Search results for "unilateral renal agenesis"

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

320 hits were found for 'unilateral renal agenesis'

# Family MCID Name MIFTS Score
1
ANR016 Aniridia Renal Agenesis Psychomotor Retardation 5 2.704
2
RNL105 Renal Agenesis, Unilateral 23 2.663
3
MCR304 Microcephaly, Congenital Heart Disease, Unilateral Renal Agenesis, and Hyposegmented Lungs 18 2.632
4
UTR057 Uterus Bicornis Bicollis with Partial Vaginal Septum and Unilateral Hematocolpos with Ipsilateral Renal Agenesis 17 2.493
5
ANR044 Aniridia, Partial, with Unilateral Renal Agenesis and Psychomotor Retardation 15 2.363
6
MLL021 Mullerian Duct Aplasia, Unilateral Renal Agenesis, and Cervicothoracic Somite Anomalies 17 2.090
7
MRC004 Murcs Association 29 1.880
8
ELL004 Ellis Yale Winter Syndrome 6 1.851
9
SNT001 Santos Mateus Leal Syndrome 6 1.843
10
URT010 Ureteral Obstruction 45 0.259
11
RNL078 Renal Dysplasia 45 0.192
12
CLF001 Cleft Lip 49 0.182
13
CRB009 Cerebritis 38 0.175
14
P ADN016 Adenocarcinoma 69 0.165
15
P THY032 Thyroiditis 54 0.162
16
P HPT021 Hepatitis 70 0.162
17
P RNL100 Renal Hypodysplasia/aplasia 1 54 0.155
18
P PNC044 Pancreatitis 60 0.154
19
VGN023 Vaginitis 42 0.151
20
P CRV039 Cervicitis 44 0.150
21
HYD002 Hydronephrosis 47 0.148
22
ADN018 Adenoma 59 0.147
23
RTN023 Retinitis 49 0.141
24
END072 Endotheliitis 42 0.134
25
P NRP001 Neuropathy 60 0.131
26
ANR040 Aneurysm 57 0.131
27
P GLM007 Glomerulonephritis 56 0.129
28
P HRT032 Heart Disease 76 0.129
29
RNL025 Renal Hypoplasia 41 0.125
30
ANG018 Angiomyolipoma 46 0.124
31
CRY002 Cryptorchidism 62 0.122
32
URT001 Urethritis 40 0.121
33
P VSC005 Vesicoureteral Reflux 54 0.120
34
HRS011 Horseshoe Kidney 35 0.114
35
SYN005 Synostosis 45 0.109
36
P PLY006 Polydactyly 55 0.109
37
P HYP069 Hyperparathyroidism 57 0.109
38
P EPL164 Epilepsy 66 0.106
39
NRN002 Neuronitis 42 0.105
40
FBR032 Fibromuscular Dysplasia 45 0.103
41
SPS057 Spasticity 42 0.102
42
GLM011 Glomerulosclerosis 44 0.101
43
PRS047 Prostatitis 56 0.101
44
HYP015 Hyperlucent Lung 34 0.101
45
P ESP024 Esophagitis 62 0.100
46
ANR004 Anuria 46 0.099
47
P HYP086 Hypothyroidism 65 0.098
48
PNL023 Penile Agenesis 20 0.096
49
SNS001 Sensorineural Hearing Loss 57 0.091
50
MLT084 Multicystic Dysplastic Kidney 37 0.088
51
P HYD006 Hydrocephalus 67 0.088
52
P PLM037 Pulmonary Hypertension 79 0.087
53
CRB045 Cerebellar Hypoplasia 48 0.085
54
BRT030 Birth Defects 43 0.084
55
PLY024 Polymicrogyria 36 0.084
56
IMP002 Imperforate Anus 52 0.083
57
TRC040 Tracheoesophageal Fistula 41 0.083
58
ALR002 Al-Raqad Syndrome 36 0.082
59
MCR103 Microtia 37 0.082
60
ACR041 Acromelic Frontonasal Dysostosis 46 0.082
61
GNG013 Gingivitis 60 0.081
62
P INF032 Infertility 61 0.080
