Search results for "[genes] FHL1"

20 hits were found for '[genes] FHL1'

# Family MCID Name MIFTS Score
1
SCP009 Scapuloperoneal Myopathy, X-Linked Dominant 30 22.126
2
MYP056 Myopathy, X-Linked, with Postural Muscle Atrophy 25 22.126
3
P EMR001 Emery-Dreifuss Muscular Dystrophy 57 20.697
4
RDC012 Reducing Body Myopathy, X-Linked 1b, with Late Childhood or Adult Onset 14 19.162
5
RDC010 Reducing Body Myopathy 32 19.162
6
P MSC005 Muscular Dystrophy 64 17.492
7
SCP010 Scapuloperoneal Myopathy 18 17.492
8
P MYP004 Myopathy 67 15.646
9
RDC011 Reducing Body Myopathy, X-Linked 1a, Severe, Infantile or Early Childhood Onset 20 13.549
10
P CRD011 Cardiomyopathy 66 11.063
11
P MSC007 Muscle Hypertrophy 55 11.063
12
FTD001 Foot Drop 34 11.063
13
c PRG106 Progressive Muscular Dystrophy 40 11.063
14
FCS012 Facioscapulohumeral Muscular Dystrophy 1 50 7.823
15
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 41 7.823
16
P EMR004 Emery-Dreifuss Muscular Dystrophy, X-Linked 27 7.823
17
CHL088 Childhood-Onset Reducing Body Myopathy, X-Linked 8 7.823
18
c FHL001 Fhl1-Related Emery-Dreifuss Muscular Dystrophy, X-Linked 10 7.823
19
ERL010 Early-Onset Severe Reducing Body Myopathy, X-Linked 3 7.823
20
c FHL002 Fhl1-Related Myofibrillar Myopathy 7 7.823