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

811 hits were found for 'twinning'

# Family MCID Name MIFTS Score
1
P TWN001 Twin-to-Twin Transfusion Syndrome 58 10.421
2
c TWN006 Twin Twin Transfusion Syndrome 40 6.388
3
c RNL090 Renal Tubular Dysgenesis Due to Twin-Twin Transfusion 6 5.079
4
PLY012 Polyhydramnios 49 0.203
5
ART109 Arterial Thoracic Outlet Syndrome 12 0.187
6
CRB009 Cerebritis 56 0.172
7
c PLY018 Polycythemia 61 0.156
8
GNR028 Generalized Essential Telangiectasia 16 0.156
9
P RNL028 Renal Tubular Dysgenesis 51 0.145
10
DWN001 Down Syndrome 62 0.143
11
FTL044 Fetal Cytomegalovirus Syndrome 28 0.132
12
P CRV039 Cervicitis 52 0.125
13
OLG003 Oligohydramnios 50 0.125
14
HYP179 Hypertrichosis Congenital Generalized X-Linked 24 0.123
15
HYD012 Hydrops Fetalis 53 0.118
16
P OBS005 Obesity 93 0.111
17
ANK002 Ankylosing Spondylitis 75 0.108
18
P HYP075 Hypertension 86 0.102
19
THR013 Thoracic Outlet Syndrome 54 0.102
20
P INF069 Infantile Neuroaxonal Dystrophy 1 32 0.102
21
NCT002 Nicotine Dependence 51 0.093
22
IMG001 Image Syndrome 34 0.093
23
P MGR002 Migraine 71 0.090
24
c THY032 Thyroiditis 67 0.090
25
CYT008 Cytomegalovirus Infection 34 0.090
26
P RTN012 Retinopathy of Prematurity 62 0.087
27
CHR005 Chorioamnionitis 56 0.087
28
P BPL003 Bipolar Disorder 80 0.084
29
c DBT009 Diabetes Mellitus 80 0.084
30
URT039 Urticaria 61 0.084
31
ALC007 Alcohol Dependence 61 0.084
32
P LKM002 Leukemia 79 0.080
33
c INT060 Intestinal Atresia 43 0.080
34
c HYP086 Hypothyroidism 68 0.076
35
ISC004 Ischemia 64 0.076
36
CRB037 Cerebral Palsy 64 0.076
37
URT008 Urticaria Pigmentosa 40 0.076
38
ENC005 Encephalomalacia 34 0.076
39
TFT003 Tufting Enteropathy 21 0.076
40
ACR022 Acardia 6 0.076
41
P ATX002 Ataxia Telangiectasia 93 0.072
42
RNL002 Renal Agenesis 77 0.072
43
ACN002 Acanthosis Nigricans 73 0.072
44
c LCL006 Localized Scleroderma 68 0.072
45
P ANR007 Anorexia Nervosa 67 0.072
46
P PRS038 Personality Disorder 64 0.072
47
URT001 Urethritis 62 0.072
48
c TXP001 Toxoplasmosis 62 0.072
49
P GND004 Gonadal Dysgenesis 52 0.072
50
PYL006 Pyloric Stenosis 49 0.072
51
CNG034 Congestive Heart Failure 81 0.068
52
P HMP004 Hemophilia B 80 0.068
53
P RBN001 Rubinstein-Taybi Syndrome 78 0.068
54
DRM006 Dermatitis 68 0.068
55
ART005 Arteriovenous Malformation 63 0.068
56
VCT001 Vacterl Association 63 0.068
57
c ACT073 Acute Leukemia 62 0.068
58
RTN023 Retinitis 61 0.068
59
MYC002 Mycobacterium Avium Complex Disease 57 0.068
60
c THN001 Thanatophoric Dysplasia 56 0.068
61
SCN006 Secondary Syphilis 55 0.068
62
P CNG021 Congenital Toxoplasmosis 54 0.068
63
IMP002 Imperforate Anus 47 0.068
64
c BPL002 Bipolar I Disorder 41 0.068
65
HYD001 Hydranencephaly 37 0.068
66
FCT013 Factor V Leiden Thrombophilia 35 0.068
67
LKM059 Leukemia, Megakaryoblastic, with or Without Down Syndrome, Somatic 33 0.068
68
PRT015 Partial Third-Nerve Palsy 26 0.068
69
CNG069 Congenital Cytomegalovirus 18 0.068
70
P MLT020 Multiple Sclerosis 82 0.064
71
BRN024 Bronchitis 76 0.064
72
P ART022 Arthritis 75 0.064
73
c LPS004 Lupus Erythematosus 73 0.064
74
c CNG006 Congenital Hypothyroidism 72 0.064
75
SPN038 Spina Bifida 70 0.064
76
KLN001 Klinefelter's Syndrome 67 0.064
77
GLD001 Goldenhar Syndrome 65 0.064
78
P PRM019 Premature Ovarian Failure 65 0.064
79
GST009 Gastroschisis 63 0.064
80
P OST009 Osteochondritis Dissecans 62 0.064
81
c MSC005 Muscular Dystrophy 62 0.064
82
P ESP024 Esophagitis 60 0.064
83
P MJR001 Major Depressive Disorder 58 0.064
84
PRV004 Periventricular Leukomalacia 58 0.064
85
P MYP004 Myopathy 58 0.064
86
P DBT005 Diabetes Insipidus 57 0.064
87
ESP020 Esophageal Atresia 56 0.064
88
NSY001 N Syndrome 55 0.064
89
TRN007 Transsexualism 53 0.064
90
HYP009 Hypertrophic Pyloric Stenosis 50 0.064
91
SYN053 Syndromic Diarrhea 42 0.064
92
CNN001 Cannabis Dependence 39 0.064
93
P NRF002 Neurofibromatosis 100 0.059
94
PRT036 Peritonitis 78 0.059
95
PLM033 Pulmonary Embolism 68 0.059
96
DMN002 Dementia 66 0.059
97
P BCK002 Beckwith-Wiedemann Syndrome 65 0.059
98
ACQ007 Acquired Immunodeficiency Syndrome 63 0.059
99
BLM002 Bulimia Nervosa 62 0.059
100
CND002 Conduct Disorder 59 0.059
101
