Search results for nr3c1

58 hits were found for nr3c1

# Family MCID Name MIFTS Score
1
GLC106 Glucocorticoid Resistance, Generalized 41 5.045
2
CNN003 Conn's Syndrome 70 3.675
3
P BRS047 Breast Cancer 100 3.646
4
AST005 Asthma 83 3.374
5
MDD011 Mood Disorder 64 3.293
6
P ACT010 Acth-Secreting Pituitary Adenoma 58 3.293
7
OCL006 Ocular Hypertension 51 3.293
8
P OST002 Osteoporosis 75 3.261
9
ANX010 Anxiety 72 3.261
10
CHR066 Chronic Fatigue Syndrome 67 3.261
11
P RHN004 Rhinitis 62 3.261
12
PST028 Post-Traumatic Stress Disorder 59 3.261
13
P INF037 Inflammatory Bowel Disease 52 3.261
14
NLS001 Nelson Syndrome 49 3.261
15
P BPL003 Bipolar Disorder 61 2.893
16
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 2.824
17
P ACT074 Acute Lymphocytic Leukemia 61 2.824
18
LYM019 Lymphosarcoma 58 2.824
19
c HYP731 Hyperaldosteronism, Familial, Type I 56 2.824
20
APP015 Apparent Mineralocorticoid Excess 54 2.824
21
ADR013 Adrenal Gland Hyperfunction 54 2.824
22
LDD002 Liddle Syndrome 53 2.824
23
ACT103 Acute Lymphoblastic Leukemia, Childhood 53 2.824
24
END040 Endogenous Depression 53 2.824
25
BRD004 Borderline Personality Disorder 50 2.824
26
CRT046 Corticosteroid-Binding Globulin Deficiency 43 2.824
27
P MJR001 Major Depressive Disorder 70 2.386
28
BLS007 Blastic Plasmacytoid Dendritic Cell 45 2.349
29
c HYP595 Hypertension, Essential 78 2.306
30
BDY004 Body Mass Index Quantitative Trait Locus 11 75 2.306
31
HMN044 Human Immunodeficiency Virus Type 1 71 2.306
32
c INS002 in Situ Carcinoma 56 2.306
33
OST016 Osteochondrosis 52 2.306
34
ADR012 Adrenal Gland Disease 51 2.306
35
ADL002 Adult Syndrome 48 2.306
36
c ACT078 Acute Porphyria 48 2.306
37
ADR009 Adrenal Cortex Disease 40 2.306
38
ATS008 Autosomal Dominant Disease 39 2.306
39
c RTN142 Retinitis Pigmentosa 38 38 2.306
40
ALL007 Allergic Urticaria 25 2.306
41
c RNL016 Renal Infectious Disease 11 2.306
42
MNT002 Mental Depression 60 1.631
43
P ALC004 Alcohol Abuse 63 0.096
44
P NPH012 Nephrotic Syndrome 60 0.096
45
MYL069 Myeloma, Multiple 86 0.068
46
P MLT020 Multiple Sclerosis 85 0.068
47
CRH001 Crohn's Disease 80 0.068
48
P CRN018 Coronary Artery Anomaly 69 0.068
49
P THR014 Thrombocytopenia 65 0.068
50
ADN018 Adenoma 63 0.068
51
P PTT006 Pituitary Adenoma 57 0.068
52
P PMP005 Pemphigus Vulgaris 56 0.068
53
P PMP001 Pemphigus 55 0.068
54
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.068
55
GRW007 Growth Hormone Deficiency 52 0.068
56
ART140 Arteries, Anomalies of 51 0.068
57
NRN002 Neuronitis 43 0.068
58
c PMP006 Pemphigus Vulgaris, Familial 26 0.068
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