{
"@context": "/terms/",
"@id": "/phenotype-terms/MONDO_0014222/",
"@type": [
"PhenotypeTerm",
"OntologyTerm",
"Item"
],
"ancestors": [
"immune system disorder",
"experimental factor",
"inborn error of immunity",
"immunodeficiency 14",
"agammaglobulinemia",
"characteristic",
"continuant",
"hematologic disorder",
"entity",
"immunodeficiency disease",
"immune system disease",
"human disease",
"leukocyte disorder",
"realizable",
"activated PI3K-delta syndrome",
"genetic disorder",
"hereditary disease",
"disease",
"hematologic disease",
"disposition",
"B cell deficiency",
"immune deficiency disease"
],
"audit": {},
"creation_timestamp": "2023-11-03T21:56:49.042595+00:00",
"name": "MONDO_0014222",
"ontology": "MONDO",
"release_timestamp": "2023-11-06T21:07:43.784307+00:00",
"schema_version": "4",
"status": "released",
"submitted_by": {
"@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
"title": "Ingrid Youngworth"
},
"summary": "immunodeficiency 14",
"synonyms": [
"immunodeficiency 14A, autosomal dominant",
"immunodeficiency 14",
"Activated Phosphoinositide 3-Kinase Delta Syndrome (APDS)",
"immunodeficiency type 14"
],
"term_id": "MONDO:0014222",
"term_name": "immunodeficiency 14",
"uuid": "eb159419-f5bb-45df-b4ff-23268067249b"
}