c HYP065 Hyperaldosteronism 59 0.059
102
CTN014 Cutaneous Mastocytosis 58 0.059
103
PTH002 Pathological Gambling 58 0.059
104
P LYM026 Lymphoblastic Leukemia 56 0.059
105
RFR003 Refractive Error 53 0.059
106
THY089 Thymic Epithelial Neoplasm 52 0.059
107
PLY024 Polymicrogyria 48 0.059
108
ENT001 Enterocele 42 0.059
109
PLM070 Pulmonic Stenosis 37 0.059
110
ERL004 Early Yaws 33 0.059
111
P BRS047 Breast Cancer 105 0.054
112
P RHM011 Rheumatoid Arthritis 91 0.054
113
P SYS001 Systemic Lupus Erythematosus 87 0.054
114
P SCH015 Schizophrenia 77 0.054
115
P CNG026 Congenital Heart Defect 73 0.054
116
P NRB001 Neuroblastoma 71 0.054
117
P ANG001 Angelman Syndrome 70 0.054
118
ART019 Aortic Valve Stenosis 68 0.054
119
MYS005 Myositis 67 0.054
120
GST033 Gestational Diabetes 67 0.054
121
P DRM007 Dermatitis Herpetiformis 66 0.054
122
ECL001 Eclampsia 63 0.054
123
P HLP001 Holoprosencephaly 61 0.054
124
ALP008 Alopecia 60 0.054
125
HLL004 Hellp Syndrome 57 0.054
126
PSD009 Pseudohermaphroditism 57 0.054
127
P HYP055 Hypoplastic Left Heart Syndrome 56 0.054
128
ATT002 Attention Deficit Hyperactivity Disorder 54 0.054
129
PLC007 Placental Abruption 53 0.054
130
MGR001 Migraine Without Aura 52 0.054
131
c CRN015 Cornelia De Lange Syndrome 51 0.054
132
P CHN005 Choanal Atresia 49 0.054
133
MTS001 Mutism 46 0.054
134
AST006 Astigmatism 41 0.054
135
c MYP006 Myopia 41 0.054
136
BRX001 Bruxism 41 0.054
137
EST005 Esotropia 36 0.054
138
CYS001 Cystic Fibrosis 103 0.048
139
P ALZ001 Alzheimer's Disease 103 0.048
140
P MYC007 Myocardial Infarction 88 0.048
141
TBR010 Tuberculosis 84 0.048
142
PTZ001 Peutz-Jeghers Syndrome 83 0.048
143
P PRM021 Primary Pulmonary Hypertension 82 0.048
144
c HPT021 Hepatitis 75 0.048
145
P ATM003 Autoimmune Thyroiditis 70 0.048
146
P FNC001 Fanconi's Anemia 67 0.048
147
DFC004 Deficiency Anemia 66 0.048
148
WST001 West Syndrome 64 0.048
149
P GRV001 Graves' Disease 63 0.048
150
DDN006 Duodenitis 62 0.048
151
SMT015 Smith Magenis Syndrome 62 0.048
152
P GTR002 Goiter 61 0.048
153
c HYP076 Hyperthyroidism 61 0.048
154
PSR002 Psoriasis 60 0.048
155
EPD016 Epidermolysis Bullosa 59 0.048
156
P GLC007 Glaucoma 58 0.048
157
P ATS007 Autism Spectrum Disorder 57 0.048
158
P ALC004 Alcohol Abuse 57 0.048
159
ACR012 Aicardi Syndrome 53 0.048
160
P MGR003 Migraine with Aura 53 0.048
161
c CNG018 Congenital Heart Block 52 0.048
162
DYS018 Dysostosis 49 0.048
163
END020 Endocardial Fibroelastosis 49 0.048
164
GND002 Gender Identity Disorder 48 0.048
165
c ART084 Arteriovenous Fistula 47 0.048
166
PLC005 Placental Insufficiency 44 0.048
167
P ATX010 Ataxia Neuropathy Spectrum 44 0.048
168
TXC012 Toxic Epidermal Necrolysis 38 0.048
169
TRN044 Transposition of the Great Arteries 36 0.048
170
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.048
171
ANS004 Anisometropia 26 0.048
172
P HYP078 Hypertrophy of Breast 26 0.048
173
NNS006 Non-Suppurative Otitis Media 26 0.048
174
PL2001 Pla2g6-Associated Neurodegeneration 21 0.048
175
c BNG076 Benign Exophthalmos Syndrome 21 0.048
176
AND005 Androgen Insensitivity Syndrome, Mild 18 0.048
177
CMV001 Cmv Antenatal Infection 13 0.048
178
FTL016 Fetal Edema 9 0.048
179
AND002 Androgen Insensitivity Syndrome 88 0.042
180
MCC001 Mccune Albright Syndrome 82 0.042
181
P TRN020 Turner Syndrome 77 0.042
182
ANX002 Anxiety Disorder 75 0.042
183
LNG024 Langerhans-Cell Histiocytosis 75 0.042
184
PRC016 Pre-Eclampsia 75 0.042
185
KWS002 Kawasaki Disease 74 0.042
186
P CLC005 Celiac Disease 73 0.042
187
VSC007 Vascular Disease 72 0.042
188
P HST010 Histiocytosis 71 0.042
189
ANR002 Aniridia 71 0.042
190
ATH003 Atherosclerosis 71 0.042
191
OVR029 Ovarian Hyperstimulation Syndrome 70 0.042
192
c HMP007 Hemophilia 68 0.042
193
c THL005 Thalassemia 68 0.042
194
c NPH012 Nephrotic Syndrome 66 0.042
195
c NTR004 Neutropenia 65 0.042
196
P MLN008 Melanoma 65 0.042
197
P CTS001 Cutis Laxa 63 0.042
198
CLB001 Coloboma 63 0.042
199
BRN029 Brain Disease 62 0.042
200
P AGM001 Agammaglobulinemia 61 0.042
201
c AXN002 Axenfeld-Rieger Syndrome 60 0.042
202
P ADN016 Adenocarcinoma 60 0.042
203
P NPH009 Nephrolithiasis 59 0.042
204
P CLF002 Cleft Palate 59 0.042
205
