Search results for unilateral renal agenesis

410 hits were found for unilateral renal agenesis

# Family MCID Name MIFTS Score
1
RNL105 Renal Agenesis, Unilateral 35 3.131
2
ANR016 Aniridia Renal Agenesis Psychomotor Retardation 10 2.684
3
MCR304 Microcephaly, Congenital Heart Disease, Unilateral Renal Agenesis, and Hyposegmented Lungs 21 2.622
4
UTR057 Uterus Bicornis Bicollis with Partial Vaginal Septum and Unilateral Hematocolpos with Ipsilateral Renal Agenesis 24 2.487
5
ANR044 Aniridia, Partial, with Unilateral Renal Agenesis and Psychomotor Retardation 18 2.346
6
MLL021 Mullerian Duct Aplasia, Unilateral Renal Agenesis, and Cervicothoracic Somite Anomalies 25 2.089
7
MRC004 Murcs Association 31 1.855
8
SNT001 Santos Mateus Leal Syndrome 9 1.855
9
ELL004 Ellis Yale Winter Syndrome 8 1.829
10
P RNL100 Renal Hypodysplasia/aplasia 1 57 0.571
11
P KDN018 Kidney Disease 69 0.384
12
URN009 Urinary System Disease 58 0.295
13
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.275
14
URT010 Ureteral Obstruction 49 0.270
15
c BLD140 Blood Group, I System 37 0.230
16
P ADN016 Adenocarcinoma 71 0.210
17
RNL078 Renal Dysplasia 49 0.207
18
P DBT009 Diabetes Mellitus 72 0.194
19
CRB009 Cerebritis 41 0.190
20
CLF001 Cleft Lip 54 0.190
21
P HPT021 Hepatitis 75 0.176
22
P THY032 Thyroiditis 56 0.174
23
AGN016 Aging 65 0.164
24
P PNC044 Pancreatitis 64 0.162
25
HYD002 Hydronephrosis 49 0.159
26
P CRV039 Cervicitis 49 0.158
27
ADN018 Adenoma 63 0.157
28
VGN023 Vaginitis 59 0.155
29
P GLM007 Glomerulonephritis 61 0.154
30
END072 Endotheliitis 46 0.152
31
THR024 Thrombosis 61 0.152
32
RTN023 Retinitis 52 0.147
33
ANR040 Aneurysm 61 0.146
34
ANG018 Angiomyolipoma 50 0.144
35
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.142
36
P NRP001 Neuropathy 63 0.139
37
P HRT032 Heart Disease 80 0.134
38
URT001 Urethritis 44 0.133
39
RNL025 Renal Hypoplasia 37 0.132
40
P ANR048 Aniridia 1 68 0.132
41
c BRN108 Branchiootic Syndrome 1 47 0.130
42
P PLY014 Polycystic Kidney Disease 60 0.128
43
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.127
44
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.126
45
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.126
46
BLD137 Blood Group--Ahonen 17 0.126
47
ANR038 Anorexia Nervosa 1 21 0.126
48
P HYP069 Hyperparathyroidism 58 0.123
49
c VSC019 Vesicoureteral Reflux 1 54 0.122
50
c WLM011 Wilms Tumor 6 44 0.121
51
HRS011 Horseshoe Kidney 35 0.121
52
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.121
53
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.117
54
P TBR001 Tuberous Sclerosis 69 0.116
55
FBR032 Fibromuscular Dysplasia 53 0.115
56
P PLY006 Polydactyly 57 0.115
57
ANR004 Anuria 49 0.114
58
PRS047 Prostatitis 59 0.112
59
CLB010 Coloboma of Macula 52 0.112
60
P EPL164 Epilepsy 70 0.111
61
NRN002 Neuronitis 43 0.109
62
P ESP024 Esophagitis 64 0.108
63
SPS057 Spasticity 41 0.108
64
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.108
65
P LPS004 Lupus Erythematosus 69 0.106
66
PNL023 Penile Agenesis 25 0.105
67
