Search results for gja5

89 hits were found for gja5

# Family MCID Name MIFTS Score
1
c ATR059 Atrial Fibrillation, Familial, 11 22 42.817
2
c ATR087 Atrial Standstill 1 74 33.338
3
c FML001 Familial Atrial Fibrillation 65 25.718
4
1Q2003 1q21.1 Recurrent Microdeletion 22 23.269
5
P ATR011 Atrial Fibrillation 66 22.845
6
P TTR001 Tetralogy of Fallot 69 21.674
7
P ATR081 Atrial Standstill 31 20.636
8
P HRT032 Heart Disease 81 16.437
9
P HYP061 Hypertrophic Cardiomyopathy 69 11.213
10
c PRG126 Progressive Familial Heart Block 58 10.612
11
c PRG042 Progressive Familial Heart Block, Type Ia 66 10.334
12
LPP008 Lipoprotein Quantitative Trait Locus 65 9.662
13
RHM028 Rheumatic Heart Disease 56 9.662
14
c HYP595 Hypertension, Essential 85 9.662
15
P NNN008 Noonan Syndrome 1 77 9.662
16
c DLT002 Dilated Cardiomyopathy 78 9.662
17
HRT011 Heart Septal Defect 49 7.995
18
ATR057 Atrioventricular Block 54 7.782
19
P OCL013 Oculodentodigital Dysplasia 67 7.504
20
P ATR001 Atrioventricular Septal Defect 55 7.504
21
P SCK002 Sick Sinus Syndrome 55 7.504
22
P PLM158 Palmoplantar Keratoderma and Congenital Alopecia 1 42 6.832
23
RGH009 Right Atrial Isomerism 57 6.832
24
P BRG001 Brugada Syndrome 69 6.832
25
THR099 Third-Degree Atrioventricular Block 42 6.832
26
SNT005 Sinoatrial Node Disease 47 6.832
27
HLT001 Holt-Oram Syndrome 66 6.832
28
EBS001 Ebstein Anomaly 55 6.832
29
CLS005 Clouston Syndrome 58 6.832
30
c MYS051 Myasthenic Syndrome, Congenital, 5 53 6.832
31
P LFT003 Left Ventricular Noncompaction 57 6.832
32
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 6.832
33
c HRD100 Hereditary Lymphedema Ic 28 6.832
34
P CNG001 Congenital Myasthenic Syndrome 68 6.832
35
HRT008 Heart Conduction Disease 44 6.832
36
P ATR010 Atrial Heart Septal Defect 58 6.832
37
DBL002 Double Outlet Right Ventricle 57 6.832
38
PTN001 Patent Foramen Ovale 62 6.832
39
P HYP055 Hypoplastic Left Heart Syndrome 65 6.832
40
CRD223 Cardiac Arrhythmia 63 4.168
41
CHR583 Chromosome 1q21.1 Deletion Syndrome, 1.35-Mb 39 2.222
42
CRD132 Cardiac Conduction Defect 60 2.037
43
c TLN011 Telangiectasia, Hereditary Hemorrhagic, Type 2 45 1.776
44
P HRD008 Hereditary Hemorrhagic Telangiectasia 65 1.776
45
TLN003 Telangiectasis 51 1.776
46
P ART005 Arteriovenous Malformation 65 1.776
47
WLF001 Wolff-Parkinson-White Syndrome 65 1.551
48
P SCH015 Schizophrenia 74 1.544
49
P VNT002 Ventricular Septal Defect 58 1.343
50
P CRN300 Coronary Heart Disease 1 73 0.950
51
WLL001 Williams-Beuren Syndrome 61 0.950
52
P MGL010 Megalencephalic Leukoencephalopathy with Subcortical Cysts 2a 40 0.950
53
c NPH031 Nephronophthisis 3 46 0.950
54
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.950
55
OST159 Osteogenic Sarcoma 66 0.950
56
c NMN014 Niemann-Pick Disease, Type C2 49 0.950
57
P MYP004 Myopathy 67 0.950
58
HRT012 Heart Valve Disease 53 0.950
59
P CTR002 Cataract 60 0.950
60
c NTR031 Neutropenia, Severe Congenital, 5, Autosomal Recessive 36 0.950
61
VSC002 Vascular Dementia 60 0.950
62
CYT002 Cytokine Deficiency 43 0.950
63
P BRS047 Breast Cancer 98 0.873
64
SNG003 Single Ventricular Heart 30 0.671
65
c ART115 Aortic Valve Disease 1 74 0.671
66
SMT008 Smith-Magenis Syndrome 54 0.671
67
SDD001 Sudden Infant Death Syndrome 60 0.671
68
P PLY006 Polydactyly 59 0.671
69
c BRD011 Bardet-Biedl Syndrome 10 49 0.671
70
c NTR047 Neutropenia, Severe Congenital, 1, Autosomal Dominant 37 0.671
71
MLL018 Miller-Dieker Lissencephaly Syndrome 52 0.671
72
c ATR026 Atrial Fibrillation, Familial, 1 21 0.671
73
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.671
74
WLF002 Wolf-Hirschhorn Syndrome 57 0.671
75
RNL078 Renal Dysplasia 46 0.671
76
P NRB001 Neuroblastoma 66 0.671
77
SBV001 Subvalvular Aortic Stenosis 30 0.671
78
P MSC005 Muscular Dystrophy 67 0.671
79
OLG003 Oligohydramnios 51 0.671
80
OST016 Osteochondrosis 52 0.671
81
EMB004 Embryonal Carcinoma 56 0.671
82
P MYT002 Myotonic Dystrophy 51 0.671
84
MYT011 Myotonia 39 0.671
85
HYP266 Hypoxia 57 0.671
86
P ATS364 Autism 69 0.504
87
P OVR042 Ovarian Cancer 88 0.504
88
CKT002 Cakut 47 0.504
89
P PNC035 Pancreatic Cancer 86 0.504
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