Search results for "unilateral renal agenesis"

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

325 hits were found for 'unilateral renal agenesis'

# Family MCID Name MIFTS Score
1
ANR016 Aniridia Renal Agenesis Psychomotor Retardation 5 2.714
2
RNL105 Renal Agenesis, Unilateral 21 2.672
3
MCR304 Microcephaly, Congenital Heart Disease, Unilateral Renal Agenesis, and Hyposegmented Lungs 19 2.634
4
UTR057 Uterus Bicornis Bicollis with Partial Vaginal Septum and Unilateral Hematocolpos with Ipsilateral Renal Agenesis 17 2.491
5
ANR044 Aniridia, Partial, with Unilateral Renal Agenesis and Psychomotor Retardation 15 2.369
6
MLL021 Mullerian Duct Aplasia, Unilateral Renal Agenesis, and Cervicothoracic Somite Anomalies 17 2.089
7
MRC004 Murcs Association 33 1.897
8
ELL004 Ellis Yale Winter Syndrome 6 1.869
9
SNT001 Santos Mateus Leal Syndrome 6 1.855
10
P KDN018 Kidney Disease 64 0.285
11
URT010 Ureteral Obstruction 45 0.258
12
RNL078 Renal Dysplasia 48 0.208
13
CRB009 Cerebritis 36 0.184
14
P RNL100 Renal Hypodysplasia/aplasia 1 54 0.182
15
CLF001 Cleft Lip 48 0.178
16
P HPT021 Hepatitis 74 0.170
17
P THY032 Thyroiditis 57 0.166
18
P PNC044 Pancreatitis 62 0.163
19
P ADN016 Adenocarcinoma 69 0.161
20
P CRV039 Cervicitis 45 0.159
21
VGN023 Vaginitis 41 0.156
22
HYD002 Hydronephrosis 48 0.152
23
ADN018 Adenoma 59 0.151
24
RTN023 Retinitis 49 0.144
25
END072 Endotheliitis 41 0.141
26
ANR040 Aneurysm 56 0.140
27
ANG018 Angiomyolipoma 46 0.138
28
P NRP001 Neuropathy 57 0.137
29
P GLM007 Glomerulonephritis 56 0.134
30
c CNG401 Congenital Heart Disease 67 0.134
31
P PLY006 Polydactyly 56 0.130
32
RNL025 Renal Hypoplasia 40 0.130
33
URT001 Urethritis 39 0.127
34
P VSC005 Vesicoureteral Reflux 53 0.125
35
CRY002 Cryptorchidism 61 0.124
36
P EPL164 Epilepsy 60 0.119
37
SYN005 Synostosis 44 0.117
38
HRS011 Horseshoe Kidney 34 0.117
39
P PLY014 Polycystic Kidney Disease 60 0.114
40
ALR002 Al-Raqad Syndrome 36 0.113
41
P AMY004 Amyloidosis 63 0.113
42
NRN002 Neuronitis 40 0.111
43
P HYP069 Hyperparathyroidism 57 0.111
44
HYP015 Hyperlucent Lung 35 0.109
45
P HRT032 Heart Disease 64 0.109
46
SPS057 Spasticity 41 0.108
47
P TBR001 Tuberous Sclerosis 68 0.108
48
P TRC086 Trichohepatoenteric Syndrome 1 46 0.107
49
FBR032 Fibromuscular Dysplasia 39 0.106
50
P ESP024 Esophagitis 62 0.105
51
P HYP086 Hypothyroidism 63 0.105
52
GLM011 Glomerulosclerosis 41 0.104
53
PRS047 Prostatitis 56 0.104
54
ANR004 Anuria 46 0.102
55
P CHN005 Choanal Atresia 42 0.101
56
PNL023 Penile Agenesis 21 0.100
57
BRT030 Birth Defects 44 0.097
58
P HYD006 Hydrocephalus 68 0.094
59
P PLM037 Pulmonary Hypertension 78 0.094
60
CRB045 Cerebellar Hypoplasia 47 0.093
61
PLY024 Polymicrogyria 34 0.091
62
P MCR010 Microcephaly 60 0.090
63
TRC040 Tracheoesophageal Fistula 41 0.085
