Search results for hoxa13

139 hits were found for hoxa13

# Family MCID Name MIFTS Score
1
HND004 Hand-Foot-Genital Syndrome 48 50.050
2
PRX093 Preaxial Deficiency, Postaxial Polydactyly, and Hypospadias 33 38.329
3
P GST053 Gastric Cancer 82 18.119
4
P HYP040 Hypospadias 51 18.016
5
P PLY006 Polydactyly 58 14.862
6
P HPT023 Hepatocellular Carcinoma 95 14.408
7
P SYN012 Synpolydactyly 41 8.891
8
P PLV020 Pelvic Organ Prolapse 57 8.836
9
CHR619 Chromosome 2q35 Duplication Syndrome 64 8.796
10
CRY035 Cryptorchidism, Unilateral or Bilateral 57 7.884
11
c SYN059 Syndactyly, Type V 40 7.586
12
ATH001 Athabaskan Brainstem Dysgenesis Syndrome 52 7.586
13
CNT097 Central Hypoventilation Syndrome, Congenital 70 7.586
14
c ECT064 Ectodermal Dysplasia 5, Hair/nail Type 27 7.586
15
c ECT068 Ectodermal Dysplasia 6, Hair/nail Type 27 7.586
16
c ECT065 Ectodermal Dysplasia 7, Hair/nail Type 32 7.586
17
c ECT066 Ectodermal Dysplasia 9, Hair/nail Type 33 7.586
18
ISL125 Isolated Growth Hormone Deficiency Type Iii 39 7.586
19
SQM006 Squamous Cell Carcinoma 59 2.300
20
P PRS040 Prostate Cancer 95 1.880
21
P PNC035 Pancreatic Cancer 87 1.801
22
P OVR042 Ovarian Cancer 88 1.687
23
ESP021 Esophageal Cancer 84 1.618
24
P LKM062 Leukemia, Acute Lymphoblastic 69 1.601
25
P MYL006 Myeloid Leukemia 60 1.548
26
RNL077 Renal Fibrosis 46 1.468
27
P LNG064 Lung Cancer Susceptibility 3 69 1.403
28
P ADN016 Adenocarcinoma 63 1.403
29
P BRC006 Brachydactyly 52 1.346
30
P MYR002 Mayer-Rokitansky-Kuster-Hauser Syndrome 59 1.316
31
c LKM063 Leukemia, Chronic Myeloid 70 1.316
32
P BLD134 Bladder Cancer 79 1.250
33
c LKM061 Leukemia, Acute Myeloid 83 1.250
34
TRS030 Tarsal Coalition 25 1.249
35
P INF032 Infertility 60 1.210
36
PNC041 Pancreatic Ductal Adenocarcinoma 51 1.167
37
BNN005 Bunion 32 1.162
38
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.120
39
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 1.120
40
GLB002 Glioblastoma 67 1.094
41
HGH043 High Grade Glioma 46 1.094
42
HYD002 Hydronephrosis 58 1.094
43
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 1.094
44
GLM045 Glioma 62 1.094
45
GLL048 Glial Tumor 51 1.094
46
c SML038 Small Cell Cancer of the Lung 68 1.038
47
PHM001 Phimosis 37 1.038
48
LRY018 Laryngeal Squamous Cell Carcinoma 47 1.038
49
c BRC109 Brachydactyly, Type E1 45 1.006
50
c BRC062 Brachydactyly, Type D 37 1.006
51
P LKM002 Leukemia 65 1.006
52
CNG034 Congestive Heart Failure 69 1.006
53
c PRC016 Pre-Eclampsia 64 1.006
54
c SVR005 Severe Pre-Eclampsia 49 1.006
55
SPT023 Septate Uterus 31 1.006
56
PLY150 Polykaryocytosis Inducer 29 0.971
57
P HRS035 Hirschsprung Disease 1 66 0.971
58
CRV035 Cervical Cancer 72 0.971
59
P END044 Endometriosis 62 0.931
60
CNG587 Congenital Limb Malformation 12 0.931
61
MYL009 Myelodysplastic Syndrome 67 0.884
62
OST159 Osteogenic Sarcoma 66 0.884
63
AMN001 Amenorrhea 53 0.884
64
c SYN084 Synpolydactyly 1 36 0.822
65
P UTR058 Uterine Anomalies 47 0.822
66
c SPL067 Split-Hand/foot Malformation 1 46 0.822
67
ISL121 Isolated Split Hand-Split Foot Malformation 42 0.822
68
P BRS047 Breast Cancer 97 0.681
69
P GND004 Gonadal Dysgenesis 46 0.673
70
P CLR023 Colorectal Cancer 100 0.482
