Search results for "twinning"

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

1277 hits were found for 'twinning'

# Family MCID Name MIFTS Score
1
TWN001 Twin-to-Twin Transfusion Syndrome 47 12.708
2
c RNL090 Renal Tubular Dysgenesis Due to Twin-Twin Transfusion 6 3.797
3
P PLY018 Polycythemia 58 0.151
4
PLY012 Polyhydramnios 45 0.150
5
CRB009 Cerebritis 36 0.144
6
ANN002 Anencephaly 50 0.134
7
PLC008 Placenta Disease 33 0.117
8
P HRT032 Heart Disease 64 0.109
9
c CNG401 Congenital Heart Disease 67 0.105
10
P CRV039 Cervicitis 45 0.104
11
OLG003 Oligohydramnios 52 0.100
12
HYD012 Hydrops Fetalis 45 0.098
13
P OBS005 Obesity 91 0.095
14
P CRD011 Cardiomyopathy 66 0.089
15
CYT008 Cytomegalovirus Infection 51 0.087
16
CHL071 Child Syndrome 58 0.083
17
KDS001 Kid Syndrome 53 0.083
18
CNG069 Congenital Cytomegalovirus 34 0.083
19
CHR005 Chorioamnionitis 47 0.080
20
DWN001 Down Syndrome 65 0.078
21
CCN007 Cocoon Syndrome 32 0.078
22
P THY032 Thyroiditis 57 0.078
23
ISC004 Ischemia 56 0.076
24
P PLM037 Pulmonary Hypertension 78 0.073
25
SRN002 Sirenomelia 26 0.073
26
P LKM002 Leukemia 70 0.071
27
DFC004 Deficiency Anemia 64 0.068
28
P HYP086 Hypothyroidism 63 0.068
29
URT039 Urticaria 58 0.066
30
P PRS038 Personality Disorder 60 0.066
31
ECT026 Ectopic Pregnancy 46 0.066
32
NNT011 Neonatal Anemia 34 0.066
33
OMP004 Omphalocele 51 0.063
34
PYL006 Pyloric Stenosis 46 0.063
35
INT060 Intestinal Atresia 37 0.063
36
CRB037 Cerebral Palsy 54 0.060
37
P ENC008 Encephalocele 48 0.060
38
P ECL001 Eclampsia 55 0.060
39
c PRC016 Pre-Eclampsia 57 0.060
40
P THR014 Thrombocytopenia 63 0.060
41
P EPL164 Epilepsy 60 0.060
42
PRT082 Preterm Premature Rupture of the Membranes 46 0.060
43
P TRT010 Teratoma 49 0.060
44
URT008 Urticaria Pigmentosa 37 0.060
45
AMN009 Amniotic Band Syndrome 26 0.060
46
ENC005 Encephalomalacia 26 0.060
47
P TYS001 Tay-Sachs Disease 72 0.057
48
P NRC002 Narcolepsy 62 0.057
49
DRM006 Dermatitis 58 0.057
50
P MYP004 Myopathy 67 0.057
51
VCT001 Vacterl Association 47 0.057
52
P LPS004 Lupus Erythematosus 63 0.057
53
ART005 Arteriovenous Malformation 63 0.057
54
P TXP001 Toxoplasmosis 61 0.057
55
WLL006 Wells Syndrome 57 0.057
56
PRV004 Periventricular Leukomalacia 51 0.057
57
P GND004 Gonadal Dysgenesis 51 0.057
58
P APL006 Aplasia Cutis Congenita 48 0.057
59
P UTR038 Uterine Disease 38 0.057
60
URT001 Urethritis 39 0.057
61
GDS001 Good Syndrome 46 0.057
62
c PST041 Posterior Urethral Valves 46 0.057
63
PNT005 Pentalogy of Cantrell 22 0.057
64
P HYP009 Hypertrophic Pyloric Stenosis 40 0.057
65
GST009 Gastroschisis 31 0.057
66
PLC005 Placental Insufficiency 50 0.057
67
LKM006 Leukomalacia 41 0.057
68
P RBN001 Rubinstein-Taybi Syndrome 65 0.054
69
PLM033 Pulmonary Embolism 59 0.054
70
CHR322 Choreoathetosis, Hypothyroidism, and Neonatal Respiratory Distress 43 0.054
71
P ART022 Arthritis 73 0.054
72
c ACT210 Acute Respiratory Distress Syndrome 55 0.054
73
NWB001 Newborn Respiratory Distress Syndrome 47 0.054
74
THR013 Thoracic Outlet Syndrome 48 0.054
75
PRP027 Peripheral Vascular Disease 69 0.054
76
PST028 Post-Traumatic Stress Disorder 55 0.054
77
c CNG006 Congenital Hypothyroidism 59 0.054
78
ATN011 Autoinflammation with Infantile Enterocolitis 36 0.054
79
IMP002 Imperforate Anus 54 0.054
80
P ADL010 Adult Respiratory Distress Syndrome 60 0.054
81
RSP007 Respiratory Distress Syndrome, Infant 26 0.054
82
P ESP024 Esophagitis 62 0.054
83
P LYM026 Lymphoblastic Leukemia 60 0.054
84
KLN001 Klinefelter's Syndrome 52 0.054
85
CND002 Conduct Disorder 54 0.054
86
P DBT005 Diabetes Insipidus 53 0.054
87
P HYP065 Hyperaldosteronism 52 0.054
88
HYD001 Hydranencephaly 35 0.054
89
GST033 Gestational Diabetes 54 0.054
90
PRN019 Perinatal Necrotizing Enterocolitis 47 0.054
91
TRN044 Transposition of the Great Arteries 48 0.054
92
c CNG021 Congenital Toxoplasmosis 46 0.054
93
RFR003 Refractive Error 39 0.054
94
BRT030 Birth Defects 44 0.054
95
c BPL002 Bipolar I Disorder 45 0.054
96
RTN023 Retinitis 49 0.054
97
DPR014 Diprosopus 18 0.054
98
ACR022 Acardia 12 0.054
99
c ADL080 Adult Acute Respiratory Distress Syndrome 21 0.054
100
P MYC007 Myocardial Infarction 80 0.050
101
P CRN211 Coronary Artery Disease 74 0.050
102
P PRM019 Premature Ovarian Failure 65 0.050
103
ALC007 Alcohol Dependence 66 0.050
104
ANX002 Anxiety Disorder 67 0.050
105
P DYS154 Dystonia 62 0.050
106
P NRF002 Neurofibromatosis 66 0.050
107
P OST009 Osteochondritis Dissecans 51 0.050
108
P MSC005 Muscular Dystrophy 64 0.050
109
PRT036 Peritonitis 65 0.050
110
P HLP001 Holoprosencephaly 62 0.050
111
C3D001 C3 Deficiency 50 0.050
112
P MST009 Mastocytosis 54 0.050
113
P RNL028 Renal Tubular Dysgenesis 52 0.050
114
c BLD124 Bleeding Disorder, Platelet-Type, 11 37 0.050
115
MTS001 Mutism 38 0.050
116
ALR002 Al-Raqad Syndrome 36 0.050
117
ESP020 Esophageal Atresia 48 0.050
118
PTH002 Pathological Gambling 50 0.050
119
URN010 Urinary Tract Obstruction 53 0.050
120
ISC006 Ischemic Heart Disease 54 0.050
121
ART111 Artery Disease 56 0.050
122
TRN007 Transsexualism 41 0.050
123
SCR024 Sacrococcygeal Teratoma 25 0.050
124
LMB062 Limb Ischemia 48 0.050
125
P SCH015 Schizophrenia 78 0.046
126
ATT013 Attention Deficit-Hyperactivity Disorder 69 0.046
127
c SYS001 Systemic Lupus Erythematosus 87 0.046
128
P RHM011 Rheumatoid Arthritis 87 0.046
129
P NRB001 Neuroblastoma 70 0.046
130
P BCK002 Beckwith-Wiedemann Syndrome 56 0.046
131
CRZ001 Crouzon Syndrome 70 0.046
132
ADL002 Adult Syndrome 53 0.046
133
DMN002 Dementia 62 0.046
134
JJN004 Jejunal Atresia 31 0.046
135
P MYS005 Myositis 57 0.046
