{
    "disease_id": "DOID:6683", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010589", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010589", 
            "name": "Aarskog-Scott syndrome, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010589", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010589", 
            "name": "Aarskog-Scott syndrome; AAS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010589", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010589", 
            "name": "faciogenital dysplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010589", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010589", 
            "name": "FGD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010589", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010589", 
            "name": "faciodigitogenital syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010589", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010589", 
            "name": "mental retardation, X-linked, syndromic 16, included"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010589", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010589", 
            "name": "Aarskog syndrome, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010589", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010589", 
            "name": "AAS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010589", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010589", 
            "name": "FGDY"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010589", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010589", 
            "name": "mental retardation, X-linked, syndromic 16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010589", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010589", 
            "name": "MRXS16, included"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010589", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010589", 
            "name": "Aarskog syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010589", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010589", 
            "name": "faciodigitogenital syndrome, recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010589", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010589", 
            "name": "Aarskog Scott syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010589", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010589", 
            "name": "faciogenital dysplasia with attention Deficit-hyperactivity disorder"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010589", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010589", 
            "name": "Aarskog-Scott syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010589", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010589", 
            "name": "Scott Aarskog syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010589", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010589", 
            "name": "Aarskog-like syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010589", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010589", 
            "name": "Aarskog disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010589", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010589", 
            "name": "facio-digito-genital dysplasia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:6683", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:6683", 
            "name": "Aarskog-Scott syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:6683", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:6683", 
            "name": "Greig's syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:6683", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:6683", 
            "name": "faciogenital dysplasia"
        }, 
        {
            "url": "https://www.omim.org/entry/305400", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:305400", 
            "name": "Aarskog-Scott syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:6683", 
        "description": "A syndromic X-linked intellectual disability affects a person's height, muscles, skeleton, genitals, and appearance of the face.", 
        "resource": "Disease Ontology", 
        "id": "DOID:6683", 
        "name": "X-linked Aarskog syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/305400", 
            "id": "305400", 
            "database": "MIM"
        }
    ]
}