Search results for unilateral renal agenesis

434 hits were found for unilateral renal agenesis

# Family MCID Name MIFTS Score
1
ANR016 Aniridia Renal Agenesis Psychomotor Retardation 6 2.714
2
RNL105 Renal Agenesis, Unilateral 25 2.688
3
MCR304 Microcephaly, Congenital Heart Disease, Unilateral Renal Agenesis, and Hyposegmented Lungs 19 2.638
4
UTR057 Uterus Bicornis Bicollis with Partial Vaginal Septum and Unilateral Hematocolpos with Ipsilateral Renal Agenesis 16 2.499
5
ANR044 Aniridia, Partial, with Unilateral Renal Agenesis and Psychomotor Retardation 17 2.375
6
MLL021 Mullerian Duct Aplasia, Unilateral Renal Agenesis, and Cervicothoracic Somite Anomalies 19 2.109
7
MRC004 Murcs Association 31 1.876
8
ELL004 Ellis Yale Winter Syndrome 6 1.852
9
SNT001 Santos Mateus Leal Syndrome 6 1.841
10
P KDN018 Kidney Disease 65 0.343
11
URN009 Urinary System Disease 49 0.263
12
URT010 Ureteral Obstruction 44 0.259
13
P ADN016 Adenocarcinoma 69 0.194
14
RNL078 Renal Dysplasia 50 0.186
15
CRB009 Cerebritis 39 0.180
16
CLF001 Cleft Lip 49 0.175
17
P HPT021 Hepatitis 68 0.162
18
P RNL100 Renal Hypodysplasia/aplasia 1 50 0.160
19
P THY032 Thyroiditis 53 0.158
20
ADN018 Adenoma 58 0.147
21
HYD002 Hydronephrosis 46 0.147
22
P PNC044 Pancreatitis 60 0.146
23
P CRV039 Cervicitis 45 0.143
24
THR024 Thrombosis 43 0.140
25
RTN023 Retinitis 49 0.139
26
VGN023 Vaginitis 41 0.139
27
END072 Endotheliitis 41 0.138
28
P GLM007 Glomerulonephritis 55 0.136
29
LNG054 Lung Agenesis 32 0.135
30
ANR040 Aneurysm 57 0.133
31
VSC007 Vascular Disease 65 0.133
32
ANG018 Angiomyolipoma 45 0.128
33
P NRP001 Neuropathy 57 0.127
34
RNL025 Renal Hypoplasia 39 0.126
35
BRT030 Birth Defects 44 0.119
36
URT001 Urethritis 40 0.118
37
CRY002 Cryptorchidism 61 0.117
38
P VSC005 Vesicoureteral Reflux 52 0.115
39
P PLY014 Polycystic Kidney Disease 52 0.112
40
HRS011 Horseshoe Kidney 33 0.112
41
P HYP069 Hyperparathyroidism 56 0.111
42
P HRT032 Heart Disease 75 0.109
43
P TBR001 Tuberous Sclerosis 67 0.106
44
P EPL164 Epilepsy 65 0.105
45
SYN005 Synostosis 45 0.104
46
FBR032 Fibromuscular Dysplasia 46 0.104
47
ANR004 Anuria 44 0.103
48
CLB001 Coloboma 54 0.101
49
P ESP024 Esophagitis 59 0.100
50
NRN002 Neuronitis 39 0.099
51
P PLY006 Polydactyly 54 0.099
52
PRS047 Prostatitis 55 0.099
53
SPS057 Spasticity 42 0.099
54
PNL023 Penile Agenesis 23 0.097
55
P PNC045 Pancreatic Agenesis 43 0.096
56
P LKM002 Leukemia 72 0.095
57
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.092
58
HYP015 Hyperlucent Lung 35 0.091
59
SNS001 Sensorineural Hearing Loss 54 0.091
60
P HYP086 Hypothyroidism 60 0.088
61
P ART022 Arthritis 72 0.085
62