P HYP086 Hypothyroidism 62 0.105
68
P ENC018 Encephalopathy 58 0.103
69
P ART022 Arthritis 77 0.101
70
P NPH012 Nephrotic Syndrome 60 0.100
71
c WLM018 Wilms Tumor 5 49 0.098
72
SYN005 Synostosis 50 0.098
73
SNS001 Sensorineural Hearing Loss 59 0.097
74
ALR002 Al-Raqad Syndrome 30 0.096
75
CHN065 Choanal Atresia, Posterior 43 0.094
76
RNL094 Renal Dysplasia, Cystic 29 0.094
77
HYP015 Hyperlucent Lung 36 0.092
78
c FCL025 Focal Segmental Glomerulosclerosis 1 59 0.092
79
MCR103 Microtia 39 0.092
80
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.091
81
c SYS001 Systemic Lupus Erythematosus 86 0.090
82
P HYD006 Hydrocephalus 68 0.090
83
HMF006 Hemifacial Microsomia 58 0.090
84
P INF032 Infertility 59 0.089
85
ANS023 Anus, Imperforate 50 0.089
86
P PLM037 Pulmonary Hypertension 79 0.089
87
TRC040 Tracheoesophageal Fistula 47 0.088
88
HPT082 Hepatic Adenomas, Familial 52 0.088
89
MCR013 Microphthalmia 61 0.086
90
MYR002 Mayer-Rokitansky-Kuster-Hauser Syndrome 59 0.086
91
P CNG499 Congenital Anomalies of Kidney and Urinary Tract 2 41 0.086
92
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 51 0.085
93
P CTR002 Cataract 60 0.085
94
MLT084 Multicystic Dysplastic Kidney 36 0.085
95
P HYP024 Hypoparathyroidism 55 0.085
96
URT020 Ureterocele 37 0.085
97
GNG013 Gingivitis 64 0.085
98
CRB045 Cerebellar Hypoplasia 48 0.084
99
P TRT010 Teratoma 53 0.083
100
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.083
101
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.083
102
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.083
103
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.083
104
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.083
105
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.083
106
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.083
107
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.083
108
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.083
109
P JBR020 Joubert Syndrome 1 68 0.083
110
PLY024 Polymicrogyria 36 0.083
111
P MCR010 Microcephaly 57 0.082
112
P HLP001 Holoprosencephaly 67 0.081
113
P HMN010 Hemangioma 61 0.081
114
P NRV007 Nervous System Disease 75 0.081
115
DXT001 Dextrocardia 55 0.080
116
RNL051 Renal Cysts and Diabetes Syndrome 45 0.080
117
P KLL001 Kallmann Syndrome 63 0.079
118
P FCL005 Focal Segmental Glomerulosclerosis 60 0.079
119
SQM006 Squamous Cell Carcinoma 74 0.078
120
ESP020 Esophageal Atresia 54 0.077
121
P MMB011 Membranous Nephropathy 55 0.076
122
PLY110 Polymicrogyria, Bilateral Temporooccipital 32 0.076
123
PNM008 Pneumothorax 57 0.076
124
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 51 0.076
125
CLF027 Cleft Palate, Isolated 61 0.075
126
c FRS014 Fraser Syndrome 1 51 0.075
127
P SNS014 Sinusitis 62 0.074
128
P KLP003 Klippel-Feil Syndrome 46 0.074
129
P TTR001 Tetralogy of Fallot 70 0.074
130
ALP046 Alport Syndrome, X-Linked 74 0.074
131
PLN006 Poland Syndrome 50 0.073
132
P PHC003 Pheochromocytoma 72 0.073
133
c MNN043 Meningioma, Familial 69 0.072
134
P LNG032 Lung Cancer 99 0.072
135