64
IMP002 Imperforate Anus 54 0.085
65
P NPH012 Nephrotic Syndrome 55 0.085
66
ACR041 Acromelic Frontonasal Dysostosis 45 0.085
67
TTR001 Tetralogy of Fallot 69 0.085
68
MCR103 Microtia 37 0.085
69
GNG013 Gingivitis 61 0.084
70
P SCH018 Schizencephaly 51 0.083
71
MLT084 Multicystic Dysplastic Kidney 31 0.083
72
c BRN108 Branchiootic Syndrome 1 36 0.082
73
MYR002 Mayer-Rokitansky-Kuster-Hauser Syndrome 55 0.082
74
P HMN010 Hemangioma 62 0.082
75
P OBS005 Obesity 91 0.082
76
P INF032 Infertility 61 0.081
77
ESP020 Esophageal Atresia 48 0.081
78
CLR003 Clear Cell Adenocarcinoma 52 0.081
79
P NRV006 Nervous System Cancer 62 0.081
80
MCR013 Microphthalmia 57 0.081
81
P CTR002 Cataract 57 0.079
82
DXT001 Dextrocardia 44 0.079
83
P SNS014 Sinusitis 66 0.078
84
P LRY019 Laryngitis 55 0.077
85
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 27 0.076
86
P SYN001 Syndactyly 49 0.076
87
P HLP001 Holoprosencephaly 62 0.076
88
P TRT010 Teratoma 49 0.075
89
PLV005 Pelviureteric Junction Obstruction 43 0.074
90
PTN002 Patent Ductus Arteriosus 50 0.074
91
P KLP003 Klippel-Feil Syndrome 47 0.074
92
P FCL005 Focal Segmental Glomerulosclerosis 59 0.073
93
MDL009 Medullary Sponge Kidney 41 0.073
94
DDN006 Duodenitis 44 0.072
95
HDC001 Headache 52 0.072
96
CRY010 Cryptophthalmos 23 0.072
97
P PHC003 Pheochromocytoma 72 0.071
98
MSC004 Muscle Tissue Disease 35 0.071
99
P PLY019 Polyneuropathy 53 0.070
100
PPL002 Papillary Carcinoma 50 0.070
101
P AST005 Asthma 80 0.070
102
P MYM002 Moyamoya Disease 60 0.070
103
PLG004 Plagiocephaly 40 0.070
104
P RSP003 Respiratory Failure 68 0.070
105
URT020 Ureterocele 29 0.070
106
ANR002 Aniridia 62 0.070
107
LPM004 Lipoma 59 0.070
108
P TRM003 Tremor 54 0.070
109
P CNJ013 Conjunctivitis 65 0.070
110
PNM008 Pneumothorax 51 0.069
111
P KLL001 Kallmann Syndrome 61 0.069
112
c PRM005 Primary Hyperparathyroidism 56 0.069
113
P HYP265 Hypotonia 39 0.068
114
P LNG032 Lung Cancer 92 0.068
115
ING001 Inguinal Hernia 57 0.068
116
P HYP024 Hypoparathyroidism 52 0.068
117
P LYD001 Leydig Cell Tumor 40 0.068
118
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.067
119
P CRD011 Cardiomyopathy 66 0.067
120
P FRS003 Fraser Syndrome 58 0.066
121
PHY002 Physical Disorder 43 0.066
122
HMF006 Hemifacial Microsomia 54 0.065
123
P CLR023 Colorectal Cancer 96 0.065
124
P CRN037 Craniosynostosis 66 0.065
125
DYS018 Dysostosis 43 0.065
126
MMB002 Membranous Glomerulonephritis 47 0.064
127
P END044 Endometriosis 53 0.064
128
P MNN013 Meningitis 66 0.064
129
P ART084 Arteriovenous Fistula 40 0.064
130
P NRF002 Neurofibromatosis 66 0.064
131
MDS022 Mediastinitis 37 0.063
132
OTP003 Oto-Palatal-Digital Syndrome 14 0.063
133
P CNG015 Congenital Diaphragmatic Hernia 58 0.063
134
GNG012 Gingival Overgrowth 52 0.062
