.027
558
TRD003 Taurodontism 27 0.027
559
RNL008 Renal Artery Atheroma 27 0.027
560
HMN031 Human Venous Malformation 27 0.027
561
LKM059 Leukemia, Megakaryoblastic, with or Without Down Syndrome, Somatic 26 0.027
562
NNT018 Neonatal Herpes 26 0.027
563
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 26 0.027
564
OSC001 Oeis Complex 26 0.027
565
SVN001 Sveinsson Choreoretinal Atrophy 26 0.027
566
HNM002 Hinman Syndrome 25 0.027
567
NNT021 Neonatal Meningitis 24 0.027
568
c CRN214 Coronary Heart Disease 5 23 0.027
569
RHH001 Rohhad 22 0.027
570
CDL005 Caudal Duplication Anomaly 22 0.027
571
VSC009 Vascular Skin Disease 22 0.027
572
CLC002 Calcaneonavicular Coalition 21 0.027
573
TRG006 Trigger Thumb 20 0.027
574
TGF006 Tgfb2-Related Loeys-Dietz Syndrome 17 0.027
575
AND005 Androgen Insensitivity Syndrome, Mild 16 0.027
576
LMB009 Lambdoid Synostosis 15 0.027
577
CLP002 Colpocephaly 15 0.027
578
ECT085 Ectopia Cordis 15 0.027
579
WLS002 Wilson-Mikity Syndrome 14 0.027
580
LNR009 Linear Atrophoderma of Moulin 14 0.027
581
NNT002 Neonatal Urinary Tract Infectious Disease 13 0.027
582
SYM006 Symmetrical Thalamic Calcifications 11 0.027
583
FBL005 Fibular Aplasia 10 0.027
584
P CLR023 Colorectal Cancer 97 0.019
585
P ALZ034 Alzheimer Disease 93 0.019
586
P PRS040 Prostate Cancer 89 0.019
587
P OST012 Osteoarthritis 82 0.019
588
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.019
589
P MLT019 Multiple Myeloma 80 0.019
590
P RTN008 Retinitis Pigmentosa 79 0.019
591
STR067 Stroke, Ischemic 77 0.019
592
P ATX030 Ataxia-Telangiectasia 76 0.019
593
P OVR042 Ovarian Cancer 75 0.019
594
END057 Endometrial Cancer 75 0.019
595
c DLT002 Dilated Cardiomyopathy 75 0.019
596
P RTN024 Retinoblastoma 75 0.019
597
P NRF019 Neurofibromatosis, Type 2 73 0.019
598
HDG012 Hodgkin Lymphoma 73 0.019
599
CMP005 Campomelic Dysplasia 72 0.019
600
c HPT073 Hepatitis C Virus 72 0.019
601
P WSK001 Wiskott-Aldrich Syndrome 72 0.019
602
P PRK057 Parkinson Disease, Late-Onset 72 0.019
603
MLT021 Multiple System Atrophy 71 0.019
604
P NRV007 Nervous System Disease 71 0.019
605
P MTC003 Metachromatic Leukodystrophy 71 0.019
606
TST021 Testicular Germ Cell Tumor 70 0.019
607
KRT004 Keratitis 70 0.019
608
FBR012 Fabry Disease 69 0.019
609
CST001 Costello Syndrome 69 0.019
610
P ALP004 Alport Syndrome 68 0.019
611
P DMN001 Diamond-Blackfan Anemia 68 0.019
612
c MLT136 Multiple Endocrine Neoplasia 1 68 0.019
613
P LPR003 Leprosy 68 0.019
614
P FRG001 Fragile X Syndrome 68 0.019
615
c HPT001 Hepatitis C 68 0.019
616
P CWD006 Cowden Syndrome 1 68 0.019
617
P ESS003 Essential Thrombocythemia 68 0.019
618
PLM001 Pulmonary Tuberculosis 68 0.019
619
BCK001 Becker Muscular Dystrophy 68 0.019
620
