{
    "disease_id": "DOID:2476", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:2476", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2476", 
            "name": "French settlement disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2476", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2476", 
            "name": "Strumpell-Lorrain disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2476", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2476", 
            "name": "hereditary spastic paraparesis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2476", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2476", 
            "name": "familial spastic paraplegia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010559", 
            "description": "MASA syndrome (Mental retardation, Aphasia, Spastic paraplegia, Adducted thumbs) is a historical term used to describe a phenotype now considered to be part of the X-linked L1 clinical spectrum (L1 syndrome, see this term). MASA is characterized by mild to moderate intellectual deficit, delayed development of speech, hypotonia progressing to spasticity or spastic paraplegia, adducted thumbs, and mild to moderate distension of the cerebral ventricles.", 
            "resource": "MONDO", 
            "id": "MONDO:0010559", 
            "name": "MASA syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010559", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010559", 
            "name": "SPG1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010559", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010559", 
            "name": "crash syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010559", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010559", 
            "name": "L1 syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010559", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010559", 
            "name": "spastic paraplegia, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010559", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010559", 
            "name": "hereditary spastic paraplegia 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010559", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010559", 
            "name": "intellectual disability-aphasia-shuffling gait-adducted thumbs syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010559", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010559", 
            "name": "X-linked corpus callosum agenesis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010559", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010559", 
            "name": "mental retardation aphasia shuffling Gait adducted thumbs (MASA)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010559", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010559", 
            "name": "Gareis-Mason syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010559", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010559", 
            "name": "thumb, congenital Clasped, with mental retardation"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010559", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010559", 
            "name": "adducted thumb with mental retardation"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010559", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010559", 
            "name": "spastic paraplegia 1, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010559", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010559", 
            "name": "thumb congenital clasped with mental retardation"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010559", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010559", 
            "name": "mental retardation, aphasia, shuffling Gait, and adducted thumbs"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010559", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010559", 
            "name": "X-linked spastic paraplegia 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010559", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010559", 
            "name": "spastic paraplegia 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010559", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010559", 
            "name": "Clasped thumb and mental retardation"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010559", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010559", 
            "name": "MASA syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010559", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010559", 
            "name": "X-linked complicated hereditary spastic paraplegia type 1"
        }, 
        {
            "url": "https://www.omim.org/entry/303350", 
            "description": "Mental retardation, aphasia, shuffling gait, and adducted thumbs syndrome", 
            "resource": "MIM", 
            "id": "MIM:303350", 
            "name": "Mental retardation, aphasia, shuffling gait, and adducted thumbs syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:2476", 
        "description": "A paraplegia that is characterized by progressive stiffness and contraction (spasticity) in the lower limbs.", 
        "resource": "Disease Ontology", 
        "id": "DOID:2476", 
        "name": "hereditary spastic paraplegia"
    }
}