P HYP040 Hypospadias 59 0.042
206
CLF001 Cleft Lip 59 0.042
207
ARR001 Arrhythmogenic Right Ventricular Dysplasia 59 0.042
208
c SCL016 Scleroderma 59 0.042
209
HYP013 Hypohidrotic Ectodermal Dysplasia 58 0.042
210
ARC002 Arachnoiditis 57 0.042
211
GYN001 Gynecomastia 57 0.042
212
P DND001 Dandy-Walker Syndrome 56 0.042
213
PNM008 Pneumothorax 55 0.042
214
URN010 Urinary Tract Obstruction 55 0.042
215
c CNG015 Congenital Diaphragmatic Hernia 55 0.042
216
P PLY006 Polydactyly 54 0.042
217
SBS004 Substance Dependence 54 0.042
218
VGN023 Vaginitis 54 0.042
219
c NNT009 Neonatal Diabetes Mellitus 54 0.042
220
c VNT002 Ventricular Septal Defect 53 0.042
221
c CTR002 Cataract 53 0.042
222
CHN016 Cohen Syndrome 53 0.042
223
SVR005 Severe Pre-Eclampsia 52 0.042
224
PPL021 Papilledema 52 0.042
225
c SYN005 Synostosis 51 0.042
226
P JVN003 Juvenile Xanthogranuloma 50 0.042
227
PRP016 Paraplegia 48 0.042
228
c FTL001 Fetal Alcohol Syndrome 44 0.042
229
DGN001 Degenerative Disc Disease 41 0.042
230
TTH002 Tooth Agenesis 40 0.042
231
CNN002 Cannabis Abuse 35 0.042
232
P MLT015 Multiple Intestinal Atresia 32 0.042
233
FRM001 Freemartinism 22 0.042
234
P PRK002 Parkinson's Disease 92 0.034
235
VNH001 Von Hippel-Lindau Disease 89 0.034
236
P AST005 Asthma 88 0.034
237
21H001 21-Hydroxylase Deficiency 87 0.034
238
ADR007 Adrenoleukodystrophy 86 0.034
239
CRH001 Crohn's Disease 83 0.034
240
BLM001 Bloom Syndrome 82 0.034
241
P TYS001 Tay-Sachs Disease 82 0.034
242
P MDL005 Medulloblastoma 82 0.034
243
P MNN012 Meningioma 79 0.034
244
P MYS003 Myasthenia Gravis 79 0.034
245
P PNM007 Pneumonia 79 0.034
246
CRZ001 Crouzon Syndrome 79 0.034
247
INC002 Inclusion Body Myositis 78 0.034
248
DCH001 Duchenne Muscular Dystrophy 78 0.034
249
NPH007 Nephrogenic Diabetes Insipidus 77 0.034
250
P OST002 Osteoporosis 77 0.034
251
PRG004 Progeria 77 0.034
252
TTR001 Tetralogy of Fallot 76 0.034
253
P ALP006 Alpha Thalassemia 75 0.034
254
VNW001 Von Willebrand's Disease 74 0.034
255
P HYP035 Hypophosphatasia 73 0.034
256
c MNN013 Meningitis 71 0.034
257
P SDD001 Sudden Infant Death Syndrome 70 0.034
258
DNY001 Denys-Drash Syndrome 70 0.034
259
c OST005 Osteogenesis Imperfecta 70 0.034
260
P END044 Endometriosis 69 0.034
261
P HMN010 Hemangioma 68 0.034
262
P ATP001 Atopic Dermatitis 68 0.034
263
P PLY011 Polycystic Ovary Syndrome 68 0.034
264
c THR014 Thrombocytopenia 67 0.034
265
P UVT001 Uveitis 67 0.034
266
P RCK004 Rickets 67 0.034
267
PRP030 Purpura 67 0.034
268
ADN018 Adenoma 67 0.034
269
P DGR001 Digeorge Syndrome 67 0.034
270
c CRN037 Craniosynostosis 67 0.034
271
P GLM007 Glomerulonephritis 66 0.034
272
HYP056 Hypoglycemia 66 0.034
273
P PNC025 Panic Disorder 65 0.034
274
P RHN004 Rhinitis 65 0.034
275
CHR066 Chronic Fatigue Syndrome 65 0.034
276
ELL001 Ellis-Van Creveld Syndrome 64 0.034
277
NRN002 Neuronitis 64 0.034
278
VLV011 Vulvovaginal Candidiasis 64 0.034
279
P HRP006 Herpes Simplex 63 0.034
280
P SLV001 Silver-Russell Syndrome 63 0.034
281
ART001 Arterial Tortuosity Syndrome 62 0.034
282
PPL002 Papillary Carcinoma 61 0.034
283
P KLL001 Kallmann Syndrome 61 0.034
284
P CNG042 Congenital Central Hypoventilation Syndrome 61 0.034
285
HYP014 Hyperuricemia 61 0.034
286
NRP001 Neuropathy 61 0.034
287
LPM004 Lipoma 60 0.034
288
CLR003 Clear Cell Adenocarcinoma 60 0.034
289
RTN017 Retinal Detachment 60 0.034
290
P HYP080 Hypogonadism 60 0.034
291
KRT006 Keratoconjunctivitis 60 0.034
292
c MLG069 Malignant Hypertension 60 0.034
293
P PPL020 Papillary Thyroid Carcinoma 59 0.034
294
CHR001 Churg-Strauss Syndrome 59 0.034
295
P RBL001 Rubella 59 0.034
296
EDW001 Edwards Syndrome 59 0.034
297
WLL003 Williams Syndrome 58 0.034
298
c KDN018 Kidney Disease 58 0.034
299
c SBC007 Subacute Thyroiditis 58 0.034
300
SCL003 Social Phobia 57 0.034
301
ANT011 Antisocial Personality Disorder 57 0.034
302
SCH012 Schizoaffective Disorder 57 0.034
303
DRG003 Drug Dependence 57 0.034
304
c BRG001 Brugada Syndrome 56 0.034
305
P PRT008 Proteus Syndrome 56 0.034
306
P STR020 Strabismus 56 0.034
307
STS002 Situs Inversus 56 0.034
308
SPR004 Supravalvular Aortic Stenosis 55 0.034
309
GNR004 Generalized Anxiety Disorder 55 0.034
310