P CTR002 Cataract 57 0.083
63
MLT084 Multicystic Dysplastic Kidney 37 0.083
64
P NPH012 Nephrotic Syndrome 59 0.082
65
TRC040 Tracheoesophageal Fistula 46 0.081
66
P PLM037 Pulmonary Hypertension 77 0.081
67
P HYD006 Hydrocephalus 66 0.080
68
PLY024 Polymicrogyria 36 0.080
69
P INF032 Infertility 57 0.080
70
GNG013 Gingivitis 61 0.079
71
P OBS005 Obesity 91 0.078
72
MCR103 Microtia 39 0.078
73
IMP002 Imperforate Anus 52 0.077
74
CRB045 Cerebellar Hypoplasia 50 0.077
75
P FCL005 Focal Segmental Glomerulosclerosis 60 0.076
76
ALR002 Al-Raqad Syndrome 29 0.075
77
P HMN010 Hemangioma 59 0.075
78
P TRC086 Trichohepatoenteric Syndrome 1 51 0.075
79
HMF006 Hemifacial Microsomia 54 0.075
80
PRP030 Purpura 57 0.074
81
MYR002 Mayer-Rokitansky-Kuster-Hauser Syndrome 57 0.074
82
CLR003 Clear Cell Adenocarcinoma 53 0.074
83
RNL051 Renal Cysts and Diabetes Syndrome 46 0.073
84
MCR013 Microphthalmia 59 0.073
85
AND005 Androgen Insensitivity Syndrome, Mild 16 0.072
86
P NRV007 Nervous System Disease 70 0.072
87
P SCH018 Schizencephaly 52 0.072
88
PLN006 Poland Syndrome 54 0.071
89
P TRT010 Teratoma 51 0.071
90
TTR001 Tetralogy of Fallot 69 0.071
91
URT020 Ureterocele 31 0.071
92
DXT001 Dextrocardia 43 0.070
93
P HLP001 Holoprosencephaly 65 0.070
94
P MCR010 Microcephaly 58 0.070
95
P SNS014 Sinusitis 59 0.069
96
HDC001 Headache 53 0.069
97
PRP019 Peripheral Nervous System Disease 53 0.069
98
ESP020 Esophageal Atresia 50 0.069
99
P PHC003 Pheochromocytoma 72 0.069
100
P HYP024 Hypoparathyroidism 52 0.068
101
P LNG032 Lung Cancer 94 0.068
102
CHL071 Child Syndrome 59 0.068
103
SQM006 Squamous Cell Carcinoma 69 0.068
104
PPL002 Papillary Carcinoma 47 0.068
105
P PTS002 Ptosis 52 0.067
106
P LRY019 Laryngitis 53 0.067
107
P MYM002 Moyamoya Disease 60 0.066
108
P CNJ013 Conjunctivitis 63 0.065
109
P AST005 Asthma 81 0.065
110
RDC002 Radiculopathy 50 0.065
111
P KLL001 Kallmann Syndrome 62 0.065
112
NLL002 Null Syndrome 26 0.065
113
P ATX004 Ataxia 52 0.064
114
DDN006 Duodenitis 40 0.064
115
ING001 Inguinal Hernia 57 0.063
116
P TRM003 Tremor 53 0.063
117
PNM008 Pneumothorax 53 0.062
118
CLF004 Cleft Lip/palate 45 0.062
119
MCN001 Mucinous Adenocarcinoma 49 0.061
120
P END044 Endometriosis 53 0.061
121
P HYP265 Hypotonia 39 0.061
122
P ART084 Arteriovenous Fistula 43 0.061
123
P PTN002 Patent Ductus Arteriosus 48 0.060
124
CRY010 Cryptophthalmos 24 0.060
125
P CRD011 Cardiomyopathy 67 0.060
126
P NNT009 Neonatal Diabetes Mellitus 51 0.060
127
GNG012 Gingival Overgrowth 51 0.059
128
MVM001 Movement Disease 52 0.058
129
PLG004 Plagiocephaly 42 0.058
130
P INF038 Influenza 71 0.058
131
P MNN013 Meningitis 65 0.058
