Search results for tbx4

57 hits were found for tbx4

# Family MCID Name MIFTS Score
1
ISC020 Ischiocoxopodopatellar Syndrome with or Without Pulmonary Arterial Hypertension 54 6.482
2
P PLM037 Pulmonary Hypertension 67 3.656
3
AML066 Amelia, Posterior, with Pelvic and Pulmonary Hypoplasia Syndrome 37 3.264
4
HYD002 Hydronephrosis 60 3.188
5
AML065 Amelia 30 3.126
6
P HRT032 Heart Disease 75 3.089
7
CHR381 Chromosome 17q23.1-Q23.2 Deletion Syndrome 34 2.764
8
P HYP055 Hypoplastic Left Heart Syndrome 63 2.636
9
P MCR010 Microcephaly 59 2.636
10
CLB002 Clubfoot 51 2.636
11
P CMP005 Campomelic Dysplasia 64 2.522
12
P BND020 Bone Disease 59 2.522
13
PLM184 Pulmonary Arterial Hypertension Associated with Congenital Heart Disease 42 2.181
14
CHR363 Chromosome 17q23.1-Q23.2 Duplication Syndrome 17 1.884
15
HLT001 Holt-Oram Syndrome 63 1.841
16
HRT015 Heritable Pulmonary Arterial Hypertension 44 1.841
17
TRC097 Tracheomalacia 42 1.841
18
P PLM025 Pulmonary Venoocclusive Disease 42 1.841
19
NNT004 Neonatal Respiratory Failure 36 1.841
20
c DPH024 Diaphragmatic Hernia, Congenital 63 1.783
21
P LRS001 Larsen Syndrome 62 1.783
22
LCR014 Lacrimoauriculodentodigital Syndrome 61 1.783
23
ULN003 Ulnar-Mammary Syndrome 57 1.783
24
VRT007 Vertical Talus, Congenital 48 1.783
25
c ATS204 Autosomal Recessive Non-Syndromic Intellectual Disability 44 1.783
26
P MLT072 Multiple Synostoses Syndrome 39 1.783
27
TRC026 Tracheal Disease 38 1.783
28
c EXD012 Exudative Vitreoretinopathy 7 35 1.783
29
P BND014 Bone Development Disease 33 1.783
30
LPD001 Lipid Pneumonia 28 1.783
31
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.346
32
P PLM182 Pulmonary Hypoplasia, Primary 32 0.155
33
P RSP003 Respiratory Failure 74 0.138
34
LNG099 Lung Disease 60 0.138
35
P PLM036 Pulmonary Fibrosis 65 0.098
36
ESP020 Esophageal Atresia 62 0.098
37
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.098
38
P LNG032 Lung Cancer 98 0.069
39
c PRM196 Premature Ovarian Failure 1 67 0.069
40
c SML038 Small Cell Cancer of the Lung 65 0.069
41
P ADN016 Adenocarcinoma 64 0.069
42
P ECT006 Ectodermal Dysplasia 62 0.069
43
INT066 Interstitial Lung Disease 60 0.069
44
P SNS001 Sensorineural Hearing Loss 60 0.069
45
P PTN014 Patent Ductus Arteriosus 1 60 0.069
46
NLP001 Nail-Patella Syndrome 60 0.069
47
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.069
48
P SZR006 Seizure Disorder 56 0.069
49
OPT070 Optic Nerve Hypoplasia, Bilateral 56 0.069
50
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 55 0.069
51
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.069
52
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.069
53
SYN005 Synostosis 45 0.069
54
SPS057 Spasticity 45 0.069
55
GNT031 Genitopatellar Syndrome 42 0.069
56
P DVL012 Developmental Dysplasia of the Hip 1 38 0.069
57
PTL010 Patella Aplasia-Hypoplasia 22 0.069
Content
Loading form....