{
    "disease_id": "DOID:0061133",
    "recommended_name": {
        "id": "DOID:0061133",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061133",
        "name": "autosomal recessive limb-girdle muscular dystrophy type 27",
        "description": "An autosomal recessive limb-girdle muscular dystrophy characterized by progressive muscle weakness primarily affecting the lower limbs and resulting in walking difficulty or loss of ambulation that has_material_basis_in homozygous or compound heterozygous mutation in the JAG2 gene on chromosome 14q32."
    },
    "synonyms": [
        {
            "id": "DOID:0061133",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0061133",
            "name": "LGMDR27",
            "description": ""
        },
        {
            "id": "MONDO:0030456",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030456",
            "name": "muscular dystrophy, limb-girdle, autosomal recessive 27",
            "description": ""
        },
        {
            "id": "MONDO:0030456",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030456",
            "name": "LGMDR27",
            "description": ""
        },
        {
            "id": "MIM:619566",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619566",
            "name": "Muscular dystrophy, limb-girdle, autosomal recessive 27",
            "description": "Muscular dystrophy, limb-girdle, autosomal recessive 27"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061133"
    ],
    "unlinked_id_list": []
}