Search results for lemd3

73 hits were found for lemd3

# Family MCID Name MIFTS Score
1
BSC001 Buschke-Ollendorff Syndrome 56 57.864
2
OST014 Osteopoikilosis 41 35.057
3
MLR003 Melorheostosis 48 21.192
4
MLR010 Melorheostosis with Osteopoikilosis 23 20.064
5
END081 Endosteal Hyperostosis, Autosomal Dominant 54 10.393
7
ODN023 Odontochondrodysplasia 70 10.393
8
P EMR001 Emery-Dreifuss Muscular Dystrophy 62 10.393
9
ART141 Arteriovenous Malformations of the Brain 58 9.980
10
ELS005 Elastoma 17 8.899
11
12Q002 12q14 Microdeletion Syndrome 28 8.882
12
c EMR018 Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant 54 7.349
13
c CNG551 Congenital Muscular Dystrophy-Dystroglycanopathy A7 29 7.349
14
FBR010 Fibrogenesis Imperfecta Ossium 25 7.349
15
GRN013 Greenberg Dysplasia 54 7.349
16
c CNG411 Congenital Disorder of Glycosylation, Type in 66 7.349
17
AXL003 Axial Osteomalacia 31 7.349
18
P PLG001 Pelger-Huet Anomaly 52 7.349
19
HTC003 Hutchinson-Gilford Progeria Syndrome 65 7.349
20
WLK001 Walker-Warburg Syndrome 62 7.349
21
VRT003 Vertebrobasilar Insufficiency 31 7.349
22
ORN001 Ornithosis 39 7.349
23
P EMR017 Emery-Dreifuss Muscular Dystrophy 1, X-Linked 48 7.349
24
c CRD069 Cardiomyopathy, Dilated, 1h 41 7.349
25
P DCR004 Dacryocystitis 36 7.349
26
P ACT070 Acute Inflammation of Lacrimal Passage 18 7.349
27
MLR023 Melorheostosis, Isolated 32 3.388
28
P BND020 Bone Disease 60 1.691
29
HYP068 Hyperostosis 47 1.636
30
DYS018 Dysostosis 43 1.395
31
c EXS019 Exostoses, Multiple, Type I 54 1.291
32
EXS001 Exostosis 49 1.291
33
P SYS005 Systemic Scleroderma 73 1.291
34
SKL017 Skeletal Dysplasias 41 1.159
35
c LCL006 Localized Scleroderma 64 1.159
36
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 1.118
37
BCK006 Back Pain 43 1.072
38
DWR001 Dwarfism 45 0.955
39
GRM010 Germ Cells Tumors 33 0.946
40
MXD032 Mixed Germ Cell Tumor 24 0.946
41
MCR103 Microtia 40 0.946
42
CLL041 Collagenoma, Familial Cutaneous 20 0.773
43
P ALP008 Alopecia 53 0.773
44
P BRS047 Breast Cancer 97 0.533
45
P ATS364 Autism 72 0.533
46
P PNC035 Pancreatic Cancer 86 0.533
47
P SLV027 Silver-Russell Syndrome 1 52 0.423
48
DNC004 Diencephalic Syndrome 36 0.423
49
PRM334 Primary Bone Dysplasia with Increased Bone Density 15 0.423
50
ISL014 Isolated Growth Hormone Deficiency, Type Ia 54 0.345
51
c SLV031 Silver-Russell Syndrome 5 24 0.345
52
NVS017 Nevus, Epidermal 66 0.345
53
c THR092 Thrombophilia Due to Thrombin Defect 74 0.345
54
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 50 0.299
55
P CHN059 Chondrocalcinosis 51 0.299
56
LRN003 Learning Disability 49 0.299
57
c SML038 Small Cell Cancer of the Lung 69 0.244
58
c UNP012 Uniparental Disomy of Chromosome 7 14 0.244
59
MTR087 Maternal Uniparental Disomy 27 0.244
60
P LNG032 Lung Cancer 98 0.173
61
CST001 Costello Syndrome 68 0.173
62
TRC118 Trichodentoosseous Syndrome 42 0.173
63
FBR054 Fibroma 44 0.173
64
P NNN008 Noonan Syndrome 1 76 0.173
65
CLF027 Cleft Palate, Isolated 64 0.173
66
P ART005 Arteriovenous Malformation 65 0.173
67
SPN027 Spinal Stenosis 59 0.173
68
P OSS001 Ossifying Fibroma 42 0.173
69
LYS002 Lysosomal Storage Disease 51 0.173
70
CLF001 Cleft Lip 54 0.173
71
KLD004 Keloid Disorder 39 0.173
72
ERY069 Erythrokeratoderma ''en Cocardes'' 26 0.173
73
c PSD047 Pseudo-Turner Syndrome 52 0.173
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