{
"@context": "/terms/",
"@id": "/phenotype-terms/MONDO_0008564/",
"@type": [
"PhenotypeTerm",
"OntologyTerm",
"Item"
],
"ancestors": [
"heart disorder",
"chromosome 22q deletion",
"nervous system disorder",
"developmental defect during embryogenesis",
"cardiovascular disease",
"entity",
"multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome",
"immunodeficiency disease",
"22q11.2 deletion syndrome",
"multiple congenital anomalies/dysmorphic syndrome",
"hereditary disease",
"experimental factor",
"congenital T-cell immunodeficiency",
"realizable",
"human disease",
"immune system disease",
"disorder of development or morphogenesis",
"cardiogenetic disease",
"neurocristopathy",
"genetic disorder",
"chromosomal disorder",
"continuant",
"DiGeorge syndrome",
"T-cell immunodeficiency",
"cardiovascular disorder",
"hereditary neurological disease",
"syndrome caused by partial chromosomal deletion",
"congenital nervous system disorder",
"characteristic",
"nervous system disease",
"immune system disorder",
"heart disease",
"disposition",
"disease"
],
"audit": {},
"creation_timestamp": "2023-03-10T01:05:45.657458+00:00",
"name": "MONDO_0008564",
"ontology": "MONDO",
"release_timestamp": "2023-06-20T18:43:36.402022+00:00",
"schema_version": "4",
"status": "released",
"submitted_by": {
"@id": "/users/43f2f757-5cbf-490a-9787-a1ee85a4cdcd/",
"title": "Jennifer Jou"
},
"summary": "DiGeorge syndrome",
"synonyms": [
"pharyngeal pouch syndrome",
"DGS",
"DiGeorge anomaly",
"22q11.2 Deletion syndrome",
"Di-George syndrome",
"DiGeorge syndrome",
"22q deletion syndrome(s)",
"DGS1",
"DiGeorge syndrome type 1",
"DiGeorge's syndrome"
],
"term_id": "MONDO:0008564",
"term_name": "DiGeorge syndrome",
"uuid": "fe463bf9-edd2-4a32-867e-8aca19cf443f"
}