{
    "disease_id": "DOID:0080056", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008702", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008702", 
            "name": "achondrogenesis, type II; ACG2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008702", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008702", 
            "name": "ACG2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008702", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008702", 
            "name": "achondrogenesis, type IB, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008702", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008702", 
            "name": "achondrogenesis, type II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008702", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008702", 
            "name": "achondrogenesis, type IB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008702", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008702", 
            "name": "chondrogenesis imperfecta"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008702", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008702", 
            "name": "achondrogenesis, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008702", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008702", 
            "name": "hypochondrogenesis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008702", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008702", 
            "name": "achondrogenesis, Langer-Saldino type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008702", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008702", 
            "name": "achondrogenesis type 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080056", 
        "description": "An achondrogenesis that has_material_basis_in mutations in the COL2A1 gene which results_in underdeveloped lungs, hydrops fetalis, a prominent forehead and abnormal ossification of the located_in vertebral column or located_in pelvis.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080056", 
        "name": "achondrogenesis type II"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080056#disease-associations", 
            "id": "0080056", 
            "database": "Alliance of Genome Resources"
        }
    ]
}