Search results for "unilateral renal agenesis"

The MalaCard for "unilateral renal agenesis" has been retired.
Searching MalaCards for entries containing "unilateral renal agenesis"

375 hits were found for 'unilateral renal agenesis'

# Family MCID Name MIFTS Score
1
ANR016 Aniridia Renal Agenesis Psychomotor Retardation 5 2.699
2
RNL105 Renal Agenesis, Unilateral 21 2.656
3
MCR304 Microcephaly, Congenital Heart Disease, Unilateral Renal Agenesis, and Hyposegmented Lungs 17 2.626
4
UTR057 Uterus Bicornis Bicollis with Partial Vaginal Septum and Unilateral Hematocolpos with Ipsilateral Renal Agenesis 14 2.486
5
ANR044 Aniridia, Partial, with Unilateral Renal Agenesis and Psychomotor Retardation 15 2.365
6
MLL021 Mullerian Duct Aplasia, Unilateral Renal Agenesis, and Cervicothoracic Somite Anomalies 17 2.097
7
MRC004 Murcs Association 31 1.876
8
ELL004 Ellis Yale Winter Syndrome 6 1.848
9
SNT001 Santos Mateus Leal Syndrome 6 1.841
10
P KDN018 Kidney Disease 66 0.259
11
URT010 Ureteral Obstruction 45 0.242
12
P URF003 Urofacial Syndrome 1 50 0.197
13
URN009 Urinary System Disease 50 0.196
14
RNL078 Renal Dysplasia 45 0.185
15
TTH002 Tooth Agenesis 54 0.179
16
CRB009 Cerebritis 39 0.166
17
CLF001 Cleft Lip 50 0.166
18
P HPT021 Hepatitis 69 0.161
19
P ADN016 Adenocarcinoma 69 0.160
20
P THY032 Thyroiditis 54 0.155
21
P RNL100 Renal Hypodysplasia/aplasia 1 53 0.151
22
P PNC044 Pancreatitis 61 0.149
23
VGN023 Vaginitis 42 0.144
24
ADN018 Adenoma 58 0.142
25
HYD002 Hydronephrosis 47 0.141
26
P CRV039 Cervicitis 45 0.141
27
THR024 Thrombosis 57 0.137
28
LNG054 Lung Agenesis 32 0.136
29
P GLM007 Glomerulonephritis 59 0.135
30
END072 Endotheliitis 42 0.133
31
RTN023 Retinitis 50 0.132
32
ANR040 Aneurysm 57 0.130
33
P HRT032 Heart Disease 75 0.126
34
RNL025 Renal Hypoplasia 42 0.125
35
ANG018 Angiomyolipoma 46 0.125
36
P NRP001 Neuropathy 59 0.125
37
URT001 Urethritis 41 0.118
38
CRY002 Cryptorchidism 60 0.115
39
HRS011 Horseshoe Kidney 33 0.113
40
P VSC005 Vesicoureteral Reflux 53 0.111
41
P HYP069 Hyperparathyroidism 58 0.107
42
P PLY014 Polycystic Kidney Disease 53 0.106
43
P EPL164 Epilepsy 66 0.103
44
P TBR001 Tuberous Sclerosis 67 0.103
45
FBR032 Fibromuscular Dysplasia 43 0.101
46
P PNC045 Pancreatic Agenesis 42 0.101
47
PNL023 Penile Agenesis 21 0.101
48
P PLY006 Polydactyly 56 0.100
49
PRS047 Prostatitis 56 0.100
50
NRN002 Neuronitis 41 0.099
51
P ESP024 Esophagitis 61 0.097
52
ANR004 Anuria 45 0.096
53
P HYP086 Hypothyroidism 64 0.095
54
SPS057 Spasticity 42 0.094
55
PRT036 Peritonitis 63 0.093
56
SYN005 Synostosis 46 0.092
57
c ATS347 Autosomal Dominant Polycystic Kidney Disease 63 0.091
58
P NPH012 Nephrotic Syndrome 59 0.089
59
HYP015 Hyperlucent Lung 36 0.087
60
