{
    "disease_id": "DOID:1858", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:1858", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1858", 
            "name": "fibrous dysplasia of bone"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1858", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1858", 
            "name": "polyostotic fibrous dysplasia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1858", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1858", 
            "name": "osteitis fibrosa disseminata"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0018919", 
            "description": "McCune-Albright syndrome (MAS) is classically defined by the clinical triad of fibrous dysplasia of bone (FD), cafC)-au-lait skin spots, and precocious puberty (PP).", 
            "resource": "MONDO", 
            "id": "MONDO:0018919", 
            "name": "McCune-Albright syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0018919", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0018919", 
            "name": "MAS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0018919", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0018919", 
            "name": "polyostotic fibrous dysplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0018919", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0018919", 
            "name": "PFD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0018919", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0018919", 
            "name": "POFD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0018919", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0018919", 
            "name": "gonadotropin-independent female-limited sexual precocity"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0018919", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0018919", 
            "name": "McCune Albright syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0018919", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0018919", 
            "name": "Albright's disease"
        }, 
        {
            "url": "https://www.omim.org/entry/174800", 
            "description": "McCune-Albright syndrome", 
            "resource": "MIM", 
            "id": "MIM:174800", 
            "name": "McCune-Albright syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:1858", 
        "description": "A syndrome that is characterized by polyostotic fibrous dysplasia, precocious puberty, and caf-au-lait spots and has_material_basis_in spontaneous post zygotic missense mutation at ARG201 or Gln227 of the GNAS gene during embryogenesis.", 
        "resource": "Disease Ontology", 
        "id": "DOID:1858", 
        "name": "McCune Albright syndrome"
    }
}