{
    "disease_id": "DOID:0111571",
    "recommended_name": {
        "id": "DOID:0111571",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111571",
        "name": "Weyers acrofacial dysostosis",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0111571",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111571",
            "name": "Curry-Hall syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111571",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111571",
            "name": "WAD",
            "description": ""
        },
        {
            "id": "DOID:0111571",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111571",
            "name": "Weyers acrodental dysostosis",
            "description": ""
        },
        {
            "id": "DOID:0111571",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111571",
            "name": "acrofacial dysostosis, Weyers type",
            "description": ""
        },
        {
            "id": "MONDO:0008673",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008673",
            "name": "acrofacial dysostosis, Weyers type",
            "description": "Acrofacialdysostosis, Weyers type (WAD) is a rare ectodermal dysplasia syndrome with bone abnormalities characterized by onychodystrophy; anomalies of the lower jaw, oral vestibule and dentition; post-axialpolydactyly; moderately restricted growth with short limbs; and normal intelligence. Although it closely resembles Ellis-van Creveld syndrome (see this term), an allelic disorder and another type of ciliopathy, WAD is usually a milder disease without the presence of heart abnormalities and is inherited in an autosomal dominant manner."
        },
        {
            "id": "MONDO:0008673",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008673",
            "name": "Weyers acrodental dysostosis",
            "description": ""
        },
        {
            "id": "MONDO:0008673",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008673",
            "name": "curry Hall syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008673",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008673",
            "name": "Weyers acrofacial dysostosis",
            "description": ""
        },
        {
            "id": "MONDO:0008673",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008673",
            "name": "Weyers acrofacial dysostosis; wad",
            "description": ""
        },
        {
            "id": "MONDO:0008673",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008673",
            "name": "wad",
            "description": ""
        },
        {
            "id": "MONDO:0008673",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008673",
            "name": "acrofacial dysostosis of Weyers",
            "description": ""
        },
        {
            "id": "MONDO:0008673",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008673",
            "name": "acrodental dysostosis of Weyers",
            "description": ""
        },
        {
            "id": "MONDO:0008673",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008673",
            "name": "curry-Hall syndrome",
            "description": ""
        },
        {
            "id": "MIM:193530",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/193530",
            "name": "Acrofacial dysostosis, Weyers type",
            "description": "Acrofacial dysostosis, Weyers type"
        }
    ]
}