{
    "disease_id": "DOID:0111818",
    "recommended_name": {
        "id": "DOID:0111818",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111818",
        "name": "syndactyly type 4",
        "description": "A syndactyly characterized by complete bilateral syndactyly involving all digits 1 to 5 that has_material_basis_in heterozygous mutation of a SHH regulatory element in intron 5 of the LMBR1 gene on chromosome 7q36.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111818",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111818",
            "name": "Haas type syndactyly",
            "description": ""
        },
        {
            "id": "DOID:0111818",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111818",
            "name": "SDTY4",
            "description": ""
        },
        {
            "id": "DOID:0111818",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111818",
            "name": "polysyndactyly, Haas type",
            "description": ""
        },
        {
            "id": "MONDO:0008515",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008515",
            "name": "syndactyly type 4",
            "description": "A very rare congenital distal limb malformation characterized by complete bilateral syndactyly (involving all digits 1 to 5)."
        },
        {
            "id": "MONDO:0008515",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008515",
            "name": "LMBR1 non-syndromic syndactyly",
            "description": ""
        },
        {
            "id": "MONDO:0008515",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008515",
            "name": "non-syndromic syndactyly caused by mutation in LMBR1",
            "description": ""
        },
        {
            "id": "MONDO:0008515",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008515",
            "name": "polysyndactyly, Haas type",
            "description": ""
        },
        {
            "id": "MONDO:0008515",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008515",
            "name": "SDTY4",
            "description": ""
        },
        {
            "id": "MONDO:0008515",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008515",
            "name": "polysyndactyly type Haas",
            "description": ""
        },
        {
            "id": "MONDO:0008515",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008515",
            "name": "syndactyly, type IV",
            "description": ""
        },
        {
            "id": "MIM:186200",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/186200",
            "name": "Syndactyly 4",
            "description": "Syndactyly 4"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111818"
    ],
    "unlinked_id_list": []
}