CMM004 Common Variable Immunodeficiency 67 0.019
621
P MYL005 Myelofibrosis 67 0.019
622
PSY004 Psychotic Disorder 67 0.019
623
SMT004 Smith-Lemli-Opitz Syndrome 67 0.019
624
P NSP012 Nasopharyngeal Carcinoma 67 0.019
625
APR006 Apert Syndrome 66 0.019
626
OBS061 Obstructive Sleep Apnea 66 0.019
627
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.019
628
KPS004 Kaposi Sarcoma 66 0.019
629
P CHR071 Charcot-Marie-Tooth Disease 66 0.019
630
OBS002 Obsessive-Compulsive Disorder 66 0.019
631
SRC014 Sarcoma 66 0.019
632
ACR007 Acromegaly 65 0.019
633
c HRD010 Hereditary Spastic Paraplegia 65 0.019
634
c MLT024 Multiple Endocrine Neoplasia Iia 65 0.019
635
TBR024 Tuberous Sclerosis-1 65 0.019
636
PRT037 Pertussis 64 0.019
637
c HPT016 Hepatitis B 64 0.019
638
P AMY004 Amyloidosis 64 0.019
639
PSR001 Psoriatic Arthritis 64 0.019
640
c HMP029 Hemophilia a 64 0.019
641
P ALX003 Alexander Disease 64 0.019
642
PTR006 Peters Anomaly 64 0.019
643
AND015 Androgen Insensitivity 63 0.019
644
MTH009 Mouth Disease 63 0.019
645
P HMP002 Hemophagocytic Lymphohistiocytosis 63 0.019
646
P ART023 Arthropathy 63 0.019
647
LPT001 Leptospirosis 63 0.019
648
CRD119 Cardiac Arrest 63 0.019
649
P NRV006 Nervous System Cancer 62 0.019
650
P CLD001 Cleidocranial Dysplasia 62 0.019
651
c MYT021 Myotonic Dystrophy 1 62 0.019
652
CNT047 Contact Dermatitis 62 0.019
653
P VLC001 Velocardiofacial Syndrome 62 0.019
654
P ADD001 Addison's Disease 62 0.019
655
CRY002 Cryptorchidism 62 0.019
656
VSC011 Vasculitis 62 0.019
657
OCL009 Ocular Cancer 62 0.019
658
GST092 Gastroesophageal Reflux 61 0.019
659
MDD011 Mood Disorder 61 0.019
660
P ESN007 Eosinophilia 61 0.019
661
WST001 West Syndrome 61 0.019
662
P ENC004 Encephalitis 61 0.019
663
CHR063 Chronic Mucocutaneous Candidiasis 61 0.019
664
MNK001 Menkes Disease 61 0.019
665
LPD011 Lipoid Adrenal Hyperplasia 61 0.019
666
P IDP010 Idiopathic Generalized Epilepsy 61 0.019
667
P INT068 Intestinal Disease 61 0.019
668
P ANG001 Angelman Syndrome 61 0.019
669
TNG002 Tangier Disease 61 0.019
670
P SLP006 Sleep Apnea 61 0.019
671
P MYM002 Moyamoya Disease 60 0.019
672
SHW002 Shwachman-Diamond Syndrome 60 0.019
673
P ASP006 Aspergillosis 60 0.019
674
P PNC044 Pancreatitis 60 0.019
675
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.019
676
CRB011 Cerebrotendinous Xanthomatosis 60 0.019
677
FTT001 Fatty Liver Disease 60 0.019
678
P LBR001 Leber Congenital Amaurosis 60 0.019
679
ETN001 Eating Disorder 60 0.019
680
INC021 Incontinentia Pigmenti 60 0.019
681
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.019
682
KRN002 Kearns-Sayre Syndrome 59 0.019
683
SPT004 Septic Arthritis 59 0.019
684
ASP002 Aspartylglucosaminuria 59 0.019
685
