Search results for "COMP"

37 hits were found for 'COMP'

# Family MCID Name MIFTS Score
1
c MLT043 Multiple Epiphyseal Dysplasia 1 17 12.811
2
PSD012 Pseudoachondroplasia 68 9.877
3
P MLT007 Multiple Epiphyseal Dysplasia 73 9.023
4
P ART023 Arthropathy 64 4.137
5
c MLT030 Multiple Epiphyseal Dysplasia, Dominant 23 4.137
6
RLP001 Relapsing Polychondritis 72 2.975
7
TND004 Tendinopathy 38 2.975
8
c THN001 Thanatophoric Dysplasia 62 2.926
9
DST005 Diastrophic Dysplasia 59 2.926
10
SPN008 Spondyloepiphyseal Dysplasia Congenita 56 2.926
11
SPN250 Spondyloepimetaphyseal Dysplasia 51 2.926
12
TND005 Tendinitis 45 2.926
13
HMP018 Hemophilic Arthropathy 41 2.926
14
LNG040 Langer Mesomelic Dysplasia 39 2.926
15
P FNC025 Fanconi Anemia, Complementation Group J 55 2.069
16
c FNC027 Fanconi Anemia, Complementation Group a 41 2.069
17
P ART022 Arthritis 75 0.290
18
P RHM011 Rheumatoid Arthritis 94 0.257
19
P OST012 Osteoarthritis 76 0.245
20
P MYP004 Myopathy 62 0.110
21
P PNC035 Pancreatic Cancer 93 0.078
22
NNH001 Non-Hodgkin Lymphoma 73 0.078
23
c PNC044 Pancreatitis 69 0.078
24
P SHR002 Short Stature 68 0.078
25
P ADN016 Adenocarcinoma 59 0.078
26
INT066 Interstitial Lung Disease 53 0.078
27
END072 Endotheliitis 51 0.078
28
RNL077 Renal Fibrosis 49 0.078
29
URT010 Ureteral Obstruction 47 0.078
30
BNF002 Bone Fracture 45 0.078
31
LNG029 Lung Adenocarcinoma 44 0.078
32
CHN015 Chondrodysplasia 44 0.078
33
P ALP005 Alpha Chain Disease 25 0.078
34
THR067 Thrombophilia Due to Protein C Deficiency, Autosomal Dominant 24 0.078
35
HLS001 Heel Spur 20 0.078
36
KSH004 Kashin–beck Disease 11 0.078
37
THR088 Thrombophilia Due to Protein S Deficiency, Autosomal Recessive 8 0.078