63
CLR003 Clear Cell Adenocarcinoma 54 0.079
64
P CTR002 Cataract 57 0.078
65
P HMN010 Hemangioma 60 0.078
66
MCR013 Microphthalmia 59 0.076
67
P SCH018 Schizencephaly 51 0.076
68
MYR002 Mayer-Rokitansky-Kuster-Hauser Syndrome 55 0.076
69
P OBS005 Obesity 93 0.076
70
P MCR010 Microcephaly 58 0.075
71
TTR001 Tetralogy of Fallot 71 0.074
72
ESP020 Esophageal Atresia 49 0.073
73
DXT001 Dextrocardia 44 0.073
74
P SNS014 Sinusitis 60 0.073
75
P TRC086 Trichohepatoenteric Syndrome 1 46 0.072
76
P FCL005 Focal Segmental Glomerulosclerosis 59 0.071
77
P HLP001 Holoprosencephaly 62 0.071
78
P LRY019 Laryngitis 55 0.070
79
LPM004 Lipoma 58 0.070
80
P MYM002 Moyamoya Disease 60 0.070
81
P PHC003 Pheochromocytoma 71 0.069
82
ING001 Inguinal Hernia 57 0.069
83
URT020 Ureterocele 31 0.068
84
P PTN002 Patent Ductus Arteriosus 52 0.067
85
PPL002 Papillary Carcinoma 49 0.067
86
P RSP003 Respiratory Failure 70 0.067
87
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 41 0.067
88
DDN006 Duodenitis 44 0.066
89
PLV005 Pelviureteric Junction Obstruction 45 0.066
90
CRY010 Cryptophthalmos 24 0.066
91
SCR035 Sacral Agenesis with Vertebral Anomalies 33 0.066
92
NTR005 Nutritional Deficiency Disease 39 0.066
93
P CNJ013 Conjunctivitis 65 0.065
94
P KLP003 Klippel-Feil Syndrome 46 0.065
95
MDL009 Medullary Sponge Kidney 40 0.065
96
P FRS003 Fraser Syndrome 57 0.065
97
P KLL001 Kallmann Syndrome 60 0.065
98
P TRT010 Teratoma 52 0.065
99
P HYP024 Hypoparathyroidism 52 0.065
100
PNM008 Pneumothorax 52 0.065
101
P TRM003 Tremor 54 0.064
102
P END044 Endometriosis 53 0.064
103
P AST005 Asthma 82 0.064
104
PLN006 Poland Syndrome 48 0.063
105
P LNG032 Lung Cancer 94 0.063
106
P ART084 Arteriovenous Fistula 44 0.063
107
P NRV007 Nervous System Disease 71 0.063
108
P ATX004 Ataxia 53 0.063
109
P PTS002 Ptosis 56 0.063
110
CLF004 Cleft Lip/palate 46 0.062
111
HMF006 Hemifacial Microsomia 54 0.062
112
PLG004 Plagiocephaly 42 0.062
113
c BRN108 Branchiootic Syndrome 1 36 0.061
114
P ATR011 Atrial Fibrillation 64 0.061
115
RNL051 Renal Cysts and Diabetes Syndrome 47 0.061
116
P CLR023 Colorectal Cancer 97 0.060
117
P ENC008 Encephalocele 47 0.060
118
c RNL099 Renal Hypodysplasia/aplasia 2 18 0.060
119
NRG002 Neurogenic Bladder 50 0.059
120
P MNN013 Meningitis 65 0.059
121
GNG012 Gingival Overgrowth 52 0.059
122
P CRN037 Craniosynostosis 65 0.059
123
MDS022 Mediastinitis 41 0.059
124
PHY002 Physical Disorder 44 0.058
125
VCS001 Vici Syndrome 44 0.058
126
DYS018 Dysostosis 44 0.058
127
SMN007 Seminoma 42 0.058
128
DWN001 Down Syndrome 65 0.058
129
P CRD011 Cardiomyopathy 67 0.058
130
P CNG015 Congenital Diaphragmatic Hernia 58 0.058
131
P MYS005 Myositis 56 0.058
132
MSC004 Muscle Tissue Disease 36 0.058
133