135
CHR078 Chorioretinitis 41 0.062
136
PLN006 Poland Syndrome 48 0.062
137
P ATX004 Ataxia 53 0.062
138
c RNL099 Renal Hypodysplasia/aplasia 2 18 0.062
139
RNL051 Renal Cysts and Diabetes Syndrome 46 0.061
140
P ENC008 Encephalocele 48 0.061
141
OBS001 Obstructive Jaundice 47 0.061
142
NRG002 Neurogenic Bladder 47 0.060
143
P GND004 Gonadal Dysgenesis 51 0.060
144
SMN007 Seminoma 45 0.060
145
VCS001 Vici Syndrome 50 0.060
146
DWN001 Down Syndrome 65 0.060
147
CYS009 Cystadenoma 40 0.060
148
P LMY004 Leiomyosarcoma 54 0.059
149
c THR092 Thrombophilia Due to Thrombin Defect 56 0.059
150
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.059
151
STS002 Situs Inversus 43 0.059
152
STT001 Status Epilepticus 59 0.058
153
P PRD008 Periodontitis 46 0.058
154
RNL104 Renal Hypodysplasia 29 0.058
155
DBL008 Double Uterus-Hemivagina-Renal Agenesis 3 0.058
156
ACR008 Acrocallosal Syndrome 51 0.058
157
P INF038 Influenza 71 0.058
158
P GRV001 Graves' Disease 62 0.057
159
APR006 Apert Syndrome 66 0.057
160
P VNT002 Ventricular Septal Defect 59 0.057
161
PRP019 Peripheral Nervous System Disease 52 0.057
162
ACH004 Achondroplasia 64 0.057
163
PLM014 Pleomorphic Adenoma 51 0.057
164
MYL020 Myelomeningocele 50 0.057
165
DND001 Dandy-Walker Syndrome 42 0.057
166
P PRG013 Paraganglioma 54 0.056
167
OPT037 Optic Nerve Hypoplasia 50 0.056
168
SRN002 Sirenomelia 26 0.056
169
RNL108 Renal Hypoplasia, Unilateral 6 0.056
170
P ORF002 Orofacial Cleft 38 0.056
171
PRN038 Prune Belly Syndrome 46 0.056
172
c CLD010 Cold-Induced Sweating Syndrome 1 43 0.055
173
KRT008 Keratopathy 49 0.055
174
INV006 Inverted Papilloma 43 0.055
175
PTR006 Peters Anomaly 64 0.054
176
P PRT013 Portal Hypertension 61 0.054
177
PLY012 Polyhydramnios 45 0.054
178
c JVN024 Juvenile Hereditary Hemochromatosis 30 0.054
179
P MNN007 Meningocele 37 0.053
180
VCT001 Vacterl Association 47 0.053
181
P LYM025 Lymphedema 60 0.053
182
BRN022 Bronchiectasis 55 0.053
183
CRC006 Carcinoid Syndrome 51 0.053
184
PLM068 Pulmonary Vein Stenosis 39 0.053
185
P AST007 Astrocytoma 66 0.053
186
MCN001 Mucinous Adenocarcinoma 48 0.053
187
CHR103 Charge Syndrome 64 0.053
188
CHL071 Child Syndrome 58 0.052
189
NRF007 Neurofibroma 53 0.052
190
RDL002 Radioulnar Synostosis 45 0.051
191
ANG011 Angiodysplasia 44 0.051
192
HRS039 Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness 14 0.051
193
PLL001 Pallister-Hall Syndrome 56 0.051
194
P CPL006 Capillary Hemangioma 53 0.051
195
WRN001 Werner Syndrome 69 0.050
196
P DGR001 Digeorge Syndrome 52 0.050
197
CHR072 Chordoma 60 0.050
198
HYP077 Hypertrichosis 52 0.049
199
c PLY057 Polydactyly, Postaxial, Types A1 and B 29 0.049
200
P SCL018 Scoliosis 56 0.049
201
FCL009 Focal Dermal Hypoplasia 52 0.049
202
P MSC005 Muscular Dystrophy 64 0.049
