{
    "disease_id": "DOID:0060857",
    "recommended_name": {
        "id": "DOID:0060857",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060857",
        "name": "septooptic dysplasia",
        "description": "A syndrome characterized by the classical triad of optic nerve hypoplasia, pituitary gland hypoplasia and midline brain defects that has_material_basis_in heterozygous, homozygous, or compound heterozygous mutation in the homeobox gene HESX1 on chromosome 3p14."
    },
    "synonyms": [
        {
            "id": "DOID:0060857",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060857",
            "name": "De Morsier syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060857",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060857",
            "name": "SOD",
            "description": ""
        },
        {
            "id": "DOID:0060857",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060857",
            "name": "septo-optic dysplasia",
            "description": ""
        },
        {
            "id": "MONDO:0008428",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008428",
            "name": "septooptic dysplasia",
            "description": "Septooptic dysplasia (SOD) is a clinically heterogeneous disorder characterized by the classical triad of optic nerve hypoplasia, pituitary hormone abnormalities and midline brain defects."
        },
        {
            "id": "MONDO:0008428",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008428",
            "name": "De Morsier syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008428",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008428",
            "name": "SOD",
            "description": ""
        },
        {
            "id": "MONDO:0008428",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008428",
            "name": "septo-optic dysplasia",
            "description": ""
        },
        {
            "id": "MONDO:0008428",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008428",
            "name": "septo-optic dysplasia sequence",
            "description": ""
        },
        {
            "id": "MONDO:0008428",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008428",
            "name": "septooptic dysplasia",
            "description": ""
        },
        {
            "id": "MONDO:0008428",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008428",
            "name": "hypopituitarism and septooptic 'dysplasia'",
            "description": ""
        },
        {
            "id": "MONDO:0008428",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008428",
            "name": "septo-optic dysplasia with growth hormone deficiency",
            "description": ""
        },
        {
            "id": "MIM:182230",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/182230",
            "name": "Septooptic dysplasia",
            "description": "Septooptic dysplasia"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060857"
    ],
    "unlinked_id_list": []
}