{
    "disease_id": "DOID:3911", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008310", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008310", 
            "name": "Hutchinson-Gilford progeria syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008310", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008310", 
            "name": "premature senility syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008310", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008310", 
            "name": "HGPS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008310", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008310", 
            "name": "Hutchinson-Gilford disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008310", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008310", 
            "name": "progeria syndrome, childhood-onset"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008310", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008310", 
            "name": "Hutchinson Gilford syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008310", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008310", 
            "name": "Hutchinson-Gilford progeria syndrome; HGPS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008310", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008310", 
            "name": "Hutchinson Gilford progeria syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3911", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3911", 
            "name": "HGPS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3911", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3911", 
            "name": "Hutchinson Gilford syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3911", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3911", 
            "name": "Hutchinson-Gilford Progeria syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3911", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3911", 
            "name": "Hutchinson-Gilford disease"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:3911", 
        "description": "A syndrome characterized by extreme short stature, low body weight, early loss of hair, lipodystrophy, scleroderma, decreased joint mobility, osteolysis, and facial features that resemble aged persons that has_material_basis_in mutation in LMNA on chromosome 1q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:3911", 
        "name": "progeria"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/3911#disease-associations", 
            "id": "3911", 
            "database": "Alliance of Genome Resources"
        }
    ]
}