P CCK001 Cockayne Syndrome 59 0.019
686
PLM070 Pulmonic Stenosis 59 0.019
687
CHL123 Chlamydia 59 0.019
688
P MSC007 Muscle Hypertrophy 59 0.019
689
VRL011 Viral Infectious Disease 59 0.019
690
MSS002 Mass Syndrome 59 0.019
691
OST017 Osteomyelitis 59 0.019
692
ADM013 Adamantinoma of Long Bones 59 0.019
693
c FML001 Familial Atrial Fibrillation 59 0.019
694
c SYS004 Systemic Mastocytosis 59 0.019
695
STT001 Status Epilepticus 59 0.019
696
P ANT006 Antiphospholipid Syndrome 58 0.019
697
P GT001 Gout 58 0.019
698
P SYS005 Systemic Scleroderma 58 0.019
699
LPD008 Lipid Metabolism Disorder 58 0.019
700
P MCR010 Microcephaly 58 0.019
701
P LKD001 Leukodystrophy 58 0.019
702
P PRP029 Porphyria 58 0.019
703
P MCP010 Mucopolysaccharidosis 58 0.019
704
P RTH001 Rothmund-Thomson Syndrome 57 0.019
705
ALP001 Alopecia Universalis 57 0.019
706
ACS001 Acoustic Neuroma 57 0.019
707
RHM027 Rheumatic Disease 57 0.019
708
P FRS003 Fraser Syndrome 57 0.019
709
MLG056 Malignant Hyperthermia 57 0.019
710
PLY023 Polycystic Liver Disease 57 0.019
711
P CND004 Candidiasis 57 0.019
712
ACN002 Acanthosis Nigricans 57 0.019
713
P INT143 Interstitial Cystitis 57 0.019
714
CNS004 Constipation 57 0.019
715
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 57 0.019
716
P SZR006 Seizure Disorder 57 0.019
717
WLF001 Wolff-Parkinson-White Syndrome 57 0.019
718
P PND002 Pendred Syndrome 56 0.019
719
STR026 Star Syndrome 56 0.019
720
STF001 Stiff-Person Syndrome 56 0.019
721
BLS001 Blau Syndrome 56 0.019
722
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 56 0.019
723
SFT003 Soft Tissue Sarcoma 56 0.019
724
JNT002 Joint Disorders 56 0.019
725
WLM001 Wolman Disease 56 0.019
726
c CHR536 Charcot-Marie-Tooth Disease, Type 1a 56 0.019
727
P PTS002 Ptosis 56 0.019
728
BRN002 Bronchiolitis 56 0.019
729
P BDD001 Budd-Chiari Syndrome 56 0.019
730
PRS047 Prostatitis 56 0.019
731
P MMB011 Membranous Nephropathy 56 0.019
732
MLN007 Male Infertility 56 0.019
733
CNC002 Cinca Syndrome 56 0.019
734
MNK003 Muenke Syndrome 55 0.019
735
P GRS014 Griscelli Syndrome, Type 2 55 0.019
736
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.019
737
P OVR049 Ovarian Disease 55 0.019
738
CHL014 Cholera 55 0.019
739
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 55 0.019
740
c PND001 Pain Disorder 55 0.019
741
DMY004 Demyelinating Disease 55 0.019
742
BLD034 Bile Duct Carcinoma 55 0.019
743
c PRK031 Parkinson Disease 1 55 0.019
744
GLC003 Glucose Intolerance 55 0.019
745
PTT006 Pituitary Adenoma 55 0.019
746
P FND001 Fundus Albipunctatus 55 0.019
747
P OLG002 Oligodendroglioma 55 0.019
748
SCR008 Scrub Typhus 54 0.019
749
MVM001 Movement Disease 54 0.019
750
LST001 Listeriosis 54 0.019
751
VSC002 Vascular Dementia 54 0.019
