Cathepsin F deficiency

Synonym(s)
- Autosomal recessive Kufs disease type B,
- CLN13 disease
Type

Disease
External link(s)
- IEMbase
Gene
- CTSF / Cathepsin F
  11q13.2
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Cathepsin F
Disease group(s)
- 20.4 Neuronal ceroid lipofuscinoses (NCL)