136
ALP008 Alopecia 56 0.046
137
c LCL006 Localized Scleroderma 60 0.046
138
ART021 Arteriosclerosis 59 0.046
139
BLM002 Bulimia Nervosa 54 0.046
140
P THR003 Thoracic Aortic Aneurysm 57 0.046
141
CTN014 Cutaneous Mastocytosis 49 0.046
142
TNP003 Tn Polyagglutination Syndrome, Somatic 30 0.046
143
HLL004 Hellp Syndrome 48 0.046
144
PLC007 Placental Abruption 46 0.046
145
PLY024 Polymicrogyria 34 0.046
146
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 34 0.046
147
PRT086 Partial Hydatidiform Mole 24 0.046
148
BRN071 Brain Injury 51 0.046
149
P ART084 Arteriovenous Fistula 40 0.046
150
PTZ001 Peutz-Jeghers Syndrome 71 0.042
151
NRL016 Neural Tube Defects 76 0.042
152
INS024 Insulin-Like Growth Factor I 75 0.042
153
P PRC031 Preeclampsia/eclampsia 1 53 0.042
154
P HPT021 Hepatitis 74 0.042
155
ACR041 Acromelic Frontonasal Dysostosis 45 0.042
156
P BPL003 Bipolar Disorder 58 0.042
157
EPD016 Epidermolysis Bullosa 59 0.042
158
P INF032 Infertility 61 0.042
159
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 45 0.042
160
ALL026 Allergic Hypersensitivity Disease 53 0.042
161
P CRN015 Cornelia De Lange Syndrome 65 0.042
162
BRX001 Bruxism 45 0.042
163
P HYP055 Hypoplastic Left Heart Syndrome 60 0.042
164
P MYP006 Myopia 58 0.042
165
BWN001 Bowen-Conradi Syndrome 51 0.042
166
P HYP076 Hyperthyroidism 59 0.042
167
ATH003 Atherosclerosis 63 0.042
168
P PNM007 Pneumonia 67 0.042
169
P DRM007 Dermatitis Herpetiformis 48 0.042
170
EST005 Esotropia 39 0.042
171
LNG099 Lung Disease 63 0.042
172
AST006 Astigmatism 42 0.042
173
P CHN005 Choanal Atresia 42 0.042
174
VND001 Vein Disease 51 0.042
175
TBR006 Tuberculoid Leprosy 44 0.042
176
P ALC004 Alcohol Abuse 57 0.042
177
PHC006 Phacomatosis Pigmentovascularis 26 0.042
178
VRN004 Vernal Keratoconjunctivitis 48 0.042
179
ANR040 Aneurysm 56 0.042
180
GND002 Gender Identity Disorder 44 0.042
181
PSD009 Pseudohermaphroditism 39 0.042
182
SPS057 Spasticity 41 0.042
183
c SVR005 Severe Pre-Eclampsia 48 0.042
184
ANS004 Anisometropia 27 0.042
185
c CRN173 Coronary Heart Disease 8 19 0.042
186
ECT006 Ectodermal Dysplasia 46 0.042
187
EPG004 Epignathus 17 0.042
188
END072 Endotheliitis 41 0.042
189
P BRS047 Breast Cancer 100 0.038
190
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.038
191
c HYP595 Hypertension, Essential 69 0.038
192
P AST005 Asthma 80 0.038
193
CYS001 Cystic Fibrosis 87 0.038
194
HV1006 Hiv-1 80 0.038
195
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 60 0.038
196
c INF069 Infantile Neuroaxonal Dystrophy 1 44 0.038
197
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.038
198
RBR001 Roberts Syndrome 61 0.038
199
SMT008 Smith-Magenis Syndrome 49 0.038
200
MRF001 Marfan Syndrome 73 0.038
201
ANR002 Aniridia 62 0.038
202
RSP006 Respiratory System Disease 61 0.038
203
VHW001 Vohwinkel Syndrome 47 0.038
204
TBR010 Tuberculosis 70 0.038
205
P SHR029 Short Syndrome 60 0.038
206
P PSR002 Psoriasis 63 0.038
207
c NRF018 Neurofibromatosis, Type 1 69 0.038
208
NTR005 Nutritional Deficiency Disease 51 0.038
209
ACR012 Aicardi Syndrome 45 0.038
210
LYS017 Loeys-Dietz Syndrome 4 37 0.038
211
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.038
212
PRN038 Prune Belly Syndrome 46 0.038
213
RSP019 Respiratory Distress Syndrome in Premature Infants 43 0.038
214
P PLY006 Polydactyly 56 0.038
215
P GRV001 Graves' Disease 62 0.038
216
LYS001 Loeys-Dietz Syndrome 53 0.038
217
STF002 Stiff Skin Syndrome 51 0.038
218
GTR002 Goiter 54 0.038
219
EYD002 Eye Disease 62 0.038
220
END020 Endocardial Fibroelastosis 44 0.038
221
IMM102 Immunodeficiency 14 33 0.038
222
P ATS007 Autism Spectrum Disorder 64 0.038
223
VSC007 Vascular Disease 51 0.038
224
VTR013 Vitreoretinopathy, Neovascular Inflammatory 50 0.038
225
HPT074 Hepatic Adenoma, Somatic 35 0.038
226
P ENC018 Encephalopathy 59 0.038
227
SVN001 Sveinsson Choreoretinal Atrophy 28 0.038
228
P MGR003 Migraine with Aura 52 0.038
229
ACQ007 Acquired Immunodeficiency Syndrome 60 0.038
230
ACD009 Acid-Labile Subunit, Deficiency of 37 0.038
231
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 35 0.038
232
PYR010 Peyronie's Disease 52 0.038
233
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 27 0.038
234
GYN001 Gynecomastia 49 0.038
235
NPH018 Nephrogenic Systemic Fibrosis 51 0.038
236
HYP041 Hypochondrogenesis 40 0.038
237
P NNT009 Neonatal Diabetes Mellitus 50 0.038
238
DDN006 Duodenitis 44 0.038
239
P CRN178 Coronary Heart Disease 6 22 0.038
240
BRN004 Brain Edema 51 0.038
241
MCR103 Microtia 37 0.038
242
BRW006 Brown Syndrome 31 0.038
243
HMN014 Human Immunodeficiency Virus Infectious Disease 46 0.038
244
PNL013 Penile Disease 38 0.038
245
P ATX004 Ataxia 53 0.038
246
CRV043 Cervical Dystonia 43 0.038
247
MLK006 Milk Allergy 50 0.038
248
BFD003 Bifid Uvula 40 0.038
249
URT031 Ureteral Disease 45 0.038
250
DBT062 Diabetic Foot Ulcers 55 0.038
251
NPH010 Nephrosclerosis 44 0.038
252
DYS018 Dysostosis 43 0.038
253
CLN022 Colonic Atresia 23 0.038
254
BRS050 Breast Cyst 43 0.038
255
KLD001 Keloids 50 0.038
256
AND005 Androgen Insensitivity Syndrome, Mild 14 0.038
257
BLL004 Bullous Keratopathy 45 0.038
258
KRT008 Keratopathy 49 0.038
259
c CHR054 Chronic Closed-Angle Glaucoma 38 0.038
260
MLT003 Multilocular Clear Cell Renal Cell Carcinoma 28 0.038
261
MCL003 Macular Holes 43 0.038
262
FTL016 Fetal Edema 14 0.038
263
SYN005 Synostosis 44 0.038
264
TCL003 T Cell Deficiency 44 0.038
265
BRN080 Brain Ischemia 42 0.038
266
JMC001 Jamaican Vomiting Sickness 10 0.038
267
CRS001 Crescentic Glomerulonephritis 41 0.038
268
CRB031 Cerebral Arterial Disease 31 0.038