752
P EPD009 Epidermolysis Bullosa Dystrophica 54 0.019
753
MVL001 Mevalonic Aciduria 54 0.019
754
P PLY019 Polyneuropathy 54 0.019
755
RST001 Restless Legs Syndrome 54 0.019
756
VSC006 Vascular Cancer 54 0.019
757
P INT030 Intracranial Aneurysm 54 0.019
758
HST011 Histoplasmosis 54 0.019
759
FDL002 Food Allergy 54 0.019
760
P STC001 Stickler Syndrome 54 0.019
761
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.019
762
APH002 Aphasia 53 0.019
763
P INT063 Intellectual Disability 53 0.019
764
RSC001 Rosacea 53 0.019
765
P EMR001 Emery-Dreifuss Muscular Dystrophy 53 0.019
766
SLP005 Sleep Disorder 53 0.019
767
P SYP003 Syphilis 53 0.019
768
ALP014 Alpha-Thalassemia/mental Retardation Syndrome 53 0.019
769
NNL002 Nonalcoholic Steatohepatitis 53 0.019
770
P CNT005 Central Nervous System Lymphoma 53 0.019
771
P ANG015 Angioedema 53 0.019
772
P CYS018 Cystitis 53 0.019
773
P HLL001 Hallermann-Streiff Syndrome 53 0.019
774
c RCS002 Recessive Dystrophic Epidermolysis Bullosa 52 0.019
775
P PYL005 Pyelonephritis 52 0.019
776
P DGR001 Digeorge Syndrome 52 0.019
777
P HYP027 Hypobetalipoproteinemia 52 0.019
778
P BRC006 Brachydactyly 52 0.019
779
TRM010 Traumatic Brain Injury 52 0.019
780
NTH001 Netherton Syndrome 52 0.019
781
TTH006 Tooth Disease 52 0.019
782
CRH005 Crohn's Colitis 52 0.019
783
TMR010 Tumor Predisposition Syndrome 52 0.019
784
PRS042 Prostate Disease 52 0.019
785
QDR001 Quadriplegia 52 0.019
786
MST017 Mast Cell Disease 52 0.019
787
VGT001 Vogt-Koyanagi-Harada Disease 52 0.019
788
OCL020 Ocular Cicatricial Pemphigoid 52 0.019
789
HYP077 Hypertrichosis 52 0.019
790
WGR001 Wagr Syndrome 52 0.019
791
ARS001 Aarskog-Scott Syndrome 52 0.019
792
P ALT001 Alternating Hemiplegia of Childhood 52 0.019
793
c INT064 Intermediate Uveitis 52 0.019
794
P PRM006 Primary Biliary Cirrhosis 52 0.019
795
NRF007 Neurofibroma 52 0.019
796
CYS005 Cysticercosis 52 0.019
797
MYM001 Myoma 51 0.019
798
CYS010 Cystinosis 51 0.019
799
BLR001 Biliary Atresia 51 0.019
800
TMP001 Temporal Lobe Epilepsy 51 0.019
801
THY030 Thyroid Gland Disease 51 0.019
802
ALL009 Allergic Conjunctivitis 51 0.019
803
DSM004 Desmoid Tumor 51 0.019
804
MGL013 Megalencephaly 51 0.019
805
P WVR001 Weaver Syndrome 51 0.019
806
P MSC003 Muscular Atrophy 51 0.019
807
P PLY041 Polymyositis 51 0.019
808
PRT011 Protein C Deficiency 51 0.019
809
P LRS001 Larsen Syndrome 51 0.019
810
DSS009 Disseminated Intravascular Coagulation 51 0.019
811
P DDN001 Duodenal Ulcer 51 0.019
812
c INF067 Inflammatory Bowel Disease 10 51 0.019
813
CCT002 Cicatricial Pemphigoid 51 0.019
814
LRN003 Learning Disability 51 0.019
815
CHL069 Cholesteatoma 51 0.019
816
c INF071 Inflammatory Bowel Disease 1 51 0.019
817
