{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007804", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007804", 
            "name": "ano-cerebro-digital syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007804", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007804", 
            "name": "hypothalamic hamartoblastoma syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007804", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007804", 
            "name": "hypothalamic hamartoblastoma, hypopituitarism, imperforate anus, and postaxial polydactyly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007804", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007804", 
            "name": "Pallister-Hall syndrome; PHS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007804", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007804", 
            "name": "PHS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007804", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007804", 
            "name": "Pallister Hall syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:9248", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:9248", 
            "name": "A syndrome that is characterized by hypothalamic hamartoma, pituitary dysfunction, central polydactyly, and visceral malformations and has_material_basis_in autosomal dominant heterozygous mutation in the GLI3 gene on chromosome 7p14."
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:9248", 
        "description": "", 
        "resource": "Disease Ontology", 
        "id": "DOID:9248", 
        "name": "Pallister-Hall syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/146510", 
            "id": "146510", 
            "database": "MIM"
        }
    ]
}