SNS001 Sensorineural Hearing Loss 57 0.087
61
BRT030 Birth Defects 43 0.086
62
PRD011 Proud Syndrome 42 0.085
63
ALR002 Al-Raqad Syndrome 36 0.085
64
P PLM037 Pulmonary Hypertension 79 0.084
65
P HYD006 Hydrocephalus 66 0.082
66
ACR041 Acromelic Frontonasal Dysostosis 45 0.081
67
P FCL005 Focal Segmental Glomerulosclerosis 60 0.081
68
GNG013 Gingivitis 61 0.081
69
P INF032 Infertility 59 0.081
70
CLR003 Clear Cell Adenocarcinoma 56 0.080
71
IMP002 Imperforate Anus 52 0.079
72
CRB045 Cerebellar Hypoplasia 48 0.079
73
TRN018 Transitional Cell Carcinoma 53 0.079
74
MLT084 Multicystic Dysplastic Kidney 39 0.079
75
TRC040 Tracheoesophageal Fistula 45 0.078
76
PLY024 Polymicrogyria 35 0.077
77
P TRC086 Trichohepatoenteric Syndrome 1 48 0.077
78
P HMN010 Hemangioma 59 0.077
79
MCR103 Microtia 37 0.077
80
P OBS005 Obesity 92 0.075
81
MYR002 Mayer-Rokitansky-Kuster-Hauser Syndrome 55 0.074
82
CYT008 Cytomegalovirus Infection 52 0.073
83
P MCR010 Microcephaly 58 0.073
84
P CTR002 Cataract 58 0.073
85
P RSP003 Respiratory Failure 71 0.072
86
P HLP001 Holoprosencephaly 63 0.071
87
MCR013 Microphthalmia 60 0.071
88
P MMB011 Membranous Nephropathy 54 0.071
89
P SNS014 Sinusitis 60 0.069
90
TTR001 Tetralogy of Fallot 71 0.069
91
AND005 Androgen Insensitivity Syndrome, Mild 16 0.069
92
DXT001 Dextrocardia 43 0.069
93
NTR005 Nutritional Deficiency Disease 36 0.068
94
MDL009 Medullary Sponge Kidney 41 0.068
95
HMF006 Hemifacial Microsomia 55 0.067
96
P KLL001 Kallmann Syndrome 61 0.067
97
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.067
98
P TRT010 Teratoma 52 0.066
99
LPM004 Lipoma 60 0.066
100
P PHC003 Pheochromocytoma 71 0.066
101
SQM006 Squamous Cell Carcinoma 70 0.066
102
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.066
103
URT020 Ureterocele 32 0.066
104
PPL002 Papillary Carcinoma 51 0.065
105
RNL051 Renal Cysts and Diabetes Syndrome 47 0.065
106
P NNT009 Neonatal Diabetes Mellitus 52 0.065
107
P HYP024 Hypoparathyroidism 53 0.065
108
P LRY019 Laryngitis 54 0.065
109
ESP020 Esophageal Atresia 50 0.064
110
P PTN002 Patent Ductus Arteriosus 52 0.064
111
DDN006 Duodenitis 42 0.064
112
HDC001 Headache 54 0.064
113
ING001 Inguinal Hernia 58 0.063
114
PLV005 Pelviureteric Junction Obstruction 38 0.062
115
P FRS003 Fraser Syndrome 56 0.062
116
P KLP003 Klippel-Feil Syndrome 46 0.062
117
P MYM002 Moyamoya Disease 61 0.062
118
LPD004 Lipoid Nephrosis 48 0.062
119
PNM008 Pneumothorax 53 0.062
120
P LNG032 Lung Cancer 95 0.061
121
CRY010 Cryptophthalmos 24 0.061
122
P TRM003 Tremor 54 0.060
123
P ART084 Arteriovenous Fistula 44 0.060
124
P CNJ013 Conjunctivitis 64 0.060
125
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.060
126
ATN002 Autonomic Nervous System Disease 48 0.060
127
