{
"@context": "/terms/",
"@id": "/phenotype-terms/MONDO_0011842/",
"@type": [
"PhenotypeTerm",
"OntologyTerm",
"Item"
],
"ancestors": [
"disease",
"nervous system disease",
"psychiatric disorder",
"brain disease",
"Primary progressive aphasia",
"hereditary neurological disease",
"frontotemporal dementia",
"cognitive disorder",
"central nervous system disorder",
"entity",
"mental or behavioural disorder",
"human disease",
"central nervous system disease",
"continuant",
"nervous system disorder",
"dementia",
"characteristic",
"genetic disorder",
"hereditary disease",
"neurodegenerative disease",
"disposition",
"hereditary dementia",
"experimental factor",
"inherited neurodegenerative disorder",
"realizable",
"GRN-related frontotemporal lobar degeneration with Tdp43 inclusions",
"primary progressive aphasia"
],
"audit": {},
"creation_timestamp": "2023-11-03T21:50:10.985559+00:00",
"name": "MONDO_0011842",
"ontology": "MONDO",
"release_timestamp": "2023-11-06T21:33:07.528501+00:00",
"schema_version": "4",
"status": "released",
"submitted_by": {
"@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
"title": "Ingrid Youngworth"
},
"summary": "GRN-related frontotemporal lobar degeneration with Tdp43 inclusions",
"synonyms": [],
"term_id": "MONDO:0011842",
"term_name": "GRN-related frontotemporal lobar degeneration with Tdp43 inclusions",
"uuid": "e6fc221f-f04a-45ae-9df8-3dc11822fe81"
}