{
    "disease_id": "DOID:0111607",
    "recommended_name": {
        "id": "DOID:0111607",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111607",
        "name": "distal arthrogryposis type 3",
        "description": "A distal arthrogryposis characterized by distal arthrogryposis with short stature and cleft palate that has_material_basis_in heterozygous mutation in the PIEZO2 gene on chromosome 18p11.22-p11.21."
    },
    "synonyms": [
        {
            "id": "DOID:0111607",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111607",
            "name": "DA3",
            "description": ""
        },
        {
            "id": "DOID:0111607",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111607",
            "name": "Gordon syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111607",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111607",
            "name": "camptodactyly-cleft palate-clubfoot syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111607",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111607",
            "name": "distal arthrogryposis multiplex congenita type IIA",
            "description": ""
        },
        {
            "id": "MONDO:0007252",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007252",
            "name": "Gordon syndrome",
            "description": "An extremely rare multiple congenital malformation syndrome characterized by congenital contractures of hand and feet with variable degrees of severity of camptodactyly, clubfoot and, less frequently, cleft palate. Intelligence is normal but in some cases, additional abnormalities, such as short stature, kyphoscoliosis, ptosis, micrognathia, and cryptorchidism may also be present. Gordon syndrome, Marden-Walker syndrome and arthrogryposis with oculomotor limitation and electroretinal anomalies clinically and genetically overlap, and could represent variable expressions of the same condition."
        },
        {
            "id": "MONDO:0007252",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007252",
            "name": "Gordon syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007252",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007252",
            "name": "camptodactyly-cleft palate-clubfoot syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007252",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007252",
            "name": "distal arthrogryposis type 3",
            "description": ""
        },
        {
            "id": "MONDO:0007252",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007252",
            "name": "distal arthrogryposis type IIA",
            "description": ""
        },
        {
            "id": "MONDO:0007252",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007252",
            "name": "DA3",
            "description": ""
        },
        {
            "id": "MONDO:0007252",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007252",
            "name": "arthrogryposis distal type 3",
            "description": ""
        },
        {
            "id": "MONDO:0007252",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007252",
            "name": "arthrogryposis, distal, type 3",
            "description": ""
        },
        {
            "id": "MIM:114300",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/114300",
            "name": "Arthrogryposis, distal, 3",
            "description": "Arthrogryposis, distal, 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111607"
    ],
    "unlinked_id_list": []
}