CHR078 Chorioretinitis 41 0.057
134
ACR008 Acrocallosal Syndrome 51 0.057
135
P GND004 Gonadal Dysgenesis 53 0.057
136
MCN001 Mucinous Adenocarcinoma 50 0.056
137
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 38 0.055
138
P LYD001 Leydig Cell Tumor 44 0.055
139
CHL071 Child Syndrome 58 0.055
140
ANR002 Aniridia 60 0.055
141
P PLY019 Polyneuropathy 54 0.055
142
P HYP265 Hypotonia 39 0.054
143
RNL108 Renal Hypoplasia, Unilateral 6 0.054
144
OPT037 Optic Nerve Hypoplasia 52 0.054
145
OBS001 Obstructive Jaundice 48 0.054
146
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 34 0.054
147
P LYM025 Lymphedema 61 0.053
148
PTR006 Peters Anomaly 64 0.053
149
P MNN007 Meningocele 36 0.053
150
P PRD008 Periodontitis 46 0.053
151
PRN038 Prune Belly Syndrome 45 0.053
152
P GRV001 Graves' Disease 61 0.053
153
PLM014 Pleomorphic Adenoma 50 0.053
154
SRN002 Sirenomelia 25 0.053
155
STT001 Status Epilepticus 59 0.052
156
DND001 Dandy-Walker Syndrome 44 0.052
157
RNL104 Renal Hypodysplasia 30 0.052
158
KRT008 Keratopathy 46 0.051
159
c THR092 Thrombophilia Due to Thrombin Defect 56 0.051
160
P ORF002 Orofacial Cleft 38 0.051
161
P LMY004 Leiomyosarcoma 53 0.051
162
HRS039 Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness 14 0.051
163
P PRT013 Portal Hypertension 59 0.051
164
P AST007 Astrocytoma 65 0.051
165
P VNT002 Ventricular Septal Defect 59 0.050
166
MYL020 Myelomeningocele 50 0.050
167
DBL008 Double Uterus-Hemivagina-Renal Agenesis 4 0.050
168
CYS009 Cystadenoma 40 0.050
169
VGN031 Vaginal Atresia 23 0.049
170
ADP007 Adie Pupil 34 0.049
171
BRN022 Bronchiectasis 47 0.049
172
P RHN004 Rhinitis 61 0.049
173
ANG011 Angiodysplasia 44 0.049
174
CHR103 Charge Syndrome 64 0.049
175
HYP077 Hypertrichosis 52 0.049
176
FCL009 Focal Dermal Hypoplasia 54 0.049
177
P CPL006 Capillary Hemangioma 52 0.049
178
P DGR001 Digeorge Syndrome 52 0.048
179
ACH004 Achondroplasia 66 0.048
180
P TRC005 Tracheal Stenosis 38 0.048
181
NRF007 Neurofibroma 52 0.047
182
INV006 Inverted Papilloma 40 0.047
183
P PRP019 Peripheral Nervous System Disease 54 0.046
184
P OST001 Osteopetrosis 62 0.046
185
c BSL007 Basal Cell Carcinoma 64 0.046
186
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 29 0.046
187
PLM068 Pulmonary Vein Stenosis 39 0.046
188
P TRN020 Turner Syndrome 64 0.046
189
CRC006 Carcinoid Syndrome 51 0.045
190
JJN004 Jejunal Atresia 28 0.045
191
TRN045 True Unicornuate Uterus 11 0.045
192
c LRG001 Large Cell Carcinoma 51 0.045
193
ALB002 Albinism 43 0.044
194
PYL006 Pyloric Stenosis 46 0.044
195
SPN369 Spinal Disease 41 0.043
196
PLY012 Polyhydramnios 47 0.043
197
ART031 Aortic Coarctation 42 0.043
198
P MSC005 Muscular Dystrophy 64 0.043
199
APR006 Apert Syndrome 66 0.043
200
