Neuronal Ceroid Lipofuscinosis

About the Disease
Neuronal Ceroid Lipofuscinosis, also known as hereditary ceroid lipofuscinosis, is related to ceroid lipofuscinosis, neuronal, 10 and ceroid lipofuscinosis, neuronal, 3, and has symptoms including myoclonus, seizures and abnormality of extrapyramidal motor function. An important gene associated with Neuronal Ceroid Lipofuscinosis is CLN3 (CLN3 Lysosomal/Endosomal Transmembrane Protein, Battenin). The drugs Cysteamine and Acetylcysteine have been mentioned in the context of this disorder. Affiliated tissues include retina, brain and spleen, and related phenotypes are no effect and no effect

Common Targets
NPM1 | CTSF | TPP1 | CLN3 | KCTD7 | CLN6 | TGM2 | CLN8 | CLCN2 | RORB | CLN5 | GRN | Glutamate Receptor Ionotropic AMPA Receptor | TTPA | MFSD8 | PPARA | PPT1 | DNAJC5 | RARS2 | CTSD

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Common Variable Immunodeficiency