{
    "disease_id": "DOID:0111208",
    "recommended_name": {
        "id": "DOID:0111208",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111208",
        "name": "distal hereditary motor neuronopathy type 2A",
        "description": "A distal hereditary motor neuropathy type 2 that has_material_basis_in heterozygous mutation in HSPB8 on 12q24.23."
    },
    "synonyms": [
        {
            "id": "DOID:0111208",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111208",
            "name": "autosomal dominant adult spinal muscular atrophy IIA",
            "description": ""
        },
        {
            "id": "DOID:0111208",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111208",
            "name": "HMN IIA",
            "description": ""
        },
        {
            "id": "DOID:0111208",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111208",
            "name": "HMN2A",
            "description": ""
        },
        {
            "id": "DOID:0111208",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111208",
            "name": "distal hereditary motor neuropathy type IIA",
            "description": ""
        },
        {
            "id": "DOID:0111208",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111208",
            "name": "spinal Charcot-Marie-Tooth disease IIA",
            "description": ""
        },
        {
            "id": "MONDO:0008025",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008025",
            "name": "neuronopathy, distal hereditary motor, type 2A",
            "description": "Any neuronopathy, distal hereditary motor in which the cause of the disease is a mutation in the HSPB8 gene."
        },
        {
            "id": "MONDO:0008025",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008025",
            "name": "neuronopathy, distal hereditary motor caused by mutation in HSPB8",
            "description": ""
        },
        {
            "id": "MONDO:0008025",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008025",
            "name": "spinal muscular atrophy, distal, adult, autosomal dominant, 2A",
            "description": ""
        },
        {
            "id": "MONDO:0008025",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008025",
            "name": "HMN 2A",
            "description": ""
        },
        {
            "id": "MONDO:0008025",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008025",
            "name": "neuronopathy, distal hereditary motor, type IIA; HMN2A",
            "description": ""
        },
        {
            "id": "MONDO:0008025",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008025",
            "name": "HMN2A",
            "description": ""
        },
        {
            "id": "MONDO:0008025",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008025",
            "name": "neuropathy, distal hereditary motor, type 2A",
            "description": ""
        },
        {
            "id": "MONDO:0008025",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008025",
            "name": "HSPB8 neuronopathy, distal hereditary motor",
            "description": ""
        },
        {
            "id": "MONDO:0008025",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008025",
            "name": "neuronopathy, distal hereditary motor, type IIA",
            "description": ""
        },
        {
            "id": "MONDO:0008025",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008025",
            "name": "Charcot-Marie-Tooth disease, spinal, 2A",
            "description": ""
        },
        {
            "id": "MIM:158590",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/158590",
            "name": "Neuronopathy, distal hereditary motor, 2A",
            "description": "Neuronopathy, distal hereditary motor, 2A"
        }
    ]
}