Search results for CITED2

68 hits were found for CITED2

# Family MCID Name MIFTS Score
1
c ATR065 Atrial Septal Defect 8 24 4.548
2
HYP266 Hypoxia 57 4.372
3
c VNT026 Ventricular Septal Defect 2 24 4.014
4
P HRT032 Heart Disease 75 3.488
5
P VNT002 Ventricular Septal Defect 60 2.959
6
P TTR001 Tetralogy of Fallot 70 2.892
7
NRL016 Neural Tube Defects 82 2.838
8
PTN001 Patent Foramen Ovale 60 2.773
9
EXN003 Exencephaly 31 2.092
10
HRT011 Heart Septal Defect 50 2.027
11
P ATR010 Atrial Heart Septal Defect 60 1.985
12
DBL002 Double Outlet Right Ventricle 56 1.985
13
DXT002 Dextrocardia with Situs Inversus 39 1.985
14
ATR019 Atrial Septal Defect Sinus Venosus 22 1.985
15
RGH009 Right Atrial Isomerism 60 1.931
16
ESN011 Eisenmenger Syndrome 55 1.931
17
CHR101 Char Syndrome 55 1.931
18
c 46X049 46,xy Sex Reversal 2 48 1.931
19
c HYP549 Hypogonadotropic Hypogonadism 5 with or Without Anosmia 47 1.931
20
c 46X082 46,xy Sex Reversal 46 1.931
21
P BRS047 Breast Cancer 97 0.145
22
P PRS040 Prostate Cancer 97 0.092
23
c LKM061 Leukemia, Acute Myeloid 84 0.092
24
HYP066 Hyperglycemia 61 0.092
25
P CLR023 Colorectal Cancer 99 0.065
26
P GST053 Gastric Cancer 83 0.065
27
STR067 Stroke, Ischemic 81 0.065
28
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.065
29
ULC004 Ulcerative Colitis 73 0.065
30
P RTN024 Retinoblastoma 73 0.065
31
c CHR684 Chronic Kidney Disease 70 0.065
32
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.065
33
CHR593 Chromosome 16p13.3 Deletion Syndrome, Proximal 66 0.065
34
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.065
35
P THY023 Thymoma 65 0.065
36
CNT061 Conotruncal Heart Malformations 63 0.065
37
PTR032 Peters-Plus Syndrome 63 0.065
38
CLT003 Colitis 62 0.065
39
GST033 Gestational Diabetes 61 0.065
40
c OTP006 Otopalatodigital Syndrome, Type I 60 0.065
41
THY029 Thyroid Carcinoma 59 0.065
42
ISC004 Ischemia 58 0.065
43
P GLL018 Gallbladder Cancer 57 0.065
44
P INF032 Infertility 57 0.065
45
P PLY011 Polycystic Ovary Syndrome 56 0.065
46
DXT001 Dextrocardia 55 0.065
47
c FML008 Familial Retinoblastoma 53 0.065
48
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.065
49
P MSC003 Muscular Atrophy 52 0.065
50
c THY107 Thymoma, Familial 52 0.065
51
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.065
52
P SPP010 Suppressor of Tumorigenicity 3 51 0.065
53
URM002 Uremia 49 0.065
54
ADR016 Adrenal Cortical Carcinoma 48 0.065
55
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.065
56
HLX001 Helix Syndrome 47 0.065
57
CRN027 Corneal Neovascularization 47 0.065
58
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.065
59
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.065
60
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.065
61
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.065
62
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.065
63
P PRS062 Persistent Hyperplastic Primary Vitreous 44 0.065
64
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.065
65
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.065
66
CYT002 Cytokine Deficiency 42 0.065
67
INT276 Interatrial Communication 42 0.065
68
ADR004 Adrenal Cortical Adenocarcinoma 39 0.065
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