{
"@context": "/terms/",
"@id": "/phenotype-terms/MONDO_0018958/",
"@type": [
"PhenotypeTerm",
"OntologyTerm",
"Item"
],
"ancestors": [
"characteristic",
"disease",
"muscle tissue disorder",
"skeletal muscle disorder",
"myopathy",
"musculoskeletal system disorder",
"genetic disorder",
"nemaline myopathy",
"experimental factor",
"congenital myopathy",
"realizable",
"human disease",
"hereditary skeletal muscle disorder",
"disposition",
"muscular disease",
"hereditary disease",
"congenital structural myopathy",
"musculoskeletal system disease",
"continuant",
"entity"
],
"audit": {},
"creation_timestamp": "2023-11-03T21:57:52.995254+00:00",
"name": "MONDO_0018958",
"ontology": "MONDO",
"release_timestamp": "2023-11-06T21:09:54.954869+00:00",
"schema_version": "4",
"status": "released",
"submitted_by": {
"@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
"title": "Ingrid Youngworth"
},
"summary": "nemaline myopathy",
"synonyms": [
"NEM",
"nemaline body disease",
"NM",
"nemaline myopathy",
"nemaline rod myopathy",
"rod myopathy"
],
"term_id": "MONDO:0018958",
"term_name": "nemaline myopathy",
"uuid": "eff96d19-0968-4417-b425-e03814ebe884"
}