269
c BNG076 Benign Exophthalmos Syndrome 15 0.038
270
PHC005 Phacomatosis Pigmentokeratotica 12 0.038
271
SLP010 Slipped Capital Femoral Epiphysis 32 0.038
272
CRN073 Coronary Arteries Congenital Malformation 11 0.038
273
CD4004 Cd4 Deficiency 15 0.038
274
RNL077 Renal Fibrosis 48 0.038
275
TGF006 Tgfb2-Related Loeys-Dietz Syndrome 18 0.038
276
VSC047 Vascular Malformation 45 0.038
277
INC002 Inclusion Body Myositis 64 0.033
278
P MDL005 Medulloblastoma 76 0.033
279
SKN016 Skin Disease 69 0.033
280
BRN024 Bronchitis 67 0.033
281
P OST005 Osteogenesis Imperfecta 68 0.033
282
P ALG002 Alagille Syndrome 70 0.033
283
P CLC005 Celiac Disease 67 0.033
284
WLL001 Williams-Beuren Syndrome 61 0.033
285
MLN008 Melanoma 61 0.033
286
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 77 0.033
287
CRH001 Crohn's Disease 76 0.033
288
P ATP001 Atopic Dermatitis 60 0.033
289
CDL003 Caudal Regression Syndrome 52 0.033
290
PCK002 Pick Disease 66 0.033
291
VND002 Van Der Woude Syndrome 50 0.033
292
KWS002 Kawasaki Disease 70 0.033
293
TST014 Testicular Cancer 55 0.033
294
P TRN020 Turner Syndrome 64 0.033
295
CHN016 Cohen Syndrome 55 0.033
296
LNG024 Langerhans-Cell Histiocytosis 64 0.033
297
P SLV001 Silver-Russell Syndrome 54 0.033
298
P RCK004 Rickets 59 0.033
299
DND001 Dandy-Walker Syndrome 42 0.033
300
VNW007 Von Willebrand Disease 57 0.033
301
P PLY011 Polycystic Ovary Syndrome 64 0.033
302
P NPH012 Nephrotic Syndrome 55 0.033
303
P CNG015 Congenital Diaphragmatic Hernia 58 0.033
304
P ANR007 Anorexia Nervosa 63 0.033
305
OVR029 Ovarian Hyperstimulation Syndrome 59 0.033
306
ATP002 Atopy 62 0.033
307
P RHN004 Rhinitis 59 0.033
308
P LYM118 Lymphoma 68 0.033
309
P INT001 Intrahepatic Cholestasis 58 0.033
310
P INF038 Influenza 71 0.033
311
MCN017 Meconium Ileus 53 0.033
312
P THL005 Thalassemia 61 0.033
313
PPL021 Papilledema 47 0.033
314
P VNT002 Ventricular Septal Defect 59 0.033
315
INC022 Inclusion-Cell Disease 46 0.033
316
P CTS001 Cutis Laxa 57 0.033
317
P HYP040 Hypospadias 58 0.033
318
P HMP007 Hemophilia 55 0.033
319
P NTR004 Neutropenia 59 0.033
320
P MNN013 Meningitis 66 0.033
321
IMM068 Immunodeficiency 8 32 0.033
322
CNV002 Conversion Disorder 45 0.033
323
CHL068 Cholestasis 57 0.033
324
ALN001 Aland Island Eye Disease 45 0.033
325
P NPH009 Nephrolithiasis 59 0.033
326
P HST010 Histiocytosis 56 0.033
327
PRP016 Paraplegia 49 0.033
328
HTR003 Heterotaxy 41 0.033
329
ARC007 Arachnoid Cysts 39 0.033
330
P ADN016 Adenocarcinoma 69 0.033
331
TTH002 Tooth Agenesis 54 0.033
332
GST045 Gastroenteritis 59 0.033
333
P DRR001 Diarrhea 60 0.033
334
PNM008 Pneumothorax 51 0.033
335
NSY001 N Syndrome 42 0.033
336
TRP014 Triploidy 39 0.033
337
P CTR002 Cataract 57 0.033
338
c ANR038 Anorexia Nervosa 1 28 0.033
339
P MYT002 Myotonic Dystrophy 46 0.033
340
TRC040 Tracheoesophageal Fistula 41 0.033
341
CYT004 Cytomegalic Inclusion Disease 29 0.033
342
CNN005 Connective Tissue Disease 60 0.033
343
DGN001 Degenerative Disc Disease 53 0.033
344
SCL003 Social Phobia 45 0.033
345
P PLN008 Peeling Skin Syndrome 45 0.033
346
ARC002 Arachnoiditis 38 0.033
347
c JVN003 Juvenile Xanthogranuloma 41 0.033
348
P HYP071 Hypersensitivity Reaction Type Ii Disease 46 0.033
349
RNL078 Renal Dysplasia 48 0.033
350
ANT011 Antisocial Personality Disorder 46 0.033
351
P MNN007 Meningocele 37 0.033
352
VGN023 Vaginitis 41 0.033
353
SXL003 Sexual Disorder 45 0.033
354
CRV069 Cervix Disease 31 0.033
355
P AGM001 Agammaglobulinemia 63 0.033
356
BRN056 Bronchopulmonary Dysplasia 56 0.033
357
P FTL001 Fetal Alcohol Syndrome 53 0.033
358
GRW007 Growth Hormone Deficiency 49 0.033
359
CLF001 Cleft Lip 48 0.033
360
GNR004 Generalized Anxiety Disorder 49 0.033
361
HYP266 Hypoxia 55 0.033
362
OCC011 Occipital Encephalocele 24 0.033
363
CNN002 Cannabis Abuse 37 0.033
364
CNN001 Cannabis Dependence 37 0.033
365
SBS004 Substance Dependence 48 0.033
366
GLC008 Glucose Metabolism Disease 44 0.033
367
GST058 Gestational Diabetes Insipidus 12 0.033
368
SPS090 Sepsis in Premature Infants 22 0.033
369
P HMP006 Hemiplegic Migraine 45 0.033
370
FRM001 Freemartinism 22 0.033
371
ATM012 Autoimmune Disease of Blood 36 0.033
372
TYP015 Type 2b Von Willebrand Disease 29 0.033
373
ADR007 Adrenoleukodystrophy 74 0.027
374
P HYP607 Hypercholesterolemia, Familial 77 0.027
375
P RTT002 Rett Syndrome 77 0.027
376
P OST002 Osteoporosis 63 0.027
377
BRN028 Brain Cancer 69 0.027
378
P PFF001 Pfeiffer Syndrome 73 0.027
379
P HMC003 Hemochromatosis 71 0.027
380
THY028 Thyroid Cancer 71 0.027
381
ALL003 Allergic Rhinitis 67 0.027
382
P LVR013 Liver Disease 76 0.027
383
DCH001 Duchenne Muscular Dystrophy 81 0.027
384
P HYP035 Hypophosphatasia 56 0.027
385
CNG034 Congestive Heart Failure 72 0.027
386
P TBR001 Tuberous Sclerosis 68 0.027
387
c EXD008 Exudative Vitreoretinopathy 1 58 0.027
388
ART002 Arts Syndrome 53 0.027
389
BLM001 Bloom Syndrome 63 0.027
390
ACH004 Achondroplasia 64 0.027
391
P KDN018 Kidney Disease 64 0.027
392
P NMN002 Niemann-Pick Disease 63 0.027
393
P EPS003 Episodic Ataxia 58 0.027
394
TTR001 Tetralogy of Fallot 69 0.027
395
P MYS003 Myasthenia Gravis 64 0.027
396
P STR020 Strabismus 55 0.027
397
ART016 Aortic Aneurysm 67 0.027
398
P PNC025 Panic Disorder 60 0.027
399
ELL001 Ellis-Van Creveld Syndrome 56 0.027
400
P TMT001 Timothy Syndrome 58 0.027
401
DNY001 Denys-Drash Syndrome 53 0.027
402
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 40 0.027
403
P SDD001 Sudden Infant Death Syndrome 60 0.027
404
ULC004 Ulcerative Colitis 74 0.027
405
P PRM011 Primary Ciliary Dyskinesia 56 0.027
