{
    "disease_id": "DOID:0110965", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007216", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007216", 
            "name": "Brachymesophalangy 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007216", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007216", 
            "name": "Mohr-Wriedt type brachydactyly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007216", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007216", 
            "name": "brachydactyly, Mohr-Wriedt type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007216", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007216", 
            "name": "brachydactyly, type A2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007216", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007216", 
            "name": "brachydactyly, type A2; BDA2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007216", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007216", 
            "name": "brachymesophalangy II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007216", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007216", 
            "name": "Brachymesophalangy type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007216", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007216", 
            "name": "BDA2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110965", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110965", 
            "name": "BDA2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110965", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110965", 
            "name": "Mohr-Wriedt type brachydactyly"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110965", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110965", 
            "name": "brachymesophalangy II"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110965", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110965", 
        "name": "brachydactyly type A2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110965#disease-associations", 
            "id": "0110965", 
            "database": "Alliance of Genome Resources"
        }
    ]
}