Search results for hoxb1

78 hits were found for hoxb1

# Family MCID Name MIFTS Score
1
c FCL056 Facial Paresis, Hereditary Congenital, 3 24 37.556
2
CNG490 Congenital Hereditary Facial Paralysis-Variable Hearing Loss Syndrome 11 25.552
3
P ATS364 Autism 69 16.066
4
P HRD043 Hereditary Congenital Facial Paresis 18 15.267
5
c ATS007 Autism Spectrum Disorder 72 15.109
6
P STR020 Strabismus 56 14.906
7
P VNT002 Ventricular Septal Defect 58 14.387
8
FCL012 Facial Paralysis 49 12.910
9
TKL001 Tukel Syndrome 52 9.013
10
ATH001 Athabaskan Brainstem Dysgenesis Syndrome 52 7.882
11
HND004 Hand-Foot-Genital Syndrome 47 7.882
12
PRX093 Preaxial Deficiency, Postaxial Polydactyly, and Hypospadias 34 7.882
13
FCL011 Facial Nerve Disease 38 7.882
14
BLL003 Bell's Palsy 48 7.882
15
EMB004 Embryonal Carcinoma 56 3.928
16
MCH006 Mechanical Strabismus 40 3.759
17
MBS002 Moebius Syndrome 54 3.517
18
GLL048 Glial Tumor 52 3.114
19
GLM045 Glioma 63 3.114
20
HLX001 Helix Syndrome 48 2.921
21
c LKM061 Leukemia, Acute Myeloid 83 2.719
22
c FCL030 Facial Paresis, Hereditary Congenital, 1 19 2.359
23
c FCL050 Facial Paresis, Hereditary Congenital, 2 15 2.359
24
HRT011 Heart Septal Defect 49 2.220
25
DBL002 Double Outlet Right Ventricle 57 2.220
26
HMN047 Human Cytomegalovirus Infection 57 2.066
27
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.891
28
P SNS001 Sensorineural Hearing Loss 59 1.891
29
P PNC035 Pancreatic Cancer 86 1.704
30
OST159 Osteogenic Sarcoma 66 1.683
31
c SPN225 Spondyloarthropathy 1 70 1.306
32
SPN051 Spondylitis 51 1.306
33
INF009 Inflammatory Spondylopathy 30 1.306
34
PNC129 Pancreatic Adenocarcinoma 65 1.131
35
TRT001 Teratocarcinoma 42 1.131
36
PNC041 Pancreatic Ductal Adenocarcinoma 51 1.131
37
GST092 Gastroesophageal Reflux 61 0.923
38
c LKM063 Leukemia, Chronic Myeloid 71 0.923
39
SMN007 Seminoma 42 0.923
40
P MLN007 Male Infertility 56 0.923
41
ALT003 Alternating Exotropia 33 0.923
42
ING001 Inguinal Hernia 59 0.923
43
EXT022 Exotropia 42 0.923
44
P PTS002 Ptosis 52 0.923
45
P BRN022 Bronchiectasis 60 0.923
46
P BRS047 Breast Cancer 98 0.811
47
P RTT002 Rett Syndrome 79 0.760
48
END057 Endometrial Cancer 72 0.653
49
c DNR003 Duane Retraction Syndrome 1 37 0.653
50
NRL016 Neural Tube Defects 81 0.653
51
RNL051 Renal Cysts and Diabetes Syndrome 57 0.653
52
c BRN108 Branchiootic Syndrome 1 62 0.653
53
c RNL122 Renal Hypodysplasia/aplasia 3 44 0.653
54
c VNW005 Von Willebrand Disease, Type 1 45 0.653
55
P SPP010 Suppressor of Tumorigenicity 3 51 0.653
56
DGR001 Digeorge Syndrome 62 0.653
57
P RNL100 Renal Hypodysplasia/aplasia 1 63 0.653
58
P KBK002 Kabuki Syndrome 1 65 0.653
59
GZP005 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 30 0.653
60
P SCL018 Scoliosis 57 0.653
61
ORL015 Oral Squamous Cell Carcinoma 43 0.653
62
P VNW001 Von Willebrand's Disease 65 0.653
63
P PLY041 Polymyositis 59 0.653
64
P NRB001 Neuroblastoma 66 0.653
65
c CHR684 Chronic Kidney Disease 69 0.653
66
P MYP004 Myopathy 67 0.653
67
P PTT006 Pituitary Adenoma 55 0.653
68
ADN018 Adenoma 59 0.653
69
P DRM010 Dermatomyositis 61 0.653
70
P RSP003 Respiratory Failure 74 0.653
71
BRW002 Brown's Tendon Sheath Syndrome 27 0.653
72
P INF032 Infertility 57 0.653
73
OCL011 Ocular Motility Disease 44 0.653
74
CHL028 Childhood Type Dermatomyositis 59 0.653
75
P HRZ002 Horizontal Gaze Palsy with Progressive Scoliosis 37 0.653
76
JVN046 Juvenile Polymyositis 17 0.653
77
ORL011 Oral Cancer 60 0.653
78
P OVR042 Ovarian Cancer 88 0.573
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