{
    "disease_id": "DOID:0080050", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011275", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011275", 
            "name": "acromesomelic dysplasia, Maroteaux type; AMDM"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011275", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011275", 
            "name": "acromesomelic dwarfism Maroteux type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011275", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011275", 
            "name": "acromesomelic dysplasia Maroteaux type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011275", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011275", 
            "name": "St. Helena dysplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011275", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011275", 
            "name": "AMDM"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080050", 
        "description": "An acromesomelic dysplasia that has_material_basis_in mutation in NPR-B receptor which results_in severe dwarfism, abnormalities of the vertebral column and shortening of the limb middle and distal segments.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080050", 
        "name": "acromesomelic dysplasia, Maroteaux type"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/602875", 
            "id": "602875", 
            "database": "MIM"
        }
    ]
}