{
    "disease_id": "DOID:0050600", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010895", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010895", 
            "name": "albinism, black lock, cell migration disorder of the Neurocytes of the gut, and deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010895", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010895", 
            "name": "albinism, block lock, cell migration disorder of the neurocytes of the gut, and deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010895", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010895", 
            "name": "ABCD syndrome; ABCDS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010895", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010895", 
            "name": "ABCDS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050600", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050600", 
            "name": "ABCDS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050600", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050600", 
            "name": "albinism, black lock, cell migration disorder of the neurocytes of the gut, and deafness"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050600", 
        "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).", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050600", 
        "name": "ABCD syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/600501", 
            "id": "600501", 
            "database": "MIM"
        }
    ]
}