ING001 Inguinal Hernia 59 0.072
136
c CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 53 0.072
137
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.072
138
P RNL123 Renal Agenesis, Bilateral 25 0.072
139
CHR008 Choroiditis 47 0.071
140
c PRM005 Primary Hyperparathyroidism 59 0.071
141
P TRC086 Trichohepatoenteric Syndrome 1 54 0.071
142
c THR092 Thrombophilia Due to Thrombin Defect 61 0.071
143
HDC001 Headache 55 0.071
144
P LRY019 Laryngitis 57 0.071
145
P END044 Endometriosis 71 0.071
146
DDN006 Duodenitis 46 0.070
147
GYN001 Gynecomastia 47 0.070
148
c DPH024 Diaphragmatic Hernia, Congenital 63 0.070
149
P MYP004 Myopathy 69 0.070
150
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 36 0.069
151
P PTS002 Ptosis 50 0.069
152
AST005 Asthma 83 0.069
153
P HYP265 Hypotonia 40 0.069
154
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.068
155
CRY010 Cryptophthalmos 26 0.068
156
VRC001 Varicocele 52 0.067
157
PPL002 Papillary Carcinoma 51 0.067
158
VTR016 Vater/vacterl Association 37 0.066
159
P TRM003 Tremor 54 0.066
160
DWN001 Down Syndrome 70 0.066
161
MCR310 Microgastria-Limb Reduction Defects Association 23 0.066
162
BFD002 Bifid Nose with or Without Anorectal and Renal Anomalies 24 0.066
163
P ART084 Arteriovenous Fistula 46 0.066
164
P MYM013 Moyamoya Disease 1 50 0.065
165
c MCR256 Microphthalmia, Syndromic 9 48 0.065
166
P HRD009 Hereditary Wilms' Tumor 46 0.065
167
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.065
168
CLF004 Cleft Lip/palate 49 0.065
169
CHR619 Chromosome 2q35 Duplication Syndrome 62 0.065
170
c LPM012 Lipomatosis, Multiple 64 0.065
171
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 51 0.065
172
P CNJ013 Conjunctivitis 67 0.065
173
EXS017 Exstrophy of Bladder 45 0.064
174
NRF026 Neurofibromatosis, Type Iv, of Riccardi 72 0.064
175
HYP080 Hypogonadism 54 0.064
176
NRG002 Neurogenic Bladder 53 0.064
177
HYP730 Hypogonadotropic Hypogonadism 56 0.064
178
P STS008 Sotos Syndrome 1 56 0.064
179
HRS039 Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness 18 0.064
180
MYL020 Myelomeningocele 54 0.064
181
P ATR011 Atrial Fibrillation 68 0.064
182
GNG012 Gingival Overgrowth 52 0.064
183
P HYP040 Hypospadias 60 0.063
184
VCS001 Vici Syndrome 46 0.063
185
ADR054 Adrenocortical Carcinoma, Hereditary 63 0.063
186
NRL016 Neural Tube Defects 79 0.063
187
P MNN013 Meningitis 71 0.063
188
P INF038 Influenza 77 0.062
189
HYP748 Hypertelorism 46 0.062
190
ACR008 Acrocallosal Syndrome 56 0.062
191
OVR029 Ovarian Hyperstimulation Syndrome 64 0.062
192
c RNL099 Renal Hypodysplasia/aplasia 2 18 0.061
193
BLD163 Blood Group, Dombrock System 23 0.061
194
P ENC008 Encephalocele 48 0.061
195
NRF010 Neurofaciodigitorenal Syndrome 21 0.061
196
SMN007 Seminoma 49 0.061
197
MCN001 Mucinous Adenocarcinoma 54 0.061
198
MDS022 Mediastinitis 44 0.061
199
P LYD001 Leydig Cell Tumor 47 0.061
200
LNG099 Lung Disease 67 0.061
201
PTR032 Peters-Plus Syndrome 60 0.060
202
STS002 Situs Inversus 48 0.060
203
PRN038 Prune Belly Syndrome 55 0.060
204
