Search results for hoxa1

168 hits were found for hoxa1

# Family MCID Name MIFTS Score
1
ATH001 Athabaskan Brainstem Dysgenesis Syndrome 52 67.270
2
P ATS364 Autism 69 21.763
3
c ATS007 Autism Spectrum Disorder 72 19.576
4
EMB004 Embryonal Carcinoma 56 19.300
5
P ASP001 Asperger Syndrome 48 11.828
6
MCR103 Microtia 44 11.477
7
P DNR001 Duane Retraction Syndrome 53 11.477
8
MCR119 Microtia, Hearing Impairment, and Cleft Palate 29 11.035
9
TKL001 Tukel Syndrome 52 10.352
10
ACC003 Accommodative Esotropia 24 7.956
11
EST005 Esotropia 43 7.956
12
DPN001 Dependent Personality Disorder 27 7.956
13
c SML038 Small Cell Cancer of the Lung 69 5.484
14
P LNG032 Lung Cancer 98 4.700
15
c BRN108 Branchiootic Syndrome 1 62 3.975
16
CRV035 Cervical Cancer 73 3.584
17
c LKM061 Leukemia, Acute Myeloid 83 3.460
18
ISL019 Isolated Duane Retraction Syndrome 21 3.455
19
ORL011 Oral Cancer 60 3.388
20
P GST053 Gastric Cancer 83 3.179
21
P SNS001 Sensorineural Hearing Loss 59 3.175
22
P HPT023 Hepatocellular Carcinoma 96 2.972
23
P VNT002 Ventricular Septal Defect 58 2.940
24
P MLN008 Melanoma 76 2.940
25
P PRS040 Prostate Cancer 95 2.908
26
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 2.890
27
DSS008 Disease of Mental Health 74 2.890
28
P PNC035 Pancreatic Cancer 86 2.819
29
GLL048 Glial Tumor 52 2.672
30
GLB002 Glioblastoma 67 2.672
31
HGH043 High Grade Glioma 45 2.672
32
GLM045 Glioma 63 2.672
33
ORL015 Oral Squamous Cell Carcinoma 43 2.627
34
END057 Endometrial Cancer 72 2.578
35
NRL016 Neural Tube Defects 81 2.578
36
c PCH010 Pachyonychia Congenita 3 43 2.578
37
SQM006 Squamous Cell Carcinoma 60 2.578
38
P OVR042 Ovarian Cancer 88 2.573
39
ESP021 Esophageal Cancer 83 2.489
40
TRT001 Teratocarcinoma 42 2.489
41
P NSP012 Nasopharyngeal Carcinoma 61 2.468
42
OST012 Osteoarthritis 77 2.468
43
HRT011 Heart Septal Defect 49 2.396
44
P LNG064 Lung Cancer Susceptibility 3 70 2.396
45
c DNR003 Duane Retraction Syndrome 1 37 2.355
46
CLF027 Cleft Palate, Isolated 64 2.297
47
P BCL017 B-Cell Lymphoma 59 2.297
48
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 2.297
49
MCR013 Microphthalmia 60 2.297
50
P TTR001 Tetralogy of Fallot 69 2.192
51
P MYL006 Myeloid Leukemia 61 2.192
52
ABR001 Aberrant Subclavian Artery 22 2.192
53
ART030 Aortic Arch Interruption 25 2.192
54
P BLD134 Bladder Cancer 79 2.150
55
c TYP008 Type 1 Diabetes Mellitus 70 2.079
56
DNR006 Duane Retraction Syndrome 3 with or Without Deafness 20 2.079
57
PRT234 Partial Duplication of Chromosome 7 7 2.079
58
P LKM002 Leukemia 67 2.079
59
HMN014 Human Immunodeficiency Virus Infectious Disease 54 2.079
60
RFR003 Refractive Error 41 2.079
61
c FML056 Familial Deafness 14 2.079
62
P MLN069 Melanoma, Uveal 61 1.956
63
ATH013 Atherosclerosis Susceptibility 63 1.911
64
P INS002 in Situ Carcinoma 53 1.822
65
P RTN024 Retinoblastoma 73 1.820
66
BNG036 Bone Giant Cell Tumor 49 1.820
67
SPT007 Spitz Nevus 34 1.820
68
FTL029 Fetal Thalidomide Syndrome 27 1.820
69
PLY150 Polykaryocytosis Inducer 29 1.665
70
CHL065 Cholangiocarcinoma 58 1.411
71
INT079 Intrahepatic Cholangiocarcinoma 51 1.411
72
c HPT073 Hepatitis C Virus 71 1.288
73
WLF002 Wolf-Hirschhorn Syndrome 57 1.288
74
P STR020 Strabismus 56 1.288
75
P SCL018 Scoliosis 57 1.288
76
MCH006 Mechanical Strabismus 40 1.288
77
c HPT001 Hepatitis C 62 1.288
78
P ADN016 Adenocarcinoma 63 1.288
79
ASP026 Asplenia, Isolated Congenital 43 1.244
80
MYL069 Myeloma, Multiple 77 1.244
81
P CLR023 Colorectal Cancer 100 1.220
82
c DFN159 Deafness, Autosomal Dominant 5 31 1.152
83
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 1.152
84
MBS002 Moebius Syndrome 54 1.152
85
ALT003 Alternating Exotropia 33 1.152
86
EXT022 Exotropia 42 1.152
