MONDO:0008564

released
1{
2    "@context": "/terms/",
3    "@id": "/phenotype-terms/MONDO_0008564/",
4    "@type": [
5        "PhenotypeTerm",
6        "OntologyTerm",
7        "Item"
8    ],
9    "ancestors": [
10        "hereditary neurological disease",
11        "22q11.2 deletion syndrome",
12        "developmental defect during embryogenesis",
13        "syndrome caused by partial chromosomal deletion",
14        "cardiogenetic disease",
15        "entity",
16        "experimental factor",
17        "disease",
18        "chromosomal disorder",
19        "human disease",
20        "characteristic",
21        "nervous system disease",
22        "disorder of development or morphogenesis",
23        "hereditary disease",
24        "DiGeorge syndrome",
25        "realizable",
26        "multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome",
27        "heart disease",
28        "cardiovascular disorder",
29        "immune system disease",
30        "chromosome 22q deletion",
31        "genetic disorder",
32        "multiple congenital anomalies/dysmorphic syndrome",
33        "immunodeficiency disease",
34        "congenital T-cell immunodeficiency",
35        "neurocristopathy",
36        "immune system disorder",
37        "continuant",
38        "heart disorder",
39        "nervous system disorder",
40        "cardiovascular disease",
41        "T-cell immunodeficiency",
42        "congenital nervous system disorder",
43        "disposition"
44    ],
45    "audit": {},
46    "creation_timestamp": "2023-03-10T01:05:45.657458+00:00",
47    "name": "MONDO_0008564",
48    "ontology": "MONDO",
49    "release_timestamp": "2023-06-20T18:43:36.402022+00:00",
50    "schema_version": "4",
51    "status": "released",
52    "submitted_by": {
53        "@id": "/users/43f2f757-5cbf-490a-9787-a1ee85a4cdcd/",
54        "title": "Jennifer Jou"
55    },
56    "summary": "DiGeorge syndrome",
57    "synonyms": [
58        "22q11.2 Deletion syndrome",
59        "pharyngeal pouch syndrome",
60        "DiGeorge syndrome",
61        "DiGeorge anomaly",
62        "DGS",
63        "DiGeorge's syndrome",
64        "DiGeorge syndrome type 1",
65        "DGS1",
66        "22q deletion syndrome(s)",
67        "Di-George syndrome"
68    ],
69    "term_id": "MONDO:0008564",
70    "term_name": "DiGeorge syndrome",
71    "uuid": "fe463bf9-edd2-4a32-867e-8aca19cf443f"
72}