{
"@context": "/terms/",
"@id": "/phenotype-terms/MONDO_0010420/",
"@type": [
"PhenotypeTerm",
"OntologyTerm",
"Item"
],
"ancestors": [
"hepatic porphyria",
"liver disorder",
"hereditary skin disorder",
"skin disease",
"entity",
"hereditary disease",
"liver disease",
"endocrine system disorder",
"experimental factor",
"integumentary system disorder",
"erythropoietic protoporphyria",
"hepatobiliary disorder",
"inborn errors of metabolism",
"digestive system disorder",
"porphyria",
"realizable",
"human disease",
"metabolic disease",
"genetic disorder",
"continuant",
"hepatobiliary disease",
"skin disorder",
"X-linked disease",
"X-linked erythropoietic protoporphyria",
"digestive system disease",
"porphyrin metabolism disease",
"integumentary system disease",
"inherited porphyria",
"inborn disorder of porphyrin metabolism",
"endocrine system disease",
"characteristic",
"disposition",
"disease",
"hereditary photodermatosis"
],
"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 protoporphyria",
"XLPP",
"XLDPP",
"erythropoietic protoporphyria, X-linked",
"X-linked dominant erythropoietic protoporphyria"
],
"term_id": "MONDO:0010420",
"term_name": "X-linked erythropoietic protoporphyria",
"uuid": "f7caba37-1bcb-47e9-9607-2ea6394a77aa"
}