132
NRF010 Neurofaciodigitorenal Syndrome 19 0.058
133
c RNL099 Renal Hypodysplasia/aplasia 2 18 0.057
134
MDS022 Mediastinitis 40 0.057
135
ACR008 Acrocallosal Syndrome 55 0.057
136
BFD002 Bifid Nose with or Without Anorectal and Renal Anomalies 23 0.057
137
P ATR011 Atrial Fibrillation 65 0.057
138
P KLP003 Klippel-Feil Syndrome 44 0.056
139
NRG002 Neurogenic Bladder 50 0.056
140
c CNG499 Congenital Anomalies of Kidney and Urinary Tract 2 33 0.056
141
HYP066 Hyperglycemia 59 0.056
142
P MYS005 Myositis 56 0.056
143
P PLY019 Polyneuropathy 54 0.056
144
SMN007 Seminoma 42 0.055
145
P ENC008 Encephalocele 48 0.055
146
CHR078 Chorioretinitis 37 0.055
147
VCS001 Vici Syndrome 46 0.055
148
HYP291 Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia 46 0.055
149
DWN001 Down Syndrome 69 0.054
150
c MCR256 Microphthalmia, Syndromic 9 43 0.054
151
P CNG015 Congenital Diaphragmatic Hernia 60 0.054
152
DYS018 Dysostosis 42 0.054
153
P LMY004 Leiomyosarcoma 54 0.054
154
STS002 Situs Inversus 45 0.054
155
CYS009 Cystadenoma 40 0.054
156
P RTN014 Retinal Artery Occlusion 42 0.054
157
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 43 0.053
158
HRS039 Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness 15 0.053
159
P LYM025 Lymphedema 60 0.053
160
EXS017 Exstrophy of Bladder 41 0.053
161
P BLD051 Blood Coagulation Disease 43 0.052
162
P ANR002 Aniridia 66 0.052
163
PRN038 Prune Belly Syndrome 48 0.052
164
ACR058 Acrofacial Dysostosis 1, Nager Type 41 0.051
165
VTR017 Vater-Like Defects with Pulmonary Hypertension, Laryngeal Webs, and Growth Deficiency 16 0.051
166
RNL108 Renal Hypoplasia, Unilateral 6 0.051
167
FCL009 Focal Dermal Hypoplasia 56 0.051
168
P LYD001 Leydig Cell Tumor 44 0.051
169
FRY002 Fryns Syndrome 40 0.051
170
P OST012 Osteoarthritis 79 0.051
171
P PRD008 Periodontitis 46 0.051
172
EMN001 Emanuel Syndrome 41 0.051
173
P AST007 Astrocytoma 63 0.051
174
OPT037 Optic Nerve Hypoplasia 51 0.051
175
P LYM026 Lymphoblastic Leukemia 60 0.051
176
ADP007 Adie Pupil 35 0.051
177
RSP006 Respiratory System Disease 60 0.050
178
PRP027 Peripheral Vascular Disease 65 0.050
179
P GND004 Gonadal Dysgenesis 51 0.050
180
SRN002 Sirenomelia 33 0.050
181
PLM014 Pleomorphic Adenoma 50 0.049
182
STT001 Status Epilepticus 58 0.049
183
VCT001 Vacterl Association 40 0.049
184
P MNN007 Meningocele 35 0.049
185
P LCH002 Lichen Planus 52 0.049
186
BLD053 Blood Platelet Disease 46 0.049
187
INT075 Intracranial Hypertension 48 0.049
188
P RHN004 Rhinitis 59 0.049
189
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 33 0.048
190
P CRN037 Craniosynostosis 65 0.048
191