BLL001 Baller-Gerold Syndrome 51 0.019
818
FML038 Female Reproductive Organ Cancer 51 0.019
819
FML037 Female Breast Cancer 51 0.019
820
P SJG002 Sjogren-Larsson Syndrome 51 0.019
821
CLN019 Colonic Disease 50 0.019
822
QBC001 Quebec Platelet Disorder 50 0.019
823
STM006 Stomach Disease 50 0.019
824
PRC012 Pericardial Effusion 50 0.019
825
IMM136 Immune System Disease 50 0.019
826
SCT005 Scott Syndrome 50 0.019
827
RNL007 Renal Tubular Acidosis 50 0.019
828
NRG002 Neurogenic Bladder 50 0.019
829
DBT084 Diabetes Mellitus, Ketosis-Prone 50 0.019
830
SPN019 Spondylolisthesis 50 0.019
831
MGC001 Megacolon 50 0.019
832
MRG003 Marginal Zone B-Cell Lymphoma 50 0.019
833
RHM001 Rheumatic Fever 50 0.019
834
BCL002 B Cell Deficiency 50 0.019
835
HRT007 Heart Cancer 50 0.019
836
ASP001 Asperger Syndrome 49 0.019
837
P CLL015 Collagen Disease 49 0.019
838
CHN055 Chanarin-Dorfman Syndrome 49 0.019
839
ESN005 Eosinophilic Gastroenteritis 49 0.019
840
P EPD002 Epidermolytic Hyperkeratosis 49 0.019
841
SPN020 Spondylosis 49 0.019
842
HMG002 Hemoglobinuria 49 0.019
843
BRD001 Brody Myopathy 49 0.019
844
P ALL008 Allergic Bronchopulmonary Aspergillosis 49 0.019
845
c PRM226 Primary Central Nervous System Lymphoma 49 0.019
846
P LSS002 Lissencephaly 49 0.019
847
OST011 Osteomalacia 48 0.019
848
PRN023 Prion Disease 48 0.019
849
HND002 Hand, Foot and Mouth Disease 48 0.019
850
MTB004 Metabolic Acidosis 48 0.019
851
NRM004 Neuroma 48 0.019
852
ACR003 Acrodermatitis Enteropathica 48 0.019
853
P CNG046 Congenital Fiber-Type Disproportion 48 0.019
854
PLM041 Pulmonary Valve Stenosis 48 0.019
855
RSP002 Respiratory Syncytial Virus Infectious Disease 48 0.019
856
PLS009 Plasma Cell Neoplasm 48 0.019
857
GNG002 Ganglioneuroma 48 0.019
858
MTN003 Motion Sickness 48 0.019
859
PPL018 Papillary Adenocarcinoma 48 0.019
860
P FBR025 Fibrochondrogenesis 48 0.019
861
KRT010 Kartagener Syndrome 48 0.019
862
SLD003 Sialadenitis 48 0.019
863
BNF002 Bone Fracture 47 0.019
864
c PSD066 Pseudohypoparathyroidism, Type Ib 47 0.019
865
SYN036 Syncope 47 0.019
866
PLC003 Placental Site Trophoblastic Tumor 47 0.019
867
CRD118 Cardiovascular Cancer 47 0.019
868
CCN002 Cocaine Abuse 47 0.019
869
XNT003 Xanthomatosis 47 0.019
870
c HMG001 Hemoglobin C Disease 47 0.019
871
CD4003 Cd40 Ligand Deficiency 47 0.019
872
c MLG069 Malignant Hypertension 47 0.019
873
PSD007 Pseudomyxoma Peritonei 47 0.019
874
LPM005 Lipomatosis 47 0.019
875
MLR006 Male Reproductive Organ Cancer 47 0.019
876
P SYR001 Syringomyelia 47 0.019
877
FLL008 Folliculitis 47 0.019
878
CNJ012 Conjunctival Disease 46 0.019
879
SPC010 Speech and Communication Disorders 46 0.019
880
MLT006 Multidrug-Resistant Tuberculosis 46 0.019
881
P PRD008 Periodontitis 46 0.019
