{
    "disease_id": "DOID:0060783",
    "recommended_name": {
        "id": "DOID:0060783",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060783",
        "name": "ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3",
        "description": "An EEC syndrome characterized by autosomal dominant inheritance of absence of the central parts of the hands and feet, resulting in split-hand/foot malformation, ectodermal dysplasia, and cleft lip with or without cleft palate that has_material_basis_in heterozygous mutation in the TP63 gene on chromosome 3q28."
    },
    "synonyms": [
        {
            "id": "DOID:0060783",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060783",
            "name": "EEC syndrome 3",
            "description": ""
        },
        {
            "id": "DOID:0060783",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060783",
            "name": "EEC3",
            "description": ""
        },
        {
            "id": "MONDO:0011428",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011428",
            "name": "ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3",
            "description": "Any EEC syndrome in which the cause of the disease is a mutation in the TP63 gene."
        },
        {
            "id": "MONDO:0011428",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011428",
            "name": "EEC syndrome 3",
            "description": ""
        },
        {
            "id": "MONDO:0011428",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011428",
            "name": "EEC syndrome caused by mutation in TP63",
            "description": ""
        },
        {
            "id": "MONDO:0011428",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011428",
            "name": "EEC3",
            "description": ""
        },
        {
            "id": "MONDO:0011428",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011428",
            "name": "TP63 EEC syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011428",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011428",
            "name": "ectrodactyly, ectodermal dysplasia, and cleft Lip/palate syndrome type 3",
            "description": ""
        },
        {
            "id": "MONDO:0011428",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011428",
            "name": "ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome type 3",
            "description": ""
        },
        {
            "id": "MONDO:0011428",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011428",
            "name": "ectrodactyly, ectodermal dysplasia, and cleft LIP/palate syndrome 3",
            "description": ""
        },
        {
            "id": "MIM:604292",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/604292",
            "name": "Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3",
            "description": "Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060783"
    ],
    "unlinked_id_list": []
}