{
    "disease_id": "DOID:0060732", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008013", 
            "name": "9p- syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008013", 
            "name": "9p syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008013", 
            "name": "9p deletion syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008013", 
            "name": "deletion 9p"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008013", 
            "name": "monosomy 9P syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008013", 
            "name": "9p deletion"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008013", 
            "name": "monosomy 9p"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008013", 
            "name": "9p monosomy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008013", 
            "name": "Alfi syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008013", 
            "name": "chromosome 9p deletion"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008013", 
            "name": "partial monosomy 9p"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008013", 
            "name": "monosomy type 9p"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060732", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060732", 
            "name": "9p syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060732", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060732", 
            "name": "Alfi syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060732", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060732", 
            "name": "monosomy 9p syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060732", 
        "description": "A chromosomal deletion syndrome characterized by trigonocephaly, flattened occiput midface hypoplasia, long philtrum, prominent forehead, broad flat nasal bridge, anteverted nares, malformed external ears, hypertelorism, hypertonia, delayed psychomotor development and that has_material_basis_in a contiguous gene deletion on the short arm of chromosome 9.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060732", 
        "name": "chromosome 9p deletion syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060732#disease-associations", 
            "id": "0060732", 
            "database": "Alliance of Genome Resources"
        }
    ]
}