406
P FTL009 Fetal Akinesia Deformation Sequence 51 0.027
407
FCT003 Factor X Deficiency 62 0.027
408
P KLL001 Kallmann Syndrome 61 0.027
409
c HMP004 Hemophilia B 61 0.027
410
P HYP061 Hypertrophic Cardiomyopathy 64 0.027
411
KBG001 Kbg Syndrome 50 0.027
412
MSC006 Muscle Glycogenosis 49 0.027
413
P CNJ013 Conjunctivitis 65 0.027
414
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 59 0.027
415
P HRD011 Hereditary Spherocytosis 51 0.027
416
LPM004 Lipoma 59 0.027
417
c FML023 Familial Hemiplegic Migraine 55 0.027
418
CRB039 Cerebrovascular Disease 49 0.027
419
P BRG001 Brugada Syndrome 59 0.027
420
P DRM010 Dermatomyositis 59 0.027
421
ATS001 Autistic Disorder 60 0.027
422
P ATR011 Atrial Fibrillation 63 0.027
423
c PLN018 Peeling Skin Syndrome 2 36 0.027
424
BLD044 Bladder Disease 50 0.027
425
SVR004 Severe Combined Immunodeficiency 71 0.027
426
PTY003 Pityriasis Rubra Pilaris 46 0.027
427
CHR066 Chronic Fatigue Syndrome 63 0.027
428
P NPH005 Nephronophthisis 55 0.027
429
P ALP009 Alopecia Areata 62 0.027
430
TTN003 Tetanus 62 0.027
431
P SCH018 Schizencephaly 51 0.027
432
P KLP003 Klippel-Feil Syndrome 47 0.027
433
P PRV002 Periventricular Nodular Heterotopia 46 0.027
434
PRG004 Progeria 54 0.027
435
P INT070 Intestinal Obstruction 55 0.027
436
P CRN037 Craniosynostosis 66 0.027
437
INT007 Intermediate Coronary Syndrome 52 0.027
438
c ACT068 Acute Cystitis 50 0.027
439
TRC010 Trichotillomania 39 0.027
440
P HRP006 Herpes Simplex 65 0.027
441
APR001 Apraxia 50 0.027
442
P RBL001 Rubella 54 0.027
443
ADR038 Adermatoglyphia 39 0.027
444
IMM065 Immunodeficiency 10 39 0.027
445
IMM082 Immunodeficiency 18 31 0.027
446
c MCR129 Microvascular Complications of Diabetes 1 55 0.027
447
c ATM003 Autoimmune Thyroiditis 59 0.027
448
EXF001 Exfoliation Syndrome 56 0.027
449
HYP080 Hypogonadism 54 0.027
450
HYP056 Hypoglycemia 60 0.027
451
P END044 Endometriosis 53 0.027
452
P HMN010 Hemangioma 62 0.027
453
NNT012 Neonatal Jaundice 49 0.027
454
c DGT005 Digital Arthropathy-Brachydactyly, Familial 36 0.027
455
FRY002 Fryns Syndrome 37 0.027
456
PLN006 Poland Syndrome 48 0.027
457
P FBR031 Febrile Seizures 53 0.027
458
P KRT007 Keratoconus 48 0.027
459
RTN018 Retinal Disease 55 0.027
460
P LFT003 Left Ventricular Noncompaction 48 0.027
461
PRP030 Purpura 60 0.027
462
BLP004 Blepharophimosis 38 0.027
463
SCB001 Scabies 45 0.027
464
OCY001 Oocyte Maturation Defect 31 0.027
465
P HML001 Hemolytic-Uremic Syndrome 50 0.027
466
PMP001 Pemphigus 49 0.027
467
HMP005 Hemiplegia 52 0.027
468
NSD001 Nose Disease 51 0.027
469
DDN011 Duodenal Atresia 40 0.027
470
NRM005 Neuromuscular Disease 56 0.027
471
RPR002 Reproductive System Disease 45 0.027
472
OBS015 Obesity, Hyperphagia, and Developmental Delay 35 0.027
473
CDS001 Cadasil 50 0.027
474
AMN001 Amenorrhea 51 0.027
475
VTR016 Vater/vacterl Association 37 0.027
476
c PLN021 Peeling Skin Syndrome 3 30 0.027
477
P VSC005 Vesicoureteral Reflux 53 0.027
478
RTN017 Retinal Detachment 58 0.027
479
P SCL018 Scoliosis 56 0.027
480
P GLY013 Glycogen Storage Disease 58 0.027
481
IMM076 Immunodeficiency 24 27 0.027
482
P OCL002 Oculocutaneous Albinism 51 0.027
483
PRV006 Pervasive Developmental Disorder 49 0.027
484
RFL001 Reflex Sympathetic Dystrophy 45 0.027
485
P BCL006 B-Cell Lymphomas 64 0.027
486
RGH009 Right Atrial Isomerism 31 0.027
487
CDL005 Caudal Duplication Anomaly 23 0.027
488
MYL020 Myelomeningocele 50 0.027
489
P OVR046 Ovarian Cyst 48 0.027
490
P HYP014 Hyperuricemia 49 0.027
491
P SPN016 Spondylocostal Dysostosis 36 0.027
492
TRD003 Taurodontism 28 0.027
493
P PRN026 Porencephaly 47 0.027
494
IMP004 Impetigo 41 0.027
495
CLS010 Cluster Headache 43 0.027
496
FXF002 Fox-Fordyce Disease 37 0.027
497
TRN012 Transient Global Amnesia 38 0.027
498
P MSC033 Muscle Disorders 52 0.027
499
ANR004 Anuria 46 0.027
500
STS002 Situs Inversus 43 0.027
501
P HYP060 Hyperinsulinism 58 0.027
502
P CMP008 Compartment Syndrome 46 0.027
503
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.027
504
P MLT074 Multiple Endocrine Neoplasia 55 0.027
505
c CNG124 Congenital Rubella 40 0.027
506
CLR003 Clear Cell Adenocarcinoma 52 0.027
507
P UVT001 Uveitis 60 0.027
508
P MYC008 Myocarditis 56 0.027
509
c CRN214 Coronary Heart Disease 5 22 0.027
510
HMG005 Hemoglobinopathy 49 0.027
511
DXT001 Dextrocardia 44 0.027
512
HDC001 Headache 52 0.027
513
PRP021 Peripheral Nervous System Neoplasm 49 0.027
514
P PNC001 Pancytopenia 53 0.027
515
ANR018 Anorchia 35 0.027
516
ADN018 Adenoma 59 0.027
517
BLN002 Balanitis Xerotica Obliterans 38 0.027
518
IRT001 Iritis 36 0.027
519
CHR001 Churg-Strauss Syndrome 48 0.027
520
LTT002 Letterer-Siwe Disease 32 0.027
521
c SBC007 Subacute Thyroiditis 42 0.027
522
DRG003 Drug Dependence 53 0.027
523
TLN003 Telangiectasis 50 0.027
524
ANK001 Ankylosis 52 0.027
525
HYP458 Hyper Ige Syndrome 43 0.027
526
MYC033 Myoclonus 41 0.027
527
P GLM007 Glomerulonephritis 56 0.027
528
ALB002 Albinism 43 0.027
529
P NRP001 Neuropathy 57 0.027
530
P MRC003 Mercury Poisoning 38 0.027
531
LCH009 Lichen Sclerosus 43 0.027
532
AVD001 Avoidant Personality Disorder 38 0.027
533
CRV025 Cervical Incompetence 39 0.027
534
PHC013 Phaeochromocytoma 47 0.027
535
OSC001 Oeis Complex 27 0.027
536
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 19 0.027
537
P PRS062 Persistent Hyperplastic Primary Vitreous 38 0.027
538
CRN025 Corneal Dystrophy 40 0.027
539
CLT003 Colitis 56 0.027
540
TRG003 Trigeminal Nerve Disease 25 0.027
541
FCL044 Fecal Incontinence 34 0.027
542
KRT006 Keratoconjunctivitis 51 0.027
543
