Gene table: search width pubmed_id = 18952429


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Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Reducing body myopathy (1A and 1B) - (XD)
5.33
18274675
18952429
FHL1 (Xq26.3)
Four and a half LIM domain 1
* Scapuloperoneal myopathy, X-linked dominant - SPM
* Emery-dreifuss muscular dystrophy 6 - EDMD6
* X-linked myopathy with postural muscle atrophy - XMPMA
* Myopathy, reducing body, X-linked, childhood-onset
* Rigid spine syndrome related to FHL1 - RSS
* Myopathy, reducing body, X-linked, severe early-onset
* Rigid spine syndrome - RSMD1