{
"@context": "/terms/",
"@id": "/phenotype-terms/MONDO_0007885/",
"@type": [
"PhenotypeTerm",
"OntologyTerm",
"Item"
],
"ancestors": [
"skeletal system disease",
"type 2 collagenopathy",
"bone disorder",
"bone disease",
"syndromic disease",
"experimental factor",
"realizable",
"disposition",
"continuant",
"skeletal dysplasia",
"musculoskeletal system disorder",
"collagenopathy",
"human disease",
"disease",
"Legg-Calve-Perthes disease",
"genetic disorder",
"entity",
"skeletal system disorder",
"connective tissue disease",
"musculoskeletal system disease",
"connective tissue disorder",
"characteristic",
"osteonecrosis of genetic origin",
"osteochondrosis",
"hereditary disease",
"osteonecrosis",
"hereditary disorder of connective tissue",
"dysplasia of the proximal femoral epiphyses"
],
"audit": {},
"creation_timestamp": "2023-11-03T21:54:55.157565+00:00",
"name": "MONDO_0007885",
"ontology": "MONDO",
"release_timestamp": "2023-11-06T21:03:53.744092+00:00",
"schema_version": "4",
"status": "released",
"submitted_by": {
"@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
"title": "Ingrid Youngworth"
},
"summary": "Legg-Calve-Perthes disease",
"synonyms": [
"Legg-Calve-Perthes symptom",
"Legg-CALVE-Perthes disease",
"Legg-Calve-Perthes syndrome",
"juvenile osteochondrosis of hip and/or pelvis",
"Legg-Calvé-Perthes disease",
"Perthe's disease",
"juvenile osteochondrosis of hip and pelvis",
"Legg-Calve-Perthes disease",
"osteochondritis of the capital femoral epiphysis",
"Calve - Perthes' disease",
"juvenile osteochond-hip/pelvis",
"Pseudocoxalgia",
"Osteochondrosis of the capital femoral epiphysis",
"Legg Calvé Perthes Disease",
"aseptic necrosis of the capital femoral epiphysis",
"Perthes disease",
"coxa plana",
"Legg-Perthes disease",
"pseudocoxalgia",
"osteochondrosis of Legg-Calve-Perthes"
],
"term_id": "MONDO:0007885",
"term_name": "Legg-Calve-Perthes disease",
"uuid": "fbd03092-71a1-4292-a154-d9cbef0be84e"
}