PLN006 Poland Syndrome 54 0.060
128
P END044 Endometriosis 66 0.060
129
P AST005 Asthma 82 0.060
130
P CRD011 Cardiomyopathy 68 0.060
131
P ATX004 Ataxia 53 0.060
132
P MNN013 Meningitis 67 0.059
133
P PTS002 Ptosis 51 0.059
134
P NRF002 Neurofibromatosis 71 0.059
135
GNG012 Gingival Overgrowth 52 0.058
136
P HYP265 Hypotonia 38 0.058
137
MCN001 Mucinous Adenocarcinoma 50 0.058
138
P CNG015 Congenital Diaphragmatic Hernia 60 0.058
139
P CLR023 Colorectal Cancer 97 0.058
140
OPT009 Optic Neuritis 50 0.058
141
P SYN001 Syndactyly 53 0.058
142
c BRN108 Branchiootic Syndrome 1 34 0.058
143
c RNL099 Renal Hypodysplasia/aplasia 2 18 0.058
144
CLF004 Cleft Lip/palate 46 0.058
145
VCS001 Vici Syndrome 43 0.057
146
NRG002 Neurogenic Bladder 50 0.057
147
SMN007 Seminoma 45 0.057
148
P ENC008 Encephalocele 48 0.057
149
P NRV007 Nervous System Disease 71 0.056
150
P PLY019 Polyneuropathy 56 0.056
151
P PRD008 Periodontitis 63 0.056
152
MSC004 Muscle Tissue Disease 34 0.056
153
P ATR011 Atrial Fibrillation 66 0.056
154
OBS001 Obstructive Jaundice 48 0.056
155
HYP066 Hyperglycemia 61 0.056
156
ATR060 Atrial Standstill, Digenic 51 0.056
157
DWN001 Down Syndrome 66 0.055
158
MDS022 Mediastinitis 41 0.055
159
CHR078 Chorioretinitis 40 0.054
160
ACR008 Acrocallosal Syndrome 52 0.054
161
STS002 Situs Inversus 46 0.054
162
CYS009 Cystadenoma 40 0.054
163
P MYS005 Myositis 57 0.054
164
c LRG001 Large Cell Carcinoma 51 0.053
165
BRN022 Bronchiectasis 50 0.052
166
P INF038 Influenza 72 0.052
167
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 33 0.052
168
PRN038 Prune Belly Syndrome 45 0.052
169
CHL071 Child Syndrome 58 0.051
170
SRN002 Sirenomelia 29 0.051
171
P CYS018 Cystitis 52 0.051
172
RNL108 Renal Hypoplasia, Unilateral 6 0.051
173
ADP007 Adie Pupil 34 0.051
174
P ANR002 Aniridia 64 0.051
175
P LYM025 Lymphedema 61 0.051
176
P GND004 Gonadal Dysgenesis 51 0.051
177
RNL104 Renal Hypodysplasia 29 0.050
178
PTR006 Peters Anomaly 65 0.050
179
P LYD001 Leydig Cell Tumor 44 0.050
180
P MNN007 Meningocele 36 0.050
181
DND001 Dandy-Walker Syndrome 44 0.050
182
P RHN004 Rhinitis 60 0.049
183
DYS018 Dysostosis 44 0.049
184
PRP019 Peripheral Nervous System Disease 55 0.049
185
c CNG031 Congenital Nervous System Abnormality 37 0.049
186
P PRT013 Portal Hypertension 60 0.049
187
FCL009 Focal Dermal Hypoplasia 54 0.049
188
HRP004 Herpes Zoster 56 0.049
189
STT001 Status Epilepticus 59 0.049
190
SPN369 Spinal Disease 39 0.049
191
c THR092 Thrombophilia Due to Thrombin Defect 54 0.049
192
P ORF002 Orofacial Cleft 38 0.048
193
PLM014 Pleomorphic Adenoma 52 0.048
194
KRT008 Keratopathy 44 0.048
195
P GRV001 Graves' Disease 59 0.048
196
ANG011 Angiodysplasia 44 0.048
197
P VNT002 Ventricular Septal Defect 60 0.047
