{
    "disease_id": "DOID:0050943", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013354", 
            "name": "autosomal recessive spastic ataxia 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013354", 
            "name": "spastic ataxia 4, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013354", 
            "name": "autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013354", 
            "name": "autosomal recessive spastic ataxia type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013354", 
            "name": "MTPAP autosomal recessive spastic ataxia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013354", 
            "name": "spastic ataxia type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013354", 
            "name": "SPAX4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013354", 
            "name": "autosomal recessive spastic ataxia - optic atrophy - dysarthria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013354", 
            "name": "autosomal recessive spastic ataxia caused by mutation in MTPAP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013354", 
            "name": "spastic ataxia 4, autosomal recessive; SPAX4"
        }, 
        {
            "url": "https://www.omim.org/entry/613672", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:613672", 
            "name": "Spastic ataxia 4, autosomal recessive"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050943", 
        "description": "A spastic ataxia that is characterized by cerebellar ataxia, spasticity, dysarthria and optic atrophy, has_material_basis_in homozygous mutation in the MTPAP gene on chromosome 10p11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050943", 
        "name": "spastic ataxia 4"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613672", 
            "id": "613672", 
            "database": "MIM"
        }
    ]
}