LKC003 Leukocyte Disease 45 0.027
544
VSC009 Vascular Skin Disease 21 0.027
545
CLC002 Calcaneonavicular Coalition 22 0.027
546
IMP001 Impetigo Herpetiformis 29 0.027
547
FRZ001 Frozen Shoulder 40 0.027
548
CRN088 Craniorachischisis 31 0.027
549
PHY002 Physical Disorder 43 0.027
550
MYS001 Myositis Ossificans 40 0.027
551
BLN010 Balanitis 29 0.027
552
HMH002 Hemihypertrophy 37 0.027
553
HYP043 Hyperandrogenism 46 0.027
554
MYF001 Myofibroma 34 0.027
555
SPL040 Split Hand 35 0.027
556
RNL008 Renal Artery Atheroma 26 0.027
557
CRB090 Cerebral Hypoxia 45 0.027
558
HYP391 Hyperammonemia 38 0.027
559
BRD004 Borderline Personality Disorder 46 0.027
560
LMB009 Lambdoid Synostosis 14 0.027
561
RNL097 Renal Artery Disease 44 0.027
562
NRC003 Narcissistic Personality Disorder 25 0.027
563
NNT019 Neonatal Hypothyroidism 34 0.027
564
TRG006 Trigger Thumb 19 0.027
565
WLS002 Wilson-Mikity Syndrome 15 0.027
566
PLC001 Placenta Accreta 39 0.027
567
NNT018 Neonatal Herpes 26 0.027
568
FNS001 Funisitis 39 0.027
569
P PMP005 Pemphigus Vulgaris 47 0.027
570
RHH001 Rohhad 14 0.027
571
P RNL015 Renal Hypertension 47 0.027
572
P NNT042 Neonatal Lupus Erythematosus 34 0.027
573
CLP002 Colpocephaly 15 0.027
574
P CHR342 Chiari Malformation 36 0.027
575
HRM002 Hermaphroditism 37 0.027
576
CND006 Candida Glabrata 35 0.027
577
NNT002 Neonatal Urinary Tract Infectious Disease 12 0.027
578
NNT021 Neonatal Meningitis 23 0.027
579
NRN002 Neuronitis 40 0.027
580
ART031 Aortic Coarctation 42 0.027
581
HMT018 Hematopoietic Stem Cell Transplantation 39 0.027
582
P PST059 Pustular Psoriasis 33 0.027
583
SYM006 Symmetrical Thalamic Calcifications 11 0.027
584
LNR009 Linear Atrophoderma of Moulin 11 0.027
585
RTR008 Root Resorption 41 0.027
586
c ATM007 Autoimmune Disease of Central Nervous System 29 0.027
587
ECT085 Ectopia Cordis 14 0.027
588
HMN031 Human Venous Malformation 16 0.027
589
FBL005 Fibular Aplasia 10 0.027
590
PDT040 Pediatric Hypertension 30 0.027
591
MTG002 Mutagen Sensitivity 35 0.027
592
P ALZ034 Alzheimer Disease 92 0.019
593
P PRS040 Prostate Cancer 89 0.019
594
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.019
595
P PRK057 Parkinson Disease, Late-Onset 72 0.019
596
c MLT019 Multiple Myeloma 77 0.019
597
STR067 Stroke, Ischemic 74 0.019
598
FBR012 Fabry Disease 68 0.019
599
P STM004 Stomach Cancer 73 0.019
600
P CLR023 Colorectal Cancer 96 0.019
601
P OVR042 Ovarian Cancer 73 0.019
602
P FRG001 Fragile X Syndrome 68 0.019
603
PSY004 Psychotic Disorder 62 0.019
604
HDG012 Hodgkin Lymphoma 75 0.019
605
P MTC003 Metachromatic Leukodystrophy 71 0.019
606
P ATX030 Ataxia-Telangiectasia 78 0.019
607
KPS004 Kaposi Sarcoma 69 0.019
608
WLF001 Wolff-Parkinson-White Syndrome 58 0.019
609
P RTN024 Retinoblastoma 75 0.019
610
OBS002 Obsessive-Compulsive Disorder 66 0.019
611
P GCH001 Gaucher's Disease 63 0.019
612
MVL001 Mevalonic Aciduria 53 0.019
613
P VLC001 Velocardiofacial Syndrome 64 0.019
614
KRN002 Kearns-Sayre Syndrome 60 0.019
615
CMP005 Campomelic Dysplasia 60 0.019
616
SMT004 Smith-Lemli-Opitz Syndrome 66 0.019
617
ASP002 Aspartylglucosaminuria 55 0.019
618
WLM001 Wolman Disease 55 0.019
619
MNK001 Menkes Disease 61 0.019
620
c MLT024 Multiple Endocrine Neoplasia Iia 64 0.019
621
WST001 West Syndrome 61 0.019
622
P SJG002 Sjogren-Larsson Syndrome 51 0.019
623
P FNG005 Feingold Syndrome 43 0.019
624
P ANG001 Angelman Syndrome 62 0.019
625
c TBR024 Tuberous Sclerosis-1 50 0.019
626
P ADD001 Addison's Disease 60 0.019
627
P CLD001 Cleidocranial Dysplasia 62 0.019
628
P WVR001 Weaver Syndrome 54 0.019
629
P WSK001 Wiskott-Aldrich Syndrome 70 0.019
630
ETH011 Ethylmalonic Encephalopathy 57 0.019
631
c MLT136 Multiple Endocrine Neoplasia 1 68 0.019
632
c CHR536 Charcot-Marie-Tooth Disease, Type 1a 55 0.019
633
P CHR071 Charcot-Marie-Tooth Disease 66 0.019
634
CST001 Costello Syndrome 68 0.019
635
P EPD002 Epidermolytic Hyperkeratosis 51 0.019
636
BLS001 Blau Syndrome 59 0.019
637
KRT004 Keratitis 70 0.019
638
INC021 Incontinentia Pigmenti 57 0.019
639
P ALT001 Alternating Hemiplegia of Childhood 52 0.019
640
c DLT002 Dilated Cardiomyopathy 75 0.019
641
P OST012 Osteoarthritis 81 0.019
642
TNG002 Tangier Disease 61 0.019
643
AND015 Androgen Insensitivity 64 0.019
644
P LPR003 Leprosy 70 0.019
645
GST092 Gastroesophageal Reflux 62 0.019
646
P ESS003 Essential Thrombocythemia 66 0.019
647
c TYR013 Tyrosinemia, Type Ii 44 0.019
648
c MYT021 Myotonic Dystrophy 1 64 0.019
649
c TRC092 Trichorhinophalangeal Syndrome, Type I 44 0.019
650
P SZR006 Seizure Disorder 56 0.019
651
END057 Endometrial Cancer 75 0.019
652
c HRD010 Hereditary Spastic Paraplegia 66 0.019
653
P ALX003 Alexander Disease 64 0.019
654
BCK001 Becker Muscular Dystrophy 68 0.019
655
ARS001 Aarskog-Scott Syndrome 52 0.019
656
WGR001 Wagr Syndrome 53 0.019
657
c CWD006 Cowden Syndrome 1 43 0.019
658
APR006 Apert Syndrome 66 0.019
659
SHW002 Shwachman-Diamond Syndrome 59 0.019
660
P PND002 Pendred Syndrome 52 0.019
661
P KLF001 Kleefstra Syndrome 41 0.019
662
PSR001 Psoriatic Arthritis 64 0.019
663
c INF071 Inflammatory Bowel Disease 1 51 0.019
664
STT001 Status Epilepticus 59 0.019
665
MLG056 Malignant Hyperthermia 60 0.019
666
CHN055 Chanarin-Dorfman Syndrome 48 0.019
667
ARM002 Aromatic L-Amino Acid Decarboxylase Deficiency 36 0.019
668
ACR007 Acromegaly 66 0.019
669
CNG035 Congenital Bilateral Absence of Vas Deferens 40 0.019
670
GST050 Gastrointestinal System Disease 58 0.019
671
P ALP004 Alport Syndrome 68 0.019
672
P FND001 Fundus Albipunctatus 52 0.019
673
P LRS001 Larsen Syndrome 53 0.019
674