P ANT006 Antiphospholipid Syndrome 54 0.048
192
P PRT013 Portal Hypertension 58 0.048
193
APR006 Apert Syndrome 68 0.048
194
DSS009 Disseminated Intravascular Coagulation 50 0.048
195
DND001 Dandy-Walker Syndrome 44 0.048
196
ANG011 Angiodysplasia 43 0.048
197
KRT008 Keratopathy 39 0.048
198
P GRV001 Graves' Disease 57 0.048
199
RNL104 Renal Hypodysplasia 29 0.047
200
P VNT002 Ventricular Septal Defect 58 0.047
201
P THR005 Thrombotic Thrombocytopenic Purpura 57 0.047
202
P CPL006 Capillary Hemangioma 50 0.047
203
CHR501 Chromosome 17q12 Deletion Syndrome 30 0.047
204
ACN002 Acanthosis Nigricans 56 0.047
205
HYP077 Hypertrichosis 48 0.047
206
P DGR001 Digeorge Syndrome 54 0.047
207
SPN369 Spinal Disease 38 0.047
208
P PRG013 Paraganglioma 54 0.046
209
P ORF002 Orofacial Cleft 40 0.046
210
BLL006 Bullous Pemphigoid 59 0.046
211
BRN022 Bronchiectasis 49 0.046
212
VGN031 Vaginal Atresia 23 0.046
213
MYL020 Myelomeningocele 50 0.046
214
DBL008 Double Uterus-Hemivagina-Renal Agenesis 4 0.046
215
STR026 Star Syndrome 59 0.046
216
PLY012 Polyhydramnios 46 0.046
217
INV006 Inverted Papilloma 41 0.046
218
P TRN020 Turner Syndrome 65 0.045
219
P OST001 Osteopetrosis 63 0.045
220
SKN016 Skin Disease 64 0.045
221
KRT006 Keratoconjunctivitis 52 0.045
222
TND004 Tendinopathy 40 0.045
223
P FRS014 Fraser Syndrome 1 51 0.045
224
ACH004 Achondroplasia 66 0.045
225
c BSL007 Basal Cell Carcinoma 64 0.045
226
PLM033 Pulmonary Embolism 59 0.045
227
JJN004 Jejunal Atresia 29 0.045
228
BFD001 Bifid Nose 26 0.045
229
MCR310 Microgastria-Limb Reduction Defects Association 17 0.045
230
NRF007 Neurofibroma 58 0.045
231
P PLY041 Polymyositis 52 0.044
232
GLC003 Glucose Intolerance 54 0.044
233
c BRN108 Branchiootic Syndrome 1 35 0.044
234
HYP080 Hypogonadism 52 0.044
235
c LRG001 Large Cell Carcinoma 50 0.044
236
HMH002 Hemihypertrophy 40 0.044
237
BRN002 Bronchiolitis 52 0.044
238
PMP001 Pemphigus 49 0.044
239
P TRC005 Tracheal Stenosis 36 0.043
240
SPN060 Spondylocarpotarsal Synostosis Syndrome 40 0.043
241
P RSP003 Respiratory Failure 68 0.043
242
P NRV006 Nervous System Cancer 59 0.043
243
LSH001 Leishmaniasis 66 0.043
244
P VLC001 Velocardiofacial Syndrome 64 0.043
245
MLL011 Mullerian Aplasia and Hyperandrogenism 26 0.043
246
CYL001 Cayler Cardiofacial Syndrome 32 0.043
247
RGH009 Right Atrial Isomerism 48 0.042
248
P HYP040 Hypospadias 58 0.042
249
CHR103 Charge Syndrome 65 0.042
250
c DMN029 Diamond-Blackfan Anemia 11 28 0.042
251
TRN045 True Unicornuate Uterus 11 0.042
252
HLL004 Hellp Syndrome 48 0.042
253
ART031 Aortic Coarctation 43 0.042
254
P CRB042 Cerebellar Ataxia 69 0.042
255
P MSC005 Muscular Dystrophy 65 0.042
