Search results for col11a1

90 hits were found for col11a1

# Family MCID Name MIFTS Score
1
c STC013 Stickler Syndrome, Type Ii 36 6.765
2
MRS002 Marshall Syndrome 58 6.476
3
c FBR029 Fibrochondrogenesis 1 40 5.990
4
c DFN379 Deafness, Autosomal Dominant 37 20 4.075
5
P STC001 Stickler Syndrome 56 3.998
6
P MYP006 Myopia 55 3.890
7
P FBR025 Fibrochondrogenesis 48 3.775
8
P BRS047 Breast Cancer 97 3.641
9
CNN005 Connective Tissue Disease 68 3.075
10
CLF027 Cleft Palate, Isolated 64 2.936
11
INT146 Intervertebral Disc Disease 63 2.936
12
P SNS001 Sensorineural Hearing Loss 60 2.915
13
RTN017 Retinal Detachment 61 2.893
14
P CTR002 Cataract 60 2.814
15
ART016 Aortic Aneurysm 69 2.781
16
PRM024 Primary Angle-Closure Glaucoma 40 2.397
17
HYP748 Hypertelorism 50 2.343
18
MGL003 Megalocornea 48 2.343
19
SPN027 Spinal Stenosis 59 2.310
20
P ECT006 Ectodermal Dysplasia 62 2.271
21
P MLT007 Multiple Epiphyseal Dysplasia 58 2.271
22
P STR020 Strabismus 55 2.271
23
EST005 Esotropia 42 2.271
24
PHR008 Pharynx Squamous Cell Carcinoma 16 2.271
25
P OST122 Osteogenesis Imperfecta, Type Iii 57 1.695
26
TLC001 Telecanthus 35 1.695
27
c PNT032 Pontocerebellar Hypoplasia, Type 9 41 1.656
28
c ATS076 Autosomal Recessive Stickler Syndrome 32 1.656
29
P VTR008 Vitreoretinal Degeneration 29 1.656
30
ATS292 Autosomal Dominant Myopia-Midfacial Retrusion-Sensorineural Hearing Loss-Rhizomelic Dysplasia Syndrome 13 1.656
31
ODN023 Odontochondrodysplasia 68 1.606
32
SPN209 Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations 66 1.606
33
DHY002 Dihydropyrimidine Dehydrogenase Deficiency 58 1.606
34
c OTS013 Otospondylomegaepiphyseal Dysplasia, Autosomal Recessive 57 1.606
35
FND002 Fundus Dystrophy 55 1.606
36
KNS001 Kniest Dysplasia 53 1.606
37
P OTS014 Otospondylomegaepiphyseal Dysplasia, Autosomal Dominant 52 1.606
39
MCR037 Macroglossia 45 1.606
40
P ORF002 Orofacial Cleft 44 1.606
41
SCH030 Schneckenbecken Dysplasia 44 1.606
42
RTN002 Retinal Perforation 38 1.606
43
CLF028 Cleft Soft Palate 37 1.606
44
VTR002 Vitreous Syneresis 31 1.606
45
KHL001 Kohler's Disease 30 1.606
46
VTR001 Vitreoretinal Dystrophy 22 1.606
47
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.236
48
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.202
49
P CLR023 Colorectal Cancer 99 0.122
50
P LNG032 Lung Cancer 98 0.122
51
P OVR042 Ovarian Cancer 88 0.122
52
OST012 Osteoarthritis 78 0.122
53
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.122
54
P PNC035 Pancreatic Cancer 84 0.086
55
P GST053 Gastric Cancer 83 0.086
56
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.086
57
c BRN108 Branchiootic Syndrome 1 62 0.086
58
P SCL018 Scoliosis 60 0.086
59
ADN018 Adenoma 59 0.086
60
c STC015 Stickler Syndrome, Type I 40 0.086
61
SYN143 Syndromic Telecanthus 9 0.086
62
P LNG064 Lung Cancer Susceptibility 3 78 0.061
63
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.061
64
SVR004 Severe Combined Immunodeficiency 73 0.061
65
P SYS005 Systemic Scleroderma 68 0.061
66
c SML038 Small Cell Cancer of the Lung 65 0.061
67
P PLM036 Pulmonary Fibrosis 65 0.061
68
CLR108 Colorectal Adenoma 64 0.061
69
P ADN016 Adenocarcinoma 64 0.061
70
P PLY014 Polycystic Kidney Disease 62 0.061
71
OST024 Osteoporosis-Pseudoglioma Syndrome 60 0.061
72
P INF037 Inflammatory Bowel Disease 54 0.061
73
P BRC006 Brachydactyly 53 0.061
74
OST016 Osteochondrosis 53 0.061
75
P PRR016 Pierre Robin Syndrome 52 0.061
76
SPN019 Spondylolisthesis 51 0.061
77
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.061
78
DGN001 Degenerative Disc Disease 48 0.061
79
HLX001 Helix Syndrome 47 0.061
80
AST006 Astigmatism 47 0.061
81
P PNT019 Pontocerebellar Hypoplasia 46 0.061
82
DVR002 Diverticulitis 43 0.061
83
P HYP265 Hypotonia 43 0.061
84
P NNS072 Nonsyndromic Hearing Loss 41 0.061
85
SKL017 Skeletal Dysplasias 40 0.061
86
VTR003 Vitreous Detachment 39 0.061
87
c NNS007 Nonsyndromic Deafness 35 0.061
88
ISL075 Isolated Pierre Robin Sequence 29 0.061
89
SPL005 Splenic Artery Aneurysm 25 0.061
90
P LTH050 Lethal Chondrodysplasia 14 0.061
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