{
"@context": "/terms/",
"@id": "/phenotype-terms/MONDO_0008476/",
"@type": [
"PhenotypeTerm",
"OntologyTerm",
"Item"
],
"ancestors": [
"collagenopathy",
"osteochondrodysplasia",
"hereditary disease",
"experimental factor",
"syndromic disease",
"bone disorder",
"disorder of development or morphogenesis",
"entity",
"human disease",
"connective tissue disease",
"disease",
"characteristic",
"musculoskeletal system disorder",
"skeletal system disease",
"hereditary disorder of connective tissue",
"bone disease",
"skeletal dysplasia",
"spondylometaphyseal dysplasia",
"spondyloepimetaphyseal dysplasia, Strudwick type",
"connective tissue disorder",
"disposition",
"spondyloepimetaphyseal dysplasia",
"type 2 collagenopathy",
"realizable",
"bone development disease",
"musculoskeletal system disease",
"skeletal system disorder",
"genetic disorder",
"continuant"
],
"audit": {},
"creation_timestamp": "2023-11-03T21:55:01.071663+00:00",
"name": "MONDO_0008476",
"ontology": "MONDO",
"release_timestamp": "2023-11-06T21:04:03.171507+00:00",
"schema_version": "4",
"status": "released",
"submitted_by": {
"@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
"title": "Ingrid Youngworth"
},
"summary": "spondyloepimetaphyseal dysplasia, Strudwick type",
"synonyms": [
"spondyloepimetaphyseal dysplasia, Strudwick type"
],
"term_id": "MONDO:0008476",
"term_name": "spondyloepimetaphyseal dysplasia, Strudwick type",
"uuid": "f06d9da9-70f3-4070-8f6d-5af498c7dbc9"
}