{
    "disease_id": "DOID:0110148", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007309", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007309", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007309", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007309", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007309", 
            "name": "Charcot-Marie-Tooth neuropathy, type 1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007309", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007309", 
            "name": "CMT 1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007309", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007309", 
            "name": "Charcot Marie Tooth disease type 1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007309", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007309", 
            "name": "CMT1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007309", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007309", 
            "name": "autosomal dominant Charcot-Marie-Tooth disease with focally folded myelin sheaths type 1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007309", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007309", 
            "name": "Charcot-Marie-Tooth disease, demyelinating, type 1A; CMT1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007309", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007309", 
            "name": "HMSN 1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007309", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007309", 
            "name": "Charcot-Marie-Tooth disease, demyelinating, type 1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007309", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007309", 
            "name": "hereditary motor and sensory neuropathy 1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007309", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007309", 
            "name": "microduplication 17p12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007309", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007309", 
            "name": "Charcot-Marie-Tooth neuropathy type 1A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110148", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110148", 
            "name": "CMT1A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110148", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110148", 
            "name": "Charcot-Marie-Tooth neuropathy type 1A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110148", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110148", 
            "name": "HMSN1A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110148", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110148", 
            "name": "hereditary motor and sensory neuropathy 1A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110148", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110148", 
            "name": "microduplication 17p12"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110148", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110148", 
            "name": "autosomal dominant Charcot-Marie-Tooth disease with focally folded myelin sheaths type 1A"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110148", 
        "description": "A Charcot-Marie-Tooth disease type 1 that has_material_basis_in duplication of, or mutation in, the gene encoding peripheral myelin protein-22 (PMP22).", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110148", 
        "name": "Charcot-Marie-Tooth disease type 1A"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110148#disease-associations", 
            "id": "0110148", 
            "database": "Alliance of Genome Resources"
        }
    ]
}