ADP007 Adie Pupil 41 0.060
205
P LYM025 Lymphedema 63 0.059
206
P PLY019 Polyneuropathy 58 0.059
207
P UTR058 Uterine Anomalies 55 0.058
208
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 40 0.058
209
P CRN037 Craniosynostosis 68 0.058
210
SRN002 Sirenomelia 33 0.058
211
PLL001 Pallister-Hall Syndrome 59 0.058
212
ACR058 Acrofacial Dysostosis 1, Nager Type 46 0.057
213
c BSL007 Basal Cell Carcinoma 66 0.057
214
c BRT038 Baraitser-Winter Syndrome 1 37 0.057
215
P PTN014 Patent Ductus Arteriosus 1 45 0.057
216
P PRD008 Periodontitis 67 0.056
217
P ICH004 Ichthyosis 54 0.056
218
ICH054 Ichthyosis, X-Linked 59 0.056
219
P GND004 Gonadal Dysgenesis 50 0.056
220
PNS014 Penis Agenesis 29 0.056
221
APR006 Apert Syndrome 69 0.056
222
FRY002 Fryns Syndrome 43 0.056
223
FCL009 Focal Dermal Hypoplasia 57 0.055
224
CHR078 Chorioretinitis 41 0.055
225
DYS018 Dysostosis 48 0.055
226
P RSP003 Respiratory Failure 71 0.055
227
EMN001 Emanuel Syndrome 37 0.055
228
VTR017 Vater-Like Defects with Pulmonary Hypertension, Laryngeal Webs, and Growth Deficiency 17 0.055
229
RNL108 Renal Hypoplasia, Unilateral 6 0.054
230
P AST007 Astrocytoma 66 0.054
231
P PRT013 Portal Hypertension 59 0.054
232
SPT006 Septooptic Dysplasia 54 0.054
233
TRN045 True Unicornuate Uterus 13 0.053
234
IRN002 Iron Metabolism Disease 45 0.053
235
ACH004 Achondroplasia 67 0.053
236
VCT001 Vacterl Association 41 0.053
237
P CPL006 Capillary Hemangioma 56 0.053
238
P PRT008 Proteus Syndrome 67 0.052
239
P TRN020 Turner Syndrome 69 0.052
240
CLR003 Clear Cell Adenocarcinoma 57 0.052
241
P RHN004 Rhinitis 62 0.052
242
P SCL018 Scoliosis 56 0.052
243
P FRN036 Frontonasal Dysplasia 1 39 0.052
244
DND001 Dandy-Walker Syndrome 41 0.052
245
VGN031 Vaginal Atresia 20 0.052
246
P MNN007 Meningocele 38 0.052
247
CHR501 Chromosome 17q12 Deletion Syndrome 34 0.051
248
ANG011 Angiodysplasia 48 0.051
249
PLY012 Polyhydramnios 47 0.051
250
AYM001 Ayme-Gripp Syndrome 40 0.051
251
STT001 Status Epilepticus 60 0.051
252
TST014 Testicular Cancer 54 0.051
253
WLL012 Williams-Beuren Region Duplication Syndrome 26 0.051
254
P CYS018 Cystitis 57 0.050
255
HYP064 Hypogonadotropism 38 0.050
256
PLM014 Pleomorphic Adenoma 55 0.050
257
KRT008 Keratopathy 44 0.050
258
WBR001 Weber Syndrome 40 0.050
259
CNG184 Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects 50 0.050
260
P ORF002 Orofacial Cleft 41 0.050
261
c LPR012 Leopard Syndrome 1 33 0.050
262
DGR001 Digeorge Syndrome 55 0.050
263
PNM010 Pneumothorax, Primary Spontaneous 41 0.050
264
DBL008 Double Uterus-Hemivagina-Renal Agenesis 4 0.050
265
P GRV001 Graves' Disease 62 0.050
266
P OST001 Osteopetrosis 70 0.049
267
HYP077 Hypertrichosis 49 0.049
268
HYP056 Hypoglycemia 62 0.049
269
P TRC005 Tracheal Stenosis 39 0.049
270
BRN022 Bronchiectasis 55 0.049
271
P VNT002 Ventricular Septal Defect 59 0.048
272
PYL006 Pyloric Stenosis 47 0.048
273
JJN004 Jejunal Atresia 33 0.048
274
BCK006 Back Pain 46 0.048
275
ART031 Aortic Coarctation 48 0.047
276
CMP079 Complete Septate Uterus 14 0.047
277
