Search results for tfap2a

67 hits were found for tfap2a

# Family MCID Name MIFTS Score
1
BRN003 Branchiooculofacial Syndrome 51 6.195
2
P LNG032 Lung Cancer 98 4.517
3
P BRS047 Breast Cancer 97 3.851
4
P PRS040 Prostate Cancer 97 3.797
5
MCR013 Microphthalmia 57 3.550
6
P MLN008 Melanoma 69 3.396
7
CLF001 Cleft Lip 53 3.109
8
CHR074 Choriocarcinoma 47 2.977
9
CLF027 Cleft Palate, Isolated 64 2.565
10
CLF056 Cleft Lip with or Without Cleft Palate 47 2.539
11
HYP748 Hypertelorism 50 2.510
12
AMB002 Amblyopia 49 2.510
13
EST005 Esotropia 42 2.510
14
EPC005 Epicanthus 40 2.510
15
LNS001 Lens Subluxation 38 2.510
16
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 2.401
17
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 2.401
18
LNG039 Lung Squamous Cell Carcinoma 66 2.401
19
CLB010 Coloboma of Macula 52 1.831
20
PTH003 Pathologic Nystagmus 52 1.831
21
P CLB034 Coloboma, Ocular, Autosomal Dominant 47 1.831
22
CLB009 Coloboma of Iris 28 1.831
23
CLB026 Colobomatous Microphthalmia 47 1.753
24
P ORF002 Orofacial Cleft 44 1.753
25
ERM002 Ear Malformation 39 1.753
26
LCR001 Lacrimal Duct Obstruction 26 1.753
27
ECT003 Ectopic Thymus 25 1.753
28
CHR103 Charge Syndrome 67 1.698
29
P PTN014 Patent Ductus Arteriosus 1 60 1.698
30
P BRN019 Bernard-Soulier Syndrome 60 1.698
31
P VND007 Van Der Woude Syndrome 1 58 1.698
32
PPL025 Popliteal Pterygium Syndrome 56 1.698
33
CHR101 Char Syndrome 55 1.698
34
ORB013 Orbital Disease 42 1.698
35
c HYP608 Hypocalciuric Hypercalcemia, Familial, Type Iii 41 1.698
36
ENP001 Enophthalmos 35 1.698
37
EXN003 Exencephaly 31 1.698
38
TTN003 Tetanus 65 0.115
39
FRY006 Fryns Microphthalmia Syndrome 52 0.115
40
NRL016 Neural Tube Defects 82 0.094
41
P LNG064 Lung Cancer Susceptibility 3 78 0.094
42
END057 Endometrial Cancer 74 0.094
43
P SKN015 Skin Carcinoma 66 0.094
44
P ADN016 Adenocarcinoma 64 0.094
45
P CTR002 Cataract 60 0.094
46
P GST053 Gastric Cancer 83 0.066
47
P NRB001 Neuroblastoma 72 0.066
48
P OLG002 Oligodendroglioma 67 0.066
49
P NSP012 Nasopharyngeal Carcinoma 66 0.066
50
P ATR011 Atrial Fibrillation 66 0.066
51
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.066
52
GT001 Gout 64 0.066
53
P GLM045 Glioma 63 0.066
54
c PRC016 Pre-Eclampsia 63 0.066
55
c BRN108 Branchiootic Syndrome 1 62 0.066
56
P GLL018 Gallbladder Cancer 57 0.066
57
P PLY011 Polycystic Ovary Syndrome 56 0.066
58
P PTS002 Ptosis 53 0.066
59
DFN245 Deafness, Autosomal Recessive 4, with Enlarged Vestibular Aqueduct 51 0.066
60
HYP043 Hyperandrogenism 48 0.066
61
P ENC008 Encephalocele 47 0.066
62
GLL048 Glial Tumor 45 0.066
63
MLT084 Multicystic Dysplastic Kidney 42 0.066
64
UNL014 Unilateral Multicystic Dysplastic Kidney 18 0.066
65
c ATR027 Atrial Fibrillation, Familial, 5 15 0.066
66
BRN050 Branchial Arch Defects 10 0.066
67
DMN008 Dominant Cleft Palate 5 0.066
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