c GRS014 Griscelli Syndrome, Type 2 50 0.019
675
MNK003 Muenke Syndrome 55 0.019
676
CRD119 Cardiac Arrest 63 0.019
677
P MYL005 Myelofibrosis 67 0.019
678
P NRV007 Nervous System Disease 71 0.019
679
P RTH001 Rothmund-Thomson Syndrome 56 0.019
680
P HMP002 Hemophagocytic Lymphohistiocytosis 64 0.019
681
NTH001 Netherton Syndrome 52 0.019
682
P DMN001 Diamond-Blackfan Anemia 69 0.019
683
P FRS003 Fraser Syndrome 58 0.019
684
ALV007 Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins 45 0.019
685
FMR004 Fumarase Deficiency 38 0.019
686
CYS010 Cystinosis 51 0.019
687
P RTN008 Retinitis Pigmentosa 78 0.019
688
BLL003 Bell's Palsy 47 0.019
689
c FML001 Familial Atrial Fibrillation 59 0.019
690
CRY002 Cryptorchidism 61 0.019
691
OCL069 Ocular Motor Apraxia 44 0.019
692
CSY001 C Syndrome 49 0.019
693
PRD011 Proud Syndrome 42 0.019
694
P SYS005 Systemic Scleroderma 60 0.019
695
VRL011 Viral Infectious Disease 56 0.019
696
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.019
697
MLT021 Multiple System Atrophy 71 0.019
698
c DBT064 Diabetes Mellitus, Transient Neonatal, 1 44 0.019
699
P LBR001 Leber Congenital Amaurosis 61 0.019
700
P DGR001 Digeorge Syndrome 52 0.019
701
P MYM002 Moyamoya Disease 60 0.019
702
LPT001 Leptospirosis 65 0.019
703
c PRK031 Parkinson Disease 1 54 0.019
704
c PSD066 Pseudohypoparathyroidism, Type Ib 49 0.019
705
P BDD001 Budd-Chiari Syndrome 52 0.019
706
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 59 0.019
707
TST021 Testicular Germ Cell Tumor 67 0.019
708
BLL001 Baller-Gerold Syndrome 52 0.019
709
ACS001 Acoustic Neuroma 56 0.019
710
ALP014 Alpha-Thalassemia/mental Retardation Syndrome 54 0.019
711
P GNG009 Gangliosidosis 58 0.019
712
OHT001 Ohtahara Syndrome 49 0.019
713
INT259 Interleukin 1 Receptor Antagonist Deficiency 34 0.019
714
c HMP029 Hemophilia a 61 0.019
715
BRD001 Brody Myopathy 49 0.019
716
MLN007 Male Infertility 56 0.019
717
c JVN010 Juvenile Rheumatoid Arthritis 65 0.019
718
WDM004 Wiedemann-Steiner Syndrome 40 0.019
719
TYP011 Typhus 57 0.019
720
STF001 Stiff-Person Syndrome 54 0.019
721
JHN001 Johanson-Blizzard Syndrome 47 0.019
722
P NSP012 Nasopharyngeal Carcinoma 59 0.019
723
CHD004 Chudley-Mccullough Syndrome 32 0.019
724
CMM004 Common Variable Immunodeficiency 68 0.019
725
P PTS002 Ptosis 56 0.019
726
P ASP006 Aspergillosis 61 0.019
727
HST011 Histoplasmosis 54 0.019
728
P LNG028 Long Qt Syndrome 67 0.019
729
HYP101 Hyperinsulinism-Hyperammonemia Syndrome 41 0.019
730
MST006 Mast Syndrome 44 0.019
731
KRT010 Kartagener Syndrome 48 0.019
732
c HPT001 Hepatitis C 68 0.019
733
PRP019 Peripheral Nervous System Disease 52 0.019
734
CHR063 Chronic Mucocutaneous Candidiasis 61 0.019
735
PRT037 Pertussis 63 0.019
736
P D2H001 D-2-Hydroxyglutaric Aciduria 45 0.019
737
P HYP027 Hypobetalipoproteinemia 52 0.019
738
MGL001 Megaloblastic Anemia 51 0.019
739
c MTB001 Metabolic Syndrome X 61 0.019
740
MTH009 Mouth Disease 63 0.019
741
P CNG046 Congenital Fiber-Type Disproportion 49 0.019
742
P ART023 Arthropathy 63 0.019
743
IVC001 Ivic Syndrome 28 0.019
744
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 55 0.019
745
P RBN002 Robinow Syndrome 47 0.019
746
P HRM001 Hermansky-Pudlak Syndrome 56 0.019
747
HYP077 Hypertrichosis 52 0.019
748
TST015 Testicular Disease 47 0.019
749
BND015 Band-Like Calcification with Simplified Gyration and Polymicrogyria 45 0.019
750
P GT001 Gout 58 0.019
751
MDY003 Mody, Type Ii 36 0.019
752
P IDP010 Idiopathic Generalized Epilepsy 61 0.019
753
c HPT016 Hepatitis B 61 0.019
754
ALP001 Alopecia Universalis 57 0.019
755
P HLL001 Hallermann-Streiff Syndrome 53 0.019
756
P MYL006 Myeloid Leukemia 67 0.019
757
PLM070 Pulmonic Stenosis 59 0.019
758
P MCR010 Microcephaly 60 0.019
759
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 55 0.019
760
RST001 Restless Legs Syndrome 51 0.019
761
CTS002 Cat-Scratch Disease 46 0.019
762
CCT002 Cicatricial Pemphigoid 50 0.019
763
P CCK001 Cockayne Syndrome 58 0.019
764
SLP005 Sleep Disorder 52 0.019
765
P EMR001 Emery-Dreifuss Muscular Dystrophy 57 0.019
766
MCR037 Macroglossia 45 0.019
767
c HRD002 Hereditary Angioedema 52 0.019
768
CNG048 Congenital Hepatic Fibrosis 47 0.019
769
ART035 Arterial Calcification of Infancy 40 0.019
770
MTN003 Motion Sickness 48 0.019
771
CNT047 Contact Dermatitis 62 0.019
772
SCT005 Scott Syndrome 51 0.019
773
MSS002 Mass Syndrome 49 0.019
774
c CLD010 Cold-Induced Sweating Syndrome 1 43 0.019
775
ACR003 Acrodermatitis Enteropathica 49 0.019
776
NRG002 Neurogenic Bladder 47 0.019
777
c HPT073 Hepatitis C Virus 72 0.019
778
MDD011 Mood Disorder 60 0.019
779
QBC001 Quebec Platelet Disorder 51 0.019
780
IDP024 Idiopathic Inflammatory Myopathy 50 0.019
781
RSC001 Rosacea 54 0.019
782
OLM001 Olmsted Syndrome 33 0.019
783
c BRC082 Brachydactyly, Type E 39 0.019
784
c HYP163 Hyperlipidemia Type 3 52 0.019
785
SCH072 Scheuermann Disease 37 0.019
786
c NRC009 Narcolepsy 1 28 0.019
787
HRT007 Heart Cancer 51 0.019
788
IMM066 Immunodeficiency 9 30 0.019
789
SPT004 Septic Arthritis 60 0.019
790
P LKD001 Leukodystrophy 58 0.019
791
P STC001 Stickler Syndrome 53 0.019
792
STR026 Star Syndrome 57 0.019
793
TMR010 Tumor Predisposition Syndrome 58 0.019
794
PLY023 Polycystic Liver Disease 57 0.019
795
CNG064 Congenital Chloride Diarrhea 34 0.019
796
P PRP029 Porphyria 56 0.019
797
LST001 Listeriosis 53 0.019
798
SRC014 Sarcoma 66 0.019
799
CYS005 Cysticercosis 52 0.019
800
ACN002 Acanthosis Nigricans 59 0.019
801
BHR001 Behr Syndrome 43 0.019
802
OLV001 Olivopontocerebellar Atrophy 53 0.019
803
P INT143 Interstitial Cystitis 57 0.019
