Search results for zic3

118 hits were found for zic3

# Family MCID Name MIFTS Score
1
HTR014 Heterotaxy, Visceral, 1, X-Linked 40 48.812
2
P VSC013 Visceral Heterotaxy 53 41.506
3
VCT005 Vacterl Association, X-Linked, with or Without Hydrocephalus 40 40.008
4
HTR003 Heterotaxy 43 21.572
5
P HRT032 Heart Disease 84 19.510
6
VCT002 Vacterl Association with Hydrocephaly, X-Linked 15 17.961
7
P VCT008 Vacterl with Hydrocephalus 33 17.961
8
NRL016 Neural Tube Defects 80 17.330
9
VCT001 Vacterl Association 46 15.149
10
P HYD006 Hydrocephalus 62 11.765
11
P OMP004 Omphalocele 47 11.148
12
DBL002 Double Outlet Right Ventricle 56 10.782
13
P VNT002 Ventricular Septal Defect 58 9.876
14
P MCK013 Meckel Syndrome, Type 1 64 9.762
15
HYD002 Hydronephrosis 58 9.606
16
VTR016 Vater/vacterl Association 50 9.268
17
P DXT004 Dextro-Looped Transposition of the Great Arteries 58 9.107
18
ISL054 Isolated Congenitally Uncorrected Transposition of the Great Arteries 12 8.160
19
P TTR001 Tetralogy of Fallot 69 7.968
20
DXT001 Dextrocardia 54 7.883
21
ANS023 Anus, Imperforate 56 7.813
22
P HLP001 Holoprosencephaly 68 7.813
23
KRT010 Kartagener Syndrome 49 7.394
24
HRT011 Heart Septal Defect 49 7.062
25
P ATR001 Atrioventricular Septal Defect 54 7.013
26
TRC062 Tricuspid Atresia 54 6.948
27
DDN011 Duodenal Atresia 47 6.948
28
P ATR010 Atrial Heart Septal Defect 58 6.948
29
P PRM011 Primary Ciliary Dyskinesia 68 6.948
30
P TWN003 Townes-Brocks Syndrome 55 6.793
31
c VSC019 Vesicoureteral Reflux 1 56 6.793
32
RGH009 Right Atrial Isomerism 57 6.793
33
HLT001 Holt-Oram Syndrome 66 6.793
34
TTL012 Total Anomalous Pulmonary Venous Return 1 58 6.793
35
P PTN014 Patent Ductus Arteriosus 1 59 6.793
36
P RNL100 Renal Hypodysplasia/aplasia 1 63 6.793
37
c SHR064 Short-Rib Thoracic Dysplasia 10 with or Without Polydactyly 44 6.793
38
P ACR072 Acrorenal Syndrome 34 6.793
39
JCB001 Jacobsen Syndrome 50 6.793
40
PHY002 Physical Disorder 40 6.793
41
PTN001 Patent Foramen Ovale 61 6.793
42
PLM041 Pulmonary Valve Stenosis 50 6.793
43
P PLM040 Pulmonary Valve Disease 40 6.793
44
P HYP055 Hypoplastic Left Heart Syndrome 65 6.793
45
STS002 Situs Inversus 44 1.906
46
DXT002 Dextrocardia with Situs Inversus 43 1.605
47
HMF006 Hemifacial Microsomia 55 1.564
48
ESP020 Esophageal Atresia 59 1.564
49
CRN051 Craniofacial Microsomia 28 1.564
50
P SCL018 Scoliosis 57 1.201
51
ECT085 Ectopia Cordis 18 1.201
52
P PLY006 Polydactyly 58 1.149
53
c TRN038 Transposition of the Great Arteries, Dextro-Looped 1 39 1.149
54
P PLL001 Pallister-Hall Syndrome 62 1.121
55
P TRT010 Teratoma 50 1.121
56
DBL004 Double Discordia 20 1.090
57
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 52 1.057
58
CRN088 Craniorachischisis 35 1.057
59
c HTR010 Heterotaxy, Visceral, 4, Autosomal 30 1.020
60
VCT004 Vacterl Association with Hydrocephalus 33 1.020
61
EXN003 Exencephaly 30 1.020
62
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.978
63
P JBR020 Joubert Syndrome 1 74 0.978
64
c HTR021 Heterotaxy, Visceral, 5, Autosomal 38 0.978
65
ART016 Aortic Aneurysm 68 0.978
66
ANR040 Aneurysm 60 0.978
67
P SPN237 Spina Bifida Aperta 19 0.978
68
47X002 47,xyy 47 0.864
69
P PNC035 Pancreatic Cancer 87 0.822
70
BRS099 Breast Ductal Carcinoma 61 0.737
71
P LNG021 Lung Occult Small Cell Carcinoma 20 0.737
72
LNG019 Lung Combined Type Small Cell Carcinoma 34 0.737
73
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.737
74
HLX001 Helix Syndrome 47 0.382
75
P LSS002 Lissencephaly 52 0.382
76
P HYP265 Hypotonia 42 0.312
77
DWN001 Down Syndrome 70 0.220
78
P BRS047 Breast Cancer 97 0.220
79
P AST005 Asthma 75 0.220
80
ATR088 Atrial Septal Defect 7 with or Without Atrioventricular Conduction Defects 30 0.220
81
ATR093 Atrial Heart Septal Defect 7 22 0.220
82
P NPH005 Nephronophthisis 59 0.220
83
MCR103 Microtia 40 0.220
84
CBB005 Cobblestone Lissencephaly 31 0.220
85
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.156
86
c HTR009 Heterotaxy, Visceral, 2, Autosomal 27 0.156
87
P SCH015 Schizophrenia 74 0.156
88
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.156
89
P MDL005 Medulloblastoma 75 0.156
90
LYM133 Lymphoma, Hodgkin, Classic 69 0.156
91
P ART028 Aortic Aneurysm, Familial Thoracic 4 61 0.156
92
PTT046 Pituitary Hormone Deficiency, Combined, 2 62 0.156
93
P CLR023 Colorectal Cancer 100 0.156
94
P GST053 Gastric Cancer 82 0.156
95
P ATX030 Ataxia-Telangiectasia 80 0.156
96
c SPN101 Spinocerebellar Ataxia 29 58 0.156
97
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.156
98
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.156
99
MNN043 Meningioma, Familial 79 0.156
100
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.156
101
c ATR067 Atrioventricular Septal Defect 4 26 0.156
102
BRK010 Burkitt Lymphoma 65 0.156
103
RTN020 Retinal Vascular Disease 45 0.156
104
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.156
105
BLR001 Biliary Atresia 55 0.156
106
SCR001 Secretory Meningioma 40 0.156
107
PPL018 Papillary Adenocarcinoma 44 0.156
108
P NNT058 Neonatal Diabetes 52 0.156
109
INT395 Intracranial Meningioma 47 0.156
110
TLN003 Telangiectasis 51 0.156
111
SBV001 Subvalvular Aortic Stenosis 31 0.156
112
CLF001 Cleft Lip 54 0.156
113
P BCL017 B-Cell Lymphoma 57 0.156
115
P CRB059 Cerebellar Degeneration 36 0.156
116
CHR178 Chromosomal Triplication 33 0.156
117
c JVN041 Juvenile Nephronophthisis 45 0.156
118
CLF004 Cleft Lip/palate 56 0.156
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