{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008961", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008961", 
            "name": "autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008961", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008961", 
            "name": "Charcot-Marie-Tooth disease, demyelinating, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008961", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008961", 
            "name": "Charcot-Marie-Tooth neuropathy, type 4A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008961", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008961", 
            "name": "Charcot-Marie-Tooth disease, demyelinating, autosomal recessive, type 4A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008961", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008961", 
            "name": "Charcot-Marie-Tooth disease type 4 caused by mutation in GDAP1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008961", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008961", 
            "name": "Charcot Marie Tooth disease type 4A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008961", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008961", 
            "name": "Charcot-Marie-Tooth disease, type 4A; CMT4A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008961", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008961", 
            "name": "GDAP1 Charcot-Marie-Tooth disease type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008961", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008961", 
            "name": "CMT4A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008961", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008961", 
            "name": "Charcot-Marie-Tooth neuropathy type 4A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008961", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008961", 
            "name": "Charcot-Marie-Tooth disease, type 4A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110185", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110185", 
            "name": "CMT4A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110185", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110185", 
            "name": "Charcot-Marie-Tooth neuropathy type 4A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110185", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110185", 
            "name": "autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4A"
        }, 
        {
            "url": "https://www.omim.org/entry/214400", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:214400", 
            "name": "Charcot-Marie-Tooth disease 4A"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110185", 
        "description": "A Charcot-Marie-Tooth disease type 4 that has_material_basis_in mutation in the gene encoding ganglioside-induced differentiation-associated protein-1 (GDAP1) on chromosome 8q21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110185", 
        "name": "Charcot-Marie-Tooth disease type 4A"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/214400", 
            "id": "214400", 
            "database": "MIM"
        }
    ]
}