ANN002 Anencephaly 52 0.043
201
P HYP040 Hypospadias 57 0.043
202
HMH002 Hemihypertrophy 39 0.042
203
P SCL018 Scoliosis 56 0.042
204
CHR072 Chordoma 59 0.042
205
PTT037 Pituitary Tumors 45 0.042
206
HYD012 Hydrops Fetalis 44 0.042
207
LYM035 Lymphangiectasis 28 0.042
208
PYR004 Pyuria 34 0.041
209
ACR007 Acromegaly 65 0.041
210
PLL001 Pallister-Hall Syndrome 54 0.041
211
KLN001 Klinefelter's Syndrome 55 0.041
212
CRT028 Cor Triatriatum 21 0.041
213
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 39 0.041
214
SPR035 Superior Vena Cava Syndrome 32 0.041
215
P PLM036 Pulmonary Fibrosis 68 0.041
216
LYM022 Lymphangioma 54 0.041
217
P VLC001 Velocardiofacial Syndrome 62 0.041
218
OMP004 Omphalocele 50 0.041
219
ACR058 Acrofacial Dysostosis 1, Nager Type 36 0.041
220
NRF010 Neurofaciodigitorenal Syndrome 16 0.041
221
VTR017 Vater-Like Defects with Pulmonary Hypertension, Laryngeal Webs, and Growth Deficiency 13 0.041
222
TTH006 Tooth Disease 52 0.041
223
DDN011 Duodenal Atresia 39 0.040
224
ADN027 Adenomyosis 46 0.040
225
RDL002 Radioulnar Synostosis 44 0.040
226
MCR021 Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies 34 0.040
227
HYP080 Hypogonadism 54 0.040
228
P CRB042 Cerebellar Ataxia 64 0.040
229
P RBL001 Rubella 56 0.039
230
SPN060 Spondylocarpotarsal Synostosis Syndrome 35 0.039
231
DPH006 Diaphragmatic Eventration 27 0.039
232
WRN001 Werner Syndrome 67 0.039
233
PMP001 Pemphigus 49 0.038
234
CYL001 Cayler Cardiofacial Syndrome 30 0.038
235
P DYS007 Dyskeratosis Congenita 63 0.038
236
LDD001 Ladd Syndrome 60 0.038
237
P MST009 Mastocytosis 54 0.038
238
PRT029 Parathyroid Adenoma 47 0.038
239
c MCR263 Microphthalmia, Syndromic 1 34 0.038
240
ECT026 Ectopic Pregnancy 47 0.037
241
NSP002 Nasopharyngitis 41 0.037
242
CMB021 Combined Pituitary Hormone Deficiency 36 0.037
243
TRS012 Trisomy 22 26 0.037
244
P FRN036 Frontonasal Dysplasia 1 31 0.037
245
P OST005 Osteogenesis Imperfecta 67 0.037
246
DVL001 Developmental Coordination Disorder 37 0.037
247
P ESS003 Essential Thrombocythemia 68 0.037
248
DRR010 Darier Disease 61 0.037
249
RGH009 Right Atrial Isomerism 32 0.037
250
MCR310 Microgastria-Limb Reduction Defects Association 16 0.037
251
URG002 Urogenital Adysplasia 6 0.037
252
ICH054 Ichthyosis, X-Linked 48 0.036
253
CRZ001 Crouzon Syndrome 70 0.035
254
DRM013 Dermoid Cyst 43 0.035
255
c MCR247 Microcephaly 1, Primary, Autosomal Recessive 34 0.035
256
MLL011 Mullerian Aplasia and Hyperandrogenism 25 0.035
257
CHR501 Chromosome 17q12 Deletion Syndrome 26 0.035
258
OBS015 Obesity, Hyperphagia, and Developmental Delay 46 0.035
259
LRY029 Laryngomalacia 39 0.035
260
c PLY057 Polydactyly, Postaxial, Types A1 and B 31 0.035
261
INT309 Intellectual Developmental Disorder with Persistence of Fetal Hemoglobin 29 0.035
