{
"@context": "/terms/",
"@id": "/phenotype-terms/MONDO_0008379/",
"@type": [
"PhenotypeTerm",
"OntologyTerm",
"Item"
],
"ancestors": [
"eye disease",
"retinitis pigmentosa 10",
"inborn errors of metabolism",
"nervous system disorder",
"experimental factor",
"psychiatric disorder",
"retinopathy",
"realizable",
"genetic disorder",
"disorder of orbital region",
"retinal disorder",
"inborn disorder of amino acid metabolism",
"amino acid metabolism disease",
"characteristic",
"inherited retinal dystrophy",
"disease of orbital region",
"hereditary disease",
"human disease",
"inborn disorder of amino acid transport",
"nervous system disease",
"perceptual disorders",
"retinal degeneration",
"retinitis pigmentosa",
"hereditary neurological disease",
"head and neck disorder",
"metabolic disease",
"continuant",
"disposition",
"IMPDH1-related retinopathy",
"disease",
"entity",
"eye disorder",
"disorder of visual system"
],
"audit": {},
"creation_timestamp": "2023-11-03T21:55:55.443807+00:00",
"name": "MONDO_0008379",
"ontology": "MONDO",
"release_timestamp": "2023-11-06T21:05:57.585945+00:00",
"schema_version": "4",
"status": "released",
"submitted_by": {
"@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
"title": "Ingrid Youngworth"
},
"summary": "retinitis pigmentosa 10",
"synonyms": [
"retinitis pigmentosa 10",
"retinitis pigmentosa type 10",
"RP10",
"IMPDH1 retinitis pigmentosa",
"retinitis pigmentosa caused by mutation in IMPDH1"
],
"term_id": "MONDO:0008379",
"term_name": "retinitis pigmentosa 10",
"uuid": "f9cd437e-2a50-4a3f-8fcc-a114bfe7cd09"
}