Search results for hoxa1

168 hits were found for hoxa1

# Family MCID Name MIFTS Score
1
ATH001 Athabaskan Brainstem Dysgenesis Syndrome 52 65.511
2
P ATS364 Autism 72 19.378
3
EMB004 Embryonal Carcinoma 55 17.646
4
c ATS007 Autism Spectrum Disorder 71 16.663
5
P SNS001 Sensorineural Hearing Loss 60 12.767
6
P ASP001 Asperger Syndrome 48 11.409
7
MCR119 Microtia, Hearing Impairment, and Cleft Palate 28 9.781
8
P DNR001 Duane Retraction Syndrome 53 9.555
9
TKL001 Tukel Syndrome 52 9.066
10
DPN001 Dependent Personality Disorder 26 7.965
11
ACC003 Accommodative Esotropia 24 7.965
12
EST005 Esotropia 43 7.965
13
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 2.934
14
DSS008 Disease of Mental Health 74 2.934
15
c SML038 Small Cell Cancer of the Lung 68 2.492
16
P BRS047 Breast Cancer 97 2.266
17
c BRN108 Branchiootic Syndrome 1 63 1.996
18
P LNG032 Lung Cancer 98 1.996
19
P PNC035 Pancreatic Cancer 87 1.956
20
SQM006 Squamous Cell Carcinoma 59 1.785
21
c LKM061 Leukemia, Acute Myeloid 83 1.733
22
ORL015 Oral Squamous Cell Carcinoma 43 1.731
23
CRV035 Cervical Cancer 72 1.605
24
MCR103 Microtia 40 1.589
25
ISL019 Isolated Duane Retraction Syndrome 21 1.573
26
ORL011 Oral Cancer 60 1.556
27
P PRS040 Prostate Cancer 95 1.476
28
P VNT002 Ventricular Septal Defect 58 1.444
29
P MLN008 Melanoma 75 1.444
30
GLB002 Glioblastoma 67 1.377
31
HGH043 High Grade Glioma 46 1.377
32
GLM045 Glioma 62 1.377
33
GLL048 Glial Tumor 51 1.377
34
P OVR042 Ovarian Cancer 88 1.352
35
P NSP012 Nasopharyngeal Carcinoma 60 1.326
36
OST012 Osteoarthritis 77 1.326
37
c DNR003 Duane Retraction Syndrome 1 39 1.298
38
P GST053 Gastric Cancer 82 1.296
39
P BLD134 Bladder Cancer 79 1.286
40
P HPT023 Hepatocellular Carcinoma 95 1.245
41
P CLR023 Colorectal Cancer 100 1.220
42
NRL016 Neural Tube Defects 80 1.146
43
c PCH010 Pachyonychia Congenita 3 43 1.146
44
END057 Endometrial Cancer 76 1.146
45
ESP021 Esophageal Cancer 84 1.124
46
TRT001 Teratocarcinoma 41 1.124
47
P LNG064 Lung Cancer Susceptibility 3 69 1.100
48
HRT011 Heart Septal Defect 49 1.100
49
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.076
50
CLF027 Cleft Palate, Isolated 64 1.076
51
MCR013 Microphthalmia 59 1.076
52
P BCL017 B-Cell Lymphoma 57 1.076
53
P TTR001 Tetralogy of Fallot 69 1.049
54
ABR001 Aberrant Subclavian Artery 22 1.049
55
ART030 Aortic Arch Interruption 25 1.049
56
DNR006 Duane Retraction Syndrome 3 with or Without Deafness 19 1.021
57
c TYP008 Type 1 Diabetes Mellitus 77 1.021
58
HMN014 Human Immunodeficiency Virus Infectious Disease 54 1.021
59
c FML056 Familial Deafness 15 1.021
60
RFR003 Refractive Error 41 1.021
61
PRT234 Partial Duplication of Chromosome 7 7 1.021
62
P MLN069 Melanoma, Uveal 59 0.990
63
P MYL006 Myeloid Leukemia 60 0.990
64
P RTN024 Retinoblastoma 72 0.956
65
BNG036 Bone Giant Cell Tumor 48 0.956
66
FTL029 Fetal Thalidomide Syndrome 27 0.956
67
SPT007 Spitz Nevus 34 0.956
68
P LNG021 Lung Occult Small Cell Carcinoma 20 0.941
69
LNG019 Lung Combined Type Small Cell Carcinoma 34 0.941
70
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.941
71
PLY150 Polykaryocytosis Inducer 29 0.918
72
ASP026 Asplenia, Isolated Congenital 43 0.812
73
MYL069 Myeloma, Multiple 76 0.812
74
P LKM062 Leukemia, Acute Lymphoblastic 69 0.677
75
P CRD246 Cardiovascular System Disease 55 0.611
76
ATH013 Atherosclerosis Susceptibility 63 0.478
77
RNL065 Renal Cell Carcinoma, Papillary, 1 79 0.471
78
P INS002 in Situ Carcinoma 52 0.456
79
CHL065 Cholangiocarcinoma 57 0.353
80
INT079 Intrahepatic Cholangiocarcinoma 51 0.353
81
MYL009 Myelodysplastic Syndrome 67 0.330
82
LMY014 Leiomyoma, Uterine 55 0.330
83
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.330
