{
    "disease_id": "DOID:0110777", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012213", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012213", 
            "name": "hereditary spastic paraplegia type 26"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012213", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012213", 
            "name": "autosomal recessive spastic paraplegia 26"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012213", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012213", 
            "name": "GM2 synthase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012213", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012213", 
            "name": "spastic paraplegia 26, autosomal recessive; SPG26"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012213", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012213", 
            "name": "spastic paraplegia 26, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012213", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012213", 
            "name": "autosomal recessive spastic paraplegia type 26"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012213", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012213", 
            "name": "spastic paraplegia 26"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012213", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012213", 
            "name": "SPG26"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110777", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110777", 
            "name": "GM2 synthase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110777", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110777", 
            "name": "SPG26"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110777", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110777", 
            "name": "autosomal recessive spastic paraplegia 26"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110777", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110777", 
            "name": "autosomal recessive spastic paraplegia type 26"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110777", 
        "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the B4GALNT1 gene on chromosome 12q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110777", 
        "name": "hereditary spastic paraplegia 26"
    }, 
    "evidence": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012213", 
            "id": "0012213", 
            "database": "MONDO"
        }, 
        {
            "url": "https://www.omim.org/entry/609195", 
            "id": "609195", 
            "database": "MIM"
        }
    ]
}