VLC001 Velocardiofacial Syndrome 64 0.047
278
c ACT210 Acute Respiratory Distress Syndrome 63 0.047
279
SPN060 Spondylocarpotarsal Synostosis Syndrome 41 0.047
280
CYL001 Cayler Cardiofacial Syndrome 36 0.046
281
CHR103 Charge Syndrome 59 0.046
282
LYM035 Lymphangiectasis 31 0.046
283
FRS002 Frasier Syndrome 51 0.046
284
SPN051 Spondylitis 55 0.046
285
MLL011 Mullerian Aplasia and Hyperandrogenism 26 0.046
286
P FNC043 Fanconi Anemia, Complementation Group E 52 0.046
287
KLL015 Kallmann Syndrome with Spastic Paraplegia 14 0.046
288
ALP072 Alpha-Fetoprotein Deficiency 32 0.046
289
c BSL024 Basal Cell Carcinoma 1 42 0.046
290
CHR178 Chromosomal Triplication 35 0.045
291
HMF010 Hemifacial Microsomia with Radial Defects 31 0.045
292
LNT004 Lentigines 52 0.045
293
c SPN225 Spondyloarthropathy 1 71 0.045
294
PYR004 Pyuria 34 0.045
295
PRT029 Parathyroid Adenoma 50 0.045
296
c MCR263 Microphthalmia, Syndromic 1 41 0.045
297
P RBL001 Rubella 61 0.044
298
ANN002 Anencephaly 57 0.044
299
P OMP004 Omphalocele 51 0.044
300
LPM007 Lipomyelomeningocele 26 0.044
301
c DMN029 Diamond-Blackfan Anemia 11 21 0.044
302
ACR045 Acro-Pectoro-Renal Field Defect 7 0.044
303
RGH009 Right Atrial Isomerism 48 0.044
304
PRS042 Prostate Disease 56 0.044
305
P ATR010 Atrial Heart Septal Defect 45 0.043
306
PHN003 Phenylketonuria 73 0.043
307
SCR024 Sacrococcygeal Teratoma 32 0.043
308
ADR004 Adrenal Cortical Adenocarcinoma 47 0.043
309
HRM002 Hermaphroditism 42 0.043
310
P KBK002 Kabuki Syndrome 1 62 0.043
311
LYM022 Lymphangioma 53 0.043
312
WRN001 Werner Syndrome 70 0.042
313
HYD012 Hydrops Fetalis 50 0.042
314
HYD059 Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect 34 0.042
315
THY111 Thyroid Carcinoma, Familial Medullary 63 0.042
316
HMH004 Hemihyperplasia, Isolated 43 0.042
317
HYP513 Hypogonadotropic Hypogonadism 1 with or Without Anosmia 40 0.042
318
PRP019 Peripheral Nervous System Disease 53 0.041
319
DPH006 Diaphragmatic Eventration 29 0.041
320
ACR007 Acromegaly 70 0.041
321
P EHL001 Ehlers-Danlos Syndrome 61 0.041
322
c RNL122 Renal Hypodysplasia/aplasia 3 10 0.041
323
P CHL069 Cholesteatoma 52 0.041
324
CRT028 Cor Triatriatum 25 0.041
325
MYM001 Myoma 56 0.041
326
DWR001 Dwarfism 48 0.041
327
BDY007 Body Mass Index Quantitative Trait Locus 1 23 0.041
328
GST009 Gastroschisis 55 0.041
329
PTT046 Pituitary Hormone Deficiency, Combined, 2 57 0.040
330
SHR082 Short Stature, Microcephaly, and Endocrine Dysfunction 22 0.040
331
ATR053 Atresia of Urethra 13 0.040
332
BRT054 Brittle Bone Disorder 67 0.040
333
TTL012 Total Anomalous Pulmonary Venous Return 1 42 0.040
334
P ESS003 Essential Thrombocythemia 71 0.040
335
DDN011 Duodenal Atresia 39 0.040
336
PSD009 Pseudohermaphroditism 42 0.040
337
P MSC005 Muscular Dystrophy 66 0.039
338
P ATX024 Ataxia-Oculomotor Apraxia 3 47 0.039
339
P CYS017 Cystic Teratoma 40 0.039
340
LRY029 Laryngomalacia 43 0.039
341
P PLY011 Polycystic Ovary Syndrome 65 0.039
342
PLX004 Plexopathy 37 0.039
343
CCC001 Coccidioidomycosis 60 0.039
344
DRM013 Dermoid Cyst 43 0.039
345
