Search results for col11a1

73 hits were found for col11a1

# Family MCID Name MIFTS Score
1
MRS002 Marshall Syndrome 47 7.111
2
P FBR025 Fibrochondrogenesis 52 6.791
3
c FBR029 Fibrochondrogenesis 1 29 6.130
4
c STC013 Stickler Syndrome, Type Ii 40 5.863
5
P STC001 Stickler Syndrome 53 4.748
6
P MYP006 Myopia 58 4.611
7
c DFN379 Deafness, Autosomal Dominant 37 15 4.137
8
RTN017 Retinal Detachment 62 3.633
9
INT146 Intervertebral Disc Disease 64 3.261
10
P SNS001 Sensorineural Hearing Loss 62 3.215
11
PRM024 Primary Angle-Closure Glaucoma 39 3.215
12
HYP748 Hypertelorism 50 3.162
13
P CTR002 Cataract 62 3.131
14
DHY002 Dihydropyrimidine Dehydrogenase Deficiency 58 3.096
15
EST005 Esotropia 44 3.096
16
PHR008 Pharynx Squamous Cell Carcinoma 24 3.096
17
CLF027 Cleft Palate, Isolated 67 2.662
18
MGL003 Megalocornea 39 2.604
19
TLC001 Telecanthus 34 2.604
20
P VTR008 Vitreoretinal Degeneration 30 2.569
21
DNN002 Donnai-Barrow Syndrome 57 2.528
22
P STR020 Strabismus 57 2.528
23
P OTS002 Otospondylomegaepiphyseal Dysplasia 47 2.528
24
MCR037 Macroglossia 46 2.528
25
CLF028 Cleft Soft Palate 34 2.528
26
VTR002 Vitreous Syneresis 32 2.528
27
VTR001 Vitreoretinal Dystrophy 26 2.528
28
c ATS409 Autosomal Recessive Nonsyndromic Deafness 32 17 2.528
29
c ATS076 Autosomal Recessive Stickler Syndrome 30 1.841
30
ATS292 Autosomal Dominant Myopia-Midfacial Retrusion-Sensorineural Hearing Loss-Rhizomelic Dysplasia Syndrome 10 1.841
31
CNN005 Connective Tissue Disease 68 0.511
32
PRD012 Periodic Fever, Aphthous Stomatitis, Pharyngitis and Adenitis 30 0.205
33
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.184
34
P LNG032 Lung Cancer 99 0.130
35
P OVR042 Ovarian Cancer 89 0.130
36
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.130
37
P CLR023 Colorectal Cancer 100 0.112
38
OST012 Osteoarthritis 80 0.112
39
c STC015 Stickler Syndrome, Type I 40 0.112
40
P BRS047 Breast Cancer 99 0.092
41
P PNC035 Pancreatic Cancer 86 0.092
42
P GST053 Gastric Cancer 85 0.092
43
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.092
44
c BRN108 Branchiootic Syndrome 1 62 0.092
45
P SCL018 Scoliosis 61 0.092
46
ADN018 Adenoma 60 0.092
47
SYN143 Syndromic Telecanthus 10 0.092
48
P LNG064 Lung Cancer Susceptibility 3 79 0.065
49
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.065
50
SVR004 Severe Combined Immunodeficiency 74 0.065
51
P SYS005 Systemic Scleroderma 68 0.065
52
c SML038 Small Cell Cancer of the Lung 67 0.065
53
P PLM036 Pulmonary Fibrosis 66 0.065
54
P ADN016 Adenocarcinoma 65 0.065
55
IDP011 Idiopathic Interstitial Pneumonia 65 0.065
56
CLR108 Colorectal Adenoma 64 0.065
57
P PLY014 Polycystic Kidney Disease 61 0.065
58
SPN027 Spinal Stenosis 58 0.065
59
P INF037 Inflammatory Bowel Disease 57 0.065
60
OST024 Osteoporosis-Pseudoglioma Syndrome 55 0.065
61
OST016 Osteochondrosis 55 0.065
62
P BRC006 Brachydactyly 54 0.065
63
SPN019 Spondylolisthesis 54 0.065
64
P PRR016 Pierre Robin Syndrome 53 0.065
65
c NNS007 Nonsyndromic Deafness 51 0.065
66
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.065
67
HLX001 Helix Syndrome 46 0.065
68
DVR002 Diverticulitis 44 0.065
69
SKL017 Skeletal Dysplasias 41 0.065
70
VTR003 Vitreous Detachment 41 0.065
71
ISL075 Isolated Pierre Robin Sequence 30 0.065
72
c STC007 Stickler Syndrome, Type 3 21 0.065
73
P LTH050 Lethal Chondrodysplasia 15 0.065
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