804
SCR008 Scrub Typhus 55 0.019
805
LPD008 Lipid Metabolism Disorder 42 0.019
806
P EPD009 Epidermolysis Bullosa Dystrophica 55 0.019
807
ETN001 Eating Disorder 59 0.019
808
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 35 0.019
809
BLN001 Blount's Disease 46 0.019
810
RHM001 Rheumatic Fever 50 0.019
811
QDR001 Quadriplegia 51 0.019
812
P PRM001 Primary Cutaneous Amyloidosis 54 0.019
813
P JNC001 Junctional Epidermolysis Bullosa 52 0.019
814
MHC001 Mhc Class Ii Deficiency 39 0.019
815
SPC010 Speech and Communication Disorders 42 0.019
816
RHM027 Rheumatic Disease 55 0.019
817
CHL069 Cholesteatoma 51 0.019
818
LYM009 Lymphocytic Choriomeningitis 49 0.019
819
P ESN007 Eosinophilia 61 0.019
820
GRN016 Grant Syndrome 30 0.019
821
P ALL008 Allergic Bronchopulmonary Aspergillosis 50 0.019
822
LBN004 Liebenberg Syndrome 28 0.019
823
P CRB154 Cerebrocostomandibular Syndrome 33 0.019
824
CNC002 Cinca Syndrome 55 0.019
825
GGR001 Geographic Tongue 45 0.019
826
IRN001 Iron Deficiency Anemia 51 0.019
827
PSD007 Pseudomyxoma Peritonei 51 0.019
828
LND001 Landau-Kleffner Syndrome 36 0.019
829
P MMB011 Membranous Nephropathy 53 0.019
830
P NRV006 Nervous System Cancer 62 0.019
831
VSC011 Vasculitis 62 0.019
832
c PLM127 Pulmonary Hypertension, Primary, 3 31 0.019
833
RNL007 Renal Tubular Acidosis 50 0.019
834
PRR031 Pruritic Urticarial Papules and Plaques of Pregnancy 23 0.019
835
IMM025 Immunoglobulin a Deficiency 2 27 0.019
836
MVM001 Movement Disease 45 0.019
837
DBW001 Dubowitz Syndrome 48 0.019
838
P FBR025 Fibrochondrogenesis 49 0.019
839
P MCP010 Mucopolysaccharidosis 58 0.019
840
P DDN001 Duodenal Ulcer 51 0.019
841
SPS004 Spastic Quadriplegia 36 0.019
842
P AML002 Amelogenesis Imperfecta 43 0.019
843
VGT001 Vogt-Koyanagi-Harada Disease 54 0.019
844
PRS042 Prostate Disease 50 0.019
845
OCL009 Ocular Cancer 61 0.019
846
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.019
847
CD4003 Cd40 Ligand Deficiency 47 0.019
848
CHL014 Cholera 56 0.019
849
PLM124 Pulmonary Hypertension, Neonatal 25 0.019
850
c SYS004 Systemic Mastocytosis 60 0.019
851
c PND001 Pain Disorder 53 0.019
852
PRL009 Prolactinoma 63 0.019
853
PLM041 Pulmonary Valve Stenosis 48 0.019
854
TRN030 Transient Erythroblastopenia of Childhood 35 0.019
855
TTH006 Tooth Disease 52 0.019
856
c MTR002 Mitral Valve Insufficiency 42 0.019
857
P ANT006 Antiphospholipid Syndrome 60 0.019
858
CHL123 Chlamydia 60 0.019
859
BLD034 Bile Duct Carcinoma 56 0.019
860
P PNC044 Pancreatitis 62 0.019
861
PRM013 Premature Menopause 45 0.019
862
P MLG086 Malignant Hyperthermia Susceptibility 45 0.019
863
MST017 Mast Cell Disease 52 0.019
864
P CND004 Candidiasis 58 0.019
865
STM006 Stomach Disease 48 0.019
866
P MSC007 Muscle Hypertrophy 55 0.019
867
SMT001 Somatization Disorder 44 0.019
868
NTR006 Neutrophil Immunodeficiency Syndrome 36 0.019
869
IPX001 Ipex Syndrome 35 0.019
870
c DBT044 Diabetes Mellitus, Transient Neonatal, 3 32 0.019
871
P PRM006 Primary Biliary Cirrhosis 55 0.019
872
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.019
873
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.019
874
ADM013 Adamantinoma of Long Bones 57 0.019
875
ASP001 Asperger Syndrome 49 0.019
876
P VTL001 Vitelliform Macular Dystrophy 41 0.019
877
P ENC004 Encephalitis 60 0.019
878
DBT084 Diabetes Mellitus, Ketosis-Prone 28 0.019
879
c CNT035 Central Nervous System Disease 60 0.019
880
OBS061 Obstructive Sleep Apnea 61 0.019
881
TBL008 Tibial Hemimelia 26 0.019
882
P OVR049 Ovarian Disease 54 0.019
883
DFF021 Diffuse Mesangial Sclerosis 40 0.019
884
EST007 Estrogen Resistance 43 0.019
885
P HYP004 Hypercalcemia 54 0.019
886
YCH001 Y Chromosome Infertility 28 0.019
887
CNS004 Constipation 57 0.019
888
LPD011 Lipoid Adrenal Hyperplasia 53 0.019
889
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.019
890
P INT068 Intestinal Disease 60 0.019
891
OST017 Osteomyelitis 60 0.019
892
P TYR004 Tyrosinemia 44 0.019
893
BLR001 Biliary Atresia 52 0.019
894
P PLY019 Polyneuropathy 53 0.019
895
DRM011 Dermatophytosis 44 0.019
896
P SYR001 Syringomyelia 44 0.019
897
CLR033 Color Vision Deficiency 28 0.019
898
IMM071 Immunodeficiency 12 27 0.019
899
APH002 Aphasia 52 0.019
900
ALL009 Allergic Conjunctivitis 51 0.019
901
RTT001 Ritter's Disease 35 0.019
902
CVR006 Cavernous Hemangioma 46 0.019
903
DSS009 Disseminated Intravascular Coagulation 52 0.019
904
P ANG015 Angioedema 53 0.019
905
P PLY014 Polycystic Kidney Disease 60 0.019
906
P CYS018 Cystitis 54 0.019
907
P OLG002 Oligodendroglioma 55 0.019
908
P SYP003 Syphilis 51 0.019
909
SYS006 Say Syndrome 29 0.019
910
MYM001 Myoma 51 0.019
911
AND001 Anodontia 40 0.019
912
THY030 Thyroid Gland Disease 52 0.019
913
P SLP006 Sleep Apnea 60 0.019
914
EPD006 Epidermolysis Bullosa Acquisita 46 0.019
915
SLD003 Sialadenitis 45 0.019
916
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.019
917
EXS013 Exstrophy-Epispadias Complex 33 0.019
918
MLR006 Male Reproductive Organ Cancer 46 0.019
919
DFF003 Diffuse Scleroderma 39 0.019
920
DNT012 Dental Caries 45 0.019
921
FTT001 Fatty Liver Disease 60 0.019
922
c HMG001 Hemoglobin C Disease 46 0.019
923
P INT063 Intellectual Disability 46 0.019
924
PLM001 Pulmonary Tuberculosis 69 0.019
925
CHL109 Childhood Apraxia of Speech 29 0.019
926
c MLT124 Multiple Sclerosis 5 24 0.019
927
TLP001 Talipes Equinovarus 34 0.019
928
HYP068 Hyperostosis 39 0.019
929
c CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 28 0.019
930
ASP004 Asphyxia Neonatorum 38 0.019
931
OCL020 Ocular Cicatricial Pemphigoid 51 0.019
932
