neuronal ceroid lipofuscinosis 13

Summary
Synonym
  • CLN13
  • neuronal ceroid lipofuscinosis 13 Kufs type
Definition
A neuronal ceroid lipofuscinosis that is characterized by autosomal recessive inheritance with adult onset of progressive cognitive decline and motor dysfunction leading to dementia and often early death and has_material_basis_in homozygous or compound heterozygous mutation in the CTSF gene on chromosome 11q13.
Super Class
autosomal recessive disease neuronal ceroid lipofuscinosis
Disease Ontology
DOID:0110727
Mondo Disease Ontology
ORDO
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
8722 CTSF cathepsin F
Displaying 1 entry
Gene ID Gene Symbol Description Source
56464 Ctsf cathepsin F
Displaying 1 entry
Gene ID Gene Symbol Description Source
40628 CtsF Cathepsin F
Displaying 1 entry
Gene ID Gene Symbol Description Source
179240 tag-196 Cathepsin F
The Human Phenotype Ontology
Displaying entry 21 - 21 of 21 in total
HPO ID HPO Term
HP:0002312 Clumsiness
Displaying 1 entry
Gene ID Gene Symbol Description
5538 PPT1 palmitoyl-protein thioesterase 1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024