Search results for PITX2

59 hits were found for PITX2

# Family MCID Name MIFTS Score
1
P AXN002 Axenfeld-Rieger Syndrome 53 6.263
2
c ANT071 Anterior Segment Dysgenesis 4 37 5.935
3
c AXN009 Axenfeld-Rieger Syndrome, Type 1 46 5.841
4
RNG003 Ring Dermoid of Cornea 21 5.826
5
PTR032 Peters-Plus Syndrome 62 5.166
6
P CTR002 Cataract 60 3.952
7
P HRT032 Heart Disease 74 3.926
8
P ANT088 Anterior Segment Dysgenesis 38 3.546
9
c FML001 Familial Atrial Fibrillation 54 3.517
10
c ANT077 Anterior Segment Dysgenesis 1 42 3.433
11
FCH001 Fuchs' Endothelial Dystrophy 49 3.055
12
INT060 Intestinal Atresia 43 3.055
13
P CRN249 Cornea Plana 30 3.055
14
TTH002 Tooth Agenesis 53 3.019
15
ATS008 Autosomal Dominant Disease 39 3.019
16
P TTR001 Tetralogy of Fallot 69 2.508
17
c GLC097 Glaucoma 3, Primary Congenital, a 52 2.508
18
P PRS062 Persistent Hyperplastic Primary Vitreous 40 2.508
19
P ANR048 Aniridia 1 65 2.465
20
GLC098 Glaucoma-Related Pigment Dispersion Syndrome 47 2.465
21
P VSC013 Visceral Heterotaxy 46 2.465
22
P JVN008 Juvenile Glaucoma 41 2.465
23
c AXN010 Axenfeld-Rieger Syndrome, Type 3 39 2.465
24
c BRD017 Bardet-Biedl Syndrome 5 37 2.465
25
c PRM032 Primary Congenital Glaucoma 36 2.465
26
c AXN012 Axenfeld-Rieger Syndrome, Type 2 34 2.465
27
IRS003 Iris Disease 33 2.465
28
HYD007 Hydrophthalmos 29 2.465
29
c ERL012 Early-Onset Glaucoma 27 2.465
30
CGN001 Cogan-Reese Syndrome 23 2.465
31
INT323 Intraocular Pressure Quantitative Trait Locus 22 2.465
32
c ANT085 Anterior Segment Dysgenesis 5 24 0.571
33
P PRS040 Prostate Cancer 90 0.261
34
PRS047 Prostatitis 60 0.223
35
WLF001 Wolff-Parkinson-White Syndrome 59 0.135
36
SQM006 Squamous Cell Carcinoma 59 0.135
37
NRN002 Neuronitis 41 0.135
38
P BRS047 Breast Cancer 100 0.117
39
P ATR011 Atrial Fibrillation 68 0.117
40
P THY032 Thyroiditis 55 0.117
41
P ESP024 Esophagitis 63 0.095
42
P OMP004 Omphalocele 51 0.095
43
P LNG032 Lung Cancer 98 0.067
44
P CLR023 Colorectal Cancer 97 0.067
45
P OVR042 Ovarian Cancer 81 0.067
46
c SML038 Small Cell Cancer of the Lung 68 0.067
47
DMN002 Dementia 68 0.067
48
AGN016 Aging 64 0.067
49
P KDN017 Kidney Cancer 58 0.067
50
P MCR010 Microcephaly 57 0.067
51
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.067
52
P SHR029 Short Syndrome 51 0.067
53
END072 Endotheliitis 45 0.067
54
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 45 0.067
55
CRB009 Cerebritis 41 0.067
56
TRN044 Transposition of the Great Arteries 40 0.067
57
AML004 Ameloblastic Carcinoma 34 0.067
58
P CRN233 Corneal Dystrophy, Fuchs Endothelial, 1 34 0.067
59
AXN011 Axenfeld-Rieger Anomaly with Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, and Skeletal Abnormalities 18 0.067
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