{
    "disease_id": "DOID:0111266", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009271", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009271", 
            "name": "geroderma osteodysplastica"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009271", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009271", 
            "name": "GERODERMA OSTEODYSPLASTICUM; GO"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009271", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009271", 
            "name": "Gerodermia osteodysplastica"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009271", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009271", 
            "name": "GO"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009271", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009271", 
            "name": "Walt Disney dwarfism"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111266", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111266", 
            "name": "GO"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111266", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111266", 
            "name": "Walt Disney dwarfism"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111266", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111266", 
            "name": "geroderma osteodysplastica"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111266", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111266", 
            "name": "gerodermia osteodysplastica"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111266", 
        "description": "A syndrome characterized by lax and wrinkled skin, progeroid features, hip dislocation, joint laxity, severe short stature/dwarfism, severe osteoporosis, vertebral abnormalities and spontaneous fractures, and developmental delay and mild intellectual deficit that has_material_basis_in homozygous or compound heterozygous mutation in GORAB on 1q24.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111266", 
        "name": "geroderma osteodysplasticum"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111266#disease-associations", 
            "id": "0111266", 
            "database": "Alliance of Genome Resources"
        }
    ]
}