{
    "disease_id": "DOID:0110786", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012866", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "fatty acid hydroxylase-associated neurodegeneration"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012866", 
            "name": "autosomal recessive spastic paraplegia type 35"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012866", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012866", 
            "name": "leukodystrophy, dysmyelinating and spastic paraparesis with or without dystonia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012866", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012866", 
            "name": "spastic paraplegia 35, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012866", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012866", 
            "name": "autosomal recessive spastic paraplegia 35"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012866", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012866", 
            "name": "FA2H hereditary spastic paraplegia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012866", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012866", 
            "name": "hereditary spastic paraplegia caused by mutation in FA2H"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012866", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012866", 
            "name": "leukodystrophy, dysmyelinating, and spastic paraparesis with or without dystonia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012866", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012866", 
            "name": "spastic paraplegia 35, autosomal recessive; SPG35"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012866", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012866", 
            "name": "hereditary spastic paraplegia type 35"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012866", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012866", 
            "name": "FAHN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012866", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012866", 
            "name": "SPG35"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110786", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110786", 
            "name": "FAHN"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110786", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110786", 
            "name": "leukodystrophy, dysmyelinating and spastic paraparesis with or without dystonia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110786", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110786", 
            "name": "SPG35"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110786", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110786", 
            "name": "autosomal recessive spastic paraplegia 35"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110786", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110786", 
            "name": "autosomal recessive spastic paraplegia type 35"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110786", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110786", 
            "name": "fatty acid hydroxylase-associated neurodegeneration"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110786", 
        "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the FA2H gene on chromosome 16q23.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110786", 
        "name": "hereditary spastic paraplegia 35"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110786#disease-associations", 
            "id": "0110786", 
            "database": "Alliance of Genome Resources"
        }
    ]
}