Search results for "[genes] FHL1"

21 hits were found for '[genes] FHL1'

# Family MCID Name MIFTS Score
1
SCP009 Scapuloperoneal Myopathy, X-Linked Dominant 29 22.033
2
MYP056 Myopathy, X-Linked, with Postural Muscle Atrophy 27 22.033
3
P EMR001 Emery-Dreifuss Muscular Dystrophy 55 20.610
4
RDC010 Reducing Body Myopathy 31 19.081
5
RDC012 Reducing Body Myopathy, X-Linked 1b, with Late Childhood or Adult Onset 13 19.081
6
P MYP004 Myopathy 67 17.418
7
RDC011 Reducing Body Myopathy, X-Linked 1a, Severe, Infantile or Early Childhood Onset 19 17.418
8
SCP010 Scapuloperoneal Myopathy 19 17.418
9
P MSC007 Muscle Hypertrophy 58 15.579
10
P MYF003 Myofibrillar Myopathy 42 13.492
11
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 39 13.492
12
P EMR004 Emery-Dreifuss Muscular Dystrophy, X-Linked 25 13.492
13
c FHL001 Fhl1-Related Emery-Dreifuss Muscular Dystrophy, X-Linked 10 13.492
14
CHL088 Childhood-Onset Reducing Body Myopathy, X-Linked 8 13.492
15
c FHL002 Fhl1-Related Myofibrillar Myopathy 7 13.492
16
ERL010 Early-Onset Severe Reducing Body Myopathy, X-Linked 2 13.492
17
P HMP002 Hemophagocytic Lymphohistiocytosis 64 11.016
18
P CRD194 Cardiomyopathy, Familial Hypertrophic 62 11.016
19
MSC051 Muscular Dystrophy, Rigid Spine, 1 45 11.016
20
c PRG106 Progressive Muscular Dystrophy 40 11.016
21
FTD001 Foot Drop 33 11.016