256
c MCR263 Microphthalmia, Syndromic 1 37 0.042
257
P CYS017 Cystic Teratoma 38 0.041
258
P CMP008 Compartment Syndrome 44 0.041
259
P ICH004 Ichthyosis 53 0.041
260
DRR010 Darier Disease 59 0.041
261
LYM022 Lymphangioma 51 0.041
262
TLP001 Talipes Equinovarus 40 0.041
263
ACR045 Acro-Pectoro-Renal Field Defect 6 0.041
264
PYL006 Pyloric Stenosis 45 0.041
265
ICH054 Ichthyosis, X-Linked 49 0.041
266
ANN002 Anencephaly 53 0.040
267
WLL012 Williams-Beuren Region Duplication Syndrome 22 0.040
268
GST019 Gastrointestinal Stromal Tumor 74 0.040
269
WRN001 Werner Syndrome 68 0.040
270
P HMF004 Hemifacial Spasm 37 0.040
271
LYM035 Lymphangiectasis 27 0.040
272
DPH006 Diaphragmatic Eventration 27 0.040
273
P SCL018 Scoliosis 56 0.039
274
HYP513 Hypogonadotropic Hypogonadism 1 with or Without Anosmia 38 0.039
275
c LPR012 Leopard Syndrome 1 33 0.039
276
HYP666 Hypoparathyroidism-Deafness-Renal Disease Syndrome 34 0.039
277
PYR004 Pyuria 31 0.039
278
P THR015 Thrombophilia 58 0.039
279
LDD001 Ladd Syndrome 60 0.039
280
HYD012 Hydrops Fetalis 43 0.039
281
PRT029 Parathyroid Adenoma 49 0.039
282
SPR035 Superior Vena Cava Syndrome 29 0.039
283
CRT028 Cor Triatriatum 23 0.039
284
ACR007 Acromegaly 66 0.039
285
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 28 0.039
286
PNC034 Pancreas Disease 55 0.038
287
P OST005 Osteogenesis Imperfecta 68 0.038
288
SHR082 Short Stature, Microcephaly, and Endocrine Dysfunction 24 0.038
289
P FNC043 Fanconi Anemia, Complementation Group E 51 0.038
290
P MYL006 Myeloid Leukemia 64 0.038
291
GNG002 Ganglioneuroma 48 0.038
292
OMP004 Omphalocele 51 0.038
293
P MSC003 Muscular Atrophy 49 0.037
294
P RBL001 Rubella 53 0.037
295
PMP004 Pemphigus Foliaceus 42 0.037
296
RDL002 Radioulnar Synostosis 45 0.037
297
c ACT073 Acute Leukemia 61 0.037
298
VSC047 Vascular Malformation 43 0.037
299
DDN011 Duodenal Atresia 37 0.037
300
c NTR039 Neutropenia, Severe Congenital 4, Autosomal Recessive 32 0.036
301
c CTS041 Cutis Laxa, Autosomal Dominant 3 24 0.036
302
SCH025 Schisis Association 22 0.036
303
DST055 Distal 22q11.2 Microduplication Syndrome 16 0.036
304
EPD016 Epidermolysis Bullosa 55 0.036
305
ADR005 Adrenal Carcinoma 54 0.036
306
P ESS003 Essential Thrombocythemia 70 0.036
307
ADN027 Adenomyosis 45 0.036
308
MRB003 Morbid Obesity 58 0.035
309
P HMP007 Hemophilia 55 0.035
310
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 51 0.035
311
NSP002 Nasopharyngitis 40 0.035
312
LNS003 Lens Disease 35 0.035
313
SPN185 Spinal Cord Infarction 33 0.035
314
P MMP001 Mumps 54 0.035
315
MCP006 Mucoepidermoid Carcinoma 47 0.035
316
CMP079 Complete Septate Uterus 12 0.035
