{
"@context": "/terms/",
"@id": "/phenotype-terms/MONDO_0008296/",
"@type": [
"PhenotypeTerm",
"OntologyTerm",
"Item"
],
"ancestors": [
"dermatitis",
"endocrine system disease",
"inherited porphyria",
"digestive system disease",
"inborn disorder of porphyrin metabolism",
"experimental factor",
"realizable",
"skin disorder",
"disposition",
"liver disease",
"continuant",
"hereditary skin disorder",
"hepatic porphyria",
"human disease",
"hereditary photodermatosis",
"skin disease",
"disease",
"hepatobiliary disease",
"liver disorder",
"porphyria",
"genetic disorder",
"entity",
"porphyrin metabolism disease",
"inborn errors of metabolism",
"metabolic disease",
"porphyria cutanea tarda",
"endocrine system disorder",
"inflammatory disease",
"characteristic",
"digestive system disorder",
"hepatobiliary disorder",
"hereditary disease",
"integumentary system disorder",
"familial porphyria cutanea tarda",
"integumentary system disease",
"UROD-related inherited porphyria"
],
"audit": {},
"creation_timestamp": "2023-11-03T21:58:03.765105+00:00",
"name": "MONDO_0008296",
"ontology": "MONDO",
"release_timestamp": "2023-11-06T21:10:16.176394+00:00",
"schema_version": "4",
"status": "released",
"submitted_by": {
"@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
"title": "Ingrid Youngworth"
},
"summary": "familial porphyria cutanea tarda",
"synonyms": [
"porphyria cutanea tarda, susceptibility to",
"porphyria cutanea tarda type II",
"hereditary porphyria cutanea tarda"
],
"term_id": "MONDO:0008296",
"term_name": "familial porphyria cutanea tarda",
"uuid": "ee458e00-2d0e-40a9-b98a-4e983f590472"
}