An instance of dementia that is caused by an inherited genomic modification in an individual. [ MONDO:patterns/hereditary ]
Synonyms: genetic dementia
Term information
- Orphanet:158124 (MONDO:equivalentTo)
- GARD:20028 (MONDO:GARD)
- UMLS:C5680680 (MONDO:equivalentTo)
- MEDGEN:1842422 (MONDO:equivalentTo)
gard_rare, matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, otar, matrix_excluded, matrix_llm__tag_qualy_lost_other, disease_grouping, mondo_top_grouping_member, matrix_llm__medical_specialization_other, matrix_llm__txgnn_other, mondo_top_grouping_hereditary_disease, harrisons_view_psychiatric_disorder, matrix_llm__tag_existing_treatment_other, mondo_top_grouping_psychiatric_disorder, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, matrix_txgnn_grouping_member, rare, harrisons_view_member, matrix_txgnn_grouping_psychiatric_disorder, harrisons_view_hereditary_disease, ordo_group_of_disorders
http://identifiers.org/medgen/1842422
http://linkedlifedata.com/resource/umls/id/C5680680
http://www.orpha.net/ORDO/Orphanet_158124
https://github.com/monarch-initiative/mondo/issues/5952
https://github.com/monarch-initiative/mondo/issues/5114