c GLY013 Glycogen Storage Disease 55 0.034
311
ANR004 Anuria 55 0.034
312
c EPS003 Episodic Ataxia 55 0.034
313
c MYT002 Myotonic Dystrophy 54 0.034
314
P HML001 Hemolytic-Uremic Syndrome 54 0.034
315
c DRR001 Diarrhea 54 0.034
316
HMP005 Hemiplegia 54 0.034
317
BRD004 Borderline Personality Disorder 53 0.034
318
SBC001 Subacute Sclerosing Panencephalitis 53 0.034
319
c PRM011 Primary Ciliary Dyskinesia 53 0.034
320
P EPS020 Episodic Ataxia Type 1 53 0.034
321
HMG005 Hemoglobinopathy 53 0.034
322
c NPH005 Nephronophthisis 53 0.034
323
c TRC011 Treacher Collins Syndrome 53 0.034
324
APR001 Apraxia 53 0.034
325
WLL001 Williams-Beuren Syndrome 52 0.034
326
ADL002 Adult Syndrome 52 0.034
327
DNT012 Dental Caries 51 0.034
328
c FML023 Familial Hemiplegic Migraine 51 0.034
329
c SPN016 Spondylocostal Dysostosis 51 0.034
330
c VSC005 Vesicoureteral Reflux 51 0.034
331
SCB001 Scabies 51 0.034
332
CNN003 Conn's Syndrome 50 0.034
333
ANK001 Ankylosis 50 0.034
334
PTS001 Patau Syndrome 50 0.034
335
CNV002 Conversion Disorder 50 0.034
336
P INF037 Inflammatory Bowel Disease 50 0.034
337
IRN002 Iron Metabolism Disease 50 0.034
338
HRM002 Hermaphroditism 49 0.034
339
P KLP003 Klippel-Feil Syndrome 49 0.034
340
FRZ001 Frozen Shoulder 49 0.034
341
FRY002 Fryns Syndrome 49 0.034
342
PHC013 Phaeochromocytoma 49 0.034
343
DXT001 Dextrocardia 48 0.034
344
c KBK001 Kabuki Syndrome 48 0.034
345
P FCS001 Facioscapulohumeral Muscular Dystrophy 47 0.034
346
PTY003 Pityriasis Rubra Pilaris 47 0.034
347
NNT012 Neonatal Jaundice 46 0.034
348
TLN003 Telangiectasis 46 0.034
349
c OPT004 Optic Atrophy 46 0.034
350
IMP004 Impetigo 45 0.034
351
PLC001 Placenta Accreta 44 0.034
352
KLN002 Kleine-Levin Syndrome 44 0.034
353
HYD028 Hydrops, Ectopic Calcification, Moth-Eaten Skeletal Dysplasia 43 0.034
354
GDS001 Good Syndrome 43 0.034
355
AND003 Andersen-Tawil Syndrome 43 0.034
356
P ACT020 Acute T Cell Leukemia 43 0.034
357
RTR008 Root Resorption 43 0.034
358
RFL001 Reflex Sympathetic Dystrophy 43 0.034
359
MYS001 Myositis Ossificans 43 0.034
360
TRN012 Transient Global Amnesia 42 0.034
361
BLP004 Blepharophimosis 41 0.034
362
IRT001 Iritis 41 0.034
363
LTT002 Letterer-Siwe Disease 41 0.034
364
BLN010 Balanitis 40 0.034
365
PRN019 Perinatal Necrotizing Enterocolitis 39 0.034
366
P PRV002 Periventricular Nodular Heterotopia 39 0.034
367
CRB028 Cerebellar Medulloblastoma 38 0.034
368
P MNN007 Meningocele 37 0.034
369
TRC010 Trichotillomania 37 0.034
370
MYF001 Myofibroma 37 0.034
371
CRV025 Cervical Incompetence 37 0.034
372
KBG001 Kbg Syndrome 36 0.034
373
P SLP004 Salpingo-Oophoritis 31 0.034
374
GLC004 Galactokinase Deficiency 30 0.034
375
NNT011 Neonatal Anemia 29 0.034
376
AMN009 Amniotic Band Syndrome 28 0.034
377
P SCH009 Scheuermann's Disease 28 0.034
378
ART007 Aorta Atresia 27 0.034
379
NRC003 Narcissistic Personality Disorder 25 0.034
380
FXF001 Fox Fordyce Disease 25 0.034
381
BLN002 Balanitis Xerotica Obliterans 23 0.034
382
P KRN003 Kernicterus Due to Isoimmunization 21 0.034
383
c HMP017 Hemophilia a, Congenital 21 0.034
384
CLC002 Calcaneonavicular Coalition 20 0.034
385
IMP001 Impetigo Herpetiformis 19 0.034
386
P ISC010 Isochromosome Yp 14 0.034
387
TRG003 Trigeminal Nerve Disease 12 0.034
388
P ACT019 Acute Myeloid Leukemia 94 0.024
389
CDS001 Cadasil 92 0.024
390
P PRS040 Prostate Cancer 91 0.024
391
P TBR001 Tuberous Sclerosis 91 0.024
392
P MLT019 Multiple Myeloma 89 0.024
393
FBR012 Fabry Disease 88 0.024
394
MTC003 Metachromatic Leukodystrophy 87 0.024
395
P NMN002 Niemann-Pick Disease 87 0.024
396
P WSK001 Wiskott-Aldrich Syndrome 87 0.024
397
P RTN024 Retinoblastoma 86 0.024
398
P RTT002 Rett Syndrome 85 0.024
399
SVR004 Severe Combined Immunodeficiency 85 0.024
400
P SMT004 Smith-Lemli-Opitz Syndrome 84 0.024
401
ACH004 Achondroplasia 83 0.024
402
P ALG002 Alagille Syndrome 83 0.024
403
P RTN008 Retinitis Pigmentosa 81 0.024
404
P HMC003 Hemochromatosis 80 0.024
405
c MCP002 Mucopolysaccharidosis I 80 0.024
406
CST001 Costello Syndrome 79 0.024
407
P GCH001 Gaucher's Disease 79 0.024
408
CLD001 Cleidocranial Dysplasia 78 0.024
409
P CRN008 Carney Complex 78 0.024
410
P LPR003 Leprosy 78 0.024
