{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012644", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012644", 
            "name": "short-rib thoracic dysplasia 2 with or without polydactyly; SRTD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012644", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012644", 
            "name": "ATD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012644", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012644", 
            "name": "Jeune syndrome caused by mutation in IFT80"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012644", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012644", 
            "name": "asphyxiating thoracic dystrophy type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012644", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012644", 
            "name": "SRTD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012644", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012644", 
            "name": "short-rib thoracic dysplasia 2 with or without polydactyly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012644", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012644", 
            "name": "IFT80 Jeune syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110086", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110086", 
            "name": "short-rib thoracic dysplasia 2 with or without polydactyly"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110086", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110086", 
            "name": "ATD2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110086", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110086", 
            "name": "SRTD2"
        }, 
        {
            "url": "https://www.omim.org/entry/611263", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:611263", 
            "name": "Short-rib thoracic dysplasia 2 with or without polydactyly"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110086", 
        "description": "An asphyxiating thoracic dystrophy that has_material_basis_in homozygous mutation in the IFT80 gene on chromosome 3q25.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110086", 
        "name": "asphyxiating thoracic dystrophy 2"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/611263", 
            "id": "611263", 
            "database": "MIM"
        }
    ]
}