{
"@context": "/terms/",
"@id": "/phenotype-terms/MONDO_0010420/",
"@type": [
"PhenotypeTerm",
"OntologyTerm",
"Item"
],
"ancestors": [
"hepatobiliary disease",
"skin disorder",
"hepatic porphyria",
"disease",
"continuant",
"endocrine system disease",
"endocrine system disorder",
"disposition",
"hereditary photodermatosis",
"digestive system disease",
"integumentary system disease",
"experimental factor",
"hereditary disease",
"X-linked disease",
"X-linked erythropoietic protoporphyria",
"erythropoietic protoporphyria",
"realizable",
"genetic disorder",
"liver disease",
"skin disease",
"entity",
"inborn disorder of porphyrin metabolism",
"digestive system disorder",
"hepatobiliary disorder",
"liver disorder",
"hereditary skin disorder",
"metabolic disease",
"porphyria",
"integumentary system disorder",
"inborn errors of metabolism",
"inherited porphyria",
"porphyrin metabolism disease",
"human disease",
"characteristic"
],
"audit": {},
"creation_timestamp": "2023-11-03T21:54:44.009619+00:00",
"name": "MONDO_0010420",
"ontology": "MONDO",
"release_timestamp": "2023-11-06T21:03:30.035664+00:00",
"schema_version": "4",
"status": "released",
"submitted_by": {
"@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
"title": "Ingrid Youngworth"
},
"summary": "X-linked erythropoietic protoporphyria",
"synonyms": [
"X-linked dominant erythropoietic protoporphyria",
"X-linked dominant protoporphyria",
"erythropoietic protoporphyria, X-linked",
"XLDPP",
"XLPP"
],
"term_id": "MONDO:0010420",
"term_name": "X-linked erythropoietic protoporphyria",
"uuid": "f7caba37-1bcb-47e9-9607-2ea6394a77aa"
}