Gene table: search width pubmed_id = 23933735


Grey lines background indicate newly added items
Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Congenital Myopathy 11 - (AR)
3.39
23933735
HACD1 (10p12.33)
Protein tyrosine phosphatase-like (3-Hydroxyacyl-CoA dehydratase
* Arrhythmogenic right ventricular cardiomyopathy 6 - ARVC6
* Arrhythmogenic right ventricular dysplasia, familial, 6 - ARVD6
* Congenital Myopathy 11 - CMYP11