{
    "disease_id": "DOID:0061134",
    "recommended_name": {
        "id": "DOID:0061134",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0061134",
        "name": "autosomal recessive limb-girdle muscular dystrophy type 29",
        "description": "An autosomal recessive limb-girdle muscular dystrophy characterized by onset of muscle weakness predominantly affecting the proximal lower limbs, although upper limb involvement also occurs that has_material_basis_in homozygous or compound heterozygous mutation in the SNUPN gene on chromosome 15q24."
    },
    "synonyms": [
        {
            "id": "DOID:0061134",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0061134",
            "name": "LGMDR29",
            "description": ""
        },
        {
            "id": "MONDO:0971171",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0971171",
            "name": "muscular dystrophy, limb-girdle, autosomal recessive 29",
            "description": ""
        },
        {
            "id": "MIM:620793",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620793",
            "name": "Muscular dystrophy, limb-girdle, autosomal recessive 29",
            "description": "Muscular dystrophy, limb-girdle, autosomal recessive 29"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061134"
    ],
    "unlinked_id_list": []
}