{
    "disease_id": "DOID:0111724", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009269", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009269", 
            "name": "geleophysic dysplasia 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009269", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009269", 
            "name": "GPHYSD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009269", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009269", 
            "name": "ADAMTSL2 geleophysic dysplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009269", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009269", 
            "name": "Geleophysic dysplasia type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009269", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009269", 
            "name": "geleophysic dysplasia caused by mutation in ADAMTSL2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009269", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009269", 
            "name": "GELEOPHYSIC dysplasia 1; GPHYSD1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111724", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111724", 
            "name": "GPHYSD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111724", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111724", 
            "name": "geleophysic dwarfism"
        }, 
        {
            "url": "https://www.omim.org/entry/231050", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:231050", 
            "name": "Geleophysic dysplasia 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111724", 
        "description": "A bone development disease characterized by short-limb dwarfism, brachydactyly, cardiac valvular disease, characteristic facial appearance, skin thickening, and laryngotracheal stenosis.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111724", 
        "name": "geleophysic dysplasia"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/231050", 
            "id": "231050", 
            "database": "MIM"
        }
    ]
}