Search results for AGTR2

41 hits were found for AGTR2

# Family MCID Name MIFTS Score
1
P HRT032 Heart Disease 75 4.017
2
CNN003 Conn's Syndrome 79 3.593
3
P KDN018 Kidney Disease 72 3.593
4
c PRC016 Pre-Eclampsia 63 3.188
5
c HYP595 Hypertension, Essential 84 3.111
6
P MYC007 Myocardial Infarction 70 3.111
7
P ANG015 Angioedema 57 3.111
8
OBS082 Obstructive Nephropathy 42 3.111
9
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 2.540
10
STR067 Stroke, Ischemic 81 2.540
11
P RNL100 Renal Hypodysplasia/aplasia 1 63 2.540
12
c SVR001 Severe Acute Respiratory Syndrome 62 2.540
13
HYD002 Hydronephrosis 60 2.540
14
c VSC019 Vesicoureteral Reflux 1 57 2.540
15
P CRD246 Cardiovascular System Disease 57 2.540
16
CKT002 Cakut 48 2.540
17
MYC005 Myocardial Stunning 46 2.540
18
URT010 Ureteral Obstruction 45 2.540
19
CVD001 Covid-19 44 2.540
20
NNS032 Non-Syndromic X-Linked Intellectual Disability 43 1.859
21
PLM134 Pulmonary Fibrosis, Idiopathic 77 1.796
22
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 1.796
23
P CNG499 Congenital Anomalies of Kidney and Urinary Tract 2 52 1.796
24
P RNL015 Renal Hypertension 47 1.796
25
MLT084 Multicystic Dysplastic Kidney 42 1.796
26
c PST041 Posterior Urethral Valves 41 1.796
27
c FTL072 Fetal Akinesia Deformation Sequence 4 38 1.796
28
c AML047 Amelogenesis Imperfecta, Type Ia 35 1.796
29
PLN003 Plantar Fascial Fibromatosis 33 1.796
30
P FML284 Familial Vesicoureteral Reflux 27 1.796
31
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.107
32
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.107
33
P OVR042 Ovarian Cancer 88 0.076
34
CYS001 Cystic Fibrosis 81 0.076
35
c PRM196 Premature Ovarian Failure 1 67 0.076
36
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.076
37
P PRV006 Pervasive Developmental Disorder 57 0.076
38
P RNG032 Ring Chromosome 42 0.076
39
OVR094 Ovarian Epithelial Cancer 38 0.076
40
HYP114 Hypertensive Nephropathy 36 0.076
41
c RNG016 Ring Chromosome 20 27 0.076
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