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neuronal intranuclear inclusion disease

Go to external page http://purl.obolibrary.org/obo/MONDO_0011327

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. [ Orphanet:2289 ]

Synonyms: neuronal intranuclear inclusion disease

This is just here as a test because I lose it

Term information

database cross reference
  • icd11.foundation:693937860 (MONDO:equivalentTo)
  • SCTID:715437003 (MONDO:equivalentTo)
  • Orphanet:2289 (OMIM:603472)
  • DOID:0081294 (MONDO:equivalentTo)
  • OMIM:603472 (Orphanet:2289/e)
  • UMLS:C1863843 (MONDO:equivalentTo)
  • NCIT:C122655 (MONDO:equivalentTo)
  • GARD:3971 (MONDO:GARD)
  • MESH:C537395 (Orphanet:2289/e)
  • MEDGEN:355075 (MONDO:equivalentTo)
Subsets

matrix_llm__is_cancer_other, gard_rare, ordo_disorder, matrix_llm__txgnn_other, mondo_top_grouping_member, harrisons_view_psychiatric_disorder, matrix_included, nord_rare, matrix_txgnn_grouping_member, rare, matrix_txgnn_grouping_psychiatric_disorder, orphanet_rare, harrisons_view_nervous_system_disorder, matrix_llm__is_glucose_dysfunction_other, otar, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, matrix_txgnn_grouping_neurodegenerative_disease, matrix_llm__tag_existing_treatment_other, mondo_top_grouping_psychiatric_disorder, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_member, mondo_top_grouping_nervous_system_disorder, harrisons_view_hereditary_disease

exactMatch

http://identifiers.org/snomedct/715437003

http://identifiers.org/medgen/355075

http://linkedlifedata.com/resource/umls/id/C1863843

http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/693937860

https://omim.org/entry/603472

http://purl.obolibrary.org/obo/DOID_0081294

http://identifiers.org/mesh/C537395

http://purl.obolibrary.org/obo/NCIT_C122655

http://www.orpha.net/ORDO/Orphanet_2289

has related synonym

Niid

neuronal intranuclear hyaline inclusion disease

id

MONDO:0011327

seeAlso

https://rarediseases.info.nih.gov/diseases/3971/neuronal-intranuclear-inclusion-disease