{
    "disease_id": "DOID:0110087",
    "recommended_name": {
        "id": "DOID:0110087",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110087",
        "name": "asphyxiating thoracic dystrophy 3",
        "description": "An asphyxiating thoracic dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the DYNC2H1 gene on chromosome 11q22."
    },
    "synonyms": [
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            "url": "http://disease-ontology.org/term/DOID:0110087",
            "name": "ATD3",
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            "url": "http://disease-ontology.org/term/DOID:0110087",
            "name": "SRPS1",
            "description": ""
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            "url": "http://disease-ontology.org/term/DOID:0110087",
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            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110087",
            "name": "Saldino-Noonan syndrome",
            "description": ""
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        {
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            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110087",
            "name": "Verma-Naumoff syndrome",
            "description": ""
        },
        {
            "id": "DOID:0110087",
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            "url": "http://disease-ontology.org/term/DOID:0110087",
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            "description": ""
        },
        {
            "id": "DOID:0110087",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110087",
            "name": "short rib-polydactyly syndrome, type I",
            "description": ""
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        {
            "id": "DOID:0110087",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110087",
            "name": "short rib-polydactyly syndrome, type IIB",
            "description": ""
        },
        {
            "id": "DOID:0110087",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110087",
            "name": "short-rib thoracic dysplasia 3 with or without polydactyly",
            "description": ""
        },
        {
            "id": "DOID:0110087",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110087",
            "name": "polydactyly with neonatal chondrodystrophy, type III",
            "description": ""
        },
        {
            "id": "MONDO:0013127",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013127",
            "name": "asphyxiating thoracic dystrophy 3",
            "description": "An asphyxiating thoracic dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the DYNC2H1 gene on chromosome 11q22."
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        },
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            "name": "short rib-polydactyly syndrome, type 2B",
            "description": ""
        },
        {
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            "name": "asphyxiating thoracic dystrophy type 3",
            "description": ""
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        {
            "id": "MONDO:0013127",
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            "description": ""
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        {
            "id": "MONDO:0013127",
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        {
            "id": "MONDO:0013127",
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            "description": ""
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        {
            "id": "MONDO:0013127",
            "resource": "MONDO",
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            "description": ""
        },
        {
            "id": "MONDO:0013127",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013127",
            "name": "short rib-polydactyly syndrome, type IIB",
            "description": ""
        },
        {
            "id": "MONDO:0013127",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013127",
            "name": "Verma-Naumoff syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0013127",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013127",
            "name": "short rib-polydactyly syndrome, type 3",
            "description": ""
        },
        {
            "id": "MONDO:0013127",
            "resource": "MONDO",
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            "name": "asphyxiating thoracic dystrophy 3",
            "description": ""
        },
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            "id": "MONDO:0013127",
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            "url": "https://monarchinitiative.org/disease/MONDO:0013127",
            "name": "short rib-polydactyly syndrome, type 1",
            "description": ""
        },
        {
            "id": "MIM:613091",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613091",
            "name": "Short-rib thoracic dysplasia 3 with or without polydactyly",
            "description": "Short-rib thoracic dysplasia 3 with or without polydactyly"
        }
    ]
}
