Gene table: search width pubmed_id = 22703880


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

protein
All allelic disease phenotypes - locus/disease symbols
Spinal muscular atrophy with progressive myoclonic epilepsy - (AR)
12.13
22703880
ASAH1 (8p22)
N-acylsphingosine amidohydrolase (acid ceramidase) 1
* Spinal muscular atrophy with progressive myoclonic epilepsy - SMAPME