{
    "disease_id": "DOID:0110190", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011475", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011475", 
            "name": "CMT4B2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011475", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011475", 
            "name": "Charcot-Marie-Tooth disease, type 4B2; CMT4B2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011475", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011475", 
            "name": "autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin sheaths type 4B2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011475", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011475", 
            "name": "Charcot-Marie-Tooth disease, with focally folded myelin sheaths, autosomal recessive, type 4B2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011475", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011475", 
            "name": "Charcot-Marie-Tooth neuropathy, type 4B2, with early-onset glaucoma"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011475", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011475", 
            "name": "Charcot Marie Tooth disease type 4B2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011475", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011475", 
            "name": "CMT 4B2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011475", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011475", 
            "name": "Charcot-Marie-Tooth disease, type 4B2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011475", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011475", 
            "name": "Charcot-Marie-Tooth neuropathy, type 4B2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011475", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011475", 
            "name": "Charcot-Marie-Tooth neuropathy type 4B2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011475", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011475", 
            "name": "Charcot-Marie-Tooth disease type 4 caused by mutation in SBF2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011475", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011475", 
            "name": "Charcot-Marie-Tooth disease, type 4B2, with early-onset glaucoma"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011475", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011475", 
            "name": "SBF2 Charcot-Marie-Tooth disease type 4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110190", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110190", 
            "name": "CMT4B2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110190", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110190", 
            "name": "Charcot-Marie-Tooth neuropathy type 4B2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110190", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110190", 
            "name": "autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin sheaths type 4B2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110190", 
        "description": "A Charcot-Marie-Tooth disease type 4 that has_material_basis_in mutation in the SBF2 gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110190", 
        "name": "Charcot-Marie-Tooth disease type 4B2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110190#disease-associations", 
            "id": "0110190", 
            "database": "Alliance of Genome Resources"
        }
    ]
}