{
    "disease_id": "DOID:0110196", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011534", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "neuropathy, hereditary motor and sensory, Russe type; HMSNR"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011534", 
            "name": "Charcot-Marie-Tooth disease, type 4G"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011534", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011534", 
            "name": "Charcot-Marie-Tooth disease, autosomal recessive, type 4G"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011534", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011534", 
            "name": "Charcot-Marie-Tooth neuropathy type 4G"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011534", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011534", 
            "name": "Charcot-Marie-Tooth disease type 4 caused by mutation in HK1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011534", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011534", 
            "name": "CMT4G"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011534", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011534", 
            "name": "hereditary motor and sensory neuropathy Russe type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011534", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011534", 
            "name": "neuropathy, hereditary motor and sensory, Russe type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011534", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011534", 
            "name": "autosomal recessive Charcot-Marie-Tooth disease type 4G"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011534", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011534", 
            "name": "Charcot-Marie-Tooth neuropathy, type 4G"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011534", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011534", 
            "name": "HK1 Charcot-Marie-Tooth disease type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011534", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011534", 
            "name": "hereditary motor and sensory neuropathy, Russe type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011534", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011534", 
            "name": "HMSNR"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110196", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110196", 
            "name": "autosomal recessive Charcot-Marie-Tooth disease type 4G"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110196", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110196", 
            "name": "CMT4G"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110196", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110196", 
            "name": "Charcot-Marie-Tooth neuropathy type 4G"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110196", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110196", 
            "name": "HMSNR"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110196", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110196", 
            "name": "hereditary motor and sensory neuropathy Russe type"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110196", 
        "description": "A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous mutation in the HK1 gene on chromosome 10q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110196", 
        "name": "Charcot-Marie-Tooth disease type 4G"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110196#disease-associations", 
            "id": "0110196", 
            "database": "Alliance of Genome Resources"
        }
    ]
}