{
    "disease_id": "DOID:0060812", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010286", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010286", 
            "name": "MRXSSD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010286", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010286", 
            "name": "Siderius Hamel syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010286", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010286", 
            "name": "Siderius X-linked mental retardation syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010286", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010286", 
            "name": "X-linked intellectual disability, Siderius type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010286", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010286", 
            "name": "intellectual deficit X-linked Siderius type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010286", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010286", 
            "name": "X-linked mental retardation Hamel type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010286", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010286", 
            "name": "mental retardation syndrome, X-linked, Siderius type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010286", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010286", 
            "name": "Siderius-Hamel syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010286", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010286", 
            "name": "mental retardation X-linked Siderius type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010286", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010286", 
            "name": "mental retardation, X-linked, syndromic, Siderius type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010286", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010286", 
            "name": "Siderius X-linked mental retardation syndrome; MRXSSD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060812", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060812", 
            "name": "mental retardation syndrome, X-linked, Siderius type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060812", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060812", 
            "name": "MRXSSD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060812", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060812", 
            "name": "Siderius X-linked mental retardation syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060812", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060812", 
            "name": "Siderius-Hamel syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060812", 
        "description": "A syndromic X-linked intellectual disability characterized by mild to moderate intellectual disability, long face and a broad nasal tip with in some cases cleft lip/palate, preaxial polydactyly and cryptorchidism that has_material_basis_in mutation in the PHF8 gene on chromosome Xp11.22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060812", 
        "name": "syndromic X-linked intellectual disability Siderius type"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060812#disease-associations", 
            "id": "0060812", 
            "database": "Alliance of Genome Resources"
        }
    ]
}