Progranulin deficiency

Synonym(s)
- CLN11 disease
Type

Disease
External link(s)
- IEMbase
Gene
- GRN / Granulin
  17q21.31
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Granulin
Disease group(s)
- 20.4 Neuronal ceroid lipofuscinoses (NCL)
Child entries
- Frontotemporal lobar degeneration with TDP-43 inclusions