Search results for hoxa3

87 hits were found for hoxa3

# Family MCID Name MIFTS Score
1
PNL012 Penile Cancer 57 12.140
2
HND004 Hand-Foot-Genital Syndrome 48 8.811
3
DGR001 Digeorge Syndrome 62 8.584
4
PNL025 Penile Benign Neoplasm 31 8.584
5
ECT003 Ectopic Thymus 26 8.584
6
CNG005 Congenital Aphakia 23 8.584
7
CHR100 Chronic Ulcer of Skin 57 1.637
8
P LKM062 Leukemia, Acute Lymphoblastic 69 1.542
9
P LNG064 Lung Cancer Susceptibility 3 69 1.445
10
P ADN016 Adenocarcinoma 63 1.445
11
LNG039 Lung Squamous Cell Carcinoma 57 1.426
12
MLN065 Melanocytic Nevus Syndrome, Congenital 62 1.331
13
BRS099 Breast Ductal Carcinoma 61 1.331
14
SKN019 Skin Melanoma 70 1.331
15
VTR016 Vater/vacterl Association 50 1.246
16
ESP020 Esophageal Atresia 59 1.246
17
VCT001 Vacterl Association 46 1.246
18
RNL114 Renal Cell Carcinoma, Nonpapillary 79 1.157
19
GLB002 Glioblastoma 67 1.157
20
CLR030 Clear Cell Renal Cell Carcinoma 53 1.157
21
LYM040 Lymphoblastic Lymphoma 53 1.123
22
GLM045 Glioma 62 1.123
23
GLL048 Glial Tumor 51 1.123
24
P GST053 Gastric Cancer 82 1.085
25
P LKM002 Leukemia 65 1.085
26
HGH043 High Grade Glioma 46 1.085
27
HPT022 Hepatoblastoma 54 1.085
28
P LYM118 Lymphoma 66 1.042
29
DSS032 Disease by Infectious Agent 55 1.042
30
P MYC007 Myocardial Infarction 69 1.042
31
c ACT075 Acute Myocardial Infarction 55 1.042
32
THY029 Thyroid Carcinoma 55 1.042
33
P BRS047 Breast Cancer 97 0.939
34
P CLR023 Colorectal Cancer 100 0.778
35
P PNC035 Pancreatic Cancer 87 0.711
36
c HYP595 Hypertension, Essential 84 0.424
37
P ALZ034 Alzheimer Disease 87 0.359
38
c LKM061 Leukemia, Acute Myeloid 83 0.321
39
c DPH024 Diaphragmatic Hernia, Congenital 63 0.321
40
P HYP040 Hypospadias 51 0.321
41
c HMP012 Hemophagocytic Lymphohistiocytosis, Familial, 2 47 0.278
42
SVR004 Severe Combined Immunodeficiency 70 0.278
43
P MYL006 Myeloid Leukemia 60 0.278
44
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.227
45
c EPD076 Epidermolysis Bullosa Dystrophica, Autosomal Recessive 51 0.227
46
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.227
47
AGN016 Aging 53 0.227
48
P NSP012 Nasopharyngeal Carcinoma 60 0.227
49
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 58 0.227
50
c DFN159 Deafness, Autosomal Dominant 5 31 0.227
51
c RTN041 Retinitis Pigmentosa 11 43 0.227
52
P RCS002 Recessive Dystrophic Epidermolysis Bullosa 62 0.227
53
P EPD016 Epidermolysis Bullosa 53 0.227
54
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.227
55
SKN016 Skin Disease 63 0.227
56
OST012 Osteoarthritis 77 0.227
57
P FML187 Familial Hypertension 34 0.227
58
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.160
59
VLC001 Velocardiofacial Syndrome 57 0.160
60
DWN001 Down Syndrome 70 0.160
61
c TYP009 Type 2 Diabetes Mellitus 91 0.160
62
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.160
63
ATS010 Autosomal Recessive Disease 42 0.160
64
ALP099 Alopecia, Congenital 23 0.160
65
MNN043 Meningioma, Familial 79 0.160
66
CMB007 Combined Immunodeficiency 56 0.160
67
P BNG030 Benign Ependymoma 51 0.160
68
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.160
69
CLL010 Cellular Ependymoma 58 0.160
70
P SPN042 Spinal Cord Ependymoma 30 0.160
71
P END044 Endometriosis 62 0.160
72
SCR001 Secretory Meningioma 40 0.160
73
P PLM036 Pulmonary Fibrosis 65 0.160
74
TRT001 Teratocarcinoma 41 0.160
75
INT395 Intracranial Meningioma 47 0.160
76
CRV025 Cervical Incompetence 35 0.160
77
LNG099 Lung Disease 62 0.160
78
48X005 48,xyyy 39 0.160
79
ORL011 Oral Cancer 60 0.160
80
P ALP008 Alopecia 53 0.160
81
CHR178 Chromosomal Triplication 33 0.160
82
ACT114 Acute Myeloblastic Leukemia Without Maturation 26 0.160
83
P RRT020 Rare Tumor 39 0.160
84
HYP266 Hypoxia 56 0.160
85
BCR002 Bicornuate Uterus 24 0.160
86
P OVR082 Overgrowth Syndrome 41 0.160
87
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 0.160
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