{
    "disease_id": "DOID:0111259",
    "recommended_name": {
        "id": "DOID:0111259",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111259",
        "name": "postaxial acrofacial dysostosis",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0111259",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111259",
            "name": "Miller syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111259",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111259",
            "name": "POADS",
            "description": ""
        },
        {
            "id": "DOID:0111259",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111259",
            "name": "Postaxial acrodysostosis",
            "description": ""
        },
        {
            "id": "DOID:0111259",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111259",
            "name": "acrofacial dysostosis, Genee-Wiedmann type",
            "description": ""
        },
        {
            "id": "DOID:0111259",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111259",
            "name": "mandibulfacial dysostosis with postaxial limb anomalies",
            "description": ""
        },
        {
            "id": "MONDO:0009903",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009903",
            "name": "postaxial acrofacial dysostosis",
            "description": "Postaxial acrofacial dysostosis (POADS) is a type of acrofacial dysostosis (see this term) characterised by mandibular and malar hypoplasia, small and cup-shaped ears, lower lid ectropion, and symmetrical postaxial limb deficiencies with absence of the fifth digital ray and ulnar hypoplasia."
        },
        {
            "id": "MONDO:0009903",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009903",
            "name": "Mandibulfacial dysostosis with postaxial limb anomalies",
            "description": ""
        },
        {
            "id": "MONDO:0009903",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009903",
            "name": "Genee-Wiedemann syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009903",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009903",
            "name": "Wildervanck-Smith syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009903",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009903",
            "name": "postaxial acrofacial dysostosis",
            "description": ""
        },
        {
            "id": "MONDO:0009903",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009903",
            "name": "postaxial acrodysostosis",
            "description": ""
        },
        {
            "id": "MONDO:0009903",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009903",
            "name": "POADS",
            "description": ""
        },
        {
            "id": "MONDO:0009903",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009903",
            "name": "acrofacial dysostosis, Genee-Wiedmann type",
            "description": ""
        },
        {
            "id": "MONDO:0009903",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009903",
            "name": "Genee-Wiedemann acrofacial dysostosis",
            "description": ""
        },
        {
            "id": "MONDO:0009903",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009903",
            "name": "POADS syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009903",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009903",
            "name": "postaxial acrofacial dysostosis (POADS) syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009903",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009903",
            "name": "GWAFD",
            "description": ""
        },
        {
            "id": "MONDO:0009903",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009903",
            "name": "Miller syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009903",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009903",
            "name": "postaxial acrofacial dysostosis; POADS",
            "description": ""
        },
        {
            "id": "MIM:263750",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/263750",
            "name": "Postaxial acrofacial dysostosis",
            "description": "Postaxial acrofacial dysostosis"
        }
    ]
}