411
INF030 Infectious Mononucleosis 78 0.024
412
TNG002 Tangier Disease 78 0.024
413
c TYP008 Type 1 Diabetes Mellitus 77 0.024
414
OLV001 Olivopontocerebellar Atrophy 77 0.024
415
c NNN003 Noonan Syndrome 77 0.024
416
MLT021 Multiple System Atrophy 76 0.024
417
P MYL005 Myelofibrosis 75 0.024
418
P NRC002 Narcolepsy 75 0.024
419
P FRG001 Fragile X Syndrome 75 0.024
420
ADD001 Addison's Disease 75 0.024
421
P ALX003 Alexander Disease 74 0.024
422
P PRM006 Primary Biliary Cirrhosis 74 0.024
423
P OST012 Osteoarthritis 73 0.024
424
P BLD042 Bladder Carcinoma 73 0.024
425
BLS001 Blau Syndrome 73 0.024
426
P CLR023 Colorectal Cancer 73 0.024
427
ASP006 Aspergillosis 73 0.024
428
c MYL006 Myeloid Leukemia 72 0.024
429
P PND002 Pendred Syndrome 72 0.024
430
ULC004 Ulcerative Colitis 72 0.024
431
ATS001 Autistic Disorder 72 0.024
432
CRN211 Coronary Artery Disease 72 0.024
433
c ESS002 Essential Hypertension 71 0.024
434
PRN023 Prion Disease 71 0.024
435
P EPD002 Epidermolytic Hyperkeratosis 71 0.024
436
PRL009 Prolactinoma 71 0.024
437
P DRM010 Dermatomyositis 70 0.024
438
P LVR013 Liver Disease 70 0.024
439
P SYS004 Systemic Mastocytosis 70 0.024
440
ALP004 Alport Syndrome 69 0.024
441
BCK001 Becker Muscular Dystrophy 69 0.024
442
P SYS005 Systemic Scleroderma 69 0.024
443
P INF038 Influenza 69 0.024
444
P PRP001 Propionic Acidemia 69 0.024
445
PSY004 Psychotic Disorder 69 0.024
446
HYP004 Hypercalcemia 69 0.024
447
c SRC013 Sarcoidosis 69 0.024
448
c CHR071 Charcot-Marie-Tooth Disease 69 0.024
449
ISC006 Ischemic Heart Disease 69 0.024
450
P DDN001 Duodenal Ulcer 68 0.024
451
CMP005 Campomelic Dysplasia 68 0.024
452
P RTH001 Rothmund-Thomson Syndrome 67 0.024
453
P ATY010 Atypical Hemolytic-Uremic Syndrome 67 0.024
454
P PLY014 Polycystic Kidney Disease 67 0.024
455
KLP002 Klippel-Trenaunay Syndrome 67 0.024
456
c PNC044 Pancreatitis 67 0.024
457
ANT006 Antiphospholipid Syndrome 67 0.024
458
VSC011 Vasculitis 67 0.024
459
BLR001 Biliary Atresia 67 0.024
460
P CLN016 Colon Cancer 67 0.024
461
c XRD001 Xeroderma Pigmentosum 67 0.024
462
GST034 Gastroesophageal Reflux Disease 67 0.024
463
P OLG002 Oligodendroglioma 67 0.024
464
c JVN010 Juvenile Rheumatoid Arthritis 67 0.024
465
CMM004 Common Variable Immunodeficiency 66 0.024
466
STT001 Status Epilepticus 66 0.024
467
ALP001 Alopecia Universalis 66 0.024
468
DSS009 Disseminated Intravascular Coagulation 66 0.024
469
ALL003 Allergic Rhinitis 66 0.024
470
CRY002 Cryptorchidism 66 0.024
471
KRT004 Keratitis 66 0.024
472
P HRD011 Hereditary Spherocytosis 66 0.024
473
P PRD008 Periodontitis 66 0.024
474
P VTL001 Vitelliform Macular Dystrophy 66 0.024
475
P GT001 Gout 66 0.024
476
P HMP002 Hemophagocytic Lymphohistiocytosis 66 0.024
477
P AMY004 Amyloidosis 65 0.024
478
MLG056 Malignant Hyperthermia 65 0.024
479
HST011 Histoplasmosis 65 0.024
480
MXD005 Mixed Connective Tissue Disease 65 0.024
481
LWY001 Lewy Body Dementia 65 0.024
482
VRG001 Variegate Porphyria 65 0.024
483
P STM004 Stomach Cancer 65 0.024
484
RHM001 Rheumatic Fever 65 0.024
485
ARS001 Aarskog-Scott Syndrome 65 0.024
486
ALL008 Allergic Bronchopulmonary Aspergillosis 64 0.024
487
c OST026 Osteogenesis Imperfecta Type I 64 0.024
488
CCT002 Cicatricial Pemphigoid 64 0.024
489
CYS005 Cysticercosis 64 0.024
490
c PRP029 Porphyria 64 0.024
491
PRT037 Pertussis 64 0.024
492
FCT003 Factor X Deficiency 64 0.024
493
P PLY019 Polyneuropathy 64 0.024
494
PTT006 Pituitary Adenoma 64 0.024
495
c ENC004 Encephalitis 64 0.024
496
c GLY007 Glycogen Storage Disease Iv 64 0.024
497
CHL068 Cholestasis 63 0.024
498
ACR003 Acrodermatitis Enteropathica 63 0.024
499
AMN001 Amenorrhea 63 0.024
500
NTH001 Netherton Syndrome 63 0.024
501
P CND004 Candidiasis 63 0.024
502
ETN001 Eating Disorder 63 0.024
503
CHR063 Chronic Mucocutaneous Candidiasis 63 0.024
504
GRW001 Growth Hormone Secreting Pituitary Adenoma 63 0.024
505
PLM001 Pulmonary Tuberculosis 63 0.024
506
GLC003 Glucose Intolerance 63 0.024
507
PMP001 Pemphigus 63 0.024
508
c SPN046 Spinal Muscular Atrophy 63 0.024
509
CHR452 Chorea-Acanthocytosis 62 0.024
510
ART016 Aortic Aneurysm 62 0.024
511
FMR011 Fumarate Hydratase Deficiency 62 0.024
