Search results for hoxa3

80 hits were found for hoxa3

# Family MCID Name MIFTS Score
1
PNL012 Penile Cancer 57 11.938
2
HND004 Hand-Foot-Genital Syndrome 47 9.365
3
TCL025 T-Cell Immunodeficiency with Thymic Aplasia 42 8.442
4
DGR001 Digeorge Syndrome 62 8.442
5
ECT003 Ectopic Thymus 25 8.442
6
CNG005 Congenital Aphakia 23 8.442
7
PNL025 Penile Benign Neoplasm 31 8.442
8
P LNG064 Lung Cancer Susceptibility 3 70 3.538
9
P ADN016 Adenocarcinoma 63 3.538
10
LNG039 Lung Squamous Cell Carcinoma 57 3.460
11
CHR100 Chronic Ulcer of Skin 57 3.348
12
VTR016 Vater/vacterl Association 49 2.727
13
ESP020 Esophageal Atresia 60 2.727
14
VCT001 Vacterl Association 47 2.727
15
RNL114 Renal Cell Carcinoma, Nonpapillary 80 2.367
16
GLB002 Glioblastoma 67 2.367
17
CLR030 Clear Cell Renal Cell Carcinoma 54 2.367
18
P LKM062 Leukemia, Acute Lymphoblastic 69 2.242
19
GLL048 Glial Tumor 52 2.228
20
LYM040 Lymphoblastic Lymphoma 53 2.228
21
GLM045 Glioma 63 2.228
22
P GST053 Gastric Cancer 83 2.074
23
P LKM002 Leukemia 67 2.074
24
HGH043 High Grade Glioma 45 2.074
25
P LYM118 Lymphoma 67 1.899
26
P MYC007 Myocardial Infarction 70 1.899
27
DSS032 Disease by Infectious Agent 55 1.899
28
THY029 Thyroid Carcinoma 51 1.899
29
c ACT075 Acute Myocardial Infarction 56 1.899
30
c HYP595 Hypertension, Essential 85 1.727
31
MLN065 Melanocytic Nevus Syndrome, Congenital 62 1.335
32
SKN019 Skin Melanoma 71 1.335
33
BRS099 Breast Ductal Carcinoma 61 1.335
34
c LKM061 Leukemia, Acute Myeloid 83 1.306
35
c DPH024 Diaphragmatic Hernia, Congenital 64 1.306
36
P HYP040 Hypospadias 51 1.306
37
P CLR023 Colorectal Cancer 100 1.204
38
P PNC035 Pancreatic Cancer 86 1.204
39
P ALZ034 Alzheimer Disease 87 1.131
40
P MYL006 Myeloid Leukemia 61 1.131
41
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.923
42
P NSP012 Nasopharyngeal Carcinoma 61 0.923
43
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 58 0.923
44
AGN016 Aging 54 0.923
45
c DFN159 Deafness, Autosomal Dominant 5 31 0.923
46
c RTN041 Retinitis Pigmentosa 11 42 0.923
47
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.923
48
OST012 Osteoarthritis 77 0.923
49
P FML187 Familial Hypertension 34 0.923
50
P BRS047 Breast Cancer 98 0.779
51
P RRT020 Rare Tumor 39 0.653
52
P OVR082 Overgrowth Syndrome 49 0.653
53
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 0.653
54
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.653
55
ALP099 Alopecia, Congenital 23 0.653
56
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.653
57
ATS010 Autosomal Recessive Disease 42 0.653
58
DWN001 Down Syndrome 70 0.653
59
VLC001 Velocardiofacial Syndrome 57 0.653
60
c TYP009 Type 2 Diabetes Mellitus 92 0.653
61
MNN043 Meningioma, Familial 79 0.653
62
P SPN042 Spinal Cord Ependymoma 29 0.653
63
CLL010 Cellular Ependymoma 57 0.653
64
CRV025 Cervical Incompetence 35 0.653
65
P ALP008 Alopecia 54 0.653
66
BCR002 Bicornuate Uterus 24 0.653
67
TRT001 Teratocarcinoma 42 0.653
68
P PLM036 Pulmonary Fibrosis 66 0.653
69
SCR001 Secretory Meningioma 40 0.653
70
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.653
71
LNG099 Lung Disease 62 0.653
72
P BNG030 Benign Ependymoma 51 0.653
73
CMB007 Combined Immunodeficiency 57 0.653
74
P END044 Endometriosis 62 0.653
75
SVR004 Severe Combined Immunodeficiency 72 0.653
76
SPN021 Spinal Meningioma 50 0.653
77
ACT114 Acute Myeloblastic Leukemia Without Maturation 26 0.653
78
48X005 48,xyyy 39 0.653
79
HYP266 Hypoxia 57 0.653
80
CHR178 Chromosomal Triplication 34 0.653
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