203
ACR015 Acrocephalosyndactylia 38 0.049
204
P PLM036 Pulmonary Fibrosis 69 0.048
205
c LRG001 Large Cell Carcinoma 49 0.048
206
P OST001 Osteopetrosis 63 0.048
207
SPR035 Superior Vena Cava Syndrome 31 0.048
208
P TRN020 Turner Syndrome 64 0.048
209
P TRC005 Tracheal Stenosis 36 0.048
210
LDD001 Ladd Syndrome 60 0.048
211
ACR007 Acromegaly 66 0.048
212
PYL006 Pyloric Stenosis 46 0.048
213
c BSL007 Basal Cell Carcinoma 66 0.047
214
c LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 41 0.047
215
ANN002 Anencephaly 50 0.047
216
ALB002 Albinism 43 0.046
217
VGN031 Vaginal Atresia 22 0.046
218
TTH006 Tooth Disease 52 0.046
219
END035 Endocrine Gland Cancer 50 0.046
220
P MST009 Mastocytosis 54 0.046
221
ART031 Aortic Coarctation 42 0.045
222
CRZ001 Crouzon Syndrome 70 0.045
223
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 28 0.045
224
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 51 0.045
225
TRN045 True Unicornuate Uterus 12 0.045
226
P STH001 Saethre-Chotzen Syndrome 61 0.045
227
PGM003 Pigmentation Disease 34 0.045
228
HMH002 Hemihypertrophy 37 0.045
229
P VLC001 Velocardiofacial Syndrome 64 0.044
230
OMP004 Omphalocele 51 0.044
231
P HYP040 Hypospadias 58 0.044
232
DDN011 Duodenal Atresia 40 0.044
233
P DYS007 Dyskeratosis Congenita 64 0.044
234
PYR004 Pyuria 33 0.043
235
CMB021 Combined Pituitary Hormone Deficiency 36 0.043
236
P CYS017 Cystic Teratoma 40 0.043
237
HYD012 Hydrops Fetalis 45 0.042
238
RGH009 Right Atrial Isomerism 31 0.042
239
MNK003 Muenke Syndrome 55 0.042
240
LYM022 Lymphangioma 55 0.042
241
LYM035 Lymphangiectasis 28 0.042
242
c MLG077 Malignant Peripheral Nerve Sheath Tumor 56 0.042
243
ADN027 Adenomyosis 45 0.042
244
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 38 0.041
245
KLN001 Klinefelter's Syndrome 52 0.041
246
CRT028 Cor Triatriatum 22 0.041
247
P OST005 Osteogenesis Imperfecta 68 0.041
248
ACR058 Acrofacial Dysostosis 1, Nager Type 39 0.041
249
ANT003 Antley-Bixler Syndrome 43 0.041
250
NRF010 Neurofaciodigitorenal Syndrome 17 0.041
251
VTR017 Vater-Like Defects with Pulmonary Hypertension, Laryngeal Webs, and Growth Deficiency 13 0.041
252
ACR014 Acral Lentiginous Melanoma 44 0.041
253
HYP080 Hypogonadism 54 0.041
254
P ESS003 Essential Thrombocythemia 66 0.040
255
MCR021 Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies 33 0.040
256
NSP002 Nasopharyngitis 39 0.040
257
ECT026 Ectopic Pregnancy 46 0.040
258
DPH006 Diaphragmatic Eventration 28 0.040
259
CTN014 Cutaneous Mastocytosis 49 0.040
260
P PRN022 Perineurioma 37 0.040
261
SYN036 Syncope 45 0.040
262
c MCR263 Microphthalmia, Syndromic 1 35 0.039
263
PRT029 Parathyroid Adenoma 46 0.039
264
JCK001 Jackson-Weiss Syndrome 50 0.039
265
HYP042 Hypochondroplasia 55 0.039
266
