Search results for TBX1

37 hits were found for TBX1

# Family MCID Name MIFTS Score
1
VLC001 Velocardiofacial Syndrome 63 7.924
2
DGR001 Digeorge Syndrome 55 7.535
3
P TTR001 Tetralogy of Fallot 69 5.110
4
CNT061 Conotruncal Heart Malformations 61 4.959
5
P HRT032 Heart Disease 74 4.017
6
ING001 Inguinal Hernia 59 3.524
7
CHR659 Chromosome 22q11.2 Duplication Syndrome 36 3.488
8
HLT001 Holt-Oram Syndrome 61 3.448
9
ULN003 Ulnar-Mammary Syndrome 50 3.448
10
DBL002 Double Outlet Right Ventricle 49 3.448
11
P ATR001 Atrioventricular Septal Defect 56 2.815
12
HRT011 Heart Septal Defect 43 2.815
13
CHR386 Chromosome 6pter-P24 Deletion Syndrome 40 2.815
14
ESP029 Esophageal Atresia/tracheoesophageal Fistula 33 2.815
15
c CHR565 Chromosomal Deletion Syndrome 22 2.815
16
P ORF002 Orofacial Cleft 41 1.991
17
P CHR084 Chromosomal Disease 40 1.991
18
PHR003 Pharyngitis 59 0.151
19
P RTT002 Rett Syndrome 82 0.076
20
c PRM196 Premature Ovarian Failure 1 71 0.076
21
P SCH015 Schizophrenia 69 0.076
22
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.076
23
CLF027 Cleft Palate, Isolated 63 0.076
24
MLN008 Melanoma 62 0.076
25
P CLD001 Cleidocranial Dysplasia 62 0.076
26
c ATS007 Autism Spectrum Disorder 61 0.076
27
P VNT002 Ventricular Septal Defect 58 0.076
28
AST006 Astigmatism 49 0.076
29
HYP748 Hypertelorism 47 0.076
30
ADT003 Auditory System Disease 45 0.076
31
END072 Endotheliitis 45 0.076
32
VTR016 Vater/vacterl Association 45 0.076
33
UMB002 Umbilical Hernia 42 0.076
34
ERM002 Ear Malformation 40 0.076
35
VCT001 Vacterl Association 39 0.076
36
PLT007 Palatopharyngeal Incompetence 31 0.076
37
FML216 Familial Isolated Clinodactyly of Fingers 4 0.076
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