71
P LNG032 Lung Cancer 98 0.482
72
ADN011 Adenoid Cystic Carcinoma 68 0.482
73
PLM019 Pleomorphic Liposarcoma 39 0.482
74
c ACT068 Acute Cystitis 60 0.447
75
P URN019 Urinary Tract Infection 48 0.394
76
c DFN159 Deafness, Autosomal Dominant 5 31 0.333
77
TRN018 Transitional Cell Carcinoma 56 0.333
78
BCR002 Bicornuate Uterus 24 0.333
79
P HPT021 Hepatitis 68 0.298
80
c HPT016 Hepatitis B 62 0.298
81
INT020 Intravenous Leiomyomatosis 35 0.258
82
LMY003 Leiomyomatosis 43 0.258
83
INV004 Invasive Bladder Transitional Cell Carcinoma 32 0.258
84
MYM001 Myoma 54 0.258
85
c VSC019 Vesicoureteral Reflux 1 56 0.211
86
IMM167 Immune Deficiency Disease 76 0.211
87
c SPL025 Split-Hand/foot Malformation 5 29 0.211
88
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.211
89
P TMR010 Tumor Predisposition Syndrome 69 0.211
90
STH001 Saethre-Chotzen Syndrome 65 0.211
91
P CNG499 Congenital Anomalies of Kidney and Urinary Tract 2 52 0.211
92
BCL016 B-Cell Immunodeficiency, Distal Limb Anomalies, and Urogenital Malformations 13 0.211
93
P CRN037 Craniosynostosis 67 0.211
94
P PYL005 Pyelonephritis 56 0.211
95
BLD131 Bladder Urothelial Carcinoma 59 0.211
96
c CHR098 Chronic Pyelonephritis 34 0.211
97
CHR074 Choriocarcinoma 46 0.211
98
CRV025 Cervical Incompetence 35 0.211
99
LNG081 Longitudinal Vaginal Septum 14 0.211
100
INH023 Inherited Cancer-Predisposing Syndrome 53 0.211
101
CLT003 Colitis 63 0.149
102
P SCL018 Scoliosis 57 0.149
103
IDP070 Idiopathic Scoliosis 41 0.149
104
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.149
105
P INF037 Inflammatory Bowel Disease 53 0.149
106
TNG002 Tangier Disease 63 0.149
107
P OST002 Osteoporosis 76 0.149
108
P SCL057 Scoliosis, Isolated 1 40 0.149
109
MCK005 Mckusick-Kaufman Syndrome 61 0.149
110
c INF078 Inflammatory Bowel Disease 2 28 0.149
111
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.149
112
KSH004 Kashin-Beck Disease 37 0.149
113
P SPP010 Suppressor of Tumorigenicity 3 50 0.149
114
P RNL100 Renal Hypodysplasia/aplasia 1 63 0.149
115
P LKM071 Leukemia, Chronic Lymphocytic 74 0.149
116
HRW001 Hair Whorl 35 0.149
117
c INF088 Inflammatory Bowel Disease 5 29 0.149
118
CHL149 Childhood Acute Myeloid Leukemia 42 0.149
119
MNT001 Mantle Cell Lymphoma 65 0.149
120
P SPL061 Split Hand-Foot Malformation 43 0.149
121
BRR014 Barrett Esophagus 66 0.149
122
P MLN007 Male Infertility 56 0.149
123
P PLY011 Polycystic Ovary Syndrome 57 0.149
124
MYF001 Myofibroma 42 0.149
125
HMT002 Hematologic Cancer 61 0.149
126
EMB004 Embryonal Carcinoma 55 0.149
127
TST014 Testicular Cancer 51 0.149
128
P CRN015 Cornelia De Lange Syndrome 67 0.149
129
MCR013 Microphthalmia 59 0.149
130
LMY002 Leiomyoma 51 0.149
131
PRM013 Premature Menopause 57 0.149
132
EMB006 Embryonal Testis Carcinoma 31 0.149
133
ULC004 Ulcerative Colitis 74 0.149
134
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.149
135
OVR094 Ovarian Epithelial Cancer 39 0.149
136
ORL011 Oral Cancer 60 0.149
137
RFR010 Refractory Anemia 49 0.149
138
VGN031 Vaginal Atresia 19 0.149
139
RFR007 Refractory Anemia with Excess Blasts in Transformation 26 0.149
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