317
KMR001 Kimura Disease 50 0.034
318
c HYP058 Hypervitaminosis a 37 0.034
319
GST033 Gestational Diabetes 55 0.034
320
HYP064 Hypogonadotropism 35 0.034
321
URG002 Urogenital Adysplasia 6 0.034
322
c TRS012 Trisomy 22 27 0.034
323
MLG077 Malignant Peripheral Nerve Sheath Tumor 55 0.033
324
FLL008 Folliculitis 45 0.033
325
c RTS003 Ritscher-Schinzel Syndrome 1 34 0.033
326
VRR004 Verrucous Carcinoma 50 0.033
327
PRS039 Prostate Adenocarcinoma 45 0.033
328
LRY029 Laryngomalacia 41 0.033
329
THR009 Thrombocytopenia-Absent Radius Syndrome 58 0.032
330
HYP730 Hypogonadotropic Hypogonadism 52 0.032
331
P PRN026 Porencephaly 48 0.032
332
UND005 Undifferentiated Pleomorphic Sarcoma 44 0.032
333
DRM013 Dermoid Cyst 44 0.032
334
PNT005 Pentalogy of Cantrell 30 0.032
335
INN003 Iniencephaly 27 0.032
336
BRN028 Brain Cancer 67 0.032
337
P SHR029 Short Syndrome 61 0.032
338
P CHR285 Chronic Myelomonocytic Leukemia 58 0.032
339
GST045 Gastroenteritis 57 0.032
340
P OLG002 Oligodendroglioma 55 0.032
341
OPT007 Optic Nerve Glioma 41 0.032
342
P CRB059 Cerebellar Degeneration 37 0.032
343
GRV012 Grover's Disease 35 0.032
344
c DLT002 Dilated Cardiomyopathy 74 0.031
345
P STH001 Saethre-Chotzen Syndrome 60 0.031
346
BLD034 Bile Duct Carcinoma 55 0.031
347
MYM001 Myoma 51 0.031
348
TTH006 Tooth Disease 51 0.031
349
GNG008 Ganglioneuroblastoma 40 0.031
350
c SML034 Small Cell Neuroendocrine Carcinoma 36 0.031
351
P ATX010 Ataxia Neuropathy Spectrum 27 0.031
352
CRZ001 Crouzon Syndrome 70 0.030
353
THR016 Thrombophlebitis 52 0.030
354
c ATS275 Autosomal Recessive Primary Microcephaly 46 0.030
355
ANR018 Anorchia 37 0.030
356
CMB021 Combined Pituitary Hormone Deficiency 36 0.030
357
BLP004 Blepharophimosis 36 0.030
358
ACR017 Acrofacial Dysostosis 21 0.030
359
LPM007 Lipomyelomeningocele 21 0.030
360
ARS001 Aarskog-Scott Syndrome 54 0.030
361
VRN004 Vernal Keratoconjunctivitis 52 0.030
362
P ESN008 Eosinophilic Pneumonia 51 0.030
363
GNG004 Ganglioglioma 49 0.030
364
P CRB088 Cerebral Atrophy 39 0.030
365
P CHR342 Chiari Malformation 38 0.030
366
HRM002 Hermaphroditism 38 0.030
367
CRN033 Cranial Nerve Malignant Neoplasm 31 0.030
368
TRP015 Triphalangeal Thumb 27 0.030
369
CNG039 Congenital Absence of the Vas Deferens 21 0.030
370
P DYS007 Dyskeratosis Congenita 66 0.030
371
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 56 0.030
372
ANT003 Antley-Bixler Syndrome 50 0.030
373
CRC006 Carcinoid Syndrome 48 0.030
374
HMR002 Hemarthrosis 47 0.030
375
P ORF001 Orofaciodigital Syndrome 45 0.030
376
ATR060 Atrial Standstill, Digenic 43 0.030
377
DDF001 Dedifferentiated Liposarcoma 43 0.030
378