198
MYL020 Myelomeningocele 51 0.047
199
HRS039 Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness 13 0.047
200
DBL008 Double Uterus-Hemivagina-Renal Agenesis 4 0.047
201
P AST007 Astrocytoma 65 0.047
202
P CRN037 Craniosynostosis 66 0.047
203
c ACT027 Acute Pancreatitis 57 0.047
204
PNC034 Pancreas Disease 58 0.047
205
NLP001 Nail-Patella Syndrome 54 0.047
206
VGN031 Vaginal Atresia 24 0.047
207
P DGR001 Digeorge Syndrome 53 0.047
208
APP008 Appendicitis 60 0.047
209
PLY012 Polyhydramnios 47 0.046
210
HYP077 Hypertrichosis 44 0.046
211
P TRN020 Turner Syndrome 65 0.046
212
P CPL006 Capillary Hemangioma 51 0.046
213
P OST001 Osteopetrosis 63 0.045
214
ACR058 Acrofacial Dysostosis 1, Nager Type 38 0.045
215
NRF010 Neurofaciodigitorenal Syndrome 16 0.045
216
VTR017 Vater-Like Defects with Pulmonary Hypertension, Laryngeal Webs, and Growth Deficiency 13 0.045
217
ACN002 Acanthosis Nigricans 57 0.045
218
P RBL001 Rubella 57 0.045
219
LYM022 Lymphangioma 54 0.045
220
PYL006 Pyloric Stenosis 46 0.045
221
P TRC005 Tracheal Stenosis 39 0.045
222
THR004 Thrombocytosis 55 0.044
223
TTH006 Tooth Disease 52 0.044
224
c ATS275 Autosomal Recessive Primary Microcephaly 48 0.044
225
HYP080 Hypogonadism 53 0.044
226
HMH002 Hemihypertrophy 41 0.043
227
MCR021 Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies 32 0.043
228
RGH009 Right Atrial Isomerism 44 0.043
229
JJN004 Jejunal Atresia 29 0.043
230
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 27 0.043
231
PYR004 Pyuria 32 0.042
232
c BSL007 Basal Cell Carcinoma 65 0.042
233
CHR103 Charge Syndrome 62 0.042
234
TRN045 True Unicornuate Uterus 11 0.042
235
PYD002 Pyoderma 48 0.041
236
AND001 Anodontia 43 0.041
237
ICH054 Ichthyosis, X-Linked 46 0.041
238
P HYP040 Hypospadias 57 0.041
239
P ICH004 Ichthyosis 52 0.041
240
AYM001 Ayme-Gripp Syndrome 41 0.041
241
ANN002 Anencephaly 54 0.041
242
P VLC001 Velocardiofacial Syndrome 62 0.040
243
HYD012 Hydrops Fetalis 43 0.040
244
EMN001 Emanuel Syndrome 36 0.040
245
ART031 Aortic Coarctation 43 0.040
246
DSC009 Discoid Lupus Erythematosus 45 0.040
247
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 38 0.040
248
P MSC005 Muscular Dystrophy 65 0.040
249
P SCL018 Scoliosis 55 0.040
250
ACR007 Acromegaly 66 0.039
251
P FNC043 Fanconi Anemia, Complementation Group E 55 0.039
252
WRN001 Werner Syndrome 67 0.039
253
P PNV001 Panuveitis 50 0.039
254
LYM035 Lymphangiectasis 28 0.039
255
SPR035 Superior Vena Cava Syndrome 31 0.039
256
VGT001 Vogt-Koyanagi-Harada Disease 55 0.039
257
OMP004 Omphalocele 50 0.039
258
MLL011 Mullerian Aplasia and Hyperandrogenism 25 0.039
259
INT066 Interstitial Lung Disease 59 0.039
260
DNY001 Denys-Drash Syndrome 52 0.039
261
