{
    "disease_id": "DOID:0111266",
    "recommended_name": {
        "id": "DOID:0111266",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111266",
        "name": "geroderma osteodysplasticum",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0111266",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111266",
            "name": "GO",
            "description": ""
        },
        {
            "id": "DOID:0111266",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111266",
            "name": "Walt Disney dwarfism",
            "description": ""
        },
        {
            "id": "DOID:0111266",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111266",
            "name": "geroderma osteodysplastica",
            "description": ""
        },
        {
            "id": "DOID:0111266",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111266",
            "name": "gerodermia osteodysplastica",
            "description": ""
        },
        {
            "id": "MONDO:0009271",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009271",
            "name": "geroderma osteodysplastica",
            "description": "Geroderma osteodysplastica (GO) is characterized by lax and wrinkled skin (especially on the dorsum of the hands and feet and abdomen), progeroid features, hip dislocation, joint laxity, severe short stature/dwarfism, severe osteoporosis, vertebral abnormalities and spontaneous fractures, and developmental delay and mild intellectual deficit."
        },
        {
            "id": "MONDO:0009271",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009271",
            "name": "geroderma osteodysplastica",
            "description": ""
        },
        {
            "id": "MONDO:0009271",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009271",
            "name": "GERODERMA OSTEODYSPLASTICUM",
            "description": ""
        },
        {
            "id": "MONDO:0009271",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009271",
            "name": "GO",
            "description": ""
        },
        {
            "id": "MONDO:0009271",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009271",
            "name": "Geroderma osteodysplasticum",
            "description": ""
        },
        {
            "id": "MIM:231070",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/231070",
            "name": "Geroderma osteodysplasticum",
            "description": "Geroderma osteodysplasticum"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111266"
    ],
    "unlinked_id_list": []
}