512
MVL001 Mevalonic Aciduria 62 0.024
513
RBR001 Roberts Syndrome 62 0.024
514
P JVN004 Juvenile Myelomonocytic Leukemia 62 0.024
515
LST001 Listeriosis 62 0.024
516
FLT001 Felty's Syndrome 62 0.024
517
PSD007 Pseudomyxoma Peritonei 62 0.024
518
PRS047 Prostatitis 62 0.024
519
P WVR001 Weaver Syndrome 62 0.024
520
CRB039 Cerebrovascular Disease 61 0.024
521
P ALP009 Alopecia Areata 61 0.024
522
c DMN001 Diamond-Blackfan Anemia 61 0.024
523
c MCP010 Mucopolysaccharidosis 61 0.024
524
P PRM030 Permanent Neonatal Diabetes Mellitus 61 0.024
525
MNK003 Muenke Syndrome 61 0.024
526
c LNG028 Long Qt Syndrome 61 0.024
527
P EPD009 Epidermolysis Bullosa Dystrophica 61 0.024
528
P CNJ013 Conjunctivitis 61 0.024
529
c HYP061 Hypertrophic Cardiomyopathy 61 0.024
530
EPD006 Epidermolysis Bullosa Acquisita 61 0.024
531
c CCK001 Cockayne Syndrome 61 0.024
532
P CNG046 Congenital Fiber-Type Disproportion 61 0.024
533
P SJG002 Sjogren-Larsson Syndrome 61 0.024
534
P MMB002 Membranous Glomerulonephritis 60 0.024
535
P VLC001 Velocardiofacial Syndrome 60 0.024
536
RNL015 Renal Hypertension 60 0.024
537
c OCL002 Oculocutaneous Albinism 60 0.024
538
PLM034 Pulmonary Emphysema 60 0.024
539
P ESN007 Eosinophilia 60 0.024
540
EYD002 Eye Disease 60 0.024
541
PRT011 Protein C Deficiency 60 0.024
542
ACS001 Acoustic Neuroma 60 0.024
543
STF001 Stiff-Person Syndrome 60 0.024
544
P FND001 Fundus Albipunctatus 59 0.024
545
CNT047 Contact Dermatitis 59 0.024
546
SCR008 Scrub Typhus 59 0.024
547
P BRN019 Bernard-Soulier Syndrome 59 0.024
548
c HYP050 Hyperinsulinemic Hypoglycemia 59 0.024
549
OST017 Osteomyelitis 59 0.024
550
P IDP010 Idiopathic Generalized Epilepsy 59 0.024
551
c HRD002 Hereditary Angioedema 59 0.024
552
c MYL007 Myeloma 59 0.024
553
ALL009 Allergic Conjunctivitis 59 0.024
554
CHR074 Choriocarcinoma 59 0.024
555
KRN002 Kearns-Sayre Syndrome 59 0.024
556
HRD010 Hereditary Spastic Paraplegia 59 0.024
557
MYM001 Myoma 59 0.024
558
P JNC001 Junctional Epidermolysis Bullosa 58 0.024
559
TST014 Testicular Cancer 58 0.024
560
P HRD021 Hereditary Sensory Neuropathy 58 0.024
561
LRN003 Learning Disability 58 0.024
562
P RNL007 Renal Tubular Acidosis 58 0.024
563
TYP011 Typhus 58 0.024
564
CHL069 Cholesteatoma 58 0.024
565
LKD001 Leukodystrophy 58 0.024
566
OST011 Osteomalacia 57 0.024
567
VSC002 Vascular Dementia 57 0.024
568
EPL002 Epilepsy Syndrome 57 0.024
569
CNN005 Connective Tissue Disease 57 0.024
570
P FML001 Familial Atrial Fibrillation 57 0.024
571
CHR008 Choroiditis 57 0.024
572
c TMP001 Temporal Lobe Epilepsy 57 0.024
573
P PSR001 Psoriatic Arthritis 57 0.024
574
c HRM001 Hermansky-Pudlak Syndrome 57 0.024
575
P PYL005 Pyelonephritis 57 0.024
576
c THR005 Thrombotic Thrombocytopenic Purpura 57 0.024
577
MTN003 Motion Sickness 57 0.024
578
PRT039 Proteinuria 57 0.024
579
RSC001 Rosacea 57 0.024
580
RST001 Restless Legs Syndrome 56 0.024
581
MGC001 Megacolon 56 0.024
582
OST019 Osteosclerosis 56 0.024
583
P INT030 Intracranial Aneurysm 56 0.024
584
P MYC008 Myocarditis 56 0.024
585
BLL003 Bell's Palsy 56 0.024
586
OST014 Osteopoikilosis 56 0.024
587
CCN001 Cocaine Dependence 56 0.024
588
P MYM002 Moyamoya Disease 56 0.024
589
NRG002 Neurogenic Bladder 56 0.024
590
LYM009 Lymphocytic Choriomeningitis 56 0.024
591
P SYP003 Syphilis 56 0.024
592
NPH011 Nephroblastoma 56 0.024
593
PLC003 Placental Site Trophoblastic Tumor 56 0.024
594
MLT006 Multidrug-Resistant Tuberculosis 56 0.024
595
P CNT005 Central Nervous System Lymphoma 56 0.024
596
HYP068 Hyperostosis 56 0.024
597
WGR001 Wagr Syndrome 56 0.024
598
BRS051 Breast Disease 56 0.024
599
c THR003 Thoracic Aortic Aneurysm 56 0.024
600
VGT001 Vogt-Koyanagi-Harada Disease 56 0.024
601
HMG002 Hemoglobinuria 55 0.024
602
P SYR001 Syringomyelia 55 0.024
603
P ALT001 Alternating Hemiplegia of Childhood 55 0.024
604
P PNC001 Pancytopenia 55 0.024
605
P MGL001 Megaloblastic Anemia 55 0.024
606
PNH001 Panhypopituitarism 55 0.024
607
LPT001 Leptospirosis 55 0.024
608
TTH006 Tooth Disease 55 0.024
609
BNF002 Bone Fracture 55 0.024
610
NRM004 Neuroma 55 0.024
611
WLM001 Wolman Disease 55 0.024
612
ART004 Aortic Atherosclerosis 54 0.024
