{
    "disease_id": "DOID:0060805",
    "recommended_name": {
        "id": "DOID:0060805",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060805",
        "name": "Prieto syndrome",
        "description": "A syndromic X-linked intellectual disability characterized by intellectual disability, facial dysmorphism, patella luxation, clinodactyly, subcortical cerebral atrophy, and abnormal growth of the teeth that has_material_basis_in variation in the chromosome region Xp11-q21."
    },
    "synonyms": [
        {
            "id": "DOID:0060805",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060805",
            "name": "Prieto-Badia-Mulas syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060805",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060805",
            "name": "X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010667",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010667",
            "name": "Prieto syndrome",
            "description": "This syndrome is characterised by intellectual deficit associated with facial dysmorphism, patella luxation, and abnormal growth of the teeth."
        },
        {
            "id": "MONDO:0010667",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010667",
            "name": "X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010667",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010667",
            "name": "Prieto-Badia-Mulas syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010667",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010667",
            "name": "mental retardation, X-linked, syndromic 2",
            "description": ""
        },
        {
            "id": "MONDO:0010667",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010667",
            "name": "PRS",
            "description": ""
        },
        {
            "id": "MONDO:0010667",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010667",
            "name": "mental retardation, X-linked, with Dysmorphism and cerebral atrophy",
            "description": ""
        },
        {
            "id": "MONDO:0010667",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010667",
            "name": "MRXS2",
            "description": ""
        },
        {
            "id": "MONDO:0010667",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010667",
            "name": "Prieto X-linked mental retardation syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010667",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010667",
            "name": "Prieto X-linked mental retardation syndrome; PRS",
            "description": ""
        }
    ]
}