Search results for "[genes] FHL1"

22 hits were found for '[genes] FHL1'

# Family MCID Name MIFTS Score
1
MYP056 Myopathy, X-Linked, with Postural Muscle Atrophy 25 21.971
2
P EMR001 Emery-Dreifuss Muscular Dystrophy 56 20.552
3
SCP009 Scapuloperoneal Myopathy, X-Linked Dominant 25 20.552
4
RDC010 Reducing Body Myopathy 29 19.027
5
RDC012 Reducing Body Myopathy, X-Linked 1b, with Late Childhood or Adult Onset 15 19.027
6
P MYP004 Myopathy 66 17.370
7
P MSC005 Muscular Dystrophy 64 17.370
8
SCP010 Scapuloperoneal Myopathy 26 17.370
9
RDC011 Reducing Body Myopathy, X-Linked 1a, Severe, Infantile or Early Childhood Onset 16 13.454
10
P CRD011 Cardiomyopathy 68 10.986
11
P MSC007 Muscle Hypertrophy 52 10.986
12
P MYF003 Myofibrillar Myopathy 48 10.986
13
c PRG106 Progressive Muscular Dystrophy 43 10.986
14
FTD001 Foot Drop 31 10.986
15
FCS012 Facioscapulohumeral Muscular Dystrophy 1 51 7.768
16
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 38 7.768
17
P EMR004 Emery-Dreifuss Muscular Dystrophy, X-Linked 26 7.768
18
XLN189 X-Linked Scapuloperoneal Muscular Dystrophy 14 7.768
19
c FHL001 Fhl1-Related Emery-Dreifuss Muscular Dystrophy, X-Linked 11 7.768
20
c FHL002 Fhl1-Related Myofibrillar Myopathy 8 7.768
21
CHL088 Childhood-Onset Reducing Body Myopathy, X-Linked 4 7.768
22
ERL010 Early-Onset Severe Reducing Body Myopathy, X-Linked 4 7.768