KLN001 Klinefelter's Syndrome 50 0.039
262
CRT028 Cor Triatriatum 22 0.039
263
c DLT002 Dilated Cardiomyopathy 76 0.038
264
APR006 Apert Syndrome 67 0.038
265
DDN011 Duodenal Atresia 37 0.038
266
c NPH055 Nephrotic Syndrome, Type 1 51 0.038
267
FRS002 Frasier Syndrome 47 0.038
268
CYL001 Cayler Cardiofacial Syndrome 29 0.038
269
PYD001 Pyoderma Gangrenosum 51 0.037
270
P CRB042 Cerebellar Ataxia 63 0.037
271
SPN060 Spondylocarpotarsal Synostosis Syndrome 34 0.037
272
DPH006 Diaphragmatic Eventration 27 0.037
273
SCH025 Schisis Association 19 0.037
274
DST055 Distal 22q11.2 Microduplication Syndrome 12 0.037
275
P DYS007 Dyskeratosis Congenita 63 0.036
276
ADN027 Adenomyosis 46 0.036
277
P MYS003 Myasthenia Gravis 67 0.036
278
ACH004 Achondroplasia 66 0.036
279
DRR010 Darier Disease 60 0.036
280
PRT029 Parathyroid Adenoma 48 0.036
281
c MCR263 Microphthalmia, Syndromic 1 34 0.036
282
TRS012 Trisomy 22 27 0.035
283
CCN007 Cocoon Syndrome 45 0.035
284
P CYS017 Cystic Teratoma 40 0.035
285
HYP064 Hypogonadotropism 37 0.035
286
URG002 Urogenital Adysplasia 6 0.035
287
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 52 0.035
288
P MSC003 Muscular Atrophy 50 0.035
289
ECT026 Ectopic Pregnancy 48 0.035
290
PTY001 Pityriasis Rosea 42 0.035
291
NSP002 Nasopharyngitis 40 0.035
292
P ESS003 Essential Thrombocythemia 70 0.035
293
P OST005 Osteogenesis Imperfecta 69 0.035
294
P FRN036 Frontonasal Dysplasia 1 32 0.035
295
RHM001 Rheumatic Fever 54 0.035
296
DVL001 Developmental Coordination Disorder 36 0.035
297
c EHL057 Ehlers-Danlos Syndrome, Type Iv 60 0.033
298
CHR501 Chromosome 17q12 Deletion Syndrome 26 0.033
299
c LNG031 Lung Benign Neoplasm 41 0.033
300
ANR018 Anorchia 36 0.033
301
PNT005 Pentalogy of Cantrell 26 0.033
302
INN003 Iniencephaly 25 0.033
303
ACR017 Acrofacial Dysostosis 22 0.033
304
MCR310 Microgastria-Limb Reduction Defects Association 14 0.033
305
CRV043 Cervical Dystonia 44 0.032
306
OBS015 Obesity, Hyperphagia, and Developmental Delay 41 0.032
307
LRY029 Laryngomalacia 40 0.032
308
c PLY057 Polydactyly, Postaxial, Types A1 and B 31 0.032
309
HYP711 Hypotonia, Ataxia, and Delayed Development Syndrome 26 0.032
310
P SHR029 Short Syndrome 58 0.032
311
CLN019 Colonic Disease 51 0.032
312
c BNG076 Benign Exophthalmos Syndrome 15 0.032
313
MCP006 Mucoepidermoid Carcinoma 48 0.032
314
LMT001 Limited Scleroderma 46 0.031
315
GNG008 Ganglioneuroblastoma 40 0.031
316
P ATX010 Ataxia Neuropathy Spectrum 30 0.031
317
UND005 Undifferentiated Pleomorphic Sarcoma 44 0.031
318
DRM013 Dermoid Cyst 44 0.031
319
SCL017 Sclerosing Hemangioma 41 0.031
320
HYP513 Hypogonadotropic Hypogonadism 1 with or Without Anosmia 36 0.031
321
PHN003 Phenylketonuria 72 0.030
322
MYM001 Myoma 52 0.030
323