882
SDD007 Sudden Cardiac Death 46 0.019
883
DBW001 Dubowitz Syndrome 46 0.019
884
CHR074 Choriocarcinoma 46 0.019
885
PRN011 Pernicious Anemia 46 0.019
886
c ERL020 Early-Onset Schizophrenia 46 0.019
887
ART004 Aortic Atherosclerosis 46 0.019
888
PRR002 Pure Red-Cell Aplasia 46 0.019
889
BLD053 Blood Platelet Disease 46 0.019
890
BND015 Band-Like Calcification with Simplified Gyration and Polymicrogyria 46 0.019
891
NPH003 Nephrocalcinosis 46 0.019
892
CVR006 Cavernous Hemangioma 46 0.019
893
DNT012 Dental Caries 46 0.019
894
BLL003 Bell's Palsy 46 0.019
895
HMN032 Human Herpesvirus 8 46 0.019
896
PLM035 Pulmonary Eosinophilia 46 0.019
897
PRM003 Premature Ejaculation 46 0.019
898
CRB004 Cerebral Artery Occlusion 46 0.019
899
JHN001 Johanson-Blizzard Syndrome 46 0.019
900
SMT001 Somatization Disorder 46 0.019
901
SNS023 Sensory System Cancer 46 0.019
902
ADN027 Adenomyosis 46 0.019
903
MNN009 Meningoencephalitis 45 0.019
904
CTS002 Cat-Scratch Disease 45 0.019
905
ANV001 Anovulation 45 0.019
906
P INF049 Infantile Myofibromatosis 45 0.019
907
VRN004 Vernal Keratoconjunctivitis 45 0.019
908
EST007 Estrogen Resistance 45 0.019
909
P MLG086 Malignant Hyperthermia Susceptibility 45 0.019
910
TST015 Testicular Disease 45 0.019
911
DRM011 Dermatophytosis 45 0.019
912
P CNN004 Connective Tissue Cancer 45 0.019
913
PLL012 Pollen Allergy 45 0.019
914
FBR032 Fibromuscular Dysplasia 45 0.019
915
MCR037 Macroglossia 45 0.019
916
IPX001 Ipex Syndrome 45 0.019
917
CNG048 Congenital Hepatic Fibrosis 45 0.019
918
ALV007 Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins 45 0.019
919
P TYR004 Tyrosinemia 45 0.019
920
HMP009 Haemophilus Influenzae 45 0.019
921
c TRC092 Trichorhinophalangeal Syndrome, Type I 45 0.019
922
EPD006 Epidermolysis Bullosa Acquisita 45 0.019
923
IDP024 Idiopathic Inflammatory Myopathy 45 0.019
924
c DBT064 Diabetes Mellitus, Transient Neonatal, 1 44 0.019
925
P PSD015 Pseudohypoparathyroidism 44 0.019
926
KWS001 Kwashiorkor 44 0.019
927
c MTR002 Mitral Valve Insufficiency 44 0.019
928
c TYR013 Tyrosinemia, Type Ii 44 0.019
929
P D2H001 D-2-Hydroxyglutaric Aciduria 44 0.019
930
BHR001 Behr Syndrome 44 0.019
931
GGR001 Geographic Tongue 44 0.019
932
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 44 0.019
933
FBR009 Fibrous Dysplasia 44 0.019
934
ISL003 Isolated Growth Hormone Deficiency 44 0.019
935
DSC009 Discoid Lupus Erythematosus 44 0.019
936
PRM013 Premature Menopause 44 0.019
937
OCL069 Ocular Motor Apraxia 44 0.019
938
P LYD001 Leydig Cell Tumor 44 0.019
939
OPP004 Oppositional Defiant Disorder 43 0.019
940
CHR008 Choroiditis 43 0.019
941
ANM001 Anemia of Prematurity 43 0.019
942
WRN002 Wernicke-Korsakoff Syndrome 43 0.019
