An instance of dementia that is caused by an inherited genomic modification in an individual. [ MONDO:patterns/hereditary ]
Synonyms: genetic dementia
Term information
- MEDGEN:1842422 (MONDO:equivalentTo)
- Orphanet:158124 (MONDO:equivalentTo)
- GARD:20028 (MONDO:GARD)
- UMLS:C5680680 (MONDO:equivalentTo)
gard_rare, otar, disease_grouping, rare, ordo_group_of_disorders
https://github.com/monarch-initiative/mondo/issues/5952
https://github.com/monarch-initiative/mondo/issues/5114
http://identifiers.org/medgen/1842422
http://linkedlifedata.com/resource/umls/id/C5680680
http://www.orpha.net/ORDO/Orphanet_158124