Search results for "COMP"

36 hits were found for 'COMP'

# Family MCID Name MIFTS Score
1
c EPP016 Epiphyseal Dysplasia, Multiple 1 27 31.409
2
PSD012 Pseudoachondroplasia 60 10.413
3
P MLT007 Multiple Epiphyseal Dysplasia 57 6.870
4
P ART023 Arthropathy 54 4.214
5
c MLT030 Multiple Epiphyseal Dysplasia, Dominant 20 4.214
6
c EPP014 Epiphyseal Dysplasia, Multiple, 4 34 3.452
7
RLP001 Relapsing Polychondritis 63 3.029
8
TND004 Tendinopathy 32 3.029
9
KSH004 Kashin-Beck Disease 24 3.029
10
DST005 Diastrophic Dysplasia 53 2.980
11
SPN250 Spondyloepimetaphyseal Dysplasia 51 2.980
12
TND005 Tendinitis 38 2.980
13
LNG040 Langer Mesomelic Dysplasia 35 2.980
14
HMP018 Hemophilic Arthropathy 34 2.980
15
P ART022 Arthritis 65 0.289
16
P RHM011 Rheumatoid Arthritis 94 0.256
17
P OST012 Osteoarthritis 80 0.244
18
P MYP004 Myopathy 53 0.109
19
P PNC035 Pancreatic Cancer 82 0.077
20
HDG012 Hodgkin Lymphoma 79 0.077
21
P PNC044 Pancreatitis 59 0.077
22
PLM001 Pulmonary Tuberculosis 60 0.077
23
ALC006 Alcoholic Hepatitis 58 0.077
24
P ADN016 Adenocarcinoma 49 0.077
25
INT066 Interstitial Lung Disease 44 0.077
26
END072 Endotheliitis 44 0.077
27
RNL077 Renal Fibrosis 41 0.077
28
SPL004 Splenic Marginal Zone Lymphoma 40 0.077
29
URT010 Ureteral Obstruction 39 0.077
30
BNF002 Bone Fracture 39 0.077
31
CHN015 Chondrodysplasia 37 0.077
32
c LNG064 Lung Cancer Susceptibility 3 32 0.077
33
c ALP005 Alpha Chain Disease 20 0.077
34
THR067 Thrombophilia Due to Protein C Deficiency, Autosomal Dominant 17 0.077
35
HLS001 Heel Spur 15 0.077
36
THR088 Thrombophilia Due to Protein S Deficiency, Autosomal Recessive 11 0.077