943
LYM009 Lymphocytic Choriomeningitis 43 0.019
944
NDL021 Nodular Lymphocyte Predominant Hodgkin Lymphoma 43 0.019
945
AGR002 Agoraphobia 43 0.019
946
MST006 Mast Syndrome 43 0.019
947
P AML002 Amelogenesis Imperfecta 43 0.019
948
NVS001 Neovascular Glaucoma 43 0.019
949
P PSD003 Pseudohypoaldosteronism 43 0.019
950
GST052 Gestational Choriocarcinoma 43 0.019
951
P FNG005 Feingold Syndrome 43 0.019
952
BSL008 Basal Ganglia Disease 43 0.019
953
GND003 Gonadal Disease 43 0.019
954
CRB085 Cerebral Hemorrhage 43 0.019
955
RNL012 Renal Tuberculosis 43 0.019
956
c CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 43 0.019
957
PRD011 Proud Syndrome 42 0.019
958
ANH002 Anhidrosis 42 0.019
959
c ACT076 Acute Myocarditis 42 0.019
960
BLN001 Blount's Disease 42 0.019
961
CMP034 Complete Androgen Insensitivity Syndrome 42 0.019
962
PLG004 Plagiocephaly 42 0.019
963
BCK006 Back Pain 42 0.019
964
MTR010 Mature Teratoma 42 0.019
965
FCL041 Focal Myositis 42 0.019
966
SBP004 Subependymoma 42 0.019
967
PRS012 Pars Planitis 42 0.019
968
GND001 Gonadoblastoma 42 0.019
969
RTT001 Ritter's Disease 41 0.019
970
P CNG390 Congenital Pulmonary Airway Malformation 41 0.019
971
CHR078 Chorioretinitis 41 0.019
972
DFF001 Diffuse Cutaneous Mastocytosis 41 0.019
973
NSP002 Nasopharyngitis 41 0.019
974
PRD003 Periodontosis 41 0.019
975
PRP009 Peripartum Cardiomyopathy 41 0.019
976
PRT019 Protein-Losing Enteropathy 41 0.019
977
DFF003 Diffuse Scleroderma 41 0.019
978
P TST026 Testicular Germ Cell Cancer 41 0.019
979
PRG014 Progesterone Resistance 41 0.019
980
BDY001 Body Dysmorphic Disorder 41 0.019
981
AND001 Anodontia 41 0.019
982
P FML187 Familial Hypertension 41 0.019
983
ADR009 Adrenal Cortex Disease 41 0.019
984
P SML002 Small Cell Sarcoma 41 0.019
985
DLS001 Delusional Disorder 41 0.019
986
HYP101 Hyperinsulinism-Hyperammonemia Syndrome 41 0.019
987
RNL025 Renal Hypoplasia 41 0.019
988
NNT008 Neonatal Abstinence Syndrome 41 0.019
989
c PRG001 Progressive Muscular Atrophy 40 0.019
990
P CNG024 Congenital Nystagmus 40 0.019
991
CRD144 Cardiovascular Disease Risk Factor ) 40 0.019
992
SPN029 Spondylolysis 40 0.019
993
c CHR091 Chronic Meningitis 40 0.019
994
CHL052 Choledochal Cyst 40 0.019
995
BLD054 Blood Protein Disease 40 0.019
996
HYP068 Hyperostosis 40 0.019
997
PDT035 Pediatric Systemic Lupus Erythematosus 40 0.019
998
MNN017 Mononeuropathy 40 0.019
999
IDP070 Idiopathic Scoliosis 40 0.019
1000
PRS030 Persistent Fetal Circulation Syndrome 40 0.019
1001
ACT084 Acute Stress Disorder 40 0.019
1002
WDM004 Wiedemann-Steiner Syndrome 39 0.019
1003
RDN001 Reading Disorder 39 0.019
1004
c CNG031 Congenital Nervous System Abnormality 39 0.019
1005
SPR007 Superior Mesenteric Artery Syndrome 39 0.019