613
P ANG015 Angioedema 54 0.024
614
VNS003 Venous Insufficiency 54 0.024
615
CVR006 Cavernous Hemangioma 54 0.024
616
c GNG001 Gangliosidosis Gm1 54 0.024
617
P HLL001 Hallermann-Streiff Syndrome 54 0.024
618
PRC012 Pericardial Effusion 54 0.024
619
HYP043 Hyperandrogenism 54 0.024
620
FBR009 Fibrous Dysplasia 54 0.024
621
P CYS018 Cystitis 54 0.024
622
SPN020 Spondylosis 54 0.024
623
P LYD001 Leydig Cell Tumor 54 0.024
624
MCR010 Microcephaly 53 0.024
625
NPH003 Nephrocalcinosis 53 0.024
626
CNG048 Congenital Hepatic Fibrosis 53 0.024
627
GST045 Gastroenteritis 53 0.024
628
c EMR001 Emery-Dreifuss Muscular Dystrophy 53 0.024
629
CRN030 Coronary Stenosis 53 0.024
630
c TYR004 Tyrosinemia 53 0.024
631
P CYS010 Cystinosis 53 0.024
632
ASP002 Aspartylglucosaminuria 53 0.024
633
P HYP027 Hypobetalipoproteinemia 53 0.024
634
MRG003 Marginal Zone B-Cell Lymphoma 53 0.024
635
CCN002 Cocaine Abuse 53 0.024
636
P BLD034 Bile Duct Carcinoma 52 0.024
637
PRM003 Premature Ejaculation 52 0.024
638
PRN011 Pernicious Anemia 52 0.024
639
LPM005 Lipomatosis 52 0.024
640
P MSC003 Muscular Atrophy 52 0.024
641
P INT063 Intellectual Disability 51 0.024
642
RNL029 Renal Coloboma Syndrome 51 0.024
643
c MCK006 Meckel Syndrome 51 0.024
644
BLL001 Baller-Gerold Syndrome 51 0.024
645
CTS002 Cat-Scratch Disease 51 0.024
646
WRN002 Wernicke-Korsakoff Syndrome 51 0.024
647
P CMP008 Compartment Syndrome 51 0.024
648
c GNG009 Gangliosidosis 51 0.024
649
c JBR001 Joubert Syndrome 51 0.024
650
c SPN049 Spinocerebellar Ataxia 51 0.024
651
PRM013 Premature Menopause 51 0.024
652
PLM035 Pulmonary Eosinophilia 51 0.024
653
c FML024 Familial Melanoma 51 0.024
654
c INT001 Intrahepatic Cholestasis 51 0.024
655
c LSS002 Lissencephaly 51 0.024
656
DBW001 Dubowitz Syndrome 51 0.024
657
PPL018 Papillary Adenocarcinoma 51 0.024
658
c KRT007 Keratoconus 50 0.024
659
ALB002 Albinism 50 0.024
660
c MCL001 Mucolipidosis 50 0.024
661
SHR003 Short-Chain Acyl-Coa Dehydrogenase Deficiency 50 0.024
662
ASP001 Asperger Syndrome 50 0.024
663
P OVR046 Ovarian Cyst 50 0.024
664
CNG064 Congenital Chloride Diarrhea 50 0.024
665
c INT064 Intermediate Uveitis 50 0.024
666
MYX004 Myxedema 50 0.024
667
NSP002 Nasopharyngitis 49 0.024
668
c APH002 Aphasia 49 0.024
669
c TYR003 Tyrosinemia Type Ii 49 0.024
670
c TCL004 T-Cell Leukemia 49 0.024
671
MTB004 Metabolic Acidosis 49 0.024
672
PRV006 Pervasive Developmental Disorder 48 0.024
673
P SDR003 Sideroblastic Anemia 48 0.024
674
CD4002 Cd40 Deficiency 48 0.024
675
SCH008 Schmid Metaphyseal Chondrodysplasia 48 0.024
676
PRT019 Protein-Losing Enteropathy 48 0.024
677
c BRC006 Brachydactyly 48 0.024
678
NRX001 Neuroaxonal Dystrophy 48 0.024
679
OVR006 Ovarian Endometriosis 48 0.024
680
AND001 Anodontia 48 0.024
681
HYP064 Hypogonadotropism 48 0.024
682
PSD002 Pseudotumor Cerebri 47 0.024
683
c PRM001 Primary Cutaneous Amyloidosis 47 0.024
684
c PSD003 Pseudohypoaldosteronism 47 0.024
685
c AML002 Amelogenesis Imperfecta 47 0.024
686
KWS001 Kwashiorkor 47 0.024
687
GRN007 Granuloma Annulare 47 0.024
688
ESN005 Eosinophilic Gastroenteritis 47 0.024
689
AGR002 Agoraphobia 46 0.024
690
CHR078 Chorioretinitis 45 0.024
691
ACR005 Acrodermatitis 45 0.024
692
c CND005 Cone Dystrophy 45 0.024
693
c CNG029 Congenital Mesoblastic Nephroma 45 0.024
694
RTT001 Ritter's Disease 45 0.024
695
RNL022 Renal Vascular Disease 45 0.024
696
ALX002 Alexithymia 45 0.024
697
FND002 Fundus Dystrophy 45 0.024
698
SPN019 Spondylolisthesis 45 0.024
699
NNT016 Neonatal Hemochromatosis 44 0.024
700
c TRC004 Trichorhinophalangeal Syndrome Type I 44 0.024
701
c MLG086 Malignant Hyperthermia Susceptibility 44 0.024
702
ATR057 Atrioventricular Block 44 0.024
703
c STC001 Stickler Syndrome 44 0.024
704
c CHR098 Chronic Pyelonephritis 44 0.024
705
P D2H001 D-2-Hydroxyglutaric Aciduria 43 0.024
706
PRS012 Pars Planitis 43 0.024
707
DRM011 Dermatophytosis 43 0.024
708
FLL008 Folliculitis 43 0.024
709
MNN017 Mononeuropathy 43 0.024
710
DLS001 Delusional Disorder 43 0.024
711
c SNR001 Senior-Loken Syndrome 43 0.024
712
SPN050 Spinocerebellar Degeneration 43 0.024
713
QDR001 Quadriplegia 43 0.024
714
MHC001 Mhc Class Ii Deficiency 43 0.024
