neuronal ceroid lipofuscinosis 6A

Summary
Synonym
  • CLN6
  • neuronal ceroid lipofuscinosis 6
  • neuronal ceroid lipofuscinosis 6 variable age of onset
Definition
A neuronal ceroid lipofuscinosis that is characterized by progressive decline of neurologic function, including visual deterioration in most, cognitive impairment, loss of motor function, and seizures and has_material_basis_in homozygous mutation in the CLN6 gene on chromosome 15q21-q23.
Super Class
autosomal recessive disease neuronal ceroid lipofuscinosis
External Links
Disease Ontology
DOID:0110729
Mondo Disease Ontology
ORDO
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying entries 1 - 10 of 12 in total
Gene ID Gene Symbol Description Source
47 ACLY ATP citrate lyase
1203 CLN5 CLN5 intracellular trafficking protein
2571 GAD1 glutamate decarboxylase 1
2572 GAD2 glutamate decarboxylase 2
3956 LGALS1 galectin 1
5310 PKD1 polycystin 1, transient receptor potential channel interacting
5538 PPT1 palmitoyl-protein thioesterase 1
5660 PSAP prosaposin
6609 SMPD1 sphingomyelin phosphodiesterase 1
7957 EPM2A EPM2A glucan phosphatase, laforin
The Human Phenotype Ontology
Displaying entries 41 - 50 of 61 in total
HPO ID HPO Term
HP:0007663 Reduced visual acuity
HP:0008770 Obsessive-compulsive trait
HP:0010819 Atonic seizure
HP:0010841 Multifocal epileptiform discharges
HP:0010845 EEG with generalized slow activity
HP:0010850 EEG with spike-wave complexes
HP:0010852 EEG with photoparoxysmal response
HP:0011147 Typical absence seizure
HP:0011167 Focal tonic seizure
HP:0011194 EEG with series of focal spikes
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: August 19, 2024