{
    "disease_id": "DOID:0050467",
    "recommended_name": {
        "id": "DOID:0050467",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0050467",
        "name": "erythrokeratodermia variabilis",
        "description": "A skin disease that is characterized by areas of sharply demarcated, brown hyperkeratosis and has_material_basis_in mutations in genes encoding for connexin channels proteins in the epidermis."
    },
    "synonyms": [
        {
            "id": "DOID:0050467",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0050467",
            "name": "Erythrokeratodermia Figurata Variabilis",
            "description": ""
        },
        {
            "id": "DOID:0050467",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0050467",
            "name": "Greither Disease",
            "description": ""
        },
        {
            "id": "MONDO:0033010",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033010",
            "name": "erythrokeratodermia variabilis et progressiva 1",
            "description": ""
        },
        {
            "id": "MONDO:0033010",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033010",
            "name": "keratosis palmoplantaris transgrediens Et progrediens",
            "description": ""
        },
        {
            "id": "MONDO:0033010",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033010",
            "name": "erythrokeratodermia variabilis with erythema Gyratum Repens",
            "description": ""
        },
        {
            "id": "MONDO:0033010",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033010",
            "name": "EKVP1",
            "description": ""
        },
        {
            "id": "MONDO:0033010",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033010",
            "name": "erythrokeratodermia variabilis ET progressiva 1; EKVP1",
            "description": ""
        },
        {
            "id": "MONDO:0033010",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033010",
            "name": "erythrokeratodermia Figurata, congenital familial, in plaques",
            "description": ""
        },
        {
            "id": "MONDO:0033010",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033010",
            "name": "Greither disease",
            "description": ""
        },
        {
            "id": "MONDO:0033010",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033010",
            "name": "erythrokeratodermia variabilis Et progressiva",
            "description": ""
        },
        {
            "id": "MONDO:0033010",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033010",
            "name": "erythrokeratodermia variabilis",
            "description": ""
        },
        {
            "id": "MONDO:0033010",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033010",
            "name": "erythrokeratodermia, progressive symmetric",
            "description": ""
        },
        {
            "id": "MIM:133200",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/133200",
            "name": "Erythrokeratodermia variabilis et progressiva 1",
            "description": "Erythrokeratodermia variabilis et progressiva 1"
        }
    ]
}