{
"@context": "/terms/",
"@id": "/phenotype-terms/MONDO_0008379/",
"@type": [
"PhenotypeTerm",
"OntologyTerm",
"Item"
],
"ancestors": [
"retinopathy",
"hereditary disease",
"disorder of orbital region",
"disposition",
"entity",
"retinal degeneration",
"inborn disorder of amino acid transport",
"continuant",
"genetic disorder",
"head and neck disorder",
"amino acid metabolism disease",
"disease",
"retinal disorder",
"disorder of visual system",
"inborn disorder of amino acid metabolism",
"retinitis pigmentosa",
"eye disorder",
"psychiatric disorder",
"retinitis pigmentosa 10",
"disease of orbital region",
"nervous system disease",
"characteristic",
"nervous system disorder",
"perceptual disorders",
"inherited retinal dystrophy",
"metabolic disease",
"human disease",
"inborn errors of metabolism",
"eye disease",
"hereditary neurological disease",
"experimental factor",
"IMPDH1-related retinopathy",
"realizable"
],
"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": [
"IMPDH1 retinitis pigmentosa",
"retinitis pigmentosa type 10",
"retinitis pigmentosa caused by mutation in IMPDH1",
"retinitis pigmentosa 10",
"RP10"
],
"term_id": "MONDO:0008379",
"term_name": "retinitis pigmentosa 10",
"uuid": "f9cd437e-2a50-4a3f-8fcc-a114bfe7cd09"
}