84
c LKM063 Leukemia, Chronic Myeloid 70 0.330
85
DFF005 Diffuse Large B-Cell Lymphoma 55 0.330
86
P PSR002 Psoriasis 63 0.330
87
P SCL018 Scoliosis 57 0.322
88
WLF002 Wolf-Hirschhorn Syndrome 57 0.322
89
c HPT073 Hepatitis C Virus 70 0.322
90
P STR020 Strabismus 56 0.322
91
c HPT001 Hepatitis C 61 0.322
92
P ADN016 Adenocarcinoma 63 0.322
93
MCH006 Mechanical Strabismus 40 0.322
94
MBS002 Moebius Syndrome 53 0.288
95
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.288
96
c DFN159 Deafness, Autosomal Dominant 5 31 0.288
97
ALT003 Alternating Exotropia 33 0.288
98
EXT022 Exotropia 42 0.288
99
c DFN094 Deafness, Autosomal Dominant 28 31 0.250
100
CHN065 Choanal Atresia, Posterior 48 0.250
101
P PTS002 Ptosis 52 0.250
102
DCT002 Ductal Carcinoma in Situ 58 0.250
103
c ATS005 Autosomal Dominant Nonsyndromic Deafness 24 0.250
104
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.250
105
P RTT002 Rett Syndrome 79 0.250
107
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.250
108
FRY006 Fryns Microphthalmia Syndrome 52 0.250
109
P FTL001 Fetal Alcohol Syndrome 55 0.250
110
BRS099 Breast Ductal Carcinoma 61 0.250
111
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 40 0.250
112
P OBS001 Obstructive Jaundice 49 0.250
113
ADN012 Adenocarcinoma in Situ 41 0.250
114
P DMN002 Dementia 65 0.250
115
c BRS049 Breast Carcinoma in Situ 50 0.250
116
CLF001 Cleft Lip 54 0.250
117
CRY010 Cryptophthalmos 26 0.250
118
VSC002 Vascular Dementia 59 0.250
119
P HRZ002 Horizontal Gaze Palsy with Progressive Scoliosis 37 0.250
120
P PRV006 Pervasive Developmental Disorder 52 0.204
121
ACT119 Acute Promyelocytic Leukemia 62 0.204
122
c RTN032 Retinal Cone Dystrophy 1 24 0.204
123
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.204
124
OST159 Osteogenic Sarcoma 66 0.204
125
P BRC006 Brachydactyly 52 0.204
126
GZP005 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 30 0.204
127
P SPP010 Suppressor of Tumorigenicity 3 50 0.204
128
BLM001 Bloom Syndrome 65 0.204
129
c BRC062 Brachydactyly, Type D 37 0.204
130
BRW002 Brown's Tendon Sheath Syndrome 28 0.204
131
MYL031 Myeloproliferative Neoplasm 66 0.204
132
THR004 Thrombocytosis 52 0.204
133
P BNG032 Benign Mesothelioma 53 0.204
134
SMN007 Seminoma 42 0.204
135
P LYN001 Lynch Syndrome 76 0.204
136
P HYP040 Hypospadias 51 0.204
137
OCL011 Ocular Motility Disease 45 0.204
138
HYP266 Hypoxia 56 0.204
139
PRT213 Partial Duplication of Chromosome 19 11 0.204
140
c DNR004 Duane Retraction Syndrome 2 28 0.144
141
CHR072 Chordoma 56 0.144
142
WLD004 Wildervanck Syndrome 28 0.144
143
P FRG001 Fragile X Syndrome 70 0.144
144
c WLF013 Wolfram Syndrome 1 60 0.144
145
HLC007 Helicobacter Pylori Infection 67 0.144
146
P DST002 Distal Arthrogryposis 63 0.144
147
SPP007 Suppression Amblyopia 38 0.144
148
P LKM002 Leukemia 65 0.144
149
PPL002 Papillary Carcinoma 46 0.144
150
P LMY004 Leiomyosarcoma 62 0.144
151
AMB002 Amblyopia 49 0.144
152
P KLP003 Klippel-Feil Syndrome 47 0.144
153
P ECL001 Eclampsia 52 0.144
154
BRN015 Bronchiolo-Alveolar Adenocarcinoma 55 0.144
155
FCL012 Facial Paralysis 49 0.144
156
P END044 Endometriosis 62 0.144
157
P GST044 Gastritis 55 0.144
158
c PRC016 Pre-Eclampsia 64 0.144
159
P PRN023 Prion Disease 60 0.144
160
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.144
161
SKN019 Skin Melanoma 70 0.144
162
PTH003 Pathologic Nystagmus 52 0.144
163
47X002 47,xyy 47 0.144
164
SBM006 Submucosal Cleft Palate 14 0.144
165
OVR094 Ovarian Epithelial Cancer 39 0.144
166
CHR159 Charlie M Syndrome 21 0.144
167
CNG506 Congenital Amyoplasia 27 0.144
168
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 0.144
Content
Loading form....