A rare neurodegenerative disorder leading to dementia. It is characterized by frontotemporal lobar degeneration with accumulation of tau proteins which form Pick bodies. [ NCIT:P378 ]
Synonyms: PICK disease of brain Pick disease dementia in Pick's disease lobar atrophy of brain
Term information
- SCTID:13092008 (MONDO:equivalentTo)
- UMLS:C0236642 (MONDO:equivalentTo)
- ICD9:331.11 (MONDO:i2s)
- DOID:11870 (MONDO:equivalentTo)
- ICD10CM:G31.01 (MONDO:equivalentTo)
- MEDGEN:116020 (MONDO:equivalentTo)
- OMIM:172700 (MONDO:equivalentTo)
- NCIT:C85008 (MONDO:equivalentTo)
- MESH:D020774 (MONDO:equivalentTo)
- EFO:0003096 (MONDO:equivalentTo)
gard_rare, matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, otar, matrix_llm__tag_qualy_lost_other, mondo_top_grouping_member, matrix_llm__txgnn_other, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, matrix_txgnn_grouping_neurodegenerative_disease, harrisons_view_psychiatric_disorder, matrix_llm__tag_existing_treatment_other, matrix_included, mondo_top_grouping_psychiatric_disorder, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, icd10_billable, matrix_txgnn_grouping_member, rare, harrisons_view_member, mondo_top_grouping_nervous_system_disorder, matrix_txgnn_grouping_psychiatric_disorder, harrisons_view_hereditary_disease, harrisons_view_nervous_system_disorder
http://identifiers.org/snomedct/13092008
http://purl.bioontology.org/ontology/ICD10CM/G31.01
http://linkedlifedata.com/resource/umls/id/C0236642
http://identifiers.org/mesh/D020774
http://www.ebi.ac.uk/efo/EFO_0003096
https://omim.org/entry/172700
http://purl.obolibrary.org/obo/NCIT_C85008
http://purl.obolibrary.org/obo/DOID_11870
http://identifiers.org/medgen/116020
Pick's disease
dementia with lobar atrophy and neuronal cytoplasmic inclusions
lobar atrophy of the brain
Pick disease of the brain