{
    "disease_id": "DOID:0060878", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007797", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007797", 
            "name": "hypoparathyroidism, sensorineural deafness, and renal disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007797", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007797", 
            "name": "hypoparathyroidism, sensorineural deafness, and renal dysplasia syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007797", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007797", 
            "name": "nephrosis, nerve deafness, and hypoparathyroidism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007797", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007797", 
            "name": "hypoparathyroidism, deafness, and renal anomalies syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007797", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007797", 
            "name": "Barakat syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007797", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007797", 
            "name": "hypoparathyroidism, sensorineural deafness, and renal disease; HDR"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007797", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007797", 
            "name": "HDR syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007797", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007797", 
            "name": "hypoparathyroidism, sensorineural deafness, and renal dysplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007797", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007797", 
            "name": "HDR"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060878", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060878", 
            "name": "Barakat syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060878", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060878", 
            "name": "HDR syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060878", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060878", 
            "name": "hypoparathyroidism, sensorineural deafness, and renal disease"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060878", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060878", 
        "name": "hypoparathyroidism-deafness-renal disease syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060878#disease-associations", 
            "id": "0060878", 
            "database": "Alliance of Genome Resources"
        }
    ]
}