neuronal ceroid lipofuscinosis https://www.malacards.org/card/neuronal_ceroid_lipofuscinosis_2 NCL icd11.foundation:1568332253 ICD10CM:E75.4 MEDGEN:10326 A group of inherited progressive degenerative brain diseases characterized clinically by a decline of mental and other capacities, epilepsy, and vision loss through retinal degeneration, and histopathologically by intracellular accumulation of an autofluorescent material, ceroid lipofuscin, in the neuronal cells in the brain and in the retina. ceroid lipofuscinoses DOID:14503 OMIMPS:256730 NANDO:1200150 SCTID:42012007 NCIT:C61257 UMLS:C0027877 MONDO:0016295 NANDO:2200573 GARD:0010739 neuronal ceroid lipofuscinosis Orphanet:216 lysosomal lipid storage disorder inherited neurodegenerative disorder