Search results for PITX2

57 hits were found for PITX2

# Family MCID Name MIFTS Score
1
P AXN002 Axenfeld-Rieger Syndrome 53 5.402
2
c AXN009 Axenfeld-Rieger Syndrome, Type 1 49 5.222
3
c ANT071 Anterior Segment Dysgenesis 4 37 5.209
4
RNG003 Ring Dermoid of Cornea 25 5.130
5
PTR032 Peters-Plus Syndrome 60 4.422
6
P HRT032 Heart Disease 80 3.958
7
c FML001 Familial Atrial Fibrillation 55 3.547
8
FCH001 Fuchs' Endothelial Dystrophy 48 3.080
9
INT060 Intestinal Atresia 42 3.080
10
TTH002 Tooth Agenesis 54 3.044
11
ATS008 Autosomal Dominant Disease 39 3.044
12
P TTR001 Tetralogy of Fallot 70 2.528
13
P ANR048 Aniridia 1 68 2.528
14
TRN044 Transposition of the Great Arteries 49 2.528
15
P PRS062 Persistent Hyperplastic Primary Vitreous 41 2.528
16
CNT061 Conotruncal Heart Malformations 70 2.485
17
c GLC097 Glaucoma 3, Primary Congenital, a 51 2.485
18
P VSC013 Visceral Heterotaxy 45 2.485
19
c ANT077 Anterior Segment Dysgenesis 1 45 2.485
20
P JVN008 Juvenile Glaucoma 41 2.485
21
GLC098 Glaucoma-Related Pigment Dispersion Syndrome 40 2.485
22
c AXN010 Axenfeld-Rieger Syndrome, Type 3 39 2.485
23
c BRD017 Bardet-Biedl Syndrome 5 37 2.485
24
c PRM032 Primary Congenital Glaucoma 36 2.485
25
c AXN012 Axenfeld-Rieger Syndrome, Type 2 34 2.485
26
IRS003 Iris Disease 31 2.485
27
HYD007 Hydrophthalmos 28 2.485
28
c ERL012 Early-Onset Glaucoma 28 2.485
29
CGN001 Cogan-Reese Syndrome 23 2.485
30
INT323 Intraocular Pressure Quantitative Trait Locus 22 2.485
31
P PRS040 Prostate Cancer 88 0.204
32
PRS047 Prostatitis 59 0.204
33
P BRS047 Breast Cancer 100 0.136
34
NRN002 Neuronitis 43 0.136
35
SQM006 Squamous Cell Carcinoma 74 0.118
36
P ATR011 Atrial Fibrillation 68 0.118
37
P THY032 Thyroiditis 56 0.118
38
P OMP004 Omphalocele 51 0.096
39
P LNG032 Lung Cancer 99 0.068
40
P CLR023 Colorectal Cancer 98 0.068
41
P OVR042 Ovarian Cancer 82 0.068
42
DMN002 Dementia 68 0.068
43
c SML038 Small Cell Cancer of the Lung 67 0.068
44
AGN016 Aging 65 0.068
45
P THY109 Thyroid Cancer, Nonmedullary, 1 64 0.068
46
P ESP024 Esophagitis 64 0.068
47
P MCR010 Microcephaly 57 0.068
48
P SHR029 Short Syndrome 54 0.068
49
END072 Endotheliitis 46 0.068
50
P HRD009 Hereditary Wilms' Tumor 46 0.068
51
CRB009 Cerebritis 41 0.068
52
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.068
53
AML004 Ameloblastic Carcinoma 35 0.068
54
P CRN233 Corneal Dystrophy, Fuchs Endothelial, 1 34 0.068
55
c ATR062 Atrial Septal Defect 1 32 0.068
56
P CRN249 Cornea Plana 29 0.068
57
AXN011 Axenfeld-Rieger Anomaly with Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, and Skeletal Abnormalities 18 0.068
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