has material basis in germline mutation in disease arises from feature disease has basis in feature NOTCH2NLC movement disorder neurodegenerative disease neuronal intranuclear inclusion disease https://rarediseases.info.nih.gov/diseases/3971/neuronal-intranuclear-inclusion-disease https://www.malacards.org/card/neuronal_intranuclear_inclusion_disease MESH:C537395 DOID:0081294 MONDO:0011327 neuronal intranuclear hyaline inclusion disease Orphanet:2289 NCIT:C122655 icd11.foundation:693937860 SCTID:715437003 GARD:0003971 UMLS:C1863843 MEDGEN:355075 OMIM:603472 neuronal intranuclear inclusion disease Neuronal intranuclear inclusion disease (NIID) is a very rare multisystem neurodegenerative disorder characterized by the presence of eosinophilic intranuclear inclusions in neuronal and glial cells, and neuronal loss. hereditary dementia inherited neurodegenerative disorder