{
    "disease_id": "DOID:0110965",
    "recommended_name": {
        "id": "DOID:0110965",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110965",
        "name": "brachydactyly type A2",
        "description": "A brachydactyly characterized by autosomal dominant inheritance of malformations of the middle phalanx of the index finger and anomalies of the second toe that has_material_basis_in heterozygous mutation in the BMPR1B gene on chromosome 4q or in the GDF5 gene on chromosome 20q11 or heterozygous duplication in a regulatory element of BMP2 on chromosome 20p12."
    },
    "synonyms": [
        {
            "id": "DOID:0110965",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110965",
            "name": "BDA2",
            "description": ""
        },
        {
            "id": "DOID:0110965",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110965",
            "name": "Mohr-Wriedt type brachydactyly",
            "description": ""
        },
        {
            "id": "DOID:0110965",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110965",
            "name": "brachymesophalangy II",
            "description": ""
        },
        {
            "id": "MONDO:0007216",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007216",
            "name": "brachydactyly type A2",
            "description": "Brachydactyly type A2 (BDA2) is a congenital malformation characterized by shortening (hypoplasia or aplasia) of the middle phalanges of the index finger and, sometimes, of the little finger."
        },
        {
            "id": "MONDO:0007216",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007216",
            "name": "BDA2",
            "description": ""
        },
        {
            "id": "MONDO:0007216",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007216",
            "name": "Mohr-Wriedt type brachydactyly",
            "description": ""
        },
        {
            "id": "MONDO:0007216",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007216",
            "name": "brachydactyly, Mohr-Wriedt type",
            "description": ""
        },
        {
            "id": "MONDO:0007216",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007216",
            "name": "Brachymesophalangy type 2",
            "description": ""
        },
        {
            "id": "MONDO:0007216",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007216",
            "name": "brachydactyly, type A2",
            "description": ""
        },
        {
            "id": "MIM:112600",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/112600",
            "name": "Brachydactyly A2",
            "description": "Brachydactyly A2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110965"
    ],
    "unlinked_id_list": []
}