262
P SHR029 Short Syndrome 60 0.034
263
P OLG002 Oligodendroglioma 55 0.034
264
GNG004 Ganglioglioma 49 0.034
265
MCP006 Mucoepidermoid Carcinoma 47 0.034
266
OPT008 Optic Nerve Neoplasm 40 0.034
267
HYP513 Hypogonadotropic Hypogonadism 1 with or Without Anosmia 37 0.033
268
ANR018 Anorchia 36 0.033
269
EXS007 Exstrophy of the Bladder 33 0.033
270
ACR017 Acrofacial Dysostosis 20 0.033
271
P STH001 Saethre-Chotzen Syndrome 59 0.033
272
c MLG077 Malignant Peripheral Nerve Sheath Tumor 53 0.033
273
THR016 Thrombophlebitis 52 0.033
274
MYM001 Myoma 51 0.033
275
SYN036 Syncope 47 0.033
276
P CYS017 Cystic Teratoma 41 0.033
277
MNK003 Muenke Syndrome 55 0.032
278
HRM002 Hermaphroditism 38 0.032
279
CNG039 Congenital Absence of the Vas Deferens 22 0.032
280
BLD034 Bile Duct Carcinoma 55 0.031
281
ACR014 Acral Lentiginous Melanoma 44 0.031
282
P ORF001 Orofaciodigital Syndrome 44 0.031
283
P PRN022 Perineurioma 38 0.031
284
HYP064 Hypogonadotropism 38 0.031
285
LMB013 Limb Reduction Defect 17 0.031
286
PHN003 Phenylketonuria 73 0.030
287
BCK001 Becker Muscular Dystrophy 68 0.030
288
c MTR002 Mitral Valve Insufficiency 44 0.030
289
GRV012 Grover's Disease 38 0.030
290
CCN007 Cocoon Syndrome 35 0.030
291
HYD001 Hydranencephaly 34 0.030
292
EXS016 Exstrophy of Bladder Bladder Exstrophy and Epispadias Complex, Included 25 0.030
293
SCH025 Schisis Association 19 0.030
294
DST055 Distal 22q11.2 Microduplication Syndrome 13 0.030
295
HYP042 Hypochondroplasia 57 0.028
296
CRN036 Craniopharyngioma 52 0.028
297
BLR007 Biliary Tract Neoplasm 52 0.028
298
STR081 Stormorken Syndrome 50 0.028
299
JCK001 Jackson-Weiss Syndrome 49 0.028
300
CTN014 Cutaneous Mastocytosis 48 0.028
301
OST044 Osteoglophonic Dysplasia 47 0.028
302
TRN044 Transposition of the Great Arteries 47 0.028
303
P PRN026 Porencephaly 47 0.028
304
APL002 Aplasia of Lacrimal and Salivary Glands 44 0.028
305
OCL001 Ocular Albinism 43 0.028
306
c PFF007 Pfeiffer Syndrome Type 1 36 0.028
307
CRB038 Cerebral Ventricle Cancer 35 0.028
308
CRB028 Cerebellar Medulloblastoma 34 0.028
309
TRC097 Tracheomalacia 32 0.028
310
FGF001 Fgfr-Related Craniosynostosis Syndromes 31 0.028
311
P LPR012 Leopard Syndrome 1 30 0.028
312
P RDL006 Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia 28 0.028
313
c PFF008 Pfeiffer Syndrome Type 1, 2 and 3 28 0.028
314
c KLP007 Klippel-Feil Syndrome 1, Autosomal Dominant 26 0.028
315
OLF002 Olfactory Groove Meningioma 25 0.028
316
INN003 Iniencephaly 24 0.028
317
c CTS041 Cutis Laxa, Autosomal Dominant 3 22 0.028
318
HYP565 Hypogonadotropic Hypogonadism 3 with or Without Anosmia 21 0.028
319
LPM007 Lipomyelomeningocele 21 0.028
320
TRN046 Transverse Vaginal Septum 14 0.028