{
    "disease_id": "DOID:0112342",
    "recommended_name": {
        "id": "DOID:0112342",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112342",
        "name": "hereditary spastic paraplegia 86",
        "description": "A hereditary spastic paraplegia characterized by early childhood onset of global developmental delay and early-onset progressive spasticity mainly affecting the lower limbs but also affecting the upper lmbs that has_material_basis_in homozygous or compound heterozygous mutation in ABHD16A on chromosome 6p21.33."
    },
    "synonyms": [
        {
            "id": "DOID:0112342",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112342",
            "name": "SPG86",
            "description": ""
        },
        {
            "id": "DOID:0112342",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112342",
            "name": "spastic paraplegia 86 autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0030673",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030673",
            "name": "spastic paraplegia 86, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0030673",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030673",
            "name": "spastic paraplegia 86, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0030673",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030673",
            "name": "SPG86",
            "description": ""
        },
        {
            "id": "MIM:619735",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619735",
            "name": "Spastic paraplegia 86, autosomal recessive",
            "description": "Spastic paraplegia 86, autosomal recessive"
        }
    ]
}