{
    "disease_id": "DOID:0111259", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009903", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009903", 
            "name": "Mandibulfacial dysostosis with postaxial limb anomalies"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009903", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009903", 
            "name": "Genee-Wiedemann syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009903", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009903", 
            "name": "Wildervanck-Smith syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009903", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009903", 
            "name": "postaxial acrodysostosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009903", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009903", 
            "name": "POADS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009903", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009903", 
            "name": "acrofacial dysostosis, Genee-Wiedmann type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009903", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009903", 
            "name": "Genee-Wiedemann acrofacial dysostosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009903", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009903", 
            "name": "POADS syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009903", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009903", 
            "name": "postaxial acrofacial dysostosis (POADS) syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009903", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009903", 
            "name": "GWAFD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009903", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009903", 
            "name": "Miller syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009903", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009903", 
            "name": "postaxial acrofacial dysostosis; POADS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111259", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111259", 
            "name": "Miller syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111259", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111259", 
            "name": "POADS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111259", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111259", 
            "name": "Postaxial acrodysostosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111259", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111259", 
            "name": "acrofacial dysostosis, Genee-Wiedmann type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111259", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111259", 
            "name": "mandibulfacial dysostosis with postaxial limb anomalies"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111259", 
        "description": "A syndrome characterized by severe micrognathia, cleft lip and/or palate, hypoplasia or aplasia of the postaxial elements of the limbs, coloboma of the eyelids, cup-shaped ears, and supernumerary nipples that has_material_basis_in homozygous or compound heterozygous mutation in DHODH on 16q22.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111259", 
        "name": "postaxial acrofacial dysostosis"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/263750", 
            "id": "263750", 
            "database": "MIM"
        }
    ]
}