neuronal ceroid lipofuscinosis 8 neuronal ceroid lipofuscinosis 8 northern epilepsy variant https://github.com/monarch-initiative/mondo/issues/6406 https://rarediseases.info.nih.gov/diseases/2163/epilepsy-mental-deterioration-finnish-type https://rarediseases.info.nih.gov/diseases/4010/northern-epilepsy https://www.malacards.org/card/ceroid_lipofuscinosis_neuronal_8_northern_epilepsy_variant Orphanet:530298 CLN8 disease, Northern epilepsy variant neuronal ceroid lipofuscinosis, Northern epilepsy variant Northern epilepsy NCL, Northern epilepsy variant neuronal ceroid lipofuscinosis 8 early onset familial encephalopathy with neuroserpin inclusion bodies progressive epilepsy with intellectual disability, northern epilepsy progressive epilepsy - intellectual disability, Finnish type CLN8 disease, EPMR (subtype) UMLS:C1864923 OMIM:610003 GARD:0004010 DOID:0110724 epilepsy mental deterioration Finnish type progressive myoclonic epilepsy with neuroserpin inclusion bodies ICD10CM:G40.3 CLN8 disease, late infantile (subtype) MONDO:0012391 EPMR ceroid lipofuscinosis neuronal 8 progressive epilepsy-intellectual disability syndrome, Finnish type epilepsy, progressive, with mental retardation Progressive epilepsy-intellectual deficit, Finnish type (also known as Northern epilepsy) is a subtype of neuronal ceroid lipofuscinosis (NCL) characterized by seizures, progressive decline of intellectual capacities and variable loss of vision. MEDGEN:355328 CLN8 Orphanet:1947 monogenic epilepsy syndromic dyslipidemia progressive myoclonus epilepsy