1006
NRN008 Neuronal Intranuclear Inclusion Disease 39 0.019
1007
c BRC082 Brachydactyly, Type E 39 0.019
1008
P KLF001 Kleefstra Syndrome 39 0.019
1009
P DYS005 Dyslexia 39 0.019
1010
P SDR003 Sideroblastic Anemia 39 0.019
1011
OLG001 Oligospermia 39 0.019
1012
c CNG029 Congenital Mesoblastic Nephroma 39 0.019
1013
ASP004 Asphyxia Neonatorum 39 0.019
1014
GST007 Gastric Dilatation 39 0.019
1015
c CNG033 Congenital Syphilis 39 0.019
1016
CRL004 Caroli Disease 39 0.019
1017
MDY003 Mody, Type Ii 38 0.019
1018
MNN021 Meningococcemia 38 0.019
1019
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 38 0.019
1020
ANG016 Angiokeratoma 38 0.019
1021
P ACH011 Achondrogenesis 38 0.019
1022
HYP064 Hypogonadotropism 38 0.019
1023
P TRC005 Tracheal Stenosis 38 0.019
1024
FMR004 Fumarase Deficiency 38 0.019
1025
ARM002 Aromatic L-Amino Acid Decarboxylase Deficiency 38 0.019
1026
INT011 Interstitial Emphysema 38 0.019
1027
c CHR098 Chronic Pyelonephritis 38 0.019
1028
MYX004 Myxedema 38 0.019
1029
CND005 Cone Dystrophy 38 0.019
1030
DFF021 Diffuse Mesangial Sclerosis 38 0.019
1031
SPS004 Spastic Quadriplegia 38 0.019
1032
P PNT019 Pontocerebellar Hypoplasia 37 0.019
1033
DVL001 Developmental Coordination Disorder 37 0.019
1034
ATM014 Autoimmune Disease of Endocrine System 37 0.019
1035
LYM127 Lymphatic Malformations 37 0.019
1036
TLP001 Talipes Equinovarus 37 0.019
1037
MLR007 Male Reproductive System Disease 37 0.019
1038
CVR010 Cavernous Malformation 37 0.019
1039
ALX002 Alexithymia 37 0.019
1040
EPS026 Epispadias 37 0.019
1041
OBS003 Obsessive-Compulsive Personality Disorder 37 0.019
1042
MLG097 Malignant Mesenchymal Tumor 37 0.019
1043
VSC018 Visceral Steatosis 37 0.019
1044
P HYP120 Hypoaldosteronism 37 0.019
1045
SCH072 Scheuermann Disease 37 0.019
1046
LND001 Landau-Kleffner Syndrome 36 0.019
1047
MSC004 Muscle Tissue Disease 36 0.019
1048
CMB021 Combined Pituitary Hormone Deficiency 36 0.019
1049
PCH002 Pachygyria 36 0.019
1050
C6D001 C6 Deficiency 36 0.019
1051
NTR006 Neutrophil Immunodeficiency Syndrome 36 0.019
1052
PRP080 Peripheral Artery Disease 36 0.019
1053
CNG035 Congenital Bilateral Absence of Vas Deferens 36 0.019
1054
PRS108 Persistent Polyclonal B-Cell Lymphocytosis 36 0.019
1055
c CNN010 Connective Tissue Benign Neoplasm 35 0.019
1056
PRM129 Primary Cutaneous Marginal Zone B-Cell Lymphoma 35 0.019
1057
P HRT017 Heart Tumor 35 0.019
1058
TCL012 T-Cell/histiocyte Rich Large B Cell Lymphoma 35 0.019
1059
SML028 Semilobar Holoprosencephaly 35 0.019
1060
GRN007 Granuloma Annulare 35 0.019
1061
c ATM093 Autoimmune Disease of Peripheral Nervous System 35 0.019
1062
LCH003 Lichen Nitidus 35 0.019
1063
PDT025 Pediatric Multiple Sclerosis 35 0.019