{
    "disease_id": "DOID:0110150",
    "recommended_name": {
        "id": "DOID:0110150",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110150",
        "name": "Charcot-Marie-Tooth disease type 1D",
        "description": "A Charcot-Marie-Tooth disease type 1 that has_material_basis_in mutation in the early growth response gene-2 (EGR2)."
    },
    "synonyms": [
        {
            "id": "DOID:0110150",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110150",
            "name": "CMT1D",
            "description": ""
        },
        {
            "id": "DOID:0110150",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110150",
            "name": "Charcot-Marie-Tooth neuropathy type 1D",
            "description": ""
        },
        {
            "id": "DOID:0110150",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110150",
            "name": "HMSN ID",
            "description": ""
        },
        {
            "id": "DOID:0110150",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110150",
            "name": "HMSN1D",
            "description": ""
        },
        {
            "id": "DOID:0110150",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110150",
            "name": "hereditary motor and sensory neuropathy 1D",
            "description": ""
        },
        {
            "id": "MONDO:0011890",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011890",
            "name": "Charcot-Marie-Tooth disease type 1D",
            "description": "gene (10q21.1), with a variable severity and age of onset (from infancy to adulthood), that usually presents with gait abnormalities, progressive wasting and weakness of distal limb muscles, with possible later involvement of proximal muscles, foot deformity and severe reduction in nerve conduction velocity. Additional features may include scoliosis, cranial nerve deficits such as diplopia, and bilateral vocal cord paresis."
        },
        {
            "id": "MONDO:0011890",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011890",
            "name": "Charcot-Marie-Tooth neuropathy type 1D",
            "description": ""
        },
        {
            "id": "MONDO:0011890",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011890",
            "name": "Charcot-Marie-Tooth disease, demyelinating, type 1D",
            "description": ""
        },
        {
            "id": "MONDO:0011890",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011890",
            "name": "Charcot-Marie-Tooth neuropathy, type 1D",
            "description": ""
        },
        {
            "id": "MONDO:0011890",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011890",
            "name": "EGR2 Charcot-Marie-Tooth disease type 1",
            "description": ""
        },
        {
            "id": "MONDO:0011890",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011890",
            "name": "hereditary motor and sensory neuropathy 1D",
            "description": ""
        },
        {
            "id": "MONDO:0011890",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011890",
            "name": "Hmsn1D",
            "description": ""
        },
        {
            "id": "MONDO:0011890",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011890",
            "name": "HMSN 1D",
            "description": ""
        },
        {
            "id": "MONDO:0011890",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011890",
            "name": "HMSN1D",
            "description": ""
        },
        {
            "id": "MONDO:0011890",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011890",
            "name": "Charcot Marie Tooth disease type 1D",
            "description": ""
        },
        {
            "id": "MONDO:0011890",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011890",
            "name": "CMT 1D",
            "description": ""
        },
        {
            "id": "MONDO:0011890",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011890",
            "name": "Charcot-Marie-Tooth disease, demyelinating, type 1D; CMT1D",
            "description": ""
        },
        {
            "id": "MONDO:0011890",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011890",
            "name": "CMT1D",
            "description": ""
        },
        {
            "id": "MONDO:0011890",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011890",
            "name": "Charcot-Marie-Tooth disease type 1 caused by mutation in EGR2",
            "description": ""
        },
        {
            "id": "MONDO:0011890",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011890",
            "name": "HMSN ID",
            "description": ""
        },
        {
            "id": "MIM:607678",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/607678",
            "name": "Charcot-Marie-Tooth disease 1D",
            "description": "Charcot-Marie-Tooth disease 1D"
        }
    ]
}