{
"@context": "/terms/",
"@id": "/phenotype-terms/MONDO_0010533/",
"@type": [
"PhenotypeTerm",
"OntologyTerm",
"Item"
],
"ancestors": [
"syndromic disease",
"characteristic",
"experimental factor",
"realizable",
"disease",
"human disease",
"entity",
"disposition",
"genetic disorder",
"continuant",
"hereditary disease",
"Arts syndrome"
],
"audit": {},
"creation_timestamp": "2023-11-03T21:51:38.234413+00:00",
"name": "MONDO_0010533",
"ontology": "MONDO",
"release_timestamp": "2023-11-06T21:36:07.389148+00:00",
"schema_version": "4",
"status": "released",
"submitted_by": {
"@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
"title": "Ingrid Youngworth"
},
"summary": "Arts syndrome",
"synonyms": [
"Arts",
"syndromic X-linked intellectual disability Arts type",
"lethal ataxia with deafness and optic atrophy",
"MRXSARTS",
"syndromic X-linked mental retardation Arts type",
"MRXS18",
"Arts syndrome, X-linked recessive",
"fatal X-linked ataxia with deafness and loss of vision",
"syndromic X-linked intellectual disability 18",
"syndromic X-linked mental retardation 18",
"Arts syndrome"
],
"term_id": "MONDO:0010533",
"term_name": "Arts syndrome",
"uuid": "f5f2db9d-a2c6-4ab7-b645-c1f14b2c93f8"
}