{
    "disease_id": "DOID:0060857", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008428", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008428", 
            "name": "pituitary hormone deficiency, combined, 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008428", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008428", 
            "name": "De Morsier syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008428", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008428", 
            "name": "hypopituitarism and septooptic 'dysplasia'"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008428", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008428", 
            "name": "septo-optic dysplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008428", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008428", 
            "name": "septo-optic dysplasia sequence"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008428", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008428", 
            "name": "septo-optic dysplasia with growth hormone deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008428", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008428", 
            "name": "septo-optic dysplasia spectrum"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008428", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008428", 
            "name": "Growth hormone deficiency with pituitary anomalies"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008428", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008428", 
            "name": "SOD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060857", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060857", 
            "name": "De Morsier syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060857", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060857", 
            "name": "SOD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060857", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060857", 
            "name": "septo-optic dysplasia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060857", 
        "description": "A syndrome characterized by the classical triad of optic nerve hypoplasia, pituitary gland hypoplasia and midline brain defects that has_material_basis_in mutation in the HESX1 gene on chromosome 3p14.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060857", 
        "name": "septooptic dysplasia"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060857#disease-associations", 
            "id": "0060857", 
            "database": "Alliance of Genome Resources"
        }
    ]
}