RCT017 Rectal Disease 38 0.030
379
ECT004 Ecthyma 34 0.030
380
LRN006 Laurin-Sandrow Syndrome 33 0.030
381
BLB005 Beaulieu-Boycott-Innes Syndrome 23 0.030
382
LMB013 Limb Reduction Defect 14 0.030
383
PHN003 Phenylketonuria 72 0.028
384
c HMP029 Hemophilia a 64 0.028
385
P DBT083 Diabetes Mellitus, Permanent Neonatal 56 0.028
386
P EPD009 Epidermolysis Bullosa Dystrophica 56 0.028
387
ABL002 Ablepharon-Macrostomia Syndrome 52 0.028
388
BLR007 Biliary Tract Neoplasm 50 0.028
389
c CHR086 Chronic Conjunctivitis 45 0.028
390
P PLM085 Pulmonary Hemosiderosis 44 0.028
391
LMR001 Lemierre's Syndrome 43 0.028
392
INT078 Intracranial Thrombosis 37 0.028
393
P PRN022 Perineurioma 36 0.028
394
HYD001 Hydranencephaly 35 0.028
395
SGT001 Sagittal Sinus Thrombosis 33 0.028
396
BZR001 Bizarre Leiomyoma 31 0.028
397
ACC001 Accessory Nerve Disease 21 0.028
398
THY009 Thyroid Lymphoma 50 0.028
399
HYP042 Hypochondroplasia 58 0.026
400
BRN038 Bronchial Disease 53 0.026
401
WLK001 Walker-Warburg Syndrome 52 0.026
402
OST044 Osteoglophonic Dysplasia 49 0.026
403
JCK001 Jackson-Weiss Syndrome 49 0.026
404
ONC002 Onchocerciasis 48 0.026
405
SND002 Sneddon Syndrome 48 0.026
406
TRN044 Transposition of the Great Arteries 46 0.026
407
UPP004 Upper Respiratory Tract Disease 46 0.026
408
c MLG074 Malignant Mesenchymoma 46 0.026
409
ANL017 Anal Squamous Cell Carcinoma 45 0.026
410
c MTR002 Mitral Valve Insufficiency 45 0.026
411
OCL001 Ocular Albinism 43 0.026
412
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 42 0.026
413
ADT003 Auditory System Disease 41 0.026
414
ORL012 Oral Leukoplakia 41 0.026
415
PRN049 Paraneoplastic Pemphigus 41 0.026
416
SCL017 Sclerosing Hemangioma 39 0.026
417
c PFF007 Pfeiffer Syndrome Type 1 38 0.026
418
c BLD008 Bladder Carcinoma in Situ 35 0.026
419
SCR016 Scrotal Carcinoma 35 0.026
420
SPT007 Spitz Nevus 34 0.026
421
BRN011 Brain Stem Astrocytic Neoplasm 33 0.026
422
TRC097 Tracheomalacia 33 0.026
423
KRT003 Keratinizing Squamous Cell Carcinoma 33 0.026
424
CRB038 Cerebral Ventricle Cancer 32 0.026
425
END029 Endocervical Carcinoma 32 0.026
426
VLV034 Vulva Squamous Cell Carcinoma 28 0.026
427
FRS007 Frias Syndrome 28 0.026
428
7Q1002 7q11.23 Duplication Syndrome 28 0.026
429
c KLP007 Klippel-Feil Syndrome 1, Autosomal Dominant 28 0.026
430
P RDL006 Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia 27 0.026
431
OLF002 Olfactory Groove Meningioma 25 0.026
432
ATY007 Atypical Follicular Adenoma 24 0.026
433
HYP565 Hypogonadotropic Hypogonadism 3 with or Without Anosmia 23 0.026
434
TRN046 Transverse Vaginal Septum 13 0.026
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