{
    "disease_id": "DOID:0080844",
    "recommended_name": {
        "id": "DOID:0080844",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080844",
        "name": "omodysplasia 1",
        "description": "An omodysplasia that is characterized by severe congenital micromelia with shortening and distal tapering of the humeri and femora to give a club-like appearance and that has_material_basis_in homozygous or compound heterozygous mutation in the GPC6 gene on chromosome 13q32."
    },
    "synonyms": [
        {
            "id": "MONDO:0009779",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009779",
            "name": "autosomal recessive omodysplasia",
            "description": "Autosomal recessive form of omodysplasia."
        },
        {
            "id": "MONDO:0009779",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009779",
            "name": "autosomal recessive omodysplasia",
            "description": ""
        },
        {
            "id": "MONDO:0009779",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009779",
            "name": "micromelic dysplasia-dislocation of radius syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009779",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009779",
            "name": "omodysplasia type 1",
            "description": ""
        },
        {
            "id": "MONDO:0009779",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009779",
            "name": "omodysplasia, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0009779",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009779",
            "name": "OMOD1",
            "description": ""
        },
        {
            "id": "MONDO:0009779",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009779",
            "name": "micromelic dysplasia congenita with dislocation of radius",
            "description": ""
        },
        {
            "id": "MONDO:0009779",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009779",
            "name": "omodysplasia 1",
            "description": ""
        },
        {
            "id": "MONDO:0009779",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009779",
            "name": "omodysplasia autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0009779",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009779",
            "name": "omodysplasia generalised form",
            "description": ""
        },
        {
            "id": "MONDO:0009779",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009779",
            "name": "omodysplasia generalized form",
            "description": ""
        },
        {
            "id": "MONDO:0009779",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009779",
            "name": "omodysplasia, generalised form",
            "description": ""
        },
        {
            "id": "MIM:258315",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/258315",
            "name": "Omodysplasia 1",
            "description": "Omodysplasia 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080844"
    ],
    "unlinked_id_list": []
}