715
SPS007 Spastic Cerebral Palsy 42 0.024
716
OCL001 Ocular Albinism 42 0.024
717
GND001 Gonadoblastoma 41 0.024
718
NVS001 Neovascular Glaucoma 41 0.024
719
P TRC005 Tracheal Stenosis 40 0.024
720
CD4003 Cd40 Ligand Deficiency 40 0.024
721
c PTR004 Pterygium 40 0.024
722
P CNG024 Congenital Nystagmus 40 0.024
723
IRR003 Irritant Dermatitis 40 0.024
724
c CNG033 Congenital Syphilis 40 0.024
725
c MTR002 Mitral Valve Insufficiency 39 0.024
726
NCR002 Necrobiosis Lipoidica 39 0.024
727
c ACH010 Achondrogenesis Type Ii 39 0.024
728
LND001 Landau-Kleffner Syndrome 39 0.024
729
IPX001 Ipex Syndrome 39 0.024
730
P END046 Endometritis 38 0.024
731
OLG001 Oligospermia 38 0.024
732
c ACH011 Achondrogenesis 38 0.024
733
GST052 Gestational Choriocarcinoma 38 0.024
734
URT004 Urethral Syndrome 38 0.024
735
SPC005 Speech Disorder 38 0.024
736
SPS004 Spastic Quadriplegia 38 0.024
737
RTN006 Retinal Drusen 37 0.024
738
LWT001 Low Tension Glaucoma 37 0.024
739
TBR006 Tuberculoid Leprosy 37 0.024
740
c NRC009 Narcolepsy 1 36 0.024
741
SPR007 Superior Mesenteric Artery Syndrome 36 0.024
742
P DYS005 Dyslexia 36 0.024
743
c PRG001 Progressive Muscular Atrophy 36 0.024
744
DFF001 Diffuse Cutaneous Mastocytosis 35 0.024
745
RNL012 Renal Tuberculosis 35 0.024
746
GST007 Gastric Dilatation 34 0.024
747
SMT001 Somatization Disorder 34 0.024
748
OHT001 Ohtahara Syndrome 33 0.024
749
P PTT002 Potter's Syndrome 33 0.024
750
ANG004 Angioid Streaks 33 0.024
751
SCH011 Schizotypal Personality Disorder 33 0.024
752
ATR003 Atrophic Rhinitis 32 0.024
753
ENM001 Enamel Caries 32 0.024
754
C3D001 C3 Deficiency 32 0.024
755
FCL003 Facial Hemiatrophy 32 0.024
756
c FML034 Familial Dystonia 32 0.024
757
BLN001 Blount's Disease 31 0.024
758
LTM002 Luteoma 30 0.024
759
SPN029 Spondylolysis 30 0.024
760
BDY001 Body Dysmorphic Disorder 30 0.024
761
DYS012 Dyshidrosis 30 0.024
762
c GNR001 Generalized Arterial Calcification of Infancy 30 0.024
763
SPR012 Separation Anxiety Disorder 30 0.024
764
NRW001 Norwegian Scabies 29 0.024
765
DVL001 Developmental Coordination Disorder 28 0.024
766
BMR002 Beemer-Langer Syndrome 28 0.024
767
c HMP008 Hemophagocytic Lymphohistiocytosis, Familial 28 0.024
768
c HMG001 Hemoglobin C Disease 28 0.024
769
3HY001 3-Hydroxyisobutyric Aciduria 28 0.024
770
DDN009 Duodenal Obstruction 27 0.024
771
LCH003 Lichen Nitidus 27 0.024
772
P HYP163 Hyperlipidemia Type 3 27 0.024
773
c ENL009 Enlarged Parietal Foramina 27 0.024
774
INT011 Interstitial Emphysema 26 0.024
775
c PRM032 Primary Congenital Glaucoma 26 0.024
776
CRN051 Craniofacial Microsomia 26 0.024
777
VSL002 Visual Epilepsy 25 0.024
778
c SPN081 Spondylocostal Dysostosis, Autosomal Recessive 25 0.024
779
PNT005 Pentalogy of Cantrell 24 0.024
780
CHL109 Childhood Apraxia of Speech 24 0.024
781
CLC003 Cloacogenic Carcinoma 24 0.024
782
ACC003 Accommodative Esotropia 24 0.024
783
AVD001 Avoidant Personality Disorder 24 0.024
784
PHC006 Phacomatosis Pigmentovascularis 23 0.024
785
BLD052 Blood Group Incompatibility 22 0.024
786
PLN001 Plantar Wart 22 0.024
787
RTN019 Retinal Telangiectasia 21 0.024
788
FTS001 Fetishism 21 0.024
789
PRR001 Periarthritis 21 0.024
790
LBY003 Labyrinthine Disease 20 0.024
791
PRD003 Periodontosis 20 0.024
792
DCR002 Dacryocystocele 18 0.024
793
TRC035 Tracheal Agenesis 17 0.024
794
HYP015 Hyperlucent Lung 17 0.024
795
c MLG039 Malignant Essential Hypertension 17 0.024
796
HCS001 Hec Syndrome 17 0.024
797
CMB002 Combat Disorder 17 0.024
798
c NNT006 Neonatal Myasthenia Gravis 16 0.024
799
HYP018 Hyperglobulinemic Purpura 16 0.024
800
FXC001 Foix Chavany Marie Syndrome 15 0.024
801
FBL006 Fibular Aplasia Ectrodactyly 15 0.024
802
TBR007 Tuberculum Sellae Meningioma 14 0.024
803
VLF002 Velo-Facial-Skeletal Syndrome 13 0.024
804
MCH006 Mechanical Strabismus 13 0.024
805
VLK001 Volkmann Contracture 13 0.024
806
KZL001 Kozlowski Brown Hardwick Syndrome 12 0.024
807
LCH012 Lichstenstein Syndrome 11 0.024
808
FSD001 Fused Mandibular Incisors 10 0.024
809
HLC002 Holoacardius Amorphus 9 0.024
810
HMF003 Hemifacial Myohyperplasia 9 0.024
811
OBS014 Obsessive-Compulsive Disorder, Protection Against 6 0.024