DSM004 Desmoid Tumor 55 0.019
933
HMG002 Hemoglobinuria 49 0.019
934
MYX004 Myxedema 36 0.019
935
LMB014 Limb-Body Wall Complex 26 0.019
936
CRL004 Caroli Disease 40 0.019
937
LRN003 Learning Disability 49 0.019
938
RDN001 Reading Disorder 39 0.019
939
P PRD008 Periodontitis 46 0.019
940
PRR002 Pure Red-Cell Aplasia 47 0.019
941
SKN027 Skin Conditions 44 0.019
942
PRS012 Pars Planitis 43 0.019
943
GND001 Gonadoblastoma 44 0.019
944
C6D001 C6 Deficiency 37 0.019
945
PCH002 Pachygyria 39 0.019
946
SPN019 Spondylolisthesis 50 0.019
947
MXD005 Mixed Connective Tissue Disease 63 0.019
948
FTZ005 Fitzsimmons-Guilbert Syndrome 20 0.019
949
PHT008 Photosensitive Epilepsy 34 0.019
950
P MSC003 Muscular Atrophy 51 0.019
951
VSC006 Vascular Cancer 51 0.019
952
VSC002 Vascular Dementia 41 0.019
953
WRN002 Wernicke-Korsakoff Syndrome 41 0.019
954
P INT030 Intracranial Aneurysm 52 0.019
955
ATM052 Autoimmune Disease 1 26 0.019
956
PRS108 Persistent Polyclonal B-Cell Lymphocytosis 37 0.019
957
NPH003 Nephrocalcinosis 47 0.019
958
DFF001 Diffuse Cutaneous Mastocytosis 42 0.019
959
P LSS002 Lissencephaly 48 0.019
960
PRN011 Pernicious Anemia 41 0.019
961
MGC001 Megacolon 50 0.019
962
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 35 0.019
963
SFT003 Soft Tissue Sarcoma 55 0.019
964
PRS030 Persistent Fetal Circulation Syndrome 38 0.019
965
SPR007 Superior Mesenteric Artery Syndrome 37 0.019
966
PRN023 Prion Disease 44 0.019
967
FML039 Female Reproductive System Disease 49 0.019
968
HND002 Hand, Foot and Mouth Disease 49 0.019
969
P HRD021 Hereditary Sensory Neuropathy 42 0.019
970
KWS001 Kwashiorkor 45 0.019
971
P PTT002 Potter's Syndrome 42 0.019
972
NRN008 Neuronal Intranuclear Inclusion Disease 41 0.019
973
PLS009 Plasma Cell Neoplasm 47 0.019
974
WRT001 Worth's Syndrome 37 0.019
975
CLN019 Colonic Disease 50 0.019
976
ANG016 Angiokeratoma 43 0.019
977
PLC003 Placental Site Trophoblastic Tumor 48 0.019
978
P CNG024 Congenital Nystagmus 39 0.019
979
c PRM226 Primary Central Nervous System Lymphoma 51 0.019
980
NRF007 Neurofibroma 53 0.019
981
P CLL015 Collagen Disease 49 0.019
982
FTL007 Fetal Hydantoin Syndrome 28 0.019
983
c RNG018 Ring Chromosome 22 21 0.019
984
TMP001 Temporal Lobe Epilepsy 47 0.019
985
SPN029 Spondylolysis 39 0.019
986
DVL001 Developmental Coordination Disorder 36 0.019
987
P AMY004 Amyloidosis 63 0.019
988
GLC003 Glucose Intolerance 56 0.019
989
MGL013 Megalencephaly 50 0.019
990
MST005 Mastitis 53 0.019
991
SPR035 Superior Vena Cava Syndrome 31 0.019
992
P DYS005 Dyslexia 38 0.019
993
SBP004 Subependymoma 41 0.019
994
SPN020 Spondylosis 48 0.019
995
CHR074 Choriocarcinoma 45 0.019
996
MNN017 Mononeuropathy 37 0.019
997
ELC001 Elective Mutism 17 0.019
998
ANH002 Anhidrosis 42 0.019
999
NRG004 Neurogenic Diabetes Insipidus 26 0.019
1000
OBS003 Obsessive-Compulsive Personality Disorder 36 0.019
1001
c MLG069 Malignant Hypertension 46 0.019
1002
P BRC006 Brachydactyly 53 0.019
1003
CMP034 Complete Androgen Insensitivity Syndrome 42 0.019
1004
c CNG033 Congenital Syphilis 39 0.019
1005
FDL002 Food Allergy 56 0.019
1006
c RNG014 Ring Chromosome 19 13 0.019
1007
NSP002 Nasopharyngitis 39 0.019
1008
MLR007 Male Reproductive System Disease 36 0.019
1009
MSC016 Mosaic Trisomy 14 23 0.019
1010
TTR014 Tetrasomy 18p 22 0.019
1011
ISL003 Isolated Growth Hormone Deficiency 39 0.019
1012
c RCS002 Recessive Dystrophic Epidermolysis Bullosa 47 0.019
1013
HYP064 Hypogonadotropism 38 0.019
1014
c DBT082 Diabetes Mellitus, Insulin-Dependent, 12 23 0.019
1015
P GRS003 Griscelli Syndrome 48 0.019
1016
c INF067 Inflammatory Bowel Disease 10 31 0.019
1017
ACT084 Acute Stress Disorder 38 0.019
1018
TTH021 Tethered Cord Syndrome 22 0.019
1019
CRH005 Crohn's Colitis 50 0.019
1020
AGR002 Agoraphobia 41 0.019
1021
P SDR003 Sideroblastic Anemia 40 0.019
1022
FML038 Female Reproductive Organ Cancer 50 0.019
1023
PRC012 Pericardial Effusion 50 0.019
1024
OST011 Osteomalacia 48 0.019
1025
PTT006 Pituitary Adenoma 54 0.019
1026
PRT011 Protein C Deficiency 52 0.019
1027
SPN221 Spina Bifida Occulta 32 0.019
1028
CRN051 Craniofacial Microsomia 26 0.019
1029
DMY004 Demyelinating Disease 52 0.019
1030
HMF003 Hemifacial Myohyperplasia 11 0.019
1031
PLN001 Plantar Wart 31 0.019
1032
RSP002 Respiratory Syncytial Virus Infectious Disease 31 0.019
1033
BRN002 Bronchiolitis 56 0.019
1034
P PNT019 Pontocerebellar Hypoplasia 39 0.019
1035
NRW001 Norwegian Scabies 31 0.019
1036
MCR039 Macrophagic Myofasciitis 23 0.019
1037
SPR034 Superior Limbic Keratoconjunctivitis 29 0.019
1038
PRM003 Premature Ejaculation 45 0.019
1039
BDY001 Body Dysmorphic Disorder 41 0.019
1040
ATR003 Atrophic Rhinitis 30 0.019
1041
FXC001 Foix Chavany Marie Syndrome 22 0.019
1042
CNG133 Congenital Varicella Syndrome 19 0.019
1043
LPM005 Lipomatosis 46 0.019
1044
PPL018 Papillary Adenocarcinoma 48 0.019
1045
MTB004 Metabolic Acidosis 49 0.019
1046
NCR002 Necrobiosis Lipoidica 33 0.019
1047
DCR002 Dacryocystocele 20 0.019
1048
OLG001 Oligospermia 39 0.019
1049
RNL025 Renal Hypoplasia 40 0.019
1050
VSC018 Visceral Steatosis 37 0.019
1051
GRN007 Granuloma Annulare 35 0.019
1052
P INF049 Infantile Myofibromatosis 44 0.019
1053
PNS015 Penoscrotal Transposition 22 0.019
1054
PRP009 Peripartum Cardiomyopathy 41 0.019
1055
LYM127 Lymphatic Malformations 38 0.019
1056
JNT002 Joint Disorders 55 0.019
1057
P MYL007 Myeloma 52 0.019
1058
GNG002 Ganglioneuroma 41 0.019
1059
c CNN010 Connective Tissue Benign Neoplasm 31 0.019
1060
P CNT005 Central Nervous System Lymphoma 51 0.019
1061
P ACH011 Achondrogenesis 39 0.019