87
P BRS047 Breast Cancer 98 1.109
88
P LKM062 Leukemia, Acute Lymphoblastic 69 1.109
89
P CRD246 Cardiovascular System Disease 56 1.043
90
P RTT002 Rett Syndrome 79 0.998
91
FRY006 Fryns Microphthalmia Syndrome 52 0.998
92
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.998
93
CHN065 Choanal Atresia, Posterior 48 0.998
95
c ATS005 Autosomal Dominant Nonsyndromic Deafness 24 0.998
96
P FTL001 Fetal Alcohol Syndrome 55 0.998
97
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 40 0.998
98
c DFN094 Deafness, Autosomal Dominant 28 31 0.998
99
RNL114 Renal Cell Carcinoma, Nonpapillary 80 0.998
100
DCT002 Ductal Carcinoma in Situ 58 0.998
101
ADN012 Adenocarcinoma in Situ 43 0.998
102
CLF001 Cleft Lip 53 0.998
103
c BRS049 Breast Carcinoma in Situ 50 0.998
104
P DMN002 Dementia 66 0.998
105
BRS099 Breast Ductal Carcinoma 61 0.998
106
P OBS001 Obstructive Jaundice 48 0.998
107
P PTS002 Ptosis 52 0.998
108
OCL011 Ocular Motility Disease 44 0.998
109
VSC002 Vascular Dementia 60 0.998
110
P HRZ002 Horizontal Gaze Palsy with Progressive Scoliosis 37 0.998
111
CRY010 Cryptophthalmos 25 0.998
112
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.944
113
P LNG021 Lung Occult Small Cell Carcinoma 20 0.944
114
LNG019 Lung Combined Type Small Cell Carcinoma 32 0.944
115
P PRV006 Pervasive Developmental Disorder 52 0.815
116
P BRC006 Brachydactyly 51 0.815
117
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.815
118
ACT119 Acute Promyelocytic Leukemia 62 0.815
119
BLM001 Bloom Syndrome 65 0.815
120
P SPP010 Suppressor of Tumorigenicity 3 51 0.815
121
c RTN032 Retinal Cone Dystrophy 1 24 0.815
122
OST159 Osteogenic Sarcoma 66 0.815
123
c BRC062 Brachydactyly, Type D 35 0.815
124
GZP005 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 30 0.815
125
PRT213 Partial Duplication of Chromosome 19 12 0.815
126
P LYN001 Lynch Syndrome 76 0.815
127
SMN007 Seminoma 42 0.815
128
MYL031 Myeloproliferative Neoplasm 66 0.815
129
THR004 Thrombocytosis 53 0.815
130
P HYP040 Hypospadias 51 0.815
131
BRW002 Brown's Tendon Sheath Syndrome 27 0.815
132
P BNG032 Benign Mesothelioma 53 0.815
133
HYP266 Hypoxia 57 0.815
134
c WLF013 Wolfram Syndrome 1 60 0.576
135
CNG506 Congenital Amyoplasia 27 0.576
136
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 0.576
137
P FRG001 Fragile X Syndrome 70 0.576
138
WLD004 Wildervanck Syndrome 28 0.576
139
P DST002 Distal Arthrogryposis 65 0.576
140
HLC007 Helicobacter Pylori Infection 67 0.576
141
c DNR004 Duane Retraction Syndrome 2 28 0.576
142
CHR072 Chordoma 57 0.576
143
SKN019 Skin Melanoma 71 0.576
144
SBM006 Submucosal Cleft Palate 14 0.576
145
47X002 47,xyy 48 0.576
146
P GST044 Gastritis 55 0.576
147
SPP007 Suppression Amblyopia 38 0.576
148
AMB002 Amblyopia 50 0.576
149
P KLP003 Klippel-Feil Syndrome 47 0.576
150
c PRC016 Pre-Eclampsia 65 0.576
151
PPL002 Papillary Carcinoma 46 0.576
152
P ECL001 Eclampsia 52 0.576
153
FCL012 Facial Paralysis 49 0.576
154
P END044 Endometriosis 62 0.576
155
P PRN023 Prion Disease 60 0.576
156
BRN015 Bronchiolo-Alveolar Adenocarcinoma 55 0.576
157
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.576
158
P LMY004 Leiomyosarcoma 62 0.576
159
PTH003 Pathologic Nystagmus 52 0.576
160
CHR159 Charlie M Syndrome 21 0.576
161
OVR094 Ovarian Epithelial Cancer 39 0.576
162
RNL065 Renal Cell Carcinoma, Papillary, 1 79 0.470
163
SQM013 Squamous Cell Carcinoma, Head and Neck 73 0.330
164
c LKM063 Leukemia, Chronic Myeloid 71 0.330
165
MYL009 Myelodysplastic Syndrome 67 0.330
166
DFF005 Diffuse Large B-Cell Lymphoma 54 0.330
167
LMY014 Leiomyoma, Uterine 56 0.330
168
P PSR002 Psoriasis 63 0.330
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