Search results for rxrg

81 hits were found for rxrg

# Family MCID Name MIFTS Score
1
P LNG032 Lung Cancer 98 21.851
2
P HYP838 Hyperlipidemia, Familial Combined, 3 61 13.010
3
P CNR004 Cone-Rod Dystrophy 2 74 12.616
4
P RTN008 Retinitis Pigmentosa 79 8.921
5
P BRS047 Breast Cancer 97 2.455
6
ADN018 Adenoma 58 1.263
7
P PTT006 Pituitary Adenoma 55 1.182
8
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 1.131
9
FML168 Familial Isolated Pituitary Adenoma 33 1.131
10
P PNC035 Pancreatic Cancer 87 0.602
11
LPD008 Lipid Metabolism Disorder 61 0.509
12
P CRN300 Coronary Heart Disease 1 73 0.426
13
c MJR022 Major Affective Disorder 8 37 0.360
14
c MJR024 Major Affective Disorder 9 40 0.360
15
P SPR119 Spermatogenic Failure, X-Linked, 1 36 0.360
16
P MLN007 Male Infertility 56 0.360
17
P BPL003 Bipolar Disorder 56 0.360
18
TXC005 Toxic Shock Syndrome 61 0.360
19
P INF032 Infertility 60 0.360
20
ANX010 Anxiety 70 0.322
21
RCK004 Rickets 64 0.322
22
P END046 Endometritis 46 0.322
23
P MLN008 Melanoma 75 0.322
24
THY029 Thyroid Carcinoma 55 0.322
25
P MLN069 Melanoma, Uveal 59 0.279
26
FLL031 Follicular Adenoma 40 0.279
27
GST033 Gestational Diabetes 60 0.279
28
SKN019 Skin Melanoma 70 0.279
29
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.228
30
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.228
31
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.228
32
P HRT032 Heart Disease 84 0.228
33
ALL003 Allergic Rhinitis 66 0.161
34
AND014 Androgenic Alopecia 46 0.161
35
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 55 0.161
36
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.161
37
NRL016 Neural Tube Defects 80 0.161
38
P ALP061 Alopecia, Androgenetic, 1 48 0.161
39
c BRN108 Branchiootic Syndrome 1 63 0.161
40
c DFN163 Deafness, Autosomal Dominant 7 31 0.161
41
AGN016 Aging 53 0.161
42
P FML012 Familial Partial Lipodystrophy 54 0.161
43
c MCR133 Microvascular Complications of Diabetes 4 41 0.161
44
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.161
45
CNG495 Congenital Anomalies of Kidney and Urinary Tract Syndrome with or Without Hearing Loss, Abnormal Ears, or Developmental Delay 26 0.161
46
c MCR113 Microvascular Complications of Diabetes 3 52 0.161
47
c MCR130 Microvascular Complications of Diabetes 6 41 0.161
48
c MCR120 Microvascular Complications of Diabetes 7 47 0.161
49
HLX001 Helix Syndrome 47 0.161
50
c THY107 Thymoma, Familial 42 0.161
51
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.161
52
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.161
53
P MNR014 Menarche, Age at, Quantitative Trait Locus 2 7 0.161
54
c MNR015 Menarche, Age at, Quantitative Trait Locus 3 6 0.161
55
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.161
56
IGR001 Ige Responsiveness, Atopic 58 0.161
57
c LPD015 Lipodystrophy, Familial Partial, Type 2 61 0.161
58
HMN044 Human Immunodeficiency Virus Type 1 76 0.161
59
P THY023 Thymoma 64 0.161
60
END035 Endocrine Gland Cancer 42 0.161
61
P LTR001 Lateral Sclerosis 57 0.161
62
P MYP006 Myopia 55 0.161
63
RNL025 Renal Hypoplasia 46 0.161
64
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.161
65
P RHN004 Rhinitis 56 0.161
66
THY123 Thyroid Gland Follicular Carcinoma 53 0.161
67
ALL029 Allergic Disease 61 0.161
68
P HYP040 Hypospadias 51 0.161
69
P MCR010 Microcephaly 59 0.161
70
P ART022 Arthritis 70 0.161
71
SCR011 Scrapie 39 0.161
72
P PRN023 Prion Disease 60 0.161
73
P NRF002 Neurofibromatosis 60 0.161
74
END086 End Stage Renal Disease 54 0.161
75
CYT002 Cytokine Deficiency 43 0.161
76
FTT001 Fatty Liver Disease 61 0.161
77
P HYP076 Hyperthyroidism 53 0.161
78
DFF036 Differentiated Thyroid Carcinoma 51 0.161
79
ORL011 Oral Cancer 60 0.161
80
P ALP008 Alopecia 53 0.161
81
P ENC018 Encephalopathy 62 0.161
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