Gene table: search width pubmed_id = 25193783


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
Isolated mitochondrial myopathy - (AD)
16.63
25193783
CHCHD10 (22q11.2-q13.2)
Coiled-coil-helix-coiled-coil-helix domain containing 10(M)
* Amyotrophic lateral sclerosis and/or frontotemporal dementia - FTDALS2
* late-onset spinal motor neuronopathy, Jokela type - SMAJ