{
    "disease_id": "DOID:0110873", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012563", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012563", 
            "name": "pituitary anomalies with holoprosencephaly-like features"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012563", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012563", 
            "name": "holoprosencephaly with microphthalmia and first branchial arch anomalies"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012563", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012563", 
            "name": "holoprosencephaly 9; HPE9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012563", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012563", 
            "name": "holoprosencephaly caused by mutation in GLI2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012563", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012563", 
            "name": "holoprosencephaly type 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012563", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012563", 
            "name": "GLI2 holoprosencephaly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012563", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012563", 
            "name": "HPE9"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110873", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110873", 
            "name": "pituitary anomalies with holoprosencephaly-like features"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110873", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110873", 
            "name": "HPE9"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110873", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110873", 
            "name": "holoprosencephaly with microphthalmia and first branchial arch anomalies"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110873", 
        "description": "A holoprosencephaly that has_material_basis_in heterozygous mutation in the GLI2 gene on chromosome 2q14.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110873", 
        "name": "holoprosencephaly 9"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110873#disease-associations", 
            "id": "0110873", 
            "database": "Alliance of Genome Resources"
        }
    ]
}