LONP1 deficiency

Synonym(s)
- Cerebral, ocular, dental, auricular, and skeletal (CODAS) syndrome
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- LONP1 / Lon Peptidase 1, Mitochondrial
  19p13.2
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Lon protease homolog, mitochondrial
Disease group(s)
- 11.3 Disorders of mitochondrial protein quality control