P HRS035 Hirschsprung Disease 1 64 0.039
346
GRW036 Growth Control, Y-Chromosome Influenced 33 0.039
347
c TRS012 Trisomy 22 26 0.039
348
ACR017 Acrofacial Dysostosis 24 0.039
349
P MSC003 Muscular Atrophy 55 0.039
350
c CTS041 Cutis Laxa, Autosomal Dominant 3 25 0.039
351
SCH025 Schisis Association 21 0.039
352
DST055 Distal 22q11.2 Microduplication Syndrome 17 0.039
353
ACR006 Aceruloplasminemia 65 0.038
354
GST033 Gestational Diabetes 62 0.038
355
ADN027 Adenomyosis 57 0.038
356
VGN019 Vaginal Discharge 34 0.038
357
KLP010 Klippel-Trenaunay-Weber Syndrome 60 0.037
358
SPN369 Spinal Disease 42 0.037
359
P ATS364 Autism 70 0.037
360
URG002 Urogenital Adysplasia 8 0.037
361
NSP002 Nasopharyngitis 46 0.036
362
P OVR049 Ovarian Disease 58 0.036
363
CNT061 Conotruncal Heart Malformations 70 0.036
364
ANR018 Anorchia 40 0.036
365
MCP006 Mucoepidermoid Carcinoma 51 0.035
366
c MTR002 Mitral Valve Insufficiency 46 0.035
367
c RTS003 Ritscher-Schinzel Syndrome 1 36 0.035
368
PNT005 Pentalogy of Cantrell 32 0.035
369
INN003 Iniencephaly 30 0.035
370
GND003 Gonadal Disease 32 0.034
371
CRP001 Carpal Tunnel Syndrome 64 0.034
372
AMN001 Amenorrhea 55 0.033
373
P PRC019 Precocious Puberty 52 0.033
374
c LCL006 Localized Scleroderma 66 0.033
375
P PLM006 Pulmonary Alveolar Proteinosis 49 0.033
376
LMB013 Limb Reduction Defect 16 0.033
377
THR009 Thrombocytopenia-Absent Radius Syndrome 58 0.032
378
c ATS275 Autosomal Recessive Primary Microcephaly 43 0.032
379
ADR007 Adrenoleukodystrophy 72 0.032
380
P DYS007 Dyskeratosis Congenita 68 0.032
381
P TRC072 Treacher Collins Syndrome 1 61 0.032
382
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 46 0.032
383
P ORF001 Orofaciodigital Syndrome 46 0.032
384
HYD001 Hydranencephaly 36 0.032
385
VSD002 Vas Deferens, Congenital Bilateral Aplasia of 34 0.032
386
BLB005 Beaulieu-Boycott-Innes Syndrome 25 0.032
387
P PRD006 Prader-Willi Syndrome 66 0.031
388
c CNG124 Congenital Rubella 47 0.031
389
RTR008 Root Resorption 44 0.031
390
P CRB088 Cerebral Atrophy 38 0.031
391
c MSC047 Muscular Dystrophy-Dystroglycanopathy , Type a, 1 53 0.030
392
P THR117 Three M Syndrome 1 52 0.030
393
P PRN026 Porencephaly 50 0.030
394
TRN044 Transposition of the Great Arteries 49 0.030
395
P TST026 Testicular Germ Cell Cancer 44 0.030
396
TRC097 Tracheomalacia 32 0.030
397
TRN046 Transverse Vaginal Septum 15 0.030
398
ABL002 Ablepharon-Macrostomia Syndrome 55 0.027
399
TTH006 Tooth Disease 54 0.027
400
THR016 Thrombophlebitis 53 0.027
401
ANV001 Anovulation 48 0.027
402
P RBN002 Robinow Syndrome 48 0.027
403
P OCL001 Ocular Albinism 46 0.027
404
SWT003 Sweat Gland Disease 42 0.027
405
c CRN278 Craniosynostosis 1 41 0.027
406
c NTR050 Neutropenia, Severe Congenital, 4, Autosomal Recessive 32 0.027
407
7Q1002 7q11.23 Duplication Syndrome 31 0.027
408
FRS007 Frias Syndrome 29 0.027
409
c KLP007 Klippel-Feil Syndrome 1, Autosomal Dominant 26 0.027
410
HYP565 Hypogonadotropic Hypogonadism 3 with or Without Anosmia 24 0.027
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