P FRN036 Frontonasal Dysplasia 1 31 0.039
267
OST044 Osteoglophonic Dysplasia 49 0.039
268
P RDL006 Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia 28 0.039
269
GNG004 Ganglioglioma 46 0.039
270
c PFF007 Pfeiffer Syndrome Type 1 35 0.039
271
FGF001 Fgfr-Related Craniosynostosis Syndromes 33 0.039
272
CYL001 Cayler Cardiofacial Syndrome 30 0.039
273
P SHR029 Short Syndrome 60 0.038
274
ABL002 Ablepharon-Macrostomia Syndrome 51 0.038
275
URG002 Urogenital Adysplasia 6 0.038
276
DRR010 Darier Disease 60 0.037
277
EXS007 Exstrophy of the Bladder 31 0.037
278
TRS012 Trisomy 22 26 0.037
279
BCK001 Becker Muscular Dystrophy 68 0.037
280
MCR310 Microgastria-Limb Reduction Defects Association 16 0.037
281
THR016 Thrombophlebitis 55 0.036
282
ICH054 Ichthyosis, X-Linked 46 0.036
283
MCP006 Mucoepidermoid Carcinoma 50 0.036
284
CHR501 Chromosome 17q12 Deletion Syndrome 26 0.035
285
STR081 Stormorken Syndrome 50 0.035
286
c MCR247 Microcephaly 1, Primary, Autosomal Recessive 30 0.035
287
MLL011 Mullerian Aplasia and Hyperandrogenism 26 0.035
288
c MTR002 Mitral Valve Insufficiency 42 0.035
289
GRV012 Grover's Disease 39 0.035
290
CRB038 Cerebral Ventricle Cancer 34 0.035
291
NRL005 Neurilemmoma 47 0.035
292
OLF002 Olfactory Groove Meningioma 25 0.035
293
P EPN001 Ependymoblastoma 38 0.035
294
SCL017 Sclerosing Hemangioma 41 0.035
295
CRB028 Cerebellar Medulloblastoma 33 0.035
296
LRY029 Laryngomalacia 40 0.035
297
BLD034 Bile Duct Carcinoma 56 0.034
298
MYM001 Myoma 51 0.034
299
HYP513 Hypogonadotropic Hypogonadism 1 with or Without Anosmia 35 0.033
300
ANR018 Anorchia 35 0.033
301
ACR017 Acrofacial Dysostosis 21 0.033
302
LMB013 Limb Reduction Defect 14 0.033
303
DVL001 Developmental Coordination Disorder 36 0.032
304
HRM002 Hermaphroditism 37 0.032
305
CNG039 Congenital Absence of the Vas Deferens 23 0.032
306
P ORF001 Orofaciodigital Syndrome 43 0.032
307
HYP064 Hypogonadotropism 38 0.032
308
DRM013 Dermoid Cyst 39 0.032
309
PHN003 Phenylketonuria 71 0.030
310
OCL001 Ocular Albinism 46 0.030
311
HYD001 Hydranencephaly 35 0.030
312
P PRN026 Porencephaly 47 0.030
313
EXS016 Exstrophy of Bladder Bladder Exstrophy and Epispadias Complex, Included 26 0.030
314
SCH025 Schisis Association 17 0.030
315
DST055 Distal 22q11.2 Microduplication Syndrome 13 0.030
316
c LPR012 Leopard Syndrome 1 29 0.028
317
c KLP007 Klippel-Feil Syndrome 1, Autosomal Dominant 32 0.028
318
TRC097 Tracheomalacia 33 0.028
319
CCN007 Cocoon Syndrome 32 0.028
320
TRN044 Transposition of the Great Arteries 48 0.028
321
c CTS041 Cutis Laxa, Autosomal Dominant 3 22 0.028
322
HYP565 Hypogonadotropic Hypogonadism 3 with or Without Anosmia 22 0.028
323
INN003 Iniencephaly 25 0.028
324
LPM007 Lipomyelomeningocele 20 0.028
325
TRN046 Transverse Vaginal Septum 14 0.028