{
    "disease_id": "DOID:0111196", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010338", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "X-linked distal spinal muscular atrophy type 3"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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            "name": "spinal muscular atrophy caused by mutation in ATP7A"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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            "name": "spinal muscular atrophy, distal, X-linked recessive"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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            "name": "SMAX3"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010338", 
            "name": "X-linked distal hereditary motor neuropathy type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010338", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010338", 
            "name": "spinal muscular atrophy, distal, X-linked type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010338", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010338", 
            "name": "X-linked dSMA3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010338", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010338", 
            "name": "spinal muscular atrophy, distal, X-linked 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010338", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010338", 
            "name": "X-linked dHMN3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010338", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010338", 
            "name": "Dsmax"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010338", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010338", 
            "name": "ATP7A-related distal motor neuropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010338", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010338", 
            "name": "X-linked dSMA type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010338", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010338", 
            "name": "ATP7A spinal muscular atrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010338", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010338", 
            "name": "X-linked dHMN type 3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111196", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111196", 
            "name": "ATP7A-related distal motor neuropathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111196", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111196", 
            "name": "DSMAX"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111196", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111196", 
            "name": "SMAX3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111196", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111196", 
            "name": "X-linked dHMN3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111196", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111196", 
            "name": "X-linked dSMA3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111196", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111196", 
            "name": "X-linked distal hereditary motor neuropathy type 3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111196", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111196", 
            "name": "X-linked recessive distal spinal muscular atrophy"
        }, 
        {
            "url": "https://www.omim.org/entry/300489", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:300489", 
            "name": "Distal spinal muscular atrophy, X-linked, 3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111196", 
        "description": "A spinal muscular atrophy characterized by slowly progressive atrophy and weakness of distal muscles of hands and feet with absence of cognitive, pyramidal, or sensory impairment that has_material_basis_in homozygous or hemizygous mutation in ATP7A on Xq21.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111196", 
        "name": "X-linked distal spinal muscular atrophy 3"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/300489", 
            "id": "300489", 
            "database": "MIM"
        }
    ]
}