{
    "disease_id": "DOID:0060878",
    "recommended_name": {
        "id": "DOID:0060878",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060878",
        "name": "hypoparathyroidism-deafness-renal disease syndrome",
        "description": "A chromosomal deletion syndrome that is characterized by autosomal dominant inheritance of hypoparathyroidism, sensorineural deafness and progressive renal failure and that has_material_basis_in chromosome deletion that results in haploinsufficiency of the GATA3 gene on chromosome 10p14."
    },
    "synonyms": [
        {
            "id": "DOID:0060878",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060878",
            "name": "Barakat syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060878",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060878",
            "name": "HDR syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060878",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060878",
            "name": "hypoparathyroidism, sensorineural deafness, and renal disease",
            "description": ""
        },
        {
            "id": "MONDO:0007797",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007797",
            "name": "hypoparathyroidism-deafness-renal disease syndrome",
            "description": "The HDR syndrome is an inherited condition consisting of hypoparathyroidism, sensorineural deafness and renal disease."
        },
        {
            "id": "MONDO:0007797",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007797",
            "name": "Barakat Syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007797",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007797",
            "name": "Barakat syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007797",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007797",
            "name": "HDR syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007797",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007797",
            "name": "hypoparathyroidism, deafness, and renal anomalies syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007797",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007797",
            "name": "hypoparathyroidism, sensorineural deafness, and renal disease",
            "description": ""
        },
        {
            "id": "MONDO:0007797",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007797",
            "name": "hypoparathyroidism-deafness-renal disease syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007797",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007797",
            "name": "HDR",
            "description": ""
        },
        {
            "id": "MONDO:0007797",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007797",
            "name": "hypoparathyroidism, sensorineural deafness, and renal dysplasia",
            "description": ""
        },
        {
            "id": "MIM:146255",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/146255",
            "name": "Hypoparathyroidism, sensorineural deafness, and renal disease",
            "description": "Hypoparathyroidism, sensorineural deafness, and renal disease"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060878"
    ],
    "unlinked_id_list": []
}