MYL003 Myeloid Sarcoma 48 0.030
324
P ORF001 Orofaciodigital Syndrome 47 0.030
325
P PLM085 Pulmonary Hemosiderosis 44 0.030
326
LMB013 Limb Reduction Defect 16 0.030
327
SCT005 Scott Syndrome 53 0.030
328
HRM002 Hermaphroditism 38 0.030
329
CRN033 Cranial Nerve Malignant Neoplasm 28 0.030
330
CNG039 Congenital Absence of the Vas Deferens 22 0.030
331
CNS004 Constipation 57 0.028
332
c MLG077 Malignant Peripheral Nerve Sheath Tumor 56 0.028
333
BLD034 Bile Duct Carcinoma 56 0.028
334
P DBT083 Diabetes Mellitus, Permanent Neonatal 55 0.028
335
P PRN026 Porencephaly 48 0.028
336
MCR191 Microscopic Colitis 47 0.028
337
c CHR283 Chronic Inflammatory Demyelinating Polyneuropathy 40 0.028
338
PRN049 Paraneoplastic Pemphigus 40 0.028
339
c FML015 Familial Nephrotic Syndrome 36 0.028
340
HYD001 Hydranencephaly 35 0.028
341
SHR082 Short Stature, Microcephaly, and Endocrine Dysfunction 26 0.028
342
EXS016 Exstrophy of Bladder Bladder Exstrophy and Epispadias Complex, Included 25 0.028
343
DCH001 Duchenne Muscular Dystrophy 79 0.026
344
BCK001 Becker Muscular Dystrophy 69 0.026
345
c MLT024 Multiple Endocrine Neoplasia Iia 64 0.026
346
P ANG001 Angelman Syndrome 61 0.026
347
THR016 Thrombophlebitis 53 0.026
348
c EHL055 Ehlers-Danlos Syndrome, Type Iii 50 0.026
349
TRN044 Transposition of the Great Arteries 48 0.026
350
MMM001 Mammary Paget's Disease 45 0.026
351
c MTR002 Mitral Valve Insufficiency 44 0.026
352
DDN010 Duodenum Cancer 43 0.026
353
OCL001 Ocular Albinism 42 0.026
354
APL002 Aplasia of Lacrimal and Salivary Glands 42 0.026
355
RTR008 Root Resorption 42 0.026
356
RCR004 Recurrent Respiratory Papillomatosis 42 0.026
357
LCH009 Lichen Sclerosus 41 0.026
358
CHR466 Chronic Thromboembolic Pulmonary Hypertension 39 0.026
359
P AXN001 Axonal Neuropathy 38 0.026
360
MTR007 Motor Peripheral Neuropathy 37 0.026
361
c ATR022 Atrial Septal Defect 3 36 0.026
362
TRC097 Tracheomalacia 34 0.026
363
c LPR012 Leopard Syndrome 1 30 0.026
364
CNG116 Congenital Nephrotic Syndrome Finnish Type 28 0.026
365
ADT002 Auditory System Cancer 26 0.026
366
c KLP007 Klippel-Feil Syndrome 1, Autosomal Dominant 26 0.026
367
ACR034 Acrogeria, Gottron Type 25 0.026
368
CHR367 Chromosome 7q11.23 Duplication Syndrome 24 0.026
369
7Q1002 7q11.23 Duplication Syndrome 23 0.026
370
c FML269 Familial Idiopathic Steroid-Resistant Nephrotic Syndrome with Focal Segmental Hyalinosis 23 0.026
371
c CTS041 Cutis Laxa, Autosomal Dominant 3 22 0.026
372
LPM007 Lipomyelomeningocele 21 0.026
373
HYP565 Hypogonadotropic Hypogonadism 3 with or Without Anosmia 20 0.026
374
P SPR076 Sporadic Idiopathic Steroid-Resistant Nephrotic Syndrome with Focal Segmental Hyalinosis 14 0.026
375
TRN046 Transverse Vaginal Septum 14 0.026