{
    "disease_id": "DOID:0060306",
    "recommended_name": {
        "id": "DOID:0060306",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060306",
        "name": "Meier-Gorlin syndrome",
        "description": "A syndrome that is characterized by bilateral underdevelopment of the external ear, short stature, absent or underdeveloped patellae and severe prenatal and postnatal growth retardation."
    },
    "synonyms": [
        {
            "id": "DOID:0060306",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060306",
            "name": "ear-patella-short stature syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009143",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009143",
            "name": "Meier-Gorlin syndrome 1",
            "description": "Any Meier-Gorlin syndrome in which the cause of the disease is a mutation in the ORC1 gene."
        },
        {
            "id": "MONDO:0009143",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009143",
            "name": "Meier-GORLIN syndrome 1; MGORS1",
            "description": ""
        },
        {
            "id": "MONDO:0009143",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009143",
            "name": "ORC1 Meier-Gorlin syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009143",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009143",
            "name": "Meier-Gorlin syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0009143",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009143",
            "name": "Meier-Gorlin syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009143",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009143",
            "name": "microtia, absent patellae, micrognathia syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009143",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009143",
            "name": "Ear, patella, short stature syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009143",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009143",
            "name": "Meier-Gorlin syndrome type 1",
            "description": ""
        },
        {
            "id": "MONDO:0009143",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009143",
            "name": "MGORS1",
            "description": ""
        },
        {
            "id": "MONDO:0009143",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009143",
            "name": "Meier-Gorlin syndrome caused by mutation in ORC1",
            "description": ""
        },
        {
            "id": "MIM:224690",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/224690",
            "name": "Meier-Gorlin syndrome 1",
            "description": "Meier-Gorlin syndrome 1"
        }
    ]
}