{
    "disease_id": "DOID:0111571", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008673", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008673", 
            "name": "acrofacial dysostosis, Weyers type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008673", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008673", 
            "name": "Weyers acrodental dysostosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008673", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008673", 
            "name": "curry Hall syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008673", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008673", 
            "name": "Weyers acrofacial dysostosis; wad"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008673", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008673", 
            "name": "wad"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008673", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008673", 
            "name": "acrofacial dysostosis of Weyers"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008673", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008673", 
            "name": "acrodental dysostosis of Weyers"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008673", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008673", 
            "name": "curry-Hall syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111571", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111571", 
            "name": "Curry-Hall syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111571", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111571", 
            "name": "WAD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111571", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111571", 
            "name": "Weyers acrodental dysostosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111571", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111571", 
            "name": "acrofacial dysostosis, Weyers type"
        }, 
        {
            "url": "https://www.omim.org/entry/193530", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:193530", 
            "name": "Acrofacial dysostosis, Weyers type"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111571", 
        "description": "An acrofacial dysostosis characterized by dental anomalies, nail dystrophy, postaxial polydactyly, and mild short stature that has_material_basis_in heterozygous mutation in the genes EVC2 or EVC on chromosome 4p16.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111571", 
        "name": "Weyers acrofacial dysostosis"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/193530", 
            "id": "193530", 
            "database": "MIM"
        }
    ]
}