{
    "disease_id": "DOID:0050600",
    "recommended_name": {
        "id": "DOID:0050600",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0050600",
        "name": "ABCD syndrome",
        "description": "A syndrome that is characterized by albinism, black lock, cell migration disorder of the neurocytes of the gut and sensorineural deafness and has_material_basis_in a mutation in the endothelin B receptor gene (EDNRB)."
    },
    "synonyms": [
        {
            "id": "DOID:0050600",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0050600",
            "name": "ABCDS",
            "description": ""
        },
        {
            "id": "DOID:0050600",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0050600",
            "name": "albinism, black lock, cell migration disorder of the neurocytes of the gut, and deafness",
            "description": ""
        },
        {
            "id": "MONDO:0010895",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010895",
            "name": "ABCD syndrome",
            "description": "An autosomal recessive disease that is characterized by albinism, black lock, cell migration disorder of the neurocytes of the gut and sensorineural deafness and has_material_basis_in a mutation in the endothelin B receptor gene (EDNRB)."
        },
        {
            "id": "MONDO:0010895",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010895",
            "name": "albinism, black lock, cell migration disorder of the Neurocytes of the gut, and deafness",
            "description": ""
        },
        {
            "id": "MONDO:0010895",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010895",
            "name": "albinism, block lock, cell migration disorder of the neurocytes of the gut, and deafness",
            "description": ""
        },
        {
            "id": "MONDO:0010895",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010895",
            "name": "ABCD syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010895",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010895",
            "name": "ABCD syndrome; ABCDS",
            "description": ""
        },
        {
            "id": "MONDO:0010895",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010895",
            "name": "ABCDS",
            "description": ""
        },
        {
            "id": "MIM:600501",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/600501",
            "name": "ABCD syndrome",
            "description": "ABCD syndrome"
        }
    ]
}