{
    "disease_id": "DOID:0111596", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0111596", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111596", 
            "name": "digitotalar dysmorphism"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111596", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111596", 
            "name": "DA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007458", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007458", 
            "name": "digitotalar dysmorphism; ulnar drift, hereditary"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007458", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007458", 
            "name": "digitotalar dysmorphism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007458", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007458", 
            "name": "ulnar drift, hereditary"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111596", 
        "description": "A distal arthrogryposis characterized by autosomal domiant inheritance of contractures of the distal regions of the hands and feet with no facial involvement or other anomalies.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111596", 
        "name": "distal arthrogryposis type 1"
    }
}